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'en:chromosomal translocation'
(id=6891111 ; fe=en:chromosomal translocation ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=10591 creation date=2017-06-25 touchdate=2025-07-20 16:32:40.000)
≈ 220 relations sortantes

  1. en:chromosomal translocation -- r_associated #0: 42 / 1 -> en:rearrangement of 3q
    n1=en:chromosomal translocation | n2=en:rearrangement of 3q | rel=r_associated | relid=0 | w=42
  2. en:chromosomal translocation -- r_associated #0: 42 / 1 -> en:sex chromosome aberrations
    n1=en:chromosomal translocation | n2=en:sex chromosome aberrations | rel=r_associated | relid=0 | w=42
  3. en:chromosomal translocation -- r_associated #0: 41 / 0.976 -> en:tissue mosaicism
    n1=en:chromosomal translocation | n2=en:tissue mosaicism | rel=r_associated | relid=0 | w=41
  4. en:chromosomal translocation -- r_associated #0: 40 / 0.952 -> en:complete trisomy 18 syndrome
    n1=en:chromosomal translocation | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=40
  5. en:chromosomal translocation -- r_associated #0: 39 / 0.929 -> en:emanuel syndrome
    n1=en:chromosomal translocation | n2=en:emanuel syndrome | rel=r_associated | relid=0 | w=39
  6. en:chromosomal translocation -- r_associated #0: 38 / 0.905 -> en:homogeneously staining region
    n1=en:chromosomal translocation | n2=en:homogeneously staining region | rel=r_associated | relid=0 | w=38
  7. en:chromosomal translocation -- r_associated #0: 36 / 0.857 -> en:balanced autosomal translocation
    n1=en:chromosomal translocation | n2=en:balanced autosomal translocation | rel=r_associated | relid=0 | w=36
  8. en:chromosomal translocation -- r_associated #0: 36 / 0.857 -> en:chromosome replaced with ring or dicentric
    n1=en:chromosomal translocation | n2=en:chromosome replaced with ring or dicentric | rel=r_associated | relid=0 | w=36
  9. en:chromosomal translocation -- r_associated #0: 36 / 0.857 -> en:giant rod chromosome
    n1=en:chromosomal translocation | n2=en:giant rod chromosome | rel=r_associated | relid=0 | w=36
  10. en:chromosomal translocation -- r_associated #0: 36 / 0.857 -> en:meretoja syndrome
    n1=en:chromosomal translocation | n2=en:meretoja syndrome | rel=r_associated | relid=0 | w=36
  11. en:chromosomal translocation -- r_associated #0: 36 / 0.857 -> en:rearrangement of 6q13
    n1=en:chromosomal translocation | n2=en:rearrangement of 6q13 | rel=r_associated | relid=0 | w=36
  12. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:angelman syndrome
    n1=en:chromosomal translocation | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=35
  13. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:anomaly of chromosome x
    n1=en:chromosomal translocation | n2=en:anomaly of chromosome x | rel=r_associated | relid=0 | w=35
  14. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:aspects of radiation effects
    n1=en:chromosomal translocation | n2=en:aspects of radiation effects | rel=r_associated | relid=0 | w=35
  15. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:bloom syndrome
    n1=en:chromosomal translocation | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=35
  16. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition
    n1=en:chromosomal translocation | n2=en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition | rel=r_associated | relid=0 | w=35
  17. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:chromosomal alterations of group b
    n1=en:chromosomal translocation | n2=en:chromosomal alterations of group b | rel=r_associated | relid=0 | w=35
  18. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:chromosomal insertion
    n1=en:chromosomal translocation | n2=en:chromosomal insertion | rel=r_associated | relid=0 | w=35
  19. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:chromosomal instability
    n1=en:chromosomal translocation | n2=en:chromosomal instability | rel=r_associated | relid=0 | w=35
  20. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:cri du chat syndrome
    n1=en:chromosomal translocation | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=35
  21. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:ddit3 wt allele
    n1=en:chromosomal translocation | n2=en:ddit3 wt allele | rel=r_associated | relid=0 | w=35
  22. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:dicentric chromosome
    n1=en:chromosomal translocation | n2=en:dicentric chromosome | rel=r_associated | relid=0 | w=35
  23. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:gene rearrangement
    n1=en:chromosomal translocation | n2=en:gene rearrangement | rel=r_associated | relid=0 | w=35
  24. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:oligosomy
    n1=en:chromosomal translocation | n2=en:oligosomy | rel=r_associated | relid=0 | w=35
  25. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:philadelphia chromosome
    n1=en:chromosomal translocation | n2=en:philadelphia chromosome | rel=r_associated | relid=0 | w=35
  26. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:rearrangement of 21q
    n1=en:chromosomal translocation | n2=en:rearrangement of 21q | rel=r_associated | relid=0 | w=35
  27. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:rearrangement of 8q11-13
    n1=en:chromosomal translocation | n2=en:rearrangement of 8q11-13 | rel=r_associated | relid=0 | w=35
  28. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:site-directed mutagenesis
    n1=en:chromosomal translocation | n2=en:site-directed mutagenesis | rel=r_associated | relid=0 | w=35
  29. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:triploidy, diploidy, mixoploidy syndrome
    n1=en:chromosomal translocation | n2=en:triploidy, diploidy, mixoploidy syndrome | rel=r_associated | relid=0 | w=35
  30. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:trisomy and partial trisomy of autosome
    n1=en:chromosomal translocation | n2=en:trisomy and partial trisomy of autosome | rel=r_associated | relid=0 | w=35
  31. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> en:williams syndrome
    n1=en:chromosomal translocation | n2=en:williams syndrome | rel=r_associated | relid=0 | w=35
  32. en:chromosomal translocation -- r_associated #0: 35 / 0.833 -> translocation génétique
    n1=en:chromosomal translocation | n2=translocation génétique | rel=r_associated | relid=0 | w=35
  33. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:chimerism
    n1=en:chromosomal translocation | n2=en:chimerism | rel=r_associated | relid=0 | w=34
  34. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:chromosomal rearrangement
    n1=en:chromosomal translocation | n2=en:chromosomal rearrangement | rel=r_associated | relid=0 | w=34
  35. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:chromosome 9 inversion or duplication
    n1=en:chromosomal translocation | n2=en:chromosome 9 inversion or duplication | rel=r_associated | relid=0 | w=34
  36. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:chromosome breakage
    n1=en:chromosomal translocation | n2=en:chromosome breakage | rel=r_associated | relid=0 | w=34
  37. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:ddit3 gene
    n1=en:chromosomal translocation | n2=en:ddit3 gene | rel=r_associated | relid=0 | w=34
  38. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:digeorge syndrome
    n1=en:chromosomal translocation | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=34
  39. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:fragile x syndrome
    n1=en:chromosomal translocation | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=34
  40. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:gelatinous droplike corneal dystrophy
    n1=en:chromosomal translocation | n2=en:gelatinous droplike corneal dystrophy | rel=r_associated | relid=0 | w=34
  41. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:genetic aspects
    n1=en:chromosomal translocation | n2=en:genetic aspects | rel=r_associated | relid=0 | w=34
  42. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:genomic_region_amplification
    n1=en:chromosomal translocation | n2=en:genomic_region_amplification | rel=r_associated | relid=0 | w=34
  43. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:gonadal dysgenesis
    n1=en:chromosomal translocation | n2=en:gonadal dysgenesis | rel=r_associated | relid=0 | w=34
  44. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:indel mutation
    n1=en:chromosomal translocation | n2=en:indel mutation | rel=r_associated | relid=0 | w=34
  45. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:pseudotrisomy 18
    n1=en:chromosomal translocation | n2=en:pseudotrisomy 18 | rel=r_associated | relid=0 | w=34
  46. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:rearrangement of 11q
    n1=en:chromosomal translocation | n2=en:rearrangement of 11q | rel=r_associated | relid=0 | w=34
  47. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:rearrangement of 8q21
    n1=en:chromosomal translocation | n2=en:rearrangement of 8q21 | rel=r_associated | relid=0 | w=34
  48. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:russell-silver syndrome
    n1=en:chromosomal translocation | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=34
  49. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:sotos syndrome
    n1=en:chromosomal translocation | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=34
  50. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:translocation down syndrome
    n1=en:chromosomal translocation | n2=en:translocation down syndrome | rel=r_associated | relid=0 | w=34
  51. en:chromosomal translocation -- r_associated #0: 34 / 0.81 -> en:xyy syndrome
    n1=en:chromosomal translocation | n2=en:xyy syndrome | rel=r_associated | relid=0 | w=34
  52. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication
    n1=en:chromosomal translocation | n2=en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication | rel=r_associated | relid=0 | w=32
  53. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:chromosomal alterations of group g and y
    n1=en:chromosomal translocation | n2=en:chromosomal alterations of group g and y | rel=r_associated | relid=0 | w=32
  54. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:complete trisomy 13 syndrome
    n1=en:chromosomal translocation | n2=en:complete trisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  55. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:deimmunization
    n1=en:chromosomal translocation | n2=en:deimmunization | rel=r_associated | relid=0 | w=32
  56. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:ethics qualifier
    n1=en:chromosomal translocation | n2=en:ethics qualifier | rel=r_associated | relid=0 | w=32
  57. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:isochromosome
    n1=en:chromosomal translocation | n2=en:isochromosome | rel=r_associated | relid=0 | w=32
  58. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:physiological aspects
    n1=en:chromosomal translocation | n2=en:physiological aspects | rel=r_associated | relid=0 | w=32
  59. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:rearrangement of 11q13-21
    n1=en:chromosomal translocation | n2=en:rearrangement of 11q13-21 | rel=r_associated | relid=0 | w=32
  60. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:rubinstein-taybi syndrome
    n1=en:chromosomal translocation | n2=en:rubinstein-taybi syndrome | rel=r_associated | relid=0 | w=32
  61. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:trim24 wt allele
    n1=en:chromosomal translocation | n2=en:trim24 wt allele | rel=r_associated | relid=0 | w=32
  62. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:triploidy and polyploidy
    n1=en:chromosomal translocation | n2=en:triploidy and polyploidy | rel=r_associated | relid=0 | w=32
