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'en:mental retardation, autosomal dominant 29'
(id=7269051 ; fe=en:mental retardation, autosomal dominant 29 ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1742 creation date=2017-06-26 touchdate=2025-05-30 15:23:13.000)
≈ 34 relations sortantes

  1. en:mental retardation, autosomal dominant 29 -- r_associated #0: 36 / 1 -> en:setbp1, 1-bp del
    n1=en:mental retardation, autosomal dominant 29 | n2=en:setbp1, 1-bp del | rel=r_associated | relid=0 | w=36
  2. en:mental retardation, autosomal dominant 29 -- r_associated #0: 32 / 0.889 -> en:setbp1, arg625ter
    n1=en:mental retardation, autosomal dominant 29 | n2=en:setbp1, arg625ter | rel=r_associated | relid=0 | w=32
  3. en:mental retardation, autosomal dominant 29 -- r_associated #0: 31 / 0.861 -> en:setbp1, ser1011ter
    n1=en:mental retardation, autosomal dominant 29 | n2=en:setbp1, ser1011ter | rel=r_associated | relid=0 | w=31
  4. en:mental retardation, autosomal dominant 29 -- r_associated #0: 28 / 0.778 -> en:attention deficit hyperactivity disorder
    n1=en:mental retardation, autosomal dominant 29 | n2=en:attention deficit hyperactivity disorder | rel=r_associated | relid=0 | w=28
  5. en:mental retardation, autosomal dominant 29 -- r_associated #0: 27 / 0.75 -> en:autosomal dominant inheritance
    n1=en:mental retardation, autosomal dominant 29 | n2=en:autosomal dominant inheritance | rel=r_associated | relid=0 | w=27
  6. en:mental retardation, autosomal dominant 29 -- r_associated #0: 26 / 0.722 -> en:setbp1, arg626ter
    n1=en:mental retardation, autosomal dominant 29 | n2=en:setbp1, arg626ter | rel=r_associated | relid=0 | w=26
  7. en:mental retardation, autosomal dominant 29 -- r_associated #0: 26 / 0.722 -> en:setbp1, trp532ter
    n1=en:mental retardation, autosomal dominant 29 | n2=en:setbp1, trp532ter | rel=r_associated | relid=0 | w=26
  8. en:mental retardation, autosomal dominant 29 -- r_associated #0: 25 / 0.694 -> en:mental
    n1=en:mental retardation, autosomal dominant 29 | n2=en:mental | rel=r_associated | relid=0 | w=25
  9. en:mental retardation, autosomal dominant 29 -- r_associated #0: 22 / 0.611 -> en:ptosis
    n1=en:mental retardation, autosomal dominant 29 | n2=en:ptosis | rel=r_associated | relid=0 | w=22
  10. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> blépharophimosis-ptosis-épicanthus inversus (syndrome)
    n1=en:mental retardation, autosomal dominant 29 | n2=blépharophimosis-ptosis-épicanthus inversus (syndrome) | rel=r_associated | relid=0 | w=20
  11. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> colobome de l'iris avec ptosis, hypertélorisme et retard mental
    n1=en:mental retardation, autosomal dominant 29 | n2=colobome de l'iris avec ptosis, hypertélorisme et retard mental | rel=r_associated | relid=0 | w=20
  12. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:absent corpus callosum
    n1=en:mental retardation, autosomal dominant 29 | n2=en:absent corpus callosum | rel=r_associated | relid=0 | w=20
  13. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:brachycephalies
    n1=en:mental retardation, autosomal dominant 29 | n2=en:brachycephalies | rel=r_associated | relid=0 | w=20
  14. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:byzanthine arch palate
    n1=en:mental retardation, autosomal dominant 29 | n2=en:byzanthine arch palate | rel=r_associated | relid=0 | w=20
  15. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:diaphragmatic hernia
    n1=en:mental retardation, autosomal dominant 29 | n2=en:diaphragmatic hernia | rel=r_associated | relid=0 | w=20
  16. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:drooping eyelid
    n1=en:mental retardation, autosomal dominant 29 | n2=en:drooping eyelid | rel=r_associated | relid=0 | w=20
  17. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:hypertelorism
    n1=en:mental retardation, autosomal dominant 29 | n2=en:hypertelorism | rel=r_associated | relid=0 | w=20
  18. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:long narrow head
    n1=en:mental retardation, autosomal dominant 29 | n2=en:long narrow head | rel=r_associated | relid=0 | w=20
  19. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:pointed chin
    n1=en:mental retardation, autosomal dominant 29 | n2=en:pointed chin | rel=r_associated | relid=0 | w=20
  20. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:telecanthus
    n1=en:mental retardation, autosomal dominant 29 | n2=en:telecanthus | rel=r_associated | relid=0 | w=20
  21. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:thin upper lips
    n1=en:mental retardation, autosomal dominant 29 | n2=en:thin upper lips | rel=r_associated | relid=0 | w=20
  22. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> en:tooth crowding
    n1=en:mental retardation, autosomal dominant 29 | n2=en:tooth crowding | rel=r_associated | relid=0 | w=20
  23. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle
    n1=en:mental retardation, autosomal dominant 29 | n2=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | rel=r_associated | relid=0 | w=20
  24. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> hyperactivité avec déficit de l'attention
    n1=en:mental retardation, autosomal dominant 29 | n2=hyperactivité avec déficit de l'attention | rel=r_associated | relid=0 | w=20
  25. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> hypertélorisme
