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'en:chromosome deletion'
(id=9991648 ; fe=en:chromosome deletion ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=5596 creation date=2018-02-22 touchdate=2025-08-27 16:59:39.000)
≈ 218 relations sortantes

  1. en:chromosome deletion -- r_associated #0: 140 / 1 -> délétion chromosomique
    n1=en:chromosome deletion | n2=délétion chromosomique | rel=r_associated | relid=0 | w=140
  2. en:chromosome deletion -- r_associated #0: 140 / 1 -> processus pathologique
    n1=en:chromosome deletion | n2=processus pathologique | rel=r_associated | relid=0 | w=140
  3. en:chromosome deletion -- r_associated #0: 124 / 0.886 -> en:loss of heterozygosity
    n1=en:chromosome deletion | n2=en:loss of heterozygosity | rel=r_associated | relid=0 | w=124
  4. en:chromosome deletion -- r_associated #0: 115 / 0.821 -> en:7p2 monosomy syndrome
    n1=en:chromosome deletion | n2=en:7p2 monosomy syndrome | rel=r_associated | relid=0 | w=115
  5. en:chromosome deletion -- r_associated #0: 115 / 0.821 -> en:chromosomal mutation
    n1=en:chromosome deletion | n2=en:chromosomal mutation | rel=r_associated | relid=0 | w=115
  6. en:chromosome deletion -- r_associated #0: 115 / 0.821 -> en:deafness, sensorineural, and male infertility
    n1=en:chromosome deletion | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=115
  7. en:chromosome deletion -- r_associated #0: 114 / 0.814 -> en:10p deletion syndrome (partial)
    n1=en:chromosome deletion | n2=en:10p deletion syndrome (partial) | rel=r_associated | relid=0 | w=114
  8. en:chromosome deletion -- r_associated #0: 114 / 0.814 -> en:chromosome 20, deletion 20p
    n1=en:chromosome deletion | n2=en:chromosome 20, deletion 20p | rel=r_associated | relid=0 | w=114
  9. en:chromosome deletion -- r_associated #0: 114 / 0.814 -> en:sequence deletion
    n1=en:chromosome deletion | n2=en:sequence deletion | rel=r_associated | relid=0 | w=114
  10. en:chromosome deletion -- r_associated #0: 113 / 0.807 -> en:1p36 deletion syndrome
    n1=en:chromosome deletion | n2=en:1p36 deletion syndrome | rel=r_associated | relid=0 | w=113
  11. en:chromosome deletion -- r_associated #0: 113 / 0.807 -> en:chromosome 10, monosomy 10q
    n1=en:chromosome deletion | n2=en:chromosome 10, monosomy 10q | rel=r_associated | relid=0 | w=113
  12. en:chromosome deletion -- r_associated #0: 113 / 0.807 -> en:chromosome 15q13.3 microdeletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 15q13.3 microdeletion syndrome | rel=r_associated | relid=0 | w=113
  13. en:chromosome deletion -- r_associated #0: 113 / 0.807 -> en:chromosome 1q43-q44 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 1q43-q44 deletion syndrome | rel=r_associated | relid=0 | w=113
  14. en:chromosome deletion -- r_associated #0: 113 / 0.807 -> en:chromosome 3, monosomy 3p
    n1=en:chromosome deletion | n2=en:chromosome 3, monosomy 3p | rel=r_associated | relid=0 | w=113
  15. en:chromosome deletion -- r_associated #0: 113 / 0.807 -> en:chromosome 6, deletion 6q13 q15
    n1=en:chromosome deletion | n2=en:chromosome 6, deletion 6q13 q15 | rel=r_associated | relid=0 | w=113
  16. en:chromosome deletion -- r_associated #0: 113 / 0.807 -> en:deletion 6q16 q21
    n1=en:chromosome deletion | n2=en:deletion 6q16 q21 | rel=r_associated | relid=0 | w=113
  17. en:chromosome deletion -- r_associated #0: 113 / 0.807 -> en:monosomy 16
    n1=en:chromosome deletion | n2=en:monosomy 16 | rel=r_associated | relid=0 | w=113
  18. en:chromosome deletion -- r_associated #0: 113 / 0.807 -> en:mutagenic effect
    n1=en:chromosome deletion | n2=en:mutagenic effect | rel=r_associated | relid=0 | w=113
  19. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:15q24 microdeletion
    n1=en:chromosome deletion | n2=en:15q24 microdeletion | rel=r_associated | relid=0 | w=112
  20. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 1, monosomy 1p22 p13
    n1=en:chromosome deletion | n2=en:chromosome 1, monosomy 1p22 p13 | rel=r_associated | relid=0 | w=112
  21. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 1, monosomy 1q32 q42
    n1=en:chromosome deletion | n2=en:chromosome 1, monosomy 1q32 q42 | rel=r_associated | relid=0 | w=112
  22. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 10q23 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 10q23 deletion syndrome | rel=r_associated | relid=0 | w=112
  23. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 10q26 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 10q26 deletion syndrome | rel=r_associated | relid=0 | w=112
  24. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 14q, terminal deletion
    n1=en:chromosome deletion | n2=en:chromosome 14q, terminal deletion | rel=r_associated | relid=0 | w=112
  25. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 17q21.31 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=112
  26. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 2q32-q33 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 2q32-q33 deletion syndrome | rel=r_associated | relid=0 | w=112
  27. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 2q37 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 2q37 deletion syndrome | rel=r_associated | relid=0 | w=112
  28. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 3, monosomy 3q13
    n1=en:chromosome deletion | n2=en:chromosome 3, monosomy 3q13 | rel=r_associated | relid=0 | w=112
  29. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 3, monosomy 3q27
    n1=en:chromosome deletion | n2=en:chromosome 3, monosomy 3q27 | rel=r_associated | relid=0 | w=112
  30. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome 4, 4q terminal deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 4, 4q terminal deletion syndrome | rel=r_associated | relid=0 | w=112
  31. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:chromosome breakage
    n1=en:chromosome deletion | n2=en:chromosome breakage | rel=r_associated | relid=0 | w=112
  32. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:monosomy 3
    n1=en:chromosome deletion | n2=en:monosomy 3 | rel=r_associated | relid=0 | w=112
  33. en:chromosome deletion -- r_associated #0: 112 / 0.8 -> en:tissue mosaicism
    n1=en:chromosome deletion | n2=en:tissue mosaicism | rel=r_associated | relid=0 | w=112
  34. en:chromosome deletion -- r_associated #0: 111 / 0.793 -> en:chimerism
    n1=en:chromosome deletion | n2=en:chimerism | rel=r_associated | relid=0 | w=111
  35. en:chromosome deletion -- r_associated #0: 111 / 0.793 -> en:chromosome 11p deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 11p deletion syndrome | rel=r_associated | relid=0 | w=111
  36. en:chromosome deletion -- r_associated #0: 111 / 0.793 -> en:chromosome 2, monosomy 2pter p24
    n1=en:chromosome deletion | n2=en:chromosome 2, monosomy 2pter p24 | rel=r_associated | relid=0 | w=111
  37. en:chromosome deletion -- r_associated #0: 111 / 0.793 -> en:chromosome 6, monosomy 6q2
    n1=en:chromosome deletion | n2=en:chromosome 6, monosomy 6q2 | rel=r_associated | relid=0 | w=111
  38. en:chromosome deletion -- r_associated #0: 111 / 0.793 -> en:chromothripsis
    n1=en:chromosome deletion | n2=en:chromothripsis | rel=r_associated | relid=0 | w=111
  39. en:chromosome deletion -- r_associated #0: 111 / 0.793 -> en:giant rod chromosome
    n1=en:chromosome deletion | n2=en:giant rod chromosome | rel=r_associated | relid=0 | w=111
  40. en:chromosome deletion -- r_associated #0: 111 / 0.793 -> en:monosomy 8
    n1=en:chromosome deletion | n2=en:monosomy 8 | rel=r_associated | relid=0 | w=111
  41. en:chromosome deletion -- r_associated #0: 111 / 0.793 -> en:rearrangement of 11q
    n1=en:chromosome deletion | n2=en:rearrangement of 11q | rel=r_associated | relid=0 | w=111
  42. en:chromosome deletion -- r_associated #0: 111 / 0.793 -> en:trisomy
    n1=en:chromosome deletion | n2=en:trisomy | rel=r_associated | relid=0 | w=111
  43. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> délétion chromosomale
    n1=en:chromosome deletion | n2=délétion chromosomale | rel=r_associated | relid=0 | w=110
  44. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosomal abnormalities nec
    n1=en:chromosome deletion | n2=en:chromosomal abnormalities nec | rel=r_associated | relid=0 | w=110
  45. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosomal insertion
    n1=en:chromosome deletion | n2=en:chromosomal insertion | rel=r_associated | relid=0 | w=110
  46. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 1, monosomy 1q25 q32
    n1=en:chromosome deletion | n2=en:chromosome 1, monosomy 1q25 q32 | rel=r_associated | relid=0 | w=110
  47. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 11p, partial deletion
    n1=en:chromosome deletion | n2=en:chromosome 11p, partial deletion | rel=r_associated | relid=0 | w=110
  48. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 12p partial deletion
    n1=en:chromosome deletion | n2=en:chromosome 12p partial deletion | rel=r_associated | relid=0 | w=110
  49. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 15q, partial deletion
    n1=en:chromosome deletion | n2=en:chromosome 15q, partial deletion | rel=r_associated | relid=0 | w=110