  63. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:trisomy
    n1=en:chromosomal translocation | n2=en:trisomy | rel=r_associated | relid=0 | w=32
  64. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:turner syndrome
    n1=en:chromosomal translocation | n2=en:turner syndrome | rel=r_associated | relid=0 | w=32
  65. en:chromosomal translocation -- r_associated #0: 32 / 0.762 -> en:wolf-hirschhorn syndrome
    n1=en:chromosomal translocation | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=32
  66. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:aberrant chromosome 1
    n1=en:chromosomal translocation | n2=en:aberrant chromosome 1 | rel=r_associated | relid=0 | w=31
  67. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:abnormal karyotype
    n1=en:chromosomal translocation | n2=en:abnormal karyotype | rel=r_associated | relid=0 | w=31
  68. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:amino acid substitution
    n1=en:chromosomal translocation | n2=en:amino acid substitution | rel=r_associated | relid=0 | w=31
  69. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:b lymphoblastic leukemia/lymphoma, not otherwise specified
    n1=en:chromosomal translocation | n2=en:b lymphoblastic leukemia/lymphoma, not otherwise specified | rel=r_associated | relid=0 | w=31
  70. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:chromosomal alterations of group a
    n1=en:chromosomal translocation | n2=en:chromosomal alterations of group a | rel=r_associated | relid=0 | w=31
  71. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:drug effect
    n1=en:chromosomal translocation | n2=en:drug effect | rel=r_associated | relid=0 | w=31
  72. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:klinefelter syndrome
    n1=en:chromosomal translocation | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=31
  73. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:large-scale state transition
    n1=en:chromosomal translocation | n2=en:large-scale state transition | rel=r_associated | relid=0 | w=31
  74. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:polyploidy
    n1=en:chromosomal translocation | n2=en:polyploidy | rel=r_associated | relid=0 | w=31
  75. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:prader-willi syndrome
    n1=en:chromosomal translocation | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=31
  76. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:rearrangement of 2p23
    n1=en:chromosomal translocation | n2=en:rearrangement of 2p23 | rel=r_associated | relid=0 | w=31
  77. en:chromosomal translocation -- r_associated #0: 31 / 0.738 -> en:xxyy syndrome
    n1=en:chromosomal translocation | n2=en:xxyy syndrome | rel=r_associated | relid=0 | w=31
  78. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:autosomal translocation
    n1=en:chromosomal translocation | n2=en:autosomal translocation | rel=r_associated | relid=0 | w=30
  79. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:balanced chromosomal translocation
    n1=en:chromosomal translocation | n2=en:balanced chromosomal translocation | rel=r_associated | relid=0 | w=30
  80. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg
    n1=en:chromosomal translocation | n2=en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg | rel=r_associated | relid=0 | w=30
  81. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:chromosomal alterations of group d
    n1=en:chromosomal translocation | n2=en:chromosomal alterations of group d | rel=r_associated | relid=0 | w=30
  82. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:chromosomal inversion
    n1=en:chromosomal translocation | n2=en:chromosomal inversion | rel=r_associated | relid=0 | w=30
  83. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:chromosome disorders, autosomal
    n1=en:chromosomal translocation | n2=en:chromosome disorders, autosomal | rel=r_associated | relid=0 | w=30
  84. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:cytogenetic abnormality
    n1=en:chromosomal translocation | n2=en:cytogenetic abnormality | rel=r_associated | relid=0 | w=30
  85. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:deletion mutagenesis
    n1=en:chromosomal translocation | n2=en:deletion mutagenesis | rel=r_associated | relid=0 | w=30
  86. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:duplication seen only at prometaphase
    n1=en:chromosomal translocation | n2=en:duplication seen only at prometaphase | rel=r_associated | relid=0 | w=30
  87. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:extra unidentified structurally abnormal chromosome (disorder)
    n1=en:chromosomal translocation | n2=en:extra unidentified structurally abnormal chromosome (disorder) | rel=r_associated | relid=0 | w=30
  88. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:fetus with chromosomal abnormality
    n1=en:chromosomal translocation | n2=en:fetus with chromosomal abnormality | rel=r_associated | relid=0 | w=30
  89. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:immunology aspects
    n1=en:chromosomal translocation | n2=en:immunology aspects | rel=r_associated | relid=0 | w=30
  90. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:intracellular translocation
    n1=en:chromosomal translocation | n2=en:intracellular translocation | rel=r_associated | relid=0 | w=30
  91. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:mosaicism
    n1=en:chromosomal translocation | n2=en:mosaicism | rel=r_associated | relid=0 | w=30
  92. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:rearrangement of 17p11-13
    n1=en:chromosomal translocation | n2=en:rearrangement of 17p11-13 | rel=r_associated | relid=0 | w=30
  93. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:sequence deletion
    n1=en:chromosomal translocation | n2=en:sequence deletion | rel=r_associated | relid=0 | w=30
  94. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> en:suppression, genetic
    n1=en:chromosomal translocation | n2=en:suppression, genetic | rel=r_associated | relid=0 | w=30
  95. en:chromosomal translocation -- r_associated #0: 30 / 0.714 -> translocations chromosomiques
    n1=en:chromosomal translocation | n2=translocations chromosomiques | rel=r_associated | relid=0 | w=30
  96. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:balanced rearrangement and structural marker
    n1=en:chromosomal translocation | n2=en:balanced rearrangement and structural marker | rel=r_associated | relid=0 | w=29
  97. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:beckwith-wiedemann syndrome
    n1=en:chromosomal translocation | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  98. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:insertional mutagenesis
    n1=en:chromosomal translocation | n2=en:insertional mutagenesis | rel=r_associated | relid=0 | w=29
  99. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:jacobsen syndrome
    n1=en:chromosomal translocation | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=29
  100. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:linker-scanning mutagenesis
    n1=en:chromosomal translocation | n2=en:linker-scanning mutagenesis | rel=r_associated | relid=0 | w=29
  101. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:mosaic variegated aneuploidy syndrome
    n1=en:chromosomal translocation | n2=en:mosaic variegated aneuploidy syndrome | rel=r_associated | relid=0 | w=29
  102. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:mutagenesis
    n1=en:chromosomal translocation | n2=en:mutagenesis | rel=r_associated | relid=0 | w=29
  103. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:numerical chromosomal abnormality
    n1=en:chromosomal translocation | n2=en:numerical chromosomal abnormality | rel=r_associated | relid=0 | w=29
  104. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:other conditions due to autosomal anomalies
    n1=en:chromosomal translocation | n2=en:other conditions due to autosomal anomalies | rel=r_associated | relid=0 | w=29
  105. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:rearrangement of 1p11-q11
    n1=en:chromosomal translocation | n2=en:rearrangement of 1p11-q11 | rel=r_associated | relid=0 | w=29
  106. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:rearrangement of 6q25
    n1=en:chromosomal translocation | n2=en:rearrangement of 6q25 | rel=r_associated | relid=0 | w=29
  107. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:unbalanced translocation and insertion
    n1=en:chromosomal translocation | n2=en:unbalanced translocation and insertion | rel=r_associated | relid=0 | w=29
  108. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome
    n1=en:chromosomal translocation | n2=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | rel=r_associated | relid=0 | w=29
  109. en:chromosomal translocation -- r_associated #0: 29 / 0.69 -> translocation chromosomique
    n1=en:chromosomal translocation | n2=translocation chromosomique | rel=r_associated | relid=0 | w=29
  110. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:46, xx true hermaphrodite
    n1=en:chromosomal translocation | n2=en:46, xx true hermaphrodite | rel=r_associated | relid=0 | w=28
  111. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:absence of sex chromosome
    n1=en:chromosomal translocation | n2=en:absence of sex chromosome | rel=r_associated | relid=0 | w=28
  112. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:autosomal deletion syndromes
    n1=en:chromosomal translocation | n2=en:autosomal deletion syndromes | rel=r_associated | relid=0 | w=28
  113. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:chromosomal alterations of group f
    n1=en:chromosomal translocation | n2=en:chromosomal alterations of group f | rel=r_associated | relid=0 | w=28
  114. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:chromosomal duplication
    n1=en:chromosomal translocation | n2=en:chromosomal duplication | rel=r_associated | relid=0 | w=28
  115. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:chromothripsis
    n1=en:chromosomal translocation | n2=en:chromothripsis | rel=r_associated | relid=0 | w=28
  116. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:double minutes
    n1=en:chromosomal translocation | n2=en:double minutes | rel=r_associated | relid=0 | w=28
  117. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:gene amplification
    n1=en:chromosomal translocation | n2=en:gene amplification | rel=r_associated | relid=0 | w=28
  118. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:genetic duplication process
    n1=en:chromosomal translocation | n2=en:genetic duplication process | rel=r_associated | relid=0 | w=28
  119. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:group chromosomal alteration
    n1=en:chromosomal translocation | n2=en:group chromosomal alteration | rel=r_associated | relid=0 | w=28
  120. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:isodicentric chromosome
    n1=en:chromosomal translocation | n2=en:isodicentric chromosome | rel=r_associated | relid=0 | w=28
  121. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:karyotype morphology
    n1=en:chromosomal translocation | n2=en:karyotype morphology | rel=r_associated | relid=0 | w=28
  122. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:mutation
    n1=en:chromosomal translocation | n2=en:mutation | rel=r_associated | relid=0 | w=28
  123. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:polysomy
    n1=en:chromosomal translocation | n2=en:polysomy | rel=r_associated | relid=0 | w=28
  124. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:protein translocation
    n1=en:chromosomal translocation | n2=en:protein translocation | rel=r_associated | relid=0 | w=28
  125. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:rearrangement of 1p11-13
