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'en:genetic disease'
(id=15056040 ; fe=en:genetic disease ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=78756.96997070312 creation date=2020-10-11 touchdate=2026-01-08 14:17:42.000)
≈ 629 relations sortantes

  1. en:genetic disease -- r_hypo #8: 395 / 1 -> hirsutisme
    n1=en:genetic disease | n2=hirsutisme | rel=r_hypo | relid=8 | w=395
  2. en:genetic disease -- r_hypo #8: 390 / 0.987 -> goutte
    (maladie)
    n1=en:genetic disease | n2=goutte
    (maladie)
    | rel=r_hypo | relid=8 | w=390
  3. en:genetic disease -- r_hypo #8: 390 / 0.987 -> nanisme
    n1=en:genetic disease | n2=nanisme | rel=r_hypo | relid=8 | w=390
  4. en:genetic disease -- r_hypo #8: 385 / 0.975 -> myopie
    n1=en:genetic disease | n2=myopie | rel=r_hypo | relid=8 | w=385
  5. en:genetic disease -- r_hypo #8: 380 / 0.962 -> achondroplasie
    n1=en:genetic disease | n2=achondroplasie | rel=r_hypo | relid=8 | w=380
  6. en:genetic disease -- r_hypo #8: 380 / 0.962 -> albinisme
    n1=en:genetic disease | n2=albinisme | rel=r_hypo | relid=8 | w=380
  7. en:genetic disease -- r_hypo #8: 380 / 0.962 -> cancer du côlon
    n1=en:genetic disease | n2=cancer du côlon | rel=r_hypo | relid=8 | w=380
  8. en:genetic disease -- r_hypo #8: 380 / 0.962 -> chorée de Huntington
    n1=en:genetic disease | n2=chorée de Huntington | rel=r_hypo | relid=8 | w=380
  9. en:genetic disease -- r_hypo #8: 380 / 0.962 -> daltonisme
    n1=en:genetic disease | n2=daltonisme | rel=r_hypo | relid=8 | w=380
  10. en:genetic disease -- r_hypo #8: 380 / 0.962 -> drépanocytose
    n1=en:genetic disease | n2=drépanocytose | rel=r_hypo | relid=8 | w=380
  11. en:genetic disease -- r_hypo #8: 380 / 0.962 -> hémophilie
    n1=en:genetic disease | n2=hémophilie | rel=r_hypo | relid=8 | w=380
  12. en:genetic disease -- r_hypo #8: 380 / 0.962 -> maladie de Wilson
    n1=en:genetic disease | n2=maladie de Wilson | rel=r_hypo | relid=8 | w=380
  13. en:genetic disease -- r_hypo #8: 380 / 0.962 -> maladie génétique congénitale
    n1=en:genetic disease | n2=maladie génétique congénitale | rel=r_hypo | relid=8 | w=380
  14. en:genetic disease -- r_hypo #8: 380 / 0.962 -> mucoviscidose
    n1=en:genetic disease | n2=mucoviscidose | rel=r_hypo | relid=8 | w=380
  15. en:genetic disease -- r_hypo #8: 380 / 0.962 -> myopathie
    n1=en:genetic disease | n2=myopathie | rel=r_hypo | relid=8 | w=380
  16. en:genetic disease -- r_hypo #8: 380 / 0.962 -> phénylcétonurie
    n1=en:genetic disease | n2=phénylcétonurie | rel=r_hypo | relid=8 | w=380
  17. en:genetic disease -- r_hypo #8: 380 / 0.962 -> rétinoblastome
    n1=en:genetic disease | n2=rétinoblastome | rel=r_hypo | relid=8 | w=380
  18. en:genetic disease -- r_hypo #8: 380 / 0.962 -> thalassémie
    n1=en:genetic disease | n2=thalassémie | rel=r_hypo | relid=8 | w=380
  19. en:genetic disease -- r_hypo #8: 380 / 0.962 -> vitiligo
    n1=en:genetic disease | n2=vitiligo | rel=r_hypo | relid=8 | w=380
  20. en:genetic disease -- r_hypo #8: 370 / 0.937 -> galactosémie
    n1=en:genetic disease | n2=galactosémie | rel=r_hypo | relid=8 | w=370
  21. en:genetic disease -- r_hypo #8: 370 / 0.937 -> goître
    n1=en:genetic disease | n2=goître | rel=r_hypo | relid=8 | w=370
  22. en:genetic disease -- r_hypo #8: 370 / 0.937 -> phacomatose
    n1=en:genetic disease | n2=phacomatose | rel=r_hypo | relid=8 | w=370
  23. en:genetic disease -- r_hypo #8: 370 / 0.937 -> spondylarthrite ankylosante
    n1=en:genetic disease | n2=spondylarthrite ankylosante | rel=r_hypo | relid=8 | w=370
  24. en:genetic disease -- r_hypo #8: 365 / 0.924 -> céroïde lipofuscinose neuronale de type infantile tardive
    n1=en:genetic disease | n2=céroïde lipofuscinose neuronale de type infantile tardive | rel=r_hypo | relid=8 | w=365
  25. en:genetic disease -- r_hypo #8: 365 / 0.924 -> eczéma atopique
    n1=en:genetic disease | n2=eczéma atopique | rel=r_hypo | relid=8 | w=365
  26. en:genetic disease -- r_hypo #8: 365 / 0.924 -> maladie d'Ollier
    n1=en:genetic disease | n2=maladie d'Ollier | rel=r_hypo | relid=8 | w=365
  27. en:genetic disease -- r_hypo #8: 365 / 0.924 -> maladie du sirop d'érable
    n1=en:genetic disease | n2=maladie du sirop d'érable | rel=r_hypo | relid=8 | w=365
  28. en:genetic disease -- r_hypo #8: 365 / 0.924 -> mucopolysaccharidose
    n1=en:genetic disease | n2=mucopolysaccharidose | rel=r_hypo | relid=8 | w=365
  29. en:genetic disease -- r_hypo #8: 365 / 0.924 -> pachyonychie congénitale de Jadassohn-Lewandowsky
    n1=en:genetic disease | n2=pachyonychie congénitale de Jadassohn-Lewandowsky | rel=r_hypo | relid=8 | w=365
  30. en:genetic disease -- r_hypo #8: 365 / 0.924 -> sphingolipidose
    n1=en:genetic disease | n2=sphingolipidose | rel=r_hypo | relid=8 | w=365
  31. en:genetic disease -- r_hypo #8: 360 / 0.911 -> maladie génétique en néphrologie
    n1=en:genetic disease | n2=maladie génétique en néphrologie | rel=r_hypo | relid=8 | w=360
  32. en:genetic disease -- r_hypo #8: 360 / 0.911 -> neuropathie optique de Leber
    n1=en:genetic disease | n2=neuropathie optique de Leber | rel=r_hypo | relid=8 | w=360
  33. en:genetic disease -- r_hypo #8: 360 / 0.911 -> syndrome de la Tourette
    n1=en:genetic disease | n2=syndrome de la Tourette | rel=r_hypo | relid=8 | w=360
  34. en:genetic disease -- r_hypo #8: 360 / 0.911 -> syndrome de Larsen
    n1=en:genetic disease | n2=syndrome de Larsen | rel=r_hypo | relid=8 | w=360
  35. en:genetic disease -- r_hypo #8: 360 / 0.911 -> syndrome de Saethre-Chotzen
    n1=en:genetic disease | n2=syndrome de Saethre-Chotzen | rel=r_hypo | relid=8 | w=360
  36. en:genetic disease -- r_hypo #8: 355 / 0.899 -> en:laurence-moon syndrome
    n1=en:genetic disease | n2=en:laurence-moon syndrome | rel=r_hypo | relid=8 | w=355
  37. en:genetic disease -- r_hypo #8: 355 / 0.899 -> en:mehes syndrome
    n1=en:genetic disease | n2=en:mehes syndrome | rel=r_hypo | relid=8 | w=355
  38. en:genetic disease -- r_hypo #8: 355 / 0.899 -> en:rett syndrome, atypical
    n1=en:genetic disease | n2=en:rett syndrome, atypical | rel=r_hypo | relid=8 | w=355
  39. en:genetic disease -- r_hypo #8: 345 / 0.873 -> en:colon neoplasm
    n1=en:genetic disease | n2=en:colon neoplasm | rel=r_hypo | relid=8 | w=345
  40. en:genetic disease -- r_hypo #8: 345 / 0.873 -> en:colonic neoplasms
    n1=en:genetic disease | n2=en:colonic neoplasms | rel=r_hypo | relid=8 | w=345
  41. en:genetic disease -- r_hypo #8: 345 / 0.873 -> en:malignant colon neoplasm
    n1=en:genetic disease | n2=en:malignant colon neoplasm | rel=r_hypo | relid=8 | w=345
  42. en:genetic disease -- r_hypo #8: 345 / 0.873 -> en:malignant tumor of colon
    n1=en:genetic disease | n2=en:malignant tumor of colon | rel=r_hypo | relid=8 | w=345
  43. en:genetic disease -- r_hypo #8: 335 / 0.848 -> myopathie de Duchenne
    n1=en:genetic disease | n2=myopathie de Duchenne | rel=r_hypo | relid=8 | w=335
  44. en:genetic disease -- r_hypo #8: 330 / 0.835 -> maladie d'Alzheimer
    n1=en:genetic disease | n2=maladie d'Alzheimer | rel=r_hypo | relid=8 | w=330
  45. en:genetic disease -- r_hypo #8: 325 / 0.823 -> goutte
    n1=en:genetic disease | n2=goutte | rel=r_hypo | relid=8 | w=325
  46. en:genetic disease -- r_hypo #8: 315 / 0.797 -> épilepsie
    n1=en:genetic disease | n2=épilepsie | rel=r_hypo | relid=8 | w=315
  47. en:genetic disease -- r_hypo #8: 315 / 0.797 -> leucinose
    n1=en:genetic disease | n2=leucinose | rel=r_hypo | relid=8 | w=315
  48. en:genetic disease -- r_hypo #8: 315 / 0.797 -> maladie de Crohn
    n1=en:genetic disease | n2=maladie de Crohn | rel=r_hypo | relid=8 | w=315
  49. en:genetic disease -- r_hypo #8: 305 / 0.772 -> diabète sucré
    n1=en:genetic disease | n2=diabète sucré | rel=r_hypo | relid=8 | w=305
  50. en:genetic disease -- r_hypo #8: 305 / 0.772 -> maladie de Cowden
    n1=en:genetic disease | n2=maladie de Cowden | rel=r_hypo | relid=8 | w=305
  51. en:genetic disease -- r_hypo #8: 305 / 0.772 -> maladie de Huntington
    n1=en:genetic disease | n2=maladie de Huntington | rel=r_hypo | relid=8 | w=305
  52. en:genetic disease -- r_hypo #8: 305 / 0.772 -> maladie de Rendu-Osler
    n1=en:genetic disease | n2=maladie de Rendu-Osler | rel=r_hypo | relid=8 | w=305
  53. en:genetic disease -- r_hypo #8: 305 / 0.772 -> maladie de Steinert
    n1=en:genetic disease | n2=maladie de Steinert | rel=r_hypo | relid=8 | w=305
  54. en:genetic disease -- r_hypo #8: 305 / 0.772 -> maladie génétique de l'appareil digestif
    n1=en:genetic disease | n2=maladie génétique de l'appareil digestif | rel=r_hypo | relid=8 | w=305
  55. en:genetic disease -- r_hypo #8: 305 / 0.772 -> maladie génétique du système nerveux
    n1=en:genetic disease | n2=maladie génétique du système nerveux | rel=r_hypo | relid=8 | w=305
  56. en:genetic disease -- r_hypo #8: 305 / 0.772 -> naevomatose basocellulaire
    n1=en:genetic disease | n2=naevomatose basocellulaire | rel=r_hypo | relid=8 | w=305
  57. en:genetic disease -- r_hypo #8: 305 / 0.772 -> pachyonychie congénitale
    n1=en:genetic disease | n2=pachyonychie congénitale | rel=r_hypo | relid=8 | w=305
  58. en:genetic disease -- r_hypo #8: 305 / 0.772 -> progeria
    n1=en:genetic disease | n2=progeria | rel=r_hypo | relid=8 | w=305
  59. en:genetic disease -- r_hypo #8: 305 / 0.772 -> syndrome d'Aicardi
    n1=en:genetic disease | n2=syndrome d'Aicardi | rel=r_hypo | relid=8 | w=305
  60. en:genetic disease -- r_hypo #8: 305 / 0.772 -> syndrome de Greig
    n1=en:genetic disease | n2=syndrome de Greig | rel=r_hypo | relid=8 | w=305
  61. en:genetic disease -- r_hypo #8: 305 / 0.772 -> syndrome de Kallmann
    n1=en:genetic disease | n2=syndrome de Kallmann | rel=r_hypo | relid=8 | w=305
  62. en:genetic disease -- r_hypo #8: 305 / 0.772 -> syndrome de Kearns-Sayre
    n1=en:genetic disease | n2=syndrome de Kearns-Sayre | rel=r_hypo | relid=8 | w=305
  63. en:genetic disease -- r_hypo #8: 305 / 0.772 -> syndrome Larsen-Bourbon
    n1=en:genetic disease | n2=syndrome Larsen-Bourbon | rel=r_hypo | relid=8 | w=305
  64. en:genetic disease -- r_hypo #8: 300 / 0.759 -> déficit en céto-acide décarboxylase
    n1=en:genetic disease | n2=déficit en céto-acide décarboxylase | rel=r_hypo | relid=8 | w=300
  65. en:genetic disease -- r_hypo #8: 300 / 0.759 -> dermatite atopique
    n1=en:genetic disease | n2=dermatite atopique | rel=r_hypo | relid=8 | w=300
  66. en:genetic disease -- r_hypo #8: 300 / 0.759 -> enchondromatose
    n1=en:genetic disease | n2=enchondromatose | rel=r_hypo | relid=8 | w=300
  67. en:genetic disease -- r_hypo #8: 300 / 0.759 -> goitre
    (zoologie)
    n1=en:genetic disease | n2=goitre
    (zoologie)
    | rel=r_hypo | relid=8 | w=300
  68. en:genetic disease -- r_hypo #8: 300 / 0.759 -> holoprosencéphalie
    n1=en:genetic disease | n2=holoprosencéphalie | rel=r_hypo | relid=8 | w=300
  69. en:genetic disease -- r_hypo #8: 300 / 0.759 -> maladie de Gaucher
    n1=en:genetic disease | n2=maladie de Gaucher | rel=r_hypo | relid=8 | w=300
  70. en:genetic disease -- r_hypo #8: 300 / 0.759 -> maladie de Morquio
    n1=en:genetic disease | n2=maladie de Morquio | rel=r_hypo | relid=8 | w=300
  71. en:genetic disease -- r_hypo #8: 300 / 0.759 -> maladie de Recklinghausen
    n1=en:genetic disease | n2=maladie de Recklinghausen | rel=r_hypo | relid=8 | w=300
  72. en:genetic disease -- r_hypo #8: 300 / 0.759 -> maladie de Sanfilippo
    n1=en:genetic disease | n2=maladie de Sanfilippo | rel=r_hypo | relid=8 | w=300
  73. en:genetic disease -- r_hypo #8: 300 / 0.759 -> maladie génétique du métabolisme des acides aminés
    n1=en:genetic disease | n2=maladie génétique du métabolisme des acides aminés | rel=r_hypo | relid=8 | w=300
  74. en:genetic disease -- r_hypo #8: 300 / 0.759 -> maladie génétique du métabolisme des nucléotides
    n1=en:genetic disease | n2=maladie génétique du métabolisme des nucléotides | rel=r_hypo | relid=8 | w=300
  75. en:genetic disease -- r_hypo #8: 300 / 0.759 -> maladie lysosomale
    n1=en:genetic disease | n2=maladie lysosomale | rel=r_hypo | relid=8 | w=300
  76. en:genetic disease -- r_hypo #8: 300 / 0.759 -> microcéphalie
    n1=en:genetic disease | n2=microcéphalie | rel=r_hypo | relid=8 | w=300
  77. en:genetic disease -- r_hypo #8: 300 / 0.759 -> microlissencéphalie
    n1=en:genetic disease | n2=microlissencéphalie | rel=r_hypo | relid=8 | w=300
  78. en:genetic disease -- r_hypo #8: 300 / 0.759 -> neurofibromatose de type 1
    n1=en:genetic disease | n2=neurofibromatose de type 1 | rel=r_hypo | relid=8 | w=300
  79. en:genetic disease -- r_hypo #8: 300 / 0.759 -> rétinite pigmentaire
    n1=en:genetic disease | n2=rétinite pigmentaire | rel=r_hypo | relid=8 | w=300
  80. en:genetic disease -- r_hypo #8: 300 / 0.759 -> syndrome de Sanfillipo
    n1=en:genetic disease | n2=syndrome de Sanfillipo | rel=r_hypo | relid=8 | w=300
  81. en:genetic disease -- r_hypo #8: 300 / 0.759 -> syndrome de Simpson-Golabi-Behmel
    n1=en:genetic disease | n2=syndrome de Simpson-Golabi-Behmel | rel=r_hypo | relid=8 | w=300
  82. en:genetic disease -- r_hypo #8: 300 / 0.759 -> syndrome L1
    n1=en:genetic disease | n2=syndrome L1 | rel=r_hypo | relid=8 | w=300
  83. en:genetic disease -- r_hypo #8: 295 / 0.747 -> fibrodysplasie ossifiante progressive
