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'en:pseudotrisomy 13 syndrome'
(id=6819111 ; fe=en:pseudotrisomy 13 syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=97998.54998779297 creation date=2017-06-25 touchdate=2025-08-14 00:37:30.000)
≈ 1775 relations sortantes

  1. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:de sanctis-cacchione syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=43
  2. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:fetal warfarin syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fetal warfarin syndrome | rel=r_associated | relid=0 | w=43
  3. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:leri-weill dyschondrosteosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:leri-weill dyschondrosteosis | rel=r_associated | relid=0 | w=43
  4. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:mitochondrial neurogastrointestingal encephalopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:mitochondrial neurogastrointestingal encephalopathy | rel=r_associated | relid=0 | w=43
  5. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:netherton syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=43
  6. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:orofacial cleft 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:orofacial cleft 1 | rel=r_associated | relid=0 | w=43
  7. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:poems syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:poems syndrome | rel=r_associated | relid=0 | w=43
  8. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:retinoschisis
    n1=en:pseudotrisomy 13 syndrome | n2=en:retinoschisis | rel=r_associated | relid=0 | w=43
  9. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome | rel=r_associated | relid=0 | w=43
  10. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:tarsal tunnel syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:tarsal tunnel syndrome | rel=r_associated | relid=0 | w=43
  11. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:tubulointerstitial nephritis and uveitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:tubulointerstitial nephritis and uveitis | rel=r_associated | relid=0 | w=43
  12. en:pseudotrisomy 13 syndrome -- r_associated #0: 43 / 1 -> en:turner syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:turner syndrome | rel=r_associated | relid=0 | w=43
  13. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:alport syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:alport syndrome | rel=r_associated | relid=0 | w=42
  14. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:autosomal recessive muscular dystrophy with limb girdle distribution
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=42
  15. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:deafness, autosomal recessive 28
    n1=en:pseudotrisomy 13 syndrome | n2=en:deafness, autosomal recessive 28 | rel=r_associated | relid=0 | w=42
  16. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:diffuse infiltrative lymphocytosis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:diffuse infiltrative lymphocytosis syndrome | rel=r_associated | relid=0 | w=42
  17. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:gurrieri sammito bellussi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=42
  18. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:imperforate anus
    n1=en:pseudotrisomy 13 syndrome | n2=en:imperforate anus | rel=r_associated | relid=0 | w=42
  19. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:levocardia
    n1=en:pseudotrisomy 13 syndrome | n2=en:levocardia | rel=r_associated | relid=0 | w=42
  20. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:myositis
    n1=en:pseudotrisomy 13 syndrome | n2=en:myositis | rel=r_associated | relid=0 | w=42
  21. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:pelger-huet anomaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:pelger-huet anomaly | rel=r_associated | relid=0 | w=42
  22. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:phosphoenolpyruvate carboxykinase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:phosphoenolpyruvate carboxykinase deficiency | rel=r_associated | relid=0 | w=42
  23. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:rieger syndrome type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:rieger syndrome type 1 | rel=r_associated | relid=0 | w=42
  24. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:scimitar syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:scimitar syndrome | rel=r_associated | relid=0 | w=42
  25. en:pseudotrisomy 13 syndrome -- r_associated #0: 42 / 0.977 -> en:spondyloepiphyseal dysplasia tarda, toledo type
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=42
  26. en:pseudotrisomy 13 syndrome -- r_associated #0: 41 / 0.953 -> en:central sleep apnea syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:central sleep apnea syndrome | rel=r_associated | relid=0 | w=41
  27. en:pseudotrisomy 13 syndrome -- r_associated #0: 41 / 0.953 -> en:dyskeratosis congenita, autosomal recessive
    n1=en:pseudotrisomy 13 syndrome | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=41
  28. en:pseudotrisomy 13 syndrome -- r_associated #0: 41 / 0.953 -> en:erythromelalgia
    n1=en:pseudotrisomy 13 syndrome | n2=en:erythromelalgia | rel=r_associated | relid=0 | w=41
  29. en:pseudotrisomy 13 syndrome -- r_associated #0: 41 / 0.953 -> en:fibromyalgia
    n1=en:pseudotrisomy 13 syndrome | n2=en:fibromyalgia | rel=r_associated | relid=0 | w=41
  30. en:pseudotrisomy 13 syndrome -- r_associated #0: 41 / 0.953 -> en:long-chain acyl-coa dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=41
  31. en:pseudotrisomy 13 syndrome -- r_associated #0: 41 / 0.953 -> en:perthes disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:perthes disease | rel=r_associated | relid=0 | w=41
  32. en:pseudotrisomy 13 syndrome -- r_associated #0: 41 / 0.953 -> en:proteus syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:proteus syndrome | rel=r_associated | relid=0 | w=41
  33. en:pseudotrisomy 13 syndrome -- r_associated #0: 41 / 0.953 -> en:subclavian steal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:subclavian steal syndrome | rel=r_associated | relid=0 | w=41
  34. en:pseudotrisomy 13 syndrome -- r_associated #0: 40 / 0.93 -> en:acquired hyperostosis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:acquired hyperostosis syndrome | rel=r_associated | relid=0 | w=40
  35. en:pseudotrisomy 13 syndrome -- r_associated #0: 40 / 0.93 -> en:arthrogryposis
    n1=en:pseudotrisomy 13 syndrome | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=40
  36. en:pseudotrisomy 13 syndrome -- r_associated #0: 40 / 0.93 -> en:genoa syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:genoa syndrome | rel=r_associated | relid=0 | w=40
  37. en:pseudotrisomy 13 syndrome -- r_associated #0: 40 / 0.93 -> en:kimura disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:kimura disease | rel=r_associated | relid=0 | w=40
  38. en:pseudotrisomy 13 syndrome -- r_associated #0: 40 / 0.93 -> en:lissencephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:lissencephaly | rel=r_associated | relid=0 | w=40
  39. en:pseudotrisomy 13 syndrome -- r_associated #0: 40 / 0.93 -> en:malignant hyperthermia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:malignant hyperthermia syndrome | rel=r_associated | relid=0 | w=40
  40. en:pseudotrisomy 13 syndrome -- r_associated #0: 40 / 0.93 -> en:paragonimiasis
    n1=en:pseudotrisomy 13 syndrome | n2=en:paragonimiasis | rel=r_associated | relid=0 | w=40
  41. en:pseudotrisomy 13 syndrome -- r_associated #0: 40 / 0.93 -> en:progressive supranuclear palsy
    n1=en:pseudotrisomy 13 syndrome | n2=en:progressive supranuclear palsy | rel=r_associated | relid=0 | w=40
  42. en:pseudotrisomy 13 syndrome -- r_associated #0: 40 / 0.93 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
    n1=en:pseudotrisomy 13 syndrome | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=40
  43. en:pseudotrisomy 13 syndrome -- r_associated #0: 39 / 0.907 -> en:beta-methylcrotonylglycinuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:beta-methylcrotonylglycinuria | rel=r_associated | relid=0 | w=39
  44. en:pseudotrisomy 13 syndrome -- r_associated #0: 39 / 0.907 -> en:feingold syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=39
  45. en:pseudotrisomy 13 syndrome -- r_associated #0: 39 / 0.907 -> en:fibromuscular dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:fibromuscular dysplasia | rel=r_associated | relid=0 | w=39
  46. en:pseudotrisomy 13 syndrome -- r_associated #0: 39 / 0.907 -> en:fructose-1,6-bisphosphatase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=39
  47. en:pseudotrisomy 13 syndrome -- r_associated #0: 39 / 0.907 -> en:miller-dieker syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:miller-dieker syndrome | rel=r_associated | relid=0 | w=39
  48. en:pseudotrisomy 13 syndrome -- r_associated #0: 39 / 0.907 -> en:progressive muscular atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:progressive muscular atrophy | rel=r_associated | relid=0 | w=39
  49. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:achenbach syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:achenbach syndrome | rel=r_associated | relid=0 | w=38
