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'en:hereditary disease'
(id=15056041 ; fe=en:hereditary disease ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=76758.96997070312 creation date=2020-10-11 touchdate=2026-04-24 08:32:10.000)
≈ 14 relations sortantes

  1. en:hereditary disease -- r_isa #6: 450 / 1 -> maladie
    (médecine)

    n1=en:hereditary disease | n2=maladie
    (médecine)
    | rel=r_isa | relid=6 | w=450
  2. en:hereditary disease -- r_isa #6: 432 / 0.96 -> maladie
    n1=en:hereditary disease | n2=maladie | rel=r_isa | relid=6 | w=432
  3. en:hereditary disease -- r_isa #6: 390 / 0.867 -> anomalie
    n1=en:hereditary disease | n2=anomalie | rel=r_isa | relid=6 | w=390
  4. en:hereditary disease -- r_isa #6: 390 / 0.867 -> en:disease or disorder
    n1=en:hereditary disease | n2=en:disease or disorder | rel=r_isa | relid=6 | w=390
  5. en:hereditary disease -- r_isa #6: 335 / 0.744 -> en:disorder
    n1=en:hereditary disease | n2=en:disorder | rel=r_isa | relid=6 | w=335
  6. en:hereditary disease -- r_isa #6: 270 / 0.6 -> processus pathologique
    n1=en:hereditary disease | n2=processus pathologique | rel=r_isa | relid=6 | w=270
  7. en:hereditary disease -- r_isa #6: 34 / 0.076 -> en:disease
    n1=en:hereditary disease | n2=en:disease | rel=r_isa | relid=6 | w=34
  8. en:hereditary disease -- r_isa #6: 32 / 0.071 -> pathologie
    n1=en:hereditary disease | n2=pathologie | rel=r_isa | relid=6 | w=32
  9. en:hereditary disease -- r_isa #6: 32 / 0.071 -> processus
    n1=en:hereditary disease | n2=processus | rel=r_isa | relid=6 | w=32
  10. en:hereditary disease -- r_isa #6: 29 / 0.064 -> analyte
    n1=en:hereditary disease | n2=analyte | rel=r_isa | relid=6 | w=29
  11. en:hereditary disease -- r_isa #6: 29 / 0.064 -> disorder
    n1=en:hereditary disease | n2=disorder | rel=r_isa | relid=6 | w=29
  12. en:hereditary disease -- r_isa #6: 26 / 0.058 -> affection
    n1=en:hereditary disease | n2=affection | rel=r_isa | relid=6 | w=26
  13. en:hereditary disease -- r_isa #6: 26 / 0.058 -> disease
    n1=en:hereditary disease | n2=disease | rel=r_isa | relid=6 | w=26
  14. en:hereditary disease -- r_isa #6: 25 / 0.056 -> en:hereditary
    n1=en:hereditary disease | n2=en:hereditary | rel=r_isa | relid=6 | w=25
≈ 1355 relations entrantes

  1. goutte --- r_isa #6: 519.97 --> en:hereditary disease
    n1=goutte | n2=en:hereditary disease | rel=r_isa | relid=6 | w=519.97
  2. syndrome de Rett --- r_isa #6: 360 --> en:hereditary disease
    n1=syndrome de Rett | n2=en:hereditary disease | rel=r_isa | relid=6 | w=360
  3. sicklémie --- r_isa #6: 203 --> en:hereditary disease
    n1=sicklémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=203
  4. chorée rhumatismale sans atteinte cardiaque --- r_isa #6: 190 --> en:hereditary disease
    n1=chorée rhumatismale sans atteinte cardiaque | n2=en:hereditary disease | rel=r_isa | relid=6 | w=190
  5. affection à hématies falciformes --- r_isa #6: 189 --> en:hereditary disease
    n1=affection à hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=189
  6. danse de saint Guy --- r_isa #6: 184 --> en:hereditary disease
    n1=danse de saint Guy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=184
  7. dysplasie olfacto-génitale --- r_isa #6: 182 --> en:hereditary disease
    n1=dysplasie olfacto-génitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=182
  8. dysplasie olfactogénitale --- r_isa #6: 180 --> en:hereditary disease
    n1=dysplasie olfactogénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=180
  9. hypogonadisme avec anosmie --- r_isa #6: 180 --> en:hereditary disease
    n1=hypogonadisme avec anosmie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=180
  10. tumeur colique --- r_isa #6: 179 --> en:hereditary disease
    n1=tumeur colique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=179
  11. chorées --- r_isa #6: 177 --> en:hereditary disease
    n1=chorées | n2=en:hereditary disease | rel=r_isa | relid=6 | w=177
  12. chorée de Huntington --- r_isa #6: 176 --> en:hereditary disease
    n1=chorée de Huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=176
  13. en:kallmann syndrome --- r_isa #6: 175 --> en:hereditary disease
    n1=en:kallmann syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=175
  14. en:rheumatic chorea --- r_isa #6: 173 --> en:hereditary disease
    n1=en:rheumatic chorea | n2=en:hereditary disease | rel=r_isa | relid=6 | w=173
  15. Chorée --- r_isa #6: 172 --> en:hereditary disease
    n1=Chorée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=172
  16. association de tics vocaux et tics moteurs du syndrome de gilles de la tourette --- r_isa #6: 172 --> en:hereditary disease
    n1=association de tics vocaux et tics moteurs du syndrome de gilles de la tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=172
  17. dysplasie olfactogénitale de De Morsier --- r_isa #6: 171 --> en:hereditary disease
    n1=dysplasie olfactogénitale de De Morsier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=171
  18. tumeur maligne colique --- r_isa #6: 171 --> en:hereditary disease
    n1=tumeur maligne colique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=171
  19. chorée rhumatismale --- r_isa #6: 170 --> en:hereditary disease
    n1=chorée rhumatismale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=170
  20. en:colon neoplasm --- r_isa #6: 170 --> en:hereditary disease
    n1=en:colon neoplasm | n2=en:hereditary disease | rel=r_isa | relid=6 | w=170
  21. maladies de gilles de la tourette --- r_isa #6: 170 --> en:hereditary disease
    n1=maladies de gilles de la tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=170
  22. maladie de Huntington --- r_isa #6: 169 --> en:hereditary disease
    n1=maladie de Huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=169
  23. trouble de gilles de la tourette --- r_isa #6: 169 --> en:hereditary disease
    n1=trouble de gilles de la tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=169
  24. en:colonic neoplasms --- r_isa #6: 167 --> en:hereditary disease
    n1=en:colonic neoplasms | n2=en:hereditary disease | rel=r_isa | relid=6 | w=167
  25. Kallman --- r_isa #6: 166 --> en:hereditary disease
    n1=Kallman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=166
  26. non précisée, tumeur maligne du côlon --- r_isa #6: 165 --> en:hereditary disease
    n1=non précisée, tumeur maligne du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=165
  27. en:malignant tumor of colon --- r_isa #6: 163 --> en:hereditary disease
    n1=en:malignant tumor of colon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=163
  28. maladie des tics --- r_isa #6: 163 --> en:hereditary disease
    n1=maladie des tics | n2=en:hereditary disease | rel=r_isa | relid=6 | w=163
  29. en:malignant colon neoplasm --- r_isa #6: 162 --> en:hereditary disease
    n1=en:malignant colon neoplasm | n2=en:hereditary disease | rel=r_isa | relid=6 | w=162
  30. cancer colique --- r_isa #6: 161 --> en:hereditary disease
    n1=cancer colique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=161
  31. chorée de saint jean --- r_isa #6: 160 --> en:hereditary disease
    n1=chorée de saint jean | n2=en:hereditary disease | rel=r_isa | relid=6 | w=160
  32. néoplasie du côlon --- r_isa #6: 160 --> en:hereditary disease
    n1=néoplasie du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=160
  33. syndrome de Kallman-de Morsier --- r_isa #6: 158 --> en:hereditary disease
    n1=syndrome de Kallman-de Morsier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=158
  34. syndrome de tourette --- r_isa #6: 157 --> en:hereditary disease
    n1=syndrome de tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=157
  35. tumeur du côlon --- r_isa #6: 157 --> en:hereditary disease
    n1=tumeur du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=157
  36. ostéopétrose autosomique dominante de type ii --- r_isa #6: 155 --> en:hereditary disease
    n1=ostéopétrose autosomique dominante de type ii | n2=en:hereditary disease | rel=r_isa | relid=6 | w=155
  37. maladie des tics de Gilles de la Tourette --- r_isa #6: 154 --> en:hereditary disease
    n1=maladie des tics de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=154
  38. tumeur maligne du côlon --- r_isa #6: 152 --> en:hereditary disease
    n1=tumeur maligne du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=152
  39. syndrome de de Morsier-Kallmann --- r_isa #6: 151 --> en:hereditary disease
    n1=syndrome de de Morsier-Kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=151
  40. enzymopathie --- r_isa #6: 150 --> en:hereditary disease
    n1=enzymopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=150
  41. tumeur maligne du côlon non précisée --- r_isa #6: 150 --> en:hereditary disease
    n1=tumeur maligne du côlon non précisée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=150
  42. ostéopétrose autosomique dominante de type 2 --- r_isa #6: 149 --> en:hereditary disease
    n1=ostéopétrose autosomique dominante de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=149
  43. cancer du côlon --- r_isa #6: 145 --> en:hereditary disease
    n1=cancer du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=145
  44. syndrome des tics de Gilles de la Tourette --- r_isa #6: 145 --> en:hereditary disease
    n1=syndrome des tics de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=145
  45. Kallmann --- r_isa #6: 144 --> en:hereditary disease
    n1=Kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=144
  46. cholémie familiale --- r_isa #6: 144 --> en:hereditary disease
    n1=cholémie familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=144
  47. en:osteopetrosis --- r_isa #6: 144 --> en:hereditary disease
    n1=en:osteopetrosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=144
  48. syndrome de Gilles de la Tourette --- r_isa #6: 144 --> en:hereditary disease
    n1=syndrome de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=144
  49. maladie des os marmoréens --- r_isa #6: 142 --> en:hereditary disease
    n1=maladie des os marmoréens | n2=en:hereditary disease | rel=r_isa | relid=6 | w=142
  50. déficit en céto-acide décarboxylase --- r_isa #6: 140 --> en:hereditary disease
    n1=déficit en céto-acide décarboxylase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=140
  51. leucinose --- r_isa #6: 140 --> en:hereditary disease
    n1=leucinose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=140
  52. maladie de Gilbert --- r_isa #6: 140 --> en:hereditary disease
    n1=maladie de Gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=140
  53. chorée héréditaire --- r_isa #6: 139 --> en:hereditary disease
    n1=chorée héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=139
  54. en:classical maple syrup urine disease --- r_isa #6: 137 --> en:hereditary disease
    n1=en:classical maple syrup urine disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=137
  55. neuropathie motrice et sensorielle héréditaire --- r_isa #6: 136 --> en:hereditary disease
    n1=neuropathie motrice et sensorielle héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=136
  56. hyperbilirubinémie de type i --- r_isa #6: 134 --> en:hereditary disease
    n1=hyperbilirubinémie de type i | n2=en:hereditary disease | rel=r_isa | relid=6 | w=134
  57. neuropathie héréditaire sensitive et motrice --- r_isa #6: 134 --> en:hereditary disease
    n1=neuropathie héréditaire sensitive et motrice | n2=en:hereditary disease | rel=r_isa | relid=6 | w=134
  58. syndrome de la Tourette --- r_isa #6: 134 --> en:hereditary disease
    n1=syndrome de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=134
  59. en:huntington's disease --- r_isa #6: 133 --> en:hereditary disease
    n1=en:huntington's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=133
  60. en:maple syrup urine disease --- r_isa #6: 133 --> en:hereditary disease
    n1=en:maple syrup urine disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=133
  61. neuropathie héréditaire sensitivomotrice --- r_isa #6: 133 --> en:hereditary disease
    n1=neuropathie héréditaire sensitivomotrice | n2=en:hereditary disease | rel=r_isa | relid=6 | w=133
  62. ostéopétrose familiale --- r_isa #6: 133 --> en:hereditary disease
    n1=ostéopétrose familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=133
  63. chorée de Sydenham --- r_isa #6: 132 --> en:hereditary disease
    n1=chorée de Sydenham | n2=en:hereditary disease | rel=r_isa | relid=6 | w=132
  64. ictère héréditaire de gilbert --- r_isa #6: 132 --> en:hereditary disease
    n1=ictère héréditaire de gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=132
  65. hyperbilirubinémie de type indirect bénin --- r_isa #6: 131 --> en:hereditary disease
    n1=hyperbilirubinémie de type indirect bénin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=131
  66. maladie de Gilles de la Tourette --- r_isa #6: 131 --> en:hereditary disease
    n1=maladie de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=131
  67. ostéopétroses --- r_isa #6: 131 --> en:hereditary disease
    n1=ostéopétroses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=131
  68. en:thiamin-responsive maple syrup urine disease --- r_isa #6: 130 --> en:hereditary disease
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=130
  69. syndrome de Kallmann --- r_isa #6: 130 --> en:hereditary disease
    n1=syndrome de Kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=130
  70. neuropathies héréditaires sensorielles et autonomes --- r_isa #6: 129 --> en:hereditary disease
    n1=neuropathies héréditaires sensorielles et autonomes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=129
  71. neuropathie héréditaire sensitivo-motrice --- r_isa #6: 128 --> en:hereditary disease
    n1=neuropathie héréditaire sensitivo-motrice | n2=en:hereditary disease | rel=r_isa | relid=6 | w=128
  72. syndrome de de Morsier --- r_isa #6: 127 --> en:hereditary disease
    n1=syndrome de de Morsier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=127
  73. cholémie de gilbert --- r_isa #6: 126 --> en:hereditary disease
    n1=cholémie de gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=126
  74. en:tourette syndrome --- r_isa #6: 125 --> en:hereditary disease
    n1=en:tourette syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=125
  75. maladie des urines à l'odeur de sirop d'érable --- r_isa #6: 125 --> en:hereditary disease
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:hereditary disease | rel=r_isa | relid=6 | w=125
  76. maladie des os de marbre --- r_isa #6: 124 --> en:hereditary disease
    n1=maladie des os de marbre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=124
  77. subictère chronique intermittent --- r_isa #6: 124 --> en:hereditary disease
    n1=subictère chronique intermittent | n2=en:hereditary disease | rel=r_isa | relid=6 | w=124
  78. neuropathie sensitivo-motrice héréditaire --- r_isa #6: 122 --> en:hereditary disease
    n1=neuropathie sensitivo-motrice héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=122
  79. hyperbilirubinémie de type 1 --- r_isa #6: 119 --> en:hereditary disease
    n1=hyperbilirubinémie de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=119
  80. maladie des urines avec odeur de sirop erable --- r_isa #6: 119 --> en:hereditary disease
    n1=maladie des urines avec odeur de sirop erable | n2=en:hereditary disease | rel=r_isa | relid=6 | w=119
  81. neuropathie héréditaire motrice et sensorielle --- r_isa #6: 119 --> en:hereditary disease
    n1=neuropathie héréditaire motrice et sensorielle | n2=en:hereditary disease | rel=r_isa | relid=6 | w=119
  82. syndrome olfacto-génital --- r_isa #6: 119 --> en:hereditary disease
    n1=syndrome olfacto-génital | n2=en:hereditary disease | rel=r_isa | relid=6 | w=119
  83. cholémie familiale congénitale --- r_isa #6: 116 --> en:hereditary disease
    n1=cholémie familiale congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=116
  84. syndrome de Gilbert --- r_isa #6: 116 --> en:hereditary disease
    n1=syndrome de Gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=116
  85. dysfonctionnement hépatique constitutionnel --- r_isa #6: 115 --> en:hereditary disease
    n1=dysfonctionnement hépatique constitutionnel | n2=en:hereditary disease | rel=r_isa | relid=6 | w=115
  86. maladie du sirop d'érable --- r_isa #6: 114 --> en:hereditary disease
    n1=maladie du sirop d'érable | n2=en:hereditary disease | rel=r_isa | relid=6 | w=114
  87. ostéopétrose --- r_isa #6: 114 --> en:hereditary disease
    n1=ostéopétrose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=114
  88. maladie d'Albers-Schönberg --- r_isa #6: 111 --> en:hereditary disease
    n1=maladie d'Albers-Schönberg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=111
  89. syndrome de Mayer-Rokitansky-Küster-Hauser --- r_isa #6: 110 --> en:hereditary disease
    n1=syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=110
  90. hémochromatose --- r_isa #6: 109 --> en:hereditary disease
    n1=hémochromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=109
  91. neuropathie héréditaire motrice et sensitive --- r_isa #6: 109 --> en:hereditary disease
    n1=neuropathie héréditaire motrice et sensitive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=109
  92. drépanocytose --- r_isa #6: 108 --> en:hereditary disease
    n1=drépanocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=108
  93. spondylarthrite ankylosante --- r_isa #6: 107 --> en:hereditary disease
    n1=spondylarthrite ankylosante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=107
  94. syndrome de Marfan --- r_isa #6: 104 --> en:hereditary disease
    n1=syndrome de Marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=104
  95. Syndrome de Mayer-Rokitansky-Küster-Hauser --- r_isa #6: 103 --> en:hereditary disease
    n1=Syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=103
  96. trouble du métabolisme du fer --- r_isa #6: 101 --> en:hereditary disease
    n1=trouble du métabolisme du fer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=101
  97. déficit en phosphatases alcalines --- r_isa #6: 100 --> en:hereditary disease
    n1=déficit en phosphatases alcalines | n2=en:hereditary disease | rel=r_isa | relid=6 | w=100
  98. en:marfan syndrome --- r_isa #6: 100 --> en:hereditary disease
    n1=en:marfan syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=100
  99. anémie par carence en fer --- r_isa #6: 97 --> en:hereditary disease
    n1=anémie par carence en fer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=97
  100. neuropathie héréditaire avec hypersensibilité à la pression --- r_isa #6: 97 --> en:hereditary disease
    n1=neuropathie héréditaire avec hypersensibilité à la pression | n2=en:hereditary disease | rel=r_isa | relid=6 | w=97
  101. neuropathie tomaculaire --- r_isa #6: 97 --> en:hereditary disease
    n1=neuropathie tomaculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=97
  102. maladie enzymatique --- r_isa #6: 96 --> en:hereditary disease
    n1=maladie enzymatique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=96
  103. en:hemochromatosis --- r_isa #6: 95 --> en:hereditary disease
    n1=en:hemochromatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=95
  104. neuropathie sensitivomotrice héréditaire --- r_isa #6: 94 --> en:hereditary disease
    n1=neuropathie sensitivomotrice héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=94
  105. en:hypophosphatasia --- r_isa #6: 92 --> en:hereditary disease
    n1=en:hypophosphatasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=92
  106. en:mayer-rokitansky-kuster-hauser syndrome --- r_isa #6: 92 --> en:hereditary disease
    n1=en:mayer-rokitansky-kuster-hauser syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=92
  107. anémie sidéroblastique --- r_isa #6: 90 --> en:hereditary disease
    n1=anémie sidéroblastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
  108. hypophosphatasies --- r_isa #6: 90 --> en:hereditary disease
    n1=hypophosphatasies | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
  109. hémochromatose primitive --- r_isa #6: 90 --> en:hereditary disease
    n1=hémochromatose primitive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
  110. myopathie --- r_isa #6: 90 --> en:hereditary disease
    n1=myopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
  111. syndrome de Rokitansky-Küster-Hauser --- r_isa #6: 90 --> en:hereditary disease
    n1=syndrome de Rokitansky-Küster-Hauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=90
  112. en:enzymopathy --- r_isa #6: 89 --> en:hereditary disease
    n1=en:enzymopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=89
  113. syndrome de Rathbun --- r_isa #6: 89 --> en:hereditary disease
    n1=syndrome de Rathbun | n2=en:hereditary disease | rel=r_isa | relid=6 | w=89
  114. maladie de Marfan --- r_isa #6: 88 --> en:hereditary disease
    n1=maladie de Marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=88
  115. epilepsy --- r_isa #6: 86 --> en:hereditary disease
    n1=epilepsy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=86
  116. maladie du muscle --- r_isa #6: 86 --> en:hereditary disease
    n1=maladie du muscle | n2=en:hereditary disease | rel=r_isa | relid=6 | w=86
  117. diabète bronzé --- r_isa #6: 85 --> en:hereditary disease
    n1=diabète bronzé | n2=en:hereditary disease | rel=r_isa | relid=6 | w=85
  118. syndrome de Rokitansky --- r_isa #6: 85 --> en:hereditary disease
    n1=syndrome de Rokitansky | n2=en:hereditary disease | rel=r_isa | relid=6 | w=85
  119. arachnodactylie --- r_isa #6: 82 --> en:hereditary disease
    n1=arachnodactylie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=82
  120. syndrome MRKH --- r_isa #6: 81 --> en:hereditary disease
    n1=syndrome MRKH | n2=en:hereditary disease | rel=r_isa | relid=6 | w=81
  121. en:chromosome disorder --- r_isa #6: 80 --> en:hereditary disease
    n1=en:chromosome disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=80
  122. Épilepsie --- r_isa #6: 80 --> en:hereditary disease
    n1=Épilepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=80
  123. trouble chromosomique --- r_isa #6: 79 --> en:hereditary disease
    n1=trouble chromosomique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=79
  124. anomalie chromosomique --- r_isa #6: 78 --> en:hereditary disease
    n1=anomalie chromosomique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=78
  125. en:epilepsy --- r_isa #6: 78 --> en:hereditary disease
    n1=en:epilepsy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=78
  126. anormalité des chromosomes --- r_isa #6: 77 --> en:hereditary disease
    n1=anormalité des chromosomes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=77
  127. hypophosphatasie --- r_isa #6: 77 --> en:hereditary disease
    n1=hypophosphatasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=77
  128. maladie musculaire --- r_isa #6: 77 --> en:hereditary disease
    n1=maladie musculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=77
  129. épilepsie --- r_isa #6: 77 --> en:hereditary disease
    n1=épilepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=77
  130. en:arachnodactyly --- r_isa #6: 75 --> en:hereditary disease
    n1=en:arachnodactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=75
  131. en:sickle-cell anaemia --- r_isa #6: 75 --> en:hereditary disease
    n1=en:sickle-cell anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=75
  132. epilepsie --- r_isa #6: 75 --> en:hereditary disease
    n1=epilepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=75
  133. maladie génétique du métabolisme des glucides --- r_isa #6: 75 --> en:hereditary disease
    n1=maladie génétique du métabolisme des glucides | n2=en:hereditary disease | rel=r_isa | relid=6 | w=75
  134. maladie génétique musculaire --- r_isa #6: 71 --> en:hereditary disease
    n1=maladie génétique musculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=71
  135. en:sickle-cell anemia --- r_isa #6: 70 --> en:hereditary disease
    n1=en:sickle-cell anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=70
  136. Maladie de Crohn --- r_isa #6: 69 --> en:hereditary disease
    n1=Maladie de Crohn | n2=en:hereditary disease | rel=r_isa | relid=6 | w=69
  137. Maladie de Gaucher --- r_isa #6: 69 --> en:hereditary disease
    n1=Maladie de Gaucher | n2=en:hereditary disease | rel=r_isa | relid=6 | w=69
  138. naevomatose baso-cellulaire --- r_isa #6: 69 --> en:hereditary disease
    n1=naevomatose baso-cellulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=69
  139. Spondylarthrite ankylosante --- r_isa #6: 68 --> en:hereditary disease
    n1=Spondylarthrite ankylosante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=68
  140. syndrome de Gorlin --- r_isa #6: 67 --> en:hereditary disease
    n1=syndrome de Gorlin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=67
  141. naevomatose basocellulaire --- r_isa #6: 66 --> en:hereditary disease
    n1=naevomatose basocellulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=66
  142. dystrophie musculaire oculo-pharyngée --- r_isa #6: 65 --> en:hereditary disease
    n1=dystrophie musculaire oculo-pharyngée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=65
  143. en:sickle cell anaemia --- r_isa #6: 65 --> en:hereditary disease
    n1=en:sickle cell anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=65
  144. progeria --- r_isa #6: 65 --> en:hereditary disease
    n1=progeria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=65
  145. en:progeria --- r_isa #6: 64 --> en:hereditary disease
    n1=en:progeria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=64
  146. dystrophie musculaire oculopharyngée --- r_isa #6: 63 --> en:hereditary disease
    n1=dystrophie musculaire oculopharyngée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=63
  147. xanthomatose cérébrotendineuse --- r_isa #6: 62 --> en:hereditary disease
    n1=xanthomatose cérébrotendineuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=62
  148. dystrophy --- r_isa #6: 61 --> en:hereditary disease
    n1=dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
  149. en:myopathy --- r_isa #6: 61 --> en:hereditary disease
    n1=en:myopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
  150. myopathy --- r_isa #6: 61 --> en:hereditary disease
    n1=myopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
  151. polydactylie --- r_isa #6: 61 --> en:hereditary disease
    n1=polydactylie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
  152. syndrome d'Aase --- r_isa #6: 61 --> en:hereditary disease
    n1=syndrome d'Aase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=61
