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'en:osteogenesis imperfecta, type vi'
(id=8684650 ; fe=en:osteogenesis imperfecta, type vi ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1975 creation date=2017-08-18 touchdate=2025-06-08 10:16:26.000)
≈ 26 relations sortantes

  1. en:osteogenesis imperfecta, type vi -- r_associated #0: 35 / 1 -> en:serpinf1, 2-bp dup, 324ct
    n1=en:osteogenesis imperfecta, type vi | n2=en:serpinf1, 2-bp dup, 324ct | rel=r_associated | relid=0 | w=35
  2. en:osteogenesis imperfecta, type vi -- r_associated #0: 34 / 0.971 -> en:serpinf1, 2-bp del, nt1118
    n1=en:osteogenesis imperfecta, type vi | n2=en:serpinf1, 2-bp del, nt1118 | rel=r_associated | relid=0 | w=34
  3. en:osteogenesis imperfecta, type vi -- r_associated #0: 34 / 0.971 -> en:serpinf1, tyr232ter
    n1=en:osteogenesis imperfecta, type vi | n2=en:serpinf1, tyr232ter | rel=r_associated | relid=0 | w=34
  4. en:osteogenesis imperfecta, type vi -- r_associated #0: 32 / 0.914 -> en:serpinf1, 1-bp del, 653t
    n1=en:osteogenesis imperfecta, type vi | n2=en:serpinf1, 1-bp del, 653t | rel=r_associated | relid=0 | w=32
  5. en:osteogenesis imperfecta, type vi -- r_associated #0: 29 / 0.829 -> en:serpinf1, -9+2dup
    n1=en:osteogenesis imperfecta, type vi | n2=en:serpinf1, -9+2dup | rel=r_associated | relid=0 | w=29
  6. en:osteogenesis imperfecta, type vi -- r_associated #0: 29 / 0.829 -> en:serpinf1, gln378ter
    n1=en:osteogenesis imperfecta, type vi | n2=en:serpinf1, gln378ter | rel=r_associated | relid=0 | w=29
  7. en:osteogenesis imperfecta, type vi -- r_associated #0: 26 / 0.743 -> en:osteogenesis imperfecta
    n1=en:osteogenesis imperfecta, type vi | n2=en:osteogenesis imperfecta | rel=r_associated | relid=0 | w=26
  8. en:osteogenesis imperfecta, type vi -- r_associated #0: 25 / 0.714 -> en:osteogenesis
    n1=en:osteogenesis imperfecta, type vi | n2=en:osteogenesis | rel=r_associated | relid=0 | w=25
  9. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> en:blue sclera syndrome
    n1=en:osteogenesis imperfecta, type vi | n2=en:blue sclera syndrome | rel=r_associated | relid=0 | w=20
  10. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> en:brittle bone disease
    n1=en:osteogenesis imperfecta, type vi | n2=en:brittle bone disease | rel=r_associated | relid=0 | w=20
  11. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> en:brittle-bone disease
    n1=en:osteogenesis imperfecta, type vi | n2=en:brittle-bone disease | rel=r_associated | relid=0 | w=20
  12. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> en:Eddowes's disease
    n1=en:osteogenesis imperfecta, type vi | n2=en:Eddowes's disease | rel=r_associated | relid=0 | w=20
  13. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> en:OI
    n1=en:osteogenesis imperfecta, type vi | n2=en:OI | rel=r_associated | relid=0 | w=20
  14. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> en:Osteogenesis imperfecta
    n1=en:osteogenesis imperfecta, type vi | n2=en:Osteogenesis imperfecta | rel=r_associated | relid=0 | w=20
  15. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> en:osteopsathyrosis
    n1=en:osteogenesis imperfecta, type vi | n2=en:osteopsathyrosis | rel=r_associated | relid=0 | w=20
  16. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> maladie de l'homme de verre
    n1=en:osteogenesis imperfecta, type vi | n2=maladie de l'homme de verre | rel=r_associated | relid=0 | w=20
  17. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> maladie des os de verre
    n1=en:osteogenesis imperfecta, type vi | n2=maladie des os de verre | rel=r_associated | relid=0 | w=20
  18. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> Ostéogenèse imparfaite
    n1=en:osteogenesis imperfecta, type vi | n2=Ostéogenèse imparfaite | rel=r_associated | relid=0 | w=20
  19. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> ostéogénèse imparfaite
