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'en:chromosomal morphology'
(id=6862162 ; fe=en:chromosomal morphology ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=2352 creation date=2017-06-25 touchdate=2025-07-24 23:23:44.000)
≈ 86 relations sortantes

  1. en:chromosomal morphology -- r_associated #0: 42 / 1 -> en:fragile x chromosome
    n1=en:chromosomal morphology | n2=en:fragile x chromosome | rel=r_associated | relid=0 | w=42
  2. en:chromosomal morphology -- r_associated #0: 42 / 1 -> en:muscle fiber change
    n1=en:chromosomal morphology | n2=en:muscle fiber change | rel=r_associated | relid=0 | w=42
  3. en:chromosomal morphology -- r_associated #0: 42 / 1 -> en:xxxy syndrome
    n1=en:chromosomal morphology | n2=en:xxxy syndrome | rel=r_associated | relid=0 | w=42
  4. en:chromosomal morphology -- r_associated #0: 41 / 0.976 -> en:penta x syndrome
    n1=en:chromosomal morphology | n2=en:penta x syndrome | rel=r_associated | relid=0 | w=41
  5. en:chromosomal morphology -- r_associated #0: 38 / 0.905 -> en:mosaic turner syndrome
    n1=en:chromosomal morphology | n2=en:mosaic turner syndrome | rel=r_associated | relid=0 | w=38
  6. en:chromosomal morphology -- r_associated #0: 36 / 0.857 -> en:homer wright rosette
    n1=en:chromosomal morphology | n2=en:homer wright rosette | rel=r_associated | relid=0 | w=36
  7. en:chromosomal morphology -- r_associated #0: 35 / 0.833 -> en:erythrocyte inclusion
    n1=en:chromosomal morphology | n2=en:erythrocyte inclusion | rel=r_associated | relid=0 | w=35
  8. en:chromosomal morphology -- r_associated #0: 35 / 0.833 -> en:fraxf syndrome
    n1=en:chromosomal morphology | n2=en:fraxf syndrome | rel=r_associated | relid=0 | w=35
  9. en:chromosomal morphology -- r_associated #0: 35 / 0.833 -> en:fungal cytoplasmic inclusion body
    n1=en:chromosomal morphology | n2=en:fungal cytoplasmic inclusion body | rel=r_associated | relid=0 | w=35
  10. en:chromosomal morphology -- r_associated #0: 35 / 0.833 -> en:klinefelter's syndrome - male with 46 xx karyotype
    n1=en:chromosomal morphology | n2=en:klinefelter's syndrome - male with 46 xx karyotype | rel=r_associated | relid=0 | w=35
  11. en:chromosomal morphology -- r_associated #0: 35 / 0.833 -> en:margination
    n1=en:chromosomal morphology | n2=en:margination | rel=r_associated | relid=0 | w=35
  12. en:chromosomal morphology -- r_associated #0: 35 / 0.833 -> en:may-hegglin inclusion
    n1=en:chromosomal morphology | n2=en:may-hegglin inclusion | rel=r_associated | relid=0 | w=35
  13. en:chromosomal morphology -- r_associated #0: 35 / 0.833 -> en:tetrasomy x
    n1=en:chromosomal morphology | n2=en:tetrasomy x | rel=r_associated | relid=0 | w=35
  14. en:chromosomal morphology -- r_associated #0: 35 / 0.833 -> morphologies du caryotype
    n1=en:chromosomal morphology | n2=morphologies du caryotype | rel=r_associated | relid=0 | w=35
  15. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:anomaly of chromosome x
    n1=en:chromosomal morphology | n2=en:anomaly of chromosome x | rel=r_associated | relid=0 | w=34
  16. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:axonal swelling
    n1=en:chromosomal morphology | n2=en:axonal swelling | rel=r_associated | relid=0 | w=34
  17. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:cellular hormonal pattern
    n1=en:chromosomal morphology | n2=en:cellular hormonal pattern | rel=r_associated | relid=0 | w=34
  18. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:charcot-leyden crystal deposits
    n1=en:chromosomal morphology | n2=en:charcot-leyden crystal deposits | rel=r_associated | relid=0 | w=34
  19. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:clasmatodendrosis
    n1=en:chromosomal morphology | n2=en:clasmatodendrosis | rel=r_associated | relid=0 | w=34
  20. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:cytologic engulfment
    n1=en:chromosomal morphology | n2=en:cytologic engulfment | rel=r_associated | relid=0 | w=34
  21. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:flagella alteration
    n1=en:chromosomal morphology | n2=en:flagella alteration | rel=r_associated | relid=0 | w=34
  22. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:fleurette
    n1=en:chromosomal morphology | n2=en:fleurette | rel=r_associated | relid=0 | w=34
  23. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:gonadal dysgenesis, mixed
    n1=en:chromosomal morphology | n2=en:gonadal dysgenesis, mixed | rel=r_associated | relid=0 | w=34