  153. en:muscular dystrophy --- r_isa #6: 60 --> en:hereditary disease
    n1=en:muscular dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
  154. en:muscular dystrophy, oculopharyngeal --- r_isa #6: 60 --> en:hereditary disease
    n1=en:muscular dystrophy, oculopharyngeal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
  155. incontinentia pigmenti --- r_isa #6: 60 --> en:hereditary disease
    n1=incontinentia pigmenti | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
  156. maladie de Crohn --- r_isa #6: 60 --> en:hereditary disease
    n1=maladie de Crohn | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
  157. maladie de Gaucher --- r_isa #6: 60 --> en:hereditary disease
    n1=maladie de Gaucher | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
  158. maladie de forbes --- r_isa #6: 60 --> en:hereditary disease
    n1=maladie de forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
  159. xanthomatose cérébro-tendineuse --- r_isa #6: 60 --> en:hereditary disease
    n1=xanthomatose cérébro-tendineuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=60
  160. en:polydactyly --- r_isa #6: 59 --> en:hereditary disease
    n1=en:polydactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=59
  161. hirsutisme --- r_isa #6: 59 --> en:hereditary disease
    n1=hirsutisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=59
  162. maladie d'alzheimer --- r_isa #6: 59 --> en:hereditary disease
    n1=maladie d'alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=59
  163. maladie de Rendu-Osler-Weber --- r_isa #6: 59 --> en:hereditary disease
    n1=maladie de Rendu-Osler-Weber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=59
  164. en:incontinentia pigmenti --- r_isa #6: 58 --> en:hereditary disease
    n1=en:incontinentia pigmenti | n2=en:hereditary disease | rel=r_isa | relid=6 | w=58
  165. progéria --- r_isa #6: 58 --> en:hereditary disease
    n1=progéria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=58
  166. Syndrome d'Aase --- r_isa #6: 57 --> en:hereditary disease
    n1=Syndrome d'Aase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  167. dextrinose limite --- r_isa #6: 57 --> en:hereditary disease
    n1=dextrinose limite | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  168. galactosémie --- r_isa #6: 57 --> en:hereditary disease
    n1=galactosémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  169. glycogénose de type III --- r_isa #6: 57 --> en:hereditary disease
    n1=glycogénose de type III | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  170. holoprosencéphalie --- r_isa #6: 57 --> en:hereditary disease
    n1=holoprosencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  171. maladie d'Illingworth-Cori-Forbes --- r_isa #6: 57 --> en:hereditary disease
    n1=maladie d'Illingworth-Cori-Forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  172. maladie de Cori --- r_isa #6: 57 --> en:hereditary disease
    n1=maladie de Cori | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  173. maladie de Forbes --- r_isa #6: 57 --> en:hereditary disease
    n1=maladie de Forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  174. maladie de hartnup --- r_isa #6: 57 --> en:hereditary disease
    n1=maladie de hartnup | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  175. télangiectasie hémorragique familiale --- r_isa #6: 57 --> en:hereditary disease
    n1=télangiectasie hémorragique familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=57
  176. albinisme --- r_isa #6: 56 --> en:hereditary disease
    n1=albinisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=56
  177. maladie d'Alzheimer --- r_isa #6: 56 --> en:hereditary disease
    n1=maladie d'Alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=56
  178. maladie de crohn --- r_isa #6: 56 --> en:hereditary disease
    n1=maladie de crohn | n2=en:hereditary disease | rel=r_isa | relid=6 | w=56
  179. Maladie de Cori --- r_isa #6: 55 --> en:hereditary disease
    n1=Maladie de Cori | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
  180. Syndrome d'Angelman --- r_isa #6: 55 --> en:hereditary disease
    n1=Syndrome d'Angelman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
  181. adréno-leucodystrophie --- r_isa #6: 55 --> en:hereditary disease
    n1=adréno-leucodystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
  182. en:hirsutism --- r_isa #6: 55 --> en:hereditary disease
    n1=en:hirsutism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
  183. en:vitiligo --- r_isa #6: 55 --> en:hereditary disease
    n1=en:vitiligo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
  184. hyperprolinémie --- r_isa #6: 55 --> en:hereditary disease
    n1=hyperprolinémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
  185. maladie des Açores --- r_isa #6: 55 --> en:hereditary disease
    n1=maladie des Açores | n2=en:hereditary disease | rel=r_isa | relid=6 | w=55
  186. dystrophie musculaire --- r_isa #6: 54 --> en:hereditary disease
    n1=dystrophie musculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
  187. en:adrenoleukodystrophy --- r_isa #6: 54 --> en:hereditary disease
    n1=en:adrenoleukodystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
  188. en:dystrophy --- r_isa #6: 54 --> en:hereditary disease
    n1=en:dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
  189. en:holoprosencephaly --- r_isa #6: 54 --> en:hereditary disease
    n1=en:holoprosencephaly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
  190. maladie de cori --- r_isa #6: 54 --> en:hereditary disease
    n1=maladie de cori | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
  191. maladie de gaucher --- r_isa #6: 54 --> en:hereditary disease
    n1=maladie de gaucher | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
  192. myopathie primitive progressive --- r_isa #6: 54 --> en:hereditary disease
    n1=myopathie primitive progressive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
  193. neurofibromatose de type 1 --- r_isa #6: 54 --> en:hereditary disease
    n1=neurofibromatose de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
  194. pseudoxanthome élastique --- r_isa #6: 54 --> en:hereditary disease
    n1=pseudoxanthome élastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=54
  195. en:muscular dystrophy, emery-dreifuss --- r_isa #6: 53 --> en:hereditary disease
    n1=en:muscular dystrophy, emery-dreifuss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=53
  196. maladie de Hartnup --- r_isa #6: 53 --> en:hereditary disease
    n1=maladie de Hartnup | n2=en:hereditary disease | rel=r_isa | relid=6 | w=53
  197. syndrome d'angelman --- r_isa #6: 53 --> en:hereditary disease
    n1=syndrome d'angelman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=53
  198. syndrome de marfan --- r_isa #6: 53 --> en:hereditary disease
    n1=syndrome de marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=53
  199. chorée de huntington --- r_isa #6: 52 --> en:hereditary disease
    n1=chorée de huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
  200. en:albinism --- r_isa #6: 52 --> en:hereditary disease
    n1=en:albinism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
  201. maladie de Machado-Joseph --- r_isa #6: 52 --> en:hereditary disease
    n1=maladie de Machado-Joseph | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
  202. maladie des açores --- r_isa #6: 52 --> en:hereditary disease
    n1=maladie des açores | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
  203. syndrome d'Angelman --- r_isa #6: 52 --> en:hereditary disease
    n1=syndrome d'Angelman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=52
  204. dystrophie musculaire d'Emery-Dreifuss --- r_isa #6: 51 --> en:hereditary disease
    n1=dystrophie musculaire d'Emery-Dreifuss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
  205. maladie clinique de recklinghausen --- r_isa #6: 51 --> en:hereditary disease
    n1=maladie clinique de recklinghausen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
  206. pseudo-xanthome élastique --- r_isa #6: 51 --> en:hereditary disease
    n1=pseudo-xanthome élastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
  207. sphingolipidose --- r_isa #6: 51 --> en:hereditary disease
    n1=sphingolipidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
  208. syndrome de Walker-Warburg --- r_isa #6: 51 --> en:hereditary disease
    n1=syndrome de Walker-Warburg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
  209. vitiligo --- r_isa #6: 51 --> en:hereditary disease
    n1=vitiligo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=51
  210. Maladie de Hartnup --- r_isa #6: 50 --> en:hereditary disease
    n1=Maladie de Hartnup | n2=en:hereditary disease | rel=r_isa | relid=6 | w=50
  211. en:sickle cell anemia --- r_isa #6: 50 --> en:hereditary disease
    n1=en:sickle cell anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=50
  212. maladie de marfan --- r_isa #6: 50 --> en:hereditary disease
    n1=maladie de marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=50
  213. mosaïque --- r_isa #6: 50 --> en:hereditary disease
    n1=mosaïque | n2=en:hereditary disease | rel=r_isa | relid=6 | w=50
  214. en:fanconi's anaemia --- r_isa #6: 49 --> en:hereditary disease
    n1=en:fanconi's anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=49
  215. en:sicklaemia --- r_isa #6: 49 --> en:hereditary disease
    n1=en:sicklaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=49
  216. démence d'Alzheimer --- r_isa #6: 48 --> en:hereditary disease
    n1=démence d'Alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=48
  217. en:emery-dreifuss muscular dystrophy --- r_isa #6: 48 --> en:hereditary disease
    n1=en:emery-dreifuss muscular dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=48
  218. Maladie de Tay-Sachs --- r_isa #6: 47 --> en:hereditary disease
    n1=Maladie de Tay-Sachs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
  219. Syndrome de Kartagener --- r_isa #6: 47 --> en:hereditary disease
    n1=Syndrome de Kartagener | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
  220. adrénoleucodystrophie --- r_isa #6: 47 --> en:hereditary disease
    n1=adrénoleucodystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
  221. en:globoid cell leukodystrophy --- r_isa #6: 47 --> en:hereditary disease
    n1=en:globoid cell leukodystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
  222. en:walker-warburg syndrome --- r_isa #6: 47 --> en:hereditary disease
    n1=en:walker-warburg syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
  223. maladie de Rendu-Osler --- r_isa #6: 47 --> en:hereditary disease
    n1=maladie de Rendu-Osler | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
  224. nail-Patella syndrome --- r_isa #6: 47 --> en:hereditary disease
    n1=nail-Patella syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
  225. paraplégie spastique type 7 --- r_isa #6: 47 --> en:hereditary disease
    n1=paraplégie spastique type 7 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
  226. syndrome Rapadilano --- r_isa #6: 47 --> en:hereditary disease
    n1=syndrome Rapadilano | n2=en:hereditary disease | rel=r_isa | relid=6 | w=47
  227. en:Fanconi's anaemia --- r_isa #6: 46 --> en:hereditary disease
    n1=en:Fanconi's anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
  228. en:myodystrophia --- r_isa #6: 46 --> en:hereditary disease
    n1=en:myodystrophia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
  229. hémoglobinose s --- r_isa #6: 46 --> en:hereditary disease
    n1=hémoglobinose s | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
  230. hétérotaxie --- r_isa #6: 46 --> en:hereditary disease
    n1=hétérotaxie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
  231. maladie de Recklinghausen --- r_isa #6: 46 --> en:hereditary disease
    n1=maladie de Recklinghausen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
  232. syndrome de Kartagener --- r_isa #6: 46 --> en:hereditary disease
    n1=syndrome de Kartagener | n2=en:hereditary disease | rel=r_isa | relid=6 | w=46
  233. Maladie de Fabry --- r_isa #6: 45 --> en:hereditary disease
    n1=Maladie de Fabry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  234. ataxie télangiectasie --- r_isa #6: 45 --> en:hereditary disease
    n1=ataxie télangiectasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  235. dermatite atopique --- r_isa #6: 45 --> en:hereditary disease
    n1=dermatite atopique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  236. dyskératose congénitale --- r_isa #6: 45 --> en:hereditary disease
    n1=dyskératose congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  237. en:iron metabolism disorders --- r_isa #6: 45 --> en:hereditary disease
    n1=en:iron metabolism disorders | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  238. en:rett syndrome --- r_isa #6: 45 --> en:hereditary disease
    n1=en:rett syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  239. maladie d'Ollier --- r_isa #6: 45 --> en:hereditary disease
    n1=maladie d'Ollier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  240. maladie de von Recklinghausen --- r_isa #6: 45 --> en:hereditary disease
    n1=maladie de von Recklinghausen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  241. paraplégie spastique autosomique récessive type 7 --- r_isa #6: 45 --> en:hereditary disease
    n1=paraplégie spastique autosomique récessive type 7 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  242. syndrome d'aarskog --- r_isa #6: 45 --> en:hereditary disease
    n1=syndrome d'aarskog | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  243. syndrome de Cowden --- r_isa #6: 45 --> en:hereditary disease
    n1=syndrome de Cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  244. syndrome de cockayne --- r_isa #6: 45 --> en:hereditary disease
    n1=syndrome de cockayne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=45
  245. leucodystrophie à cellules globoïdes --- r_isa #6: 44 --> en:hereditary disease
    n1=leucodystrophie à cellules globoïdes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=44
  246. maladie de Tay-Sachs --- r_isa #6: 44 --> en:hereditary disease
    n1=maladie de Tay-Sachs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=44
  247. résistance à la protéine C activée --- r_isa #6: 44 --> en:hereditary disease
    n1=résistance à la protéine C activée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=44
  248. Nail-Patella syndrome --- r_isa #6: 43 --> en:hereditary disease
    n1=Nail-Patella syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
  249. Syndrome de Gilbert --- r_isa #6: 43 --> en:hereditary disease
    n1=Syndrome de Gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
  250. en:canavan disease --- r_isa #6: 43 --> en:hereditary disease
    n1=en:canavan disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
  251. en:heterotaxy --- r_isa #6: 43 --> en:hereditary disease
    n1=en:heterotaxy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
  252. microencéphalie --- r_isa #6: 43 --> en:hereditary disease
    n1=microencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
  253. myosite ossifiante progressive --- r_isa #6: 43 --> en:hereditary disease
    n1=myosite ossifiante progressive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
  254. phacomatose --- r_isa #6: 43 --> en:hereditary disease
    n1=phacomatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
  255. syndrome d'Aarskog --- r_isa #6: 43 --> en:hereditary disease
    n1=syndrome d'Aarskog | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
  256. syndrome de Greig --- r_isa #6: 43 --> en:hereditary disease
    n1=syndrome de Greig | n2=en:hereditary disease | rel=r_isa | relid=6 | w=43
  257. La tétrasomie X --- r_isa #6: 42 --> en:hereditary disease
    n1=La tétrasomie X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  258. Syndrome Rapadilano --- r_isa #6: 42 --> en:hereditary disease
    n1=Syndrome Rapadilano | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  259. en:Cowden's disease --- r_isa #6: 42 --> en:hereditary disease
    n1=en:Cowden's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  260. en:ataxia telangiectasia --- r_isa #6: 42 --> en:hereditary disease
    n1=en:ataxia telangiectasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  261. en:microcephaly --- r_isa #6: 42 --> en:hereditary disease
    n1=en:microcephaly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  262. maladie de Canavan --- r_isa #6: 42 --> en:hereditary disease
    n1=maladie de Canavan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  263. maladie des exostoses multiples --- r_isa #6: 42 --> en:hereditary disease
    n1=maladie des exostoses multiples | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  264. maladie génétique à transmission dominante liée à l'X --- r_isa #6: 42 --> en:hereditary disease
    n1=maladie génétique à transmission dominante liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  265. microcéphalie --- r_isa #6: 42 --> en:hereditary disease
    n1=microcéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  266. syndrome de Cockayne --- r_isa #6: 42 --> en:hereditary disease
    n1=syndrome de Cockayne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  267. syndrome de Zinsser-Engman-Cole --- r_isa #6: 42 --> en:hereditary disease
    n1=syndrome de Zinsser-Engman-Cole | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  268. syndrome de cheveux laineux-kératodermie palmoplantaire-cardiomyopathie dilatée --- r_isa #6: 42 --> en:hereditary disease
    n1=syndrome de cheveux laineux-kératodermie palmoplantaire-cardiomyopathie dilatée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  269. thrombophilie par mutation du facteur V --- r_isa #6: 42 --> en:hereditary disease
    n1=thrombophilie par mutation du facteur V | n2=en:hereditary disease | rel=r_isa | relid=6 | w=42
  270. Ataxie télangiectasie --- r_isa #6: 41 --> en:hereditary disease
    n1=Ataxie télangiectasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  271. Myopathie de Bethlem --- r_isa #6: 41 --> en:hereditary disease
    n1=Myopathie de Bethlem | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  272. dyskinésie ciliaire primitive --- r_isa #6: 41 --> en:hereditary disease
    n1=dyskinésie ciliaire primitive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  273. eczéma atopique --- r_isa #6: 41 --> en:hereditary disease
    n1=eczéma atopique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  274. en:congenital afibrinogenemia --- r_isa #6: 41 --> en:hereditary disease
    n1=en:congenital afibrinogenemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  275. enchondromatose --- r_isa #6: 41 --> en:hereditary disease
    n1=enchondromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  276. maladie de wilson --- r_isa #6: 41 --> en:hereditary disease
    n1=maladie de wilson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  277. maladie génétique rare --- r_isa #6: 41 --> en:hereditary disease
    n1=maladie génétique rare | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  278. syndrome d'hypercalcémie familiale-néphrocalcinose-indicanurie --- r_isa #6: 41 --> en:hereditary disease
    n1=syndrome d'hypercalcémie familiale-néphrocalcinose-indicanurie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  279. syndrome de Sanfillipo --- r_isa #6: 41 --> en:hereditary disease
    n1=syndrome de Sanfillipo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  280. syndrome de kartagener --- r_isa #6: 41 --> en:hereditary disease
    n1=syndrome de kartagener | n2=en:hereditary disease | rel=r_isa | relid=6 | w=41
  281. Maladie de Forbes --- r_isa #6: 40 --> en:hereditary disease
    n1=Maladie de Forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  282. Syndrome d'Ehlers-Danlos type classique --- r_isa #6: 40 --> en:hereditary disease
    n1=Syndrome d'Ehlers-Danlos type classique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  283. Syndrome de Saethre-Chotzen --- r_isa #6: 40 --> en:hereditary disease
    n1=Syndrome de Saethre-Chotzen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  284. aclasie diaphysaire --- r_isa #6: 40 --> en:hereditary disease
    n1=aclasie diaphysaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  285. chondrodysplasie déformante héréditaire --- r_isa #6: 40 --> en:hereditary disease
    n1=chondrodysplasie déformante héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  286. chondrodysplasie héréditaire déformante --- r_isa #6: 40 --> en:hereditary disease
    n1=chondrodysplasie héréditaire déformante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  287. en:Alzheimer's disease --- r_isa #6: 40 --> en:hereditary disease
    n1=en:Alzheimer's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  288. en:Huntington's disease --- r_isa #6: 40 --> en:hereditary disease
    n1=en:Huntington's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  289. en:cystic fibrosis --- r_isa #6: 40 --> en:hereditary disease
    n1=en:cystic fibrosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  290. en:hereditary motor and sensory neuropathies --- r_isa #6: 40 --> en:hereditary disease
    n1=en:hereditary motor and sensory neuropathies | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  291. en:hereditary multiple exostoses --- r_isa #6: 40 --> en:hereditary disease
    n1=en:hereditary multiple exostoses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  292. exostose héréditaire multiple --- r_isa #6: 40 --> en:hereditary disease
    n1=exostose héréditaire multiple | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  293. fibrodysplasie ossifiante progressive --- r_isa #6: 40 --> en:hereditary disease
    n1=fibrodysplasie ossifiante progressive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  294. maladie de Bessel-Hagen --- r_isa #6: 40 --> en:hereditary disease
    n1=maladie de Bessel-Hagen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  295. maladie de Sanfilippo --- r_isa #6: 40 --> en:hereditary disease
    n1=maladie de Sanfilippo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  296. maladie de Wilson --- r_isa #6: 40 --> en:hereditary disease
    n1=maladie de Wilson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  297. maladie exostosante multiple --- r_isa #6: 40 --> en:hereditary disease
    n1=maladie exostosante multiple | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  298. maladie ostéogénique --- r_isa #6: 40 --> en:hereditary disease
    n1=maladie ostéogénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  299. mucoviscidose --- r_isa #6: 40 --> en:hereditary disease
    n1=mucoviscidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  300. syndrome d'aase --- r_isa #6: 40 --> en:hereditary disease
    n1=syndrome d'aase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  301. syndrome de Peutz-Jeghers --- r_isa #6: 40 --> en:hereditary disease
    n1=syndrome de Peutz-Jeghers | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  302. syndrome de peutz-jeghers --- r_isa #6: 40 --> en:hereditary disease
    n1=syndrome de peutz-jeghers | n2=en:hereditary disease | rel=r_isa | relid=6 | w=40
  303. acrocéphalie-crâne asymétrique et syndactylie modérée --- r_isa #6: 39 --> en:hereditary disease
    n1=acrocéphalie-crâne asymétrique et syndactylie modérée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
  304. dystrophie musculaire congénitale, cataracte infantile et hypogonadisme --- r_isa #6: 39 --> en:hereditary disease
    n1=dystrophie musculaire congénitale, cataracte infantile et hypogonadisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
  305. en:Alzheimer's --- r_isa #6: 39 --> en:hereditary disease
    n1=en:Alzheimer's | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
  306. en:limit dextrinosis --- r_isa #6: 39 --> en:hereditary disease
    n1=en:limit dextrinosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
  307. en:progressive muscular dystrophy --- r_isa #6: 39 --> en:hereditary disease
    n1=en:progressive muscular dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
  308. maladie de Fanconi --- r_isa #6: 39 --> en:hereditary disease
    n1=maladie de Fanconi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
  309. microlissencéphalie --- r_isa #6: 39 --> en:hereditary disease
    n1=microlissencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
  310. syndrome d'Ehlers-Danlos type classique --- r_isa #6: 39 --> en:hereditary disease
    n1=syndrome d'Ehlers-Danlos type classique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=39
  311. Syndrome d'Aicardi --- r_isa #6: 38 --> en:hereditary disease
    n1=Syndrome d'Aicardi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  312. Syndrome de Marfan --- r_isa #6: 38 --> en:hereditary disease
    n1=Syndrome de Marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  313. en:anemia and sickle-shaped erythrocytes --- r_isa #6: 38 --> en:hereditary disease
    n1=en:anemia and sickle-shaped erythrocytes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  314. en:cardiomyopathy dilated with woolly hair and keratoderma --- r_isa #6: 38 --> en:hereditary disease
    n1=en:cardiomyopathy dilated with woolly hair and keratoderma | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  315. en:habit spasm --- r_isa #6: 38 --> en:hereditary disease
    n1=en:habit spasm | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  316. maladie de Minkowski-Chauffard --- r_isa #6: 38 --> en:hereditary disease
    n1=maladie de Minkowski-Chauffard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  317. maladie des langes bleus --- r_isa #6: 38 --> en:hereditary disease
    n1=maladie des langes bleus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  318. ostéopétrose par mutation du gène CLCN7 --- r_isa #6: 38 --> en:hereditary disease
    n1=ostéopétrose par mutation du gène CLCN7 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  319. syndrome de Coffin-Siris --- r_isa #6: 38 --> en:hereditary disease
    n1=syndrome de Coffin-Siris | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  320. syndrome de Saethre-Chotzen --- r_isa #6: 38 --> en:hereditary disease
    n1=syndrome de Saethre-Chotzen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=38
  321. chorée de sydenham --- r_isa #6: 37 --> en:hereditary disease
    n1=chorée de sydenham | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
  322. en:polygenic disorder --- r_isa #6: 37 --> en:hereditary disease
    n1=en:polygenic disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