  50. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 17, deletion 17q23 q24
    n1=en:chromosome deletion | n2=en:chromosome 17, deletion 17q23 q24 | rel=r_associated | relid=0 | w=110
  51. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 18, deletion 18q23
    n1=en:chromosome deletion | n2=en:chromosome 18, deletion 18q23 | rel=r_associated | relid=0 | w=110
  52. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 1q21.1 deletion syndrome, 1.35-mb
    n1=en:chromosome deletion | n2=en:chromosome 1q21.1 deletion syndrome, 1.35-mb | rel=r_associated | relid=0 | w=110
  53. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 21, monosomy 21q22
    n1=en:chromosome deletion | n2=en:chromosome 21, monosomy 21q22 | rel=r_associated | relid=0 | w=110
  54. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 22, microdeletion 22 q11
    n1=en:chromosome deletion | n2=en:chromosome 22, microdeletion 22 q11 | rel=r_associated | relid=0 | w=110
  55. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:chromosome 4, monosomy 4p14 p16
    n1=en:chromosome deletion | n2=en:chromosome 4, monosomy 4p14 p16 | rel=r_associated | relid=0 | w=110
  56. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:cytogenetic abnormality
    n1=en:chromosome deletion | n2=en:cytogenetic abnormality | rel=r_associated | relid=0 | w=110
  57. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:haploinsufficiency
    n1=en:chromosome deletion | n2=en:haploinsufficiency | rel=r_associated | relid=0 | w=110
  58. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:holoprosencephaly 10
    n1=en:chromosome deletion | n2=en:holoprosencephaly 10 | rel=r_associated | relid=0 | w=110
  59. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:il1rapl1/dmd fusion gene
    n1=en:chromosome deletion | n2=en:il1rapl1/dmd fusion gene | rel=r_associated | relid=0 | w=110
  60. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:isochromosome
    n1=en:chromosome deletion | n2=en:isochromosome | rel=r_associated | relid=0 | w=110
  61. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:kleefstra syndrome
    n1=en:chromosome deletion | n2=en:kleefstra syndrome | rel=r_associated | relid=0 | w=110
  62. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:micronuclei, chromosome-defective
    n1=en:chromosome deletion | n2=en:micronuclei, chromosome-defective | rel=r_associated | relid=0 | w=110
  63. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:monosomy 21
    n1=en:chromosome deletion | n2=en:monosomy 21 | rel=r_associated | relid=0 | w=110
  64. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:monosomy 5
    n1=en:chromosome deletion | n2=en:monosomy 5 | rel=r_associated | relid=0 | w=110
  65. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:rearrangement of 11q13-21
    n1=en:chromosome deletion | n2=en:rearrangement of 11q13-21 | rel=r_associated | relid=0 | w=110
  66. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:rearrangement of 12q13
    n1=en:chromosome deletion | n2=en:rearrangement of 12q13 | rel=r_associated | relid=0 | w=110
  67. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:rearrangement of 1p11-q11
    n1=en:chromosome deletion | n2=en:rearrangement of 1p11-q11 | rel=r_associated | relid=0 | w=110
  68. en:chromosome deletion -- r_associated #0: 110 / 0.786 -> en:rearrangement of 3q
    n1=en:chromosome deletion | n2=en:rearrangement of 3q | rel=r_associated | relid=0 | w=110
  69. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:aneuploidy
    n1=en:chromosome deletion | n2=en:aneuploidy | rel=r_associated | relid=0 | w=109
  70. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:chromosome 1, monosomy 1p31 p22
    n1=en:chromosome deletion | n2=en:chromosome 1, monosomy 1p31 p22 | rel=r_associated | relid=0 | w=109
  71. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:chromosome 3, monosomy 3p14 p11
    n1=en:chromosome deletion | n2=en:chromosome 3, monosomy 3p14 p11 | rel=r_associated | relid=0 | w=109
  72. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:chromosome 4q- syndrome
    n1=en:chromosome deletion | n2=en:chromosome 4q- syndrome | rel=r_associated | relid=0 | w=109
  73. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:chromosome disorder
    n1=en:chromosome deletion | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=109
  74. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:chromosome xq deletion
    n1=en:chromosome deletion | n2=en:chromosome xq deletion | rel=r_associated | relid=0 | w=109
  75. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:double minutes
    n1=en:chromosome deletion | n2=en:double minutes | rel=r_associated | relid=0 | w=109
  76. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:homozygous 11p15-p14 deletion syndrome
    n1=en:chromosome deletion | n2=en:homozygous 11p15-p14 deletion syndrome | rel=r_associated | relid=0 | w=109
  77. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia
    n1=en:chromosome deletion | n2=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | rel=r_associated | relid=0 | w=109
  78. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:isodicentric chromosome
    n1=en:chromosome deletion | n2=en:isodicentric chromosome | rel=r_associated | relid=0 | w=109
  79. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:oligosomy
    n1=en:chromosome deletion | n2=en:oligosomy | rel=r_associated | relid=0 | w=109
  80. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:rearrangement of 8q21
    n1=en:chromosome deletion | n2=en:rearrangement of 8q21 | rel=r_associated | relid=0 | w=109
  81. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:telomeric 22q13 monosomy syndrome
    n1=en:chromosome deletion | n2=en:telomeric 22q13 monosomy syndrome | rel=r_associated | relid=0 | w=109
  82. en:chromosome deletion -- r_associated #0: 109 / 0.779 -> en:uniparental disomy
    n1=en:chromosome deletion | n2=en:uniparental disomy | rel=r_associated | relid=0 | w=109
  83. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:abnormal karyotype
    n1=en:chromosome deletion | n2=en:abnormal karyotype | rel=r_associated | relid=0 | w=108
  84. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:chromosomal duplication
    n1=en:chromosome deletion | n2=en:chromosomal duplication | rel=r_associated | relid=0 | w=108
  85. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:chromosomal inversion
    n1=en:chromosome deletion | n2=en:chromosomal inversion | rel=r_associated | relid=0 | w=108
  86. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:chromosome 2, monosomy 2q
    n1=en:chromosome deletion | n2=en:chromosome 2, monosomy 2q | rel=r_associated | relid=0 | w=108
  87. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:chromosome 6, monosomy 6q1
    n1=en:chromosome deletion | n2=en:chromosome 6, monosomy 6q1 | rel=r_associated | relid=0 | w=108
  88. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:chromosome 8, monosomy 8q
    n1=en:chromosome deletion | n2=en:chromosome 8, monosomy 8q | rel=r_associated | relid=0 | w=108
  89. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:chromosome 8p deletion syndrome (partial)
    n1=en:chromosome deletion | n2=en:chromosome 8p deletion syndrome (partial) | rel=r_associated | relid=0 | w=108
  90. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:hypodiploidy
    n1=en:chromosome deletion | n2=en:hypodiploidy | rel=r_associated | relid=0 | w=108
  91. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:loss of chromosome 12p
    n1=en:chromosome deletion | n2=en:loss of chromosome 12p | rel=r_associated | relid=0 | w=108
  92. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:loss of chromosome 1p
    n1=en:chromosome deletion | n2=en:loss of chromosome 1p | rel=r_associated | relid=0 | w=108
  93. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:male sterility due to y-chromosome deletions
    n1=en:chromosome deletion | n2=en:male sterility due to y-chromosome deletions | rel=r_associated | relid=0 | w=108
  94. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:monosomy
    n1=en:chromosome deletion | n2=en:monosomy | rel=r_associated | relid=0 | w=108
  95. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:monosomy 11
    n1=en:chromosome deletion | n2=en:monosomy 11 | rel=r_associated | relid=0 | w=108
  96. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:monosomy 9
    n1=en:chromosome deletion | n2=en:monosomy 9 | rel=r_associated | relid=0 | w=108
  97. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:monosomy x
    n1=en:chromosome deletion | n2=en:monosomy x | rel=r_associated | relid=0 | w=108
  98. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:otodental dysplasia
    n1=en:chromosome deletion | n2=en:otodental dysplasia | rel=r_associated | relid=0 | w=108
  99. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:p2ry8/crlf2 fusion gene
    n1=en:chromosome deletion | n2=en:p2ry8/crlf2 fusion gene | rel=r_associated | relid=0 | w=108
  100. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:rearrangement of 21q
    n1=en:chromosome deletion | n2=en:rearrangement of 21q | rel=r_associated | relid=0 | w=108