    n1=en:osteogenesis imperfecta, type vi | n2=ostéogénèse imparfaite | rel=r_associated | relid=0 | w=20
  20. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> ostéogenèse imparfaite
    n1=en:osteogenesis imperfecta, type vi | n2=ostéogenèse imparfaite | rel=r_associated | relid=0 | w=20
  21. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> osteogenesis imperfecta
    n1=en:osteogenesis imperfecta, type vi | n2=osteogenesis imperfecta | rel=r_associated | relid=0 | w=20
  22. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> osteogenesis imperfecta forme oculaire
    n1=en:osteogenesis imperfecta, type vi | n2=osteogenesis imperfecta forme oculaire | rel=r_associated | relid=0 | w=20
  23. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> osteogenesis imperfecta progressivement déformante avec sclères normales
    n1=en:osteogenesis imperfecta, type vi | n2=osteogenesis imperfecta progressivement déformante avec sclères normales | rel=r_associated | relid=0 | w=20
  24. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> ostéopsathyrose
    n1=en:osteogenesis imperfecta, type vi | n2=ostéopsathyrose | rel=r_associated | relid=0 | w=20
  25. en:osteogenesis imperfecta, type vi -- r_associated #0: 20 / 0.571 -> syndrome de Lobstein-van der Hoeve
    n1=en:osteogenesis imperfecta, type vi | n2=syndrome de Lobstein-van der Hoeve | rel=r_associated | relid=0 | w=20
  26. en:osteogenesis imperfecta, type vi -- r_associated #0: 2 / 0.057 -> en:disease or syndrome
    n1=en:osteogenesis imperfecta, type vi | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=2
≈ 32 relations entrantes

  1. en:osteogenesis imperfecta --- r_associated #0: 195 --> en:osteogenesis imperfecta, type vi
    n1=en:osteogenesis imperfecta | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=195
  2. ostéogenèse imparfaite --- r_associated #0: 191 --> en:osteogenesis imperfecta, type vi
    n1=ostéogenèse imparfaite | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=191
  3. ostéogénèse imparfaite --- r_associated #0: 191 --> en:osteogenesis imperfecta, type vi
    n1=ostéogénèse imparfaite | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=191
  4. maladie des os de verre --- r_associated #0: 171 --> en:osteogenesis imperfecta, type vi
    n1=maladie des os de verre | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=171
  5. en:Osteogenesis imperfecta --- r_associated #0: 160 --> en:osteogenesis imperfecta, type vi
    n1=en:Osteogenesis imperfecta | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=160
  6. en:brittle bone disease --- r_associated #0: 145 --> en:osteogenesis imperfecta, type vi
    n1=en:brittle bone disease | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=145
  7. en:OI --- r_associated #0: 140 --> en:osteogenesis imperfecta, type vi
    n1=en:OI | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=140
  8. osteogenesis imperfecta --- r_associated #0: 68 --> en:osteogenesis imperfecta, type vi
    n1=osteogenesis imperfecta | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=68
  9. Ostéogenèse imparfaite --- r_associated #0: 50 --> en:osteogenesis imperfecta, type vi
    n1=Ostéogenèse imparfaite | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=50
  10. maladie de l'homme de verre --- r_associated #0: 50 --> en:osteogenesis imperfecta, type vi
    n1=maladie de l'homme de verre | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=50
  11. osteogenesis imperfecta forme oculaire --- r_associated #0: 40 --> en:osteogenesis imperfecta, type vi
    n1=osteogenesis imperfecta forme oculaire | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=40
  12. osteogenesis imperfecta progressivement déformante avec sclères normales --- r_associated #0: 40 --> en:osteogenesis imperfecta, type vi