    n1=en:chromosomal translocation | n2=en:rearrangement of 1p11-13 | rel=r_associated | relid=0 | w=28
  126. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:sex chromosome disorders
    n1=en:chromosomal translocation | n2=en:sex chromosome disorders | rel=r_associated | relid=0 | w=28
  127. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:smith-magenis syndrome
    n1=en:chromosomal translocation | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=28
  128. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:somatic hypermutation, immunoglobulin
    n1=en:chromosomal translocation | n2=en:somatic hypermutation, immunoglobulin | rel=r_associated | relid=0 | w=28
  129. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> en:unbalanced translocation of chromosome
    n1=en:chromosomal translocation | n2=en:unbalanced translocation of chromosome | rel=r_associated | relid=0 | w=28
  130. en:chromosomal translocation -- r_associated #0: 28 / 0.667 -> translocation
    n1=en:chromosomal translocation | n2=translocation | rel=r_associated | relid=0 | w=28
  131. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:22q11 deletion syndrome
    n1=en:chromosomal translocation | n2=en:22q11 deletion syndrome | rel=r_associated | relid=0 | w=27
  132. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:aneuploidy
    n1=en:chromosomal translocation | n2=en:aneuploidy | rel=r_associated | relid=0 | w=27
  133. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:balanced autosomal translocation in normal individual
    n1=en:chromosomal translocation | n2=en:balanced autosomal translocation in normal individual | rel=r_associated | relid=0 | w=27
  134. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:cellular translocation
    n1=en:chromosomal translocation | n2=en:cellular translocation | rel=r_associated | relid=0 | w=27
  135. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:chromosomal abnormality in fetus affecting management of mother
    n1=en:chromosomal translocation | n2=en:chromosomal abnormality in fetus affecting management of mother | rel=r_associated | relid=0 | w=27
  136. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:chromosomal alterations of group c and x
    n1=en:chromosomal translocation | n2=en:chromosomal alterations of group c and x | rel=r_associated | relid=0 | w=27
  137. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:chromosomal alterations of group e
    n1=en:chromosomal translocation | n2=en:chromosomal alterations of group e | rel=r_associated | relid=0 | w=27
  138. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:chromosomal deletion
    n1=en:chromosomal translocation | n2=en:chromosomal deletion | rel=r_associated | relid=0 | w=27
  139. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:chromosomal translocation process
    n1=en:chromosomal translocation | n2=en:chromosomal translocation process | rel=r_associated | relid=0 | w=27
  140. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:down syndrome
    n1=en:chromosomal translocation | n2=en:down syndrome | rel=r_associated | relid=0 | w=27
  141. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:holoprosencephaly
    n1=en:chromosomal translocation | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=27
  142. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:melnick-fraser syndrome
    n1=en:chromosomal translocation | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=27
  143. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:natural vs induced genetic mutation
    n1=en:chromosomal translocation | n2=en:natural vs induced genetic mutation | rel=r_associated | relid=0 | w=27
  144. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:other conditions due to chromosome anomalies
    n1=en:chromosomal translocation | n2=en:other conditions due to chromosome anomalies | rel=r_associated | relid=0 | w=27
  145. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:sequence inversion
    n1=en:chromosomal translocation | n2=en:sequence inversion | rel=r_associated | relid=0 | w=27
  146. en:chromosomal translocation -- r_associated #0: 27 / 0.643 -> en:trim24 gene
    n1=en:chromosomal translocation | n2=en:trim24 gene | rel=r_associated | relid=0 | w=27
  147. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> 614 translocations chromosomiques
    n1=en:chromosomal translocation | n2=614 translocations chromosomiques | rel=r_associated | relid=0 | w=26
  148. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:alteration of chromosome structure
    n1=en:chromosomal translocation | n2=en:alteration of chromosome structure | rel=r_associated | relid=0 | w=26
  149. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:anomaly of chromosome pair
    n1=en:chromosomal translocation | n2=en:anomaly of chromosome pair | rel=r_associated | relid=0 | w=26
  150. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:chimera disorder
    n1=en:chromosomal translocation | n2=en:chimera disorder | rel=r_associated | relid=0 | w=26
  151. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:chromosome disorder
    n1=en:chromosomal translocation | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=26
  152. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:chromosomes 1 and 2, monosomy 2q duplication 1p
    n1=en:chromosomal translocation | n2=en:chromosomes 1 and 2, monosomy 2q duplication 1p | rel=r_associated | relid=0 | w=26
  153. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:complex karyotype
    n1=en:chromosomal translocation | n2=en:complex karyotype | rel=r_associated | relid=0 | w=26
  154. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:derivative chromosome
    n1=en:chromosomal translocation | n2=en:derivative chromosome | rel=r_associated | relid=0 | w=26
  155. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:dna repeat expansion
    n1=en:chromosomal translocation | n2=en:dna repeat expansion | rel=r_associated | relid=0 | w=26
  156. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:duplication with other complex rearrangement
    n1=en:chromosomal translocation | n2=en:duplication with other complex rearrangement | rel=r_associated | relid=0 | w=26
  157. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:genetics
    n1=en:chromosomal translocation | n2=en:genetics | rel=r_associated | relid=0 | w=26
  158. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:micronuclei, chromosome-defective
    n1=en:chromosomal translocation | n2=en:micronuclei, chromosome-defective | rel=r_associated | relid=0 | w=26
  159. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:nondisjunction, genetic
    n1=en:chromosomal translocation | n2=en:nondisjunction, genetic | rel=r_associated | relid=0 | w=26
  160. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:rearrangement of 12q13
    n1=en:chromosomal translocation | n2=en:rearrangement of 12q13 | rel=r_associated | relid=0 | w=26
  161. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:supernumerary circular chromosome
    n1=en:chromosomal translocation | n2=en:supernumerary circular chromosome | rel=r_associated | relid=0 | w=26
  162. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:translocation
    n1=en:chromosomal translocation | n2=en:translocation | rel=r_associated | relid=0 | w=26
  163. en:chromosomal translocation -- r_associated #0: 26 / 0.619 -> en:uniparental disomy
    n1=en:chromosomal translocation | n2=en:uniparental disomy | rel=r_associated | relid=0 | w=26
  164. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> amplification de gènes
    n1=en:chromosomal translocation | n2=amplification de gènes | rel=r_associated | relid=0 | w=20
  165. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> anomalie chromosomique
    n1=en:chromosomal translocation | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
  166. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> anomalie cytogénétique
    n1=en:chromosomal translocation | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
  167. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> anormalité des chromosomes
    n1=en:chromosomal translocation | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
  168. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> chimérisme
    n1=en:chromosomal translocation | n2=chimérisme | rel=r_associated | relid=0 | w=20
  169. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> délétion chromosomale
    n1=en:chromosomal translocation | n2=délétion chromosomale | rel=r_associated | relid=0 | w=20
  170. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> délétion chromosomique
    n1=en:chromosomal translocation | n2=délétion chromosomique | rel=r_associated | relid=0 | w=20
  171. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> délétion de segment de chromosome
    n1=en:chromosomal translocation | n2=délétion de segment de chromosome | rel=r_associated | relid=0 | w=20
  172. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> effet d'un médicament
    n1=en:chromosomal translocation | n2=effet d'un médicament | rel=r_associated | relid=0 | w=20
  173. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:Angelman syndrome
    n1=en:chromosomal translocation | n2=en:Angelman syndrome | rel=r_associated | relid=0 | w=20
  174. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:Angelman's syndrome
    n1=en:chromosomal translocation | n2=en:Angelman's syndrome | rel=r_associated | relid=0 | w=20
  175. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:cerebral gigantism
    n1=en:chromosomal translocation | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
  176. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:chromosomal aberration
    n1=en:chromosomal translocation | n2=en:chromosomal aberration | rel=r_associated | relid=0 | w=20
  177. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:chromosomal abnormality
    n1=en:chromosomal translocation | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
  178. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:chromosome deletion
    n1=en:chromosomal translocation | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  179. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:chromosome inversion
    n1=en:chromosomal translocation | n2=en:chromosome inversion | rel=r_associated | relid=0 | w=20
  180. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:Down syndrome
    n1=en:chromosomal translocation | n2=en:Down syndrome | rel=r_associated | relid=0 | w=20
  181. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:fragile X syndrome
    n1=en:chromosomal translocation | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
  182. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:Klinefelter syndrome
    n1=en:chromosomal translocation | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20
  183. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:mosaïcism
    n1=en:chromosomal translocation | n2=en:mosaïcism | rel=r_associated | relid=0 | w=20
  184. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:Prader-Willi syndrome
    n1=en:chromosomal translocation | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
  185. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:Soto's syndrome
    n1=en:chromosomal translocation | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
  186. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:sotos' syndrome
    n1=en:chromosomal translocation | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
  187. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:Sotos' syndrome
    n1=en:chromosomal translocation | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
  188. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:structural variant:type:pt:^patient:nom
