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'syndrome de Pfeiffer'
(id=331505 ; fe=syndrome de Pfeiffer ; type=1 ; niveau=200 ; luminosité=51 ; somme entrante=15337.400024414062 creation date=2014-06-09 touchdate=2025-09-14 09:35:31.000)
≈ 78 relations sortantes

  1. syndrome de Pfeiffer -- r_associated #0: 1042 / 1 -> médecine
    n1=syndrome de Pfeiffer | n2=médecine | rel=r_associated | relid=0 | w=1042
  2. syndrome de Pfeiffer -- r_associated #0: 1025.77 / 0.984 -> maladies
    n1=syndrome de Pfeiffer | n2=maladies | rel=r_associated | relid=0 | w=1025.77
  3. syndrome de Pfeiffer -- r_associated #0: 1023.13 / 0.982 -> maladies héréditaires
    n1=syndrome de Pfeiffer | n2=maladies héréditaires | rel=r_associated | relid=0 | w=1023.13
  4. syndrome de Pfeiffer -- r_associated #0: 986.69 / 0.947 -> maladies génétiques
    n1=syndrome de Pfeiffer | n2=maladies génétiques | rel=r_associated | relid=0 | w=986.69
  5. syndrome de Pfeiffer -- r_associated #0: 566.66 / 0.544 -> maladies rares
    n1=syndrome de Pfeiffer | n2=maladies rares | rel=r_associated | relid=0 | w=566.66
  6. syndrome de Pfeiffer -- r_associated #0: 343 / 0.329 -> génétique
    n1=syndrome de Pfeiffer | n2=génétique | rel=r_associated | relid=0 | w=343
  7. syndrome de Pfeiffer -- r_associated #0: 337 / 0.323 -> maladies génétiques congénitales
    n1=syndrome de Pfeiffer | n2=maladies génétiques congénitales | rel=r_associated | relid=0 | w=337
  8. syndrome de Pfeiffer -- r_associated #0: 337 / 0.323 -> syndromes génétiques
    n1=syndrome de Pfeiffer | n2=syndromes génétiques | rel=r_associated | relid=0 | w=337
  9. syndrome de Pfeiffer -- r_associated #0: 107 / 0.103 -> Pfeiffer
    n1=syndrome de Pfeiffer | n2=Pfeiffer | rel=r_associated | relid=0 | w=107
  10. syndrome de Pfeiffer -- r_associated #0: 107 / 0.103 -> syndrome
    n1=syndrome de Pfeiffer | n2=syndrome | rel=r_associated | relid=0 | w=107
  11. syndrome de Pfeiffer -- r_associated #0: 106 / 0.102 -> syndrome de
    n1=syndrome de Pfeiffer | n2=syndrome de | rel=r_associated | relid=0 | w=106
  12. syndrome de Pfeiffer -- r_associated #0: 52 / 0.05 -> acrocéphalosyndactylie
    n1=syndrome de Pfeiffer | n2=acrocéphalosyndactylie | rel=r_associated | relid=0 | w=52
  13. syndrome de Pfeiffer -- r_associated #0: 51 / 0.049 -> spécialités médicales
    n1=syndrome de Pfeiffer | n2=spécialités médicales | rel=r_associated | relid=0 | w=51
  14. syndrome de Pfeiffer -- r_associated #0: 46 / 0.044 -> pédiatrie
    n1=syndrome de Pfeiffer | n2=pédiatrie | rel=r_associated | relid=0 | w=46
  15. syndrome de Pfeiffer -- r_associated #0: 45 / 0.043 -> anomalie de la face
    n1=syndrome de Pfeiffer | n2=anomalie de la face | rel=r_associated | relid=0 | w=45
  16. syndrome de Pfeiffer -- r_associated #0: 45 / 0.043 -> dysostoses
    n1=syndrome de Pfeiffer | n2=dysostoses | rel=r_associated | relid=0 | w=45
  17. syndrome de Pfeiffer -- r_associated #0: 45 / 0.043 -> maladie métabolique congénitale
    n1=syndrome de Pfeiffer | n2=maladie métabolique congénitale | rel=r_associated | relid=0 | w=45
  18. syndrome de Pfeiffer -- r_associated #0: 45 / 0.043 -> médecine spécialisée
    n1=syndrome de Pfeiffer | n2=médecine spécialisée | rel=r_associated | relid=0 | w=45
  19. syndrome de Pfeiffer -- r_associated #0: 45 / 0.043 -> processus pathologique
    n1=syndrome de Pfeiffer | n2=processus pathologique | rel=r_associated | relid=0 | w=45
  20. syndrome de Pfeiffer -- r_associated #0: 43 / 0.041 -> acrocéphalosyndactylie type v
    n1=syndrome de Pfeiffer | n2=acrocéphalosyndactylie type v | rel=r_associated | relid=0 | w=43
  21. syndrome de Pfeiffer -- r_associated #0: 42 / 0.04 -> acrocéphalosyndactylie type 5
    n1=syndrome de Pfeiffer | n2=acrocéphalosyndactylie type 5 | rel=r_associated | relid=0 | w=42