  24. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> en:karyotype 46, x with abnormal sex chromosome except iso (xq)
    n1=en:chromosomal morphology | n2=en:karyotype 46, x with abnormal sex chromosome except iso (xq) | rel=r_associated | relid=0 | w=34
  25. en:chromosomal morphology -- r_associated #0: 34 / 0.81 -> morphologie du caryotype
    n1=en:chromosomal morphology | n2=morphologie du caryotype | rel=r_associated | relid=0 | w=34
  26. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:cell size alteration
    n1=en:chromosomal morphology | n2=en:cell size alteration | rel=r_associated | relid=0 | w=32
  27. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:cytoplasmic accumulation
    n1=en:chromosomal morphology | n2=en:cytoplasmic accumulation | rel=r_associated | relid=0 | w=32
  28. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:degenerated herring's bodies
    n1=en:chromosomal morphology | n2=en:degenerated herring's bodies | rel=r_associated | relid=0 | w=32
  29. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:fraxa syndrome
    n1=en:chromosomal morphology | n2=en:fraxa syndrome | rel=r_associated | relid=0 | w=32
  30. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:fraxe intellectual disability syndrome
    n1=en:chromosomal morphology | n2=en:fraxe intellectual disability syndrome | rel=r_associated | relid=0 | w=32
  31. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:hyperparakeratosis
    n1=en:chromosomal morphology | n2=en:hyperparakeratosis | rel=r_associated | relid=0 | w=32
  32. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:mosaicism 45, x or other cell line with abnormal sex chromosome
    n1=en:chromosomal morphology | n2=en:mosaicism 45, x or other cell line with abnormal sex chromosome | rel=r_associated | relid=0 | w=32
  33. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:nuclear size alteration
    n1=en:chromosomal morphology | n2=en:nuclear size alteration | rel=r_associated | relid=0 | w=32
  34. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:plasma membrane globulin coating
    n1=en:chromosomal morphology | n2=en:plasma membrane globulin coating | rel=r_associated | relid=0 | w=32
  35. en:chromosomal morphology -- r_associated #0: 32 / 0.762 -> en:reticulin fibril alteration
    n1=en:chromosomal morphology | n2=en:reticulin fibril alteration | rel=r_associated | relid=0 | w=32
  36. en:chromosomal morphology -- r_associated #0: 31 / 0.738 -> en:cell content alteration
    n1=en:chromosomal morphology | n2=en:cell content alteration | rel=r_associated | relid=0 | w=31
  37. en:chromosomal morphology -- r_associated #0: 31 / 0.738 -> en:myelin body formation
    n1=en:chromosomal morphology | n2=en:myelin body formation | rel=r_associated | relid=0 | w=31
  38. en:chromosomal morphology -- r_associated #0: 31 / 0.738 -> en:nuclear lead inclusion
    n1=en:chromosomal morphology | n2=en:nuclear lead inclusion | rel=r_associated | relid=0 | w=31
  39. en:chromosomal morphology -- r_associated #0: 31 / 0.738 -> en:russell body
    n1=en:chromosomal morphology | n2=en:russell body | rel=r_associated | relid=0 | w=31
  40. en:chromosomal morphology -- r_associated #0: 31 / 0.738 -> en:turner's phenotype - ring chromosome karyotype
    n1=en:chromosomal morphology | n2=en:turner's phenotype - ring chromosome karyotype | rel=r_associated | relid=0 | w=31
  41. en:chromosomal morphology -- r_associated #0: 30 / 0.714 -> en:cell shape alteration
    n1=en:chromosomal morphology | n2=en:cell shape alteration | rel=r_associated | relid=0 | w=30
  42. en:chromosomal morphology -- r_associated #0: 30 / 0.714 -> en:cytoplasmic aggregate
    n1=en:chromosomal morphology | n2=en:cytoplasmic aggregate | rel=r_associated | relid=0 | w=30
  43. en:chromosomal morphology -- r_associated #0: 30 / 0.714 -> en:leukocytic agglutination
    n1=en:chromosomal morphology | n2=en:leukocytic agglutination | rel=r_associated | relid=0 | w=30
  44. en:chromosomal morphology -- r_associated #0: 30 / 0.714 -> en:neuronophagia
    n1=en:chromosomal morphology | n2=en:neuronophagia | rel=r_associated | relid=0 | w=30
  45. en:chromosomal morphology -- r_associated #0: 30 / 0.714 -> en:rouleaux formation
    n1=en:chromosomal morphology | n2=en:rouleaux formation | rel=r_associated | relid=0 | w=30
  46. en:chromosomal morphology -- r_associated #0: 30 / 0.714 -> en:syndromes, 49,xxxxy
    n1=en:chromosomal morphology | n2=en:syndromes, 49,xxxxy | rel=r_associated | relid=0 | w=30
  47. en:chromosomal morphology -- r_associated #0: 30 / 0.714 -> en:turner syndrome