  323. goitre
    (zoologie)
    --- r_isa #6: 37 --> en:hereditary disease

    n1=goitre
    (zoologie)
    | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
  324. goître --- r_isa #6: 37 --> en:hereditary disease
    n1=goître | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
  325. maladie de Steinert --- r_isa #6: 37 --> en:hereditary disease
    n1=maladie de Steinert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
  326. rétinoblastome --- r_isa #6: 37 --> en:hereditary disease
    n1=rétinoblastome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
  327. syndrome LEOPARD --- r_isa #6: 37 --> en:hereditary disease
    n1=syndrome LEOPARD | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
  328. syndrome de Lowe --- r_isa #6: 37 --> en:hereditary disease
    n1=syndrome de Lowe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=37
  329. dystonie avec parkinsonisme liée à l'X --- r_isa #6: 36 --> en:hereditary disease
    n1=dystonie avec parkinsonisme liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  330. dystrophie facioscapulohumérale musculaire 1A --- r_isa #6: 36 --> en:hereditary disease
    n1=dystrophie facioscapulohumérale musculaire 1A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  331. en:Tourette syndrome --- r_isa #6: 36 --> en:hereditary disease
    n1=en:Tourette syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  332. en:hereditary spherocytosis --- r_isa #6: 36 --> en:hereditary disease
    n1=en:hereditary spherocytosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  333. en:myonosus --- r_isa #6: 36 --> en:hereditary disease
    n1=en:myonosus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  334. en:retinoblastoma --- r_isa #6: 36 --> en:hereditary disease
    n1=en:retinoblastoma | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  335. idiotie amaurotique familiale --- r_isa #6: 36 --> en:hereditary disease
    n1=idiotie amaurotique familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  336. maladie de Behçet --- r_isa #6: 36 --> en:hereditary disease
    n1=maladie de Behçet | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  337. maladie de Cowden --- r_isa #6: 36 --> en:hereditary disease
    n1=maladie de Cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  338. maladie de Fabry --- r_isa #6: 36 --> en:hereditary disease
    n1=maladie de Fabry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  339. syndrome de McKusick Kaufman --- r_isa #6: 36 --> en:hereditary disease
    n1=syndrome de McKusick Kaufman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=36
  340. EPSM --- r_isa #6: 35 --> en:hereditary disease
    n1=EPSM | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  341. Maladie d'Alzheimer --- r_isa #6: 35 --> en:hereditary disease
    n1=Maladie d'Alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  342. Maladie de Canavan --- r_isa #6: 35 --> en:hereditary disease
    n1=Maladie de Canavan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  343. Myopathie de Duchenne --- r_isa #6: 35 --> en:hereditary disease
    n1=Myopathie de Duchenne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  344. Syndrome de Rett --- r_isa #6: 35 --> en:hereditary disease
    n1=Syndrome de Rett | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  345. Voir l'article --- r_isa #6: 35 --> en:hereditary disease
    n1=Voir l'article | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  346. achondroplasie --- r_isa #6: 35 --> en:hereditary disease
    n1=achondroplasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  347. atrophie optique de Leber --- r_isa #6: 35 --> en:hereditary disease
    n1=atrophie optique de Leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  348. canalopathie --- r_isa #6: 35 --> en:hereditary disease
    n1=canalopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  349. distrophie --- r_isa #6: 35 --> en:hereditary disease
    n1=distrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  350. dystrophie --- r_isa #6: 35 --> en:hereditary disease
    n1=dystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  351. en:Lowe's disease --- r_isa #6: 35 --> en:hereditary disease
    n1=en:Lowe's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  352. en:Sachs' disease --- r_isa #6: 35 --> en:hereditary disease
    n1=en:Sachs' disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  353. en:down syndrome --- r_isa #6: 35 --> en:hereditary disease
    n1=en:down syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  354. en:fanconi syndrome --- r_isa #6: 35 --> en:hereditary disease
    n1=en:fanconi syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  355. en:galactosemia --- r_isa #6: 35 --> en:hereditary disease
    n1=en:galactosemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  356. en:goiter --- r_isa #6: 35 --> en:hereditary disease
    n1=en:goiter | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  357. en:gout --- r_isa #6: 35 --> en:hereditary disease
    n1=en:gout | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  358. gangliosidose à GM2 --- r_isa #6: 35 --> en:hereditary disease
    n1=gangliosidose à GM2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  359. leucodystrophie familiale avec atteinte surrénale --- r_isa #6: 35 --> en:hereditary disease
    n1=leucodystrophie familiale avec atteinte surrénale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  360. maladie de Westphal --- r_isa #6: 35 --> en:hereditary disease
    n1=maladie de Westphal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  361. maladie génétique du métabolisme des métaux --- r_isa #6: 35 --> en:hereditary disease
    n1=maladie génétique du métabolisme des métaux | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  362. maladie héréditaire autosomique récessive --- r_isa #6: 35 --> en:hereditary disease
    n1=maladie héréditaire autosomique récessive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  363. maladie héréditaire de l'oeil --- r_isa #6: 35 --> en:hereditary disease
    n1=maladie héréditaire de l'oeil | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  364. myopathie de Duchenne --- r_isa #6: 35 --> en:hereditary disease
    n1=myopathie de Duchenne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  365. nanisme --- r_isa #6: 35 --> en:hereditary disease
    n1=nanisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  366. neuropathie optique de Leber --- r_isa #6: 35 --> en:hereditary disease
    n1=neuropathie optique de Leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  367. pycnodysostose --- r_isa #6: 35 --> en:hereditary disease
    n1=pycnodysostose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  368. syndrome FG --- r_isa #6: 35 --> en:hereditary disease
    n1=syndrome FG | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  369. syndrome de Pendred --- r_isa #6: 35 --> en:hereditary disease
    n1=syndrome de Pendred | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  370. syndrome triple A --- r_isa #6: 35 --> en:hereditary disease
    n1=syndrome triple A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  371. syringomyélie --- r_isa #6: 35 --> en:hereditary disease
    n1=syringomyélie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  372. thalassémie --- r_isa #6: 35 --> en:hereditary disease
    n1=thalassémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=35
  373. ABD --- r_isa #6: 34 --> en:hereditary disease
    n1=ABD | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  374. Dextrinose limite --- r_isa #6: 34 --> en:hereditary disease
    n1=Dextrinose limite | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  375. XLH --- r_isa #6: 34 --> en:hereditary disease
    n1=XLH | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  376. anomalie polygénique --- r_isa #6: 34 --> en:hereditary disease
    n1=anomalie polygénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  377. anémie mégaloblastique thiamine-sensible --- r_isa #6: 34 --> en:hereditary disease
    n1=anémie mégaloblastique thiamine-sensible | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  378. diabète sucré --- r_isa #6: 34 --> en:hereditary disease
    n1=diabète sucré | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  379. en:lactase deficiency --- r_isa #6: 34 --> en:hereditary disease
    n1=en:lactase deficiency | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  380. en:myopathia --- r_isa #6: 34 --> en:hereditary disease
    n1=en:myopathia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  381. en:osteosclerosis congenita --- r_isa #6: 34 --> en:hereditary disease
    n1=en:osteosclerosis congenita | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  382. en:rett syndrome, atypical --- r_isa #6: 34 --> en:hereditary disease
    n1=en:rett syndrome, atypical | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  383. fibrose kystique --- r_isa #6: 34 --> en:hereditary disease
    n1=fibrose kystique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  384. gangliosidose --- r_isa #6: 34 --> en:hereditary disease
    n1=gangliosidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  385. goitre --- r_isa #6: 34 --> en:hereditary disease
    n1=goitre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  386. hyperphosphatasie alcaline avec retard mental --- r_isa #6: 34 --> en:hereditary disease
    n1=hyperphosphatasie alcaline avec retard mental | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  387. hypophosphatémie liée à l'X --- r_isa #6: 34 --> en:hereditary disease
    n1=hypophosphatémie liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  388. hémochromatose de type 1 --- r_isa #6: 34 --> en:hereditary disease
    n1=hémochromatose de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  389. macrocéphalie - malformation capillaire --- r_isa #6: 34 --> en:hereditary disease
    n1=macrocéphalie - malformation capillaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  390. maladie de Crigler-Najjar --- r_isa #6: 34 --> en:hereditary disease
    n1=maladie de Crigler-Najjar | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  391. maladie de fabry --- r_isa #6: 34 --> en:hereditary disease
    n1=maladie de fabry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  392. sphérocytose héréditaire --- r_isa #6: 34 --> en:hereditary disease
    n1=sphérocytose héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  393. syndrome d'Aicardi --- r_isa #6: 34 --> en:hereditary disease
    n1=syndrome d'Aicardi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  394. syndrome d'aicardi --- r_isa #6: 34 --> en:hereditary disease
    n1=syndrome d'aicardi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  395. syndrome de Kearns-Sayre --- r_isa #6: 34 --> en:hereditary disease
    n1=syndrome de Kearns-Sayre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  396. syringomyelie --- r_isa #6: 34 --> en:hereditary disease
    n1=syringomyelie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=34
  397. Gilles de la Tourette --- r_isa #6: 33 --> en:hereditary disease
    n1=Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
  398. en:gangliosidosis --- r_isa #6: 33 --> en:hereditary disease
    n1=en:gangliosidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
  399. hépatite familiale juvénile avec dégénérescence du corps strié --- r_isa #6: 33 --> en:hereditary disease
    n1=hépatite familiale juvénile avec dégénérescence du corps strié | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
  400. maladie de hirschsprung --- r_isa #6: 33 --> en:hereditary disease
    n1=maladie de hirschsprung | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
  401. myopathie de Bethlem --- r_isa #6: 33 --> en:hereditary disease
    n1=myopathie de Bethlem | n2=en:hereditary disease | rel=r_isa | relid=6 | w=33
  402. Maladie de Wilson --- r_isa #6: 32 --> en:hereditary disease
    n1=Maladie de Wilson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  403. PSSM --- r_isa #6: 32 --> en:hereditary disease
    n1=PSSM | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  404. alacrymie-achalasie-addisonisme --- r_isa #6: 32 --> en:hereditary disease
    n1=alacrymie-achalasie-addisonisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  405. albinisme oculo-cutané type I --- r_isa #6: 32 --> en:hereditary disease
    n1=albinisme oculo-cutané type I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  406. déficience en entérokinase --- r_isa #6: 32 --> en:hereditary disease
    n1=déficience en entérokinase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  407. déficit en cofacteur à molybdène --- r_isa #6: 32 --> en:hereditary disease
    n1=déficit en cofacteur à molybdène | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  408. en:gilbert disease (disorder) --- r_isa #6: 32 --> en:hereditary disease
    n1=en:gilbert disease (disorder) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  409. maladie de tay-sachs --- r_isa #6: 32 --> en:hereditary disease
    n1=maladie de tay-sachs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  410. maladie génétique de l'appareil digestif --- r_isa #6: 32 --> en:hereditary disease
    n1=maladie génétique de l'appareil digestif | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  411. maladie génétique du métabolisme des nucléotides --- r_isa #6: 32 --> en:hereditary disease
    n1=maladie génétique du métabolisme des nucléotides | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  412. maladie génétique en hématologie --- r_isa #6: 32 --> en:hereditary disease
    n1=maladie génétique en hématologie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  413. maladie héréditaire de l'oreille moyenne --- r_isa #6: 32 --> en:hereditary disease
    n1=maladie héréditaire de l'oreille moyenne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  414. maladie héréditaire rare --- r_isa #6: 32 --> en:hereditary disease
    n1=maladie héréditaire rare | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  415. maladie polygénique --- r_isa #6: 32 --> en:hereditary disease
    n1=maladie polygénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  416. microsphérophakie --- r_isa #6: 32 --> en:hereditary disease
    n1=microsphérophakie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  417. microsphérophakie et/ou mégalocornée avec ectopie du cristallin et avec ou sans glaucome secondaire --- r_isa #6: 32 --> en:hereditary disease
    n1=microsphérophakie et/ou mégalocornée avec ectopie du cristallin et avec ou sans glaucome secondaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  418. mucopolysaccharidose --- r_isa #6: 32 --> en:hereditary disease
    n1=mucopolysaccharidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  419. nævomatose baso-cellulaire --- r_isa #6: 32 --> en:hereditary disease
    n1=nævomatose baso-cellulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  420. pycnose --- r_isa #6: 32 --> en:hereditary disease
    n1=pycnose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  421. syndrome L1 --- r_isa #6: 32 --> en:hereditary disease
    n1=syndrome L1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  422. syndrome d'Andermann --- r_isa #6: 32 --> en:hereditary disease
    n1=syndrome d'Andermann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  423. syndrome de Brugada --- r_isa #6: 32 --> en:hereditary disease
    n1=syndrome de Brugada | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  424. syndrome de Crigler-Najjar --- r_isa #6: 32 --> en:hereditary disease
    n1=syndrome de Crigler-Najjar | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  425. syndrome de Lujan-Fryns --- r_isa #6: 32 --> en:hereditary disease
    n1=syndrome de Lujan-Fryns | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  426. syndrome de Protée --- r_isa #6: 32 --> en:hereditary disease
    n1=syndrome de Protée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  427. syndrome de Simpson-Golabi-Behmel --- r_isa #6: 32 --> en:hereditary disease
    n1=syndrome de Simpson-Golabi-Behmel | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  428. thalassémie alpha --- r_isa #6: 32 --> en:hereditary disease
    n1=thalassémie alpha | n2=en:hereditary disease | rel=r_isa | relid=6 | w=32
  429. acidurie argininosuccinique --- r_isa #6: 31 --> en:hereditary disease
    n1=acidurie argininosuccinique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  430. affection familiale --- r_isa #6: 31 --> en:hereditary disease
    n1=affection familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  431. anémie sidéroblastique liée à l'X avec ataxie --- r_isa #6: 31 --> en:hereditary disease
    n1=anémie sidéroblastique liée à l'X avec ataxie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  432. daltonisme --- r_isa #6: 31 --> en:hereditary disease
    n1=daltonisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  433. déficit en carnitine palmitoyltransférase II --- r_isa #6: 31 --> en:hereditary disease
    n1=déficit en carnitine palmitoyltransférase II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  434. en:Wilson's disease --- r_isa #6: 31 --> en:hereditary disease
    n1=en:Wilson's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  435. en:juvenile amaurotic idiocy --- r_isa #6: 31 --> en:hereditary disease
    n1=en:juvenile amaurotic idiocy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  436. en:prune belly syndrome --- r_isa #6: 31 --> en:hereditary disease
    n1=en:prune belly syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  437. génodermatose --- r_isa #6: 31 --> en:hereditary disease
    n1=génodermatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  438. hypercholestérolémie familiale --- r_isa #6: 31 --> en:hereditary disease
    n1=hypercholestérolémie familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  439. maladie de Danon --- r_isa #6: 31 --> en:hereditary disease
    n1=maladie de Danon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  440. maladie de Mac Ardle --- r_isa #6: 31 --> en:hereditary disease
    n1=maladie de Mac Ardle | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  441. maladie de Morquio --- r_isa #6: 31 --> en:hereditary disease
    n1=maladie de Morquio | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  442. maladie de Sly --- r_isa #6: 31 --> en:hereditary disease
    n1=maladie de Sly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  443. maladie héréditaire du sang --- r_isa #6: 31 --> en:hereditary disease
    n1=maladie héréditaire du sang | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  444. maladie multigénique --- r_isa #6: 31 --> en:hereditary disease
    n1=maladie multigénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  445. myopie --- r_isa #6: 31 --> en:hereditary disease
    n1=myopie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  446. neuroacanthocytose --- r_isa #6: 31 --> en:hereditary disease
    n1=neuroacanthocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  447. neurofibromatose de type 2 --- r_isa #6: 31 --> en:hereditary disease
    n1=neurofibromatose de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  448. neurofibromatose de type II --- r_isa #6: 31 --> en:hereditary disease
    n1=neurofibromatose de type II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  449. paralysie périodique hypokaliémique --- r_isa #6: 31 --> en:hereditary disease
    n1=paralysie périodique hypokaliémique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  450. rétinoschisis juvénile lié à l'X --- r_isa #6: 31 --> en:hereditary disease
    n1=rétinoschisis juvénile lié à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  451. syndrome de Christ-Siemens-Touraine --- r_isa #6: 31 --> en:hereditary disease
    n1=syndrome de Christ-Siemens-Touraine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  452. syndrome de Hermansky-Pudlak --- r_isa #6: 31 --> en:hereditary disease
    n1=syndrome de Hermansky-Pudlak | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  453. syndrome de Larsen --- r_isa #6: 31 --> en:hereditary disease
    n1=syndrome de Larsen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  454. syndrome des plaquettes grises --- r_isa #6: 31 --> en:hereditary disease
    n1=syndrome des plaquettes grises | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  455. syndrome main pied utérus --- r_isa #6: 31 --> en:hereditary disease
    n1=syndrome main pied utérus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=31
  456. ASC3 --- r_isa #6: 30 --> en:hereditary disease
    n1=ASC3 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  457. CADASIL --- r_isa #6: 30 --> en:hereditary disease
    n1=CADASIL | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  458. Chopart (désarticulation de) --- r_isa #6: 30 --> en:hereditary disease
    n1=Chopart (désarticulation de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  459. Maladie de Sanfilippo --- r_isa #6: 30 --> en:hereditary disease
    n1=Maladie de Sanfilippo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  460. Syndrome de Gorlin --- r_isa #6: 30 --> en:hereditary disease
    n1=Syndrome de Gorlin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  461. Syndrome de Pendred --- r_isa #6: 30 --> en:hereditary disease
    n1=Syndrome de Pendred | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  462. Syndrome de Peutz-Jeghers --- r_isa #6: 30 --> en:hereditary disease
    n1=Syndrome de Peutz-Jeghers | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  463. adrénoleucodystrophie liée à l'X --- r_isa #6: 30 --> en:hereditary disease
    n1=adrénoleucodystrophie liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  464. affection congénitale --- r_isa #6: 30 --> en:hereditary disease
    n1=affection congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  465. anomalie héréditaire du métabolisme de la bilirubine --- r_isa #6: 30 --> en:hereditary disease
    n1=anomalie héréditaire du métabolisme de la bilirubine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  466. céroïde lipofuscinose neuronale de type infantile tardive --- r_isa #6: 30 --> en:hereditary disease
    n1=céroïde lipofuscinose neuronale de type infantile tardive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  467. diabète (accidents vasculaires cérébraux du) --- r_isa #6: 30 --> en:hereditary disease
    n1=diabète (accidents vasculaires cérébraux du) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  468. défaut d'adhérence des leucocytes chez les bovins --- r_isa #6: 30 --> en:hereditary disease
    n1=défaut d'adhérence des leucocytes chez les bovins | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  469. déficit en alpha-1-antitrypsine --- r_isa #6: 30 --> en:hereditary disease
    n1=déficit en alpha-1-antitrypsine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  470. en:Angelman syndrome --- r_isa #6: 30 --> en:hereditary disease
    n1=en:Angelman syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  471. en:Bechterew's disease --- r_isa #6: 30 --> en:hereditary disease
    n1=en:Bechterew's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  472. en:Crigler Najjar's disease --- r_isa #6: 30 --> en:hereditary disease
    n1=en:Crigler Najjar's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  473. en:Greig's syndrome --- r_isa #6: 30 --> en:hereditary disease
    n1=en:Greig's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  474. en:Guinon's disease --- r_isa #6: 30 --> en:hereditary disease
    n1=en:Guinon's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  475. en:Kartagener's triad --- r_isa #6: 30 --> en:hereditary disease
    n1=en:Kartagener's triad | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  476. en:achondroplasia --- r_isa #6: 30 --> en:hereditary disease
    n1=en:achondroplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  477. en:acrocephaly --- r_isa #6: 30 --> en:hereditary disease
    n1=en:acrocephaly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  478. en:alymphocytosis --- r_isa #6: 30 --> en:hereditary disease
    n1=en:alymphocytosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  479. en:alzheimer's disease --- r_isa #6: 30 --> en:hereditary disease
    n1=en:alzheimer's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  480. en:angelman syndrome --- r_isa #6: 30 --> en:hereditary disease
    n1=en:angelman syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  481. en:angiomatoma corporis diffusum --- r_isa #6: 30 --> en:hereditary disease
    n1=en:angiomatoma corporis diffusum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  482. en:bleeder's disease --- r_isa #6: 30 --> en:hereditary disease
    n1=en:bleeder's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  483. en:caducous morbus --- r_isa #6: 30 --> en:hereditary disease
    n1=en:caducous morbus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  484. en:cat cry disease --- r_isa #6: 30 --> en:hereditary disease
    n1=en:cat cry disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  485. en:drepanocytaemia --- r_isa #6: 30 --> en:hereditary disease
    n1=en:drepanocytaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  486. en:dyskeratosis congenita --- r_isa #6: 30 --> en:hereditary disease
    n1=en:dyskeratosis congenita | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  487. en:goitre --- r_isa #6: 30 --> en:hereditary disease
    n1=en:goitre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  488. en:haemochromatosis --- r_isa #6: 30 --> en:hereditary disease
    n1=en:haemochromatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  489. en:hemophilia --- r_isa #6: 30 --> en:hereditary disease
    n1=en:hemophilia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  490. en:lissencephaly --- r_isa #6: 30 --> en:hereditary disease
    n1=en:lissencephaly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  491. en:microspherophakia --- r_isa #6: 30 --> en:hereditary disease
    n1=en:microspherophakia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  492. en:multiple osteogenic exostoses --- r_isa #6: 30 --> en:hereditary disease
    n1=en:multiple osteogenic exostoses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  493. en:myotonic dystrophy --- r_isa #6: 30 --> en:hereditary disease
    n1=en:myotonic dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  494. en:oculocerebrorenal syndrome --- r_isa #6: 30 --> en:hereditary disease
    n1=en:oculocerebrorenal syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  495. en:oligodontia --- r_isa #6: 30 --> en:hereditary disease