  22. syndrome de Pfeiffer -- r_associated #0: 42 / 0.04 -> acrocéphalosyndactylies
    n1=syndrome de Pfeiffer | n2=acrocéphalosyndactylies | rel=r_associated | relid=0 | w=42
  23. syndrome de Pfeiffer -- r_associated #0: 42 / 0.04 -> en:pfeiffer syndrome
    n1=syndrome de Pfeiffer | n2=en:pfeiffer syndrome | rel=r_associated | relid=0 | w=42
  24. syndrome de Pfeiffer -- r_associated #0: 42 / 0.04 -> en:type v acrocephalosyndactyly
    n1=syndrome de Pfeiffer | n2=en:type v acrocephalosyndactyly | rel=r_associated | relid=0 | w=42
  25. syndrome de Pfeiffer -- r_associated #0: 42 / 0.04 -> syndrome d'Apert
    n1=syndrome de Pfeiffer | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=42
  26. syndrome de Pfeiffer -- r_associated #0: 41 / 0.039 -> acro-céphalo-syndactylie de type v
    n1=syndrome de Pfeiffer | n2=acro-céphalo-syndactylie de type v | rel=r_associated | relid=0 | w=41
  27. syndrome de Pfeiffer -- r_associated #0: 41 / 0.039 -> acrocéphalosyndactylie de type V
    n1=syndrome de Pfeiffer | n2=acrocéphalosyndactylie de type V | rel=r_associated | relid=0 | w=41
  28. syndrome de Pfeiffer -- r_associated #0: 41 / 0.039 -> acrocéphalosyndactylie, type iv
    n1=syndrome de Pfeiffer | n2=acrocéphalosyndactylie, type iv | rel=r_associated | relid=0 | w=41
  29. syndrome de Pfeiffer -- r_associated #0: 41 / 0.039 -> maladie génétique
    n1=syndrome de Pfeiffer | n2=maladie génétique | rel=r_associated | relid=0 | w=41
  30. syndrome de Pfeiffer -- r_associated #0: 41 / 0.039 -> maladie rare
    n1=syndrome de Pfeiffer | n2=maladie rare | rel=r_associated | relid=0 | w=41
  31. syndrome de Pfeiffer -- r_associated #0: 41 / 0.039 -> maladies métaboliques congénitales
    n1=syndrome de Pfeiffer | n2=maladies métaboliques congénitales | rel=r_associated | relid=0 | w=41
  32. syndrome de Pfeiffer -- r_associated #0: 40 / 0.038 -> anomalies de la face
    n1=syndrome de Pfeiffer | n2=anomalies de la face | rel=r_associated | relid=0 | w=40
  33. syndrome de Pfeiffer -- r_associated #0: 40 / 0.038 -> FGFR2
    n1=syndrome de Pfeiffer | n2=FGFR2 | rel=r_associated | relid=0 | w=40
  34. syndrome de Pfeiffer -- r_associated #0: 40 / 0.038 -> handicap
    n1=syndrome de Pfeiffer | n2=handicap | rel=r_associated | relid=0 | w=40
  35. syndrome de Pfeiffer -- r_associated #0: 40 / 0.038 -> maladie génétique congénitale
    n1=syndrome de Pfeiffer | n2=maladie génétique congénitale | rel=r_associated | relid=0 | w=40
  36. syndrome de Pfeiffer -- r_associated #0: 39 / 0.037 -> syndrome génétique
    n1=syndrome de Pfeiffer | n2=syndrome génétique | rel=r_associated | relid=0 | w=39
  37. syndrome de Pfeiffer -- r_associated #0: 36 / 0.035 -> acrocéphalosyndactylie de type v
    n1=syndrome de Pfeiffer | n2=acrocéphalosyndactylie de type v | rel=r_associated | relid=0 | w=36
  38. syndrome de Pfeiffer -- r_associated #0: 35 / 0.034 -> acro-céphalo-syndactylie de type 5
    n1=syndrome de Pfeiffer | n2=acro-céphalo-syndactylie de type 5 | rel=r_associated | relid=0 | w=35
  39. syndrome de Pfeiffer -- r_associated #0: 34 / 0.033 -> en:Pfeiffer's syndrome
    n1=syndrome de Pfeiffer | n2=en:Pfeiffer's syndrome | rel=r_associated | relid=0 | w=34
  40. syndrome de Pfeiffer -- r_associated #0: 30 / 0.029 -> ACS V
    n1=syndrome de Pfeiffer | n2=ACS V | rel=r_associated | relid=0 | w=30
  41. syndrome de Pfeiffer -- r_associated #0: 30 / 0.029 -> maladie héréditaire
    n1=syndrome de Pfeiffer | n2=maladie héréditaire | rel=r_associated | relid=0 | w=30
  42. syndrome de Pfeiffer -- r_associated #0: 30 / 0.029 -> Pfeiffer (syndrome de)
    n1=syndrome de Pfeiffer | n2=Pfeiffer (syndrome de) | rel=r_associated | relid=0 | w=30
  43. syndrome de Pfeiffer -- r_associated #0: 28 / 0.027 -> syndrome de Noack