  50. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:churg-strauss syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:churg-strauss syndrome | rel=r_associated | relid=0 | w=38
  51. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:epiphyseal dysplasia, multiple, 4
    n1=en:pseudotrisomy 13 syndrome | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=38
  52. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:familial renal iminoglycinuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=38
  53. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:interleukin-1 receptor-associated kinase 4 deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=38
  54. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:kallmann syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=38
  55. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:meesmann corneal dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:meesmann corneal dystrophy | rel=r_associated | relid=0 | w=38
  56. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:mulibrey nanism
    n1=en:pseudotrisomy 13 syndrome | n2=en:mulibrey nanism | rel=r_associated | relid=0 | w=38
  57. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:osteopetrosis with renal tubular acidosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:osteopetrosis with renal tubular acidosis | rel=r_associated | relid=0 | w=38
  58. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:prolidase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=38
  59. en:pseudotrisomy 13 syndrome -- r_associated #0: 38 / 0.884 -> en:variegate porphyria
    n1=en:pseudotrisomy 13 syndrome | n2=en:variegate porphyria | rel=r_associated | relid=0 | w=38
  60. en:pseudotrisomy 13 syndrome -- r_associated #0: 37 / 0.86 -> en:capillary leak syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:capillary leak syndrome | rel=r_associated | relid=0 | w=37
  61. en:pseudotrisomy 13 syndrome -- r_associated #0: 37 / 0.86 -> en:cystathioninuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:cystathioninuria | rel=r_associated | relid=0 | w=37
  62. en:pseudotrisomy 13 syndrome -- r_associated #0: 37 / 0.86 -> en:hnsha due to glutathione reductase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=37
  63. en:pseudotrisomy 13 syndrome -- r_associated #0: 37 / 0.86 -> en:holoprosencephaly type 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly type 2 | rel=r_associated | relid=0 | w=37
  64. en:pseudotrisomy 13 syndrome -- r_associated #0: 37 / 0.86 -> en:lethal congenital contracture syndrome 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=37
  65. en:pseudotrisomy 13 syndrome -- r_associated #0: 37 / 0.86 -> en:marburg virus disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:marburg virus disease | rel=r_associated | relid=0 | w=37
  66. en:pseudotrisomy 13 syndrome -- r_associated #0: 37 / 0.86 -> en:pulmonary alveolar proteinosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:pulmonary alveolar proteinosis | rel=r_associated | relid=0 | w=37
  67. en:pseudotrisomy 13 syndrome -- r_associated #0: 37 / 0.86 -> en:sudden unexplained infant death
    n1=en:pseudotrisomy 13 syndrome | n2=en:sudden unexplained infant death | rel=r_associated | relid=0 | w=37
  68. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:alper syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:alper syndrome | rel=r_associated | relid=0 | w=36
  69. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:anhidrotic ectodermal dysplasia 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:anhidrotic ectodermal dysplasia 1 | rel=r_associated | relid=0 | w=36
  70. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:bile acid synthesis defect
    n1=en:pseudotrisomy 13 syndrome | n2=en:bile acid synthesis defect | rel=r_associated | relid=0 | w=36
  71. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:congenital alpha-2-antiplasmin deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=36
  72. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:deletion 18p syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:deletion 18p syndrome | rel=r_associated | relid=0 | w=36
  73. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:fragile x tremor/ataxia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fragile x tremor/ataxia syndrome | rel=r_associated | relid=0 | w=36
  74. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:geroderma osteodysplastica
    n1=en:pseudotrisomy 13 syndrome | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=36
  75. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:giant axonal neuropathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:giant axonal neuropathy | rel=r_associated | relid=0 | w=36
  76. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:glutamate formiminotransferase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=36
  77. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:glutathione synthetase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=36
  78. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:gynatresia
    n1=en:pseudotrisomy 13 syndrome | n2=en:gynatresia | rel=r_associated | relid=0 | w=36
  79. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:hereditary fructose intolerance
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=36
  80. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=36
  81. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:kleine-levin syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:kleine-levin syndrome | rel=r_associated | relid=0 | w=36
  82. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:multiple malformation syndrome with facial-limb defects as major feature
    n1=en:pseudotrisomy 13 syndrome | n2=en:multiple malformation syndrome with facial-limb defects as major feature | rel=r_associated | relid=0 | w=36
  83. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:sex ratio - 2.3 males-to-1 female
    n1=en:pseudotrisomy 13 syndrome | n2=en:sex ratio - 2.3 males-to-1 female | rel=r_associated | relid=0 | w=36
  84. en:pseudotrisomy 13 syndrome -- r_associated #0: 36 / 0.837 -> en:wernicke-korsakoff syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:wernicke-korsakoff syndrome | rel=r_associated | relid=0 | w=36
  85. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:17q21 microdeletion syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:17q21 microdeletion syndrome | rel=r_associated | relid=0 | w=35
  86. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:3-methylglutaconic aciduria type iv
    n1=en:pseudotrisomy 13 syndrome | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=35
  87. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:acromelic frontonasal dysostosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:acromelic frontonasal dysostosis | rel=r_associated | relid=0 | w=35
  88. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:adherence syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:adherence syndrome | rel=r_associated | relid=0 | w=35
  89. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:ainhum
    n1=en:pseudotrisomy 13 syndrome | n2=en:ainhum | rel=r_associated | relid=0 | w=35
  90. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:albinism
    n1=en:pseudotrisomy 13 syndrome | n2=en:albinism | rel=r_associated | relid=0 | w=35
  91. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:albright's hereditary osteodystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:albright's hereditary osteodystrophy | rel=r_associated | relid=0 | w=35
  92. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:allan-herndon-dudley syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=35
  93. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:amelogenesis imperfecta - recessive - rough
    n1=en:pseudotrisomy 13 syndrome | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=35
  94. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:andersen syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=35
  95. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:anemia, hypochromic microcytic, with iron overload
    n1=en:pseudotrisomy 13 syndrome | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=35
  96. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:antiphospholipid syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:antiphospholipid syndrome | rel=r_associated | relid=0 | w=35
  97. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:argininosuccinic aciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=35
  98. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:arrhythmogenic right ventricular dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=35
  99. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:aspartylglycosaminuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=35
  100. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:baller-gerold syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=35
  101. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:bardet-biedl syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=35