    n1=en:genetic disease | n2=fibrodysplasie ossifiante progressive | rel=r_hypo | relid=8 | w=295
  84. en:genetic disease -- r_hypo #8: 295 / 0.747 -> myosite ossifiante progressive
    n1=en:genetic disease | n2=myosite ossifiante progressive | rel=r_hypo | relid=8 | w=295
  85. en:genetic disease -- r_hypo #8: 290 / 0.734 -> alacrymie-achalasie-addisonisme
    n1=en:genetic disease | n2=alacrymie-achalasie-addisonisme | rel=r_hypo | relid=8 | w=290
  86. en:genetic disease -- r_hypo #8: 285 / 0.722 -> maladie de Cori
    n1=en:genetic disease | n2=maladie de Cori | rel=r_hypo | relid=8 | w=285
  87. en:genetic disease -- r_hypo #8: 280 / 0.709 -> dextrinose limite
    n1=en:genetic disease | n2=dextrinose limite | rel=r_hypo | relid=8 | w=280
  88. en:genetic disease -- r_hypo #8: 280 / 0.709 -> en:canavan disease
    n1=en:genetic disease | n2=en:canavan disease | rel=r_hypo | relid=8 | w=280
  89. en:genetic disease -- r_hypo #8: 280 / 0.709 -> en:mayer-rokitansky-kuster-hauser syndrome
    n1=en:genetic disease | n2=en:mayer-rokitansky-kuster-hauser syndrome | rel=r_hypo | relid=8 | w=280
  90. en:genetic disease -- r_hypo #8: 280 / 0.709 -> maladie de Curschmann-Steinert
    n1=en:genetic disease | n2=maladie de Curschmann-Steinert | rel=r_hypo | relid=8 | w=280
  91. en:genetic disease -- r_hypo #8: 280 / 0.709 -> maladie de Forbes
    n1=en:genetic disease | n2=maladie de Forbes | rel=r_hypo | relid=8 | w=280
  92. en:genetic disease -- r_hypo #8: 280 / 0.709 -> syndrome de Mayer-Rokitansky-Küster-Hauser
    n1=en:genetic disease | n2=syndrome de Mayer-Rokitansky-Küster-Hauser | rel=r_hypo | relid=8 | w=280
  93. en:genetic disease -- r_hypo #8: 280 / 0.709 -> Syndrome de Mayer-Rokitansky-Küster-Hauser
    n1=en:genetic disease | n2=Syndrome de Mayer-Rokitansky-Küster-Hauser | rel=r_hypo | relid=8 | w=280
  94. en:genetic disease -- r_hypo #8: 275 / 0.696 -> atrophie optique de Leber
    n1=en:genetic disease | n2=atrophie optique de Leber | rel=r_hypo | relid=8 | w=275
  95. en:genetic disease -- r_hypo #8: 275 / 0.696 -> cataracte congénitale avec dysmorphie faciale et neuropathie
    n1=en:genetic disease | n2=cataracte congénitale avec dysmorphie faciale et neuropathie | rel=r_hypo | relid=8 | w=275
  96. en:genetic disease -- r_hypo #8: 275 / 0.696 -> cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse
    n1=en:genetic disease | n2=cholestase intrahépatique familiale progressive à activité gamma-glutamyl-transférase basse | rel=r_hypo | relid=8 | w=275
  97. en:genetic disease -- r_hypo #8: 275 / 0.696 -> déficit en ornithine carbamyl transférase
    n1=en:genetic disease | n2=déficit en ornithine carbamyl transférase | rel=r_hypo | relid=8 | w=275
  98. en:genetic disease -- r_hypo #8: 275 / 0.696 -> dystonie myoclonique
    n1=en:genetic disease | n2=dystonie myoclonique | rel=r_hypo | relid=8 | w=275
  99. en:genetic disease -- r_hypo #8: 275 / 0.696 -> dystrophie musculaire oculopharyngée
    n1=en:genetic disease | n2=dystrophie musculaire oculopharyngée | rel=r_hypo | relid=8 | w=275
  100. en:genetic disease -- r_hypo #8: 275 / 0.696 -> hétérotaxie
    n1=en:genetic disease | n2=hétérotaxie | rel=r_hypo | relid=8 | w=275
  101. en:genetic disease -- r_hypo #8: 275 / 0.696 -> leucodystrophie à cellules globoïdes
    n1=en:genetic disease | n2=leucodystrophie à cellules globoïdes | rel=r_hypo | relid=8 | w=275
  102. en:genetic disease -- r_hypo #8: 275 / 0.696 -> maladie génétique du métabolisme des glucides
    n1=en:genetic disease | n2=maladie génétique du métabolisme des glucides | rel=r_hypo | relid=8 | w=275
  103. en:genetic disease -- r_hypo #8: 275 / 0.696 -> maladie génétique lysosomale
    n1=en:genetic disease | n2=maladie génétique lysosomale | rel=r_hypo | relid=8 | w=275
  104. en:genetic disease -- r_hypo #8: 275 / 0.696 -> maladie génétique par atteinte du collagène
    n1=en:genetic disease | n2=maladie génétique par atteinte du collagène | rel=r_hypo | relid=8 | w=275
  105. en:genetic disease -- r_hypo #8: 275 / 0.696 -> syndrome de Peutz-Jeghers
    n1=en:genetic disease | n2=syndrome de Peutz-Jeghers | rel=r_hypo | relid=8 | w=275
  106. en:genetic disease -- r_hypo #8: 275 / 0.696 -> syndrome de Rokitansky-Küster-Hauser
    n1=en:genetic disease | n2=syndrome de Rokitansky-Küster-Hauser | rel=r_hypo | relid=8 | w=275
  107. en:genetic disease -- r_hypo #8: 270 / 0.684 -> en:retinoblastoma
    n1=en:genetic disease | n2=en:retinoblastoma | rel=r_hypo | relid=8 | w=270
  108. en:genetic disease -- r_hypo #8: 245 / 0.62 -> déficit en carnitine palmitoyltransférase II
    n1=en:genetic disease | n2=déficit en carnitine palmitoyltransférase II | rel=r_hypo | relid=8 | w=245
  109. en:genetic disease -- r_hypo #8: 245 / 0.62 -> Dextrinose limite
    n1=en:genetic disease | n2=Dextrinose limite | rel=r_hypo | relid=8 | w=245
  110. en:genetic disease -- r_hypo #8: 245 / 0.62 -> lissencéphalie
    n1=en:genetic disease | n2=lissencéphalie | rel=r_hypo | relid=8 | w=245
  111. en:genetic disease -- r_hypo #8: 245 / 0.62 -> maladie de Behçet
    n1=en:genetic disease | n2=maladie de Behçet | rel=r_hypo | relid=8 | w=245
  112. en:genetic disease -- r_hypo #8: 245 / 0.62 -> maladie de Canavan
    n1=en:genetic disease | n2=maladie de Canavan | rel=r_hypo | relid=8 | w=245
  113. en:genetic disease -- r_hypo #8: 245 / 0.62 -> Maladie de Cori
    n1=en:genetic disease | n2=Maladie de Cori | rel=r_hypo | relid=8 | w=245
  114. en:genetic disease -- r_hypo #8: 245 / 0.62 -> maladie de cori
    n1=en:genetic disease | n2=maladie de cori | rel=r_hypo | relid=8 | w=245
  115. en:genetic disease -- r_hypo #8: 245 / 0.62 -> maladie du cri du chat
    n1=en:genetic disease | n2=maladie du cri du chat | rel=r_hypo | relid=8 | w=245
  116. en:genetic disease -- r_hypo #8: 245 / 0.62 -> maladie génétique du métabolisme des métaux
    n1=en:genetic disease | n2=maladie génétique du métabolisme des métaux | rel=r_hypo | relid=8 | w=245
  117. en:genetic disease -- r_hypo #8: 245 / 0.62 -> maladie héréditaire inflammatoire
    n1=en:genetic disease | n2=maladie héréditaire inflammatoire | rel=r_hypo | relid=8 | w=245
  118. en:genetic disease -- r_hypo #8: 245 / 0.62 -> syndrome de Dubowitz
    n1=en:genetic disease | n2=syndrome de Dubowitz | rel=r_hypo | relid=8 | w=245
  119. en:genetic disease -- r_hypo #8: 245 / 0.62 -> syndrome de Lowe
    n1=en:genetic disease | n2=syndrome de Lowe | rel=r_hypo | relid=8 | w=245
  120. en:genetic disease -- r_hypo #8: 245 / 0.62 -> syringomyélie
    n1=en:genetic disease | n2=syringomyélie | rel=r_hypo | relid=8 | w=245
  121. en:genetic disease -- r_hypo #8: 240 / 0.608 -> acrocéphalie-crâne asymétrique et syndactylie modérée
    n1=en:genetic disease | n2=acrocéphalie-crâne asymétrique et syndactylie modérée | rel=r_hypo | relid=8 | w=240
  122. en:genetic disease -- r_hypo #8: 240 / 0.608 -> atrophie optique de leber
    n1=en:genetic disease | n2=atrophie optique de leber | rel=r_hypo | relid=8 | w=240
  123. en:genetic disease -- r_hypo #8: 240 / 0.608 -> en:kallmann syndrome
    n1=en:genetic disease | n2=en:kallmann syndrome | rel=r_hypo | relid=8 | w=240
  124. en:genetic disease -- r_hypo #8: 240 / 0.608 -> leucodystrophie
    n1=en:genetic disease | n2=leucodystrophie | rel=r_hypo | relid=8 | w=240
  125. en:genetic disease -- r_hypo #8: 240 / 0.608 -> maladie de behçet
    n1=en:genetic disease | n2=maladie de behçet | rel=r_hypo | relid=8 | w=240
  126. en:genetic disease -- r_hypo #8: 240 / 0.608 -> maladie de forbes
    n1=en:genetic disease | n2=maladie de forbes | rel=r_hypo | relid=8 | w=240
  127. en:genetic disease -- r_hypo #8: 240 / 0.608 -> maladie de Gilles de la Tourette
    n1=en:genetic disease | n2=maladie de Gilles de la Tourette | rel=r_hypo | relid=8 | w=240
  128. en:genetic disease -- r_hypo #8: 240 / 0.608 -> maladie de Rendu-Osler-Weber
    n1=en:genetic disease | n2=maladie de Rendu-Osler-Weber | rel=r_hypo | relid=8 | w=240
  129. en:genetic disease -- r_hypo #8: 240 / 0.608 -> maladie génétique en hématologie
    n1=en:genetic disease | n2=maladie génétique en hématologie | rel=r_hypo | relid=8 | w=240
  130. en:genetic disease -- r_hypo #8: 240 / 0.608 -> progéria
    n1=en:genetic disease | n2=progéria | rel=r_hypo | relid=8 | w=240
  131. en:genetic disease -- r_hypo #8: 240 / 0.608 -> syndrome d'angelman
    n1=en:genetic disease | n2=syndrome d'angelman | rel=r_hypo | relid=8 | w=240
  132. en:genetic disease -- r_hypo #8: 240 / 0.608 -> syndrome de Gorlin
    n1=en:genetic disease | n2=syndrome de Gorlin | rel=r_hypo | relid=8 | w=240
  133. en:genetic disease -- r_hypo #8: 240 / 0.608 -> télangiectasie hémorragique familiale
    n1=en:genetic disease | n2=télangiectasie hémorragique familiale | rel=r_hypo | relid=8 | w=240
  134. en:genetic disease -- r_hypo #8: 235 / 0.595 -> en:chromosome disorder
    n1=en:genetic disease | n2=en:chromosome disorder | rel=r_hypo | relid=8 | w=235
  135. en:genetic disease -- r_hypo #8: 235 / 0.595 -> en:down syndrome
    n1=en:genetic disease | n2=en:down syndrome | rel=r_hypo | relid=8 | w=235
  136. en:genetic disease -- r_hypo #8: 235 / 0.595 -> en:fanconi syndrome
    n1=en:genetic disease | n2=en:fanconi syndrome | rel=r_hypo | relid=8 | w=235
  137. en:genetic disease -- r_hypo #8: 235 / 0.595 -> en:hereditary disorder by system
    n1=en:genetic disease | n2=en:hereditary disorder by system | rel=r_hypo | relid=8 | w=235
  138. en:genetic disease -- r_hypo #8: 235 / 0.595 -> Maladie d'Illingworth-Cori-Forbes
    n1=en:genetic disease | n2=Maladie d'Illingworth-Cori-Forbes | rel=r_hypo | relid=8 | w=235
  139. en:genetic disease -- r_hypo #8: 205 / 0.519 -> en:cancer of the colon
    n1=en:genetic disease | n2=en:cancer of the colon | rel=r_hypo | relid=8 | w=205
  140. en:genetic disease -- r_hypo #8: 205 / 0.519 -> en:Tourette syndrome
    n1=en:genetic disease | n2=en:Tourette syndrome | rel=r_hypo | relid=8 | w=205
  141. en:genetic disease -- r_hypo #8: 185 / 0.468 -> trouble chromosomique
    n1=en:genetic disease | n2=trouble chromosomique | rel=r_hypo | relid=8 | w=185
  142. en:genetic disease -- r_hypo #8: 175 / 0.443 -> syndrome d'Angelman
    n1=en:genetic disease | n2=syndrome d'Angelman | rel=r_hypo | relid=8 | w=175
  143. en:genetic disease -- r_hypo #8: 155 / 0.392 -> affection congénitale
    n1=en:genetic disease | n2=affection congénitale | rel=r_hypo | relid=8 | w=155
  144. en:genetic disease -- r_hypo #8: 155 / 0.392 -> canalopathie
    n1=en:genetic disease | n2=canalopathie | rel=r_hypo | relid=8 | w=155
  145. en:genetic disease -- r_hypo #8: 155 / 0.392 -> ectrodactylie
    n1=en:genetic disease | n2=ectrodactylie | rel=r_hypo | relid=8 | w=155
  146. en:genetic disease -- r_hypo #8: 155 / 0.392 -> maladie de Fabry
    n1=en:genetic disease | n2=maladie de Fabry | rel=r_hypo | relid=8 | w=155
  147. en:genetic disease -- r_hypo #8: 155 / 0.392 -> maladie de Tay-Sachs
    n1=en:genetic disease | n2=maladie de Tay-Sachs | rel=r_hypo | relid=8 | w=155
  148. en:genetic disease -- r_hypo #8: 155 / 0.392 -> maladie génétique de l'oeil
    n1=en:genetic disease | n2=maladie génétique de l'oeil | rel=r_hypo | relid=8 | w=155
  149. en:genetic disease -- r_hypo #8: 155 / 0.392 -> maladie génétique du métabolisme
    n1=en:genetic disease | n2=maladie génétique du métabolisme | rel=r_hypo | relid=8 | w=155
  150. en:genetic disease -- r_hypo #8: 155 / 0.392 -> neuropathie héréditaire avec hypersensibilité à la pression
    n1=en:genetic disease | n2=neuropathie héréditaire avec hypersensibilité à la pression | rel=r_hypo | relid=8 | w=155
  151. en:genetic disease -- r_hypo #8: 155 / 0.392 -> neuropathie tomaculaire
    n1=en:genetic disease | n2=neuropathie tomaculaire | rel=r_hypo | relid=8 | w=155
  152. en:genetic disease -- r_hypo #8: 155 / 0.392 -> ostéopétrose par mutation du gène CLCN7
    n1=en:genetic disease | n2=ostéopétrose par mutation du gène CLCN7 | rel=r_hypo | relid=8 | w=155
  153. en:genetic disease -- r_hypo #8: 105 / 0.266 -> maladie héréditaire du sang
    n1=en:genetic disease | n2=maladie héréditaire du sang | rel=r_hypo | relid=8 | w=105
  154. en:genetic disease -- r_hypo #8: 95 / 0.241 -> maladie de Hartnup
    n1=en:genetic disease | n2=maladie de Hartnup | rel=r_hypo | relid=8 | w=95
  155. en:genetic disease -- r_hypo #8: 45 / 0.114 -> maladie de Hirschsprung
    n1=en:genetic disease | n2=maladie de Hirschsprung | rel=r_hypo | relid=8 | w=45
  156. en:genetic disease -- r_hypo #8: 45 / 0.114 -> maladie héréditaire rare
    n1=en:genetic disease | n2=maladie héréditaire rare | rel=r_hypo | relid=8 | w=45
  157. en:genetic disease -- r_hypo #8: 43 / 0.109 -> anémie de Fanconi
    n1=en:genetic disease | n2=anémie de Fanconi | rel=r_hypo | relid=8 | w=43
  158. en:genetic disease -- r_hypo #8: 43 / 0.109 -> anomalie héréditaire du métabolisme de la bilirubine
    n1=en:genetic disease | n2=anomalie héréditaire du métabolisme de la bilirubine | rel=r_hypo | relid=8 | w=43
  159. en:genetic disease -- r_hypo #8: 43 / 0.109 -> macrocéphalie - malformation capillaire
    n1=en:genetic disease | n2=macrocéphalie - malformation capillaire | rel=r_hypo | relid=8 | w=43
  160. en:genetic disease -- r_hypo #8: 43 / 0.109 -> maladie de westphal
    n1=en:genetic disease | n2=maladie de westphal | rel=r_hypo | relid=8 | w=43
