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'en:syndromes, 49,xxxxy'
(id=8389831 ; fe=en:syndromes, 49,xxxxy ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=956 creation date=2017-07-26 touchdate=2025-03-21 10:28:25.000)
≈ 22 relations sortantes

  1. en:syndromes, 49,xxxxy -- r_associated #0: 42 / 1 -> en:trisomy x
    n1=en:syndromes, 49,xxxxy | n2=en:trisomy x | rel=r_associated | relid=0 | w=42
  2. en:syndromes, 49,xxxxy -- r_associated #0: 32 / 0.762 -> en:fragile x chromosome
    n1=en:syndromes, 49,xxxxy | n2=en:fragile x chromosome | rel=r_associated | relid=0 | w=32
  3. en:syndromes, 49,xxxxy -- r_associated #0: 31 / 0.738 -> en:mosaicism - lines with various numbers of x chromosomes
    n1=en:syndromes, 49,xxxxy | n2=en:mosaicism - lines with various numbers of x chromosomes | rel=r_associated | relid=0 | w=31
  4. en:syndromes, 49,xxxxy -- r_associated #0: 31 / 0.738 -> en:xx male
    n1=en:syndromes, 49,xxxxy | n2=en:xx male | rel=r_associated | relid=0 | w=31
  5. en:syndromes, 49,xxxxy -- r_associated #0: 30 / 0.714 -> en:congenital
    n1=en:syndromes, 49,xxxxy | n2=en:congenital | rel=r_associated | relid=0 | w=30
  6. en:syndromes, 49,xxxxy -- r_associated #0: 30 / 0.714 -> en:gonadal dysgenesis
    n1=en:syndromes, 49,xxxxy | n2=en:gonadal dysgenesis | rel=r_associated | relid=0 | w=30
  7. en:syndromes, 49,xxxxy -- r_associated #0: 29 / 0.69 -> en:chromosomal morphology
    n1=en:syndromes, 49,xxxxy | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=29
  8. en:syndromes, 49,xxxxy -- r_associated #0: 28 / 0.667 -> en:tetrasomy x
    n1=en:syndromes, 49,xxxxy | n2=en:tetrasomy x | rel=r_associated | relid=0 | w=28
  9. en:syndromes, 49,xxxxy -- r_associated #0: 28 / 0.667 -> syndrome de Klinefelter
    n1=en:syndromes, 49,xxxxy | n2=syndrome de Klinefelter | rel=r_associated | relid=0 | w=28
  10. en:syndromes, 49,xxxxy -- r_associated #0: 27 / 0.643 -> en:klinefelter syndrome
    n1=en:syndromes, 49,xxxxy | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=27
  11. en:syndromes, 49,xxxxy -- r_associated #0: 26 / 0.619 -> en:penta x syndrome
    n1=en:syndromes, 49,xxxxy | n2=en:penta x syndrome | rel=r_associated | relid=0 | w=26
  12. en:syndromes, 49,xxxxy -- r_associated #0: 26 / 0.619 -> en:turner syndrome
    n1=en:syndromes, 49,xxxxy | n2=en:turner syndrome | rel=r_associated | relid=0 | w=26
  13. en:syndromes, 49,xxxxy -- r_associated #0: 26 / 0.619 -> en:xxxxy syndrome
    n1=en:syndromes, 49,xxxxy | n2=en:xxxxy syndrome | rel=r_associated | relid=0 | w=26
  14. en:syndromes, 49,xxxxy -- r_associated #0: 26 / 0.619 -> en:xxxy syndrome
    n1=en:syndromes, 49,xxxxy | n2=en:xxxy syndrome | rel=r_associated | relid=0 | w=26
  15. en:syndromes, 49,xxxxy -- r_associated #0: 20 / 0.476 -> congenital
    n1=en:syndromes, 49,xxxxy | n2=congenital | rel=r_associated | relid=0 | w=20
  16. en:syndromes, 49,xxxxy -- r_associated #0: 20 / 0.476 -> congénital
    n1=en:syndromes, 49,xxxxy | n2=congénital | rel=r_associated | relid=0 | w=20
  17. en:syndromes, 49,xxxxy -- r_associated #0: 20 / 0.476 -> congénitale
    n1=en:syndromes, 49,xxxxy | n2=congénitale | rel=r_associated | relid=0 | w=20
  18. en:syndromes, 49,xxxxy -- r_associated #0: 20 / 0.476 -> en:Klinefelter syndrome
    n1=en:syndromes, 49,xxxxy | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20
  19. en:syndromes, 49,xxxxy -- r_associated #0: 20 / 0.476 -> en:Klinefelter's syndrome
    n1=en:syndromes, 49,xxxxy | n2=en:Klinefelter's syndrome | rel=r_associated | relid=0 | w=20
  20. en:syndromes, 49,xxxxy -- r_associated #0: 20 / 0.476 -> nystagmus congénital isolé
    n1=en:syndromes, 49,xxxxy | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  21. en:syndromes, 49,xxxxy -- r_associated #0: 20 / 0.476 -> syndrome de klinefelter
    n1=en:syndromes, 49,xxxxy | n2=syndrome de klinefelter | rel=r_associated | relid=0 | w=20
  22. en:syndromes, 49,xxxxy -- r_associated #0: 1 / 0.024 -> en:disease or syndrome
    n1=en:syndromes, 49,xxxxy | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=1
≈ 32 relations entrantes

  1. congénital --- r_associated #0: 57 --> en:syndromes, 49,xxxxy
    n1=congénital | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=57
  2. en:Klinefelter syndrome --- r_associated #0: 57 --> en:syndromes, 49,xxxxy
    n1=en:Klinefelter syndrome | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=57
  3. en:klinefelter syndrome --- r_associated #0: 57 --> en:syndromes, 49,xxxxy
    n1=en:klinefelter syndrome | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=57
  4. congénitale --- r_associated #0: 53 --> en:syndromes, 49,xxxxy
    n1=congénitale | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=53