    n1=syndrome de Pfeiffer | n2=syndrome de Noack | rel=r_associated | relid=0 | w=28
  44. syndrome de Pfeiffer -- r_associated #0: 27 / 0.026 -> acrocéphalopolysyndactylie
    n1=syndrome de Pfeiffer | n2=acrocéphalopolysyndactylie | rel=r_associated | relid=0 | w=27
  45. syndrome de Pfeiffer -- r_associated #0: 27 / 0.026 -> acrocéphalopolysyndactylie type I
    n1=syndrome de Pfeiffer | n2=acrocéphalopolysyndactylie type I | rel=r_associated | relid=0 | w=27
  46. syndrome de Pfeiffer -- r_associated #0: 27 / 0.026 -> polydactylie
    n1=syndrome de Pfeiffer | n2=polydactylie | rel=r_associated | relid=0 | w=27
  47. syndrome de Pfeiffer -- r_associated #0: 25 / 0.024 -> anomalie héréditaire
    n1=syndrome de Pfeiffer | n2=anomalie héréditaire | rel=r_associated | relid=0 | w=25
  48. syndrome de Pfeiffer -- r_associated #0: 25 / 0.024 -> en:genetic condition
    n1=syndrome de Pfeiffer | n2=en:genetic condition | rel=r_associated | relid=0 | w=25
  49. syndrome de Pfeiffer -- r_associated #0: 25 / 0.024 -> en:genetic disease
    n1=syndrome de Pfeiffer | n2=en:genetic disease | rel=r_associated | relid=0 | w=25
  50. syndrome de Pfeiffer -- r_associated #0: 25 / 0.024 -> en:genetic disorder
    n1=syndrome de Pfeiffer | n2=en:genetic disorder | rel=r_associated | relid=0 | w=25
  51. syndrome de Pfeiffer -- r_associated #0: 25 / 0.024 -> en:genetic illness
    n1=syndrome de Pfeiffer | n2=en:genetic illness | rel=r_associated | relid=0 | w=25
  52. syndrome de Pfeiffer -- r_associated #0: 25 / 0.024 -> en:hereditary disease
    n1=syndrome de Pfeiffer | n2=en:hereditary disease | rel=r_associated | relid=0 | w=25
  53. syndrome de Pfeiffer -- r_associated #0: 25 / 0.024 -> Maladie rare
    n1=syndrome de Pfeiffer | n2=Maladie rare | rel=r_associated | relid=0 | w=25
  54. syndrome de Pfeiffer -- r_associated #0: 22 / 0.021 -> FGFR1 gene
    n1=syndrome de Pfeiffer | n2=FGFR1 gene | rel=r_associated | relid=0 | w=22
  55. syndrome de Pfeiffer -- r_associated #0: 22 / 0.021 -> FGFR2 gene
    n1=syndrome de Pfeiffer | n2=FGFR2 gene | rel=r_associated | relid=0 | w=22
  56. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> acro-céphalo-syndactylie
    n1=syndrome de Pfeiffer | n2=acro-céphalo-syndactylie | rel=r_associated | relid=0 | w=20
  57. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> acro-céphalo-syndactylies
    n1=syndrome de Pfeiffer | n2=acro-céphalo-syndactylies | rel=r_associated | relid=0 | w=20
  58. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> ACS
    n1=syndrome de Pfeiffer | n2=ACS | rel=r_associated | relid=0 | w=20
  59. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> ACS
    (acro-céphalo-syndactylie)
    n1=syndrome de Pfeiffer | n2=ACS
    (acro-céphalo-syndactylie)
    | rel=r_associated | relid=0 | w=20
  60. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> caryotype
    n1=syndrome de Pfeiffer | n2=caryotype | rel=r_associated | relid=0 | w=20
  61. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> en:acrocephalosyndactyly
    n1=syndrome de Pfeiffer | n2=en:acrocephalosyndactyly | rel=r_associated | relid=0 | w=20
  62. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> en:Apert's disease
    n1=syndrome de Pfeiffer | n2=en:Apert's disease | rel=r_associated | relid=0 | w=20
  63. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> en:inherited disease
    n1=syndrome de Pfeiffer | n2=en:inherited disease | rel=r_associated | relid=0 | w=20
  64. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> en:Noack's syndrome
    n1=syndrome de Pfeiffer | n2=en:Noack's syndrome | rel=r_associated | relid=0 | w=20
  65. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> en:pediatry
    n1=syndrome de Pfeiffer | n2=en:pediatry | rel=r_associated | relid=0 | w=20