    n1=en:oligodontia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  496. en:sphingolipidosis --- r_isa #6: 30 --> en:hereditary disease
    n1=en:sphingolipidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  497. en:st Valentines disease --- r_isa #6: 30 --> en:hereditary disease
    n1=en:st Valentines disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  498. en:systematized elastorrhexis --- r_isa #6: 30 --> en:hereditary disease
    n1=en:systematized elastorrhexis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  499. en:thalassaemia --- r_isa #6: 30 --> en:hereditary disease
    n1=en:thalassaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  500. en:von Recklinghausen's disease --- r_isa #6: 30 --> en:hereditary disease
    n1=en:von Recklinghausen's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  501. gangliosidosis --- r_isa #6: 30 --> en:hereditary disease
    n1=gangliosidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  502. holoprosencéphalie de type 2 --- r_isa #6: 30 --> en:hereditary disease
    n1=holoprosencéphalie de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  503. leucodystrophie --- r_isa #6: 30 --> en:hereditary disease
    n1=leucodystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  504. lissencéphalie --- r_isa #6: 30 --> en:hereditary disease
    n1=lissencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  505. maladie de Curschmann-Steinert --- r_isa #6: 30 --> en:hereditary disease
    n1=maladie de Curschmann-Steinert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  506. maladie de pompe --- r_isa #6: 30 --> en:hereditary disease
    n1=maladie de pompe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  507. maladie de sanfilippo --- r_isa #6: 30 --> en:hereditary disease
    n1=maladie de sanfilippo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  508. maladie de steinert --- r_isa #6: 30 --> en:hereditary disease
    n1=maladie de steinert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  509. maladie génétique par atteinte du collagène --- r_isa #6: 30 --> en:hereditary disease
    n1=maladie génétique par atteinte du collagène | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  510. nanisme mulibrey --- r_isa #6: 30 --> en:hereditary disease
    n1=nanisme mulibrey | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  511. polykystose rénale type récessif --- r_isa #6: 30 --> en:hereditary disease
    n1=polykystose rénale type récessif | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  512. siclémie (sicklémie) --- r_isa #6: 30 --> en:hereditary disease
    n1=siclémie (sicklémie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  513. syndrome Larsen-Bourbon --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome Larsen-Bourbon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  514. syndrome de Brachmann-de Lange --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de Brachmann-de Lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  515. syndrome de Cornelia de Lange --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de Cornelia de Lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  516. syndrome de Dubowitz --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de Dubowitz | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  517. syndrome de Johanson-Blizzard --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de Johanson-Blizzard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  518. syndrome de Lowry-Wood --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de Lowry-Wood | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  519. syndrome de cornelia de lange --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de cornelia de lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  520. syndrome de johanson-blizzard --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de johanson-blizzard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  521. syndrome de kallmann --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  522. syndrome de lowe --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de lowe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  523. syndrome de pendred --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de pendred | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  524. syndrome de rokitansky --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de rokitansky | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  525. syndrome de rothmund-thomson --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome de rothmund-thomson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  526. syndrome fg --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome fg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  527. syndrome leopard --- r_isa #6: 30 --> en:hereditary disease
    n1=syndrome leopard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=30
  528. MRKH syndrome --- r_isa #6: 29 --> en:hereditary disease
    n1=MRKH syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  529. Maladie de Cowden --- r_isa #6: 29 --> en:hereditary disease
    n1=Maladie de Cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  530. acrocéphalie --- r_isa #6: 29 --> en:hereditary disease
    n1=acrocéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  531. aplasie de la paroi abdominale --- r_isa #6: 29 --> en:hereditary disease
    n1=aplasie de la paroi abdominale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  532. cataracte, microcéphalie, arrêt de croissance et cyphoscoliose (syndrome) --- r_isa #6: 29 --> en:hereditary disease
    n1=cataracte, microcéphalie, arrêt de croissance et cyphoscoliose (syndrome) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  533. cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse --- r_isa #6: 29 --> en:hereditary disease
    n1=cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  534. dysplasie épiphysaire multiple --- r_isa #6: 29 --> en:hereditary disease
    n1=dysplasie épiphysaire multiple | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  535. déficit en transporteur de glucose de type 1 --- r_isa #6: 29 --> en:hereditary disease
    n1=déficit en transporteur de glucose de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  536. en:5p minus syndrome --- r_isa #6: 29 --> en:hereditary disease
    n1=en:5p minus syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  537. en:Andermann's syndrome --- r_isa #6: 29 --> en:hereditary disease
    n1=en:Andermann's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  538. en:Fabry's disease --- r_isa #6: 29 --> en:hereditary disease
    n1=en:Fabry's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  539. en:Gorlin's syndrome --- r_isa #6: 29 --> en:hereditary disease
    n1=en:Gorlin's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  540. en:MPS --- r_isa #6: 29 --> en:hereditary disease
    n1=en:MPS | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  541. en:Proteus' syndrome --- r_isa #6: 29 --> en:hereditary disease
    n1=en:Proteus' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  542. en:Tay Sachs' disease --- r_isa #6: 29 --> en:hereditary disease
    n1=en:Tay Sachs' disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  543. en:Williams syndrome --- r_isa #6: 29 --> en:hereditary disease
    n1=en:Williams syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  544. en:cadocous morbus --- r_isa #6: 29 --> en:hereditary disease
    n1=en:cadocous morbus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  545. en:carcinoma of colon --- r_isa #6: 29 --> en:hereditary disease
    n1=en:carcinoma of colon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  546. en:cholaemia --- r_isa #6: 29 --> en:hereditary disease
    n1=en:cholaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  547. en:colon cancer --- r_isa #6: 29 --> en:hereditary disease
    n1=en:colon cancer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  548. en:congenital hip dislocation --- r_isa #6: 29 --> en:hereditary disease
    n1=en:congenital hip dislocation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  549. en:crescent cell anemia --- r_isa #6: 29 --> en:hereditary disease
    n1=en:crescent cell anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  550. en:cystic fibrosis of the pancreas --- r_isa #6: 29 --> en:hereditary disease
    n1=en:cystic fibrosis of the pancreas | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  551. en:drepanocytic anaemia --- r_isa #6: 29 --> en:hereditary disease
    n1=en:drepanocytic anaemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  552. en:drepanocytic anemia --- r_isa #6: 29 --> en:hereditary disease
    n1=en:drepanocytic anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  553. en:dyschondroplasia --- r_isa #6: 29 --> en:hereditary disease
    n1=en:dyschondroplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  554. en:falling sickness --- r_isa #6: 29 --> en:hereditary disease
    n1=en:falling sickness | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  555. en:inborn error of metabolism --- r_isa #6: 29 --> en:hereditary disease
    n1=en:inborn error of metabolism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  556. en:kerasin thesaurismosis --- r_isa #6: 29 --> en:hereditary disease
    n1=en:kerasin thesaurismosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  557. en:leukodystrophy --- r_isa #6: 29 --> en:hereditary disease
    n1=en:leukodystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  558. en:mehes syndrome --- r_isa #6: 29 --> en:hereditary disease
    n1=en:mehes syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  559. en:mulibrey nanism syndrome --- r_isa #6: 29 --> en:hereditary disease
    n1=en:mulibrey nanism syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  560. en:otosclerosis --- r_isa #6: 29 --> en:hereditary disease
    n1=en:otosclerosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  561. exostosante (maladie) --- r_isa #6: 29 --> en:hereditary disease
    n1=exostosante (maladie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  562. holoprosencéphalie de type 3 --- r_isa #6: 29 --> en:hereditary disease
    n1=holoprosencéphalie de type 3 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  563. luxation congénitale de la hanche --- r_isa #6: 29 --> en:hereditary disease
    n1=luxation congénitale de la hanche | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  564. maladie de Mac Ardle-Schmid-Pearson --- r_isa #6: 29 --> en:hereditary disease
    n1=maladie de Mac Ardle-Schmid-Pearson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  565. maladie de canavan --- r_isa #6: 29 --> en:hereditary disease
    n1=maladie de canavan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  566. maladie génétique congénitale --- r_isa #6: 29 --> en:hereditary disease
    n1=maladie génétique congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  567. maladie génétique de l'oeil --- r_isa #6: 29 --> en:hereditary disease
    n1=maladie génétique de l'oeil | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  568. maladie génétique de la peau --- r_isa #6: 29 --> en:hereditary disease
    n1=maladie génétique de la peau | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  569. maladie génétique du système nerveux --- r_isa #6: 29 --> en:hereditary disease
    n1=maladie génétique du système nerveux | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  570. maladie lymphoproliférative liée à l'X --- r_isa #6: 29 --> en:hereditary disease
    n1=maladie lymphoproliférative liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  571. myopathie multicore congénitale avec ophtalmoplégie externe --- r_isa #6: 29 --> en:hereditary disease
    n1=myopathie multicore congénitale avec ophtalmoplégie externe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  572. pachyonychie congénitale --- r_isa #6: 29 --> en:hereditary disease
    n1=pachyonychie congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  573. paraplégie spastique familiale type 4 --- r_isa #6: 29 --> en:hereditary disease
    n1=paraplégie spastique familiale type 4 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  574. phénylcétonurie --- r_isa #6: 29 --> en:hereditary disease
    n1=phénylcétonurie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  575. rétinite pigmentaire --- r_isa #6: 29 --> en:hereditary disease
    n1=rétinite pigmentaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  576. rétinite pigmentaire in utero --- r_isa #6: 29 --> en:hereditary disease
    n1=rétinite pigmentaire in utero | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  577. syndrome d'Ondine --- r_isa #6: 29 --> en:hereditary disease
    n1=syndrome d'Ondine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  578. syndrome de rathbun --- r_isa #6: 29 --> en:hereditary disease
    n1=syndrome de rathbun | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  579. syndrome de shwachman-diamond --- r_isa #6: 29 --> en:hereditary disease
    n1=syndrome de shwachman-diamond | n2=en:hereditary disease | rel=r_isa | relid=6 | w=29
  580. NAD + --- r_isa #6: 28 --> en:hereditary disease
    n1=NAD + | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  581. Puumala (virus) --- r_isa #6: 28 --> en:hereditary disease
    n1=Puumala (virus) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  582. adrénoleucodystrophie de l?enfant --- r_isa #6: 28 --> en:hereditary disease
    n1=adrénoleucodystrophie de l?enfant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  583. albinisme oculocutané de type mutant jaune --- r_isa #6: 28 --> en:hereditary disease
    n1=albinisme oculocutané de type mutant jaune | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  584. alymphocytose --- r_isa #6: 28 --> en:hereditary disease
    n1=alymphocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  585. anémie de Fanconi --- r_isa #6: 28 --> en:hereditary disease
    n1=anémie de Fanconi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  586. dysplasie épiphysaire, microcéphalie et nystagmus --- r_isa #6: 28 --> en:hereditary disease
    n1=dysplasie épiphysaire, microcéphalie et nystagmus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  587. déficit en ornithine carbamyl transférase --- r_isa #6: 28 --> en:hereditary disease
    n1=déficit en ornithine carbamyl transférase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  588. en:Besnier's prurigo --- r_isa #6: 28 --> en:hereditary disease
    n1=en:Besnier's prurigo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  589. en:Gilbert's cholæmia --- r_isa #6: 28 --> en:hereditary disease
    n1=en:Gilbert's cholæmia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  590. en:Hartnup's disease --- r_isa #6: 28 --> en:hereditary disease
    n1=en:Hartnup's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  591. en:Hirschsprung's disease --- r_isa #6: 28 --> en:hereditary disease
    n1=en:Hirschsprung's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  592. en:Kearns-Sayre's syndrome --- r_isa #6: 28 --> en:hereditary disease
    n1=en:Kearns-Sayre's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  593. en:Rendu-Osler-Weber's syndrome --- r_isa #6: 28 --> en:hereditary disease
    n1=en:Rendu-Osler-Weber's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  594. en:Westphal's disease --- r_isa #6: 28 --> en:hereditary disease
    n1=en:Westphal's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  595. en:Williams-Beuren syndrome --- r_isa #6: 28 --> en:hereditary disease
    n1=en:Williams-Beuren syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  596. en:autosomal dominant disorder --- r_isa #6: 28 --> en:hereditary disease
    n1=en:autosomal dominant disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  597. en:cerebrotendinous xanthomatosis --- r_isa #6: 28 --> en:hereditary disease
    n1=en:cerebrotendinous xanthomatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  598. en:de Morsier-Kallman's syndrome --- r_isa #6: 28 --> en:hereditary disease
    n1=en:de Morsier-Kallman's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  599. en:epilepsia --- r_isa #6: 28 --> en:hereditary disease
    n1=en:epilepsia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  600. en:haemophilia --- r_isa #6: 28 --> en:hereditary disease
    n1=en:haemophilia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  601. en:heterotaxy syndrome --- r_isa #6: 28 --> en:hereditary disease
    n1=en:heterotaxy syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  602. en:laurence-moon syndrome --- r_isa #6: 28 --> en:hereditary disease
    n1=en:laurence-moon syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  603. en:marble bones disease --- r_isa #6: 28 --> en:hereditary disease
    n1=en:marble bones disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  604. en:near-sight --- r_isa #6: 28 --> en:hereditary disease
    n1=en:near-sight | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  605. en:pseudoxanthoma elasticum --- r_isa #6: 28 --> en:hereditary disease
    n1=en:pseudoxanthoma elasticum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  606. en:retinitis pigmentosa --- r_isa #6: 28 --> en:hereditary disease
    n1=en:retinitis pigmentosa | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  607. en:syringomyelia --- r_isa #6: 28 --> en:hereditary disease
    n1=en:syringomyelia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  608. fibrose congénitale des muscles oculo-moteurs --- r_isa #6: 28 --> en:hereditary disease
    n1=fibrose congénitale des muscles oculo-moteurs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  609. hyperinsulinisme familial --- r_isa #6: 28 --> en:hereditary disease
    n1=hyperinsulinisme familial | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  610. hémophilie --- r_isa #6: 28 --> en:hereditary disease
    n1=hémophilie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  611. maladie d'ollier --- r_isa #6: 28 --> en:hereditary disease
    n1=maladie d'ollier | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  612. maladie de Hirschsprung --- r_isa #6: 28 --> en:hereditary disease
    n1=maladie de Hirschsprung | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  613. maladie de Pompe --- r_isa #6: 28 --> en:hereditary disease
    n1=maladie de Pompe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  614. maladie de behçet --- r_isa #6: 28 --> en:hereditary disease
    n1=maladie de behçet | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  615. maladie génétique du métabolisme --- r_isa #6: 28 --> en:hereditary disease
    n1=maladie génétique du métabolisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  616. maladie génétique lysosomale --- r_isa #6: 28 --> en:hereditary disease
    n1=maladie génétique lysosomale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  617. maladie génétique orpheline --- r_isa #6: 28 --> en:hereditary disease
    n1=maladie génétique orpheline | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  618. nanisme à tête d'oiseau --- r_isa #6: 28 --> en:hereditary disease
    n1=nanisme à tête d'oiseau | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  619. neurofibromatose --- r_isa #6: 28 --> en:hereditary disease
    n1=neurofibromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  620. pachyonychie congénitale de Jadassohn-Lewandowsky --- r_isa #6: 28 --> en:hereditary disease
    n1=pachyonychie congénitale de Jadassohn-Lewandowsky | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  621. syndrome d'Ehlers-Danlos type arthro-chalasique --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome d'Ehlers-Danlos type arthro-chalasique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  622. syndrome de Chediak Higashi --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome de Chediak Higashi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  623. syndrome de Drummond --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome de Drummond | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  624. syndrome de Williams --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome de Williams | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  625. syndrome de brachmann-de lange --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome de brachmann-de lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  626. syndrome de gorlin --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome de gorlin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  627. syndrome de l'X fragile --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome de l'X fragile | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  628. syndrome de rett --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome de rett | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  629. syndrome des hamartomes multiples --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome des hamartomes multiples | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  630. syndrome oculo-facio-cardio-dentaire --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome oculo-facio-cardio-dentaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  631. syndrome triple a --- r_isa #6: 28 --> en:hereditary disease
    n1=syndrome triple a | n2=en:hereditary disease | rel=r_isa | relid=6 | w=28
  632. ataxie paroxystique héréditaire --- r_isa #6: 27 --> en:hereditary disease
    n1=ataxie paroxystique héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  633. atrophie optique de leber --- r_isa #6: 27 --> en:hereditary disease
    n1=atrophie optique de leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  634. cataracte congénitale avec dysmorphie faciale et neuropathie --- r_isa #6: 27 --> en:hereditary disease
    n1=cataracte congénitale avec dysmorphie faciale et neuropathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  635. comitialité --- r_isa #6: 27 --> en:hereditary disease
    n1=comitialité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  636. dysplasie campomélique --- r_isa #6: 27 --> en:hereditary disease
    n1=dysplasie campomélique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  637. ectrodactylie --- r_isa #6: 27 --> en:hereditary disease
    n1=ectrodactylie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  638. en:Alzheimer's dementia --- r_isa #6: 27 --> en:hereditary disease
    n1=en:Alzheimer's dementia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  639. en:Down syndrome --- r_isa #6: 27 --> en:hereditary disease
    n1=en:Down syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  640. en:Larsen's syndrome --- r_isa #6: 27 --> en:hereditary disease
    n1=en:Larsen's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  641. en:Lejeune's syndrome --- r_isa #6: 27 --> en:hereditary disease
    n1=en:Lejeune's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  642. en:Marfan's syndrome --- r_isa #6: 27 --> en:hereditary disease
    n1=en:Marfan's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  643. en:Marie-Strümpell's disease --- r_isa #6: 27 --> en:hereditary disease
    n1=en:Marie-Strümpell's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  644. en:Rathbun's syndrome --- r_isa #6: 27 --> en:hereditary disease
    n1=en:Rathbun's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  645. en:alacrymia-achalasia-addisonianism --- r_isa #6: 27 --> en:hereditary disease
    n1=en:alacrymia-achalasia-addisonianism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  646. en:amaurotic familial idiocy --- r_isa #6: 27 --> en:hereditary disease
    n1=en:amaurotic familial idiocy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  647. en:ankylosing spondylitis --- r_isa #6: 27 --> en:hereditary disease
    n1=en:ankylosing spondylitis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  648. en:bird-headed dwarfism --- r_isa #6: 27 --> en:hereditary disease
    n1=en:bird-headed dwarfism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  649. en:branched-chain ketoaciduria --- r_isa #6: 27 --> en:hereditary disease
    n1=en:branched-chain ketoaciduria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  650. en:cataract --- r_isa #6: 27 --> en:hereditary disease
    n1=en:cataract | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  651. en:cri du chat syndrome --- r_isa #6: 27 --> en:hereditary disease
    n1=en:cri du chat syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  652. en:drepanocytosis --- r_isa #6: 27 --> en:hereditary disease
    n1=en:drepanocytosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  653. en:familial cholemia --- r_isa #6: 27 --> en:hereditary disease
    n1=en:familial cholemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  654. en:familial epistaxis and telangiectasis --- r_isa #6: 27 --> en:hereditary disease
    n1=en:familial epistaxis and telangiectasis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  655. en:hemorrhaphilia --- r_isa #6: 27 --> en:hereditary disease
    n1=en:hemorrhaphilia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  656. en:hereditary disorder by system --- r_isa #6: 27 --> en:hereditary disease
    n1=en:hereditary disorder by system | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  657. en:maple-tree syrup disease --- r_isa #6: 27 --> en:hereditary disease
    n1=en:maple-tree syrup disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  658. en:neurofibromatosis type 1 --- r_isa #6: 27 --> en:hereditary disease
    n1=en:neurofibromatosis type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  659. en:olfacto genital dysplasia --- r_isa #6: 27 --> en:hereditary disease
    n1=en:olfacto genital dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  660. en:progerialike syndrome --- r_isa #6: 27 --> en:hereditary disease
    n1=en:progerialike syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  661. en:st Avertin's disease --- r_isa #6: 27 --> en:hereditary disease
    n1=en:st Avertin's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  662. en:uroglycosis --- r_isa #6: 27 --> en:hereditary disease
    n1=en:uroglycosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  663. goutte
    (maladie)
    --- r_isa #6: 27 --> en:hereditary disease

    n1=goutte
    (maladie)
    | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  664. leucoencéphalopathie mégalencéphalique avec kystes sub-corticaux --- r_isa #6: 27 --> en:hereditary disease