    n1=osteogenesis imperfecta progressivement déformante avec sclères normales | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=40
  13. syndrome de Lobstein-van der Hoeve --- r_associated #0: 39 --> en:osteogenesis imperfecta, type vi
    n1=syndrome de Lobstein-van der Hoeve | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=39
  14. en:serpinf1, 2-bp dup, 324ct --- r_associated #0: 35 --> en:osteogenesis imperfecta, type vi
    n1=en:serpinf1, 2-bp dup, 324ct | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=35
  15. en:serpinf1, 1-bp del, 653t --- r_associated #0: 31 --> en:osteogenesis imperfecta, type vi
    n1=en:serpinf1, 1-bp del, 653t | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=31
  16. en:serpinf1, 2-bp del, nt1118 --- r_associated #0: 31 --> en:osteogenesis imperfecta, type vi
    n1=en:serpinf1, 2-bp del, nt1118 | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=31
  17. ostéopsathyrose --- r_associated #0: 31 --> en:osteogenesis imperfecta, type vi
    n1=ostéopsathyrose | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=31
  18. en:serpinf1, gln378ter --- r_associated #0: 30 --> en:osteogenesis imperfecta, type vi
    n1=en:serpinf1, gln378ter | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=30
  19. en:blue sclera syndrome --- r_associated #0: 29 --> en:osteogenesis imperfecta, type vi
    n1=en:blue sclera syndrome | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=29
  20. en:brittle-bone disease --- r_associated #0: 29 --> en:osteogenesis imperfecta, type vi
    n1=en:brittle-bone disease | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=29
  21. en:serpinf1, tyr232ter --- r_associated #0: 29 --> en:osteogenesis imperfecta, type vi
    n1=en:serpinf1, tyr232ter | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=29
  22. en:Eddowes's disease --- r_associated #0: 28 --> en:osteogenesis imperfecta, type vi
    n1=en:Eddowes's disease | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=28
  23. en:serpinf1, -9+2dup --- r_associated #0: 27 --> en:osteogenesis imperfecta, type vi
    n1=en:serpinf1, -9+2dup | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=27
  24. en:osteopsathyrosis --- r_associated #0: 26 --> en:osteogenesis imperfecta, type vi
    n1=en:osteopsathyrosis | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=26
  25. en:Adair Dighton's syndrome --- r_associated #0: 24 --> en:osteogenesis imperfecta, type vi
    n1=en:Adair Dighton's syndrome | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=24
  26. en:spurway-eddowes syndrome --- r_associated #0: 22 --> en:osteogenesis imperfecta, type vi
    n1=en:spurway-eddowes syndrome | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=22
  27. fragilité osseuse héréditaire --- r_associated #0: 21 --> en:osteogenesis imperfecta, type vi
    n1=fragilité osseuse héréditaire | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=21
  28. en:ocular form --- r_associated #0: 10 --> en:osteogenesis imperfecta, type vi
    n1=en:ocular form | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=10
  29. en:progressively deforming --- r_associated #0: 10 --> en:osteogenesis imperfecta, type vi
    n1=en:progressively deforming | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=10
  30. en:with normal sclerae --- r_associated #0: 10 --> en:osteogenesis imperfecta, type vi
    n1=en:with normal sclerae | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=10
  31. ostéoporose-pseudogliome (syndrome) --- r_associated #0: 10 --> en:osteogenesis imperfecta, type vi
    n1=ostéoporose-pseudogliome (syndrome) | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=10
  32. Lobstein-van der Hoeve (syndrome de) --- r_associated #0: 5 --> en:osteogenesis imperfecta, type vi
    n1=Lobstein-van der Hoeve (syndrome de) | n2=en:osteogenesis imperfecta, type vi | rel=r_associated | relid=0 | w=5
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