  66. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> en:Pfeiffer-Tietze-Welte's syndrome
    n1=syndrome de Pfeiffer | n2=en:Pfeiffer-Tietze-Welte's syndrome | rel=r_associated | relid=0 | w=20
  67. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> Maladies
    n1=syndrome de Pfeiffer | n2=Maladies | rel=r_associated | relid=0 | w=20
  68. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> syndrome d'apert
    n1=syndrome de Pfeiffer | n2=syndrome d'apert | rel=r_associated | relid=0 | w=20
  69. syndrome de Pfeiffer -- r_associated #0: 20 / 0.019 -> Syndrome d'Apert
    n1=syndrome de Pfeiffer | n2=Syndrome d'Apert | rel=r_associated | relid=0 | w=20
  70. syndrome de Pfeiffer -- r_associated #0: 15 / 0.014 -> en:pediatrics
    n1=syndrome de Pfeiffer | n2=en:pediatrics | rel=r_associated | relid=0 | w=15
  71. syndrome de Pfeiffer -- r_associated #0: 15 / 0.014 -> en:sequence-abnormal facies
    n1=syndrome de Pfeiffer | n2=en:sequence-abnormal facies | rel=r_associated | relid=0 | w=15
  72. syndrome de Pfeiffer -- r_associated #0: 15 / 0.014 -> en:specialized branches of medicine
    n1=syndrome de Pfeiffer | n2=en:specialized branches of medicine | rel=r_associated | relid=0 | w=15
  73. syndrome de Pfeiffer -- r_associated #0: 15 / 0.014 -> Maladies génétiques
    n1=syndrome de Pfeiffer | n2=Maladies génétiques | rel=r_associated | relid=0 | w=15
  74. syndrome de Pfeiffer -- r_associated #0: 15 / 0.014 -> Spécialités médicales
    n1=syndrome de Pfeiffer | n2=Spécialités médicales | rel=r_associated | relid=0 | w=15
  75. syndrome de Pfeiffer -- r_associated #0: 15 / 0.014 -> syndrome de Pfeiffer-Tietze-Welte
    n1=syndrome de Pfeiffer | n2=syndrome de Pfeiffer-Tietze-Welte | rel=r_associated | relid=0 | w=15
  76. syndrome de Pfeiffer -- r_associated #0: 5 / 0.005 -> en:hereditary illness
    n1=syndrome de Pfeiffer | n2=en:hereditary illness | rel=r_associated | relid=0 | w=5
  77. syndrome de Pfeiffer -- r_associated #0: 5 / 0.005 -> Médecine
    n1=syndrome de Pfeiffer | n2=Médecine | rel=r_associated | relid=0 | w=5
  78. syndrome de Pfeiffer -- r_associated #0: 5 / 0.005 -> pædiatrie
    n1=syndrome de Pfeiffer | n2=pædiatrie | rel=r_associated | relid=0 | w=5
≈ 104 relations entrantes

  1. maladies héréditaires --- r_associated #0: 998.09 --> syndrome de Pfeiffer
    n1=maladies héréditaires | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=998.09
  2. maladies génétiques --- r_associated #0: 968.39 --> syndrome de Pfeiffer
    n1=maladies génétiques | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=968.39
  3. médecine --- r_associated #0: 865.87 --> syndrome de Pfeiffer
    n1=médecine | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=865.87
  4. maladies --- r_associated #0: 849.05 --> syndrome de Pfeiffer
    n1=maladies | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=849.05
  5. maladies rares --- r_associated #0: 682 --> syndrome de Pfeiffer
    n1=maladies rares | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=682
  6. génétique --- r_associated #0: 319 --> syndrome de Pfeiffer
    n1=génétique | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=319
  7. syndromes génétiques --- r_associated #0: 318 --> syndrome de Pfeiffer
    n1=syndromes génétiques | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=318
  8. maladies génétiques congénitales --- r_associated #0: 315 --> syndrome de Pfeiffer
    n1=maladies génétiques congénitales | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=315
  9. maladie héréditaire --- r_associated #0: 276 --> syndrome de Pfeiffer
    n1=maladie héréditaire | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=276
  10. en:hereditary disease --- r_associated #0: 275 --> syndrome de Pfeiffer