    n1=en:chromosomal translocation | n2=en:structural variant:type:pt:^patient:nom | rel=r_associated | relid=0 | w=20
  189. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> en:Williams syndrome
    n1=en:chromosomal translocation | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20
  190. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> gigantisme cérébral
    n1=en:chromosomal translocation | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
  191. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> holoprosencéphalie
    n1=en:chromosomal translocation | n2=holoprosencéphalie | rel=r_associated | relid=0 | w=20
  192. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> holoprosencéphalie de type 2
    n1=en:chromosomal translocation | n2=holoprosencéphalie de type 2 | rel=r_associated | relid=0 | w=20
  193. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> holoprosencéphalie de type 3
    n1=en:chromosomal translocation | n2=holoprosencéphalie de type 3 | rel=r_associated | relid=0 | w=20
  194. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> holoprosencéphalie de type 4
    n1=en:chromosomal translocation | n2=holoprosencéphalie de type 4 | rel=r_associated | relid=0 | w=20
  195. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> holoprosencéphalie familiale alobaire de type 1
    n1=en:chromosomal translocation | n2=holoprosencéphalie familiale alobaire de type 1 | rel=r_associated | relid=0 | w=20
  196. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> inversion chromosomique
    n1=en:chromosomal translocation | n2=inversion chromosomique | rel=r_associated | relid=0 | w=20
  197. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> isochromosome
    n1=en:chromosomal translocation | n2=isochromosome | rel=r_associated | relid=0 | w=20
  198. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> Jacobsen (syndrome de)
    n1=en:chromosomal translocation | n2=Jacobsen (syndrome de) | rel=r_associated | relid=0 | w=20
  199. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> microdélétion 5q35
    n1=en:chromosomal translocation | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20
  200. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> mosaïcisme
    n1=en:chromosomal translocation | n2=mosaïcisme | rel=r_associated | relid=0 | w=20
  201. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> mutagénèse
    n1=en:chromosomal translocation | n2=mutagénèse | rel=r_associated | relid=0 | w=20
  202. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> non disjonction génétique
    n1=en:chromosomal translocation | n2=non disjonction génétique | rel=r_associated | relid=0 | w=20
  203. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> non-disjonction génétique
    n1=en:chromosomal translocation | n2=non-disjonction génétique | rel=r_associated | relid=0 | w=20
  204. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> polyploïdie
    n1=en:chromosomal translocation | n2=polyploïdie | rel=r_associated | relid=0 | w=20
  205. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> Silver-Russell (syndrome de)
    n1=en:chromosomal translocation | n2=Silver-Russell (syndrome de) | rel=r_associated | relid=0 | w=20
  206. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> Sotos (syndrome de)
    n1=en:chromosomal translocation | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
  207. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome d'Angelman
    n1=en:chromosomal translocation | n2=syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  208. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome d'angelman
    n1=en:chromosomal translocation | n2=syndrome d'angelman | rel=r_associated | relid=0 | w=20
  209. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> Syndrome d'Angelman
    n1=en:chromosomal translocation | n2=Syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  210. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome de fragilité du chromosome X
    n1=en:chromosomal translocation | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
  211. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome de Jacobsen
    n1=en:chromosomal translocation | n2=syndrome de Jacobsen | rel=r_associated | relid=0 | w=20
  212. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome de Martin-Bell
    n1=en:chromosomal translocation | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
  213. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome de Silver-Russell
    n1=en:chromosomal translocation | n2=syndrome de Silver-Russell | rel=r_associated | relid=0 | w=20
  214. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome de silver-russell
    n1=en:chromosomal translocation | n2=syndrome de silver-russell | rel=r_associated | relid=0 | w=20
  215. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome de soto
    n1=en:chromosomal translocation | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
  216. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome de Sotos
    n1=en:chromosomal translocation | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
  217. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome de sotos
    n1=en:chromosomal translocation | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
  218. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> syndrome de Williams
    n1=en:chromosomal translocation | n2=syndrome de Williams | rel=r_associated | relid=0 | w=20
  219. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> trisomie
    n1=en:chromosomal translocation | n2=trisomie | rel=r_associated | relid=0 | w=20
  220. en:chromosomal translocation -- r_associated #0: 20 / 0.476 -> trouble chromosomique
    n1=en:chromosomal translocation | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
≈ 319 relations entrantes

  1. anormalité des chromosomes --- r_associated #0: 323 --> en:chromosomal translocation
    n1=anormalité des chromosomes | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=323
  2. en:chromosome disorder --- r_associated #0: 320 --> en:chromosomal translocation
    n1=en:chromosome disorder | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=320
  3. anomalie chromosomique --- r_associated #0: 244 --> en:chromosomal translocation
    n1=anomalie chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=244
  4. trouble chromosomique --- r_associated #0: 235 --> en:chromosomal translocation
    n1=trouble chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=235
  5. gigantisme cérébral --- r_associated #0: 201 --> en:chromosomal translocation
    n1=gigantisme cérébral | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=201
  6. en:sotos syndrome --- r_associated #0: 199 --> en:chromosomal translocation
    n1=en:sotos syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=199
  7. syndrome de Sotos --- r_associated #0: 195 --> en:chromosomal translocation
    n1=syndrome de Sotos | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=195
  8. syndrome de soto --- r_associated #0: 195 --> en:chromosomal translocation
    n1=syndrome de soto | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=195
  9. en:sotos' syndrome --- r_associated #0: 190 --> en:chromosomal translocation
    n1=en:sotos' syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=190
  10. en:chromosomal abnormality --- r_associated #0: 175 --> en:chromosomal translocation
    n1=en:chromosomal abnormality | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=175
  11. holoprosencéphalie --- r_associated #0: 101 --> en:chromosomal translocation
    n1=holoprosencéphalie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=101
  12. chimérisme --- r_associated #0: 100 --> en:chromosomal translocation
    n1=chimérisme | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=100
  13. en:chromosomal deletion --- r_associated #0: 99 --> en:chromosomal translocation
    n1=en:chromosomal deletion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=99
  14. en:holoprosencephaly --- r_associated #0: 99 --> en:chromosomal translocation
    n1=en:holoprosencephaly | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=99
  15. délétion chromosomale --- r_associated #0: 98 --> en:chromosomal translocation
    n1=délétion chromosomale | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=98
  16. en:chimerism --- r_associated #0: 98 --> en:chromosomal translocation
    n1=en:chimerism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=98
  17. délétion de segment de chromosome --- r_associated #0: 94 --> en:chromosomal translocation
    n1=délétion de segment de chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=94
  18. en:chromosome deletion --- r_associated #0: 94 --> en:chromosomal translocation
    n1=en:chromosome deletion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=94
  19. délétion chromosomique --- r_associated #0: 91 --> en:chromosomal translocation
    n1=délétion chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=91
  20. en:jacobsen syndrome --- r_associated #0: 90 --> en:chromosomal translocation
    n1=en:jacobsen syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=90
  21. syndrome de Jacobsen --- r_associated #0: 87 --> en:chromosomal translocation
    n1=syndrome de Jacobsen | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=87
  22. en:fragile x syndrome --- r_associated #0: 74 --> en:chromosomal translocation
    n1=en:fragile x syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=74
  23. en:fragile X syndrome --- r_associated #0: 70 --> en:chromosomal translocation
    n1=en:fragile X syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=70
  24. en:Klinefelter syndrome --- r_associated #0: 67 --> en:chromosomal translocation
    n1=en:Klinefelter syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=67
  25. syndrome de fragilité du chromosome X --- r_associated #0: 65 --> en:chromosomal translocation
    n1=syndrome de fragilité du chromosome X | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=65
  26. en:klinefelter syndrome --- r_associated #0: 63 --> en:chromosomal translocation
    n1=en:klinefelter syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=63
  27. anomalie cytogénétique --- r_associated #0: 60 --> en:chromosomal translocation
    n1=anomalie cytogénétique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=60
  28. en:Sotos' syndrome --- r_associated #0: 60 --> en:chromosomal translocation
    n1=en:Sotos' syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=60
  29. en:translocation --- r_associated #0: 56 --> en:chromosomal translocation
    n1=en:translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=56
  30. translocation --- r_associated #0: 55 --> en:chromosomal translocation
    n1=translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=55
  31. syndrome de silver-russell --- r_associated #0: 54 --> en:chromosomal translocation
    n1=syndrome de silver-russell | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=54
  32. en:down syndrome --- r_associated #0: 53 --> en:chromosomal translocation
    n1=en:down syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=53
  33. syndrome d'angelman --- r_associated #0: 53 --> en:chromosomal translocation
    n1=syndrome d'angelman | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=53
  34. Syndrome d'Angelman --- r_associated #0: 50 --> en:chromosomal translocation
    n1=Syndrome d'Angelman | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
  35. en:Down syndrome --- r_associated #0: 50 --> en:chromosomal translocation
    n1=en:Down syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
  36. mosaïcisme --- r_associated #0: 50 --> en:chromosomal translocation
    n1=mosaïcisme | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
  37. syndrome d'Angelman --- r_associated #0: 50 --> en:chromosomal translocation