    n1=en:chromosomal morphology | n2=en:turner syndrome | rel=r_associated | relid=0 | w=30
  48. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> 610-611 morphologies du caryotype
    n1=en:chromosomal morphology | n2=610-611 morphologies du caryotype | rel=r_associated | relid=0 | w=29
  49. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:abnormal cell structure
    n1=en:chromosomal morphology | n2=en:abnormal cell structure | rel=r_associated | relid=0 | w=29
  50. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:basement membrane-like material
    n1=en:chromosomal morphology | n2=en:basement membrane-like material | rel=r_associated | relid=0 | w=29
  51. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:cellular stain reaction
    n1=en:chromosomal morphology | n2=en:cellular stain reaction | rel=r_associated | relid=0 | w=29
  52. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:cytologic atypia
    n1=en:chromosomal morphology | n2=en:cytologic atypia | rel=r_associated | relid=0 | w=29
  53. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:dual red blood cell population
    n1=en:chromosomal morphology | n2=en:dual red blood cell population | rel=r_associated | relid=0 | w=29
  54. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:karyotype 46, x iso (xq)
    n1=en:chromosomal morphology | n2=en:karyotype 46, x iso (xq) | rel=r_associated | relid=0 | w=29
  55. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:leukocytic margination
    n1=en:chromosomal morphology | n2=en:leukocytic margination | rel=r_associated | relid=0 | w=29
  56. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:leukostasis
    n1=en:chromosomal morphology | n2=en:leukostasis | rel=r_associated | relid=0 | w=29
  57. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:satellitosis
    n1=en:chromosomal morphology | n2=en:satellitosis | rel=r_associated | relid=0 | w=29
  58. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:urothelial dysplasia
    n1=en:chromosomal morphology | n2=en:urothelial dysplasia | rel=r_associated | relid=0 | w=29
  59. en:chromosomal morphology -- r_associated #0: 29 / 0.69 -> en:xo syndrome
    n1=en:chromosomal morphology | n2=en:xo syndrome | rel=r_associated | relid=0 | w=29
  60. en:chromosomal morphology -- r_associated #0: 28 / 0.667 -> en:alteration of mitochondrial cristae
    n1=en:chromosomal morphology | n2=en:alteration of mitochondrial cristae | rel=r_associated | relid=0 | w=28
  61. en:chromosomal morphology -- r_associated #0: 28 / 0.667 -> en:cytoplasmic droplets
    n1=en:chromosomal morphology | n2=en:cytoplasmic droplets | rel=r_associated | relid=0 | w=28
  62. en:chromosomal morphology -- r_associated #0: 28 / 0.667 -> en:fraxe syndrome
    n1=en:chromosomal morphology | n2=en:fraxe syndrome | rel=r_associated | relid=0 | w=28
  63. en:chromosomal morphology -- r_associated #0: 28 / 0.667 -> en:mosaicism
    n1=en:chromosomal morphology | n2=en:mosaicism | rel=r_associated | relid=0 | w=28
  64. en:chromosomal morphology -- r_associated #0: 28 / 0.667 -> en:rosette formation
    n1=en:chromosomal morphology | n2=en:rosette formation | rel=r_associated | relid=0 | w=28
  65. en:chromosomal morphology -- r_associated #0: 28 / 0.667 -> en:turner's phenotype, partial x deletion karyotype
    n1=en:chromosomal morphology | n2=en:turner's phenotype, partial x deletion karyotype | rel=r_associated | relid=0 | w=28
  66. en:chromosomal morphology -- r_associated #0: 28 / 0.667 -> morphologies chromosomiques
    n1=en:chromosomal morphology | n2=morphologies chromosomiques | rel=r_associated | relid=0 | w=28
  67. en:chromosomal morphology -- r_associated #0: 27 / 0.643 -> 61 morphologies chromosomiques
    n1=en:chromosomal morphology | n2=61 morphologies chromosomiques | rel=r_associated | relid=0 | w=27
  68. en:chromosomal morphology -- r_associated #0: 27 / 0.643 -> en:collagen fibril alteration
    n1=en:chromosomal morphology | n2=en:collagen fibril alteration | rel=r_associated | relid=0 | w=27
  69. en:chromosomal morphology -- r_associated #0: 27 / 0.643 -> en:epithelial cell abnormality
    n1=en:chromosomal morphology | n2=en:epithelial cell abnormality | rel=r_associated | relid=0 | w=27
  70. en:chromosomal morphology -- r_associated #0: 27 / 0.643 -> en:mosaicism - lines with various numbers of x chromosomes
    n1=en:chromosomal morphology | n2=en:mosaicism - lines with various numbers of x chromosomes | rel=r_associated | relid=0 | w=27
  71. en:chromosomal morphology -- r_associated #0: 27 / 0.643 -> en:noonan syndrome