  102. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:bartter syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:bartter syndrome | rel=r_associated | relid=0 | w=35
  103. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:basilar artery syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:basilar artery syndrome | rel=r_associated | relid=0 | w=35
  104. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:cartilage hair hypoplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:cartilage hair hypoplasia | rel=r_associated | relid=0 | w=35
  105. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:chediak-higashi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chediak-higashi syndrome | rel=r_associated | relid=0 | w=35
  106. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:chilblains
    n1=en:pseudotrisomy 13 syndrome | n2=en:chilblains | rel=r_associated | relid=0 | w=35
  107. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:pseudotrisomy 13 syndrome | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=35
  108. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:chromosome 16p11.2 deletion syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chromosome 16p11.2 deletion syndrome | rel=r_associated | relid=0 | w=35
  109. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:classical phenylketonuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  110. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:cleidocranial dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=35
  111. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:combined lipase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:combined lipase deficiency | rel=r_associated | relid=0 | w=35
  112. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:congenital abnormality
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=35
  113. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:congenital adrenal hyperplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=35
  114. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:congenital disorder of glycosylation type ia
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=35
  115. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:congenital varicella syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital varicella syndrome | rel=r_associated | relid=0 | w=35
  116. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:cor triatriatum
    n1=en:pseudotrisomy 13 syndrome | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=35
  117. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:crane-heise syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:crane-heise syndrome | rel=r_associated | relid=0 | w=35
  118. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:cri du chat syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=35
  119. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:cutis laxa
    n1=en:pseudotrisomy 13 syndrome | n2=en:cutis laxa | rel=r_associated | relid=0 | w=35
  120. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:cutis laxa, autosomal recessive
    n1=en:pseudotrisomy 13 syndrome | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=35
  121. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:cytochrome-c oxidase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=35
  122. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:d-glyceric aciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:d-glyceric aciduria | rel=r_associated | relid=0 | w=35
  123. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:de toni-debre-fanconi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:de toni-debre-fanconi syndrome | rel=r_associated | relid=0 | w=35
  124. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:ellis-van creveld syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:ellis-van creveld syndrome | rel=r_associated | relid=0 | w=35
  125. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:encephalocele
    n1=en:pseudotrisomy 13 syndrome | n2=en:encephalocele | rel=r_associated | relid=0 | w=35
  126. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:endocrine syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:endocrine syndrome | rel=r_associated | relid=0 | w=35
  127. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:factor v and factor viii, combined deficiency of
    n1=en:pseudotrisomy 13 syndrome | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=35
  128. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:familial acantholysis
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=35
  129. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=35
  130. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:familial periodic paralysis
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial periodic paralysis | rel=r_associated | relid=0 | w=35
  131. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:fanconi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fanconi syndrome | rel=r_associated | relid=0 | w=35
  132. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:fibrodysplasia ossificans progressiva
    n1=en:pseudotrisomy 13 syndrome | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=35
  133. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:fibular hypoplasia and complex brachydactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=35
  134. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:glycine encephalopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:glycine encephalopathy | rel=r_associated | relid=0 | w=35
  135. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:goodpasture syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:goodpasture syndrome | rel=r_associated | relid=0 | w=35
  136. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hantavirus pulmonary syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hantavirus pulmonary syndrome | rel=r_associated | relid=0 | w=35
  137. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hemivertebra
    n1=en:pseudotrisomy 13 syndrome | n2=en:hemivertebra | rel=r_associated | relid=0 | w=35
  138. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary adrenal unresponsiveness to corticotropin
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=35
  139. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary factor x deficiency disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=35
  140. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary methemoglobinemia, enzymatic type
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=35
  141. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary mucosal leukokeratosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=35
  142. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hydroa vacciniforme
    n1=en:pseudotrisomy 13 syndrome | n2=en:hydroa vacciniforme | rel=r_associated | relid=0 | w=35
  143. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hyperglycerolemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperglycerolemia | rel=r_associated | relid=0 | w=35
  144. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hyperlysinemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperlysinemia | rel=r_associated | relid=0 | w=35
  145. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | rel=r_associated | relid=0 | w=35
  146. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:hypoplastic right heart syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypoplastic right heart syndrome | rel=r_associated | relid=0 | w=35
  147. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:incontinentia pigmenti
    n1=en:pseudotrisomy 13 syndrome | n2=en:incontinentia pigmenti | rel=r_associated | relid=0 | w=35
  148. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:insufficient breast milk syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:insufficient breast milk syndrome | rel=r_associated | relid=0 | w=35
  149. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:isaacs syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=35
  150. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:jackson-weiss syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=35
  151. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:kabuki syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=35
  152. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:kniest dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:kniest dysplasia | rel=r_associated | relid=0 | w=35
  153. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:lafora disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:lafora disease | rel=r_associated | relid=0 | w=35
  154. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:laron syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:laron syndrome | rel=r_associated | relid=0 | w=35
  155. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:leriche syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:leriche syndrome | rel=r_associated | relid=0 | w=35
  156. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:lig4 syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lig4 syndrome | rel=r_associated | relid=0 | w=35
  157. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:malformations of cortical development