  161. en:genetic disease -- r_hypo #8: 43 / 0.109 -> mucopolysaccharidose de type VII
    n1=en:genetic disease | n2=mucopolysaccharidose de type VII | rel=r_hypo | relid=8 | w=43
  162. en:genetic disease -- r_hypo #8: 42 / 0.106 -> en:polygenic disorder
    n1=en:genetic disease | n2=en:polygenic disorder | rel=r_hypo | relid=8 | w=42
  163. en:genetic disease -- r_hypo #8: 42 / 0.106 -> hyperinsulinisme familial
    n1=en:genetic disease | n2=hyperinsulinisme familial | rel=r_hypo | relid=8 | w=42
  164. en:genetic disease -- r_hypo #8: 42 / 0.106 -> maladie d'ollier
    n1=en:genetic disease | n2=maladie d'ollier | rel=r_hypo | relid=8 | w=42
  165. en:genetic disease -- r_hypo #8: 42 / 0.106 -> syndrome d'Aarskog
    n1=en:genetic disease | n2=syndrome d'Aarskog | rel=r_hypo | relid=8 | w=42
  166. en:genetic disease -- r_hypo #8: 42 / 0.106 -> syndrome de brachmann-de lange
    n1=en:genetic disease | n2=syndrome de brachmann-de lange | rel=r_hypo | relid=8 | w=42
  167. en:genetic disease -- r_hypo #8: 41 / 0.104 -> en:adrenoleukodystrophy
    n1=en:genetic disease | n2=en:adrenoleukodystrophy | rel=r_hypo | relid=8 | w=41
  168. en:genetic disease -- r_hypo #8: 41 / 0.104 -> neurofibromatose
    n1=en:genetic disease | n2=neurofibromatose | rel=r_hypo | relid=8 | w=41
  169. en:genetic disease -- r_hypo #8: 41 / 0.104 -> syndrome de Marfan
    n1=en:genetic disease | n2=syndrome de Marfan | rel=r_hypo | relid=8 | w=41
  170. en:genetic disease -- r_hypo #8: 40 / 0.101 -> maladie d'Illingworth-Cori-Forbes
    n1=en:genetic disease | n2=maladie d'Illingworth-Cori-Forbes | rel=r_hypo | relid=8 | w=40
  171. en:genetic disease -- r_hypo #8: 40 / 0.101 -> maladie de sanfilippo
    n1=en:genetic disease | n2=maladie de sanfilippo | rel=r_hypo | relid=8 | w=40
  172. en:genetic disease -- r_hypo #8: 40 / 0.101 -> otospongiose
    n1=en:genetic disease | n2=otospongiose | rel=r_hypo | relid=8 | w=40
  173. en:genetic disease -- r_hypo #8: 40 / 0.101 -> syndrome de Gilles de La Tourette
    n1=en:genetic disease | n2=syndrome de Gilles de La Tourette | rel=r_hypo | relid=8 | w=40
  174. en:genetic disease -- r_hypo #8: 39 / 0.099 -> association de tics vocaux et tics moteurs du syndrome de gilles de la tourette
    n1=en:genetic disease | n2=association de tics vocaux et tics moteurs du syndrome de gilles de la tourette | rel=r_hypo | relid=8 | w=39
  175. en:genetic disease -- r_hypo #8: 39 / 0.099 -> hypophosphatémie liée à l'X
    n1=en:genetic disease | n2=hypophosphatémie liée à l'X | rel=r_hypo | relid=8 | w=39
  176. en:genetic disease -- r_hypo #8: 39 / 0.099 -> Kallmann
    n1=en:genetic disease | n2=Kallmann | rel=r_hypo | relid=8 | w=39
  177. en:genetic disease -- r_hypo #8: 39 / 0.099 -> syndrome de rothmund-thomson
    n1=en:genetic disease | n2=syndrome de rothmund-thomson | rel=r_hypo | relid=8 | w=39
  178. en:genetic disease -- r_hypo #8: 38 / 0.096 -> pycnodysostose
    n1=en:genetic disease | n2=pycnodysostose | rel=r_hypo | relid=8 | w=38
  179. en:genetic disease -- r_hypo #8: 38 / 0.096 -> syndrome de gilles de la tourette
    n1=en:genetic disease | n2=syndrome de gilles de la tourette | rel=r_hypo | relid=8 | w=38
  180. en:genetic disease -- r_hypo #8: 38 / 0.096 -> syndrome de rokitansky
    n1=en:genetic disease | n2=syndrome de rokitansky | rel=r_hypo | relid=8 | w=38
  181. en:genetic disease -- r_hypo #8: 37 / 0.094 -> anémie sidéroblastique liée à l'X avec ataxie
    n1=en:genetic disease | n2=anémie sidéroblastique liée à l'X avec ataxie | rel=r_hypo | relid=8 | w=37
  182. en:genetic disease -- r_hypo #8: 37 / 0.094 -> en:holoprosencephaly
    n1=en:genetic disease | n2=en:holoprosencephaly | rel=r_hypo | relid=8 | w=37
  183. en:genetic disease -- r_hypo #8: 37 / 0.094 -> microsphérophakie et/ou mégalocornée avec ectopie du cristallin et avec ou sans glaucome secondaire
    n1=en:genetic disease | n2=microsphérophakie et/ou mégalocornée avec ectopie du cristallin et avec ou sans glaucome secondaire | rel=r_hypo | relid=8 | w=37
  184. en:genetic disease -- r_hypo #8: 36 / 0.091 -> en:dystrophy
    n1=en:genetic disease | n2=en:dystrophy | rel=r_hypo | relid=8 | w=36
  185. en:genetic disease -- r_hypo #8: 36 / 0.091 -> epilepsie
    n1=en:genetic disease | n2=epilepsie | rel=r_hypo | relid=8 | w=36
  186. en:genetic disease -- r_hypo #8: 36 / 0.091 -> maladie d'alzheimer
    n1=en:genetic disease | n2=maladie d'alzheimer | rel=r_hypo | relid=8 | w=36
  187. en:genetic disease -- r_hypo #8: 35 / 0.089 -> anémie à cellules falciformes
    n1=en:genetic disease | n2=anémie à cellules falciformes | rel=r_hypo | relid=8 | w=35
  188. en:genetic disease -- r_hypo #8: 35 / 0.089 -> anémie par carence en fer
    n1=en:genetic disease | n2=anémie par carence en fer | rel=r_hypo | relid=8 | w=35
  189. en:genetic disease -- r_hypo #8: 35 / 0.089 -> ataxie paroxystique héréditaire
    n1=en:genetic disease | n2=ataxie paroxystique héréditaire | rel=r_hypo | relid=8 | w=35
  190. en:genetic disease -- r_hypo #8: 35 / 0.089 -> déficit en dopamine bêta-hydroxylase
    n1=en:genetic disease | n2=déficit en dopamine bêta-hydroxylase | rel=r_hypo | relid=8 | w=35
  191. en:genetic disease -- r_hypo #8: 35 / 0.089 -> en:enzymopathy
    n1=en:genetic disease | n2=en:enzymopathy | rel=r_hypo | relid=8 | w=35
  192. en:genetic disease -- r_hypo #8: 35 / 0.089 -> en:epilepsy
    n1=en:genetic disease | n2=en:epilepsy | rel=r_hypo | relid=8 | w=35
  193. en:genetic disease -- r_hypo #8: 35 / 0.089 -> en:gout
    n1=en:genetic disease | n2=en:gout | rel=r_hypo | relid=8 | w=35
  194. en:genetic disease -- r_hypo #8: 35 / 0.089 -> en:muscular dystrophy
    n1=en:genetic disease | n2=en:muscular dystrophy | rel=r_hypo | relid=8 | w=35
  195. en:genetic disease -- r_hypo #8: 35 / 0.089 -> en:progressive muscular dystrophy
    n1=en:genetic disease | n2=en:progressive muscular dystrophy | rel=r_hypo | relid=8 | w=35
  196. en:genetic disease -- r_hypo #8: 35 / 0.089 -> en:prune belly syndrome
    n1=en:genetic disease | n2=en:prune belly syndrome | rel=r_hypo | relid=8 | w=35
  197. en:genetic disease -- r_hypo #8: 35 / 0.089 -> génodermatose
    n1=en:genetic disease | n2=génodermatose | rel=r_hypo | relid=8 | w=35
  198. en:genetic disease -- r_hypo #8: 35 / 0.089 -> glycogénose de type III
    n1=en:genetic disease | n2=glycogénose de type III | rel=r_hypo | relid=8 | w=35
  199. en:genetic disease -- r_hypo #8: 35 / 0.089 -> hémoglobinose s
    n1=en:genetic disease | n2=hémoglobinose s | rel=r_hypo | relid=8 | w=35
  200. en:genetic disease -- r_hypo #8: 35 / 0.089 -> hyperprolinémie
    n1=en:genetic disease | n2=hyperprolinémie | rel=r_hypo | relid=8 | w=35
  201. en:genetic disease -- r_hypo #8: 35 / 0.089 -> leucodystrophie métachromatique
    n1=en:genetic disease | n2=leucodystrophie métachromatique | rel=r_hypo | relid=8 | w=35
  202. en:genetic disease -- r_hypo #8: 35 / 0.089 -> luxation congénitale de la hanche
    n1=en:genetic disease | n2=luxation congénitale de la hanche | rel=r_hypo | relid=8 | w=35
  203. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie de Danon
    n1=en:genetic disease | n2=maladie de Danon | rel=r_hypo | relid=8 | w=35
  204. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie de Machado-Joseph
    n1=en:genetic disease | n2=maladie de Machado-Joseph | rel=r_hypo | relid=8 | w=35
  205. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie de marfan
    n1=en:genetic disease | n2=maladie de marfan | rel=r_hypo | relid=8 | w=35
  206. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie de morquio
    n1=en:genetic disease | n2=maladie de morquio | rel=r_hypo | relid=8 | w=35
  207. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie de Sly
    n1=en:genetic disease | n2=maladie de Sly | rel=r_hypo | relid=8 | w=35
  208. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie de tay-sachs
    n1=en:genetic disease | n2=maladie de tay-sachs | rel=r_hypo | relid=8 | w=35
  209. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie génétique à transmission dominante liée à l'X
    n1=en:genetic disease | n2=maladie génétique à transmission dominante liée à l'X | rel=r_hypo | relid=8 | w=35
  210. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie génétique rare
    n1=en:genetic disease | n2=maladie génétique rare | rel=r_hypo | relid=8 | w=35
  211. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie héréditaire autosomique récessive
    n1=en:genetic disease | n2=maladie héréditaire autosomique récessive | rel=r_hypo | relid=8 | w=35
  212. en:genetic disease -- r_hypo #8: 35 / 0.089 -> maladie polygénique
    n1=en:genetic disease | n2=maladie polygénique | rel=r_hypo | relid=8 | w=35
  213. en:genetic disease -- r_hypo #8: 35 / 0.089 -> paraplégie spastique type 7
    n1=en:genetic disease | n2=paraplégie spastique type 7 | rel=r_hypo | relid=8 | w=35
  214. en:genetic disease -- r_hypo #8: 35 / 0.089 -> polykystose rénale type récessif
    n1=en:genetic disease | n2=polykystose rénale type récessif | rel=r_hypo | relid=8 | w=35
  215. en:genetic disease -- r_hypo #8: 35 / 0.089 -> syndrome Allgrove
    n1=en:genetic disease | n2=syndrome Allgrove | rel=r_hypo | relid=8 | w=35
  216. en:genetic disease -- r_hypo #8: 35 / 0.089 -> syndrome d'hypercalcémie familiale-néphrocalcinose-indicanurie
    n1=en:genetic disease | n2=syndrome d'hypercalcémie familiale-néphrocalcinose-indicanurie | rel=r_hypo | relid=8 | w=35
  217. en:genetic disease -- r_hypo #8: 35 / 0.089 -> syndrome de Cockayne
    n1=en:genetic disease | n2=syndrome de Cockayne | rel=r_hypo | relid=8 | w=35
  218. en:genetic disease -- r_hypo #8: 35 / 0.089 -> syndrome de Crigler-Najjar
    n1=en:genetic disease | n2=syndrome de Crigler-Najjar | rel=r_hypo | relid=8 | w=35
  219. en:genetic disease -- r_hypo #8: 35 / 0.089 -> syndrome de Drummond
    n1=en:genetic disease | n2=syndrome de Drummond | rel=r_hypo | relid=8 | w=35
  220. en:genetic disease -- r_hypo #8: 35 / 0.089 -> syndrome de treacher collins
    n1=en:genetic disease | n2=syndrome de treacher collins | rel=r_hypo | relid=8 | w=35
  221. en:genetic disease -- r_hypo #8: 35 / 0.089 -> syndrome de Waardenburg type 1
    n1=en:genetic disease | n2=syndrome de Waardenburg type 1 | rel=r_hypo | relid=8 | w=35
  222. en:genetic disease -- r_hypo #8: 35 / 0.089 -> syndrome de williams
    n1=en:genetic disease | n2=syndrome de williams | rel=r_hypo | relid=8 | w=35
  223. en:genetic disease -- r_hypo #8: 35 / 0.089 -> trouble du métabolisme du fer
    n1=en:genetic disease | n2=trouble du métabolisme du fer | rel=r_hypo | relid=8 | w=35
  224. en:genetic disease -- r_hypo #8: 34 / 0.086 -> adréno-leucodystrophie
    n1=en:genetic disease | n2=adréno-leucodystrophie | rel=r_hypo | relid=8 | w=34
  225. en:genetic disease -- r_hypo #8: 34 / 0.086 -> adrénoleucodystrophie
    n1=en:genetic disease | n2=adrénoleucodystrophie | rel=r_hypo | relid=8 | w=34
  226. en:genetic disease -- r_hypo #8: 34 / 0.086 -> affection familiale
    n1=en:genetic disease | n2=affection familiale | rel=r_hypo | relid=8 | w=34
  227. en:genetic disease -- r_hypo #8: 34 / 0.086 -> alymphocytose
    n1=en:genetic disease | n2=alymphocytose | rel=r_hypo | relid=8 | w=34
  228. en:genetic disease -- r_hypo #8: 34 / 0.086 -> anomalie chromosomique
    n1=en:genetic disease | n2=anomalie chromosomique | rel=r_hypo | relid=8 | w=34
  229. en:genetic disease -- r_hypo #8: 34 / 0.086 -> chorée de huntington
    n1=en:genetic disease | n2=chorée de huntington | rel=r_hypo | relid=8 | w=34
  230. en:genetic disease -- r_hypo #8: 34 / 0.086 -> dysplasie campomélique
    n1=en:genetic disease | n2=dysplasie campomélique | rel=r_hypo | relid=8 | w=34
  231. en:genetic disease -- r_hypo #8: 34 / 0.086 -> dysplasie épiphysaire multiple
    n1=en:genetic disease | n2=dysplasie épiphysaire multiple | rel=r_hypo | relid=8 | w=34
  232. en:genetic disease -- r_hypo #8: 34 / 0.086 -> en:hemochromatosis
    n1=en:genetic disease | n2=en:hemochromatosis | rel=r_hypo | relid=8 | w=34
  233. en:genetic disease -- r_hypo #8: 34 / 0.086 -> en:heterotaxy
    n1=en:genetic disease | n2=en:heterotaxy | rel=r_hypo | relid=8 | w=34
  234. en:genetic disease -- r_hypo #8: 34 / 0.086 -> en:vitiligo
    n1=en:genetic disease | n2=en:vitiligo | rel=r_hypo | relid=8 | w=34
  235. en:genetic disease -- r_hypo #8: 34 / 0.086 -> fibrose congénitale des muscles oculo-moteurs
    n1=en:genetic disease | n2=fibrose congénitale des muscles oculo-moteurs | rel=r_hypo | relid=8 | w=34
  236. en:genetic disease -- r_hypo #8: 34 / 0.086 -> hyperkaliémie périodique paralysante
    n1=en:genetic disease | n2=hyperkaliémie périodique paralysante | rel=r_hypo | relid=8 | w=34
  237. en:genetic disease -- r_hypo #8: 34 / 0.086 -> idiotie amaurotique familiale
    n1=en:genetic disease | n2=idiotie amaurotique familiale | rel=r_hypo | relid=8 | w=34
  238. en:genetic disease -- r_hypo #8: 34 / 0.086 -> La tétrasomie X
    n1=en:genetic disease | n2=La tétrasomie X | rel=r_hypo | relid=8 | w=34
  239. en:genetic disease -- r_hypo #8: 34 / 0.086 -> maladie de crohn
    n1=en:genetic disease | n2=maladie de crohn | rel=r_hypo | relid=8 | w=34
  240. en:genetic disease -- r_hypo #8: 34 / 0.086 -> maladie de fabry