    n1=en:chromosomal morphology | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=27
  72. en:chromosomal morphology -- r_associated #0: 27 / 0.643 -> en:toxic leukocyte granulations
    n1=en:chromosomal morphology | n2=en:toxic leukocyte granulations | rel=r_associated | relid=0 | w=27
  73. en:chromosomal morphology -- r_associated #0: 27 / 0.643 -> en:xx male
    n1=en:chromosomal morphology | n2=en:xx male | rel=r_associated | relid=0 | w=27
  74. en:chromosomal morphology -- r_associated #0: 26 / 0.619 -> en:fetus with turner syndrome
    n1=en:chromosomal morphology | n2=en:fetus with turner syndrome | rel=r_associated | relid=0 | w=26
  75. en:chromosomal morphology -- r_associated #0: 26 / 0.619 -> en:flexner-wintersteiner rosette
    n1=en:chromosomal morphology | n2=en:flexner-wintersteiner rosette | rel=r_associated | relid=0 | w=26
  76. en:chromosomal morphology -- r_associated #0: 26 / 0.619 -> en:intracytoplasmic microvilli
    n1=en:chromosomal morphology | n2=en:intracytoplasmic microvilli | rel=r_associated | relid=0 | w=26
  77. en:chromosomal morphology -- r_associated #0: 26 / 0.619 -> en:mosaicism 45, x; 46, xx
    n1=en:chromosomal morphology | n2=en:mosaicism 45, x; 46, xx | rel=r_associated | relid=0 | w=26
  78. en:chromosomal morphology -- r_associated #0: 26 / 0.619 -> en:reactive cellular changes
    n1=en:chromosomal morphology | n2=en:reactive cellular changes | rel=r_associated | relid=0 | w=26
  79. en:chromosomal morphology -- r_associated #0: 26 / 0.619 -> en:trisomy x
    n1=en:chromosomal morphology | n2=en:trisomy x | rel=r_associated | relid=0 | w=26
  80. en:chromosomal morphology -- r_associated #0: 20 / 0.476 -> corps de Russell
    n1=en:chromosomal morphology | n2=corps de Russell | rel=r_associated | relid=0 | w=20
  81. en:chromosomal morphology -- r_associated #0: 20 / 0.476 -> corps de russell
    n1=en:chromosomal morphology | n2=corps de russell | rel=r_associated | relid=0 | w=20
  82. en:chromosomal morphology -- r_associated #0: 20 / 0.476 -> en:mosaïcism
    n1=en:chromosomal morphology | n2=en:mosaïcism | rel=r_associated | relid=0 | w=20
  83. en:chromosomal morphology -- r_associated #0: 20 / 0.476 -> en:Russell body
    n1=en:chromosomal morphology | n2=en:Russell body | rel=r_associated | relid=0 | w=20
  84. en:chromosomal morphology -- r_associated #0: 20 / 0.476 -> leucostase
    n1=en:chromosomal morphology | n2=leucostase | rel=r_associated | relid=0 | w=20
  85. en:chromosomal morphology -- r_associated #0: 20 / 0.476 -> mosaïcisme
    n1=en:chromosomal morphology | n2=mosaïcisme | rel=r_associated | relid=0 | w=20
  86. en:chromosomal morphology -- r_associated #0: 20 / 0.476 -> syndrome FRAXE
    n1=en:chromosomal morphology | n2=syndrome FRAXE | rel=r_associated | relid=0 | w=20
≈ 91 relations entrantes

  1. en:fraxe syndrome --- r_associated #0: 67 --> en:chromosomal morphology
    n1=en:fraxe syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=67
  2. syndrome FRAXE --- r_associated #0: 66 --> en:chromosomal morphology
    n1=syndrome FRAXE | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=66
  3. mosaïcisme --- r_associated #0: 56 --> en:chromosomal morphology
    n1=mosaïcisme | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=56
  4. en:mosaicism --- r_associated #0: 55 --> en:chromosomal morphology
    n1=en:mosaicism | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=55
  5. corps de Russell --- r_associated #0: 51 --> en:chromosomal morphology
    n1=corps de Russell | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=51
  6. en:Russell body --- r_associated #0: 50 --> en:chromosomal morphology
    n1=en:Russell body | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=50
  7. en:russell body --- r_associated #0: 45 --> en:chromosomal morphology
    n1=en:russell body | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=45
  8. en:axonal swelling --- r_associated #0: 43 --> en:chromosomal morphology
    n1=en:axonal swelling | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=43
  9. morphologies chromosomiques --- r_associated #0: 39 --> en:chromosomal morphology
    n1=morphologies chromosomiques | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=39
  10. en:mosaïcism --- r_associated #0: 37 --> en:chromosomal morphology
    n1=en:mosaïcism | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=37
  11. en:may-hegglin inclusion --- r_associated #0: 36 --> en:chromosomal morphology
    n1=en:may-hegglin inclusion | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=36