  101. en:chromosome deletion -- r_associated #0: 108 / 0.771 -> en:rearrangement of 6q25
    n1=en:chromosome deletion | n2=en:rearrangement of 6q25 | rel=r_associated | relid=0 | w=108
  102. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:chromosome 2, monosomy 2p22
    n1=en:chromosome deletion | n2=en:chromosome 2, monosomy 2p22 | rel=r_associated | relid=0 | w=107
  103. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:chromosome 8, monosomy 8p23 1
    n1=en:chromosome deletion | n2=en:chromosome 8, monosomy 8p23 1 | rel=r_associated | relid=0 | w=107
  104. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:complete trisomy 18 syndrome
    n1=en:chromosome deletion | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=107
  105. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:derivative chromosome
    n1=en:chromosome deletion | n2=en:derivative chromosome | rel=r_associated | relid=0 | w=107
  106. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:dicentric chromosome
    n1=en:chromosome deletion | n2=en:dicentric chromosome | rel=r_associated | relid=0 | w=107
  107. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:foetal chromosome abnormality
    n1=en:chromosome deletion | n2=en:foetal chromosome abnormality | rel=r_associated | relid=0 | w=107
  108. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:fragile site 16p12
    n1=en:chromosome deletion | n2=en:fragile site 16p12 | rel=r_associated | relid=0 | w=107
  109. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:large-scale state transition
    n1=en:chromosome deletion | n2=en:large-scale state transition | rel=r_associated | relid=0 | w=107
  110. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:monosomy 13q syndrome
    n1=en:chromosome deletion | n2=en:monosomy 13q syndrome | rel=r_associated | relid=0 | w=107
  111. en:chromosome deletion -- r_associated #0: 107 / 0.764 -> en:rearrangement of 2p23
    n1=en:chromosome deletion | n2=en:rearrangement of 2p23 | rel=r_associated | relid=0 | w=107
  112. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:9p partial monosomy syndrome
    n1=en:chromosome deletion | n2=en:9p partial monosomy syndrome | rel=r_associated | relid=0 | w=106
  113. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:chromosome 1, deletion q21 q25
    n1=en:chromosome deletion | n2=en:chromosome 1, deletion q21 q25 | rel=r_associated | relid=0 | w=106
  114. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:chromosome 11q partial deletion
    n1=en:chromosome deletion | n2=en:chromosome 11q partial deletion | rel=r_associated | relid=0 | w=106
  115. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:complex karyotype
    n1=en:chromosome deletion | n2=en:complex karyotype | rel=r_associated | relid=0 | w=106
  116. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:deletion 13q syndrome, partial
    n1=en:chromosome deletion | n2=en:deletion 13q syndrome, partial | rel=r_associated | relid=0 | w=106
  117. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:minimal aneuploidy
    n1=en:chromosome deletion | n2=en:minimal aneuploidy | rel=r_associated | relid=0 | w=106
  118. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:monosomy 13
    n1=en:chromosome deletion | n2=en:monosomy 13 | rel=r_associated | relid=0 | w=106
  119. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:monosomy 22
    n1=en:chromosome deletion | n2=en:monosomy 22 | rel=r_associated | relid=0 | w=106
  120. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:monosomy 7
    n1=en:chromosome deletion | n2=en:monosomy 7 | rel=r_associated | relid=0 | w=106
  121. en:chromosome deletion -- r_associated #0: 106 / 0.757 -> en:partial monosomy
    n1=en:chromosome deletion | n2=en:partial monosomy | rel=r_associated | relid=0 | w=106
  122. en:chromosome deletion -- r_associated #0: 105 / 0.75 -> en:chromosome 1, monosomy 1p34 p32
    n1=en:chromosome deletion | n2=en:chromosome 1, monosomy 1p34 p32 | rel=r_associated | relid=0 | w=105
  123. en:chromosome deletion -- r_associated #0: 105 / 0.75 -> en:chromosome 8, monosomy 8p
    n1=en:chromosome deletion | n2=en:chromosome 8, monosomy 8p | rel=r_associated | relid=0 | w=105
  124. en:chromosome deletion -- r_associated #0: 105 / 0.75 -> en:deletion 18q syndrome
    n1=en:chromosome deletion | n2=en:deletion 18q syndrome | rel=r_associated | relid=0 | w=105
  125. en:chromosome deletion -- r_associated #0: 105 / 0.75 -> en:gene mutation
    n1=en:chromosome deletion | n2=en:gene mutation | rel=r_associated | relid=0 | w=105
  126. en:chromosome deletion -- r_associated #0: 105 / 0.75 -> en:hyperploidy
    n1=en:chromosome deletion | n2=en:hyperploidy | rel=r_associated | relid=0 | w=105
  127. en:chromosome deletion -- r_associated #0: 105 / 0.75 -> en:prader-willi-like syndrome associated with chromosome 6
    n1=en:chromosome deletion | n2=en:prader-willi-like syndrome associated with chromosome 6 | rel=r_associated | relid=0 | w=105
  128. en:chromosome deletion -- r_associated #0: 105 / 0.75 -> en:rearrangement of 1p11-13
    n1=en:chromosome deletion | n2=en:rearrangement of 1p11-13 | rel=r_associated | relid=0 | w=105
  129. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:aberrant chromosome 1
    n1=en:chromosome deletion | n2=en:aberrant chromosome 1 | rel=r_associated | relid=0 | w=104
  130. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:chromosomal translocation
    n1=en:chromosome deletion | n2=en:chromosomal translocation | rel=r_associated | relid=0 | w=104
  131. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:chromosome 2, monosomy 2q24
    n1=en:chromosome deletion | n2=en:chromosome 2, monosomy 2q24 | rel=r_associated | relid=0 | w=104
  132. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:chromosome 22q11.2 deletion syndrome, distal
    n1=en:chromosome deletion | n2=en:chromosome 22q11.2 deletion syndrome, distal | rel=r_associated | relid=0 | w=104
  133. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:chromosome 3q29 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 3q29 deletion syndrome | rel=r_associated | relid=0 | w=104
  134. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:chromosome 4, monosomy 4q32
    n1=en:chromosome deletion | n2=en:chromosome 4, monosomy 4q32 | rel=r_associated | relid=0 | w=104
  135. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:chromosome 6, monosomy 6q
    n1=en:chromosome deletion | n2=en:chromosome 6, monosomy 6q | rel=r_associated | relid=0 | w=104
  136. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:chromosome 7, monosomy 7q21
    n1=en:chromosome deletion | n2=en:chromosome 7, monosomy 7q21 | rel=r_associated | relid=0 | w=104
  137. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:monosomy 6
    n1=en:chromosome deletion | n2=en:monosomy 6 | rel=r_associated | relid=0 | w=104
  138. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:mosaicism
    n1=en:chromosome deletion | n2=en:mosaicism | rel=r_associated | relid=0 | w=104
  139. en:chromosome deletion -- r_associated #0: 104 / 0.743 -> en:potocki-shaffer syndrome
    n1=en:chromosome deletion | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=104
  140. en:chromosome deletion -- r_associated #0: 102 / 0.729 -> en:chromosomal instability
    n1=en:chromosome deletion | n2=en:chromosomal instability | rel=r_associated | relid=0 | w=102
  141. en:chromosome deletion -- r_associated #0: 102 / 0.729 -> en:chromosomal rearrangement
    n1=en:chromosome deletion | n2=en:chromosomal rearrangement | rel=r_associated | relid=0 | w=102
  142. en:chromosome deletion -- r_associated #0: 102 / 0.729 -> en:chromosome 16p11.2 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 16p11.2 deletion syndrome | rel=r_associated | relid=0 | w=102
  143. en:chromosome deletion -- r_associated #0: 102 / 0.729 -> en:del(3p25)
    n1=en:chromosome deletion | n2=en:del(3p25) | rel=r_associated | relid=0 | w=102
  144. en:chromosome deletion -- r_associated #0: 102 / 0.729 -> en:numerical chromosomal abnormality
    n1=en:chromosome deletion | n2=en:numerical chromosomal abnormality | rel=r_associated | relid=0 | w=102
  145. en:chromosome deletion -- r_associated #0: 102 / 0.729 -> en:rearrangement of 17p11-13
    n1=en:chromosome deletion | n2=en:rearrangement of 17p11-13 | rel=r_associated | relid=0 | w=102
  146. en:chromosome deletion -- r_associated #0: 102 / 0.729 -> en:rearrangement of 6q13
    n1=en:chromosome deletion | n2=en:rearrangement of 6q13 | rel=r_associated | relid=0 | w=102
  147. en:chromosome deletion -- r_associated #0: 101 / 0.721 -> en:chromosome 1, monosomy 1q4
    n1=en:chromosome deletion | n2=en:chromosome 1, monosomy 1q4 | rel=r_associated | relid=0 | w=101
  148. en:chromosome deletion -- r_associated #0: 101 / 0.721 -> en:homogeneously staining region
    n1=en:chromosome deletion | n2=en:homogeneously staining region | rel=r_associated | relid=0 | w=101
  149. en:chromosome deletion -- r_associated #0: 101 / 0.721 -> en:x chromosome, monosomy xp22 pter
    n1=en:chromosome deletion | n2=en:x chromosome, monosomy xp22 pter | rel=r_associated | relid=0 | w=101
  150. en:chromosome deletion -- r_associated #0: 100 / 0.714 -> en:chromosome 2p16.1-p15 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 2p16.1-p15 deletion syndrome | rel=r_associated | relid=0 | w=100