    n1=en:hereditary disease | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=275
  11. maladie génétique --- r_associated #0: 271 --> syndrome de Pfeiffer
    n1=maladie génétique | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=271
  12. Syndrome d'Apert --- r_associated #0: 265 --> syndrome de Pfeiffer
    n1=Syndrome d'Apert | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=265
  13. syndrome d'Apert --- r_associated #0: 263 --> syndrome de Pfeiffer
    n1=syndrome d'Apert | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=263
  14. syndrome d'apert --- r_associated #0: 258 --> syndrome de Pfeiffer
    n1=syndrome d'apert | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=258
  15. en:genetic disease --- r_associated #0: 240 --> syndrome de Pfeiffer
    n1=en:genetic disease | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=240
  16. en:genetic condition --- r_associated #0: 210 --> syndrome de Pfeiffer
    n1=en:genetic condition | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=210
  17. anomalie de la face --- r_associated #0: 209 --> syndrome de Pfeiffer
    n1=anomalie de la face | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=209
  18. en:sequence-abnormal facies --- r_associated #0: 205 --> syndrome de Pfeiffer
    n1=en:sequence-abnormal facies | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=205
  19. Spécialités médicales --- r_associated #0: 165 --> syndrome de Pfeiffer
    n1=Spécialités médicales | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=165
  20. spécialités médicales --- r_associated #0: 162 --> syndrome de Pfeiffer
    n1=spécialités médicales | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=162
  21. en:Apert's disease --- r_associated #0: 145 --> syndrome de Pfeiffer
    n1=en:Apert's disease | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=145
  22. en:genetic illness --- r_associated #0: 110 --> syndrome de Pfeiffer
    n1=en:genetic illness | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=110
  23. acro-céphalo-syndactylie --- r_associated #0: 86 --> syndrome de Pfeiffer
    n1=acro-céphalo-syndactylie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=86
  24. acrocéphalosyndactylie --- r_associated #0: 82 --> syndrome de Pfeiffer
    n1=acrocéphalosyndactylie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=82
  25. ACS
    (acro-céphalo-syndactylie)
     --- r_associated #0: 75 --> syndrome de Pfeiffer
    n1=ACS
    (acro-céphalo-syndactylie)
    | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=75
  26. en:genetic disorder --- r_associated #0: 66 --> syndrome de Pfeiffer
    n1=en:genetic disorder | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=66
  27. syndrome --- r_associated #0: 58 --> syndrome de Pfeiffer
    n1=syndrome | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=58
  28. syndrome de Pfeiffer-Tietze-Welte --- r_associated #0: 53 --> syndrome de Pfeiffer
    n1=syndrome de Pfeiffer-Tietze-Welte | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=53
  29. acro-céphalo-syndactylies --- r_associated #0: 52 --> syndrome de Pfeiffer
    n1=acro-céphalo-syndactylies | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=52
  30. acrocéphalosyndactylies --- r_associated #0: 52 --> syndrome de Pfeiffer
    n1=acrocéphalosyndactylies | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=52
  31. Maladies génétiques --- r_associated #0: 50 --> syndrome de Pfeiffer
    n1=Maladies génétiques | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=50
  32. pædiatrie --- r_associated #0: 49 --> syndrome de Pfeiffer
    n1=pædiatrie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=49
  33. pédiatrie --- r_associated #0: 49 --> syndrome de Pfeiffer
    n1=pédiatrie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=49