    n1=en:pseudotrisomy 13 syndrome | n2=en:malformations of cortical development | rel=r_associated | relid=0 | w=35
  158. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:metabolic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:metabolic syndrome | rel=r_associated | relid=0 | w=35
  159. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:microcephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:microcephaly | rel=r_associated | relid=0 | w=35
  160. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:miller-mckusick-malvaux-syndrome (3m syndrome)
    n1=en:pseudotrisomy 13 syndrome | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=35
  161. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:mixed connective tissue disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:mixed connective tissue disease | rel=r_associated | relid=0 | w=35
  162. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:moyamoya disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:moyamoya disease | rel=r_associated | relid=0 | w=35
  163. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:muscle amp deaminase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=35
  164. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:neoplastic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:neoplastic syndrome | rel=r_associated | relid=0 | w=35
  165. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:norrie syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=35
  166. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:northern epilepsy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=35
  167. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:oculocutaneous albinism type 4
    n1=en:pseudotrisomy 13 syndrome | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=35
  168. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:odontohypophosphatasia (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=35
  169. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:pachyonychia congenita
    n1=en:pseudotrisomy 13 syndrome | n2=en:pachyonychia congenita | rel=r_associated | relid=0 | w=35
  170. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:panuveitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:panuveitis | rel=r_associated | relid=0 | w=35
  171. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:paraneoplastic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:paraneoplastic syndrome | rel=r_associated | relid=0 | w=35
  172. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:pentosuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:pentosuria | rel=r_associated | relid=0 | w=35
  173. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:perinatal blood aspiration syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:perinatal blood aspiration syndrome | rel=r_associated | relid=0 | w=35
  174. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome | rel=r_associated | relid=0 | w=35
  175. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:piriformis muscle syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:piriformis muscle syndrome | rel=r_associated | relid=0 | w=35
  176. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:polydactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:polydactyly | rel=r_associated | relid=0 | w=35
  177. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:primary hyperoxaluria
    n1=en:pseudotrisomy 13 syndrome | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=35
  178. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:prolonged electroretinal response suppression
    n1=en:pseudotrisomy 13 syndrome | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=35
  179. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:radiation sickness syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:radiation sickness syndrome | rel=r_associated | relid=0 | w=35
  180. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:rapadilino syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=35
  181. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:reardon hall slaney syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=35
  182. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:reiter syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:reiter syndrome | rel=r_associated | relid=0 | w=35
  183. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:respiratory distress syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:respiratory distress syndrome | rel=r_associated | relid=0 | w=35
  184. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:reye syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:reye syndrome | rel=r_associated | relid=0 | w=35
  185. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:roberts syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=35
  186. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:robinow syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=35
  187. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:russell-silver syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=35
  188. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:scleromyxedema
    n1=en:pseudotrisomy 13 syndrome | n2=en:scleromyxedema | rel=r_associated | relid=0 | w=35
  189. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:severe early childhood onset retinal dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=35
  190. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:sheehan syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sheehan syndrome | rel=r_associated | relid=0 | w=35
  191. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:shy-drager syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:shy-drager syndrome | rel=r_associated | relid=0 | w=35
  192. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:simple syndactyly of toes, first web space
    n1=en:pseudotrisomy 13 syndrome | n2=en:simple syndactyly of toes, first web space | rel=r_associated | relid=0 | w=35
  193. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:sitosterolemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:sitosterolemia | rel=r_associated | relid=0 | w=35
  194. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:spastic paraplegia 15, autosomal recessive
    n1=en:pseudotrisomy 13 syndrome | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=35
  195. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia, autosomal recessive 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=35
  196. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:spondyloenchondrodysplasia with immune dysregulation
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=35
  197. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:stickler syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=35
  198. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:succinic semialdehyde dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=35
  199. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:sudden infant death syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sudden infant death syndrome | rel=r_associated | relid=0 | w=35
  200. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:sudden unexplained death in childhood
    n1=en:pseudotrisomy 13 syndrome | n2=en:sudden unexplained death in childhood | rel=r_associated | relid=0 | w=35
  201. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:superior vena cava syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:superior vena cava syndrome | rel=r_associated | relid=0 | w=35
  202. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:supernumerary structure
    n1=en:pseudotrisomy 13 syndrome | n2=en:supernumerary structure | rel=r_associated | relid=0 | w=35
  203. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:swyer james syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:swyer james syndrome | rel=r_associated | relid=0 | w=35
  204. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:synpolydactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=35
  205. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:tay-sachs disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=35
  206. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:type ii acrocephalopolysyndactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=35
  207. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:upper limb defect with eye and ear abnormalities syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=35
  208. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:vacterl association
    n1=en:pseudotrisomy 13 syndrome | n2=en:vacterl association | rel=r_associated | relid=0 | w=35
  209. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:waterhouse-friderichsen syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:waterhouse-friderichsen syndrome | rel=r_associated | relid=0 | w=35
  210. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:williams syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:williams syndrome | rel=r_associated | relid=0 | w=35
  211. en:pseudotrisomy 13 syndrome -- r_associated #0: 35 / 0.814 -> en:xeroderma pigmentosum
    n1=en:pseudotrisomy 13 syndrome | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=35