  151. en:chromosome deletion -- r_associated #0: 99 / 0.707 -> en:chromosome 1, monosomy 1p32
    n1=en:chromosome deletion | n2=en:chromosome 1, monosomy 1p32 | rel=r_associated | relid=0 | w=99
  152. en:chromosome deletion -- r_associated #0: 99 / 0.707 -> en:chromosome 3, monosomy 3p2
    n1=en:chromosome deletion | n2=en:chromosome 3, monosomy 3p2 | rel=r_associated | relid=0 | w=99
  153. en:chromosome deletion -- r_associated #0: 98 / 0.7 -> en:chromosomal deletion
    n1=en:chromosome deletion | n2=en:chromosomal deletion | rel=r_associated | relid=0 | w=98
  154. en:chromosome deletion -- r_associated #0: 98 / 0.7 -> en:chromosome 4 short arm deletion
    n1=en:chromosome deletion | n2=en:chromosome 4 short arm deletion | rel=r_associated | relid=0 | w=98
  155. en:chromosome deletion -- r_associated #0: 98 / 0.7 -> en:nondisjunction, genetic
    n1=en:chromosome deletion | n2=en:nondisjunction, genetic | rel=r_associated | relid=0 | w=98
  156. en:chromosome deletion -- r_associated #0: 98 / 0.7 -> en:supernumerary circular chromosome
    n1=en:chromosome deletion | n2=en:supernumerary circular chromosome | rel=r_associated | relid=0 | w=98
  157. en:chromosome deletion -- r_associated #0: 97 / 0.693 -> en:chromosome 19q13.11 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 19q13.11 deletion syndrome | rel=r_associated | relid=0 | w=97
  158. en:chromosome deletion -- r_associated #0: 93 / 0.664 -> en:sex chromosome aberrations
    n1=en:chromosome deletion | n2=en:sex chromosome aberrations | rel=r_associated | relid=0 | w=93
  159. en:chromosome deletion -- r_associated #0: 90 / 0.643 -> chromosomique
    n1=en:chromosome deletion | n2=chromosomique | rel=r_associated | relid=0 | w=90
  160. en:chromosome deletion -- r_associated #0: 90 / 0.643 -> délétion
    n1=en:chromosome deletion | n2=délétion | rel=r_associated | relid=0 | w=90
  161. en:chromosome deletion -- r_associated #0: 85 / 0.607 -> monosomie partielle
    n1=en:chromosome deletion | n2=monosomie partielle | rel=r_associated | relid=0 | w=85
  162. en:chromosome deletion -- r_associated #0: 40 / 0.286 -> en:chromosome
    n1=en:chromosome deletion | n2=en:chromosome | rel=r_associated | relid=0 | w=40
  163. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:chromosome 2q31.2 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 2q31.2 deletion syndrome | rel=r_associated | relid=0 | w=35
  164. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:chromosome 3, monosomy 3q21 23
    n1=en:chromosome deletion | n2=en:chromosome 3, monosomy 3q21 23 | rel=r_associated | relid=0 | w=35
  165. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:chromosome 6pter-p24 deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 6pter-p24 deletion syndrome | rel=r_associated | relid=0 | w=35
  166. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:chromosome 7, monosomy 7q2
    n1=en:chromosome deletion | n2=en:chromosome 7, monosomy 7q2 | rel=r_associated | relid=0 | w=35
  167. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:chromosome 7, monosomy 7q3
    n1=en:chromosome deletion | n2=en:chromosome 7, monosomy 7q3 | rel=r_associated | relid=0 | w=35
  168. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:gene deletion
    n1=en:chromosome deletion | n2=en:gene deletion | rel=r_associated | relid=0 | w=35
  169. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:genomic_region_amplification
    n1=en:chromosome deletion | n2=en:genomic_region_amplification | rel=r_associated | relid=0 | w=35
  170. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:hypotriploidy
    n1=en:chromosome deletion | n2=en:hypotriploidy | rel=r_associated | relid=0 | w=35
  171. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:loss of chromosome 11p
    n1=en:chromosome deletion | n2=en:loss of chromosome 11p | rel=r_associated | relid=0 | w=35
  172. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:monosomy 10
    n1=en:chromosome deletion | n2=en:monosomy 10 | rel=r_associated | relid=0 | w=35
  173. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:monosomy 17
    n1=en:chromosome deletion | n2=en:monosomy 17 | rel=r_associated | relid=0 | w=35
  174. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:nf1 microdeletion syndrome
    n1=en:chromosome deletion | n2=en:nf1 microdeletion syndrome | rel=r_associated | relid=0 | w=35
  175. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:polysomy
    n1=en:chromosome deletion | n2=en:polysomy | rel=r_associated | relid=0 | w=35
  176. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:tetrasomy
    n1=en:chromosome deletion | n2=en:tetrasomy | rel=r_associated | relid=0 | w=35
  177. en:chromosome deletion -- r_associated #0: 35 / 0.25 -> en:x chromosome, monosomy xq28
    n1=en:chromosome deletion | n2=en:x chromosome, monosomy xq28 | rel=r_associated | relid=0 | w=35
  178. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> délétion de segment de chromosome
    n1=en:chromosome deletion | n2=délétion de segment de chromosome | rel=r_associated | relid=0 | w=30
  179. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:anomaly of chromosome x
    n1=en:chromosome deletion | n2=en:anomaly of chromosome x | rel=r_associated | relid=0 | w=30
  180. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:chromosome 14q, partial deletions
    n1=en:chromosome deletion | n2=en:chromosome 14q, partial deletions | rel=r_associated | relid=0 | w=30
  181. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:chromosome 17 deletion
    n1=en:chromosome deletion | n2=en:chromosome 17 deletion | rel=r_associated | relid=0 | w=30
  182. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:chromosome 1q21.1 duplication syndrome
    n1=en:chromosome deletion | n2=en:chromosome 1q21.1 duplication syndrome | rel=r_associated | relid=0 | w=30
  183. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:chromosome 6, monosomy 6p23
    n1=en:chromosome deletion | n2=en:chromosome 6, monosomy 6p23 | rel=r_associated | relid=0 | w=30
  184. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:chromosome 9p deletion syndrome
    n1=en:chromosome deletion | n2=en:chromosome 9p deletion syndrome | rel=r_associated | relid=0 | w=30
  185. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:deletion 18p syndrome
    n1=en:chromosome deletion | n2=en:deletion 18p syndrome | rel=r_associated | relid=0 | w=30
  186. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:hypotonia-cystinuria syndrome
    n1=en:chromosome deletion | n2=en:hypotonia-cystinuria syndrome | rel=r_associated | relid=0 | w=30
  187. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:lamin a/c gene mutation
    n1=en:chromosome deletion | n2=en:lamin a/c gene mutation | rel=r_associated | relid=0 | w=30
  188. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:monosomy 7 of bone marrow
    n1=en:chromosome deletion | n2=en:monosomy 7 of bone marrow | rel=r_associated | relid=0 | w=30
  189. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:myelodysplastic syndrome with isolated del(5q)
    n1=en:chromosome deletion | n2=en:myelodysplastic syndrome with isolated del(5q) | rel=r_associated | relid=0 | w=30
  190. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:polyploidy
    n1=en:chromosome deletion | n2=en:polyploidy | rel=r_associated | relid=0 | w=30
  191. en:chromosome deletion -- r_associated #0: 30 / 0.214 -> en:rearrangement of 8q11-13
    n1=en:chromosome deletion | n2=en:rearrangement of 8q11-13 | rel=r_associated | relid=0 | w=30
  192. en:chromosome deletion -- r_associated #0: 26 / 0.186 -> chromosome
    n1=en:chromosome deletion | n2=chromosome | rel=r_associated | relid=0 | w=26
  193. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> anomalie chromosomique
    n1=en:chromosome deletion | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
  194. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> anomalie cytogénétique
    n1=en:chromosome deletion | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
  195. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> anormalité des chromosomes
    n1=en:chromosome deletion | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
  196. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> chimérisme
    n1=en:chromosome deletion | n2=chimérisme | rel=r_associated | relid=0 | w=20
  197. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:chromosomal aberration
    n1=en:chromosome deletion | n2=en:chromosomal aberration | rel=r_associated | relid=0 | w=20
  198. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:chromosomal abnormality
    n1=en:chromosome deletion | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
  199. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:chromosomal loss
    n1=en:chromosome deletion | n2=en:chromosomal loss | rel=r_associated | relid=0 | w=20
  200. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:chromosome arm 3p loss of heterozygosity
    n1=en:chromosome deletion | n2=en:chromosome arm 3p loss of heterozygosity | rel=r_associated | relid=0 | w=20