    n1=syndrome d'Angelman | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
  38. syndrome de Silver-Russell --- r_associated #0: 50 --> en:chromosomal translocation
    n1=syndrome de Silver-Russell | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=50
  39. en:prader-willi syndrome --- r_associated #0: 48 --> en:chromosomal translocation
    n1=en:prader-willi syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=48
  40. en:mosaicism --- r_associated #0: 47 --> en:chromosomal translocation
    n1=en:mosaicism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=47
  41. polyploïdie --- r_associated #0: 47 --> en:chromosomal translocation
    n1=polyploïdie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=47
  42. en:Prader-Willi syndrome --- r_associated #0: 45 --> en:chromosomal translocation
    n1=en:Prader-Willi syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=45
  43. en:russell-silver syndrome --- r_associated #0: 45 --> en:chromosomal translocation
    n1=en:russell-silver syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=45
  44. effet d'un médicament --- r_associated #0: 44 --> en:chromosomal translocation
    n1=effet d'un médicament | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=44
  45. en:polyploidy --- r_associated #0: 44 --> en:chromosomal translocation
    n1=en:polyploidy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=44
  46. en:genetics --- r_associated #0: 43 --> en:chromosomal translocation
    n1=en:genetics | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=43
  47. en:drug effect --- r_associated #0: 42 --> en:chromosomal translocation
    n1=en:drug effect | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=42
  48. en:other conditions due to autosomal anomalies --- r_associated #0: 42 --> en:chromosomal translocation
    n1=en:other conditions due to autosomal anomalies | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=42
  49. en:autosomal deletion syndromes --- r_associated #0: 41 --> en:chromosomal translocation
    n1=en:autosomal deletion syndromes | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=41
  50. en:duplication with other complex rearrangement --- r_associated #0: 41 --> en:chromosomal translocation
    n1=en:duplication with other complex rearrangement | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=41
  51. holoprosencéphalie familiale alobaire de type 1 --- r_associated #0: 41 --> en:chromosomal translocation
    n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=41
  52. syndrome de sotos --- r_associated #0: 41 --> en:chromosomal translocation
    n1=syndrome de sotos | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=41
  53. Silver-Russell (syndrome de) --- r_associated #0: 40 --> en:chromosomal translocation
    n1=Silver-Russell (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=40
  54. en:Angelman syndrome --- r_associated #0: 40 --> en:chromosomal translocation
    n1=en:Angelman syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=40
  55. en:angelman syndrome --- r_associated #0: 40 --> en:chromosomal translocation
    n1=en:angelman syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=40
  56. en:somatic hypermutation, immunoglobulin --- r_associated #0: 40 --> en:chromosomal translocation
    n1=en:somatic hypermutation, immunoglobulin | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=40
  57. en:mosaic variegated aneuploidy syndrome --- r_associated #0: 39 --> en:chromosomal translocation
    n1=en:mosaic variegated aneuploidy syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=39
  58. holoprosencéphalie de type 4 --- r_associated #0: 39 --> en:chromosomal translocation
    n1=holoprosencéphalie de type 4 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=39
  59. non-disjonction génétique --- r_associated #0: 39 --> en:chromosomal translocation
    n1=non-disjonction génétique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=39
  60. en:sex chromosome aberrations --- r_associated #0: 38 --> en:chromosomal translocation
    n1=en:sex chromosome aberrations | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=38
  61. Sotos (syndrome de) --- r_associated #0: 37 --> en:chromosomal translocation
    n1=Sotos (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
  62. en:Soto's syndrome --- r_associated #0: 37 --> en:chromosomal translocation
    n1=en:Soto's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
  63. en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication --- r_associated #0: 37 --> en:chromosomal translocation
    n1=en:chromosomal abnormality in fetus, affecting management of mother, antepartum condition or complication | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
  64. en:nondisjunction, genetic --- r_associated #0: 37 --> en:chromosomal translocation
    n1=en:nondisjunction, genetic | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
  65. holoprosencéphalie de type 3 --- r_associated #0: 37 --> en:chromosomal translocation
    n1=holoprosencéphalie de type 3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
  66. non disjonction génétique --- r_associated #0: 37 --> en:chromosomal translocation
    n1=non disjonction génétique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=37
  67. en:absence of sex chromosome --- r_associated #0: 36 --> en:chromosomal translocation
    n1=en:absence of sex chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=36
  68. en:Williams syndrome --- r_associated #0: 35 --> en:chromosomal translocation
    n1=en:Williams syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  69. en:beckwith-wiedemann syndrome --- r_associated #0: 35 --> en:chromosomal translocation
    n1=en:beckwith-wiedemann syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  70. en:digeorge syndrome --- r_associated #0: 35 --> en:chromosomal translocation
    n1=en:digeorge syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  71. en:group chromosomal alteration --- r_associated #0: 35 --> en:chromosomal translocation
    n1=en:group chromosomal alteration | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  72. en:sex chromosome disorders --- r_associated #0: 35 --> en:chromosomal translocation
    n1=en:sex chromosome disorders | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  73. en:unbalanced translocation and insertion --- r_associated #0: 35 --> en:chromosomal translocation
    n1=en:unbalanced translocation and insertion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  74. en:williams syndrome --- r_associated #0: 35 --> en:chromosomal translocation
    n1=en:williams syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  75. en:wolf-hirschhorn syndrome --- r_associated #0: 35 --> en:chromosomal translocation
    n1=en:wolf-hirschhorn syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  76. mutagénèse --- r_associated #0: 35 --> en:chromosomal translocation
    n1=mutagénèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  77. translocation chromosomique --- r_associated #0: 35 --> en:chromosomal translocation
    n1=translocation chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=35
  78. en:b lymphoblastic leukemia/lymphoma, not otherwise specified --- r_associated #0: 34 --> en:chromosomal translocation
    n1=en:b lymphoblastic leukemia/lymphoma, not otherwise specified | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
  79. en:cellular translocation --- r_associated #0: 34 --> en:chromosomal translocation
    n1=en:cellular translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
  80. en:chromosomal instability --- r_associated #0: 34 --> en:chromosomal translocation
    n1=en:chromosomal instability | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
  81. en:gene amplification --- r_associated #0: 34 --> en:chromosomal translocation
    n1=en:gene amplification | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
  82. en:mutation --- r_associated #0: 34 --> en:chromosomal translocation
    n1=en:mutation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
  83. en:numerical chromosomal abnormality --- r_associated #0: 34 --> en:chromosomal translocation
    n1=en:numerical chromosomal abnormality | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
  84. en:polysomy --- r_associated #0: 34 --> en:chromosomal translocation
    n1=en:polysomy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
  85. isochromosome --- r_associated #0: 34 --> en:chromosomal translocation
    n1=isochromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
  86. trisomie --- r_associated #0: 34 --> en:chromosomal translocation
    n1=trisomie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=34
  87. en:cerebral gigantism --- r_associated #0: 33 --> en:chromosomal translocation
    n1=en:cerebral gigantism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=33
  88. en:abnormal karyotype --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:abnormal karyotype | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  89. en:balanced rearrangement and structural marker --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:balanced rearrangement and structural marker | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  90. en:chromosomal inversion --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:chromosomal inversion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  91. en:chromosomal rearrangement --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:chromosomal rearrangement | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  92. en:chromosomes 1 and 2, monosomy 2q duplication 1p --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:chromosomes 1 and 2, monosomy 2q duplication 1p | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  93. en:chromothripsis --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:chromothripsis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  94. en:complete trisomy 13 syndrome --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:complete trisomy 13 syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  95. en:double minutes --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:double minutes | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  96. en:emanuel syndrome --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:emanuel syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  97. en:meretoja syndrome --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:meretoja syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  98. en:mutagenesis --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  99. en:rearrangement of 6q13 --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:rearrangement of 6q13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  100. en:structural variant:type:pt:^patient:nom --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:structural variant:type:pt:^patient:nom | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  101. en:trisomy --- r_associated #0: 32 --> en:chromosomal translocation
    n1=en:trisomy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  102. mutagenèse --- r_associated #0: 32 --> en:chromosomal translocation
    n1=mutagenèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  103. translocation génétique --- r_associated #0: 32 --> en:chromosomal translocation
    n1=translocation génétique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  104. translocations chromosomiques --- r_associated #0: 32 --> en:chromosomal translocation
    n1=translocations chromosomiques | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=32
  105. en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition --- r_associated #0: 31 --> en:chromosomal translocation