    n1=en:mental retardation, autosomal dominant 29 | n2=hypertélorisme | rel=r_associated | relid=0 | w=20
  26. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> hypertélorisme-microtie-fente faciale
    n1=en:mental retardation, autosomal dominant 29 | n2=hypertélorisme-microtie-fente faciale | rel=r_associated | relid=0 | w=20
  27. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> hypertélorisme, hypospadias, polysyndactylie (syndrome)
    n1=en:mental retardation, autosomal dominant 29 | n2=hypertélorisme, hypospadias, polysyndactylie (syndrome) | rel=r_associated | relid=0 | w=20
  28. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> menton pointu
    n1=en:mental retardation, autosomal dominant 29 | n2=menton pointu | rel=r_associated | relid=0 | w=20
  29. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> ptôse
    n1=en:mental retardation, autosomal dominant 29 | n2=ptôse | rel=r_associated | relid=0 | w=20
  30. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> ptose
    n1=en:mental retardation, autosomal dominant 29 | n2=ptose | rel=r_associated | relid=0 | w=20
  31. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> ptosis
    n1=en:mental retardation, autosomal dominant 29 | n2=ptosis | rel=r_associated | relid=0 | w=20
  32. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> télécanthus
    n1=en:mental retardation, autosomal dominant 29 | n2=télécanthus | rel=r_associated | relid=0 | w=20
  33. en:mental retardation, autosomal dominant 29 -- r_associated #0: 20 / 0.556 -> télécanthus-hypertélorisme-strabisme (syndrome)
    n1=en:mental retardation, autosomal dominant 29 | n2=télécanthus-hypertélorisme-strabisme (syndrome) | rel=r_associated | relid=0 | w=20
  34. en:mental retardation, autosomal dominant 29 -- r_associated #0: 2 / 0.056 -> en:disease or syndrome
    n1=en:mental retardation, autosomal dominant 29 | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=2
≈ 85 relations entrantes

  1. menton pointu --- r_associated #0: 70 --> en:mental retardation, autosomal dominant 29
    n1=menton pointu | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=70
  2. en:pointed chin --- r_associated #0: 68 --> en:mental retardation, autosomal dominant 29
    n1=en:pointed chin | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=68
  3. ptôse --- r_associated #0: 53 --> en:mental retardation, autosomal dominant 29
    n1=ptôse | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=53
  4. ptose --- r_associated #0: 50 --> en:mental retardation, autosomal dominant 29
    n1=ptose | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=50
  5. télécanthus-hypertélorisme-strabisme (syndrome) --- r_associated #0: 48 --> en:mental retardation, autosomal dominant 29
    n1=télécanthus-hypertélorisme-strabisme (syndrome) | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=48
  6. en:hypertelorism --- r_associated #0: 46 --> en:mental retardation, autosomal dominant 29
    n1=en:hypertelorism | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=46
  7. hypertélorisme --- r_associated #0: 46 --> en:mental retardation, autosomal dominant 29
    n1=hypertélorisme | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=46
  8. en:ptosis --- r_associated #0: 45 --> en:mental retardation, autosomal dominant 29
    n1=en:ptosis | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=45
  9. ptosis --- r_associated #0: 45 --> en:mental retardation, autosomal dominant 29
    n1=ptosis | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=45
  10. hypertélorisme, hypospadias, polysyndactylie (syndrome) --- r_associated #0: 44 --> en:mental retardation, autosomal dominant 29
    n1=hypertélorisme, hypospadias, polysyndactylie (syndrome) | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=44
  11. hypertélorisme-microtie-fente faciale --- r_associated #0: 41 --> en:mental retardation, autosomal dominant 29
    n1=hypertélorisme-microtie-fente faciale | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=41
  12. en:telecanthus --- r_associated #0: 39 --> en:mental retardation, autosomal dominant 29
    n1=en:telecanthus | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=39
  13. hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle --- r_associated #0: 36 --> en:mental retardation, autosomal dominant 29
    n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=36
  14. en:drooping eyelid --- r_associated #0: 35 --> en:mental retardation, autosomal dominant 29
    n1=en:drooping eyelid | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=35
  15. en:setbp1, 1-bp del --- r_associated #0: 35 --> en:mental retardation, autosomal dominant 29
    n1=en:setbp1, 1-bp del | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=35
  16. en:setbp1, arg625ter --- r_associated #0: 35 --> en:mental retardation, autosomal dominant 29
    n1=en:setbp1, arg625ter | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=35
  17. en:setbp1, ser1011ter --- r_associated #0: 35 --> en:mental retardation, autosomal dominant 29
    n1=en:setbp1, ser1011ter | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=35
  18. en:byzanthine arch palate --- r_associated #0: 34 --> en:mental retardation, autosomal dominant 29
    n1=en:byzanthine arch palate | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=34
  19. en:tooth crowding --- r_associated #0: 32 --> en:mental retardation, autosomal dominant 29