    n1=leucoencéphalopathie mégalencéphalique avec kystes sub-corticaux | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  665. léiomyomatose familiale et cancer du rein --- r_isa #6: 27 --> en:hereditary disease
    n1=léiomyomatose familiale et cancer du rein | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  666. maladie du cri du chat --- r_isa #6: 27 --> en:hereditary disease
    n1=maladie du cri du chat | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  667. maladie génétique du métabolisme des acides aminés --- r_isa #6: 27 --> en:hereditary disease
    n1=maladie génétique du métabolisme des acides aminés | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  668. maladie génétique en néphrologie --- r_isa #6: 27 --> en:hereditary disease
    n1=maladie génétique en néphrologie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  669. maladie héréditaire inflammatoire --- r_isa #6: 27 --> en:hereditary disease
    n1=maladie héréditaire inflammatoire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  670. microcéphalie-hernie hiatale-syndrome néphrotique --- r_isa #6: 27 --> en:hereditary disease
    n1=microcéphalie-hernie hiatale-syndrome néphrotique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  671. otospongiose --- r_isa #6: 27 --> en:hereditary disease
    n1=otospongiose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  672. syndrome 4A --- r_isa #6: 27 --> en:hereditary disease
    n1=syndrome 4A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  673. syndrome de Beckwith-Wiedemann --- r_isa #6: 27 --> en:hereditary disease
    n1=syndrome de Beckwith-Wiedemann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  674. syndrome de Hartnup --- r_isa #6: 27 --> en:hereditary disease
    n1=syndrome de Hartnup | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  675. syndrome de saethre-chotzen --- r_isa #6: 27 --> en:hereditary disease
    n1=syndrome de saethre-chotzen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=27
  676. Muir-Torre --- r_isa #6: 26 --> en:hereditary disease
    n1=Muir-Torre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  677. amaurose congénitale de Leber --- r_isa #6: 26 --> en:hereditary disease
    n1=amaurose congénitale de Leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  678. dystonie myoclonique --- r_isa #6: 26 --> en:hereditary disease
    n1=dystonie myoclonique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  679. dystrophie congénitale musculaire d'Ullrich --- r_isa #6: 26 --> en:hereditary disease
    n1=dystrophie congénitale musculaire d'Ullrich | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  680. dystrophie musculaire d'emery-dreifuss --- r_isa #6: 26 --> en:hereditary disease
    n1=dystrophie musculaire d'emery-dreifuss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  681. déficit en dopamine bêta-hydroxylase --- r_isa #6: 26 --> en:hereditary disease
    n1=déficit en dopamine bêta-hydroxylase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  682. dégénérescence hépatolenticulaire --- r_isa #6: 26 --> en:hereditary disease
    n1=dégénérescence hépatolenticulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  683. en:Bechterew's arthritis --- r_isa #6: 26 --> en:hereditary disease
    n1=en:Bechterew's arthritis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  684. en:Cockayne's syndrome --- r_isa #6: 26 --> en:hereditary disease
    n1=en:Cockayne's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  685. en:Cori's disease --- r_isa #6: 26 --> en:hereditary disease
    n1=en:Cori's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  686. en:Duchenne's myopathy --- r_isa #6: 26 --> en:hereditary disease
    n1=en:Duchenne's myopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  687. en:Goldstein's disease --- r_isa #6: 26 --> en:hereditary disease
    n1=en:Goldstein's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  688. en:Steinert's disease --- r_isa #6: 26 --> en:hereditary disease
    n1=en:Steinert's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  689. en:Williams' syndrome --- r_isa #6: 26 --> en:hereditary disease
    n1=en:Williams' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  690. en:anhidrotic ectodermal dysplasia --- r_isa #6: 26 --> en:hereditary disease
    n1=en:anhidrotic ectodermal dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  691. en:autosomal recessive disease --- r_isa #6: 26 --> en:hereditary disease
    n1=en:autosomal recessive disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  692. en:cat cry syndrome --- r_isa #6: 26 --> en:hereditary disease
    n1=en:cat cry syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  693. en:glycogen storage disease type II --- r_isa #6: 26 --> en:hereditary disease
    n1=en:glycogen storage disease type II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  694. en:leucinosis --- r_isa #6: 26 --> en:hereditary disease
    n1=en:leucinosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  695. en:mucoviscidosis --- r_isa #6: 26 --> en:hereditary disease
    n1=en:mucoviscidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  696. en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_isa #6: 26 --> en:hereditary disease
    n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  697. en:primary ciliary dyskinesia --- r_isa #6: 26 --> en:hereditary disease
    n1=en:primary ciliary dyskinesia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  698. en:rheumatoid spondylitis --- r_isa #6: 26 --> en:hereditary disease
    n1=en:rheumatoid spondylitis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  699. en:stone man --- r_isa #6: 26 --> en:hereditary disease
    n1=en:stone man | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  700. en:typus amstelodamensis --- r_isa #6: 26 --> en:hereditary disease
    n1=en:typus amstelodamensis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  701. en:wilson's disease --- r_isa #6: 26 --> en:hereditary disease
    n1=en:wilson's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  702. hyperkaliémie périodique paralysante --- r_isa #6: 26 --> en:hereditary disease
    n1=hyperkaliémie périodique paralysante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  703. maladie d' Alzheimer --- r_isa #6: 26 --> en:hereditary disease
    n1=maladie d' Alzheimer | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  704. maladie lysosomale --- r_isa #6: 26 --> en:hereditary disease
    n1=maladie lysosomale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  705. microsphérocytose héréditaire --- r_isa #6: 26 --> en:hereditary disease
    n1=microsphérocytose héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  706. mucopolysaccharidose de type VII --- r_isa #6: 26 --> en:hereditary disease
    n1=mucopolysaccharidose de type VII | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  707. sirop d'érable (urine à odeur de) --- r_isa #6: 26 --> en:hereditary disease
    n1=sirop d'érable (urine à odeur de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  708. syndrome Allgrove --- r_isa #6: 26 --> en:hereditary disease
    n1=syndrome Allgrove | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  709. syndrome cataracte, microcéphalie, arrêt de croissance et cyphoscoliose --- r_isa #6: 26 --> en:hereditary disease
    n1=syndrome cataracte, microcéphalie, arrêt de croissance et cyphoscoliose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  710. syndrome de Rothmund-Thomson --- r_isa #6: 26 --> en:hereditary disease
    n1=syndrome de Rothmund-Thomson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  711. syndrome de Shwachman-Diamond --- r_isa #6: 26 --> en:hereditary disease
    n1=syndrome de Shwachman-Diamond | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  712. syndrome de gilbert --- r_isa #6: 26 --> en:hereditary disease
    n1=syndrome de gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  713. syndrome de gilles de la tourette --- r_isa #6: 26 --> en:hereditary disease
    n1=syndrome de gilles de la tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=26
  714. Maladie de Pompe --- r_isa #6: 25 --> en:hereditary disease
    n1=Maladie de Pompe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  715. Maladie du cri du chat --- r_isa #6: 25 --> en:hereditary disease
    n1=Maladie du cri du chat | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  716. Maladie génétique du métabolisme des glucides --- r_isa #6: 25 --> en:hereditary disease
    n1=Maladie génétique du métabolisme des glucides | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  717. MucoPolySaccharidose --- r_isa #6: 25 --> en:hereditary disease
    n1=MucoPolySaccharidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  718. NAD+ --- r_isa #6: 25 --> en:hereditary disease
    n1=NAD+ | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  719. albinisme avec pigmentation minime --- r_isa #6: 25 --> en:hereditary disease
    n1=albinisme avec pigmentation minime | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  720. ataxie télangiectasique --- r_isa #6: 25 --> en:hereditary disease
    n1=ataxie télangiectasique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  721. cétoacidurie à chaînes ramifiées --- r_isa #6: 25 --> en:hereditary disease
    n1=cétoacidurie à chaînes ramifiées | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  722. diphosphopyridine-nucléotide --- r_isa #6: 25 --> en:hereditary disease
    n1=diphosphopyridine-nucléotide | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  723. en:Brugada'syndrome --- r_isa #6: 25 --> en:hereditary disease
    n1=en:Brugada'syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  724. en:Forbes' disease --- r_isa #6: 25 --> en:hereditary disease
    n1=en:Forbes' disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  725. en:Kartagener's syndrome --- r_isa #6: 25 --> en:hereditary disease
    n1=en:Kartagener's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  726. en:Marie-Strümpell disease --- r_isa #6: 25 --> en:hereditary disease
    n1=en:Marie-Strümpell disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  727. en:Mayer-Rokitansky-Küster-Hauser syndrome --- r_isa #6: 25 --> en:hereditary disease
    n1=en:Mayer-Rokitansky-Küster-Hauser syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  728. en:adactylia --- r_isa #6: 25 --> en:hereditary disease
    n1=en:adactylia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  729. en:cardiomegalia glycogenica diffusa --- r_isa #6: 25 --> en:hereditary disease
    n1=en:cardiomegalia glycogenica diffusa | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  730. en:epiphyseal dysplasia --- r_isa #6: 25 --> en:hereditary disease
    n1=en:epiphyseal dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  731. en:globoid leukodystrophy --- r_isa #6: 25 --> en:hereditary disease
    n1=en:globoid leukodystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  732. en:grand mal --- r_isa #6: 25 --> en:hereditary disease
    n1=en:grand mal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  733. en:myositis ossificans progressiva --- r_isa #6: 25 --> en:hereditary disease
    n1=en:myositis ossificans progressiva | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  734. en:phenylketonuria (PKU) --- r_isa #6: 25 --> en:hereditary disease
    n1=en:phenylketonuria (PKU) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  735. en:progressive ossifying fibrodysplasia --- r_isa #6: 25 --> en:hereditary disease
    n1=en:progressive ossifying fibrodysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  736. en:rhizomelic spondylitis --- r_isa #6: 25 --> en:hereditary disease
    n1=en:rhizomelic spondylitis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  737. encéphalopathie avec calcification intracrânienne, déficience en hormone de croissance, microcéphalie et dégénérescence rétinienne --- r_isa #6: 25 --> en:hereditary disease
    n1=encéphalopathie avec calcification intracrânienne, déficience en hormone de croissance, microcéphalie et dégénérescence rétinienne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  738. ichtyose lamellaire --- r_isa #6: 25 --> en:hereditary disease
    n1=ichtyose lamellaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  739. ichtyose liée à l'X --- r_isa #6: 25 --> en:hereditary disease
    n1=ichtyose liée à l'X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  740. ichtyose vulgaire de transmission autosomique dominante --- r_isa #6: 25 --> en:hereditary disease
    n1=ichtyose vulgaire de transmission autosomique dominante | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  741. maladie d'albers-schönberg --- r_isa #6: 25 --> en:hereditary disease
    n1=maladie d'albers-schönberg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  742. maladie de morquio --- r_isa #6: 25 --> en:hereditary disease
    n1=maladie de morquio | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  743. maladie de rendu-osler --- r_isa #6: 25 --> en:hereditary disease
    n1=maladie de rendu-osler | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  744. mucopolysaccharidose de type vii --- r_isa #6: 25 --> en:hereditary disease
    n1=mucopolysaccharidose de type vii | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  745. troubles endocriniens, épilepsie et déficience mentale --- r_isa #6: 25 --> en:hereditary disease
    n1=troubles endocriniens, épilepsie et déficience mentale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  746. érythrodermie ichtyosiforme congénitale bulleuse --- r_isa #6: 25 --> en:hereditary disease
    n1=érythrodermie ichtyosiforme congénitale bulleuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=25
  747. coenzyme --- r_isa #6: 24 --> en:hereditary disease
    n1=coenzyme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  748. en:Albers Schönberg's disease --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Albers Schönberg's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  749. en:Angelman's syndrome --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Angelman's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  750. en:Behçet's disease --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Behçet's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  751. en:Dubowitz' syndrome --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Dubowitz' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  752. en:Gaucher disease --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Gaucher disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  753. en:Louis-Bar's syndrome --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Louis-Bar's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  754. en:Minkowski's-Chauffard syndrome --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Minkowski's-Chauffard syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  755. en:Münchmeyer's disease --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Münchmeyer's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  756. en:Ollier disease --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Ollier disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  757. en:Ondine ' s syndrome --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Ondine ' s syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  758. en:Peutz-Jeghers' syndrome --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Peutz-Jeghers' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  759. en:Sydenham's chorea --- r_isa #6: 24 --> en:hereditary disease
    n1=en:Sydenham's chorea | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  760. en:WBS --- r_isa #6: 24 --> en:hereditary disease
    n1=en:WBS | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  761. en:capsulitis of the labyrinth --- r_isa #6: 24 --> en:hereditary disease
    n1=en:capsulitis of the labyrinth | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  762. en:chromosome 5p deletion syndrome --- r_isa #6: 24 --> en:hereditary disease
    n1=en:chromosome 5p deletion syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  763. en:colon carcinoma --- r_isa #6: 24 --> en:hereditary disease
    n1=en:colon carcinoma | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  764. en:ectrodactyly --- r_isa #6: 24 --> en:hereditary disease
    n1=en:ectrodactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  765. en:galactosylceramidose --- r_isa #6: 24 --> en:hereditary disease
    n1=en:galactosylceramidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  766. en:genodermatosis --- r_isa #6: 24 --> en:hereditary disease
    n1=en:genodermatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  767. en:globoid cell sclerosis of the brain --- r_isa #6: 24 --> en:hereditary disease
    n1=en:globoid cell sclerosis of the brain | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  768. en:oculofaciocradiodental syndrome --- r_isa #6: 24 --> en:hereditary disease
    n1=en:oculofaciocradiodental syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  769. en:phenylketonuria --- r_isa #6: 24 --> en:hereditary disease
    n1=en:phenylketonuria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  770. en:sideroblastic anemia --- r_isa #6: 24 --> en:hereditary disease
    n1=en:sideroblastic anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  771. en:tomaculous neuropathy --- r_isa #6: 24 --> en:hereditary disease
    n1=en:tomaculous neuropathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  772. gangliosidose à gm2 --- r_isa #6: 24 --> en:hereditary disease
    n1=gangliosidose à gm2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  773. maladie de cowden --- r_isa #6: 24 --> en:hereditary disease
    n1=maladie de cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=24
  774. adrénoleucodystrophie néonatale récessive --- r_isa #6: 23 --> en:hereditary disease
    n1=adrénoleucodystrophie néonatale récessive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  775. en:Brachmann-de Lange's syndrome --- r_isa #6: 23 --> en:hereditary disease
    n1=en:Brachmann-de Lange's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  776. en:Dresbach's anemia --- r_isa #6: 23 --> en:hereditary disease
    n1=en:Dresbach's anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  777. en:GM2 gangliosidosis --- r_isa #6: 23 --> en:hereditary disease
    n1=en:GM2 gangliosidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  778. en:Johanson Blizzard's syndrome --- r_isa #6: 23 --> en:hereditary disease
    n1=en:Johanson Blizzard's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  779. en:Kallman's syndrome --- r_isa #6: 23 --> en:hereditary disease
    n1=en:Kallman's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  780. en:Morquio's disease --- r_isa #6: 23 --> en:hereditary disease
    n1=en:Morquio's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  781. en:Pompe disease --- r_isa #6: 23 --> en:hereditary disease
    n1=en:Pompe disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  782. en:Rokitansky-Küster-Hauser's syndrome --- r_isa #6: 23 --> en:hereditary disease
    n1=en:Rokitansky-Küster-Hauser's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  783. en:and mild syndactyly --- r_isa #6: 23 --> en:hereditary disease
    n1=en:and mild syndactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  784. en:bleeding sickness --- r_isa #6: 23 --> en:hereditary disease
    n1=en:bleeding sickness | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  785. en:campomelic dysplasia --- r_isa #6: 23 --> en:hereditary disease
    n1=en:campomelic dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  786. en:cephalosynpolydactyly --- r_isa #6: 23 --> en:hereditary disease
    n1=en:cephalosynpolydactyly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  787. en:mucopolysaccharidosis type VII --- r_isa #6: 23 --> en:hereditary disease
    n1=en:mucopolysaccharidosis type VII | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  788. en:olfactory genital dysplasia --- r_isa #6: 23 --> en:hereditary disease
    n1=en:olfactory genital dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  789. en:otospongiosis --- r_isa #6: 23 --> en:hereditary disease
    n1=en:otospongiosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  790. en:pendred syndrome --- r_isa #6: 23 --> en:hereditary disease
    n1=en:pendred syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  791. en:urophtisis --- r_isa #6: 23 --> en:hereditary disease
    n1=en:urophtisis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  792. hamartomes basocellulaires (syndrome des) --- r_isa #6: 23 --> en:hereditary disease
    n1=hamartomes basocellulaires (syndrome des) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  793. holoprosencéphalie de type 4 --- r_isa #6: 23 --> en:hereditary disease
    n1=holoprosencéphalie de type 4 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  794. hypophosphatémie liée à l'x --- r_isa #6: 23 --> en:hereditary disease
    n1=hypophosphatémie liée à l'x | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  795. maladie de gilbert --- r_isa #6: 23 --> en:hereditary disease
    n1=maladie de gilbert | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  796. maladie de machado-joseph --- r_isa #6: 23 --> en:hereditary disease
    n1=maladie de machado-joseph | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  797. syndrome de Joubert-Boltshauser (syndrome de) --- r_isa #6: 23 --> en:hereditary disease
    n1=syndrome de Joubert-Boltshauser (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  798. syndrome de williams --- r_isa #6: 23 --> en:hereditary disease
    n1=syndrome de williams | n2=en:hereditary disease | rel=r_isa | relid=6 | w=23
  799. Maladie de Hirschsprung --- r_isa #6: 22 --> en:hereditary disease
    n1=Maladie de Hirschsprung | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  800. NAME (syndrome) sigle pour multiple Nævus -Atrial myxoma-Myxoid neurofibroma-Ephelides --- r_isa #6: 22 --> en:hereditary disease
    n1=NAME (syndrome) sigle pour multiple Nævus -Atrial myxoma-Myxoid neurofibroma-Ephelides | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  801. adrénoleucodystrophie liée à l?X --- r_isa #6: 22 --> en:hereditary disease
    n1=adrénoleucodystrophie liée à l?X | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  802. albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception --- r_isa #6: 22 --> en:hereditary disease
    n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  803. codéshydrogénase I --- r_isa #6: 22 --> en:hereditary disease
    n1=codéshydrogénase I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  804. en:Beckwith Wiedemann's syndrome --- r_isa #6: 22 --> en:hereditary disease
    n1=en:Beckwith Wiedemann's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  805. en:Canavan's disease --- r_isa #6: 22 --> en:hereditary disease
    n1=en:Canavan's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  806. en:Coffin-Siris' syndrome --- r_isa #6: 22 --> en:hereditary disease
    n1=en:Coffin-Siris' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  807. en:Drummond's syndrome --- r_isa #6: 22 --> en:hereditary disease
    n1=en:Drummond's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  808. en:Jadassohn-Lewandowsky syndrome --- r_isa #6: 22 --> en:hereditary disease
    n1=en:Jadassohn-Lewandowsky syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  809. en:Louis-Bar?s syndrome --- r_isa #6: 22 --> en:hereditary disease
    n1=en:Louis-Bar?s syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  810. en:Lowe's syndrome --- r_isa #6: 22 --> en:hereditary disease
    n1=en:Lowe's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  811. en:Peutz-Jeghers syndrome --- r_isa #6: 22 --> en:hereditary disease
    n1=en:Peutz-Jeghers syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  812. en:Wilson disease --- r_isa #6: 22 --> en:hereditary disease
    n1=en:Wilson disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  813. en:atopic eczema --- r_isa #6: 22 --> en:hereditary disease
    n1=en:atopic eczema | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  814. en:basal cell nevus syndrome --- r_isa #6: 22 --> en:hereditary disease
    n1=en:basal cell nevus syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  815. en:cancer of the colon --- r_isa #6: 22 --> en:hereditary disease
    n1=en:cancer of the colon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  816. en:cerebroside lipoidosis --- r_isa #6: 22 --> en:hereditary disease
    n1=en:cerebroside lipoidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  817. en:chromosomal aberration --- r_isa #6: 22 --> en:hereditary disease
    n1=en:chromosomal aberration | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  818. en:dextrinosis --- r_isa #6: 22 --> en:hereditary disease
    n1=en:dextrinosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  819. en:dwarfism --- r_isa #6: 22 --> en:hereditary disease
    n1=en:dwarfism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  820. en:enzymatic disease --- r_isa #6: 22 --> en:hereditary disease
    n1=en:enzymatic disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  821. en:leukodystrophia --- r_isa #6: 22 --> en:hereditary disease
    n1=en:leukodystrophia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  822. en:mucopolysaccharidosis --- r_isa #6: 22 --> en:hereditary disease
    n1=en:mucopolysaccharidosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  823. en:mucopolysaccharidosis IV --- r_isa #6: 22 --> en:hereditary disease
    n1=en:mucopolysaccharidosis IV | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  824. en:pachyonychia congenita --- r_isa #6: 22 --> en:hereditary disease
    n1=en:pachyonychia congenita | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  825. en:septooptic dysplasia --- r_isa #6: 22 --> en:hereditary disease
    n1=en:septooptic dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  826. en:short sight --- r_isa #6: 22 --> en:hereditary disease
    n1=en:short sight | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  827. en:skull asymetry --- r_isa #6: 22 --> en:hereditary disease
    n1=en:skull asymetry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  828. leucocyte paresseux (syndrome du) --- r_isa #6: 22 --> en:hereditary disease
    n1=leucocyte paresseux (syndrome du) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  829. maladie de westphal --- r_isa #6: 22 --> en:hereditary disease
    n1=maladie de westphal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  830. syndrome de myopathie, cataracte, hypogonadisme --- r_isa #6: 22 --> en:hereditary disease
