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Le Rézo de JeuxDeMots
• Types de relations
• Types de noeuds
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'en:xx male'
(id=8389832 ; fe=en:xx male ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1167 creation date=2017-07-26 touchdate=2025-07-27 01:17:39.000)
≈ 24 relations sortantes

  1. en:xx male -- r_associated #0: 179 / 1 -> médecine
    n1=en:xx male | n2=médecine | rel=r_associated | relid=0 | w=179
  2. en:xx male -- r_associated #0: 27 / 0.151 -> en:trisomy x
    n1=en:xx male | n2=en:trisomy x | rel=r_associated | relid=0 | w=27
  3. en:xx male -- r_associated #0: 26 / 0.145 -> syndrome des hommes xx
    n1=en:xx male | n2=syndrome des hommes xx | rel=r_associated | relid=0 | w=26
  4. en:xx male -- r_associated #0: 25 / 0.14 -> en:congenital
    n1=en:xx male | n2=en:congenital | rel=r_associated | relid=0 | w=25
  5. en:xx male -- r_associated #0: 25 / 0.14 -> en:medicine
    n1=en:xx male | n2=en:medicine | rel=r_associated | relid=0 | w=25
  6. en:xx male -- r_associated #0: 24 / 0.134 -> en:klinefelter syndrome
    n1=en:xx male | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=24
  7. en:xx male -- r_associated #0: 22 / 0.123 -> en:XX male
    n1=en:xx male | n2=en:XX male | rel=r_associated | relid=0 | w=22
  8. en:xx male -- r_associated #0: 20 / 0.112 -> congénital
    n1=en:xx male | n2=congénital | rel=r_associated | relid=0 | w=20
  9. en:xx male -- r_associated #0: 20 / 0.112 -> congenital
    n1=en:xx male | n2=congenital | rel=r_associated | relid=0 | w=20
  10. en:xx male -- r_associated #0: 20 / 0.112 -> congénitale
    n1=en:xx male | n2=congénitale | rel=r_associated | relid=0 | w=20
  11. en:xx male -- r_associated #0: 20 / 0.112 -> en:chromosomal morphology
    n1=en:xx male | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  12. en:xx male -- r_associated #0: 20 / 0.112 -> en:chromosome xp22.3 microdeletion syndrome
    n1=en:xx male | n2=en:chromosome xp22.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20
  13. en:xx male -- r_associated #0: 20 / 0.112 -> en:Klinefelter syndrome
    n1=en:xx male | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20
  14. en:xx male -- r_associated #0: 20 / 0.112 -> en:male gender, self report
    n1=en:xx male | n2=en:male gender, self report | rel=r_associated | relid=0 | w=20
  15. en:xx male -- r_associated #0: 20 / 0.112 -> en:male phenotype
    n1=en:xx male | n2=en:male phenotype | rel=r_associated | relid=0 | w=20
  16. en:xx male -- r_associated #0: 20 / 0.112 -> en:male, self-reported
    n1=en:xx male | n2=en:male, self-reported | rel=r_associated | relid=0 | w=20
  17. en:xx male -- r_associated #0: 20 / 0.112 -> en:microduplication xp11.22p11.23 syndrome
    n1=en:xx male | n2=en:microduplication xp11.22p11.23 syndrome | rel=r_associated | relid=0 | w=20
  18. en:xx male -- r_associated #0: 20 / 0.112 -> en:nystagmus
    n1=en:xx male | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
  19. en:xx male -- r_associated #0: 20 / 0.112 -> en:penta x syndrome
    n1=en:xx male | n2=en:penta x syndrome | rel=r_associated | relid=0 | w=20
  20. en:xx male -- r_associated #0: 20 / 0.112 -> en:syndromes, 49,xxxxy
    n1=en:xx male | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=20
  21. en:xx male -- r_associated #0: 20 / 0.112 -> en:trisomy xq28 syndrome
    n1=en:xx male | n2=en:trisomy xq28 syndrome | rel=r_associated | relid=0 | w=20
  22. en:xx male -- r_associated #0: 20 / 0.112 -> en:x small rings
    n1=en:xx male | n2=en:x small rings | rel=r_associated | relid=0 | w=20
  23. en:xx male -- r_associated #0: 20 / 0.112 -> nystagmus congénital isolé
    n1=en:xx male | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  24. en:xx male -- r_associated #0: 5 / 0.028 -> Médecine
    n1=en:xx male | n2=Médecine | rel=r_associated | relid=0 | w=5
≈ 31 relations entrantes

  1. médecine --- r_associated #0: 130 --> en:xx male
    n1=médecine | n2=en:xx male | rel=r_associated | relid=0 | w=130
  2. en:Klinefelter syndrome --- r_associated #0: 60 --> en:xx male
    n1=en:Klinefelter syndrome | n2=en:xx male | rel=r_associated | relid=0 | w=60
  3. congénitale --- r_associated #0: 59 --> en:xx male