    n1=en:tooth crowding | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=32
  20. en:attention deficit hyperactivity disorder --- r_associated #0: 31 --> en:mental retardation, autosomal dominant 29
    n1=en:attention deficit hyperactivity disorder | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=31
  21. en:setbp1, arg626ter --- r_associated #0: 31 --> en:mental retardation, autosomal dominant 29
    n1=en:setbp1, arg626ter | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=31
  22. hyperactivité avec déficit de l'attention --- r_associated #0: 31 --> en:mental retardation, autosomal dominant 29
    n1=hyperactivité avec déficit de l'attention | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=31
  23. en:autosomal dominant inheritance --- r_associated #0: 30 --> en:mental retardation, autosomal dominant 29
    n1=en:autosomal dominant inheritance | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=30
  24. en:long narrow head --- r_associated #0: 30 --> en:mental retardation, autosomal dominant 29
    n1=en:long narrow head | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=30
  25. en:thin upper lips --- r_associated #0: 30 --> en:mental retardation, autosomal dominant 29
    n1=en:thin upper lips | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=30
  26. colobome de l'iris avec ptosis, hypertélorisme et retard mental --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 29
    n1=colobome de l'iris avec ptosis, hypertélorisme et retard mental | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=29
  27. en:diaphragmatic hernia --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 29
    n1=en:diaphragmatic hernia | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=29
  28. en:setbp1, trp532ter --- r_associated #0: 28 --> en:mental retardation, autosomal dominant 29
    n1=en:setbp1, trp532ter | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=28
  29. blépharophimosis-ptosis-épicanthus inversus (syndrome) --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 29
    n1=blépharophimosis-ptosis-épicanthus inversus (syndrome) | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=26
  30. en:absent corpus callosum --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 29
    n1=en:absent corpus callosum | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=26
  31. en:brachycephalies --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 29
    n1=en:brachycephalies | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=26
  32. télécanthus --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 29
    n1=télécanthus | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=26
  33. en:ADHD --- r_associated #0: 25 --> en:mental retardation, autosomal dominant 29
    n1=en:ADHD | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=25
  34. en:strabismus syndrome --- r_associated #0: 24 --> en:mental retardation, autosomal dominant 29
    n1=en:strabismus syndrome | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=24
  35. en:exomphalos --- r_associated #0: 23 --> en:mental retardation, autosomal dominant 29
    n1=en:exomphalos | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=23
  36. en:sagging --- r_associated #0: 23 --> en:mental retardation, autosomal dominant 29
    n1=en:sagging | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=23
  37. hyodésoxycholique (acide) --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 29
    n1=hyodésoxycholique (acide) | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=15
  38. Hypertélorisme --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=Hypertélorisme | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  39. Ptose --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=Ptose | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  40. Ptôse --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=Ptôse | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  41. en:and sensorineural deafness --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=en:and sensorineural deafness | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  42. en:blepharophimosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=en:blepharophimosis | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  43. en:facial clefting syndrome --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=en:facial clefting syndrome | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  44. en:hyodeoxycholic acid --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=en:hyodeoxycholic acid | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  45. en:hypospadias --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=en:hypospadias | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  46. en:iris coloboma with ptosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=en:iris coloboma with ptosis | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  47. en:microtia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=en:microtia | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  48. en:myopia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=en:myopia | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  49. en:polysyndactyly syndrome --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=en:polysyndactyly syndrome | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  50. hernie diaphragmatique --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=hernie