  212. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:aagenaes syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:aagenaes syndrome | rel=r_associated | relid=0 | w=34
  213. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:acrodermatitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:acrodermatitis | rel=r_associated | relid=0 | w=34
  214. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:allanson pantzar mcleod syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:allanson pantzar mcleod syndrome | rel=r_associated | relid=0 | w=34
  215. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:alpha-fetoprotein deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=34
  216. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:aminoacylase 1 deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=34
  217. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:atrophoderma vermiculatum
    n1=en:pseudotrisomy 13 syndrome | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=34
  218. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal recessive asexual dwarfism
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive asexual dwarfism | rel=r_associated | relid=0 | w=34
  219. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:barth syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:barth syndrome | rel=r_associated | relid=0 | w=34
  220. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:bietti crystalline corneoretinal dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=34
  221. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:blepharophimosis, ptosis, and epicanthus inversus (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:blepharophimosis, ptosis, and epicanthus inversus (disorder) | rel=r_associated | relid=0 | w=34
  222. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:bloom syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=34
  223. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:bothnia retinal dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=34
  224. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:brown-vialetto-van laere syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=34
  225. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:capgras syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:capgras syndrome | rel=r_associated | relid=0 | w=34
  226. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:cerebellar ataxia, cayman type
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=34
  227. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:cerebrooculofacioskeletal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebrooculofacioskeletal syndrome | rel=r_associated | relid=0 | w=34
  228. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=34
  229. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:charcot-marie-tooth disease type 4
    n1=en:pseudotrisomy 13 syndrome | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=34
  230. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:chondrodysplasia punctata
    n1=en:pseudotrisomy 13 syndrome | n2=en:chondrodysplasia punctata | rel=r_associated | relid=0 | w=34
  231. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:chromosome 15q11-q13 duplication syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chromosome 15q11-q13 duplication syndrome | rel=r_associated | relid=0 | w=34
  232. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:chromosome 17q21.31 deletion syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=34
  233. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:chylomicron retention disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=34
  234. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:congenital bilateral aplasia of the vas deferens
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital bilateral aplasia of the vas deferens | rel=r_associated | relid=0 | w=34
  235. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:congenital leptin deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=34
  236. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:connexin 26 gene anomaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:connexin 26 gene anomaly | rel=r_associated | relid=0 | w=34
  237. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:corpus callosum agenesis
    n1=en:pseudotrisomy 13 syndrome | n2=en:corpus callosum agenesis | rel=r_associated | relid=0 | w=34
  238. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:craniodiaphyseal dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=34
  239. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia
    n1=en:pseudotrisomy 13 syndrome | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=34
  240. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:dextrocardia
    n1=en:pseudotrisomy 13 syndrome | n2=en:dextrocardia | rel=r_associated | relid=0 | w=34
  241. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:down syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:down syndrome | rel=r_associated | relid=0 | w=34
  242. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:drug- and toxin-induced pulmonary arterial hypertension
    n1=en:pseudotrisomy 13 syndrome | n2=en:drug- and toxin-induced pulmonary arterial hypertension | rel=r_associated | relid=0 | w=34
  243. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:dysfunctional elimination syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dysfunctional elimination syndrome | rel=r_associated | relid=0 | w=34
  244. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=34
  245. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:ebstein anomaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:ebstein anomaly | rel=r_associated | relid=0 | w=34
  246. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:ectrodactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:ectrodactyly | rel=r_associated | relid=0 | w=34
  247. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:enterokinase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=34
  248. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:epidermolysis bullosa simplex with pyloric atresia
    n1=en:pseudotrisomy 13 syndrome | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=34
  249. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:erythropoietic porphyria
    n1=en:pseudotrisomy 13 syndrome | n2=en:erythropoietic porphyria | rel=r_associated | relid=0 | w=34
  250. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:exfoliation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:exfoliation syndrome | rel=r_associated | relid=0 | w=34
  251. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:familial alobar holoprosencephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial alobar holoprosencephaly | rel=r_associated | relid=0 | w=34
  252. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:familial hypoaldosteronism
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=34
  253. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:fatal familial insomnia
    n1=en:pseudotrisomy 13 syndrome | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=34
  254. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:fatal infantile lactic acidosis with methylmalonic aciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=34
  255. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:fetal alcohol syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fetal alcohol syndrome | rel=r_associated | relid=0 | w=34
  256. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:gasping syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:gasping syndrome | rel=r_associated | relid=0 | w=34
  257. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:gastric antral vascular ectasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:gastric antral vascular ectasia | rel=r_associated | relid=0 | w=34
  258. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:gastroschisis
    n1=en:pseudotrisomy 13 syndrome | n2=en:gastroschisis | rel=r_associated | relid=0 | w=34
  259. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:gaze palsy, familial horizontal, with progressive scoliosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=34
  260. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:genu varum
    n1=en:pseudotrisomy 13 syndrome | n2=en:genu varum | rel=r_associated | relid=0 | w=34
  261. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:glucose-6-phosphate dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=34
  262. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:gracile syndrome (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=34
  263. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:gray baby syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:gray baby syndrome | rel=r_associated | relid=0 | w=34
  264. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:griscelli syndrome type 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:griscelli syndrome type 2 | rel=r_associated | relid=0 | w=34
  265. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:harrod doman keele syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=34