  34. en:pediatrics --- r_associated #0: 45 --> syndrome de Pfeiffer
    n1=en:pediatrics | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=45
  35. anomalie héréditaire --- r_associated #0: 41 --> syndrome de Pfeiffer
    n1=anomalie héréditaire | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=41
  36. médecine spécialisée --- r_associated #0: 40 --> syndrome de Pfeiffer
    n1=médecine spécialisée | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=40
  37. en:Pfeiffer-Tietze-Welte's syndrome --- r_associated #0: 39 --> syndrome de Pfeiffer
    n1=en:Pfeiffer-Tietze-Welte's syndrome | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=39
  38. en:specialized branches of medicine --- r_associated #0: 39 --> syndrome de Pfeiffer
    n1=en:specialized branches of medicine | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=39
  39. ACS --- r_associated #0: 38 --> syndrome de Pfeiffer
    n1=ACS | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=38
  40. syndrome de Noack --- r_associated #0: 36 --> syndrome de Pfeiffer
    n1=syndrome de Noack | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=36
  41. FGFR2 --- r_associated #0: 35 --> syndrome de Pfeiffer
    n1=FGFR2 | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=35
  42. en:Noack's syndrome --- r_associated #0: 35 --> syndrome de Pfeiffer
    n1=en:Noack's syndrome | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=35
  43. acrocéphalosyndactylie type 5 --- r_associated #0: 34 --> syndrome de Pfeiffer
    n1=acrocéphalosyndactylie type 5 | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=34
  44. en:type v acrocephalosyndactyly --- r_associated #0: 34 --> syndrome de Pfeiffer
    n1=en:type v acrocephalosyndactyly | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=34
  45. Maladie rare --- r_associated #0: 32 --> syndrome de Pfeiffer
    n1=Maladie rare | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=32
  46. acrocéphalopolysyndactylie type I --- r_associated #0: 32 --> syndrome de Pfeiffer
    n1=acrocéphalopolysyndactylie type I | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=32
  47. acrocéphalosyndactylie type v --- r_associated #0: 32 --> syndrome de Pfeiffer
    n1=acrocéphalosyndactylie type v | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=32
  48. Pfeiffer (syndrome de) --- r_associated #0: 30 --> syndrome de Pfeiffer
    n1=Pfeiffer (syndrome de) | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=30
  49. acro-céphalo-syndactylie de type 5 --- r_associated #0: 30 --> syndrome de Pfeiffer
    n1=acro-céphalo-syndactylie de type 5 | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=30
  50. acro-céphalo-syndactylie de type v --- r_associated #0: 30 --> syndrome de Pfeiffer
    n1=acro-céphalo-syndactylie de type v | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=30
  51. anomalies monogéniques --- r_associated #0: 30 --> syndrome de Pfeiffer
    n1=anomalies monogéniques | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=30
  52. en:pfeiffer syndrome --- r_associated #0: 30 --> syndrome de Pfeiffer
    n1=en:pfeiffer syndrome | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=30
  53. handicap --- r_associated #0: 30 --> syndrome de Pfeiffer
    n1=handicap | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=30
  54. processus pathologique --- r_associated #0: 30 --> syndrome de Pfeiffer
    n1=processus pathologique | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=30
  55. en:Pfeiffer's syndrome --- r_associated #0: 29 --> syndrome de Pfeiffer
    n1=en:Pfeiffer's syndrome | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=29
  56. maladie rare --- r_associated #0: 29 --> syndrome de Pfeiffer
    n1=maladie rare | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=29