diaphragmatique | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  51. hypertensinase --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=hypertensinase | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  52. hypertensine --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=hypertensine | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  53. hypertensinogène --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=hypertensinogène | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  54. hypertension --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=hypertension | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  55. hypertension abdominale --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=hypertension abdominale | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  56. hypertension artérielle --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=hypertension artérielle | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  57. omphalocèle --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=omphalocèle | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  58. télécardiographie --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=télécardiographie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  59. télécardiophone --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=télécardiophone | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  60. téléclitoridie --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=téléclitoridie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  61. télécobalt --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=télécobalt | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  62. télécobalt-thérapie --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=télécobalt-thérapie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  63. téléconsultation --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=téléconsultation | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  64. télécrâne --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=télécrâne | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  65. télécæsiothérapie --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=télécæsiothérapie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  66. télédermatologie --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=télédermatologie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  67. télédiastole --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=télédiastole | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  68. télédétection --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 29
    n1=télédétection | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=10
  69. Hyper-HDLémie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=Hyper-HDLémie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  70. hyoïdien --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyoïdien | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  71. hyper-LDLémie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyper-LDLémie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  72. hyper-alpha-globulinémie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyper-alpha-globulinémie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  73. hyper-bêta-alaninémie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyper-bêta-alaninémie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  74. hyper-bêta-globulinémie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyper-bêta-globulinémie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  75. hyper-bêta-lipoprotéinémie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyper-bêta-lipoprotéinémie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  76. hyperabsorbant --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperabsorbant | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  77. hyperacanthose --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperacanthose | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  78. hyperaction d'un muscle oculomoteur --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperaction d'un muscle oculomoteur | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  79. hyperaldostéronisme --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperaldostéronisme | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  80. hyperaldostéronisme primaire --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperaldostéronisme primaire | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  81. hyperaldostéronisme secondaire --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperaldostéronisme secondaire | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  82. hyperaminoacidurie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperaminoacidurie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  83. hyperaminoacidémie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperaminoacidémie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  84. hyperammoniémie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperammoniémie | n2=en:mental retardation, autosomal dominant 29 | rel=r_associated | relid=0 | w=5
  85. hyperammoniémie congénitale --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 29
    n1=hyperammoniémie congénitale | n2=en:mental retardation, autosomal dominant 29 | 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