    n1=congénitale | n2=en:xx male | rel=r_associated | relid=0 | w=59
  4. en:congenital --- r_associated #0: 59 --> en:xx male
    n1=en:congenital | n2=en:xx male | rel=r_associated | relid=0 | w=59
  5. congenital --- r_associated #0: 58 --> en:xx male
    n1=congenital | n2=en:xx male | rel=r_associated | relid=0 | w=58
  6. en:klinefelter syndrome --- r_associated #0: 58 --> en:xx male
    n1=en:klinefelter syndrome | n2=en:xx male | rel=r_associated | relid=0 | w=58
  7. congénital --- r_associated #0: 55 --> en:xx male
    n1=congénital | n2=en:xx male | rel=r_associated | relid=0 | w=55
  8. en:XX male --- r_associated #0: 37 --> en:xx male
    n1=en:XX male | n2=en:xx male | rel=r_associated | relid=0 | w=37
  9. en:male, self-reported --- r_associated #0: 36 --> en:xx male
    n1=en:male, self-reported | n2=en:xx male | rel=r_associated | relid=0 | w=36
  10. nystagmus congénital isolé --- r_associated #0: 36 --> en:xx male
    n1=nystagmus congénital isolé | n2=en:xx male | rel=r_associated | relid=0 | w=36
  11. en:microduplication xp11.22p11.23 syndrome --- r_associated #0: 34 --> en:xx male
    n1=en:microduplication xp11.22p11.23 syndrome | n2=en:xx male | rel=r_associated | relid=0 | w=34
  12. en:x small rings --- r_associated #0: 34 --> en:xx male
    n1=en:x small rings | n2=en:xx male | rel=r_associated | relid=0 | w=34
  13. en:penta x syndrome --- r_associated #0: 32 --> en:xx male
    n1=en:penta x syndrome | n2=en:xx male | rel=r_associated | relid=0 | w=32
  14. en:chromosome xp22.3 microdeletion syndrome --- r_associated #0: 31 --> en:xx male
    n1=en:chromosome xp22.3 microdeletion syndrome | n2=en:xx male | rel=r_associated | relid=0 | w=31
  15. en:syndromes, 49,xxxxy --- r_associated #0: 31 --> en:xx male
    n1=en:syndromes, 49,xxxxy | n2=en:xx male | rel=r_associated | relid=0 | w=31
  16. syndrome des hommes xx --- r_associated #0: 31 --> en:xx male
    n1=syndrome des hommes xx | n2=en:xx male | rel=r_associated | relid=0 | w=31
  17. en:male phenotype --- r_associated #0: 29 --> en:xx male
    n1=en:male phenotype | n2=en:xx male | rel=r_associated | relid=0 | w=29
  18. en:male gender, self report --- r_associated #0: 28 --> en:xx male
    n1=en:male gender, self report | n2=en:xx male | rel=r_associated | relid=0 | w=28
  19. en:trisomy xq28 syndrome --- r_associated #0: 28 --> en:xx male
    n1=en:trisomy xq28 syndrome | n2=en:xx male | rel=r_associated | relid=0 | w=28
  20. en:chromosomal morphology --- r_associated #0: 27 --> en:xx male
    n1=en:chromosomal morphology | n2=en:xx male | rel=r_associated | relid=0 | w=27
  21. en:trisomy x --- r_associated #0: 27 --> en:xx male
    n1=en:trisomy x | n2=en:xx male | rel=r_associated | relid=0 | w=27
  22. en:nystagmus --- r_associated #0: 26 --> en:xx male
    n1=en:nystagmus | n2=en:xx male | rel=r_associated | relid=0 | w=26
  23. en:male population group --- r_associated #0: 25 --> en:xx male
    n1=en:male population group | n2=en:xx male | rel=r_associated | relid=0 | w=25
  24. contractures congénitales et arachnodactylie --- r_associated #0: 22 --> en:xx male
    n1=contractures congénitales et arachnodactylie | n2=en:xx male | rel=r_associated | relid=0 | w=22
  25. CONGÉNITALE --- r_associated #0: 10 --> en:xx male
    n1=CONGÉNITALE | n2=en:xx male | rel=r_associated | relid=0 | w=10
  26. en:contractural arachnodactyly --- r_associated #0: 10 --> en:xx male
    n1=en:contractural arachnodactyly | n2=en:xx male | rel=r_associated | relid=0 | w=10
  27. nystagmus --- r_associated #0: 10 --> en:xx male
    n1=nystagmus | n2=en:xx male | rel=r_associated | relid=0 | w=10
  28. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:xx male
    n1=nystagmus héréditaire vertical | n2=en:xx male | rel=r_associated | relid=0 | w=10
  29. nystagmus lié au sexe --- r_associated #0: 10 --> en:xx male
    n1=nystagmus lié au sexe | n2=en:xx male | rel=r_associated | relid=0 | w=10
  30. nystagmus myoclonies --- r_associated #0: 10 --> en:xx male
    n1=nystagmus myoclonies | n2=en:xx male | rel=r_associated | relid=0 | w=10
  31. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:xx male
    n1=nystagmus (zone de moindre) | n2=en:xx male | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr