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'en:mental retardation, autosomal dominant 21'
(id=7471874 ; fe=en:mental retardation, autosomal dominant 21 ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=2740 creation date=2017-06-27 touchdate=2025-12-19 15:22:55.000)
≈ 42 relations sortantes

  1. en:mental retardation, autosomal dominant 21 -- r_associated #0: 27 / 1 -> en:developmental delay
    n1=en:mental retardation, autosomal dominant 21 | n2=en:developmental delay | rel=r_associated | relid=0 | w=27
  2. en:mental retardation, autosomal dominant 21 -- r_associated #0: 25 / 0.926 -> en:mental
    n1=en:mental retardation, autosomal dominant 21 | n2=en:mental | rel=r_associated | relid=0 | w=25
  3. en:mental retardation, autosomal dominant 21 -- r_associated #0: 23 / 0.852 -> en:hypotonia
    n1=en:mental retardation, autosomal dominant 21 | n2=en:hypotonia | rel=r_associated | relid=0 | w=23
  4. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> bébé bronzé (syndrome du)
    n1=en:mental retardation, autosomal dominant 21 | n2=bébé bronzé (syndrome du) | rel=r_associated | relid=0 | w=20
  5. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> bec de lièvre
    n1=en:mental retardation, autosomal dominant 21 | n2=bec de lièvre | rel=r_associated | relid=0 | w=20
  6. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> Bec de lièvre
    n1=en:mental retardation, autosomal dominant 21 | n2=Bec de lièvre | rel=r_associated | relid=0 | w=20
  7. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:and proeminent incisors
    n1=en:mental retardation, autosomal dominant 21 | n2=en:and proeminent incisors | rel=r_associated | relid=0 | w=20
  8. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:and teething delay
    n1=en:mental retardation, autosomal dominant 21 | n2=en:and teething delay | rel=r_associated | relid=0 | w=20
  9. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:aortic coarctation, mild (rare)
    n1=en:mental retardation, autosomal dominant 21 | n2=en:aortic coarctation, mild (rare) | rel=r_associated | relid=0 | w=20
  10. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:atrial septal defect (rare)
    n1=en:mental retardation, autosomal dominant 21 | n2=en:atrial septal defect (rare) | rel=r_associated | relid=0 | w=20
  11. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:autosomal dominant inheritance
    n1=en:mental retardation, autosomal dominant 21 | n2=en:autosomal dominant inheritance | rel=r_associated | relid=0 | w=20
  12. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:cleft lip
    n1=en:mental retardation, autosomal dominant 21 | n2=en:cleft lip | rel=r_associated | relid=0 | w=20
  13. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:cleft palate
    n1=en:mental retardation, autosomal dominant 21 | n2=en:cleft palate | rel=r_associated | relid=0 | w=20
  14. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:cleft palate (in some patients)
    n1=en:mental retardation, autosomal dominant 21 | n2=en:cleft palate (in some patients) | rel=r_associated | relid=0 | w=20
  15. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:ctcf, 1-bp dup, 1186a
    n1=en:mental retardation, autosomal dominant 21 | n2=en:ctcf, 1-bp dup, 1186a | rel=r_associated | relid=0 | w=20
  16. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:ctcf, 1-bp dup, 375t
    n1=en:mental retardation, autosomal dominant 21 | n2=en:ctcf, 1-bp dup, 375t | rel=r_associated | relid=0 | w=20
  17. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:ctcf, arg567trp
    n1=en:mental retardation, autosomal dominant 21 | n2=en:ctcf, arg567trp | rel=r_associated | relid=0 | w=20
  18. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:feeding problem
    n1=en:mental retardation, autosomal dominant 21 | n2=en:feeding problem | rel=r_associated | relid=0 | w=20
  19. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:harelip
    n1=en:mental retardation, autosomal dominant 21 | n2=en:harelip | rel=r_associated | relid=0 | w=20
  20. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:hernia
    n1=en:mental retardation, autosomal dominant 21 | n2=en:hernia | rel=r_associated | relid=0 | w=20
  21. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:keratoconus posticus
    n1=en:mental retardation, autosomal dominant 21 | n2=en:keratoconus posticus | rel=r_associated | relid=0 | w=20
  22. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:labial fissure
    n1=en:mental retardation, autosomal dominant 21 | n2=en:labial fissure | rel=r_associated | relid=0 | w=20
  23. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:muscular hypotonia
    n1=en:mental retardation, autosomal dominant 21 | n2=en:muscular hypotonia | rel=r_associated | relid=0 | w=20
  24. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:obesity
    n1=en:mental retardation, autosomal dominant 21 | n2=en:obesity | rel=r_associated | relid=0 | w=20
  25. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:palate-blepharophimosis
    n1=en:mental retardation, autosomal dominant 21 | n2=en:palate-blepharophimosis | rel=r_associated | relid=0 | w=20
  26. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:patent ductus arteriosus (rare)
    n1=en:mental retardation, autosomal dominant 21 | n2=en:patent ductus arteriosus (rare) | rel=r_associated | relid=0 | w=20
  27. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:short stature
    n1=en:mental retardation, autosomal dominant 21 | n2=en:short stature | rel=r_associated | relid=0 | w=20
  28. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> en:strabismus
    n1=en:mental retardation, autosomal dominant 21 | n2=en:strabismus | rel=r_associated | relid=0 | w=20
  29. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> Fenn (diagramme de)
    n1=en:mental retardation, autosomal dominant 21 | n2=Fenn (diagramme de) | rel=r_associated | relid=0 | w=20
  30. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> fente labiale
    n1=en:mental retardation, autosomal dominant 21 | n2=fente labiale | rel=r_associated | relid=0 | w=20
  31. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> fente labiopalatine et blépharophimosis
    n1=en:mental retardation, autosomal dominant 21 | n2=fente labiopalatine et blépharophimosis | rel=r_associated | relid=0 | w=20
  32. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> hypothyroïdie (manifestations neuromusculaires dans l')
    n1=en:mental retardation, autosomal dominant 21 | n2=hypothyroïdie (manifestations neuromusculaires dans l') | rel=r_associated | relid=0 | w=20
  33. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> hypotonie
    n1=en:mental retardation, autosomal dominant 21 | n2=hypotonie | rel=r_associated | relid=0 | w=20
  34. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> Hypotonie musculaire
    n1=en:mental retardation, autosomal dominant 21 | n2=Hypotonie musculaire | rel=r_associated | relid=0 | w=20
  35. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> hypotonie musculaire
    n1=en:mental retardation, autosomal dominant 21 | n2=hypotonie musculaire | rel=r_associated | relid=0 | w=20
  36. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> hypotonie, obésité et incisives proéminentes
    n1=en:mental retardation, autosomal dominant 21 | n2=hypotonie, obésité et incisives proéminentes | rel=r_associated | relid=0 | w=20
  37. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> kératocône postérieur-fente labiale-petite taille
    n1=en:mental retardation, autosomal dominant 21 | n2=kératocône postérieur-fente labiale-petite taille | rel=r_associated | relid=0 | w=20
  38. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique
    n1=en:mental retardation, autosomal dominant 21 | n2=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | rel=r_associated | relid=0 | w=20
  39. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose
    n1=en:mental retardation, autosomal dominant 21 | n2=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | rel=r_associated | relid=0 | w=20
  40. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> petite taille, hyperextensibilité, hernie et dépression oculaire
    n1=en:mental retardation, autosomal dominant 21 | n2=petite taille, hyperextensibilité, hernie et dépression oculaire | rel=r_associated | relid=0 | w=20
  41. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> strabisme
    n1=en:mental retardation, autosomal dominant 21 | n2=strabisme | rel=r_associated | relid=0 | w=20
  42. en:mental retardation, autosomal dominant 21 -- r_associated #0: 20 / 0.741 -> strabismus
    n1=en:mental retardation, autosomal dominant 21 | n2=strabismus | rel=r_associated | relid=0 | w=20
≈ 136 relations entrantes

  1. en:hypotonia --- r_associated #0: 87 --> en:mental retardation, autosomal dominant 21
    n1=en:hypotonia | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=87
  2. hypotonie --- r_associated #0: 85 --> en:mental retardation, autosomal dominant 21
    n1=hypotonie | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=85
  3. strabismus --- r_associated #0: 59 --> en:mental retardation, autosomal dominant 21
    n1=strabismus | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=59
  4. en:strabismus --- r_associated #0: 52 --> en:mental retardation, autosomal dominant 21
    n1=en:strabismus | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=52
  5. bec de lièvre --- r_associated #0: 49 --> en:mental retardation, autosomal dominant 21
    n1=bec de lièvre | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=49
  6. hypotonie, obésité et incisives proéminentes --- r_associated #0: 49 --> en:mental retardation, autosomal dominant 21
    n1=hypotonie, obésité et incisives proéminentes | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=49
  7. hypotonie musculaire --- r_associated #0: 46 --> en:mental retardation, autosomal dominant 21
    n1=hypotonie musculaire | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=46
  8. en:cleft lip --- r_associated #0: 45 --> en:mental retardation, autosomal dominant 21
    n1=en:cleft lip | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=45
  9. en:keratoconus posticus --- r_associated #0: 45 --> en:mental retardation, autosomal dominant 21
    n1=en:keratoconus posticus | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=45
  10. fente labiopalatine et blépharophimosis --- r_associated #0: 45 --> en:mental retardation, autosomal dominant 21
    n1=fente labiopalatine et blépharophimosis | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=45
  11. kératocône postérieur-fente labiale-petite taille --- r_associated #0: 45 --> en:mental retardation, autosomal dominant 21
    n1=kératocône postérieur-fente labiale-petite taille | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=45
  12. fente labiale --- r_associated #0: 43 --> en:mental retardation, autosomal dominant 21
    n1=fente labiale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=43
  13. petite taille, hyperextensibilité, hernie et dépression oculaire --- r_associated #0: 42 --> en:mental retardation, autosomal dominant 21
    n1=petite taille, hyperextensibilité, hernie et dépression oculaire | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=42
  14. strabisme --- r_associated #0: 42 --> en:mental retardation, autosomal dominant 21
    n1=strabisme | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=42
  15. en:short stature --- r_associated #0: 40 --> en:mental retardation, autosomal dominant 21
    n1=en:short stature | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=40
  16. hypothyroïdie (manifestations neuromusculaires dans l') --- r_associated #0: 40 --> en:mental retardation, autosomal dominant 21
    n1=hypothyroïdie (manifestations neuromusculaires dans l') | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=40
  17. myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique --- r_associated #0: 39 --> en:mental retardation, autosomal dominant 21
    n1=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=39
  18. Fenn (diagramme de) --- r_associated #0: 38 --> en:mental retardation, autosomal dominant 21
    n1=Fenn (diagramme de) | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=38
  19. en:harelip --- r_associated #0: 37 --> en:mental retardation, autosomal dominant 21
    n1=en:harelip | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=37
  20. ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose --- r_associated #0: 37 --> en:mental retardation, autosomal dominant 21
    n1=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=37
  21. Hypotonie musculaire --- r_associated #0: 36 --> en:mental retardation, autosomal dominant 21
    n1=Hypotonie musculaire | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=36
  22. en:cleft palate (in some patients) --- r_associated #0: 36 --> en:mental retardation, autosomal dominant 21
    n1=en:cleft palate (in some patients) | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=36
  23. en:ctcf, 1-bp dup, 375t --- r_associated #0: 35 --> en:mental retardation, autosomal dominant 21
    n1=en:ctcf, 1-bp dup, 375t | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=35
  24. en:developmental delay --- r_associated #0: 34 --> en:mental retardation, autosomal dominant 21
    n1=en:developmental delay | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=34
  25. Bec de lièvre --- r_associated #0: 32 --> en:mental retardation, autosomal dominant 21
    n1=Bec de lièvre | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=32
  26. en:patent ductus arteriosus (rare) --- r_associated #0: 31 --> en:mental retardation, autosomal dominant 21
    n1=en:patent ductus arteriosus (rare) | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=31
  27. en:autosomal dominant inheritance --- r_associated #0: 30 --> en:mental retardation, autosomal dominant 21
    n1=en:autosomal dominant inheritance | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=30
  28. en:labial fissure --- r_associated #0: 30 --> en:mental retardation, autosomal dominant 21
    n1=en:labial fissure | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=30
  29. bébé bronzé (syndrome du) --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 21
    n1=bébé bronzé (syndrome du) | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=29
  30. en:cleft palate --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 21
    n1=en:cleft palate | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=29
  31. en:ctcf, 1-bp dup, 1186a --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 21
    n1=en:ctcf, 1-bp dup, 1186a | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=29
  32. en:ctcf, arg567trp --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 21
    n1=en:ctcf, arg567trp | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=29
  33. en:hernia --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 21
    n1=en:hernia | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=29
  34. en:obesity --- r_associated #0: 28 --> en:mental retardation, autosomal dominant 21
    n1=en:obesity | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=28
  35. en:and proeminent incisors --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 21
    n1=en:and proeminent incisors | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=27
  36. en:aortic coarctation, mild (rare) --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 21
    n1=en:aortic coarctation, mild (rare) | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=27
  37. en:muscular hypotonia --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 21
    n1=en:muscular hypotonia | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=27
  38. en:palate-blepharophimosis --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 21
    n1=en:palate-blepharophimosis | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=27
  39. en:and teething delay --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 21
    n1=en:and teething delay | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=26
  40. en:atrial septal defect (rare) --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 21
    n1=en:atrial septal defect (rare) | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=26
  41. en:feeding problem --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 21
    n1=en:feeding problem | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=26
  42. en:Rieger anomaly --- r_associated #0: 25 --> en:mental retardation, autosomal dominant 21
    n1=en:Rieger anomaly | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=25
  43. en:squinting --- r_associated #0: 25 --> en:mental retardation, autosomal dominant 21
    n1=en:squinting | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=25
  44. kératocône posticus --- r_associated #0: 25 --> en:mental retardation, autosomal dominant 21
    n1=kératocône posticus | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=25
  45. insuffisance staturale --- r_associated #0: 24 --> en:mental retardation, autosomal dominant 21
    n1=insuffisance staturale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=24
  46. en:loxophthalmus --- r_associated #0: 23 --> en:mental retardation, autosomal dominant 21
    n1=en:loxophthalmus | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=23
  47. en:and hypogonadotropic hypogonadism --- r_associated #0: 21 --> en:mental retardation, autosomal dominant 21
    n1=en:and hypogonadotropic hypogonadism | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=21
  48. en:hyperextensibility --- r_associated #0: 21 --> en:mental retardation, autosomal dominant 21
    n1=en:hyperextensibility | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=21
  49. en:multicore disease with mental retardation --- r_associated #0: 21 --> en:mental retardation, autosomal dominant 21
    n1=en:multicore disease with mental retardation | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=21
  50. en:ocular depression --- r_associated #0: 21 --> en:mental retardation, autosomal dominant 21
    n1=en:ocular depression | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=21
  51. en:ophthalmoplegia --- r_associated #0: 21 --> en:mental retardation, autosomal dominant 21
    n1=en:ophthalmoplegia | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=21
  52. Strabisme --- r_associated #0: 20 --> en:mental retardation, autosomal dominant 21
    n1=Strabisme | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=20
  53. Fente labiale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=Fente labiale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  54. en:congenital atrophy of thyroid --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=en:congenital atrophy of thyroid | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  55. en:congenital hypothyroidism --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=en:congenital hypothyroidism | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  56. en:neonatal hypothyroidism --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=en:neonatal hypothyroidism | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  57. fente labio-palatine --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=fente labio-palatine | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  58. fente labiopalatine --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=fente labiopalatine | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  59. hypothyroïdie congénitale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypothyroïdie congénitale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  60. hypothyroïdie et psychisme --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypothyroïdie et psychisme | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  61. hypothyroïdie néonatale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypothyroïdie néonatale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  62. hypotonie plasmatique --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotonie plasmatique | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  63. hypotonie sphinctérienne anale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotonie sphinctérienne anale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  64. hypotonie sphinctérienne uréthrale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotonie sphinctérienne uréthrale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  65. hypotonie utérine --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotonie utérine | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  66. hypotonie vésicale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotonie vésicale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  67. hypotonique --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotonique | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  68. hypotrichose --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotrichose | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  69. hypotrichose avec anodontie et anhidrose de Touraine --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotrichose avec anodontie et anhidrose de Touraine | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  70. hypotrichose congénitale des cils --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotrichose congénitale des cils | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  71. hypotrichose congénitale simple --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotrichose congénitale simple | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  72. hypotrichose héréditaire de Marie Unna --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotrichose héréditaire de Marie Unna | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  73. hypotrichose, atrophodermie folliculaire et épithéliomatose --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=hypotrichose, atrophodermie folliculaire et épithéliomatose | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  74. obésité --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 21
    n1=obésité | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=15
  75. BEC DE LIEVRE --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=BEC DE LIEVRE | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  76. Hypotonie --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=Hypotonie | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  77. MOMO (syndrome) --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=MOMO (syndrome) | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  78. Obésité --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=Obésité | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  79. Stormoken-Sjaatadt-Langslet (syndrome de) --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=Stormoken-Sjaatadt-Langslet (syndrome de) | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  80. atonie de l'utérus --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=atonie de l'utérus | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  81. bec de corbin --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=bec de corbin | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  82. bec de cuiller --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=bec de cuiller | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  83. bec de la prostate --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=bec de la prostate | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  84. bec de la rotule --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=bec de la rotule | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  85. bébé collodion --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=bébé collodion | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  86. division palatine --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=division palatine | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  87. en:Fenn's diagram --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:Fenn's diagram | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  88. en:anal sphincter hypotonia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:anal sphincter hypotonia | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  89. en:ataxia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:ataxia | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  90. en:bladder hypotonia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:bladder hypotonia | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  91. en:bronze baby syndrome --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:bronze baby syndrome | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  92. en:congenital eyelashes hypotrichosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:congenital eyelashes hypotrichosis | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  93. en:hypacusis and athetosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:hypacusis and athetosis | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  94. en:hypothyreosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:hypothyreosis | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  95. en:hypothyroidism and psychism --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:hypothyroidism and psychism | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  96. en:hypotonic --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:hypotonic | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  97. en:hypotrichosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:hypotrichosis | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  98. en:hypotrichosis congenita simplex --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:hypotrichosis congenita simplex | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  99. en:hypotrichosis-anodontic syndrome --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:hypotrichosis-anodontic syndrome | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  100. en:labiopalatine cleft --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:labiopalatine cleft | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  101. en:plasma hypotonia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:plasma hypotonia | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  102. en:sphincteric hypotony --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:sphincteric hypotony | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  103. en:uterine hypotonia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=en:uterine hypotonia | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  104. fente cérébrale de Bichat --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente cérébrale de Bichat | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  105. fente de Larrey --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente de Larrey | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  106. fente de la glotte --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente de la glotte | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  107. fente foetale --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente foetale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  108. fente hypophysaire --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente hypophysaire | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  109. fente interaryténoïdienne --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente interaryténoïdienne | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  110. fente interfessière --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente interfessière | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  111. fente labiopalatine et kystes muqueux de la lèvre inférieure --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente labiopalatine et kystes muqueux de la lèvre inférieure | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  112. fente labiopalatine, ectropion et dents coniques --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente labiopalatine, ectropion et dents coniques | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  113. fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  114. fente palatine --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fente palatine | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  115. fissure palatine --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fissure palatine | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  116. fénotérol --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=fénotérol | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  117. inertie utérine --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=inertie utérine | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  118. macrosomie, obésité, macrocéphalie et anomalies oculaires --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=macrosomie, obésité, macrocéphalie et anomalies oculaires | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  119. polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  120. retards de croissance et de développement avec dysmorphie faciale --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=retards de croissance et de développement avec dysmorphie faciale | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  121. strabique --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=strabique | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  122. syndrome de Treft-Sanborn-Carey --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 21
    n1=syndrome de Treft-Sanborn-Carey | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=10
  123. Hypotonique --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=Hypotonique | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  124. atrophie congénitale de la thyroïde --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=atrophie congénitale de la thyroïde | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  125. bec de perroquet --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=bec de perroquet | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  126. bec du cuboïde --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=bec du cuboïde | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  127. bec du sphénoïde --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=bec du sphénoïde | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  128. bec scléral --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=bec scléral | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  129. bécégite --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=bécégite | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  130. crétinismes --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=crétinismes | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  131. en:congenital goiter --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=en:congenital goiter | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  132. goitre congénital --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=goitre congénital | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  133. hypothyroïdisme congénital --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=hypothyroïdisme congénital | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  134. infantilisme type brissaud --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=infantilisme type brissaud | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  135. nanisme hypothyroïdien --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=nanisme hypothyroïdien | n2=en:mental retardation, autosomal dominant 21 | rel=r_associated | relid=0 | w=5
  136. syndrome d'insuffisance thyroïdienne congénitale --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 21
    n1=syndrome d'insuffisance thyroïdienne congénitale | n2=en:mental retardation, autosomal dominant 21 | 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