    n1=en:genetic disease | n2=maladie de fabry | rel=r_hypo | relid=8 | w=34
  241. en:genetic disease -- r_hypo #8: 34 / 0.086 -> maladie héréditaire de l'oeil
    n1=en:genetic disease | n2=maladie héréditaire de l'oeil | rel=r_hypo | relid=8 | w=34
  242. en:genetic disease -- r_hypo #8: 34 / 0.086 -> Muir-Torre
    n1=en:genetic disease | n2=Muir-Torre | rel=r_hypo | relid=8 | w=34
  243. en:genetic disease -- r_hypo #8: 34 / 0.086 -> Nail-Patella syndrome
    n1=en:genetic disease | n2=Nail-Patella syndrome | rel=r_hypo | relid=8 | w=34
  244. en:genetic disease -- r_hypo #8: 34 / 0.086 -> paralysie périodique hypokaliémique
    n1=en:genetic disease | n2=paralysie périodique hypokaliémique | rel=r_hypo | relid=8 | w=34
  245. en:genetic disease -- r_hypo #8: 34 / 0.086 -> PSSM
    n1=en:genetic disease | n2=PSSM | rel=r_hypo | relid=8 | w=34
  246. en:genetic disease -- r_hypo #8: 34 / 0.086 -> résistance à la protéine C activée
    n1=en:genetic disease | n2=résistance à la protéine C activée | rel=r_hypo | relid=8 | w=34
  247. en:genetic disease -- r_hypo #8: 34 / 0.086 -> rétinoschisis juvénile lié à l'X
    n1=en:genetic disease | n2=rétinoschisis juvénile lié à l'X | rel=r_hypo | relid=8 | w=34
  248. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome 4A
    n1=en:genetic disease | n2=syndrome 4A | rel=r_hypo | relid=8 | w=34
  249. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome d'Aagenaes
    n1=en:genetic disease | n2=syndrome d'Aagenaes | rel=r_hypo | relid=8 | w=34
  250. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome d'Andermann
    n1=en:genetic disease | n2=syndrome d'Andermann | rel=r_hypo | relid=8 | w=34
  251. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome de cheveux laineux-kératodermie palmoplantaire-cardiomyopathie dilatée
    n1=en:genetic disease | n2=syndrome de cheveux laineux-kératodermie palmoplantaire-cardiomyopathie dilatée | rel=r_hypo | relid=8 | w=34
  252. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome de Cornelia de Lange
    n1=en:genetic disease | n2=syndrome de Cornelia de Lange | rel=r_hypo | relid=8 | w=34
  253. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome de louis-bar
    n1=en:genetic disease | n2=syndrome de louis-bar | rel=r_hypo | relid=8 | w=34
  254. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome de lowe
    n1=en:genetic disease | n2=syndrome de lowe | rel=r_hypo | relid=8 | w=34
  255. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome fg
    n1=en:genetic disease | n2=syndrome fg | rel=r_hypo | relid=8 | w=34
  256. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome LEOPARD
    n1=en:genetic disease | n2=syndrome LEOPARD | rel=r_hypo | relid=8 | w=34
  257. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome Rapadilano
    n1=en:genetic disease | n2=syndrome Rapadilano | rel=r_hypo | relid=8 | w=34
  258. en:genetic disease -- r_hypo #8: 34 / 0.086 -> syndrome TRAPS
    n1=en:genetic disease | n2=syndrome TRAPS | rel=r_hypo | relid=8 | w=34
  259. en:genetic disease -- r_hypo #8: 34 / 0.086 -> thalassémie alpha
    n1=en:genetic disease | n2=thalassémie alpha | rel=r_hypo | relid=8 | w=34
  260. en:genetic disease -- r_hypo #8: 32 / 0.081 -> arachnodactylie
    n1=en:genetic disease | n2=arachnodactylie | rel=r_hypo | relid=8 | w=32
  261. en:genetic disease -- r_hypo #8: 32 / 0.081 -> ataxie télangiectasie
    n1=en:genetic disease | n2=ataxie télangiectasie | rel=r_hypo | relid=8 | w=32
  262. en:genetic disease -- r_hypo #8: 32 / 0.081 -> chorée de Sydenham
    n1=en:genetic disease | n2=chorée de Sydenham | rel=r_hypo | relid=8 | w=32
  263. en:genetic disease -- r_hypo #8: 32 / 0.081 -> déficit en cofacteur à molybdène
    n1=en:genetic disease | n2=déficit en cofacteur à molybdène | rel=r_hypo | relid=8 | w=32
  264. en:genetic disease -- r_hypo #8: 32 / 0.081 -> dyskératose congénitale
    n1=en:genetic disease | n2=dyskératose congénitale | rel=r_hypo | relid=8 | w=32
  265. en:genetic disease -- r_hypo #8: 32 / 0.081 -> dystrophie musculaire d'emery-dreifuss
    n1=en:genetic disease | n2=dystrophie musculaire d'emery-dreifuss | rel=r_hypo | relid=8 | w=32
  266. en:genetic disease -- r_hypo #8: 32 / 0.081 -> dystrophie musculaire oculo-pharyngée
    n1=en:genetic disease | n2=dystrophie musculaire oculo-pharyngée | rel=r_hypo | relid=8 | w=32
  267. en:genetic disease -- r_hypo #8: 32 / 0.081 -> en:congenital afibrinogenemia
    n1=en:genetic disease | n2=en:congenital afibrinogenemia | rel=r_hypo | relid=8 | w=32
  268. en:genetic disease -- r_hypo #8: 32 / 0.081 -> en:globoid cell leukodystrophy
    n1=en:genetic disease | n2=en:globoid cell leukodystrophy | rel=r_hypo | relid=8 | w=32
  269. en:genetic disease -- r_hypo #8: 32 / 0.081 -> en:muscular dystrophy, emery-dreifuss
    n1=en:genetic disease | n2=en:muscular dystrophy, emery-dreifuss | rel=r_hypo | relid=8 | w=32
  270. en:genetic disease -- r_hypo #8: 32 / 0.081 -> en:osteopetrosis
    n1=en:genetic disease | n2=en:osteopetrosis | rel=r_hypo | relid=8 | w=32
  271. en:genetic disease -- r_hypo #8: 32 / 0.081 -> Épilepsie
    n1=en:genetic disease | n2=Épilepsie | rel=r_hypo | relid=8 | w=32
  272. en:genetic disease -- r_hypo #8: 32 / 0.081 -> hémochromatose de type 1
    n1=en:genetic disease | n2=hémochromatose de type 1 | rel=r_hypo | relid=8 | w=32
  273. en:genetic disease -- r_hypo #8: 32 / 0.081 -> hémochromatose primitive
    n1=en:genetic disease | n2=hémochromatose primitive | rel=r_hypo | relid=8 | w=32
  274. en:genetic disease -- r_hypo #8: 32 / 0.081 -> Kallman
    n1=en:genetic disease | n2=Kallman | rel=r_hypo | relid=8 | w=32
  275. en:genetic disease -- r_hypo #8: 32 / 0.081 -> maladie clinique de recklinghausen
    n1=en:genetic disease | n2=maladie clinique de recklinghausen | rel=r_hypo | relid=8 | w=32
  276. en:genetic disease -- r_hypo #8: 32 / 0.081 -> Maladie de Forbes
    n1=en:genetic disease | n2=Maladie de Forbes | rel=r_hypo | relid=8 | w=32
  277. en:genetic disease -- r_hypo #8: 32 / 0.081 -> maladie de gaucher
    n1=en:genetic disease | n2=maladie de gaucher | rel=r_hypo | relid=8 | w=32
  278. en:genetic disease -- r_hypo #8: 32 / 0.081 -> maladie des tics de Gilles de la Tourette
    n1=en:genetic disease | n2=maladie des tics de Gilles de la Tourette | rel=r_hypo | relid=8 | w=32
  279. en:genetic disease -- r_hypo #8: 32 / 0.081 -> maladie génétique de la peau
    n1=en:genetic disease | n2=maladie génétique de la peau | rel=r_hypo | relid=8 | w=32
  280. en:genetic disease -- r_hypo #8: 32 / 0.081 -> maladie lymphoproliférative liée à l'X
    n1=en:genetic disease | n2=maladie lymphoproliférative liée à l'X | rel=r_hypo | relid=8 | w=32
  281. en:genetic disease -- r_hypo #8: 32 / 0.081 -> maladie multigénique
    n1=en:genetic disease | n2=maladie multigénique | rel=r_hypo | relid=8 | w=32
  282. en:genetic disease -- r_hypo #8: 32 / 0.081 -> microsphérophakie
    n1=en:genetic disease | n2=microsphérophakie | rel=r_hypo | relid=8 | w=32
  283. en:genetic disease -- r_hypo #8: 32 / 0.081 -> syndrome d'Ehlers-Danlos type arthro-chalasique
    n1=en:genetic disease | n2=syndrome d'Ehlers-Danlos type arthro-chalasique | rel=r_hypo | relid=8 | w=32
  284. en:genetic disease -- r_hypo #8: 32 / 0.081 -> syndrome de Brugada
    n1=en:genetic disease | n2=syndrome de Brugada | rel=r_hypo | relid=8 | w=32
  285. en:genetic disease -- r_hypo #8: 32 / 0.081 -> syndrome de cornelia de lange
    n1=en:genetic disease | n2=syndrome de cornelia de lange | rel=r_hypo | relid=8 | w=32
  286. en:genetic disease -- r_hypo #8: 32 / 0.081 -> syndrome de lesch-nyhan
    n1=en:genetic disease | n2=syndrome de lesch-nyhan | rel=r_hypo | relid=8 | w=32
  287. en:genetic disease -- r_hypo #8: 32 / 0.081 -> syndrome de marfan
    n1=en:genetic disease | n2=syndrome de marfan | rel=r_hypo | relid=8 | w=32
  288. en:genetic disease -- r_hypo #8: 32 / 0.081 -> syndrome de pendred
    n1=en:genetic disease | n2=syndrome de pendred | rel=r_hypo | relid=8 | w=32
  289. en:genetic disease -- r_hypo #8: 32 / 0.081 -> syndrome de saethre-chotzen
    n1=en:genetic disease | n2=syndrome de saethre-chotzen | rel=r_hypo | relid=8 | w=32
  290. en:genetic disease -- r_hypo #8: 32 / 0.081 -> syndrome FG
    n1=en:genetic disease | n2=syndrome FG | rel=r_hypo | relid=8 | w=32
  291. en:genetic disease -- r_hypo #8: 32 / 0.081 -> syndrome MRKH
    n1=en:genetic disease | n2=syndrome MRKH | rel=r_hypo | relid=8 | w=32
  292. en:genetic disease -- r_hypo #8: 32 / 0.081 -> thrombophilie par mutation du facteur V
    n1=en:genetic disease | n2=thrombophilie par mutation du facteur V | rel=r_hypo | relid=8 | w=32
  293. en:genetic disease -- r_hypo #8: 31 / 0.078 -> albinisme oculo-cutané type I
    n1=en:genetic disease | n2=albinisme oculo-cutané type I | rel=r_hypo | relid=8 | w=31
  294. en:genetic disease -- r_hypo #8: 31 / 0.078 -> anémie sidéroblastique
    n1=en:genetic disease | n2=anémie sidéroblastique | rel=r_hypo | relid=8 | w=31
  295. en:genetic disease -- r_hypo #8: 31 / 0.078 -> cholémie familiale
    n1=en:genetic disease | n2=cholémie familiale | rel=r_hypo | relid=8 | w=31
  296. en:genetic disease -- r_hypo #8: 31 / 0.078 -> déficit en alpha-1-antitrypsine
    n1=en:genetic disease | n2=déficit en alpha-1-antitrypsine | rel=r_hypo | relid=8 | w=31
  297. en:genetic disease -- r_hypo #8: 31 / 0.078 -> dystrophie myotonique de Steinert
    n1=en:genetic disease | n2=dystrophie myotonique de Steinert | rel=r_hypo | relid=8 | w=31
  298. en:genetic disease -- r_hypo #8: 31 / 0.078 -> en:inborn error of metabolism
    n1=en:genetic disease | n2=en:inborn error of metabolism | rel=r_hypo | relid=8 | w=31
  299. en:genetic disease -- r_hypo #8: 31 / 0.078 -> en:iron metabolism disorders
    n1=en:genetic disease | n2=en:iron metabolism disorders | rel=r_hypo | relid=8 | w=31
  300. en:genetic disease -- r_hypo #8: 31 / 0.078 -> en:lactase deficiency
    n1=en:genetic disease | n2=en:lactase deficiency | rel=r_hypo | relid=8 | w=31
  301. en:genetic disease -- r_hypo #8: 31 / 0.078 -> en:myopathy
    n1=en:genetic disease | n2=en:myopathy | rel=r_hypo | relid=8 | w=31
  302. en:genetic disease -- r_hypo #8: 31 / 0.078 -> en:osteosclerosis congenita
    n1=en:genetic disease | n2=en:osteosclerosis congenita | rel=r_hypo | relid=8 | w=31
  303. en:genetic disease -- r_hypo #8: 31 / 0.078 -> EPSM
    n1=en:genetic disease | n2=EPSM | rel=r_hypo | relid=8 | w=31
  304. en:genetic disease -- r_hypo #8: 31 / 0.078 -> fibrose kystique
    n1=en:genetic disease | n2=fibrose kystique | rel=r_hypo | relid=8 | w=31
  305. en:genetic disease -- r_hypo #8: 31 / 0.078 -> gangliosidose
    n1=en:genetic disease | n2=gangliosidose | rel=r_hypo | relid=8 | w=31
  306. en:genetic disease -- r_hypo #8: 31 / 0.078 -> leucodystrophie familiale avec atteinte surrénale
    n1=en:genetic disease | n2=leucodystrophie familiale avec atteinte surrénale | rel=r_hypo | relid=8 | w=31
  307. en:genetic disease -- r_hypo #8: 31 / 0.078 -> maladie de Bessel-Hagen
    n1=en:genetic disease | n2=maladie de Bessel-Hagen | rel=r_hypo | relid=8 | w=31
  308. en:genetic disease -- r_hypo #8: 31 / 0.078 -> maladie de canavan
    n1=en:genetic disease | n2=maladie de canavan | rel=r_hypo | relid=8 | w=31
  309. en:genetic disease -- r_hypo #8: 31 / 0.078 -> maladie de Shwachman
    n1=en:genetic disease | n2=maladie de Shwachman | rel=r_hypo | relid=8 | w=31
  310. en:genetic disease -- r_hypo #8: 31 / 0.078 -> maladie de wilson
    n1=en:genetic disease | n2=maladie de wilson | rel=r_hypo | relid=8 | w=31
  311. en:genetic disease -- r_hypo #8: 31 / 0.078 -> maladie des tics
    n1=en:genetic disease | n2=maladie des tics | rel=r_hypo | relid=8 | w=31
  312. en:genetic disease -- r_hypo #8: 31 / 0.078 -> maladie du muscle
    n1=en:genetic disease | n2=maladie du muscle | rel=r_hypo | relid=8 | w=31
  313. en:genetic disease -- r_hypo #8: 31 / 0.078 -> microsphérocytose héréditaire
    n1=en:genetic disease | n2=microsphérocytose héréditaire | rel=r_hypo | relid=8 | w=31
  314. en:genetic disease -- r_hypo #8: 31 / 0.078 -> nail-Patella syndrome
    n1=en:genetic disease | n2=nail-Patella syndrome | rel=r_hypo | relid=8 | w=31
  315. en:genetic disease -- r_hypo #8: 31 / 0.078 -> RPCA
    n1=en:genetic disease | n2=RPCA | rel=r_hypo | relid=8 | w=31
  316. en:genetic disease -- r_hypo #8: 31 / 0.078 -> Spondylarthrite ankylosante
    n1=en:genetic disease | n2=Spondylarthrite ankylosante | rel=r_hypo | relid=8 | w=31
  317. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de Brachmann-de Lange
    n1=en:genetic disease | n2=syndrome de Brachmann-de Lange | rel=r_hypo | relid=8 | w=31
  318. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de Christ-Siemens-Touraine
    n1=en:genetic disease | n2=syndrome de Christ-Siemens-Touraine | rel=r_hypo | relid=8 | w=31
  319. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de Cowden
    n1=en:genetic disease | n2=syndrome de Cowden | rel=r_hypo | relid=8 | w=31
  320. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de de Morsier
    n1=en:genetic disease | n2=syndrome de de Morsier | rel=r_hypo | relid=8 | w=31
  321. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de de Morsier-Kallmann
    n1=en:genetic disease | n2=syndrome de de Morsier-Kallmann | rel=r_hypo | relid=8 | w=31