  57. Maladie héréditaire --- r_associated #0: 28 --> syndrome de Pfeiffer
    n1=Maladie héréditaire | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=28
  58. en:acrocephalosyndactyly --- r_associated #0: 28 --> syndrome de Pfeiffer
    n1=en:acrocephalosyndactyly | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=28
  59. maladie génétique congénitale --- r_associated #0: 28 --> syndrome de Pfeiffer
    n1=maladie génétique congénitale | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=28
  60. syndrome génétique --- r_associated #0: 28 --> syndrome de Pfeiffer
    n1=syndrome génétique | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=28
  61. Maladies --- r_associated #0: 27 --> syndrome de Pfeiffer
    n1=Maladies | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=27
  62. en:inherited disease --- r_associated #0: 27 --> syndrome de Pfeiffer
    n1=en:inherited disease | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=27
  63. en:pediatry --- r_associated #0: 27 --> syndrome de Pfeiffer
    n1=en:pediatry | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=27
  64. anomalies de la face --- r_associated #0: 26 --> syndrome de Pfeiffer
    n1=anomalies de la face | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=26
  65. caryotype --- r_associated #0: 26 --> syndrome de Pfeiffer
    n1=caryotype | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=26
  66. hémato-immunologie --- r_associated #0: 26 --> syndrome de Pfeiffer
    n1=hémato-immunologie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=26
  67. maladies métaboliques congénitales --- r_associated #0: 26 --> syndrome de Pfeiffer
    n1=maladies métaboliques congénitales | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=26
  68. en:hereditary illness --- r_associated #0: 25 --> syndrome de Pfeiffer
    n1=en:hereditary illness | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=25
  69. Pfeiffer --- r_associated #0: 24 --> syndrome de Pfeiffer
    n1=Pfeiffer | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=24
  70. en:peds --- r_associated #0: 24 --> syndrome de Pfeiffer
    n1=en:peds | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=24
  71. Noack (syndrome de) --- r_associated #0: 23 --> syndrome de Pfeiffer
    n1=Noack (syndrome de) | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=23
  72. en:acrocephalopolysyndactyly type I --- r_associated #0: 23 --> syndrome de Pfeiffer
    n1=en:acrocephalopolysyndactyly type I | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=23
  73. maladie métabolique congénitale --- r_associated #0: 23 --> syndrome de Pfeiffer
    n1=maladie métabolique congénitale | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=23
  74. syndrome de --- r_associated #0: 23 --> syndrome de Pfeiffer
    n1=syndrome de | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=23
  75. Pfeiffer-Tietze-Welte (syndrome de) --- r_associated #0: 22 --> syndrome de Pfeiffer
    n1=Pfeiffer-Tietze-Welte (syndrome de) | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=22
  76. dysostoses --- r_associated #0: 22 --> syndrome de Pfeiffer
    n1=dysostoses | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=22
  77. ACS V --- r_associated #0: 20 --> syndrome de Pfeiffer
    n1=ACS V | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=20
  78. acrocéphalopolysyndactylie --- r_associated #0: 20 --> syndrome de Pfeiffer
    n1=acrocéphalopolysyndactylie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=20
  79. acrocéphalosyndactylie de type V --- r_associated #0: 20 --> syndrome de Pfeiffer
    n1=acrocéphalosyndactylie de type V | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=20
  80. polydactylie --- r_associated #0: 20 --> syndrome de Pfeiffer