  12. 610-611 morphologies du caryotype --- r_associated #0: 35 --> en:chromosomal morphology
    n1=610-611 morphologies du caryotype | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=35
  13. en:erythrocyte inclusion --- r_associated #0: 35 --> en:chromosomal morphology
    n1=en:erythrocyte inclusion | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=35
  14. en:flexner-wintersteiner rosette --- r_associated #0: 35 --> en:chromosomal morphology
    n1=en:flexner-wintersteiner rosette | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=35
  15. en:homer wright rosette --- r_associated #0: 35 --> en:chromosomal morphology
    n1=en:homer wright rosette | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=35
  16. 61 morphologies chromosomiques --- r_associated #0: 34 --> en:chromosomal morphology
    n1=61 morphologies chromosomiques | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=34
  17. en:gonadal dysgenesis, mixed --- r_associated #0: 34 --> en:chromosomal morphology
    n1=en:gonadal dysgenesis, mixed | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=34
  18. morphologie du caryotype --- r_associated #0: 34 --> en:chromosomal morphology
    n1=morphologie du caryotype | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=34
  19. en:mosaicism 45, x; 46, xx --- r_associated #0: 32 --> en:chromosomal morphology
    n1=en:mosaicism 45, x; 46, xx | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=32
  20. en:trisomy x --- r_associated #0: 31 --> en:chromosomal morphology
    n1=en:trisomy x | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=31
  21. corps de russell --- r_associated #0: 30 --> en:chromosomal morphology
    n1=corps de russell | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=30
  22. en:cellular hormonal pattern --- r_associated #0: 29 --> en:chromosomal morphology
    n1=en:cellular hormonal pattern | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=29
  23. en:cytoplasmic aggregate --- r_associated #0: 29 --> en:chromosomal morphology
    n1=en:cytoplasmic aggregate | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=29
  24. en:noonan syndrome --- r_associated #0: 29 --> en:chromosomal morphology
    n1=en:noonan syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=29
  25. en:syndromes, 49,xxxxy --- r_associated #0: 29 --> en:chromosomal morphology
    n1=en:syndromes, 49,xxxxy | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=29
  26. morphologies du caryotype --- r_associated #0: 29 --> en:chromosomal morphology
    n1=morphologies du caryotype | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=29
  27. en:dual red blood cell population --- r_associated #0: 28 --> en:chromosomal morphology
    n1=en:dual red blood cell population | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=28
  28. en:fraxa syndrome --- r_associated #0: 28 --> en:chromosomal morphology
    n1=en:fraxa syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=28
  29. en:hyperparakeratosis --- r_associated #0: 28 --> en:chromosomal morphology
    n1=en:hyperparakeratosis | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=28
  30. en:leukostasis --- r_associated #0: 28 --> en:chromosomal morphology
    n1=en:leukostasis | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=28
  31. leucostase --- r_associated #0: 28 --> en:chromosomal morphology
    n1=leucostase | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=28
  32. en:leukocytic agglutination --- r_associated #0: 27 --> en:chromosomal morphology
    n1=en:leukocytic agglutination | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=27
  33. en:penta x syndrome --- r_associated #0: 27 --> en:chromosomal morphology
    n1=en:penta x syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=27
  34. en:fraxe intellectual disability syndrome --- r_associated #0: 26 --> en:chromosomal morphology
    n1=en:fraxe intellectual disability syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=26
  35. en:fraxf syndrome --- r_associated #0: 26 --> en:chromosomal morphology
    n1=en:fraxf syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=26
  36. en:nuclear size alteration --- r_associated #0: 21 --> en:chromosomal morphology
    n1=en:nuclear size alteration | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=21