    n1=syndrome de myopathie, cataracte, hypogonadisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=22
  831. ARSI --- r_isa #6: 21 --> en:hereditary disease
    n1=ARSI | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  832. anémie de fanconi --- r_isa #6: 21 --> en:hereditary disease
    n1=anémie de fanconi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  833. en:Aicardi's syndrome --- r_isa #6: 21 --> en:hereditary disease
    n1=en:Aicardi's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  834. en:Cornelia de Lange' syndrome --- r_isa #6: 21 --> en:hereditary disease
    n1=en:Cornelia de Lange' syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  835. en:Danon's disease --- r_isa #6: 21 --> en:hereditary disease
    n1=en:Danon's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  836. en:Herrick's anemia --- r_isa #6: 21 --> en:hereditary disease
    n1=en:Herrick's anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  837. en:Machado-Joseph's disease --- r_isa #6: 21 --> en:hereditary disease
    n1=en:Machado-Joseph's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  838. en:Marfan's disease --- r_isa #6: 21 --> en:hereditary disease
    n1=en:Marfan's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  839. en:Ollier's disease --- r_isa #6: 21 --> en:hereditary disease
    n1=en:Ollier's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  840. en:Rothmund-Thomson's syndrome --- r_isa #6: 21 --> en:hereditary disease
    n1=en:Rothmund-Thomson's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  841. en:WS --- r_isa #6: 21 --> en:hereditary disease
    n1=en:WS | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  842. en:arachnodactily --- r_isa #6: 21 --> en:hereditary disease
    n1=en:arachnodactily | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  843. en:argininosuccinic aciduria --- r_isa #6: 21 --> en:hereditary disease
    n1=en:argininosuccinic aciduria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  844. en:colon malignancy --- r_isa #6: 21 --> en:hereditary disease
    n1=en:colon malignancy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  845. en:diabetes bronze --- r_isa #6: 21 --> en:hereditary disease
    n1=en:diabetes bronze | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  846. en:hirsuties --- r_isa #6: 21 --> en:hereditary disease
    n1=en:hirsuties | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  847. en:hyperprolinemia --- r_isa #6: 21 --> en:hereditary disease
    n1=en:hyperprolinemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  848. en:multiple enchondromatosis --- r_isa #6: 21 --> en:hereditary disease
    n1=en:multiple enchondromatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  849. en:multiple epiphysal dysplasia --- r_isa #6: 21 --> en:hereditary disease
    n1=en:multiple epiphysal dysplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  850. en:myopia --- r_isa #6: 21 --> en:hereditary disease
    n1=en:myopia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  851. en:neurofibromatosis --- r_isa #6: 21 --> en:hereditary disease
    n1=en:neurofibromatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  852. en:neuronal ceroid lipofuscinosis late infantile type --- r_isa #6: 21 --> en:hereditary disease
    n1=en:neuronal ceroid lipofuscinosis late infantile type | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  853. en:progressive ossifying myositis --- r_isa #6: 21 --> en:hereditary disease
    n1=en:progressive ossifying myositis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  854. en:pycnosis --- r_isa #6: 21 --> en:hereditary disease
    n1=en:pycnosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  855. en:pyknodysostosis --- r_isa #6: 21 --> en:hereditary disease
    n1=en:pyknodysostosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  856. en:thalassemia --- r_isa #6: 21 --> en:hereditary disease
    n1=en:thalassemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  857. en:type a 14 --- r_isa #6: 21 --> en:hereditary disease
    n1=en:type a 14 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  858. holoprosencéphalie familiale alobaire de type 1 --- r_isa #6: 21 --> en:hereditary disease
    n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  859. myopathie à axes multiples --- r_isa #6: 21 --> en:hereditary disease
    n1=myopathie à axes multiples | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  860. polydactylie postaxiale avec myopie progressive --- r_isa #6: 21 --> en:hereditary disease
    n1=polydactylie postaxiale avec myopie progressive | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  861. syndrome de dubowitz --- r_isa #6: 21 --> en:hereditary disease
    n1=syndrome de dubowitz | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  862. syndrome de larsen --- r_isa #6: 21 --> en:hereditary disease
    n1=syndrome de larsen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  863. syndrome de zinsser-engman-cole --- r_isa #6: 21 --> en:hereditary disease
    n1=syndrome de zinsser-engman-cole | n2=en:hereditary disease | rel=r_isa | relid=6 | w=21
  864. Anomalie chromosomique --- r_isa #6: 20 --> en:hereditary disease
    n1=Anomalie chromosomique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  865. Coenzyme --- r_isa #6: 20 --> en:hereditary disease
    n1=Coenzyme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  866. Epilepsie --- r_isa #6: 20 --> en:hereditary disease
    n1=Epilepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  867. Génodermatose --- r_isa #6: 20 --> en:hereditary disease
    n1=Génodermatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  868. Hémophilie --- r_isa #6: 20 --> en:hereditary disease
    n1=Hémophilie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  869. Maladie de Danon --- r_isa #6: 20 --> en:hereditary disease
    n1=Maladie de Danon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  870. Maladie lysosomale --- r_isa #6: 20 --> en:hereditary disease
    n1=Maladie lysosomale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  871. Neuropathie optique de Leber --- r_isa #6: 20 --> en:hereditary disease
    n1=Neuropathie optique de Leber | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  872. Rétinoblastome --- r_isa #6: 20 --> en:hereditary disease
    n1=Rétinoblastome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  873. SA
    (spondylarthrite ankylosante)
    --- r_isa #6: 20 --> en:hereditary disease

    n1=SA
    (spondylarthrite ankylosante)
    | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  874. Syndrome de Crigler-Najjar --- r_isa #6: 20 --> en:hereditary disease
    n1=Syndrome de Crigler-Najjar | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  875. Syndrome de Kallmann --- r_isa #6: 20 --> en:hereditary disease
    n1=Syndrome de Kallmann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  876. Syringomyélie --- r_isa #6: 20 --> en:hereditary disease
    n1=Syringomyélie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  877. Thalassémie --- r_isa #6: 20 --> en:hereditary disease
    n1=Thalassémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  878. dégénérescence hépato-lenticulaire --- r_isa #6: 20 --> en:hereditary disease
    n1=dégénérescence hépato-lenticulaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  879. ictère hémolytique congénital type minkowski-chauffard --- r_isa #6: 20 --> en:hereditary disease
    n1=ictère hémolytique congénital type minkowski-chauffard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  880. la maladie de Gilles de La Tourette --- r_isa #6: 20 --> en:hereditary disease
    n1=la maladie de Gilles de La Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  881. syndrome de Tourette --- r_isa #6: 20 --> en:hereditary disease
    n1=syndrome de Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=20
  882. Achille (tendon d') --- r_isa #6: 15 --> en:hereditary disease
    n1=Achille (tendon d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  883. Al-Aqeel-Sewairi (syndrome de) --- r_isa #6: 15 --> en:hereditary disease
    n1=Al-Aqeel-Sewairi (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  884. Albert (position d') --- r_isa #6: 15 --> en:hereditary disease
    n1=Albert (position d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  885. Alvaro-Duncan (cathéter d') --- r_isa #6: 15 --> en:hereditary disease
    n1=Alvaro-Duncan (cathéter d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  886. Alymphocytose --- r_isa #6: 15 --> en:hereditary disease
    n1=Alymphocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  887. CFUV --- r_isa #6: 15 --> en:hereditary disease
    n1=CFUV | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  888. Canalopathie --- r_isa #6: 15 --> en:hereditary disease
    n1=Canalopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  889. Cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse --- r_isa #6: 15 --> en:hereditary disease
    n1=Cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  890. Codman triangle de --- r_isa #6: 15 --> en:hereditary disease
    n1=Codman triangle de | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  891. Dermatite atopique --- r_isa #6: 15 --> en:hereditary disease
    n1=Dermatite atopique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  892. Diabète sucré --- r_isa #6: 15 --> en:hereditary disease
    n1=Diabète sucré | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  893. Diphyllobothrium latum --- r_isa #6: 15 --> en:hereditary disease
    n1=Diphyllobothrium latum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  894. Dravet (syndrome de) --- r_isa #6: 15 --> en:hereditary disease
    n1=Dravet (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  895. ECA2 --- r_isa #6: 15 --> en:hereditary disease
    n1=ECA2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  896. Epilepsy --- r_isa #6: 15 --> en:hereditary disease
    n1=Epilepsy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  897. Gennari (strie de) --- r_isa #6: 15 --> en:hereditary disease
    n1=Gennari (strie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  898. Goître --- r_isa #6: 15 --> en:hereditary disease
    n1=Goître | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  899. Hirst (réaction de) --- r_isa #6: 15 --> en:hereditary disease
    n1=Hirst (réaction de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  900. Hypercholestérolémie familiale --- r_isa #6: 15 --> en:hereditary disease
    n1=Hypercholestérolémie familiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  901. Hyperinsulinisme familial --- r_isa #6: 15 --> en:hereditary disease
    n1=Hyperinsulinisme familial | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  902. Hypophosphatasie --- r_isa #6: 15 --> en:hereditary disease
    n1=Hypophosphatasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  903. Hölmgren (triade de) --- r_isa #6: 15 --> en:hereditary disease
    n1=Hölmgren (triade de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  904. Maladie de Gilles de la Tourette --- r_isa #6: 15 --> en:hereditary disease
    n1=Maladie de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  905. Maladie de Huntington --- r_isa #6: 15 --> en:hereditary disease
    n1=Maladie de Huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  906. Maladie de Marfan --- r_isa #6: 15 --> en:hereditary disease
    n1=Maladie de Marfan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  907. Maladie de Minkowski-Chauffard --- r_isa #6: 15 --> en:hereditary disease
    n1=Maladie de Minkowski-Chauffard | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  908. Maladie de Sly --- r_isa #6: 15 --> en:hereditary disease
    n1=Maladie de Sly | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  909. Myopie --- r_isa #6: 15 --> en:hereditary disease
    n1=Myopie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  910. Polydactylie --- r_isa #6: 15 --> en:hereditary disease
    n1=Polydactylie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  911. Rétinite pigmentaire --- r_isa #6: 15 --> en:hereditary disease
    n1=Rétinite pigmentaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  912. Sphérocytose héréditaire --- r_isa #6: 15 --> en:hereditary disease
    n1=Sphérocytose héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  913. Syndrome d'Ondine --- r_isa #6: 15 --> en:hereditary disease
    n1=Syndrome d'Ondine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  914. Syndrome de Beckwith-Wiedemann --- r_isa #6: 15 --> en:hereditary disease
    n1=Syndrome de Beckwith-Wiedemann | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  915. Syndrome de Cockayne --- r_isa #6: 15 --> en:hereditary disease
    n1=Syndrome de Cockayne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  916. Syndrome de Coffin-Siris --- r_isa #6: 15 --> en:hereditary disease
    n1=Syndrome de Coffin-Siris | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  917. Syndrome de Cornelia de Lange --- r_isa #6: 15 --> en:hereditary disease
    n1=Syndrome de Cornelia de Lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  918. Syndrome de Cowden --- r_isa #6: 15 --> en:hereditary disease
    n1=Syndrome de Cowden | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  919. Syndrome de Gilles de la Tourette --- r_isa #6: 15 --> en:hereditary disease
    n1=Syndrome de Gilles de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  920. Syndrome de Rokitansky-Küster-Hauser --- r_isa #6: 15 --> en:hereditary disease
    n1=Syndrome de Rokitansky-Küster-Hauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  921. Syndrome de Walker-Warburg --- r_isa #6: 15 --> en:hereditary disease
    n1=Syndrome de Walker-Warburg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  922. anomalie cytogénétique --- r_isa #6: 15 --> en:hereditary disease
    n1=anomalie cytogénétique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  923. appareil de Codivilla --- r_isa #6: 15 --> en:hereditary disease
    n1=appareil de Codivilla | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  924. ataxie spastique des Bédouins (syndrome de l') --- r_isa #6: 15 --> en:hereditary disease
    n1=ataxie spastique des Bédouins (syndrome de l') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  925. ataxie spinocérébelleuse type 3 --- r_isa #6: 15 --> en:hereditary disease
    n1=ataxie spinocérébelleuse type 3 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  926. codéhydrase I --- r_isa #6: 15 --> en:hereditary disease
    n1=codéhydrase I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  927. codéine --- r_isa #6: 15 --> en:hereditary disease
    n1=codéine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  928. coenzyme B12 --- r_isa #6: 15 --> en:hereditary disease
    n1=coenzyme B12 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  929. diphyllobothrium latum --- r_isa #6: 15 --> en:hereditary disease
    n1=diphyllobothrium latum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  930. diplobacille de Morax --- r_isa #6: 15 --> en:hereditary disease
    n1=diplobacille de Morax | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  931. diplochromosome --- r_isa #6: 15 --> en:hereditary disease
    n1=diplochromosome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  932. diplocorie --- r_isa #6: 15 --> en:hereditary disease
    n1=diplocorie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  933. dysimmune (neuropathie) --- r_isa #6: 15 --> en:hereditary disease
    n1=dysimmune (neuropathie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  934. démence (sémiologie) --- r_isa #6: 15 --> en:hereditary disease
    n1=démence (sémiologie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  935. en:cat's cry syndrome --- r_isa #6: 15 --> en:hereditary disease
    n1=en:cat's cry syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  936. en:coenzyme --- r_isa #6: 15 --> en:hereditary disease
    n1=en:coenzyme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  937. en:granulomatous enteritis --- r_isa #6: 15 --> en:hereditary disease
    n1=en:granulomatous enteritis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  938. en:hirschsprung disease --- r_isa #6: 15 --> en:hereditary disease
    n1=en:hirschsprung disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  939. en:pendred's syndrome --- r_isa #6: 15 --> en:hereditary disease
    n1=en:pendred's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  940. fibroscopie bronchique (intubation sous) --- r_isa #6: 15 --> en:hereditary disease
    n1=fibroscopie bronchique (intubation sous) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  941. glycogénique (surcharge et infiltration) --- r_isa #6: 15 --> en:hereditary disease
    n1=glycogénique (surcharge et infiltration) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  942. idiopathique (épilepsie) --- r_isa #6: 15 --> en:hereditary disease
    n1=idiopathique (épilepsie) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  943. kallman --- r_isa #6: 15 --> en:hereditary disease
    n1=kallman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  944. syndrome de Gilles de La Tourette --- r_isa #6: 15 --> en:hereditary disease
    n1=syndrome de Gilles de La Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  945. syndrome de Warburg --- r_isa #6: 15 --> en:hereditary disease
    n1=syndrome de Warburg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  946. Érythrodermie ichtyosiforme congénitale bulleuse --- r_isa #6: 15 --> en:hereditary disease
    n1=Érythrodermie ichtyosiforme congénitale bulleuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=15
  947. Aase (syndrome d') --- r_isa #6: 10 --> en:hereditary disease
    n1=Aase (syndrome d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  948. Achondroplasie --- r_isa #6: 10 --> en:hereditary disease
    n1=Achondroplasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  949. Aicardi (syndrome d') --- r_isa #6: 10 --> en:hereditary disease
    n1=Aicardi (syndrome d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  950. Albers-Schönberg (maladie d') --- r_isa #6: 10 --> en:hereditary disease
    n1=Albers-Schönberg (maladie d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  951. Albinisme --- r_isa #6: 10 --> en:hereditary disease
    n1=Albinisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  952. Alzheimer (maladie d') --- r_isa #6: 10 --> en:hereditary disease
    n1=Alzheimer (maladie d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  953. Andermann (syndrome d') --- r_isa #6: 10 --> en:hereditary disease
    n1=Andermann (syndrome d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  954. Angelman (syndrome d') --- r_isa #6: 10 --> en:hereditary disease
    n1=Angelman (syndrome d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  955. Beckwith-Wiedemann (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Beckwith-Wiedemann (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  956. Behçet (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Behçet (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  957. Brachmann-de Lange (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Brachmann-de Lange (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  958. Brugada (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Brugada (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  959. Canavan (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Canavan (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  960. Cancer du côlon --- r_isa #6: 10 --> en:hereditary disease
    n1=Cancer du côlon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  961. Chorée de Huntington --- r_isa #6: 10 --> en:hereditary disease
    n1=Chorée de Huntington | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  962. Christ-Siemens-Touraine (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Christ-Siemens-Touraine (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  963. Cockayne (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Cockayne (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  964. Codéine --- r_isa #6: 10 --> en:hereditary disease
    n1=Codéine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  965. Coffin-Siris (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Coffin-Siris (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  966. Cori (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Cori (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  967. Cornelia de Lange (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Cornelia de Lange (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  968. Cowden (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Cowden (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  969. Crigler-Najjar (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Crigler-Najjar (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  970. Danon (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Danon (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  971. Drummond (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Drummond (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  972. Drépanocytose --- r_isa #6: 10 --> en:hereditary disease
    n1=Drépanocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  973. Dubowitz (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Dubowitz (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  974. Dystrophie musculaire --- r_isa #6: 10 --> en:hereditary disease
    n1=Dystrophie musculaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  975. Dystrophy --- r_isa #6: 10 --> en:hereditary disease
    n1=Dystrophy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  976. Fabry (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Fabry (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  977. Fanconi (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Fanconi (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  978. Fibrose kystique --- r_isa #6: 10 --> en:hereditary disease
    n1=Fibrose kystique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  979. Forbes (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Forbes (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  980. Gaucher (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Gaucher (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  981. Gilbert (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Gilbert (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  982. Gorlin (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Gorlin (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  983. Goutte
    (maladie)
    --- r_isa #6: 10 --> en:hereditary disease

    n1=Goutte
    (maladie)
    | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  984. Greig (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Greig (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  985. Hirschsprung (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Hirschsprung (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  986. Hirsutisme --- r_isa #6: 10 --> en:hereditary disease
    n1=Hirsutisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  987. Hémochromatose --- r_isa #6: 10 --> en:hereditary disease
    n1=Hémochromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  988. Johanson-Blizzard (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Johanson-Blizzard (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  989. Kallman-de Morsier (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Kallman-de Morsier (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  990. Kallmann (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Kallmann (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  991. Kartagener (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Kartagener (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  992. Larsen (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Larsen (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  993. Leucodystrophie --- r_isa #6: 10 --> en:hereditary disease
    n1=Leucodystrophie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  994. Lisfranc (fracture de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Lisfranc (fracture de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  995. Lowe (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Lowe (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  996. Machado-Joseph (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Machado-Joseph (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  997. Maladie d'Illingworth-Cori-Forbes --- r_isa #6: 10 --> en:hereditary disease
    n1=Maladie d'Illingworth-Cori-Forbes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  998. Marfan (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Marfan (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  999. Mayer-Rokitansky-Küster-Hauser (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Mayer-Rokitansky-Küster-Hauser (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1000. Minkowski-Chauffard (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Minkowski-Chauffard (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1001. Morquio (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Morquio (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1002. Mucopolysaccharidose --- r_isa #6: 10 --> en:hereditary disease
    n1=Mucopolysaccharidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1003. Mucoviscidose --- r_isa #6: 10 --> en:hereditary disease
    n1=Mucoviscidose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1004. Myopathie --- r_isa #6: 10 --> en:hereditary disease
    n1=Myopathie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1005. Neurofibromatose --- r_isa #6: 10 --> en:hereditary disease
    n1=Neurofibromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1006. Ollier (maladie d') --- r_isa #6: 10 --> en:hereditary disease
    n1=Ollier (maladie d') | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1007. PUUV --- r_isa #6: 10 --> en:hereditary disease
    n1=PUUV | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1008. Pendred (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Pendred (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1009. Phénylcétonurie --- r_isa #6: 10 --> en:hereditary disease
    n1=Phénylcétonurie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1010. Progéria --- r_isa #6: 10 --> en:hereditary disease