  201. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:chromosome arm 9p loss of heterozygosity
    n1=en:chromosome deletion | n2=en:chromosome arm 9p loss of heterozygosity | rel=r_associated | relid=0 | w=20
  202. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:chromosome inversion
    n1=en:chromosome deletion | n2=en:chromosome inversion | rel=r_associated | relid=0 | w=20
  203. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:chromosome mutation
    n1=en:chromosome deletion | n2=en:chromosome mutation | rel=r_associated | relid=0 | w=20
  204. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:confined placental mosaicism
    n1=en:chromosome deletion | n2=en:confined placental mosaicism | rel=r_associated | relid=0 | w=20
  205. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:distal monosomy 10q syndrome
    n1=en:chromosome deletion | n2=en:distal monosomy 10q syndrome | rel=r_associated | relid=0 | w=20
  206. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:loss of chromosome 3p
    n1=en:chromosome deletion | n2=en:loss of chromosome 3p | rel=r_associated | relid=0 | w=20
  207. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> en:mosaïcism
    n1=en:chromosome deletion | n2=en:mosaïcism | rel=r_associated | relid=0 | w=20
  208. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> inversion chromosomique
    n1=en:chromosome deletion | n2=inversion chromosomique | rel=r_associated | relid=0 | w=20
  209. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> isochromosome
    n1=en:chromosome deletion | n2=isochromosome | rel=r_associated | relid=0 | w=20
  210. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> monosomie
    n1=en:chromosome deletion | n2=monosomie | rel=r_associated | relid=0 | w=20
  211. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> mosaïcisme
    n1=en:chromosome deletion | n2=mosaïcisme | rel=r_associated | relid=0 | w=20
  212. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> mutation chromosomique
    n1=en:chromosome deletion | n2=mutation chromosomique | rel=r_associated | relid=0 | w=20
  213. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> non disjonction génétique
    n1=en:chromosome deletion | n2=non disjonction génétique | rel=r_associated | relid=0 | w=20
  214. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> non-disjonction génétique
    n1=en:chromosome deletion | n2=non-disjonction génétique | rel=r_associated | relid=0 | w=20
  215. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> polyploïdie
    n1=en:chromosome deletion | n2=polyploïdie | rel=r_associated | relid=0 | w=20
  216. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> remaniement chromosomique
    n1=en:chromosome deletion | n2=remaniement chromosomique | rel=r_associated | relid=0 | w=20
  217. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> tétrasomie
    n1=en:chromosome deletion | n2=tétrasomie | rel=r_associated | relid=0 | w=20
  218. en:chromosome deletion -- r_associated #0: 20 / 0.143 -> trouble chromosomique
    n1=en:chromosome deletion | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
≈ 208 relations entrantes

  1. délétion de segment de chromosome --- r_associated #0: 100 --> en:chromosome deletion
    n1=délétion de segment de chromosome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=100
  2. en:chromosomal deletion --- r_associated #0: 91 --> en:chromosome deletion
    n1=en:chromosomal deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=91
  3. délétion chromosomale --- r_associated #0: 86 --> en:chromosome deletion
    n1=délétion chromosomale | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=86
  4. délétion chromosomique --- r_associated #0: 79 --> en:chromosome deletion
    n1=délétion chromosomique | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=79
  5. en:chromosome 1q21.1 deletion syndrome, 1.35-mb --- r_associated #0: 39 --> en:chromosome deletion
    n1=en:chromosome 1q21.1 deletion syndrome, 1.35-mb | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=39
  6. en:chromosome 6, monosomy 6p23 --- r_associated #0: 37 --> en:chromosome deletion
    n1=en:chromosome 6, monosomy 6p23 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=37
  7. en:chromosome 1, monosomy 1p34 p32 --- r_associated #0: 35 --> en:chromosome deletion
    n1=en:chromosome 1, monosomy 1p34 p32 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=35
  8. en:chromosome 10q23 deletion syndrome --- r_associated #0: 35 --> en:chromosome deletion
    n1=en:chromosome 10q23 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=35
  9. en:chromosome 1q43-q44 deletion syndrome --- r_associated #0: 35 --> en:chromosome deletion
    n1=en:chromosome 1q43-q44 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=35
  10. en:chromosome 22, microdeletion 22 q11 --- r_associated #0: 35 --> en:chromosome deletion
    n1=en:chromosome 22, microdeletion 22 q11 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=35
  11. en:chromosome 22q11.2 deletion syndrome, distal --- r_associated #0: 35 --> en:chromosome deletion
    n1=en:chromosome 22q11.2 deletion syndrome, distal | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=35
  12. en:chromosome 3, monosomy 3q27 --- r_associated #0: 35 --> en:chromosome deletion
    n1=en:chromosome 3, monosomy 3q27 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=35
  13. en:chromosome 8p deletion syndrome (partial) --- r_associated #0: 35 --> en:chromosome deletion
    n1=en:chromosome 8p deletion syndrome (partial) | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=35
  14. en:confined placental mosaicism --- r_associated #0: 35 --> en:chromosome deletion
    n1=en:confined placental mosaicism | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=35
  15. en:x chromosome, monosomy xp22 pter --- r_associated #0: 35 --> en:chromosome deletion
    n1=en:x chromosome, monosomy xp22 pter | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=35
  16. en:chromosome 2, monosomy 2pter p24 --- r_associated #0: 34 --> en:chromosome deletion
    n1=en:chromosome 2, monosomy 2pter p24 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=34
  17. en:chromosome 3, monosomy 3p2 --- r_associated #0: 34 --> en:chromosome deletion
    n1=en:chromosome 3, monosomy 3p2 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=34
  18. en:7p2 monosomy syndrome --- r_associated #0: 32 --> en:chromosome deletion
    n1=en:7p2 monosomy syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=32
  19. en:chromosome 14q, terminal deletion --- r_associated #0: 32 --> en:chromosome deletion
    n1=en:chromosome 14q, terminal deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=32
  20. en:chromosome 21, monosomy 21q22 --- r_associated #0: 32 --> en:chromosome deletion
    n1=en:chromosome 21, monosomy 21q22 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=32
  21. en:chromosome arm 9p loss of heterozygosity --- r_associated #0: 32 --> en:chromosome deletion
    n1=en:chromosome arm 9p loss of heterozygosity | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=32
  22. en:deletion 6q16 q21 --- r_associated #0: 32 --> en:chromosome deletion
    n1=en:deletion 6q16 q21 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=32
  23. en:homozygous 11p15-p14 deletion syndrome --- r_associated #0: 32 --> en:chromosome deletion
    n1=en:homozygous 11p15-p14 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=32
  24. en:x chromosome, monosomy xq28 --- r_associated #0: 32 --> en:chromosome deletion
    n1=en:x chromosome, monosomy xq28 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=32
  25. en:chromosome 10, monosomy 10q --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:chromosome 10, monosomy 10q | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  26. en:chromosome 15q, partial deletion --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:chromosome 15q, partial deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  27. en:chromosome 18, deletion 18q23 --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:chromosome 18, deletion 18q23 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  28. en:chromosome 2, monosomy 2p22 --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:chromosome 2, monosomy 2p22 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  29. en:chromosome 2q31.2 deletion syndrome --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:chromosome 2q31.2 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  30. en:chromosome 3, monosomy 3q13 --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:chromosome 3, monosomy 3q13 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  31. en:chromosome 7, monosomy 7q3 --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:chromosome 7, monosomy 7q3 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  32. en:monosomy 5 --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:monosomy 5 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  33. en:rearrangement of 2p23 --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:rearrangement of 2p23 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  34. en:rearrangement of 6q25 --- r_associated #0: 31 --> en:chromosome deletion