    n1=en:chromosomal abnormality in fetus, affecting management of mother, delivered, with or without mention of antepartum condition | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  106. en:cri du chat syndrome --- r_associated #0: 31 --> en:chromosomal translocation
    n1=en:cri du chat syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  107. en:isochromosome --- r_associated #0: 31 --> en:chromosomal translocation
    n1=en:isochromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  108. en:mosaïcism --- r_associated #0: 31 --> en:chromosomal translocation
    n1=en:mosaïcism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  109. en:other conditions due to chromosome anomalies --- r_associated #0: 31 --> en:chromosomal translocation
    n1=en:other conditions due to chromosome anomalies | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  110. en:triploidy, diploidy, mixoploidy syndrome --- r_associated #0: 31 --> en:chromosomal translocation
    n1=en:triploidy, diploidy, mixoploidy syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  111. en:unbalanced translocation of chromosome --- r_associated #0: 31 --> en:chromosomal translocation
    n1=en:unbalanced translocation of chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  112. holoprosencéphalie de type 2 --- r_associated #0: 31 --> en:chromosomal translocation
    n1=holoprosencéphalie de type 2 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  113. inversion chromosomique --- r_associated #0: 31 --> en:chromosomal translocation
    n1=inversion chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  114. syndrome de Martin-Bell --- r_associated #0: 31 --> en:chromosomal translocation
    n1=syndrome de Martin-Bell | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=31
  115. TPN ou NADP --- r_associated #0: 30 --> en:chromosomal translocation
    n1=TPN ou NADP | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  116. amplification de gènes --- r_associated #0: 30 --> en:chromosomal translocation
    n1=amplification de gènes | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  117. en:22q11 deletion syndrome --- r_associated #0: 30 --> en:chromosomal translocation
    n1=en:22q11 deletion syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  118. en:chromosomal abnormality in fetus affecting management of mother --- r_associated #0: 30 --> en:chromosomal translocation
    n1=en:chromosomal abnormality in fetus affecting management of mother | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  119. en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg --- r_associated #0: 30 --> en:chromosomal translocation
    n1=en:chromosomal abnormality in fetus, affecting manag of mother, unspec as to eoc in preg | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  120. en:deimmunization --- r_associated #0: 30 --> en:chromosomal translocation
    n1=en:deimmunization | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  121. en:melnick-fraser syndrome --- r_associated #0: 30 --> en:chromosomal translocation
    n1=en:melnick-fraser syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  122. en:pseudotrisomy 18 --- r_associated #0: 30 --> en:chromosomal translocation
    n1=en:pseudotrisomy 18 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  123. en:rearrangement of 6q25 --- r_associated #0: 30 --> en:chromosomal translocation
    n1=en:rearrangement of 6q25 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  124. en:smith-magenis syndrome --- r_associated #0: 30 --> en:chromosomal translocation
    n1=en:smith-magenis syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  125. triskélion --- r_associated #0: 30 --> en:chromosomal translocation
    n1=triskélion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=30
  126. en:amino acid substitution --- r_associated #0: 29 --> en:chromosomal translocation
    n1=en:amino acid substitution | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
  127. en:physiological aspects --- r_associated #0: 29 --> en:chromosomal translocation
    n1=en:physiological aspects | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
  128. en:rearrangement of 12q13 --- r_associated #0: 29 --> en:chromosomal translocation
    n1=en:rearrangement of 12q13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
  129. en:rearrangement of 21q --- r_associated #0: 29 --> en:chromosomal translocation
    n1=en:rearrangement of 21q | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
  130. en:rearrangement of 2p23 --- r_associated #0: 29 --> en:chromosomal translocation
    n1=en:rearrangement of 2p23 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
  131. en:rearrangement of 3q --- r_associated #0: 29 --> en:chromosomal translocation
    n1=en:rearrangement of 3q | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
  132. en:trim24 wt allele --- r_associated #0: 29 --> en:chromosomal translocation
    n1=en:trim24 wt allele | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=29
  133. Jacobsen (syndrome de) --- r_associated #0: 28 --> en:chromosomal translocation
    n1=Jacobsen (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  134. en:anomaly of chromosome pair --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:anomaly of chromosome pair | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  135. en:autosomal translocation --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:autosomal translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  136. en:chromosomal aberration --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:chromosomal aberration | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  137. en:ddit3 wt allele --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:ddit3 wt allele | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  138. en:extra unidentified structurally abnormal chromosome (disorder) --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:extra unidentified structurally abnormal chromosome (disorder) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  139. en:immunology aspects --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:immunology aspects | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  140. en:oligosomy --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:oligosomy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  141. en:supernumerary circular chromosome --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:supernumerary circular chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  142. en:tissue mosaicism --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:tissue mosaicism | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  143. en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome --- r_associated #0: 28 --> en:chromosomal translocation
    n1=en:wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  144. microdélétion 5q35 --- r_associated #0: 28 --> en:chromosomal translocation
    n1=microdélétion 5q35 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=28
  145. 614 translocations chromosomiques --- r_associated #0: 27 --> en:chromosomal translocation
    n1=614 translocations chromosomiques | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
  146. en:balanced autosomal translocation in normal individual --- r_associated #0: 27 --> en:chromosomal translocation
    n1=en:balanced autosomal translocation in normal individual | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
  147. en:chromosome 9 inversion or duplication --- r_associated #0: 27 --> en:chromosomal translocation
    n1=en:chromosome 9 inversion or duplication | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
  148. en:chromosome inversion --- r_associated #0: 27 --> en:chromosomal translocation
    n1=en:chromosome inversion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
  149. en:chromosome replaced with ring or dicentric --- r_associated #0: 27 --> en:chromosomal translocation
    n1=en:chromosome replaced with ring or dicentric | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
  150. en:duplication seen only at prometaphase --- r_associated #0: 27 --> en:chromosomal translocation
    n1=en:duplication seen only at prometaphase | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
  151. en:genomic_region_amplification --- r_associated #0: 27 --> en:chromosomal translocation
    n1=en:genomic_region_amplification | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=27
  152. en:Angelman's syndrome --- r_associated #0: 26 --> en:chromosomal translocation
    n1=en:Angelman's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
  153. en:chimera disorder --- r_associated #0: 26 --> en:chromosomal translocation
    n1=en:chimera disorder | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
  154. en:complete trisomy 18 syndrome --- r_associated #0: 26 --> en:chromosomal translocation
    n1=en:complete trisomy 18 syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
  155. en:fetus with chromosomal abnormality --- r_associated #0: 26 --> en:chromosomal translocation
    n1=en:fetus with chromosomal abnormality | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
  156. en:karyotype morphology --- r_associated #0: 26 --> en:chromosomal translocation
    n1=en:karyotype morphology | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
  157. en:rearrangement of 17p11-13 --- r_associated #0: 26 --> en:chromosomal translocation
    n1=en:rearrangement of 17p11-13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
  158. syndrome de Williams --- r_associated #0: 26 --> en:chromosomal translocation
    n1=syndrome de Williams | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=26
  159. Hölmgren (triade de) --- r_associated #0: 25 --> en:chromosomal translocation
    n1=Hölmgren (triade de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=25
  160. remaniement chromosomique --- r_associated #0: 24 --> en:chromosomal translocation
    n1=remaniement chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=24
  161. en:Martin-Bell's syndrome --- r_associated #0: 23 --> en:chromosomal translocation
    n1=en:Martin-Bell's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=23
  162. maladie du cri du chat --- r_associated #0: 22 --> en:chromosomal translocation
    n1=maladie du cri du chat | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=22
  163. amplification de gène --- r_associated #0: 21 --> en:chromosomal translocation
    n1=amplification de gène | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=21
  164. amplification génique --- r_associated #0: 21 --> en:chromosomal translocation
    n1=amplification génique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=21
  165. syndrome de Prader-Willi --- r_associated #0: 21 --> en:chromosomal translocation
    n1=syndrome de Prader-Willi | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=21