  322. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de dubowitz
    n1=en:genetic disease | n2=syndrome de dubowitz | rel=r_hypo | relid=8 | w=31
  323. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de Gilbert
    n1=en:genetic disease | n2=syndrome de Gilbert | rel=r_hypo | relid=8 | w=31
  324. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de gilbert
    n1=en:genetic disease | n2=syndrome de gilbert | rel=r_hypo | relid=8 | w=31
  325. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de Johanson-Blizzard
    n1=en:genetic disease | n2=syndrome de Johanson-Blizzard | rel=r_hypo | relid=8 | w=31
  326. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de l'X fragile
    n1=en:genetic disease | n2=syndrome de l'X fragile | rel=r_hypo | relid=8 | w=31
  327. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de Lujan-Fryns
    n1=en:genetic disease | n2=syndrome de Lujan-Fryns | rel=r_hypo | relid=8 | w=31
  328. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de Rokitansky
    n1=en:genetic disease | n2=syndrome de Rokitansky | rel=r_hypo | relid=8 | w=31
  329. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome de Rothmund-Thomson
    n1=en:genetic disease | n2=syndrome de Rothmund-Thomson | rel=r_hypo | relid=8 | w=31
  330. en:genetic disease -- r_hypo #8: 31 / 0.078 -> syndrome des plaquettes grises
    n1=en:genetic disease | n2=syndrome des plaquettes grises | rel=r_hypo | relid=8 | w=31
  331. en:genetic disease -- r_hypo #8: 31 / 0.078 -> TNF receptor associated periodic syndrome
    n1=en:genetic disease | n2=TNF receptor associated periodic syndrome | rel=r_hypo | relid=8 | w=31
  332. en:genetic disease -- r_hypo #8: 31 / 0.078 -> trouble de gilles de la tourette
    n1=en:genetic disease | n2=trouble de gilles de la tourette | rel=r_hypo | relid=8 | w=31
  333. en:genetic disease -- r_hypo #8: 30 / 0.076 -> acidurie argininosuccinique
    n1=en:genetic disease | n2=acidurie argininosuccinique | rel=r_hypo | relid=8 | w=30
  334. en:genetic disease -- r_hypo #8: 30 / 0.076 -> amaurose congénitale de Leber
    n1=en:genetic disease | n2=amaurose congénitale de Leber | rel=r_hypo | relid=8 | w=30
  335. en:genetic disease -- r_hypo #8: 30 / 0.076 -> anémie falciforme
    n1=en:genetic disease | n2=anémie falciforme | rel=r_hypo | relid=8 | w=30
  336. en:genetic disease -- r_hypo #8: 30 / 0.076 -> anormalité des chromosomes
    n1=en:genetic disease | n2=anormalité des chromosomes | rel=r_hypo | relid=8 | w=30
  337. en:genetic disease -- r_hypo #8: 30 / 0.076 -> CADASIL
    n1=en:genetic disease | n2=CADASIL | rel=r_hypo | relid=8 | w=30
  338. en:genetic disease -- r_hypo #8: 30 / 0.076 -> déficit en phosphatases alcalines
    n1=en:genetic disease | n2=déficit en phosphatases alcalines | rel=r_hypo | relid=8 | w=30
  339. en:genetic disease -- r_hypo #8: 30 / 0.076 -> en:galactosemia
    n1=en:genetic disease | n2=en:galactosemia | rel=r_hypo | relid=8 | w=30
  340. en:genetic disease -- r_hypo #8: 30 / 0.076 -> en:huntington's disease
    n1=en:genetic disease | n2=en:huntington's disease | rel=r_hypo | relid=8 | w=30
  341. en:genetic disease -- r_hypo #8: 30 / 0.076 -> en:marfan syndrome
    n1=en:genetic disease | n2=en:marfan syndrome | rel=r_hypo | relid=8 | w=30
  342. en:genetic disease -- r_hypo #8: 30 / 0.076 -> en:sphingolipidosis
    n1=en:genetic disease | n2=en:sphingolipidosis | rel=r_hypo | relid=8 | w=30
  343. en:genetic disease -- r_hypo #8: 30 / 0.076 -> en:wilson's disease
    n1=en:genetic disease | n2=en:wilson's disease | rel=r_hypo | relid=8 | w=30
  344. en:genetic disease -- r_hypo #8: 30 / 0.076 -> hémochromatose
    n1=en:genetic disease | n2=hémochromatose | rel=r_hypo | relid=8 | w=30
  345. en:genetic disease -- r_hypo #8: 30 / 0.076 -> hémoglobinose S
    n1=en:genetic disease | n2=hémoglobinose S | rel=r_hypo | relid=8 | w=30
  346. en:genetic disease -- r_hypo #8: 30 / 0.076 -> hypercholestérolémie familiale
    n1=en:genetic disease | n2=hypercholestérolémie familiale | rel=r_hypo | relid=8 | w=30
  347. en:genetic disease -- r_hypo #8: 30 / 0.076 -> hyperphosphatasie alcaline avec retard mental
    n1=en:genetic disease | n2=hyperphosphatasie alcaline avec retard mental | rel=r_hypo | relid=8 | w=30
  348. en:genetic disease -- r_hypo #8: 30 / 0.076 -> maladie de cowden
    n1=en:genetic disease | n2=maladie de cowden | rel=r_hypo | relid=8 | w=30
  349. en:genetic disease -- r_hypo #8: 30 / 0.076 -> maladie de Mac Ardle
    n1=en:genetic disease | n2=maladie de Mac Ardle | rel=r_hypo | relid=8 | w=30
  350. en:genetic disease -- r_hypo #8: 30 / 0.076 -> maladie de pompe
    n1=en:genetic disease | n2=maladie de pompe | rel=r_hypo | relid=8 | w=30
  351. en:genetic disease -- r_hypo #8: 30 / 0.076 -> maladie des Açores
    n1=en:genetic disease | n2=maladie des Açores | rel=r_hypo | relid=8 | w=30
  352. en:genetic disease -- r_hypo #8: 30 / 0.076 -> maladie des exostoses multiples
    n1=en:genetic disease | n2=maladie des exostoses multiples | rel=r_hypo | relid=8 | w=30
  353. en:genetic disease -- r_hypo #8: 30 / 0.076 -> maladie musculaire
    n1=en:genetic disease | n2=maladie musculaire | rel=r_hypo | relid=8 | w=30
  354. en:genetic disease -- r_hypo #8: 30 / 0.076 -> maladie ostéogénique
    n1=en:genetic disease | n2=maladie ostéogénique | rel=r_hypo | relid=8 | w=30
  355. en:genetic disease -- r_hypo #8: 30 / 0.076 -> paraplégie spastique autosomique récessive type 7
    n1=en:genetic disease | n2=paraplégie spastique autosomique récessive type 7 | rel=r_hypo | relid=8 | w=30
  356. en:genetic disease -- r_hypo #8: 30 / 0.076 -> sphérocytose héréditaire
    n1=en:genetic disease | n2=sphérocytose héréditaire | rel=r_hypo | relid=8 | w=30
  357. en:genetic disease -- r_hypo #8: 30 / 0.076 -> syndrome de kallmann
    n1=en:genetic disease | n2=syndrome de kallmann | rel=r_hypo | relid=8 | w=30
  358. en:genetic disease -- r_hypo #8: 30 / 0.076 -> syndrome de Kartagener
    n1=en:genetic disease | n2=syndrome de Kartagener | rel=r_hypo | relid=8 | w=30
  359. en:genetic disease -- r_hypo #8: 30 / 0.076 -> syndrome de larsen
    n1=en:genetic disease | n2=syndrome de larsen | rel=r_hypo | relid=8 | w=30
  360. en:genetic disease -- r_hypo #8: 30 / 0.076 -> syndrome de Pendred
    n1=en:genetic disease | n2=syndrome de Pendred | rel=r_hypo | relid=8 | w=30
  361. en:genetic disease -- r_hypo #8: 30 / 0.076 -> syndrome de Protée
    n1=en:genetic disease | n2=syndrome de Protée | rel=r_hypo | relid=8 | w=30
  362. en:genetic disease -- r_hypo #8: 30 / 0.076 -> syndrome de Rathbun
    n1=en:genetic disease | n2=syndrome de Rathbun | rel=r_hypo | relid=8 | w=30
  363. en:genetic disease -- r_hypo #8: 30 / 0.076 -> syndrome main pied utérus
    n1=en:genetic disease | n2=syndrome main pied utérus | rel=r_hypo | relid=8 | w=30
  364. en:genetic disease -- r_hypo #8: 30 / 0.076 -> syndrome triple a
    n1=en:genetic disease | n2=syndrome triple a | rel=r_hypo | relid=8 | w=30
  365. en:genetic disease -- r_hypo #8: 30 / 0.076 -> Voir l'article
    n1=en:genetic disease | n2=Voir l'article | rel=r_hypo | relid=8 | w=30
  366. en:genetic disease -- r_hypo #8: 29 / 0.073 -> ABD
    n1=en:genetic disease | n2=ABD | rel=r_hypo | relid=8 | w=29
  367. en:genetic disease -- r_hypo #8: 29 / 0.073 -> dysplasie olfactogénitale de De Morsier
    n1=en:genetic disease | n2=dysplasie olfactogénitale de De Morsier | rel=r_hypo | relid=8 | w=29
  368. en:genetic disease -- r_hypo #8: 29 / 0.073 -> dystrophie congénitale musculaire d'Ullrich
    n1=en:genetic disease | n2=dystrophie congénitale musculaire d'Ullrich | rel=r_hypo | relid=8 | w=29
  369. en:genetic disease -- r_hypo #8: 29 / 0.073 -> en:albinism
    n1=en:genetic disease | n2=en:albinism | rel=r_hypo | relid=8 | w=29
  370. en:genetic disease -- r_hypo #8: 29 / 0.073 -> en:arachnodactyly
    n1=en:genetic disease | n2=en:arachnodactyly | rel=r_hypo | relid=8 | w=29
  371. en:genetic disease -- r_hypo #8: 29 / 0.073 -> en:autosomal dominant disorder
    n1=en:genetic disease | n2=en:autosomal dominant disorder | rel=r_hypo | relid=8 | w=29
  372. en:genetic disease -- r_hypo #8: 29 / 0.073 -> en:juvenile amaurotic idiocy
    n1=en:genetic disease | n2=en:juvenile amaurotic idiocy | rel=r_hypo | relid=8 | w=29
  373. en:genetic disease -- r_hypo #8: 29 / 0.073 -> en:rheumatic chorea
    n1=en:genetic disease | n2=en:rheumatic chorea | rel=r_hypo | relid=8 | w=29
  374. en:genetic disease -- r_hypo #8: 29 / 0.073 -> goitre
    n1=en:genetic disease | n2=goitre | rel=r_hypo | relid=8 | w=29
  375. en:genetic disease -- r_hypo #8: 29 / 0.073 -> maladie de Crigler-Najjar
    n1=en:genetic disease | n2=maladie de Crigler-Najjar | rel=r_hypo | relid=8 | w=29
  376. en:genetic disease -- r_hypo #8: 29 / 0.073 -> maladie de machado-joseph
    n1=en:genetic disease | n2=maladie de machado-joseph | rel=r_hypo | relid=8 | w=29
  377. en:genetic disease -- r_hypo #8: 29 / 0.073 -> maladie de Westphal
    n1=en:genetic disease | n2=maladie de Westphal | rel=r_hypo | relid=8 | w=29
  378. en:genetic disease -- r_hypo #8: 29 / 0.073 -> maladie des langes bleus
    n1=en:genetic disease | n2=maladie des langes bleus | rel=r_hypo | relid=8 | w=29
  379. en:genetic disease -- r_hypo #8: 29 / 0.073 -> Maladie génétique du métabolisme des glucides
    n1=en:genetic disease | n2=Maladie génétique du métabolisme des glucides | rel=r_hypo | relid=8 | w=29
  380. en:genetic disease -- r_hypo #8: 29 / 0.073 -> maladies de gilles de la tourette
    n1=en:genetic disease | n2=maladies de gilles de la tourette | rel=r_hypo | relid=8 | w=29
  381. en:genetic disease -- r_hypo #8: 29 / 0.073 -> mucopolysaccharidose de type vii
    n1=en:genetic disease | n2=mucopolysaccharidose de type vii | rel=r_hypo | relid=8 | w=29
  382. en:genetic disease -- r_hypo #8: 29 / 0.073 -> myopathie de Bethlem
    n1=en:genetic disease | n2=myopathie de Bethlem | rel=r_hypo | relid=8 | w=29
  383. en:genetic disease -- r_hypo #8: 29 / 0.073 -> pseudoxanthome élastique
    n1=en:genetic disease | n2=pseudoxanthome élastique | rel=r_hypo | relid=8 | w=29
  384. en:genetic disease -- r_hypo #8: 29 / 0.073 -> pycnose
    n1=en:genetic disease | n2=pycnose | rel=r_hypo | relid=8 | w=29
  385. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome de bloch-sulzberger
    n1=en:genetic disease | n2=syndrome de bloch-sulzberger | rel=r_hypo | relid=8 | w=29
  386. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome de Chediak Higashi
    n1=en:genetic disease | n2=syndrome de Chediak Higashi | rel=r_hypo | relid=8 | w=29
  387. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome de Hermansky-Pudlak
    n1=en:genetic disease | n2=syndrome de Hermansky-Pudlak | rel=r_hypo | relid=8 | w=29
  388. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome de Kallman-de Morsier
    n1=en:genetic disease | n2=syndrome de Kallman-de Morsier | rel=r_hypo | relid=8 | w=29
  389. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome de kartagener
    n1=en:genetic disease | n2=syndrome de kartagener | rel=r_hypo | relid=8 | w=29
  390. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome de Louis-Bar
    n1=en:genetic disease | n2=syndrome de Louis-Bar | rel=r_hypo | relid=8 | w=29
  391. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome de rathbun
    n1=en:genetic disease | n2=syndrome de rathbun | rel=r_hypo | relid=8 | w=29
  392. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome de Williams
    n1=en:genetic disease | n2=syndrome de Williams | rel=r_hypo | relid=8 | w=29
  393. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome de zinsser-engman-cole
    n1=en:genetic disease | n2=syndrome de zinsser-engman-cole | rel=r_hypo | relid=8 | w=29
  394. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome leopard
    n1=en:genetic disease | n2=syndrome leopard | rel=r_hypo | relid=8 | w=29
  395. en:genetic disease -- r_hypo #8: 29 / 0.073 -> syndrome triple A
    n1=en:genetic disease | n2=syndrome triple A | rel=r_hypo | relid=8 | w=29
  396. en:genetic disease -- r_hypo #8: 29 / 0.073 -> xanthomatose cérébrotendineuse
    n1=en:genetic disease | n2=xanthomatose cérébrotendineuse | rel=r_hypo | relid=8 | w=29
  397. en:genetic disease -- r_hypo #8: 28 / 0.071 -> anémie mégaloblastique thiamine-sensible
    n1=en:genetic disease | n2=anémie mégaloblastique thiamine-sensible | rel=r_hypo | relid=8 | w=28
  398. en:genetic disease -- r_hypo #8: 28 / 0.071 -> démence d'Alzheimer
    n1=en:genetic disease | n2=démence d'Alzheimer | rel=r_hypo | relid=8 | w=28
  399. en:genetic disease -- r_hypo #8: 28 / 0.071 -> diabète bronzé
    n1=en:genetic disease | n2=diabète bronzé | rel=r_hypo | relid=8 | w=28
  400. en:genetic disease -- r_hypo #8: 28 / 0.071 -> dyskinésie ciliaire primitive
    n1=en:genetic disease | n2=dyskinésie ciliaire primitive | rel=r_hypo | relid=8 | w=28
  401. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:emery-dreifuss muscular dystrophy
    n1=en:genetic disease | n2=en:emery-dreifuss muscular dystrophy | rel=r_hypo | relid=8 | w=28
  402. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:gustation
    n1=en:genetic disease | n2=en:gustation | rel=r_hypo | relid=8 | w=28
  403. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:incontinentia pigmenti