    n1=en:rearrangement of 6q25 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=31
  35. en:chromosome 1q21.1 duplication syndrome --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:chromosome 1q21.1 duplication syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  36. en:chromosome 6, monosomy 6q1 --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:chromosome 6, monosomy 6q1 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  37. en:chromosome 7, monosomy 7q21 --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:chromosome 7, monosomy 7q21 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  38. en:chromosome 8, monosomy 8p --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:chromosome 8, monosomy 8p | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  39. en:deletion 13q syndrome, partial --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:deletion 13q syndrome, partial | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  40. en:fragile site 16p12 --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:fragile site 16p12 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  41. en:loss of chromosome 3p --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:loss of chromosome 3p | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  42. en:rearrangement of 12q13 --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:rearrangement of 12q13 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  43. en:rearrangement of 17p11-13 --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:rearrangement of 17p11-13 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  44. en:rearrangement of 21q --- r_associated #0: 30 --> en:chromosome deletion
    n1=en:rearrangement of 21q | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=30
  45. en:chromosome 1, monosomy 1p31 p22 --- r_associated #0: 29 --> en:chromosome deletion
    n1=en:chromosome 1, monosomy 1p31 p22 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=29
  46. en:chromosome 1, monosomy 1q32 q42 --- r_associated #0: 29 --> en:chromosome deletion
    n1=en:chromosome 1, monosomy 1q32 q42 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=29
  47. en:chromosome 2q32-q33 deletion syndrome --- r_associated #0: 29 --> en:chromosome deletion
    n1=en:chromosome 2q32-q33 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=29
  48. en:chromosome arm 3p loss of heterozygosity --- r_associated #0: 29 --> en:chromosome deletion
    n1=en:chromosome arm 3p loss of heterozygosity | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=29
  49. en:nf1 microdeletion syndrome --- r_associated #0: 29 --> en:chromosome deletion
    n1=en:nf1 microdeletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=29
  50. en:chromosome 17, deletion 17q23 q24 --- r_associated #0: 28 --> en:chromosome deletion
    n1=en:chromosome 17, deletion 17q23 q24 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=28
  51. en:chromosome 2, monosomy 2q24 --- r_associated #0: 28 --> en:chromosome deletion
    n1=en:chromosome 2, monosomy 2q24 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=28
  52. en:chromosome 3, monosomy 3q21 23 --- r_associated #0: 28 --> en:chromosome deletion
    n1=en:chromosome 3, monosomy 3q21 23 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=28
  53. en:chromosome 6, deletion 6q13 q15 --- r_associated #0: 28 --> en:chromosome deletion
    n1=en:chromosome 6, deletion 6q13 q15 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=28
  54. en:rearrangement of 3q --- r_associated #0: 28 --> en:chromosome deletion
    n1=en:rearrangement of 3q | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=28
  55. en:rearrangement of 6q13 --- r_associated #0: 28 --> en:chromosome deletion
    n1=en:rearrangement of 6q13 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=28
  56. en:chromosome 20, deletion 20p --- r_associated #0: 27 --> en:chromosome deletion
    n1=en:chromosome 20, deletion 20p | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=27
  57. en:chromosome 7, monosomy 7q2 --- r_associated #0: 27 --> en:chromosome deletion
    n1=en:chromosome 7, monosomy 7q2 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=27
  58. en:hypotriploidy --- r_associated #0: 27 --> en:chromosome deletion
    n1=en:hypotriploidy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=27
  59. en:chromosome 11p, partial deletion --- r_associated #0: 26 --> en:chromosome deletion
    n1=en:chromosome 11p, partial deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=26
  60. en:chromosome 14q, partial deletions --- r_associated #0: 26 --> en:chromosome deletion
    n1=en:chromosome 14q, partial deletions | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=26
  61. en:chromosome 3, monosomy 3p14 p11 --- r_associated #0: 26 --> en:chromosome deletion
    n1=en:chromosome 3, monosomy 3p14 p11 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=26
  62. en:chromosome 6, monosomy 6q2 --- r_associated #0: 26 --> en:chromosome deletion
    n1=en:chromosome 6, monosomy 6q2 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=26
  63. en:chromosome 8, monosomy 8q --- r_associated #0: 26 --> en:chromosome deletion
    n1=en:chromosome 8, monosomy 8q | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=26
  64. en:prader-willi-like syndrome associated with chromosome 6 --- r_associated #0: 26 --> en:chromosome deletion
    n1=en:prader-willi-like syndrome associated with chromosome 6 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=26
  65. en:chromosome 3, monosomy 3p --- r_associated #0: 21 --> en:chromosome deletion
    n1=en:chromosome 3, monosomy 3p | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=21
  66. chromosome --- r_associated #0: 20 --> en:chromosome deletion
    n1=chromosome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  67. chromosomique --- r_associated #0: 20 --> en:chromosome deletion
    n1=chromosomique | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  68. délétion --- r_associated #0: 20 --> en:chromosome deletion
    n1=délétion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  69. en:10p deletion syndrome (partial) --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:10p deletion syndrome (partial) | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  70. en:15q24 microdeletion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:15q24 microdeletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  71. en:1p36 deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:1p36 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  72. en:9p partial monosomy syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:9p partial monosomy syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  73. en:aberrant chromosome 1 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:aberrant chromosome 1 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  74. en:abnormal karyotype --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:abnormal karyotype | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  75. en:aneuploidy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:aneuploidy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  76. en:anomaly of chromosome x --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:anomaly of chromosome x | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  77. en:chimerism --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chimerism | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  78. en:chromosomal abnormalities nec --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosomal abnormalities nec | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  79. en:chromosomal duplication --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosomal duplication | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  80. en:chromosomal insertion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosomal insertion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  81. en:chromosomal instability --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosomal instability | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  82. en:chromosomal inversion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosomal inversion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  83. en:chromosomal mutation --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosomal mutation | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  84. en:chromosomal rearrangement --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosomal rearrangement | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  85. en:chromosomal translocation --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosomal translocation | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  86. en:chromosome 1, deletion q21 q25 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 1, deletion q21 q25 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  87. en:chromosome 1, monosomy 1p22 p13 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 1, monosomy 1p22 p13 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  88. en:chromosome 1, monosomy 1p32 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 1, monosomy 1p32 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  