  266. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary coproporphyria
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary coproporphyria | rel=r_associated | relid=0 | w=34
  267. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:holocarboxylase synthetase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:holocarboxylase synthetase deficiency | rel=r_associated | relid=0 | w=34
  268. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:holoprosencephaly type 5
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly type 5 | rel=r_associated | relid=0 | w=34
  269. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:hurler syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hurler syndrome | rel=r_associated | relid=0 | w=34
  270. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:hypohidrotic ectodermal dysplasia with immune deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypohidrotic ectodermal dysplasia with immune deficiency | rel=r_associated | relid=0 | w=34
  271. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:hypokalemic periodic paralysis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypokalemic periodic paralysis | rel=r_associated | relid=0 | w=34
  272. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:hypomagnesemia 1, intestinal
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=34
  273. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:hypoplastic tibia and postaxial polydactyly syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=34
  274. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:ichthyosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:ichthyosis | rel=r_associated | relid=0 | w=34
  275. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:immunoglobulin a deficiency 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:immunoglobulin a deficiency 1 | rel=r_associated | relid=0 | w=34
  276. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:klinefelter syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=34
  277. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:left ventricular non-compaction syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:left ventricular non-compaction syndrome | rel=r_associated | relid=0 | w=34
  278. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:machado-joseph disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:machado-joseph disease | rel=r_associated | relid=0 | w=34
  279. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:maple syrup urine disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=34
  280. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:marshall syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:marshall syndrome | rel=r_associated | relid=0 | w=34
  281. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:megalencephalic leukoencephalopathy with subcortical cysts
    n1=en:pseudotrisomy 13 syndrome | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=34
  282. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:menopausal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:menopausal syndrome | rel=r_associated | relid=0 | w=34
  283. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:mevalonate kinase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:mevalonate kinase deficiency | rel=r_associated | relid=0 | w=34
  284. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:microcephaly, amish type (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=34
  285. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:mitochondrial trifunctional protein deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:mitochondrial trifunctional protein deficiency | rel=r_associated | relid=0 | w=34
  286. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:morm syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:morm syndrome | rel=r_associated | relid=0 | w=34
  287. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:muenke syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:muenke syndrome | rel=r_associated | relid=0 | w=34
  288. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:multiple sulfatase deficiency disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=34
  289. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:myhre syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=34
  290. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:myokymia
    n1=en:pseudotrisomy 13 syndrome | n2=en:myokymia | rel=r_associated | relid=0 | w=34
  291. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:nathalie syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=34
  292. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:nephrotic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:nephrotic syndrome | rel=r_associated | relid=0 | w=34
  293. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:neuraminidase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=34
  294. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:neurodegeneration due to cerebral folate transport deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=34
  295. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:neuroleptic malignant syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:neuroleptic malignant syndrome | rel=r_associated | relid=0 | w=34
  296. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:north american indian childhood cirrhosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=34
  297. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:oculocerebral hypopigmentation syndrome type preus
    n1=en:pseudotrisomy 13 syndrome | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=34
  298. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:oeis complex
    n1=en:pseudotrisomy 13 syndrome | n2=en:oeis complex | rel=r_associated | relid=0 | w=34
  299. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:osteopoikilosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:osteopoikilosis | rel=r_associated | relid=0 | w=34
  300. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:pick's disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:pick's disease | rel=r_associated | relid=0 | w=34
  301. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:pinta
    n1=en:pseudotrisomy 13 syndrome | n2=en:pinta | rel=r_associated | relid=0 | w=34
  302. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:porokeratosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:porokeratosis | rel=r_associated | relid=0 | w=34
  303. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:porphobilinogen synthase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=34
  304. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:potocki-lupski syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:potocki-lupski syndrome | rel=r_associated | relid=0 | w=34
  305. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:primary fanconi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:primary fanconi syndrome | rel=r_associated | relid=0 | w=34
  306. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:propionic acidemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=34
  307. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
    n1=en:pseudotrisomy 13 syndrome | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=34
  308. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:red man syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:red man syndrome | rel=r_associated | relid=0 | w=34
  309. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:short bowel syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:short bowel syndrome | rel=r_associated | relid=0 | w=34
  310. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:sicca syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sicca syndrome | rel=r_associated | relid=0 | w=34
  311. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:simpson golabi behmel syndrome type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=34
  312. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:sly syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sly syndrome | rel=r_associated | relid=0 | w=34
  313. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia with epilepsy
    n1=en:pseudotrisomy 13 syndrome | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=34
  314. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:spondyloepimetaphyseal dysplasia, sponastrime type
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondyloepimetaphyseal dysplasia, sponastrime type | rel=r_associated | relid=0 | w=34
  315. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:stargardt disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:stargardt disease | rel=r_associated | relid=0 | w=34
  316. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:subacute sclerosing panencephalitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:subacute sclerosing panencephalitis | rel=r_associated | relid=0 | w=34
  317. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:surfactant protein deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:surfactant protein deficiency | rel=r_associated | relid=0 | w=34
  318. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:syringomyelia