    n1=en:genetic disease | n2=en:incontinentia pigmenti | rel=r_hypo | relid=8 | w=28
  404. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:marble bones disease
    n1=en:genetic disease | n2=en:marble bones disease | rel=r_hypo | relid=8 | w=28
  405. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:microcephaly
    n1=en:genetic disease | n2=en:microcephaly | rel=r_hypo | relid=8 | w=28
  406. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:oligodontia
    n1=en:genetic disease | n2=en:oligodontia | rel=r_hypo | relid=8 | w=28
  407. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:polydactyly
    n1=en:genetic disease | n2=en:polydactyly | rel=r_hypo | relid=8 | w=28
  408. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:progeria
    n1=en:genetic disease | n2=en:progeria | rel=r_hypo | relid=8 | w=28
  409. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:taste perception
    n1=en:genetic disease | n2=en:taste perception | rel=r_hypo | relid=8 | w=28
  410. en:genetic disease -- r_hypo #8: 28 / 0.071 -> en:walker-warburg syndrome
    n1=en:genetic disease | n2=en:walker-warburg syndrome | rel=r_hypo | relid=8 | w=28
  411. en:genetic disease -- r_hypo #8: 28 / 0.071 -> enzymopathie
    n1=en:genetic disease | n2=enzymopathie | rel=r_hypo | relid=8 | w=28
  412. en:genetic disease -- r_hypo #8: 28 / 0.071 -> hypogonadisme avec anosmie
    n1=en:genetic disease | n2=hypogonadisme avec anosmie | rel=r_hypo | relid=8 | w=28
  413. en:genetic disease -- r_hypo #8: 28 / 0.071 -> maladie de Marfan
    n1=en:genetic disease | n2=maladie de Marfan | rel=r_hypo | relid=8 | w=28
  414. en:genetic disease -- r_hypo #8: 28 / 0.071 -> maladie héréditaire de l'oreille moyenne
    n1=en:genetic disease | n2=maladie héréditaire de l'oreille moyenne | rel=r_hypo | relid=8 | w=28
  415. en:genetic disease -- r_hypo #8: 28 / 0.071 -> naevomatose baso-cellulaire
    n1=en:genetic disease | n2=naevomatose baso-cellulaire | rel=r_hypo | relid=8 | w=28
  416. en:genetic disease -- r_hypo #8: 28 / 0.071 -> nanisme à tête d'oiseau
    n1=en:genetic disease | n2=nanisme à tête d'oiseau | rel=r_hypo | relid=8 | w=28
  417. en:genetic disease -- r_hypo #8: 28 / 0.071 -> nanisme mulibrey
    n1=en:genetic disease | n2=nanisme mulibrey | rel=r_hypo | relid=8 | w=28
  418. en:genetic disease -- r_hypo #8: 28 / 0.071 -> nævomatose baso-cellulaire
    n1=en:genetic disease | n2=nævomatose baso-cellulaire | rel=r_hypo | relid=8 | w=28
  419. en:genetic disease -- r_hypo #8: 28 / 0.071 -> neurofibromatose de type 2
    n1=en:genetic disease | n2=neurofibromatose de type 2 | rel=r_hypo | relid=8 | w=28
  420. en:genetic disease -- r_hypo #8: 28 / 0.071 -> oxalose
    n1=en:genetic disease | n2=oxalose | rel=r_hypo | relid=8 | w=28
  421. en:genetic disease -- r_hypo #8: 28 / 0.071 -> oxaloses
    n1=en:genetic disease | n2=oxaloses | rel=r_hypo | relid=8 | w=28
  422. en:genetic disease -- r_hypo #8: 28 / 0.071 -> syndrome de Beckwith-Wiedemann
    n1=en:genetic disease | n2=syndrome de Beckwith-Wiedemann | rel=r_hypo | relid=8 | w=28
  423. en:genetic disease -- r_hypo #8: 28 / 0.071 -> syndrome de Bloch-Sulzberger
    n1=en:genetic disease | n2=syndrome de Bloch-Sulzberger | rel=r_hypo | relid=8 | w=28
  424. en:genetic disease -- r_hypo #8: 28 / 0.071 -> syndrome de gorlin
    n1=en:genetic disease | n2=syndrome de gorlin | rel=r_hypo | relid=8 | w=28
  425. en:genetic disease -- r_hypo #8: 28 / 0.071 -> syndrome de Hutchinson-Gilford
    n1=en:genetic disease | n2=syndrome de Hutchinson-Gilford | rel=r_hypo | relid=8 | w=28
  426. en:genetic disease -- r_hypo #8: 28 / 0.071 -> syndrome de johanson-blizzard
    n1=en:genetic disease | n2=syndrome de johanson-blizzard | rel=r_hypo | relid=8 | w=28
  427. en:genetic disease -- r_hypo #8: 28 / 0.071 -> syndrome de peutz-jeghers
    n1=en:genetic disease | n2=syndrome de peutz-jeghers | rel=r_hypo | relid=8 | w=28
  428. en:genetic disease -- r_hypo #8: 28 / 0.071 -> syndrome de shwachman-diamond
    n1=en:genetic disease | n2=syndrome de shwachman-diamond | rel=r_hypo | relid=8 | w=28
  429. en:genetic disease -- r_hypo #8: 28 / 0.071 -> syndrome de tourette
    n1=en:genetic disease | n2=syndrome de tourette | rel=r_hypo | relid=8 | w=28
  430. en:genetic disease -- r_hypo #8: 28 / 0.071 -> syndrome oculo-facio-cardio-dentaire
    n1=en:genetic disease | n2=syndrome oculo-facio-cardio-dentaire | rel=r_hypo | relid=8 | w=28
  431. en:genetic disease -- r_hypo #8: 27 / 0.068 -> anémie de fanconi
    n1=en:genetic disease | n2=anémie de fanconi | rel=r_hypo | relid=8 | w=27
  432. en:genetic disease -- r_hypo #8: 27 / 0.068 -> chorée de sydenham
    n1=en:genetic disease | n2=chorée de sydenham | rel=r_hypo | relid=8 | w=27
  433. en:genetic disease -- r_hypo #8: 27 / 0.068 -> défaut d'adhérence des leucocytes chez les bovins
    n1=en:genetic disease | n2=défaut d'adhérence des leucocytes chez les bovins | rel=r_hypo | relid=8 | w=27
  434. en:genetic disease -- r_hypo #8: 27 / 0.068 -> déficience en entérokinase
    n1=en:genetic disease | n2=déficience en entérokinase | rel=r_hypo | relid=8 | w=27
  435. en:genetic disease -- r_hypo #8: 27 / 0.068 -> déficit en transporteur de glucose de type 1
    n1=en:genetic disease | n2=déficit en transporteur de glucose de type 1 | rel=r_hypo | relid=8 | w=27
  436. en:genetic disease -- r_hypo #8: 27 / 0.068 -> dystonie avec parkinsonisme liée à l'X
    n1=en:genetic disease | n2=dystonie avec parkinsonisme liée à l'X | rel=r_hypo | relid=8 | w=27
  437. en:genetic disease -- r_hypo #8: 27 / 0.068 -> dystrophie musculaire d'Emery-Dreifuss
    n1=en:genetic disease | n2=dystrophie musculaire d'Emery-Dreifuss | rel=r_hypo | relid=8 | w=27
  438. en:genetic disease -- r_hypo #8: 27 / 0.068 -> en:autosomal recessive disease
    n1=en:genetic disease | n2=en:autosomal recessive disease | rel=r_hypo | relid=8 | w=27
  439. en:genetic disease -- r_hypo #8: 27 / 0.068 -> en:hirsutism
    n1=en:genetic disease | n2=en:hirsutism | rel=r_hypo | relid=8 | w=27
  440. en:genetic disease -- r_hypo #8: 27 / 0.068 -> en:tourette syndrome
    n1=en:genetic disease | n2=en:tourette syndrome | rel=r_hypo | relid=8 | w=27
  441. en:genetic disease -- r_hypo #8: 27 / 0.068 -> gangliosidose à gm2
    n1=en:genetic disease | n2=gangliosidose à gm2 | rel=r_hypo | relid=8 | w=27
  442. en:genetic disease -- r_hypo #8: 27 / 0.068 -> glycogénose de type iii
    n1=en:genetic disease | n2=glycogénose de type iii | rel=r_hypo | relid=8 | w=27
  443. en:genetic disease -- r_hypo #8: 27 / 0.068 -> hypophosphatasies
    n1=en:genetic disease | n2=hypophosphatasies | rel=r_hypo | relid=8 | w=27
  444. en:genetic disease -- r_hypo #8: 27 / 0.068 -> hypophosphatémie liée à l'x
    n1=en:genetic disease | n2=hypophosphatémie liée à l'x | rel=r_hypo | relid=8 | w=27
  445. en:genetic disease -- r_hypo #8: 27 / 0.068 -> incontinentia pigmenti
    n1=en:genetic disease | n2=incontinentia pigmenti | rel=r_hypo | relid=8 | w=27
  446. en:genetic disease -- r_hypo #8: 27 / 0.068 -> léiomyomatose familiale et cancer du rein
    n1=en:genetic disease | n2=léiomyomatose familiale et cancer du rein | rel=r_hypo | relid=8 | w=27
  447. en:genetic disease -- r_hypo #8: 27 / 0.068 -> leucoencéphalopathie mégalencéphalique avec kystes sub-corticaux
    n1=en:genetic disease | n2=leucoencéphalopathie mégalencéphalique avec kystes sub-corticaux | rel=r_hypo | relid=8 | w=27
  448. en:genetic disease -- r_hypo #8: 27 / 0.068 -> maladie de Minkowski-Chauffard
    n1=en:genetic disease | n2=maladie de Minkowski-Chauffard | rel=r_hypo | relid=8 | w=27
  449. en:genetic disease -- r_hypo #8: 27 / 0.068 -> maladie de rendu-osler
    n1=en:genetic disease | n2=maladie de rendu-osler | rel=r_hypo | relid=8 | w=27
  450. en:genetic disease -- r_hypo #8: 27 / 0.068 -> maladie de steinert
    n1=en:genetic disease | n2=maladie de steinert | rel=r_hypo | relid=8 | w=27
  451. en:genetic disease -- r_hypo #8: 27 / 0.068 -> maladie génétique musculaire
    n1=en:genetic disease | n2=maladie génétique musculaire | rel=r_hypo | relid=8 | w=27
  452. en:genetic disease -- r_hypo #8: 27 / 0.068 -> maladie génétique orpheline
    n1=en:genetic disease | n2=maladie génétique orpheline | rel=r_hypo | relid=8 | w=27
  453. en:genetic disease -- r_hypo #8: 27 / 0.068 -> neuroacanthocytose
    n1=en:genetic disease | n2=neuroacanthocytose | rel=r_hypo | relid=8 | w=27
  454. en:genetic disease -- r_hypo #8: 27 / 0.068 -> sicklémie
    n1=en:genetic disease | n2=sicklémie | rel=r_hypo | relid=8 | w=27
  455. en:genetic disease -- r_hypo #8: 27 / 0.068 -> syndrome de Rett
    n1=en:genetic disease | n2=syndrome de Rett | rel=r_hypo | relid=8 | w=27
  456. en:genetic disease -- r_hypo #8: 27 / 0.068 -> syndrome de Treacher Collins
    n1=en:genetic disease | n2=syndrome de Treacher Collins | rel=r_hypo | relid=8 | w=27
  457. en:genetic disease -- r_hypo #8: 27 / 0.068 -> syndrome de Walker-Warburg
    n1=en:genetic disease | n2=syndrome de Walker-Warburg | rel=r_hypo | relid=8 | w=27
  458. en:genetic disease -- r_hypo #8: 27 / 0.068 -> syndrome de Zinsser-Engman-Cole
    n1=en:genetic disease | n2=syndrome de Zinsser-Engman-Cole | rel=r_hypo | relid=8 | w=27
  459. en:genetic disease -- r_hypo #8: 27 / 0.068 -> syndrome des tics de Gilles de la Tourette
    n1=en:genetic disease | n2=syndrome des tics de Gilles de la Tourette | rel=r_hypo | relid=8 | w=27
  460. en:genetic disease -- r_hypo #8: 27 / 0.068 -> syndrome olfacto-génital
    n1=en:genetic disease | n2=syndrome olfacto-génital | rel=r_hypo | relid=8 | w=27
  461. en:genetic disease -- r_hypo #8: 27 / 0.068 -> XLH
    n1=en:genetic disease | n2=XLH | rel=r_hypo | relid=8 | w=27
  462. en:genetic disease -- r_hypo #8: 26 / 0.066 -> affection familiale autosomique dominante
    n1=en:genetic disease | n2=affection familiale autosomique dominante | rel=r_hypo | relid=8 | w=26
  463. en:genetic disease -- r_hypo #8: 26 / 0.066 -> en:cardiomyopathy dilated with woolly hair and keratoderma
    n1=en:genetic disease | n2=en:cardiomyopathy dilated with woolly hair and keratoderma | rel=r_hypo | relid=8 | w=26
  464. en:genetic disease -- r_hypo #8: 26 / 0.066 -> en:fanconi's anaemia
    n1=en:genetic disease | n2=en:fanconi's anaemia | rel=r_hypo | relid=8 | w=26
  465. en:genetic disease -- r_hypo #8: 26 / 0.066 -> en:hypophosphatasia
    n1=en:genetic disease | n2=en:hypophosphatasia | rel=r_hypo | relid=8 | w=26
  466. en:genetic disease -- r_hypo #8: 26 / 0.066 -> en:lissencephaly
    n1=en:genetic disease | n2=en:lissencephaly | rel=r_hypo | relid=8 | w=26
  467. en:genetic disease -- r_hypo #8: 26 / 0.066 -> en:muscular dystrophy, oculopharyngeal
    n1=en:genetic disease | n2=en:muscular dystrophy, oculopharyngeal | rel=r_hypo | relid=8 | w=26
  468. en:genetic disease -- r_hypo #8: 26 / 0.066 -> en:rett syndrome
    n1=en:genetic disease | n2=en:rett syndrome | rel=r_hypo | relid=8 | w=26
  469. en:genetic disease -- r_hypo #8: 26 / 0.066 -> gangliosidose à GM2
    n1=en:genetic disease | n2=gangliosidose à GM2 | rel=r_hypo | relid=8 | w=26
  470. en:genetic disease -- r_hypo #8: 26 / 0.066 -> hypophosphatasie
    n1=en:genetic disease | n2=hypophosphatasie | rel=r_hypo | relid=8 | w=26
  471. en:genetic disease -- r_hypo #8: 26 / 0.066 -> maladie de Pompe
    n1=en:genetic disease | n2=maladie de Pompe | rel=r_hypo | relid=8 | w=26
  472. en:genetic disease -- r_hypo #8: 26 / 0.066 -> maladie enzymatique
    n1=en:genetic disease | n2=maladie enzymatique | rel=r_hypo | relid=8 | w=26
  473. en:genetic disease -- r_hypo #8: 26 / 0.066 -> mosaïque
    n1=en:genetic disease | n2=mosaïque | rel=r_hypo | relid=8 | w=26
  474. en:genetic disease -- r_hypo #8: 26 / 0.066 -> Myopathie à stockage de polysaccharides
    n1=en:genetic disease | n2=Myopathie à stockage de polysaccharides | rel=r_hypo | relid=8 | w=26
  475. en:genetic disease -- r_hypo #8: 26 / 0.066 -> neurofibromatose de type II
    n1=en:genetic disease | n2=neurofibromatose de type II | rel=r_hypo | relid=8 | w=26
  476. en:genetic disease -- r_hypo #8: 26 / 0.066 -> paraplégie spastique familiale type 4
    n1=en:genetic disease | n2=paraplégie spastique familiale type 4 | rel=r_hypo | relid=8 | w=26
  477. en:genetic disease -- r_hypo #8: 26 / 0.066 -> polydactylie
    n1=en:genetic disease | n2=polydactylie | rel=r_hypo | relid=8 | w=26
  478. en:genetic disease -- r_hypo #8: 26 / 0.066 -> rétinite pigmentaire in utero
    n1=en:genetic disease | n2=rétinite pigmentaire in utero | rel=r_hypo | relid=8 | w=26
  479. en:genetic disease -- r_hypo #8: 26 / 0.066 -> syndrome d'aicardi
    n1=en:genetic disease | n2=syndrome d'aicardi | rel=r_hypo | relid=8 | w=26
  480. en:genetic disease -- r_hypo #8: 26 / 0.066 -> syndrome d'Ehlers-Danlos type classique
    n1=en:genetic disease | n2=syndrome d'Ehlers-Danlos type classique | rel=r_hypo | relid=8 | w=26
  481. en:genetic disease -- r_hypo #8: 26 / 0.066 -> syndrome d'Ondine
    n1=en:genetic disease | n2=syndrome d'Ondine | rel=r_hypo | relid=8 | w=26
  482. en:genetic disease -- r_hypo #8: 26 / 0.066 -> syndrome de Coffin-Siris
    n1=en:genetic disease | n2=syndrome de Coffin-Siris | rel=r_hypo | relid=8 | w=26
  483. en:genetic disease -- r_hypo #8: 26 / 0.066 -> syndrome de Gilles de la Tourette