89. en:chromosome 1, monosomy 1q25 q32 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 1, monosomy 1q25 q32 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  90. en:chromosome 1, monosomy 1q4 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 1, monosomy 1q4 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  91. en:chromosome 10q26 deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 10q26 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  92. en:chromosome 11p deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 11p deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  93. en:chromosome 11q partial deletion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 11q partial deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  94. en:chromosome 12p partial deletion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 12p partial deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  95. en:chromosome 15q13.3 microdeletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 15q13.3 microdeletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  96. en:chromosome 16p11.2 deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 16p11.2 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  97. en:chromosome 17 deletion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 17 deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  98. en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 17q21.31 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  99. en:chromosome 19q13.11 deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 19q13.11 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  100. en:chromosome 2, monosomy 2q --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 2, monosomy 2q | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  101. en:chromosome 2p16.1-p15 deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 2p16.1-p15 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  102. en:chromosome 2q37 deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 2q37 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  103. en:chromosome 3q29 deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 3q29 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  104. en:chromosome 4 short arm deletion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 4 short arm deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  105. en:chromosome 4, 4q terminal deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 4, 4q terminal deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  106. en:chromosome 4, monosomy 4p14 p16 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 4, monosomy 4p14 p16 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  107. en:chromosome 4, monosomy 4q32 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 4, monosomy 4q32 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  108. en:chromosome 4q- syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 4q- syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  109. en:chromosome 6, monosomy 6q --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 6, monosomy 6q | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  110. en:chromosome 6pter-p24 deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 6pter-p24 deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  111. en:chromosome 8, monosomy 8p23 1 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 8, monosomy 8p23 1 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  112. en:chromosome 9p deletion syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome 9p deletion syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  113. en:chromosome breakage --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome breakage | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  114. en:chromosome disorder --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome disorder | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  115. en:chromosome xq deletion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromosome xq deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  116. en:chromothripsis --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:chromothripsis | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  117. en:complete trisomy 18 syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:complete trisomy 18 syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  118. en:complex karyotype --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:complex karyotype | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  119. en:cytogenetic abnormality --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:cytogenetic abnormality | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  120. en:deafness, sensorineural, and male infertility --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:deafness, sensorineural, and male infertility | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  121. en:del(3p25) --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:del(3p25) | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  122. en:deletion 18p syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:deletion 18p syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  123. en:deletion 18q syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:deletion 18q syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  124. en:derivative chromosome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:derivative chromosome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  125. en:dicentric chromosome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:dicentric chromosome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  126. en:double minutes --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:double minutes | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  127. en:foetal chromosome abnormality --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:foetal chromosome abnormality | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  128. en:gene deletion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:gene deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  129. en:gene mutation --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:gene mutation | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  130. en:genomic_region_amplification --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:genomic_region_amplification | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  131. en:giant rod chromosome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:giant rod chromosome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  132. en:haploinsufficiency --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:haploinsufficiency | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  133. en:holoprosencephaly 10 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:holoprosencephaly 10 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  134. en:homogeneously staining region --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:homogeneously staining region | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  135. en:hyperploidy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:hyperploidy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  136. en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  137. en:hypodiploidy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:hypodiploidy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  138. en:hypotonia-cystinuria syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:hypotonia-cystinuria syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  139. en:il1rapl1/dmd fusion gene --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:il1rapl1/dmd fusion gene | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  140. en:isochromosome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:isochromosome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  141. en:isodicentric chromosome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:isodicentric chromosome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  142. en:kleefstra syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:kleefstra syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  143. en:lamin a/c gene mutation --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:lamin a/c gene mutation | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  144. en:large-scale state transition --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:large-scale state transition | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  145. en:loss of chromosome 11p --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:loss of chromosome 11p | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  146. en:loss of chromosome 12p --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:loss of chromosome 12p | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  147. en:loss of chromosome 1p --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:loss of chromosome 1p | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  148. en:loss of heterozygosity --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:loss of