    n1=en:pseudotrisomy 13 syndrome | n2=en:syringomyelia | rel=r_associated | relid=0 | w=34
  319. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:thanatophoric dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:thanatophoric dysplasia | rel=r_associated | relid=0 | w=34
  320. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=34
  321. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:togaviridae infection
    n1=en:pseudotrisomy 13 syndrome | n2=en:togaviridae infection | rel=r_associated | relid=0 | w=34
  322. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:transposition of great vessels
    n1=en:pseudotrisomy 13 syndrome | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=34
  323. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:trichinosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:trichinosis | rel=r_associated | relid=0 | w=34
  324. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:tricuspid valve atresia
    n1=en:pseudotrisomy 13 syndrome | n2=en:tricuspid valve atresia | rel=r_associated | relid=0 | w=34
  325. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:uniparental disomy
    n1=en:pseudotrisomy 13 syndrome | n2=en:uniparental disomy | rel=r_associated | relid=0 | w=34
  326. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:urocanase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=34
  327. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:verloes bourguignon syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=34
  328. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:wellesley carman french syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=34
  329. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:werdnig-hoffmann disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:werdnig-hoffmann disease | rel=r_associated | relid=0 | w=34
  330. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:wolman disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:wolman disease | rel=r_associated | relid=0 | w=34
  331. en:pseudotrisomy 13 syndrome -- r_associated #0: 34 / 0.791 -> en:xerophthalmia
    n1=en:pseudotrisomy 13 syndrome | n2=en:xerophthalmia | rel=r_associated | relid=0 | w=34
  332. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:2-hydroxyglutaric aciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=32
  333. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:3-methylglutaconic aciduria type 3
    n1=en:pseudotrisomy 13 syndrome | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=32
  334. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:5-oxoprolinase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=32
  335. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:acquired immunodeficiency syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:acquired immunodeficiency syndrome | rel=r_associated | relid=0 | w=32
  336. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:acrodermatitis enteropathica
    n1=en:pseudotrisomy 13 syndrome | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=32
  337. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:adiposis dolorosa
    n1=en:pseudotrisomy 13 syndrome | n2=en:adiposis dolorosa | rel=r_associated | relid=0 | w=32
  338. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:alpha-1 antitrypsin deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=32
  339. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:alpha, alpha-trehalase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=32
  340. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=32
  341. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:ataxia telangiectasia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=32
  342. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:autoinflammation, lipodystrophy and dermatosis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:autoinflammation, lipodystrophy and dermatosis syndrome | rel=r_associated | relid=0 | w=32
  343. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:autosomal recessive idiopathic familial dystonia
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=32
  344. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:autosomal recessive sideroblastic anemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=32
  345. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:becker generalized myotonia
    n1=en:pseudotrisomy 13 syndrome | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=32
  346. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:bowen-conradi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=32
  347. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:cadasil syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=32
  348. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:carbamoyl-phosphate synthetase i deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=32
  349. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:carbohydrate-deficient glycoprotein syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:carbohydrate-deficient glycoprotein syndrome | rel=r_associated | relid=0 | w=32
  350. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:cardiorenal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cardiorenal syndrome | rel=r_associated | relid=0 | w=32
  351. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:carnosinemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:carnosinemia | rel=r_associated | relid=0 | w=32
  352. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:caroli disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:caroli disease | rel=r_associated | relid=0 | w=32
  353. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:cerebrotendinous xanthomatosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=32
  354. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:citrin deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=32
  355. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:coffin-siris syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:coffin-siris syndrome | rel=r_associated | relid=0 | w=32
  356. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:congenital disorder of glycosylation type ig
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=32
  357. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:congenital dyserythropoietic anemia, type ii
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=32
  358. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:congenital hypoplasia of kidney
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital hypoplasia of kidney | rel=r_associated | relid=0 | w=32
  359. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:congenital myasthenic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=32
  360. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:corpus callosum agenesis neuronopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=32
  361. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:cranioectodermal dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:cranioectodermal dysplasia | rel=r_associated | relid=0 | w=32
  362. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:cyclopia (5%)
    n1=en:pseudotrisomy 13 syndrome | n2=en:cyclopia (5%) | rel=r_associated | relid=0 | w=32
  363. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:cystinuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:cystinuria | rel=r_associated | relid=0 | w=32
  364. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:deficiency of glucosyltransferase 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=32
  365. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:deletion 18q syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:deletion 18q syndrome | rel=r_associated | relid=0 | w=32
  366. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:digeorge syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=32
  367. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:dry eye syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dry eye syndrome | rel=r_associated | relid=0 | w=32
  368. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:dubowitz syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dubowitz syndrome | rel=r_associated | relid=0 | w=32
  369. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:episodic pain syndrome, familial, 3
    n1=en:pseudotrisomy 13 syndrome | n2=en:episodic pain syndrome, familial, 3 | rel=r_associated | relid=0 | w=32
  370. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:familial juvenile nephronophthisis
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial juvenile nephronophthisis | rel=r_associated | relid=0 | w=32
  371. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:fetal hydantoin syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fetal hydantoin syndrome | rel=r_associated | relid=0 | w=32
  372. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:fetal macrosomia
    n1=en:pseudotrisomy 13 syndrome | n2=en:fetal macrosomia | rel=r_associated | relid=0 | w=32
  373. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:fisher syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fisher syndrome | rel=r_associated | relid=0 | w=32
  374. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:focal dermal hypoplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=32