    n1=en:genetic disease | n2=syndrome de Gilles de la Tourette | rel=r_hypo | relid=8 | w=26
  484. en:genetic disease -- r_hypo #8: 26 / 0.066 -> syndrome de Lesch-Nyhan
    n1=en:genetic disease | n2=syndrome de Lesch-Nyhan | rel=r_hypo | relid=8 | w=26
  485. en:genetic disease -- r_hypo #8: 26 / 0.066 -> syndrome de McKusick Kaufman
    n1=en:genetic disease | n2=syndrome de McKusick Kaufman | rel=r_hypo | relid=8 | w=26
  486. en:genetic disease -- r_hypo #8: 26 / 0.066 -> syndrome de rett
    n1=en:genetic disease | n2=syndrome de rett | rel=r_hypo | relid=8 | w=26
  487. en:genetic disease -- r_hypo #8: 26 / 0.066 -> syndrome de Shwachman-Diamond
    n1=en:genetic disease | n2=syndrome de Shwachman-Diamond | rel=r_hypo | relid=8 | w=26
  488. en:genetic disease -- r_hypo #8: 26 / 0.066 -> Syndrome Rapadilano
    n1=en:genetic disease | n2=Syndrome Rapadilano | rel=r_hypo | relid=8 | w=26
  489. en:genetic disease -- r_hypo #8: 25 / 0.063 -> aclasie diaphysaire
    n1=en:genetic disease | n2=aclasie diaphysaire | rel=r_hypo | relid=8 | w=25
  490. en:genetic disease -- r_hypo #8: 25 / 0.063 -> affection à hématies falciformes
    n1=en:genetic disease | n2=affection à hématies falciformes | rel=r_hypo | relid=8 | w=25
  491. en:genetic disease -- r_hypo #8: 25 / 0.063 -> albinisme avec pigmentation minime
    n1=en:genetic disease | n2=albinisme avec pigmentation minime | rel=r_hypo | relid=8 | w=25
  492. en:genetic disease -- r_hypo #8: 25 / 0.063 -> anémie drépanocytaire
    n1=en:genetic disease | n2=anémie drépanocytaire | rel=r_hypo | relid=8 | w=25
  493. en:genetic disease -- r_hypo #8: 25 / 0.063 -> anémie ss
    n1=en:genetic disease | n2=anémie ss | rel=r_hypo | relid=8 | w=25
  494. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Ataxie télangiectasie
    n1=en:genetic disease | n2=Ataxie télangiectasie | rel=r_hypo | relid=8 | w=25
  495. en:genetic disease -- r_hypo #8: 25 / 0.063 -> ataxie télangiectasique
    n1=en:genetic disease | n2=ataxie télangiectasique | rel=r_hypo | relid=8 | w=25
  496. en:genetic disease -- r_hypo #8: 25 / 0.063 -> cancer colique
    n1=en:genetic disease | n2=cancer colique | rel=r_hypo | relid=8 | w=25
  497. en:genetic disease -- r_hypo #8: 25 / 0.063 -> cholémie de gilbert
    n1=en:genetic disease | n2=cholémie de gilbert | rel=r_hypo | relid=8 | w=25
  498. en:genetic disease -- r_hypo #8: 25 / 0.063 -> chondrodysplasie déformante héréditaire
    n1=en:genetic disease | n2=chondrodysplasie déformante héréditaire | rel=r_hypo | relid=8 | w=25
  499. en:genetic disease -- r_hypo #8: 25 / 0.063 -> chondrodysplasie héréditaire déformante
    n1=en:genetic disease | n2=chondrodysplasie héréditaire déformante | rel=r_hypo | relid=8 | w=25
  500. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Chopart (désarticulation de)
    n1=en:genetic disease | n2=Chopart (désarticulation de) | rel=r_hypo | relid=8 | w=25
  501. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Chorée
    n1=en:genetic disease | n2=Chorée | rel=r_hypo | relid=8 | w=25
  502. en:genetic disease -- r_hypo #8: 25 / 0.063 -> chorée de saint jean
    n1=en:genetic disease | n2=chorée de saint jean | rel=r_hypo | relid=8 | w=25
  503. en:genetic disease -- r_hypo #8: 25 / 0.063 -> chorée héréditaire
    n1=en:genetic disease | n2=chorée héréditaire | rel=r_hypo | relid=8 | w=25
  504. en:genetic disease -- r_hypo #8: 25 / 0.063 -> chorée rhumatismale
    n1=en:genetic disease | n2=chorée rhumatismale | rel=r_hypo | relid=8 | w=25
  505. en:genetic disease -- r_hypo #8: 25 / 0.063 -> chorée rhumatismale sans atteinte cardiaque
    n1=en:genetic disease | n2=chorée rhumatismale sans atteinte cardiaque | rel=r_hypo | relid=8 | w=25
  506. en:genetic disease -- r_hypo #8: 25 / 0.063 -> chorées
    n1=en:genetic disease | n2=chorées | rel=r_hypo | relid=8 | w=25
  507. en:genetic disease -- r_hypo #8: 25 / 0.063 -> danse de saint Guy
    n1=en:genetic disease | n2=danse de saint Guy | rel=r_hypo | relid=8 | w=25
  508. en:genetic disease -- r_hypo #8: 25 / 0.063 -> diabète (accidents vasculaires cérébraux du)
    n1=en:genetic disease | n2=diabète (accidents vasculaires cérébraux du) | rel=r_hypo | relid=8 | w=25
  509. en:genetic disease -- r_hypo #8: 25 / 0.063 -> distrophie
    n1=en:genetic disease | n2=distrophie | rel=r_hypo | relid=8 | w=25
  510. en:genetic disease -- r_hypo #8: 25 / 0.063 -> drépanocytose homozygote
    n1=en:genetic disease | n2=drépanocytose homozygote | rel=r_hypo | relid=8 | w=25
  511. en:genetic disease -- r_hypo #8: 25 / 0.063 -> dysfonctionnement hépatique constitutionnel
    n1=en:genetic disease | n2=dysfonctionnement hépatique constitutionnel | rel=r_hypo | relid=8 | w=25
  512. en:genetic disease -- r_hypo #8: 25 / 0.063 -> dysplasie olfacto-génitale
    n1=en:genetic disease | n2=dysplasie olfacto-génitale | rel=r_hypo | relid=8 | w=25
  513. en:genetic disease -- r_hypo #8: 25 / 0.063 -> dysplasie olfactogénitale
    n1=en:genetic disease | n2=dysplasie olfactogénitale | rel=r_hypo | relid=8 | w=25
  514. en:genetic disease -- r_hypo #8: 25 / 0.063 -> dystrophie
    n1=en:genetic disease | n2=dystrophie | rel=r_hypo | relid=8 | w=25
  515. en:genetic disease -- r_hypo #8: 25 / 0.063 -> dystrophie facioscapulohumérale musculaire 1A
    n1=en:genetic disease | n2=dystrophie facioscapulohumérale musculaire 1A | rel=r_hypo | relid=8 | w=25
  516. en:genetic disease -- r_hypo #8: 25 / 0.063 -> dystrophie musculaire
    n1=en:genetic disease | n2=dystrophie musculaire | rel=r_hypo | relid=8 | w=25
  517. en:genetic disease -- r_hypo #8: 25 / 0.063 -> dystrophie musculaire congénitale, cataracte infantile et hypogonadisme
    n1=en:genetic disease | n2=dystrophie musculaire congénitale, cataracte infantile et hypogonadisme | rel=r_hypo | relid=8 | w=25
  518. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Dystrophie myotonique de Steinert
    n1=en:genetic disease | n2=Dystrophie myotonique de Steinert | rel=r_hypo | relid=8 | w=25
  519. en:genetic disease -- r_hypo #8: 25 / 0.063 -> dystrophy
    n1=en:genetic disease | n2=dystrophy | rel=r_hypo | relid=8 | w=25
  520. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:Alzheimer's
    n1=en:genetic disease | n2=en:Alzheimer's | rel=r_hypo | relid=8 | w=25
  521. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:Alzheimer's disease
    n1=en:genetic disease | n2=en:Alzheimer's disease | rel=r_hypo | relid=8 | w=25
  522. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:alzheimer's disease
    n1=en:genetic disease | n2=en:alzheimer's disease | rel=r_hypo | relid=8 | w=25
  523. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:anemia and sickle-shaped erythrocytes
    n1=en:genetic disease | n2=en:anemia and sickle-shaped erythrocytes | rel=r_hypo | relid=8 | w=25
  524. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:anemia, sickle cell
    n1=en:genetic disease | n2=en:anemia, sickle cell | rel=r_hypo | relid=8 | w=25
  525. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:angelman syndrome
    n1=en:genetic disease | n2=en:angelman syndrome | rel=r_hypo | relid=8 | w=25
  526. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:Angelman syndrome
    n1=en:genetic disease | n2=en:Angelman syndrome | rel=r_hypo | relid=8 | w=25
  527. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:ataxia telangiectasia
    n1=en:genetic disease | n2=en:ataxia telangiectasia | rel=r_hypo | relid=8 | w=25
  528. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:branched-chain ketoaciduria
    n1=en:genetic disease | n2=en:branched-chain ketoaciduria | rel=r_hypo | relid=8 | w=25
  529. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:classical maple syrup urine disease
    n1=en:genetic disease | n2=en:classical maple syrup urine disease | rel=r_hypo | relid=8 | w=25
  530. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:Cowden's disease
    n1=en:genetic disease | n2=en:Cowden's disease | rel=r_hypo | relid=8 | w=25
  531. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:gangliosidosis
    n1=en:genetic disease | n2=en:gangliosidosis | rel=r_hypo | relid=8 | w=25
  532. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:goiter
    n1=en:genetic disease | n2=en:goiter | rel=r_hypo | relid=8 | w=25
  533. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:Gorlin's syndrome
    n1=en:genetic disease | n2=en:Gorlin's syndrome | rel=r_hypo | relid=8 | w=25
  534. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:Hartnup's disease
    n1=en:genetic disease | n2=en:Hartnup's disease | rel=r_hypo | relid=8 | w=25
  535. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:hereditary spherocytosis
    n1=en:genetic disease | n2=en:hereditary spherocytosis | rel=r_hypo | relid=8 | w=25
  536. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:limit dextrinosis
    n1=en:genetic disease | n2=en:limit dextrinosis | rel=r_hypo | relid=8 | w=25
  537. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:Lowe's disease
    n1=en:genetic disease | n2=en:Lowe's disease | rel=r_hypo | relid=8 | w=25
  538. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:maple syrup urine disease
    n1=en:genetic disease | n2=en:maple syrup urine disease | rel=r_hypo | relid=8 | w=25
  539. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:microspherophakia
    n1=en:genetic disease | n2=en:microspherophakia | rel=r_hypo | relid=8 | w=25
  540. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:multiple lentigines syndrome
    n1=en:genetic disease | n2=en:multiple lentigines syndrome | rel=r_hypo | relid=8 | w=25
  541. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:myodystrophia
    n1=en:genetic disease | n2=en:myodystrophia | rel=r_hypo | relid=8 | w=25
  542. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:primary hyperoxaluria
    n1=en:genetic disease | n2=en:primary hyperoxaluria | rel=r_hypo | relid=8 | w=25
  543. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:sicklaemia
    n1=en:genetic disease | n2=en:sicklaemia | rel=r_hypo | relid=8 | w=25
  544. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:sickle cell anaemia
    n1=en:genetic disease | n2=en:sickle cell anaemia | rel=r_hypo | relid=8 | w=25
  545. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:sickle cell anemia
    n1=en:genetic disease | n2=en:sickle cell anemia | rel=r_hypo | relid=8 | w=25
  546. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:sickle-cell anaemia
    n1=en:genetic disease | n2=en:sickle-cell anaemia | rel=r_hypo | relid=8 | w=25
  547. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:sickle-cell anemia
    n1=en:genetic disease | n2=en:sickle-cell anemia | rel=r_hypo | relid=8 | w=25
  548. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:thiamin-responsive maple syrup urine disease
    n1=en:genetic disease | n2=en:thiamin-responsive maple syrup urine disease | rel=r_hypo | relid=8 | w=25
  549. en:genetic disease -- r_hypo #8: 25 / 0.063 -> en:von Recklinghausen's disease
    n1=en:genetic disease | n2=en:von Recklinghausen's disease | rel=r_hypo | relid=8 | w=25
  550. en:genetic disease -- r_hypo #8: 25 / 0.063 -> epilepsy
    n1=en:genetic disease | n2=epilepsy | rel=r_hypo | relid=8 | w=25
  551. en:genetic disease -- r_hypo #8: 25 / 0.063 -> exostose héréditaire multiple
    n1=en:genetic disease | n2=exostose héréditaire multiple | rel=r_hypo | relid=8 | w=25
  552. en:genetic disease -- r_hypo #8: 25 / 0.063 -> hémoglobinopathie à hématies falciformes
    n1=en:genetic disease | n2=hémoglobinopathie à hématies falciformes | rel=r_hypo | relid=8 | w=25
  553. en:genetic disease -- r_hypo #8: 25 / 0.063 -> hémoglobinose ss
    n1=en:genetic disease | n2=hémoglobinose ss | rel=r_hypo | relid=8 | w=25
  554. en:genetic disease -- r_hypo #8: 25 / 0.063 -> hépatite familiale juvénile avec dégénérescence du corps strié
    n1=en:genetic disease | n2=hépatite familiale juvénile avec dégénérescence du corps strié | rel=r_hypo | relid=8 | w=25
  555. en:genetic disease -- r_hypo #8: 25 / 0.063 -> hyperbilirubinémie de type i
    n1=en:genetic disease | n2=hyperbilirubinémie de type i | rel=r_hypo | relid=8 | w=25
  556. en:genetic disease -- r_hypo #8: 25 / 0.063 -> hyperbilirubinémie de type indirect bénin
    n1=en:genetic disease | n2=hyperbilirubinémie de type indirect bénin | rel=r_hypo | relid=8 | w=25
  557. en:genetic disease -- r_hypo #8: 25 / 0.063 -> hyperoxalurie primaire
    n1=en:genetic disease | n2=hyperoxalurie primaire | rel=r_hypo | relid=8 | w=25
  558. en:genetic disease -- r_hypo #8: 25 / 0.063 -> hyperoxalurie primitive
    n1=en:genetic disease | n2=hyperoxalurie primitive | rel=r_hypo | relid=8 | w=25
  559. en:genetic disease -- r_hypo #8: 25 / 0.063 -> ictère héréditaire de gilbert
    n1=en:genetic disease | n2=ictère héréditaire de gilbert | rel=r_hypo | relid=8 | w=25
  560. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie d'Albers-Schönberg
    n1=en:genetic disease | n2=maladie d'Albers-Schönberg | rel=r_hypo | relid=8 | w=25
  561. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Maladie de Crohn
    n1=en:genetic disease | n2=Maladie de Crohn | rel=r_hypo | relid=8 | w=25
  562. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie de Fanconi
    n1=en:genetic disease | n2=maladie de Fanconi | rel=r_hypo | relid=8 | w=25