  166. en:46, xx true hermaphrodite --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:46, xx true hermaphrodite | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  167. en:aberrant chromosome 1 --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:aberrant chromosome 1 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  168. en:alteration of chromosome structure --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:alteration of chromosome structure | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  169. en:aneuploidy --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:aneuploidy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  170. en:anomaly of chromosome x --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:anomaly of chromosome x | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  171. en:aspects of radiation effects --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:aspects of radiation effects | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  172. en:balanced autosomal translocation --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:balanced autosomal translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  173. en:balanced chromosomal translocation --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:balanced chromosomal translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  174. en:bloom syndrome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:bloom syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  175. en:chromosomal alterations of group a --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal alterations of group a | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  176. en:chromosomal alterations of group b --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal alterations of group b | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  177. en:chromosomal alterations of group c and x --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal alterations of group c and x | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  178. en:chromosomal alterations of group d --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal alterations of group d | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  179. en:chromosomal alterations of group e --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal alterations of group e | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  180. en:chromosomal alterations of group f --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal alterations of group f | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  181. en:chromosomal alterations of group g and y --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal alterations of group g and y | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  182. en:chromosomal duplication --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal duplication | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  183. en:chromosomal insertion --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal insertion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  184. en:chromosomal translocation process --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosomal translocation process | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  185. en:chromosome breakage --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosome breakage | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  186. en:chromosome disorders, autosomal --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:chromosome disorders, autosomal | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  187. en:complex karyotype --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:complex karyotype | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  188. en:cytogenetic abnormality --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:cytogenetic abnormality | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  189. en:ddit3 gene --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:ddit3 gene | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  190. en:deletion mutagenesis --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:deletion mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  191. en:derivative chromosome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:derivative chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  192. en:dicentric chromosome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:dicentric chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  193. en:dna repeat expansion --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:dna repeat expansion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  194. en:ethics qualifier --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:ethics qualifier | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  195. en:gelatinous droplike corneal dystrophy --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:gelatinous droplike corneal dystrophy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  196. en:gene rearrangement --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:gene rearrangement | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  197. en:genetic aspects --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:genetic aspects | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  198. en:genetic duplication process --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:genetic duplication process | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  199. en:giant rod chromosome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:giant rod chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  200. en:gonadal dysgenesis --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:gonadal dysgenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  201. en:homogeneously staining region --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:homogeneously staining region | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  202. en:indel mutation --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:indel mutation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  203. en:insertional mutagenesis --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:insertional mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  204. en:intracellular translocation --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:intracellular translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  205. en:isodicentric chromosome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:isodicentric chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  206. en:large-scale state transition --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:large-scale state transition | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  207. en:linker-scanning mutagenesis --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:linker-scanning mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  208. en:micronuclei, chromosome-defective --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:micronuclei, chromosome-defective | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  209. en:natural vs induced genetic mutation --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:natural vs induced genetic mutation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  210. en:philadelphia chromosome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:philadelphia chromosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  211. en:protein translocation --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:protein translocation | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  212. en:rearrangement of 11q --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:rearrangement of 11q | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  213. en:rearrangement of 11q13-21 --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:rearrangement of 11q13-21 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  214. en:rearrangement of 1p11-13 --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:rearrangement of 1p11-13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  215. en:rearrangement of 1p11-q11 --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:rearrangement of 1p11-q11 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  216. en:rearrangement of 8q11-13 --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:rearrangement of 8q11-13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  217. en:rearrangement of 8q21 --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:rearrangement of 8q21 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  218. en:rubinstein-taybi syndrome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:rubinstein-taybi syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  219. en:sequence deletion --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:sequence deletion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  220. en:sequence inversion --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:sequence inversion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  221. en:site-directed mutagenesis --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:site-directed mutagenesis | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  222. en:suppression, genetic --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:suppression, genetic | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  223. en:translocation down syndrome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:translocation down syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  224. en:trim24 gene --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:trim24 gene | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  225. en:triploidy and polyploidy --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:triploidy and polyploidy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  226. en:trisomy and partial trisomy of autosome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:trisomy and partial trisomy of autosome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  227. en:turner syndrome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:turner syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  228. en:uniparental disomy --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:uniparental disomy | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  229. en:xxyy syndrome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:xxyy syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  230. en:xyy syndrome --- r_associated #0: 20 --> en:chromosomal translocation
    n1=en:xyy syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=20
  231. trisomie 21 --- r_associated #0: 16 --> en:chromosomal translocation
    n1=trisomie 21 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=16
  232. Child-Pugh (syndrome de) --- r_associated #0: 15 --> en:chromosomal translocation
    n1=Child-Pugh (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  233. Giessen (test de) --- r_associated #0: 15 --> en:chromosomal translocation
    n1=Giessen (test de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  234. Mutagenèse --- r_associated #0: 15 --> en:chromosomal translocation
    n1=Mutagenèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  235. triple arthrodèse --- r_associated #0: 15 --> en:chromosomal translocation
    n1=triple arthrodèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  236. triple opération à la française --- r_associated #0: 15 --> en:chromosomal translocation
    n1=triple opération à la française | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  237. triploïdie --- r_associated #0: 15 --> en:chromosomal translocation
    n1=triploïdie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  238. triptans --- r_associated #0: 15 --> en:chromosomal translocation
    n1=triptans | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  239. triquétrum --- r_associated #0: 15 --> en:chromosomal translocation
    n1=triquétrum | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  240. triradialis sulcus de Turner --- r_associated #0: 15 --> en:chromosomal translocation
    n1=triradialis sulcus de Turner | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  241. tris --- r_associated #0: 15 --> en:chromosomal translocation
    n1=tris | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  242. trismus --- r_associated #0: 15 --> en:chromosomal translocation
    n1=trismus | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  243. trisomie du bras court du chromosome 3 --- r_associated #0: 15 --> en:chromosomal translocation
    n1=trisomie du bras court du chromosome 3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=15
  244. mongolisme --- r_associated #0: 11 --> en:chromosomal translocation