  5. en:congenital --- r_associated #0: 53 --> en:syndromes, 49,xxxxy
    n1=en:congenital | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=53
  6. syndrome de Klinefelter --- r_associated #0: 49 --> en:syndromes, 49,xxxxy
    n1=syndrome de Klinefelter | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=49
  7. congenital --- r_associated #0: 48 --> en:syndromes, 49,xxxxy
    n1=congenital | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=48
  8. syndrome de klinefelter --- r_associated #0: 46 --> en:syndromes, 49,xxxxy
    n1=syndrome de klinefelter | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=46
  9. en:Klinefelter's syndrome --- r_associated #0: 45 --> en:syndromes, 49,xxxxy
    n1=en:Klinefelter's syndrome | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=45
  10. en:trisomy x --- r_associated #0: 41 --> en:syndromes, 49,xxxxy
    n1=en:trisomy x | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=41
  11. nystagmus congénital isolé --- r_associated #0: 40 --> en:syndromes, 49,xxxxy
    n1=nystagmus congénital isolé | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=40
  12. en:penta x syndrome --- r_associated #0: 31 --> en:syndromes, 49,xxxxy
    n1=en:penta x syndrome | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=31
  13. en:chromosomal morphology --- r_associated #0: 30 --> en:syndromes, 49,xxxxy
    n1=en:chromosomal morphology | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=30
  14. en:xxxxy syndrome --- r_associated #0: 27 --> en:syndromes, 49,xxxxy
    n1=en:xxxxy syndrome | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=27
  15. Klinefelter (syndrome de) --- r_associated #0: 25 --> en:syndromes, 49,xxxxy
    n1=Klinefelter (syndrome de) | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=25
  16. en:nystagmus --- r_associated #0: 23 --> en:syndromes, 49,xxxxy
    n1=en:nystagmus | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=23
  17. contractures congénitales et arachnodactylie --- r_associated #0: 22 --> en:syndromes, 49,xxxxy
    n1=contractures congénitales et arachnodactylie | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=22
  18. en:fragile x chromosome --- r_associated #0: 20 --> en:syndromes, 49,xxxxy
    n1=en:fragile x chromosome | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=20
  19. en:gonadal dysgenesis --- r_associated #0: 20 --> en:syndromes, 49,xxxxy
    n1=en:gonadal dysgenesis | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=20
  20. en:mosaicism - lines with various numbers of x chromosomes --- r_associated #0: 20 --> en:syndromes, 49,xxxxy
    n1=en:mosaicism - lines with various numbers of x chromosomes | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=20
  21. en:tetrasomy x --- r_associated #0: 20 --> en:syndromes, 49,xxxxy
    n1=en:tetrasomy x | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=20
  22. en:turner syndrome --- r_associated #0: 20 --> en:syndromes, 49,xxxxy
    n1=en:turner syndrome | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=20
  23. en:xx male --- r_associated #0: 20 --> en:syndromes, 49,xxxxy
    n1=en:xx male | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=20
  24. en:xxxy syndrome --- r_associated #0: 20 --> en:syndromes, 49,xxxxy
    n1=en:xxxy syndrome | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=20
  25. Syndrome de Klinefelter --- r_associated #0: 15 --> en:syndromes, 49,xxxxy
    n1=Syndrome de Klinefelter | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=15
  26. CONGÉNITALE --- r_associated #0: 10 --> en:syndromes, 49,xxxxy
    n1=CONGÉNITALE | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=10
  27. en:contractural arachnodactyly --- r_associated #0: 10 --> en:syndromes, 49,xxxxy
    n1=en:contractural arachnodactyly | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=10
  28. nystagmus --- r_associated #0: 10 --> en:syndromes, 49,xxxxy
    n1=nystagmus | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=10
  29. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:syndromes, 49,xxxxy
    n1=nystagmus héréditaire vertical | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=10
  30. nystagmus lié au sexe --- r_associated #0: 10 --> en:syndromes, 49,xxxxy
    n1=nystagmus lié au sexe | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=10
  31. nystagmus myoclonies --- r_associated #0: 10 --> en:syndromes, 49,xxxxy
    n1=nystagmus myoclonies | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=10
  32. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:syndromes, 49,xxxxy
    n1=nystagmus (zone de moindre) | n2=en:syndromes, 49,xxxxy | 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