    n1=polydactylie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=20
  81. Maladies rares --- r_associated #0: 16 --> syndrome de Pfeiffer
    n1=Maladies rares | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=16
  82. Maladie génétique --- r_associated #0: 15 --> syndrome de Pfeiffer
    n1=Maladie génétique | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=15
  83. Pédiatrie --- r_associated #0: 15 --> syndrome de Pfeiffer
    n1=Pédiatrie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=15
  84. fgfr2 --- r_associated #0: 15 --> syndrome de Pfeiffer
    n1=fgfr2 | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=15
  85. Apert (syndrome d') --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=Apert (syndrome d') | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  86. Caryotype --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=Caryotype | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  87. Maladies héréditaires --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=Maladies héréditaires | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  88. acrocéphalosyndactylie de type v --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=acrocéphalosyndactylie de type v | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  89. acrocéphalosyndactylie, type iv --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=acrocéphalosyndactylie, type iv | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  90. en:Apert-Crouzon maladie --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:Apert-Crouzon maladie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  91. en:FGFR2 en 10q26.13.3 --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:FGFR2 en 10q26.13.3 | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  92. en:acrocéphalosyndactylie type Ia --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:acrocéphalosyndactylie type Ia | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  93. en:acrodysplasie --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:acrodysplasie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  94. en:caryotype --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:caryotype | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  95. en:cataracte --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:cataracte | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  96. en:colobome irien ou choroïdien (rare) --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:colobome irien ou choroïdien (rare) | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  97. en:exophtalmie --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:exophtalmie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  98. en:kératite --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:kératite | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  99. en:nystagmus --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:nystagmus | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  100. en:ophtalmoplégie --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:ophtalmoplégie | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  101. en:orbites étroites --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:orbites étroites | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  102. en:paediatrics --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:paediatrics | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  103. en:polydactyly --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:polydactyly | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
  104. en:strabisme --- r_associated #0: 10 --> syndrome de Pfeiffer
    n1=en:strabisme | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=10
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