    n1=mongolisme | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=11
  245. Amplification génique --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Amplification génique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  246. Angelman (syndrome d') --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Angelman (syndrome d') | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  247. Anomalie chromosomique --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Anomalie chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  248. Délétion chromosomique --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Délétion chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  249. HLP3 --- r_associated #0: 10 --> en:chromosomal translocation
    n1=HLP3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  250. HPE3 --- r_associated #0: 10 --> en:chromosomal translocation
    n1=HPE3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  251. HPE4 --- r_associated #0: 10 --> en:chromosomal translocation
    n1=HPE4 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  252. Inversion chromosomique --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Inversion chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  253. Martin-Bell (syndrome de) --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Martin-Bell (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  254. Morvan (syndrome de) --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Morvan (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  255. Mutagénèse --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Mutagénèse | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  256. Syndrome de Prader-Willi --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Syndrome de Prader-Willi | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  257. Syndrome de Sotos --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Syndrome de Sotos | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  258. Translocation chromosomique --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Translocation chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  259. Trisomie --- r_associated #0: 10 --> en:chromosomal translocation
    n1=Trisomie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  260. aberration chromosomique --- r_associated #0: 10 --> en:chromosomal translocation
    n1=aberration chromosomique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  261. amplification de triplets nucléotidiques (affections neurologiques liées à l') --- r_associated #0: 10 --> en:chromosomal translocation
    n1=amplification de triplets nucléotidiques (affections neurologiques liées à l') | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  262. aneuploïdie --- r_associated #0: 10 --> en:chromosomal translocation
    n1=aneuploïdie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  263. en:5p minus syndrome --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:5p minus syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  264. en:5q microdeletion --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:5q microdeletion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  265. en:Down's --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:Down's | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  266. en:Down's syndrome --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:Down's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  267. en:Lejeune's syndrome --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:Lejeune's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  268. en:PWS --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:PWS | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  269. en:Smith-Magenis syndrome --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:Smith-Magenis syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  270. en:Sotos's syndrome --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:Sotos's syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  271. en:WBS --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:WBS | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  272. en:Williams' syndrome --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:Williams' syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  273. en:Williams-Beuren syndrome --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:Williams-Beuren syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  274. en:cat cry disease --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:cat cry disease | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  275. en:cat cry syndrome --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:cat cry syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  276. en:chromosomal disorder --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:chromosomal disorder | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  277. en:chromosome 5p deletion syndrome --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:chromosome 5p deletion syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  278. en:increase in gene copy number --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:increase in gene copy number | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  279. en:mutagenicity --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:mutagenicity | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  280. en:trisomy 21 --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:trisomy 21 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  281. en:type 1 --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:type 1 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  282. en:type 2 --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:type 2 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  283. en:type 3 --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:type 3 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  284. en:type 4 --- r_associated #0: 10 --> en:chromosomal translocation
    n1=en:type 4 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  285. holocentromère --- r_associated #0: 10 --> en:chromosomal translocation
    n1=holocentromère | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  286. holocentromérique --- r_associated #0: 10 --> en:chromosomal translocation
    n1=holocentromérique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  287. holocrine --- r_associated #0: 10 --> en:chromosomal translocation
    n1=holocrine | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  288. holodiastolique --- r_associated #0: 10 --> en:chromosomal translocation
    n1=holodiastolique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  289. holoenzyme --- r_associated #0: 10 --> en:chromosomal translocation
    n1=holoenzyme | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  290. hologamie --- r_associated #0: 10 --> en:chromosomal translocation
    n1=hologamie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  291. hologynique --- r_associated #0: 10 --> en:chromosomal translocation
    n1=hologynique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  292. holomérocrine --- r_associated #0: 10 --> en:chromosomal translocation
    n1=holomérocrine | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  293. holophrase --- r_associated #0: 10 --> en:chromosomal translocation
    n1=holophrase | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  294. holoproencéphalie --- r_associated #0: 10 --> en:chromosomal translocation
    n1=holoproencéphalie | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  295. inversion (zone d') --- r_associated #0: 10 --> en:chromosomal translocation
    n1=inversion (zone d') | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  296. souche de référence --- r_associated #0: 10 --> en:chromosomal translocation
    n1=souche de référence | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  297. souche transduite --- r_associated #0: 10 --> en:chromosomal translocation
    n1=souche transduite | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  298. triphosphopyridine-nucléotide --- r_associated #0: 10 --> en:chromosomal translocation
    n1=triphosphopyridine-nucléotide | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  299. trisomie 9p --- r_associated #0: 10 --> en:chromosomal translocation
    n1=trisomie 9p | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=10
  300. trisomie 13 --- r_associated #0: 6 --> en:chromosomal translocation
    n1=trisomie 13 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=6
  301. trisomie 18 --- r_associated #0: 6 --> en:chromosomal translocation
    n1=trisomie 18 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=6
  302. Chilomastix mesnili --- r_associated #0: 5 --> en:chromosomal translocation
    n1=Chilomastix mesnili | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  303. Maladie du cri du chat --- r_associated #0: 5 --> en:chromosomal translocation
    n1=Maladie du cri du chat | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  304. Williams (syndrome de) --- r_associated #0: 5 --> en:chromosomal translocation
    n1=Williams (syndrome de) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  305. children apperception test --- r_associated #0: 5 --> en:chromosomal translocation
    n1=children apperception test | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  306. chimbéré --- r_associated #0: 5 --> en:chromosomal translocation
    n1=chimbéré | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  307. chimère homme-animal --- r_associated #0: 5 --> en:chromosomal translocation
    n1=chimère homme-animal | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  308. cri du chat (maladie du) --- r_associated #0: 5 --> en:chromosomal translocation
    n1=cri du chat (maladie du) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  309. disomie uniparentale --- r_associated #0: 5 --> en:chromosomal translocation
    n1=disomie uniparentale | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  310. en:cat's cry syndrome --- r_associated #0: 5 --> en:chromosomal translocation
    n1=en:cat's cry syndrome | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  311. isobare (solution) --- r_associated #0: 5 --> en:chromosomal translocation
    n1=isobare (solution) | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  312. syndrome de Child-Pugh --- r_associated #0: 5 --> en:chromosomal translocation
    n1=syndrome de Child-Pugh | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  313. syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental --- r_associated #0: 5 --> en:chromosomal translocation
    n1=syndrome tumeur de Wilms-aniridie-anomalies génito-urinaires-retard mental | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  314. translocation de protéines --- r_associated #0: 5 --> en:chromosomal translocation
    n1=translocation de protéines | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  315. translocation des protéines --- r_associated #0: 5 --> en:chromosomal translocation
    n1=translocation des protéines | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  316. translocation protéique --- r_associated #0: 5 --> en:chromosomal translocation
    n1=translocation protéique | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  317. triplet (CGG) n --- r_associated #0: 5 --> en:chromosomal translocation
    n1=triplet (CGG) n | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  318. trisomie 17p11.2 --- r_associated #0: 5 --> en:chromosomal translocation
    n1=trisomie 17p11.2 | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=5
  319. trisomie 8 --- r_associated #0: 5 --> en:chromosomal translocation
    n1=trisomie 8 | n2=en:chromosomal translocation | 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