    n1=Progéria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1011. Protée (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Protée (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1012. Pycnodysostose --- r_isa #6: 10 --> en:hereditary disease
    n1=Pycnodysostose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1013. Rathbun (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Rathbun (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1014. Recklinghausen (maladie de von) --- r_isa #6: 10 --> en:hereditary disease
    n1=Recklinghausen (maladie de von) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1015. Recklinghausen (neurofibromatose de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Recklinghausen (neurofibromatose de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1016. Rendu-Osler-Weber (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Rendu-Osler-Weber (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1017. Rokitansky-Küster-Hauser (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Rokitansky-Küster-Hauser (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1018. SA --- r_isa #6: 10 --> en:hereditary disease
    n1=SA | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1019. Saethre-Chotzen (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Saethre-Chotzen (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1020. Sly (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Sly (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1021. Steinert (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Steinert (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1022. Sydenham (chorée de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Sydenham (chorée de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1023. Syndrome de Brugada --- r_isa #6: 10 --> en:hereditary disease
    n1=Syndrome de Brugada | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1024. Syndrome de Kearns-Sayre --- r_isa #6: 10 --> en:hereditary disease
    n1=Syndrome de Kearns-Sayre | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1025. Syndrome de Lowe --- r_isa #6: 10 --> en:hereditary disease
    n1=Syndrome de Lowe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1026. Syndrome de Protée --- r_isa #6: 10 --> en:hereditary disease
    n1=Syndrome de Protée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1027. Syndrome de Rothmund-Thomson --- r_isa #6: 10 --> en:hereditary disease
    n1=Syndrome de Rothmund-Thomson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1028. Syndrome de Simpson-Golabi-Behmel --- r_isa #6: 10 --> en:hereditary disease
    n1=Syndrome de Simpson-Golabi-Behmel | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1029. Syndrome de Williams --- r_isa #6: 10 --> en:hereditary disease
    n1=Syndrome de Williams | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1030. Syndrome de l'X fragile --- r_isa #6: 10 --> en:hereditary disease
    n1=Syndrome de l'X fragile | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1031. Syndrome de la Tourette --- r_isa #6: 10 --> en:hereditary disease
    n1=Syndrome de la Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1032. Tay-Sachs (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Tay-Sachs (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1033. Vitiligo --- r_isa #6: 10 --> en:hereditary disease
    n1=Vitiligo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1034. Walker-Warburg (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Walker-Warburg (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1035. Westphal (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Westphal (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1036. Williams (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Williams (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1037. Wilson (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=Wilson (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1038. aberration chromosomique --- r_isa #6: 10 --> en:hereditary disease
    n1=aberration chromosomique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1039. adrénoleucodystrophie de l'enfant --- r_isa #6: 10 --> en:hereditary disease
    n1=adrénoleucodystrophie de l'enfant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1040. angl : MED --- r_isa #6: 10 --> en:hereditary disease
    n1=angl : MED | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1041. anémie réfractaire sidéroblastique idiopathique --- r_isa #6: 10 --> en:hereditary disease
    n1=anémie réfractaire sidéroblastique idiopathique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1042. anémie sidéroachrestique --- r_isa #6: 10 --> en:hereditary disease
    n1=anémie sidéroachrestique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1043. anémie sidéroachrestique idiopathique --- r_isa #6: 10 --> en:hereditary disease
    n1=anémie sidéroachrestique idiopathique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1044. ataxie-télangiectasie héréditaire --- r_isa #6: 10 --> en:hereditary disease
    n1=ataxie-télangiectasie héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1045. cancer du colon --- r_isa #6: 10 --> en:hereditary disease
    n1=cancer du colon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1046. cardiomégalie glycogénique --- r_isa #6: 10 --> en:hereditary disease
    n1=cardiomégalie glycogénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1047. chorde --- r_isa #6: 10 --> en:hereditary disease
    n1=chorde | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1048. chordome --- r_isa #6: 10 --> en:hereditary disease
    n1=chordome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1049. chordomésoblaste --- r_isa #6: 10 --> en:hereditary disease
    n1=chordomésoblaste | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1050. chorio-amniotite --- r_isa #6: 10 --> en:hereditary disease
    n1=chorio-amniotite | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1051. chorio-angiome --- r_isa #6: 10 --> en:hereditary disease
    n1=chorio-angiome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1052. chorio-épithéliome --- r_isa #6: 10 --> en:hereditary disease
    n1=chorio-épithéliome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1053. choriocapillaire --- r_isa #6: 10 --> en:hereditary disease
    n1=choriocapillaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1054. choriocarcinome germinal tératomateux du médiastin --- r_isa #6: 10 --> en:hereditary disease
    n1=choriocarcinome germinal tératomateux du médiastin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1055. choriocarcinome placentaire --- r_isa #6: 10 --> en:hereditary disease
    n1=choriocarcinome placentaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1056. choriocarcinome primitif du col utérin --- r_isa #6: 10 --> en:hereditary disease
    n1=choriocarcinome primitif du col utérin | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1057. choriogonadotrophine --- r_isa #6: 10 --> en:hereditary disease
    n1=choriogonadotrophine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1058. chorioméningite lymphocytaire --- r_isa #6: 10 --> en:hereditary disease
    n1=chorioméningite lymphocytaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1059. codéshydrogénase --- r_isa #6: 10 --> en:hereditary disease
    n1=codéshydrogénase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1060. coenzyme A --- r_isa #6: 10 --> en:hereditary disease
    n1=coenzyme A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1061. coenzyme Q10 --- r_isa #6: 10 --> en:hereditary disease
    n1=coenzyme Q10 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1062. cofacteur --- r_isa #6: 10 --> en:hereditary disease
    n1=cofacteur | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1063. cofacteur à molybdène --- r_isa #6: 10 --> en:hereditary disease
    n1=cofacteur à molybdène | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1064. cofacteur à molybdène (déficit en) --- r_isa #6: 10 --> en:hereditary disease
    n1=cofacteur à molybdène (déficit en) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1065. cri du chat (maladie du) --- r_isa #6: 10 --> en:hereditary disease
    n1=cri du chat (maladie du) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1066. danse de Saint Guy --- r_isa #6: 10 --> en:hereditary disease
    n1=danse de Saint Guy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1067. de Morsier (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=de Morsier (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1068. de Morsier-Kallmann (syndrome de) --- r_isa #6: 10 --> en:hereditary disease
    n1=de Morsier-Kallmann (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1069. diabète insulinodépendant --- r_isa #6: 10 --> en:hereditary disease
    n1=diabète insulinodépendant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1070. diabète lipoatrophique congénital --- r_isa #6: 10 --> en:hereditary disease
    n1=diabète lipoatrophique congénital | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1071. diabète non-insulinodépendant --- r_isa #6: 10 --> en:hereditary disease
    n1=diabète non-insulinodépendant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1072. diabète phosphaté --- r_isa #6: 10 --> en:hereditary disease
    n1=diabète phosphaté | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1073. diabète post-transplantation --- r_isa #6: 10 --> en:hereditary disease
    n1=diabète post-transplantation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1074. diabète rénal --- r_isa #6: 10 --> en:hereditary disease
    n1=diabète rénal | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1075. diabète sucré de type 2 avec surdité --- r_isa #6: 10 --> en:hereditary disease
    n1=diabète sucré de type 2 avec surdité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1076. diabète sucré et complications rénales --- r_isa #6: 10 --> en:hereditary disease
    n1=diabète sucré et complications rénales | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1077. diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale --- r_isa #6: 10 --> en:hereditary disease
    n1=diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1078. diabètes monogéniques --- r_isa #6: 10 --> en:hereditary disease
    n1=diabètes monogéniques | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1079. diabètes sucrés et insipides avec atrophie optique et surdité --- r_isa #6: 10 --> en:hereditary disease
    n1=diabètes sucrés et insipides avec atrophie optique et surdité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1080. diabétide génitale --- r_isa #6: 10 --> en:hereditary disease
    n1=diabétide génitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1081. diphtamide --- r_isa #6: 10 --> en:hereditary disease
    n1=diphtamide | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1082. diphtérie --- r_isa #6: 10 --> en:hereditary disease
    n1=diphtérie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1083. diphtérie cutanée --- r_isa #6: 10 --> en:hereditary disease
    n1=diphtérie cutanée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1084. diphtéroïde --- r_isa #6: 10 --> en:hereditary disease
    n1=diphtéroïde | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1085. diplacousie --- r_isa #6: 10 --> en:hereditary disease
    n1=diplacousie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1086. diplobacille --- r_isa #6: 10 --> en:hereditary disease
    n1=diplobacille | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1087. diploblastique --- r_isa #6: 10 --> en:hereditary disease
    n1=diploblastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1088. diplocardie --- r_isa #6: 10 --> en:hereditary disease
    n1=diplocardie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1089. diplocéphalie --- r_isa #6: 10 --> en:hereditary disease
    n1=diplocéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1090. diplogamète --- r_isa #6: 10 --> en:hereditary disease
    n1=diplogamète | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1091. diploë --- r_isa #6: 10 --> en:hereditary disease
    n1=diploë | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1092. diplégie --- r_isa #6: 10 --> en:hereditary disease
    n1=diplégie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1093. diplégie faciale --- r_isa #6: 10 --> en:hereditary disease
    n1=diplégie faciale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1094. diplégie faciale congénitale --- r_isa #6: 10 --> en:hereditary disease
    n1=diplégie faciale congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1095. diplégie laryngée --- r_isa #6: 10 --> en:hereditary disease
    n1=diplégie laryngée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1096. diplégie spastique de type infantile --- r_isa #6: 10 --> en:hereditary disease
    n1=diplégie spastique de type infantile | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1097. dyskératose congénitale de Zinsser-Cole-Engman --- r_isa #6: 10 --> en:hereditary disease
    n1=dyskératose congénitale de Zinsser-Cole-Engman | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1098. dysplasie ectodermique anhidrotique --- r_isa #6: 10 --> en:hereditary disease
    n1=dysplasie ectodermique anhidrotique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1099. dysplasie septo-optique --- r_isa #6: 10 --> en:hereditary disease
    n1=dysplasie septo-optique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1100. dystrophie myotonique --- r_isa #6: 10 --> en:hereditary disease
    n1=dystrophie myotonique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1101. en:Achillis tendo --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Achillis tendo | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1102. en:Albert's position --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Albert's position | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1103. en:Alvaro-Duncan's catheter --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Alvaro-Duncan's catheter | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1104. en:Alzheimer disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Alzheimer disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1105. en:Behçet's aphthae --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Behçet's aphthae | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1106. en:Bessel-Hagen's disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Bessel-Hagen's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1107. en:Brocq's bullous erythroderma ichthyosiformis congenita --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Brocq's bullous erythroderma ichthyosiformis congenita | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1108. en:CF --- r_isa #6: 10 --> en:hereditary disease
    n1=en:CF | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1109. en:Chopart's amputation --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Chopart's amputation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1110. en:Chotzen's syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Chotzen's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1111. en:Codivilla's lengthening apparatus --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Codivilla's lengthening apparatus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1112. en:Crohn's disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Crohn's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1113. en:Diphyllobothrium latum --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Diphyllobothrium latum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1114. en:Fanconi's anemia --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Fanconi's anemia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1115. en:Gaucher's disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Gaucher's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1116. en:Gennari'stripe --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Gennari'stripe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1117. en:Huntington's chorea --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Huntington's chorea | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1118. en:NAD + --- r_isa #6: 10 --> en:hereditary disease
    n1=en:NAD + | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1119. en:Saethre-Chotzen's syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Saethre-Chotzen's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1120. en:Sanfilippo's disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Sanfilippo's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1121. en:Sly's syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Sly's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1122. en:Tay-Sachs disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:Tay-Sachs disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1123. en:abdominal wall aplasia --- r_isa #6: 10 --> en:hereditary disease
    n1=en:abdominal wall aplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1124. en:aicardi's syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:aicardi's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1125. en:alzheimer's --- r_isa #6: 10 --> en:hereditary disease
    n1=en:alzheimer's | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1126. en:bedouin spastic ataxia syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:bedouin spastic ataxia syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1127. en:behçet's disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:behçet's disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1128. en:chromosomal disorder --- r_isa #6: 10 --> en:hereditary disease
    n1=en:chromosomal disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1129. en:codeine --- r_isa #6: 10 --> en:hereditary disease
    n1=en:codeine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1130. en:congenita lamellaris ichtyosis --- r_isa #6: 10 --> en:hereditary disease
    n1=en:congenita lamellaris ichtyosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1131. en:congenital cataract and hypogonadisme --- r_isa #6: 10 --> en:hereditary disease
    n1=en:congenital cataract and hypogonadisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1132. en:cowden disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:cowden disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1133. en:de Morsier-Kallman?s syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:de Morsier-Kallman?s syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1134. en:diabetic strokes --- r_isa #6: 10 --> en:hereditary disease
    n1=en:diabetic strokes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1135. en:diphyllobothrium latum --- r_isa #6: 10 --> en:hereditary disease
    n1=en:diphyllobothrium latum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1136. en:diplocoria --- r_isa #6: 10 --> en:hereditary disease
    n1=en:diplocoria | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1137. en:dwarfishness --- r_isa #6: 10 --> en:hereditary disease
    n1=en:dwarfishness | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1138. en:dysimmune neuropathy --- r_isa #6: 10 --> en:hereditary disease
    n1=en:dysimmune neuropathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1139. en:encephalopathy with intracranial calcification --- r_isa #6: 10 --> en:hereditary disease
    n1=en:encephalopathy with intracranial calcification | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1140. en:endocrine disorder --- r_isa #6: 10 --> en:hereditary disease
    n1=en:endocrine disorder | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1141. en:facioscapulohumeral --- r_isa #6: 10 --> en:hereditary disease
    n1=en:facioscapulohumeral | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1142. en:gaucher disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:gaucher disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1143. en:glycogen storage disease type ii --- r_isa #6: 10 --> en:hereditary disease
    n1=en:glycogen storage disease type ii | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1144. en:grey platelet syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:grey platelet syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1145. en:growth hormone deficiency --- r_isa #6: 10 --> en:hereditary disease
    n1=en:growth hormone deficiency | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1146. en:hepatolenticular degeneration --- r_isa #6: 10 --> en:hereditary disease
    n1=en:hepatolenticular degeneration | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1147. en:hereditary multiple ossifying ecchondromata --- r_isa #6: 10 --> en:hereditary disease
    n1=en:hereditary multiple ossifying ecchondromata | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1148. en:hyperprolinemia. --- r_isa #6: 10 --> en:hereditary disease
    n1=en:hyperprolinemia. | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1149. en:idiopathic epilepsy --- r_isa #6: 10 --> en:hereditary disease
    n1=en:idiopathic epilepsy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1150. en:intubation with bronchial fibroscopy --- r_isa #6: 10 --> en:hereditary disease
    n1=en:intubation with bronchial fibroscopy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1151. en:kallman's syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:kallman's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1152. en:lazy leukocyte syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:lazy leukocyte syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1153. en:luxuriant exostosis --- r_isa #6: 10 --> en:hereditary disease
    n1=en:luxuriant exostosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1154. en:marble bone disease --- r_isa #6: 10 --> en:hereditary disease
    n1=en:marble bone disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1155. en:mental deficiency --- r_isa #6: 10 --> en:hereditary disease
    n1=en:mental deficiency | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1156. en:methylmorphine --- r_isa #6: 10 --> en:hereditary disease
    n1=en:methylmorphine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1157. en:microplasia --- r_isa #6: 10 --> en:hereditary disease
    n1=en:microplasia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1158. en:minimal pigment type --- r_isa #6: 10 --> en:hereditary disease
    n1=en:minimal pigment type | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1159. en:mucopolysaccharidosis iv --- r_isa #6: 10 --> en:hereditary disease
    n1=en:mucopolysaccharidosis iv | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1160. en:mucopolysaccharidosis type III --- r_isa #6: 10 --> en:hereditary disease
    n1=en:mucopolysaccharidosis type III | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1161. en:multiple core myopathy --- r_isa #6: 10 --> en:hereditary disease
    n1=en:multiple core myopathy | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1162. en:multiple hamartoma syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:multiple hamartoma syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1163. en:naevoid basal cell carcinoma syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:naevoid basal cell carcinoma syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1164. en:nanosoma --- r_isa #6: 10 --> en:hereditary disease
    n1=en:nanosoma | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1165. en:nanosomia --- r_isa #6: 10 --> en:hereditary disease
    n1=en:nanosomia | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1166. en:nanosomus --- r_isa #6: 10 --> en:hereditary disease
    n1=en:nanosomus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1167. en:near-sightedness --- r_isa #6: 10 --> en:hereditary disease
    n1=en:near-sightedness | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1168. en:neurofibromatosis type II --- r_isa #6: 10 --> en:hereditary disease
    n1=en:neurofibromatosis type II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1169. en:nevoid basal cell carcinoma syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:nevoid basal cell carcinoma syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1170. en:pancytopenia with congenital defects --- r_isa #6: 10 --> en:hereditary disease
    n1=en:pancytopenia with congenital defects | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1171. en:peutz-jeghers syndrome --- r_isa #6: 10 --> en:hereditary disease
    n1=en:peutz-jeghers syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1172. en:phakomatosis --- r_isa #6: 10 --> en:hereditary disease
    n1=en:phakomatosis | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1173. en:polydactylism --- r_isa #6: 10 --> en:hereditary disease
    n1=en:polydactylism | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1174. en:tendo calcaneus --- r_isa #6: 10 --> en:hereditary disease
    n1=en:tendo calcaneus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1175. en:type 1A --- r_isa #6: 10 --> en:hereditary disease
    n1=en:type 1A | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1176. fibrose kystique du pancréas --- r_isa #6: 10 --> en:hereditary disease
    n1=fibrose kystique du pancréas | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1177. glycogénose de type iii --- r_isa #6: 10 --> en:hereditary disease
    n1=glycogénose de type iii | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1178. hyperprolinémie de type I --- r_isa #6: 10 --> en:hereditary disease
    n1=hyperprolinémie de type I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1179. maladie de Behcet --- r_isa #6: 10 --> en:hereditary disease
    n1=maladie de Behcet | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1180. maladie de Bowen --- r_isa #6: 10 --> en:hereditary disease
    n1=maladie de Bowen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1181. maladie de Derry --- r_isa #6: 10 --> en:hereditary disease
    n1=maladie de Derry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1182. maladie de Forbe --- r_isa #6: 10 --> en:hereditary disease
    n1=maladie de Forbe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1183. maladie de Gilles de La Tourette --- r_isa #6: 10 --> en:hereditary disease
    n1=maladie de Gilles de La Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1184. maladie de Moeller-Barlow (maladie de) --- r_isa #6: 10 --> en:hereditary disease
    n1=maladie de Moeller-Barlow (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1185. maladie de Tay-sachs --- r_isa #6: 10 --> en:hereditary disease