  37. en:abnormal cell structure --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:abnormal cell structure | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  38. en:alteration of mitochondrial cristae --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:alteration of mitochondrial cristae | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  39. en:anomaly of chromosome x --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:anomaly of chromosome x | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  40. en:basement membrane-like material --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:basement membrane-like material | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  41. en:cell content alteration --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:cell content alteration | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  42. en:cell shape alteration --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:cell shape alteration | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  43. en:cell size alteration --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:cell size alteration | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  44. en:cellular stain reaction --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:cellular stain reaction | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  45. en:charcot-leyden crystal deposits --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:charcot-leyden crystal deposits | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  46. en:clasmatodendrosis --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:clasmatodendrosis | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  47. en:collagen fibril alteration --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:collagen fibril alteration | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  48. en:cytologic atypia --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:cytologic atypia | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  49. en:cytologic engulfment --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:cytologic engulfment | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  50. en:cytoplasmic accumulation --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:cytoplasmic accumulation | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  51. en:cytoplasmic droplets --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:cytoplasmic droplets | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  52. en:degenerated herring's bodies --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:degenerated herring's bodies | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  53. en:epithelial cell abnormality --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:epithelial cell abnormality | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  54. en:fetus with turner syndrome --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:fetus with turner syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  55. en:flagella alteration --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:flagella alteration | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  56. en:fleurette --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:fleurette | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  57. en:fragile x chromosome --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:fragile x chromosome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  58. en:fungal cytoplasmic inclusion body --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:fungal cytoplasmic inclusion body | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  59. en:intracytoplasmic microvilli --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:intracytoplasmic microvilli | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  60. en:karyotype 46, x iso (xq) --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:karyotype 46, x iso (xq) | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  61. en:karyotype 46, x with abnormal sex chromosome except iso (xq) --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:karyotype 46, x with abnormal sex chromosome except iso (xq) | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  62. en:klinefelter's syndrome - male with 46 xx karyotype --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:klinefelter's syndrome - male with 46 xx karyotype | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  63. en:leukocytic margination --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:leukocytic margination | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  64. en:margination --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:margination | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  65. en:mosaic turner syndrome --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:mosaic turner syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  66. en:mosaicism - lines with various numbers of x chromosomes --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:mosaicism - lines with various numbers of x chromosomes | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  67. en:mosaicism 45, x or other cell line with abnormal sex chromosome --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:mosaicism 45, x or other cell line with abnormal sex chromosome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  68. en:muscle fiber change --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:muscle fiber change | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  69. en:myelin body formation --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:myelin body formation | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  70. en:neuronophagia --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:neuronophagia | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  71. en:nuclear lead inclusion --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:nuclear lead inclusion | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  72. en:plasma membrane globulin coating --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:plasma membrane globulin coating | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  73. en:reactive cellular changes --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:reactive cellular changes | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  74. en:reticulin fibril alteration --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:reticulin fibril alteration | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  75. en:rosette formation --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:rosette formation | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  76. en:rouleaux formation --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:rouleaux formation | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  77. en:satellitosis --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:satellitosis | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  78. en:tetrasomy x --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:tetrasomy x | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  79. en:toxic leukocyte granulations --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:toxic leukocyte granulations | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  80. en:turner syndrome --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:turner syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  81. en:turner's phenotype - ring chromosome karyotype --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:turner's phenotype - ring chromosome karyotype | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  82. en:turner's phenotype, partial x deletion karyotype --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:turner's phenotype, partial x deletion karyotype | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  83. en:urothelial dysplasia --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:urothelial dysplasia | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  84. en:xo syndrome --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:xo syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  85. en:xx male --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:xx male | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  86. en:xxxy syndrome --- r_associated #0: 20 --> en:chromosomal morphology
    n1=en:xxxy syndrome | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=20
  87. Morvan (syndrome de) --- r_associated #0: 10 --> en:chromosomal morphology
    n1=Morvan (syndrome de) | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=10
  88. margination --- r_associated #0: 10 --> en:chromosomal morphology
    n1=margination | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=10
  89. Leucostase --- r_associated #0: 5 --> en:chromosomal morphology
    n1=Leucostase | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=5
  90. margination leucocytaire --- r_associated #0: 5 --> en:chromosomal morphology
    n1=margination leucocytaire | n2=en:chromosomal morphology | rel=r_associated | relid=0 | w=5
  91. modifications des fibres musculaires --- r_associated #0: 5 --> en:chromosomal morphology
    n1=modifications des fibres musculaires | n2=en:chromosomal morphology | 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