heterozygosity | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  149. en:male sterility due to y-chromosome deletions --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:male sterility due to y-chromosome deletions | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  150. en:micronuclei, chromosome-defective --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:micronuclei, chromosome-defective | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  151. en:minimal aneuploidy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:minimal aneuploidy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  152. en:monosomy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  153. en:monosomy 10 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 10 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  154. en:monosomy 11 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 11 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  155. en:monosomy 13 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 13 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  156. en:monosomy 13q syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 13q syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  157. en:monosomy 16 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 16 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  158. en:monosomy 17 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 17 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  159. en:monosomy 21 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 21 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  160. en:monosomy 22 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 22 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  161. en:monosomy 3 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 3 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  162. en:monosomy 6 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 6 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  163. en:monosomy 7 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 7 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  164. en:monosomy 7 of bone marrow --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 7 of bone marrow | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  165. en:monosomy 8 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 8 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  166. en:monosomy 9 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy 9 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  167. en:monosomy x --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:monosomy x | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  168. en:mosaicism --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:mosaicism | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  169. en:mutagenic effect --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:mutagenic effect | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  170. en:myelodysplastic syndrome with isolated del(5q) --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:myelodysplastic syndrome with isolated del(5q) | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  171. en:nondisjunction, genetic --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:nondisjunction, genetic | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  172. en:numerical chromosomal abnormality --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:numerical chromosomal abnormality | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  173. en:oligosomy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:oligosomy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  174. en:otodental dysplasia --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:otodental dysplasia | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  175. en:p2ry8/crlf2 fusion gene --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:p2ry8/crlf2 fusion gene | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  176. en:partial monosomy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:partial monosomy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  177. en:polyploidy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:polyploidy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  178. en:polysomy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:polysomy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  179. en:potocki-shaffer syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:potocki-shaffer syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  180. en:rearrangement of 11q --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:rearrangement of 11q | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  181. en:rearrangement of 11q13-21 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:rearrangement of 11q13-21 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  182. en:rearrangement of 1p11-13 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:rearrangement of 1p11-13 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  183. en:rearrangement of 1p11-q11 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:rearrangement of 1p11-q11 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  184. en:rearrangement of 8q11-13 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:rearrangement of 8q11-13 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  185. en:rearrangement of 8q21 --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:rearrangement of 8q21 | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  186. en:sequence deletion --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:sequence deletion | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  187. en:sex chromosome aberrations --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:sex chromosome aberrations | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  188. en:supernumerary circular chromosome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:supernumerary circular chromosome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  189. en:telomeric 22q13 monosomy syndrome --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:telomeric 22q13 monosomy syndrome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  190. en:tetrasomy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:tetrasomy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  191. en:tissue mosaicism --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:tissue mosaicism | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  192. en:trisomy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:trisomy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  193. en:uniparental disomy --- r_associated #0: 20 --> en:chromosome deletion
    n1=en:uniparental disomy | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  194. monosomie partielle --- r_associated #0: 20 --> en:chromosome deletion
    n1=monosomie partielle | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  195. processus pathologique --- r_associated #0: 20 --> en:chromosome deletion
    n1=processus pathologique | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=20
  196. Délétion chromosomique --- r_associated #0: 10 --> en:chromosome deletion
    n1=Délétion chromosomique | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  197. aneuploïdie --- r_associated #0: 10 --> en:chromosome deletion
    n1=aneuploïdie | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  198. anomalie chromosomique --- r_associated #0: 10 --> en:chromosome deletion
    n1=anomalie chromosomique | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  199. anormalité des chromosomes --- r_associated #0: 10 --> en:chromosome deletion
    n1=anormalité des chromosomes | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  200. chimérisme --- r_associated #0: 10 --> en:chromosome deletion
    n1=chimérisme | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  201. hypodiploïdie --- r_associated #0: 10 --> en:chromosome deletion
    n1=hypodiploïdie | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  202. mosaïcisme --- r_associated #0: 10 --> en:chromosome deletion
    n1=mosaïcisme | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  203. non disjonction génétique --- r_associated #0: 10 --> en:chromosome deletion
    n1=non disjonction génétique | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  204. trisomie --- r_associated #0: 10 --> en:chromosome deletion
    n1=trisomie | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  205. tétrasomie --- r_associated #0: 10 --> en:chromosome deletion
    n1=tétrasomie | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=10
  206. disomie uniparentale --- r_associated #0: 5 --> en:chromosome deletion
    n1=disomie uniparentale | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=5
  207. en:chromosome --- r_associated #0: 5 --> en:chromosome deletion
    n1=en:chromosome | n2=en:chromosome deletion | rel=r_associated | relid=0 | w=5
  208. trouble chromosomique --- r_associated #0: 5 --> en:chromosome deletion
    n1=trouble chromosomique | n2=en:chromosome deletion | 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