    n1=maladie de Tay-sachs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1186. microgéodes phalangiennes (syndrome des) --- r_isa #6: 10 --> en:hereditary disease
    n1=microgéodes phalangiennes (syndrome des) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1187. micromélie rhizomélique --- r_isa #6: 10 --> en:hereditary disease
    n1=micromélie rhizomélique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1188. mongolisme --- r_isa #6: 10 --> en:hereditary disease
    n1=mongolisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1189. myopathe (anesthésie d'un) --- r_isa #6: 10 --> en:hereditary disease
    n1=myopathe (anesthésie d'un) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1190. myotonie atrophique --- r_isa #6: 10 --> en:hereditary disease
    n1=myotonie atrophique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1191. méthylmorphine --- r_isa #6: 10 --> en:hereditary disease
    n1=méthylmorphine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1192. nanisme en tête d'oiseau --- r_isa #6: 10 --> en:hereditary disease
    n1=nanisme en tête d'oiseau | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1193. neurofibromatose de Recklinghausen --- r_isa #6: 10 --> en:hereditary disease
    n1=neurofibromatose de Recklinghausen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1194. nicotinamide-adénine-dinucléotide --- r_isa #6: 10 --> en:hereditary disease
    n1=nicotinamide-adénine-dinucléotide | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1195. opération de Codivilla --- r_isa #6: 10 --> en:hereditary disease
    n1=opération de Codivilla | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1196. otodentaire (syndrome) --- r_isa #6: 10 --> en:hereditary disease
    n1=otodentaire (syndrome) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1197. pelvispondylite rhumatismale --- r_isa #6: 10 --> en:hereditary disease
    n1=pelvispondylite rhumatismale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1198. profondeur de l'anesthésie (stade de) --- r_isa #6: 10 --> en:hereditary disease
    n1=profondeur de l'anesthésie (stade de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1199. pseudothalidomide (syndrome) --- r_isa #6: 10 --> en:hereditary disease
    n1=pseudothalidomide (syndrome) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1200. situs inversus --- r_isa #6: 10 --> en:hereditary disease
    n1=situs inversus | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1201. spondylite rhumatismale --- r_isa #6: 10 --> en:hereditary disease
    n1=spondylite rhumatismale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1202. syndrome d'Andersen --- r_isa #6: 10 --> en:hereditary disease
    n1=syndrome d'Andersen | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1203. syndrome de Coffin-Lowry --- r_isa #6: 10 --> en:hereditary disease
    n1=syndrome de Coffin-Lowry | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1204. syndrome de Cornelia De Lange --- r_isa #6: 10 --> en:hereditary disease
    n1=syndrome de Cornelia De Lange | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1205. syndrome de Laurence-Moon --- r_isa #6: 10 --> en:hereditary disease
    n1=syndrome de Laurence-Moon | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1206. syndrome de Neill-Dingwall --- r_isa #6: 10 --> en:hereditary disease
    n1=syndrome de Neill-Dingwall | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1207. syndrome de Ruiter-Pompen-Wyers --- r_isa #6: 10 --> en:hereditary disease
    n1=syndrome de Ruiter-Pompen-Wyers | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1208. syndrome de diplégie brachiale --- r_isa #6: 10 --> en:hereditary disease
    n1=syndrome de diplégie brachiale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1209. syndrome du cil immobile --- r_isa #6: 10 --> en:hereditary disease
    n1=syndrome du cil immobile | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1210. syndrome hétérotaxique --- r_isa #6: 10 --> en:hereditary disease
    n1=syndrome hétérotaxique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1211. thalamique (syndrome) --- r_isa #6: 10 --> en:hereditary disease
    n1=thalamique (syndrome) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1212. trichomégalie-cataracte-sphérocytose --- r_isa #6: 10 --> en:hereditary disease
    n1=trichomégalie-cataracte-sphérocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1213. vitesse circulatoire (mesure de la) --- r_isa #6: 10 --> en:hereditary disease
    n1=vitesse circulatoire (mesure de la) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1214. xanthique (lithiase) --- r_isa #6: 10 --> en:hereditary disease
    n1=xanthique (lithiase) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1215. élastorrhexie systématisée --- r_isa #6: 10 --> en:hereditary disease
    n1=élastorrhexie systématisée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=10
  1216. Bessel-Hagen (maladie de) --- r_isa #6: 5 --> en:hereditary disease
    n1=Bessel-Hagen (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1217. CRAP --- r_isa #6: 5 --> en:hereditary disease
    n1=CRAP | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1218. Codivilla (appareil de) --- r_isa #6: 5 --> en:hereditary disease
    n1=Codivilla (appareil de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1219. Gusberg et Kaplan (classification de) --- r_isa #6: 5 --> en:hereditary disease
    n1=Gusberg et Kaplan (classification de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1220. Nance-Horan syndrome de --- r_isa #6: 5 --> en:hereditary disease
    n1=Nance-Horan syndrome de | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1221. Peutz-Jeghers (syndrome de) --- r_isa #6: 5 --> en:hereditary disease
    n1=Peutz-Jeghers (syndrome de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1222. Sanfilippo (maladie de) --- r_isa #6: 5 --> en:hereditary disease
    n1=Sanfilippo (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1223. Syndrome de Tourette --- r_isa #6: 5 --> en:hereditary disease
    n1=Syndrome de Tourette | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1224. Thalassémie alpha --- r_isa #6: 5 --> en:hereditary disease
    n1=Thalassémie alpha | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1225. achillodynie --- r_isa #6: 5 --> en:hereditary disease
    n1=achillodynie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1226. achlorhydrie --- r_isa #6: 5 --> en:hereditary disease
    n1=achlorhydrie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1227. achondrogénèses --- r_isa #6: 5 --> en:hereditary disease
    n1=achondrogénèses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1228. achondroplase --- r_isa #6: 5 --> en:hereditary disease
    n1=achondroplase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1229. acidoses lactiques (classification selon Cohen et Woods) --- r_isa #6: 5 --> en:hereditary disease
    n1=acidoses lactiques (classification selon Cohen et Woods) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1230. ala hama --- r_isa #6: 5 --> en:hereditary disease
    n1=ala hama | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1231. alacrymie --- r_isa #6: 5 --> en:hereditary disease
    n1=alacrymie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1232. alacrymie congénitale --- r_isa #6: 5 --> en:hereditary disease
    n1=alacrymie congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1233. albinisme avec immunodéficience et troubles hématologiques --- r_isa #6: 5 --> en:hereditary disease
    n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1234. albinisme avec surdité --- r_isa #6: 5 --> en:hereditary disease
    n1=albinisme avec surdité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1235. alvéole dentale --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéole dentale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1236. alvéole pulmonaire --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéole pulmonaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1237. alvéoles de la mandibule --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéoles de la mandibule | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1238. alvéoles dentaires --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéoles dentaires | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1239. alvéoles du maxillaire --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéoles du maxillaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1240. alvéolite allergique extrinsèque --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéolite allergique extrinsèque | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1241. alvéolite lipoprotéique --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéolite lipoprotéique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1242. alvéolite luminale --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéolite luminale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1243. alvéolite murale --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéolite murale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1244. alvéolite pulmonaire --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéolite pulmonaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1245. alvéologramme aérien --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéologramme aérien | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1246. alvéolyse --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéolyse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1247. alvéus de l'hippocampe --- r_isa #6: 5 --> en:hereditary disease
    n1=alvéus de l'hippocampe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1248. ataxie spastique, de type Charlevoix-Saguenay --- r_isa #6: 5 --> en:hereditary disease
    n1=ataxie spastique, de type Charlevoix-Saguenay | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1249. ataxie spinale héréditaire --- r_isa #6: 5 --> en:hereditary disease
    n1=ataxie spinale héréditaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1250. ataxie spinocérébeelleuse --- r_isa #6: 5 --> en:hereditary disease
    n1=ataxie spinocérébeelleuse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1251. ataxie spinocérébelleuse avec cécité et surdité --- r_isa #6: 5 --> en:hereditary disease
    n1=ataxie spinocérébelleuse avec cécité et surdité | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1252. ataxie spinocérébelleuse et dysmorphie craniofaciale --- r_isa #6: 5 --> en:hereditary disease
    n1=ataxie spinocérébelleuse et dysmorphie craniofaciale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1253. ataxie spinocérébelleuse type 1 --- r_isa #6: 5 --> en:hereditary disease
    n1=ataxie spinocérébelleuse type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1254. chorial, ale --- r_isa #6: 5 --> en:hereditary disease
    n1=chorial, ale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1255. chorio-adénome destruens --- r_isa #6: 5 --> en:hereditary disease
    n1=chorio-adénome destruens | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1256. chorée fibrillaire de Morvan --- r_isa #6: 5 --> en:hereditary disease
    n1=chorée fibrillaire de Morvan | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1257. chorée gravidique --- r_isa #6: 5 --> en:hereditary disease
    n1=chorée gravidique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1258. choréo-acanthocytose --- r_isa #6: 5 --> en:hereditary disease
    n1=choréo-acanthocytose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1259. codéïne --- r_isa #6: 5 --> en:hereditary disease
    n1=codéïne | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1260. coefficient kappa (?) --- r_isa #6: 5 --> en:hereditary disease
    n1=coefficient kappa (?) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1261. diabète de type 1 --- r_isa #6: 5 --> en:hereditary disease
    n1=diabète de type 1 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1262. diabète de type 2 --- r_isa #6: 5 --> en:hereditary disease
    n1=diabète de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1263. diabète et psychisme --- r_isa #6: 5 --> en:hereditary disease
    n1=diabète et psychisme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1264. diabète et surdité d'origine mitochondriale --- r_isa #6: 5 --> en:hereditary disease
    n1=diabète et surdité d'origine mitochondriale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1265. diabète gestationnel --- r_isa #6: 5 --> en:hereditary disease
    n1=diabète gestationnel | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1266. diabète gras --- r_isa #6: 5 --> en:hereditary disease
    n1=diabète gras | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1267. diabète insipide --- r_isa #6: 5 --> en:hereditary disease
    n1=diabète insipide | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1268. diabète insipide néphrogénique --- r_isa #6: 5 --> en:hereditary disease
    n1=diabète insipide néphrogénique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1269. diabète insulino-requérant --- r_isa #6: 5 --> en:hereditary disease
    n1=diabète insulino-requérant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1270. dyskaliémie --- r_isa #6: 5 --> en:hereditary disease
    n1=dyskaliémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1271. dyskèle --- r_isa #6: 5 --> en:hereditary disease
    n1=dyskèle | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1272. dyskératome verruqueux --- r_isa #6: 5 --> en:hereditary disease
    n1=dyskératome verruqueux | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1273. dyskératose --- r_isa #6: 5 --> en:hereditary disease
    n1=dyskératose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1274. dyskératose acantholytique focale --- r_isa #6: 5 --> en:hereditary disease
    n1=dyskératose acantholytique focale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1275. dyskératose bénigne héréditaire intraépithéliale --- r_isa #6: 5 --> en:hereditary disease
    n1=dyskératose bénigne héréditaire intraépithéliale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1276. dyskératose héréditaire bénigne intraépithéliale --- r_isa #6: 5 --> en:hereditary disease
    n1=dyskératose héréditaire bénigne intraépithéliale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1277. en:Cole's syndrome --- r_isa #6: 5 --> en:hereditary disease
    n1=en:Cole's syndrome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1278. enzyme de conversion de l?angiotensine de type 2 --- r_isa #6: 5 --> en:hereditary disease
    n1=enzyme de conversion de l?angiotensine de type 2 | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1279. enzyme de défilement --- r_isa #6: 5 --> en:hereditary disease
    n1=enzyme de défilement | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1280. enzyme de restriction --- r_isa #6: 5 --> en:hereditary disease
    n1=enzyme de restriction | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1281. enzyme lysosomale --- r_isa #6: 5 --> en:hereditary disease
    n1=enzyme lysosomale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1282. enzyme pancréatique --- r_isa #6: 5 --> en:hereditary disease
    n1=enzyme pancréatique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1283. enzymes cardiaques --- r_isa #6: 5 --> en:hereditary disease
    n1=enzymes cardiaques | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1284. fibrose avec rétraction isolée du droit inférieur --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose avec rétraction isolée du droit inférieur | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1285. fibrose cardiaque du nourrisson --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose cardiaque du nourrisson | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1286. fibrose cervico-faciale --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose cervico-faciale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1287. fibrose cervicocéphalique --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose cervicocéphalique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1288. fibrose congénitale des muscles oculaires extrinsèques --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose congénitale des muscles oculaires extrinsèques | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1289. fibrose cutanée --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose cutanée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1290. fibrose du quadriceps --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose du quadriceps | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1291. fibrose généralisée des muscles oculomoteurs --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose généralisée des muscles oculomoteurs | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1292. fibrose hépatique --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose hépatique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1293. fibrose hépatique congénitale --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose hépatique congénitale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1294. fibrose hépatique-rein polykystique-colobome --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose hépatique-rein polykystique-colobome | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1295. fibrose élastigène --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose élastigène | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1296. fibrose élastique --- r_isa #6: 5 --> en:hereditary disease
    n1=fibrose élastique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1297. glycogénogénèse --- r_isa #6: 5 --> en:hereditary disease
    n1=glycogénogénèse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1298. glycogénolyse --- r_isa #6: 5 --> en:hereditary disease
    n1=glycogénolyse | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1299. glycogénose --- r_isa #6: 5 --> en:hereditary disease
    n1=glycogénose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1300. glycogénose de type I --- r_isa #6: 5 --> en:hereditary disease
    n1=glycogénose de type I | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1301. glycogénose de type II --- r_isa #6: 5 --> en:hereditary disease
    n1=glycogénose de type II | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1302. génochondromatose --- r_isa #6: 5 --> en:hereditary disease
    n1=génochondromatose | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1303. holocentromère --- r_isa #6: 5 --> en:hereditary disease
    n1=holocentromère | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1304. holocentromérique --- r_isa #6: 5 --> en:hereditary disease
    n1=holocentromérique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1305. holocrine --- r_isa #6: 5 --> en:hereditary disease
    n1=holocrine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1306. holodiastolique --- r_isa #6: 5 --> en:hereditary disease
    n1=holodiastolique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1307. holoenzyme --- r_isa #6: 5 --> en:hereditary disease
    n1=holoenzyme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1308. hologamie --- r_isa #6: 5 --> en:hereditary disease
    n1=hologamie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1309. hologynique --- r_isa #6: 5 --> en:hereditary disease
    n1=hologynique | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1310. holomérocrine --- r_isa #6: 5 --> en:hereditary disease
    n1=holomérocrine | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1311. holophrase --- r_isa #6: 5 --> en:hereditary disease
    n1=holophrase | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1312. holoproencéphalie --- r_isa #6: 5 --> en:hereditary disease
    n1=holoproencéphalie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1313. idiot savant --- r_isa #6: 5 --> en:hereditary disease
    n1=idiot savant | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1314. leucocyte polymorphe --- r_isa #6: 5 --> en:hereditary disease
    n1=leucocyte polymorphe | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1315. leucocyte polynucléaire --- r_isa #6: 5 --> en:hereditary disease
    n1=leucocyte polynucléaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1316. leucocytoclasie --- r_isa #6: 5 --> en:hereditary disease
    n1=leucocytoclasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1317. leucocytopénie --- r_isa #6: 5 --> en:hereditary disease
    n1=leucocytopénie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1318. leucocyturie --- r_isa #6: 5 --> en:hereditary disease
    n1=leucocyturie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1319. leucoderma acquisitum centrifugum --- r_isa #6: 5 --> en:hereditary disease
    n1=leucoderma acquisitum centrifugum | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1320. leucodermie --- r_isa #6: 5 --> en:hereditary disease
    n1=leucodermie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1321. leucodermie lenticulaire disséminée de Argüelles-Casals --- r_isa #6: 5 --> en:hereditary disease
    n1=leucodermie lenticulaire disséminée de Argüelles-Casals | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1322. leucodysplasie --- r_isa #6: 5 --> en:hereditary disease
    n1=leucodysplasie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1323. nanisme avec sixième doigt --- r_isa #6: 5 --> en:hereditary disease
    n1=nanisme avec sixième doigt | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1324. pycnolepsie --- r_isa #6: 5 --> en:hereditary disease
    n1=pycnolepsie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1325. syndrome de Al-Aqeel-Sewairi --- r_isa #6: 5 --> en:hereditary disease
    n1=syndrome de Al-Aqeel-Sewairi | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1326. syndrome de Dravet --- r_isa #6: 5 --> en:hereditary disease
    n1=syndrome de Dravet | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1327. syndrome de Jadassohn-Lewandowsky --- r_isa #6: 5 --> en:hereditary disease
    n1=syndrome de Jadassohn-Lewandowsky | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1328. syndrome de Kaposi-Juliusberg --- r_isa #6: 5 --> en:hereditary disease
    n1=syndrome de Kaposi-Juliusberg | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1329. syndrome de Kawasaki --- r_isa #6: 5 --> en:hereditary disease
    n1=syndrome de Kawasaki | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1330. syndrome de syndrome de Joubert-Boltshauser --- r_isa #6: 5 --> en:hereditary disease
    n1=syndrome de syndrome de Joubert-Boltshauser | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1331. von Recklinghausen (maladie de) --- r_isa #6: 5 --> en:hereditary disease
    n1=von Recklinghausen (maladie de) | n2=en:hereditary disease | rel=r_isa | relid=6 | w=5
  1332. Anémie falciforme --- r_isa #6: -5 --> en:hereditary disease
    n1=Anémie falciforme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-5
  1333. chorde dorsale --- r_isa #6: -10 --> en:hereditary disease
    n1=chorde dorsale | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-10
  1334. en:taste perception --- r_isa #6: -41 --> en:hereditary disease
    n1=en:taste perception | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-41
  1335. gustation --- r_isa #6: -41 --> en:hereditary disease
    n1=gustation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-41
  1336. gout --- r_isa #6: -46 --> en:hereditary disease
    n1=gout | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-46
  1337. en:gustation --- r_isa #6: -50 --> en:hereditary disease
    n1=en:gustation | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-50
  1338. anémie drépanocytaire --- r_isa #6: -122 --> en:hereditary disease
    n1=anémie drépanocytaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-122
  1339. drépanocytoses --- r_isa #6: -139 --> en:hereditary disease
    n1=drépanocytoses | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-139
  1340. sicklanémie --- r_isa #6: -189 --> en:hereditary disease
    n1=sicklanémie | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-189
  1341. anémie à cellules falciformes --- r_isa #6: -198 --> en:hereditary disease
    n1=anémie à cellules falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-198
  1342. anémie drépanocytaire non précisée --- r_isa #6: -201 --> en:hereditary disease
    n1=anémie drépanocytaire non précisée | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-201
  1343. en:anemia, sickle cell --- r_isa #6: -201 --> en:hereditary disease
    n1=en:anemia, sickle cell | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-201
  1344. en:sickle cell disease --- r_isa #6: -202 --> en:hereditary disease
    n1=en:sickle cell disease | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-202
  1345. maladie des hématies falciformes --- r_isa #6: -203 --> en:hereditary disease
    n1=maladie des hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-203
  1346. bêta-thalassémie à hématies falciformes --- r_isa #6: -205 --> en:hereditary disease
    n1=bêta-thalassémie à hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-205
  1347. anémie falciforme --- r_isa #6: -206 --> en:hereditary disease
    n1=anémie falciforme | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-206
  1348. drépanocytose homozygote --- r_isa #6: -206 --> en:hereditary disease
    n1=drépanocytose homozygote | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-206
  1349. hémoglobinose S --- r_isa #6: -207 --> en:hereditary disease
    n1=hémoglobinose S | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-207
  1350. non précisée, anémie drépanocytaire --- r_isa #6: -210 --> en:hereditary disease
    n1=non précisée, anémie drépanocytaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-210
  1351. hémoglobinose ss --- r_isa #6: -211 --> en:hereditary disease
    n1=hémoglobinose ss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-211
  1352. anémie ss --- r_isa #6: -214 --> en:hereditary disease
    n1=anémie ss | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-214
  1353. maladie drépanocytaire --- r_isa #6: -214 --> en:hereditary disease
    n1=maladie drépanocytaire | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-214
  1354. anémie à hématies falciformes --- r_isa #6: -216 --> en:hereditary disease
    n1=anémie à hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-216
  1355. hémoglobinopathie à hématies falciformes --- r_isa #6: -218 --> en:hereditary disease
    n1=hémoglobinopathie à hématies falciformes | n2=en:hereditary disease | rel=r_isa | relid=6 | w=-218
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