  563. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Maladie de Gaucher
    n1=en:genetic disease | n2=Maladie de Gaucher | rel=r_hypo | relid=8 | w=25
  564. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie de Gilbert
    n1=en:genetic disease | n2=maladie de Gilbert | rel=r_hypo | relid=8 | w=25
  565. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Maladie de Hartnup
    n1=en:genetic disease | n2=Maladie de Hartnup | rel=r_hypo | relid=8 | w=25
  566. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie de hartnup
    n1=en:genetic disease | n2=maladie de hartnup | rel=r_hypo | relid=8 | w=25
  567. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie de von Recklinghausen
    n1=en:genetic disease | n2=maladie de von Recklinghausen | rel=r_hypo | relid=8 | w=25
  568. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie des açores
    n1=en:genetic disease | n2=maladie des açores | rel=r_hypo | relid=8 | w=25
  569. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie des hématies falciformes
    n1=en:genetic disease | n2=maladie des hématies falciformes | rel=r_hypo | relid=8 | w=25
  570. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie des os de marbre
    n1=en:genetic disease | n2=maladie des os de marbre | rel=r_hypo | relid=8 | w=25
  571. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie des os marmoréens
    n1=en:genetic disease | n2=maladie des os marmoréens | rel=r_hypo | relid=8 | w=25
  572. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:genetic disease | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_hypo | relid=8 | w=25
  573. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie des urines avec odeur de sirop erable
    n1=en:genetic disease | n2=maladie des urines avec odeur de sirop erable | rel=r_hypo | relid=8 | w=25
  574. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie drépanocytaire
    n1=en:genetic disease | n2=maladie drépanocytaire | rel=r_hypo | relid=8 | w=25
  575. en:genetic disease -- r_hypo #8: 25 / 0.063 -> maladie exostosante multiple
    n1=en:genetic disease | n2=maladie exostosante multiple | rel=r_hypo | relid=8 | w=25
  576. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Myopathie de Bethlem
    n1=en:genetic disease | n2=Myopathie de Bethlem | rel=r_hypo | relid=8 | w=25
  577. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Myopathie de Duchenne
    n1=en:genetic disease | n2=Myopathie de Duchenne | rel=r_hypo | relid=8 | w=25
  578. en:genetic disease -- r_hypo #8: 25 / 0.063 -> néoplasie du côlon
    n1=en:genetic disease | n2=néoplasie du côlon | rel=r_hypo | relid=8 | w=25
  579. en:genetic disease -- r_hypo #8: 25 / 0.063 -> neuropathie héréditaire motrice et sensitive
    n1=en:genetic disease | n2=neuropathie héréditaire motrice et sensitive | rel=r_hypo | relid=8 | w=25
  580. en:genetic disease -- r_hypo #8: 25 / 0.063 -> neuropathie héréditaire motrice et sensorielle
    n1=en:genetic disease | n2=neuropathie héréditaire motrice et sensorielle | rel=r_hypo | relid=8 | w=25
  581. en:genetic disease -- r_hypo #8: 25 / 0.063 -> neuropathie héréditaire sensitive et motrice
    n1=en:genetic disease | n2=neuropathie héréditaire sensitive et motrice | rel=r_hypo | relid=8 | w=25
  582. en:genetic disease -- r_hypo #8: 25 / 0.063 -> neuropathie héréditaire sensitivo-motrice
    n1=en:genetic disease | n2=neuropathie héréditaire sensitivo-motrice | rel=r_hypo | relid=8 | w=25
  583. en:genetic disease -- r_hypo #8: 25 / 0.063 -> neuropathie héréditaire sensitivomotrice
    n1=en:genetic disease | n2=neuropathie héréditaire sensitivomotrice | rel=r_hypo | relid=8 | w=25
  584. en:genetic disease -- r_hypo #8: 25 / 0.063 -> neuropathie motrice et sensorielle héréditaire
    n1=en:genetic disease | n2=neuropathie motrice et sensorielle héréditaire | rel=r_hypo | relid=8 | w=25
  585. en:genetic disease -- r_hypo #8: 25 / 0.063 -> neuropathie sensitivo-motrice héréditaire
    n1=en:genetic disease | n2=neuropathie sensitivo-motrice héréditaire | rel=r_hypo | relid=8 | w=25
  586. en:genetic disease -- r_hypo #8: 25 / 0.063 -> neuropathie sensitivomotrice héréditaire
    n1=en:genetic disease | n2=neuropathie sensitivomotrice héréditaire | rel=r_hypo | relid=8 | w=25
  587. en:genetic disease -- r_hypo #8: 25 / 0.063 -> neuropathies héréditaires sensorielles et autonomes
    n1=en:genetic disease | n2=neuropathies héréditaires sensorielles et autonomes | rel=r_hypo | relid=8 | w=25
  588. en:genetic disease -- r_hypo #8: 25 / 0.063 -> non précisée, anémie drépanocytaire
    n1=en:genetic disease | n2=non précisée, anémie drépanocytaire | rel=r_hypo | relid=8 | w=25
  589. en:genetic disease -- r_hypo #8: 25 / 0.063 -> non précisée, tumeur maligne du côlon
    n1=en:genetic disease | n2=non précisée, tumeur maligne du côlon | rel=r_hypo | relid=8 | w=25
  590. en:genetic disease -- r_hypo #8: 25 / 0.063 -> ostéopétrose autosomique dominante de type 2
    n1=en:genetic disease | n2=ostéopétrose autosomique dominante de type 2 | rel=r_hypo | relid=8 | w=25
  591. en:genetic disease -- r_hypo #8: 25 / 0.063 -> ostéopétrose autosomique dominante de type ii
    n1=en:genetic disease | n2=ostéopétrose autosomique dominante de type ii | rel=r_hypo | relid=8 | w=25
  592. en:genetic disease -- r_hypo #8: 25 / 0.063 -> ostéopétrose familiale
    n1=en:genetic disease | n2=ostéopétrose familiale | rel=r_hypo | relid=8 | w=25
  593. en:genetic disease -- r_hypo #8: 25 / 0.063 -> ostéopétroses
    n1=en:genetic disease | n2=ostéopétroses | rel=r_hypo | relid=8 | w=25
  594. en:genetic disease -- r_hypo #8: 25 / 0.063 -> oxalose primitive
    n1=en:genetic disease | n2=oxalose primitive | rel=r_hypo | relid=8 | w=25
  595. en:genetic disease -- r_hypo #8: 25 / 0.063 -> pseudo-xanthome élastique
    n1=en:genetic disease | n2=pseudo-xanthome élastique | rel=r_hypo | relid=8 | w=25
  596. en:genetic disease -- r_hypo #8: 25 / 0.063 -> sicklanémie
    n1=en:genetic disease | n2=sicklanémie | rel=r_hypo | relid=8 | w=25
  597. en:genetic disease -- r_hypo #8: 25 / 0.063 -> siclémie (sicklémie)
    n1=en:genetic disease | n2=siclémie (sicklémie) | rel=r_hypo | relid=8 | w=25
  598. en:genetic disease -- r_hypo #8: 25 / 0.063 -> subictère chronique intermittent
    n1=en:genetic disease | n2=subictère chronique intermittent | rel=r_hypo | relid=8 | w=25
  599. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Syndrome d'Angelman
    n1=en:genetic disease | n2=Syndrome d'Angelman | rel=r_hypo | relid=8 | w=25
  600. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Syndrome d'Ehlers-Danlos type classique
    n1=en:genetic disease | n2=Syndrome d'Ehlers-Danlos type classique | rel=r_hypo | relid=8 | w=25
  601. en:genetic disease -- r_hypo #8: 25 / 0.063 -> Syndrome de Kartagener
    n1=en:genetic disease | n2=Syndrome de Kartagener | rel=r_hypo | relid=8 | w=25
  602. en:genetic disease -- r_hypo #8: 25 / 0.063 -> tumeur colique
    n1=en:genetic disease | n2=tumeur colique | rel=r_hypo | relid=8 | w=25
  603. en:genetic disease -- r_hypo #8: 25 / 0.063 -> tumeur du côlon
    n1=en:genetic disease | n2=tumeur du côlon | rel=r_hypo | relid=8 | w=25
  604. en:genetic disease -- r_hypo #8: 25 / 0.063 -> tumeur maligne colique
    n1=en:genetic disease | n2=tumeur maligne colique | rel=r_hypo | relid=8 | w=25
  605. en:genetic disease -- r_hypo #8: 25 / 0.063 -> tumeur maligne du côlon
    n1=en:genetic disease | n2=tumeur maligne du côlon | rel=r_hypo | relid=8 | w=25
  606. en:genetic disease -- r_hypo #8: 25 / 0.063 -> tumeur maligne du côlon non précisée
    n1=en:genetic disease | n2=tumeur maligne du côlon non précisée | rel=r_hypo | relid=8 | w=25
  607. en:genetic disease -- r_hypo #8: 25 / 0.063 -> xanthomatose cérébro-tendineuse
    n1=en:genetic disease | n2=xanthomatose cérébro-tendineuse | rel=r_hypo | relid=8 | w=25
  608. en:genetic disease -- r_hypo #8: 20 / 0.051 -> en:goitre
    n1=en:genetic disease | n2=en:goitre | rel=r_hypo | relid=8 | w=20
  609. en:genetic disease -- r_hypo #8: 20 / 0.051 -> en:Guinon's disease
    n1=en:genetic disease | n2=en:Guinon's disease | rel=r_hypo | relid=8 | w=20
  610. en:genetic disease -- r_hypo #8: 20 / 0.051 -> en:Huntington's disease
    n1=en:genetic disease | n2=en:Huntington's disease | rel=r_hypo | relid=8 | w=20
  611. en:genetic disease -- r_hypo #8: 20 / 0.051 -> Maladie de Canavan
    n1=en:genetic disease | n2=Maladie de Canavan | rel=r_hypo | relid=8 | w=20
  612. en:genetic disease -- r_hypo #8: 15 / 0.038 -> en:hereditary multiple exostoses
    n1=en:genetic disease | n2=en:hereditary multiple exostoses | rel=r_hypo | relid=8 | w=15
  613. en:genetic disease -- r_hypo #8: 15 / 0.038 -> microencéphalie
    n1=en:genetic disease | n2=microencéphalie | rel=r_hypo | relid=8 | w=15
  614. en:genetic disease -- r_hypo #8: 15 / 0.038 -> protoporphyrie érythropoïétique
    n1=en:genetic disease | n2=protoporphyrie érythropoïétique | rel=r_hypo | relid=8 | w=15
  615. en:genetic disease -- r_hypo #8: 11 / 0.028 -> en:Fanconi's anaemia
    n1=en:genetic disease | n2=en:Fanconi's anaemia | rel=r_hypo | relid=8 | w=11
  616. en:genetic disease -- r_hypo #8: 10 / 0.025 -> en:Wilson's disease
    n1=en:genetic disease | n2=en:Wilson's disease | rel=r_hypo | relid=8 | w=10
  617. en:genetic disease -- r_hypo #8: 10 / 0.025 -> syndrome de Joubert
    n1=en:genetic disease | n2=syndrome de Joubert | rel=r_hypo | relid=8 | w=10
  618. en:genetic disease -- r_hypo #8: 5 / 0.013 -> myopathy
    n1=en:genetic disease | n2=myopathy | rel=r_hypo | relid=8 | w=5
  619. en:genetic disease -- r_hypo #8: 2 / 0.005 -> anémie à hématies falciformes
    n1=en:genetic disease | n2=anémie à hématies falciformes | rel=r_hypo | relid=8 | w=2
  620. en:genetic disease -- r_hypo #8: 2 / 0.005 -> en:sickle cell disease
    n1=en:genetic disease | n2=en:sickle cell disease | rel=r_hypo | relid=8 | w=2
  621. en:genetic disease -- r_hypo #8: 1 / 0.003 -> bêta-thalassémie à hématies falciformes
    n1=en:genetic disease | n2=bêta-thalassémie à hématies falciformes | rel=r_hypo | relid=8 | w=1
  622. en:genetic disease -- r_hypo #8: 1 / 0.003 -> cholémie familiale congénitale
    n1=en:genetic disease | n2=cholémie familiale congénitale | rel=r_hypo | relid=8 | w=1
  623. en:genetic disease -- r_hypo #8: 1 / 0.003 -> en:cystic fibrosis
    n1=en:genetic disease | n2=en:cystic fibrosis | rel=r_hypo | relid=8 | w=1
  624. en:genetic disease -- r_hypo #8: 1 / 0.003 -> hyperbilirubinémie de type 1
    n1=en:genetic disease | n2=hyperbilirubinémie de type 1 | rel=r_hypo | relid=8 | w=1
  625. en:genetic disease -- r_hypo #8: 1 / 0.003 -> myopathie primitive progressive
    n1=en:genetic disease | n2=myopathie primitive progressive | rel=r_hypo | relid=8 | w=1
  626. en:genetic disease -- r_hypo #8: 1 / 0.003 -> ostéopétrose
    n1=en:genetic disease | n2=ostéopétrose | rel=r_hypo | relid=8 | w=1
  627. en:genetic disease -- r_hypo #8: -1 / -0.003 -> gout
    n1=en:genetic disease | n2=gout | rel=r_hypo | relid=8 | w=-1
  628. en:genetic disease -- r_hypo #8: -25 / -0.063 -> anémie drépanocytaire non précisée
    n1=en:genetic disease | n2=anémie drépanocytaire non précisée | rel=r_hypo | relid=8 | w=-25
  629. en:genetic disease -- r_hypo #8: -25 / -0.063 -> drépanocytoses
    n1=en:genetic disease | n2=drépanocytoses | rel=r_hypo | relid=8 | w=-25
≈ 14 relations entrantes

  1. en:genetic --- r_hypo #8: 25 --> en:genetic disease
    n1=en:genetic | n2=en:genetic disease | rel=r_hypo | relid=8 | w=25
  2. anomalie --- r_hypo #8: 7 --> en:genetic disease
    n1=anomalie | n2=en:genetic disease | rel=r_hypo | relid=8 | w=7
  3. en:disease or disorder --- r_hypo #8: 7 --> en:genetic disease
    n1=en:disease or disorder | n2=en:genetic disease | rel=r_hypo | relid=8 | w=7
  4. en:disorder --- r_hypo #8: 7 --> en:genetic disease
    n1=en:disorder | n2=en:genetic disease | rel=r_hypo | relid=8 | w=7
  5. maladie --- r_hypo #8: 7 --> en:genetic disease
    n1=maladie | n2=en:genetic disease | rel=r_hypo | relid=8 | w=7
  6. maladie
    (médecine)
     --- r_hypo #8: 7 --> en:genetic disease
    n1=maladie
    (médecine)
    | n2=en:genetic disease | rel=r_hypo | relid=8 | w=7
  7. processus pathologique --- r_hypo #8: 7 --> en:genetic disease
    n1=processus pathologique | n2=en:genetic disease | rel=r_hypo | relid=8 | w=7
  8. analyte --- r_hypo #8: 1 --> en:genetic disease
    n1=analyte | n2=en:genetic disease | rel=r_hypo | relid=8 | w=1
  9. disease --- r_hypo #8: 1 --> en:genetic disease
    n1=disease | n2=en:genetic disease | rel=r_hypo | relid=8 | w=1
  10. disorder --- r_hypo #8: 1 --> en:genetic disease
    n1=disorder | n2=en:genetic disease | rel=r_hypo | relid=8 | w=1
  11. en:analyte --- r_hypo #8: 1 --> en:genetic disease
    n1=en:analyte | n2=en:genetic disease | rel=r_hypo | relid=8 | w=1
  12. en:disease --- r_hypo #8: 1 --> en:genetic disease
    n1=en:disease | n2=en:genetic disease | rel=r_hypo | relid=8 | w=1
  13. pathologie --- r_hypo #8: 1 --> en:genetic disease
    n1=pathologie | n2=en:genetic disease | rel=r_hypo | relid=8 | w=1
  14. processus --- r_hypo #8: 1 --> en:genetic disease
    n1=processus | n2=en:genetic disease | rel=r_hypo | relid=8 | w=1
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