  375. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:fraser syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fraser syndrome | rel=r_associated | relid=0 | w=32
  376. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:frasier syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:frasier syndrome | rel=r_associated | relid=0 | w=32
  377. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:fronto-facio-nasal dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=32
  378. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:fryns syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fryns syndrome | rel=r_associated | relid=0 | w=32
  379. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate
    n1=en:pseudotrisomy 13 syndrome | n2=en:growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate | rel=r_associated | relid=0 | w=32
  380. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:gyrate atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:gyrate atrophy | rel=r_associated | relid=0 | w=32
  381. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:haspeslagh fryns muelenaere syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=32
  382. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:hereditary benign intraepithelial dyskeratosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=32
  383. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:hereditary palmoplantar keratoderma gamborg nielsen type
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=32
  384. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:heritable pulmonary arterial hypertension
    n1=en:pseudotrisomy 13 syndrome | n2=en:heritable pulmonary arterial hypertension | rel=r_associated | relid=0 | w=32
  385. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:high molecular weight kininogen deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:high molecular weight kininogen deficiency | rel=r_associated | relid=0 | w=32
  386. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:hmg-coa lyase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=32
  387. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:hnsha due to aldolase a deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:hnsha due to aldolase a deficiency | rel=r_associated | relid=0 | w=32
  388. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:hnsha due to pyrimidine-5'-nucleotidase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | rel=r_associated | relid=0 | w=32
  389. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:holmes-adie syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:holmes-adie syndrome | rel=r_associated | relid=0 | w=32
  390. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:hypophosphatasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypophosphatasia | rel=r_associated | relid=0 | w=32
  391. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:idiopathic cd4-positive t-lymphocytopenia
    n1=en:pseudotrisomy 13 syndrome | n2=en:idiopathic cd4-positive t-lymphocytopenia | rel=r_associated | relid=0 | w=32
  392. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:infantile uterus
    n1=en:pseudotrisomy 13 syndrome | n2=en:infantile uterus | rel=r_associated | relid=0 | w=32
  393. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:jeune syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:jeune syndrome | rel=r_associated | relid=0 | w=32
  394. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:kernicterus
    n1=en:pseudotrisomy 13 syndrome | n2=en:kernicterus | rel=r_associated | relid=0 | w=32
  395. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:klippel-trenaunay-weber syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=32
  396. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:knobloch syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=32
  397. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:leigh disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:leigh disease | rel=r_associated | relid=0 | w=32
  398. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:lethal multiple pterygium syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lethal multiple pterygium syndrome | rel=r_associated | relid=0 | w=32
  399. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:lipoid proteinosis of urbach and wiethe
    n1=en:pseudotrisomy 13 syndrome | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=32
  400. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:lobar holoprosencephalies
    n1=en:pseudotrisomy 13 syndrome | n2=en:lobar holoprosencephalies | rel=r_associated | relid=0 | w=32
  401. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:macrophage activation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:macrophage activation syndrome | rel=r_associated | relid=0 | w=32
  402. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:malignant atrophic papulosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:malignant atrophic papulosis | rel=r_associated | relid=0 | w=32
  403. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:mansonelliasis
    n1=en:pseudotrisomy 13 syndrome | n2=en:mansonelliasis | rel=r_associated | relid=0 | w=32
  404. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:maxillonasal dysplasia, binder type
    n1=en:pseudotrisomy 13 syndrome | n2=en:maxillonasal dysplasia, binder type | rel=r_associated | relid=0 | w=32
  405. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:meconium plug syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:meconium plug syndrome | rel=r_associated | relid=0 | w=32
  406. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=32
  407. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:methylmalonyl-coenzyme a mutase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=32
  408. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:migrating partial seizures in infancy
    n1=en:pseudotrisomy 13 syndrome | n2=en:migrating partial seizures in infancy | rel=r_associated | relid=0 | w=32
  409. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:mitochondrial dna depletion syndrome 2 (myopathic type)
    n1=en:pseudotrisomy 13 syndrome | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=32
  410. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:mmih syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
  411. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:multiple acyl-coa dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=32
  412. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:nail-patella syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=32
  413. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:nephrogenic fibrosing dermopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:nephrogenic fibrosing dermopathy | rel=r_associated | relid=0 | w=32
  414. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:neurocysticercosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:neurocysticercosis | rel=r_associated | relid=0 | w=32
  415. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:organic brain syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:organic brain syndrome | rel=r_associated | relid=0 | w=32
  416. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:pearson marrow-pancreas syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pearson marrow-pancreas syndrome | rel=r_associated | relid=0 | w=32
  417. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:pemphigoid gestationis
    n1=en:pseudotrisomy 13 syndrome | n2=en:pemphigoid gestationis | rel=r_associated | relid=0 | w=32
  418. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:phenylketonuria ii
    n1=en:pseudotrisomy 13 syndrome | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=32
  419. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:piebaldism
    n1=en:pseudotrisomy 13 syndrome | n2=en:piebaldism | rel=r_associated | relid=0 | w=32
  420. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:pre-excitation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pre-excitation syndrome | rel=r_associated | relid=0 | w=32
  421. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:progressive bulbar palsy
    n1=en:pseudotrisomy 13 syndrome | n2=en:progressive bulbar palsy | rel=r_associated | relid=0 | w=32
  422. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:pseudoachondroplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:pseudoachondroplasia | rel=r_associated | relid=0 | w=32
  423. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:pseudocholinesterase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=32
  424. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:pyruvate dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=32
  425. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:renal cysts and diabetes syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:renal cysts and diabetes syndrome | rel=r_associated | relid=0 | w=32
  426. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:renal tubulopathy with encephalopathy and liver failure syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=32
  427. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:saldino-noonan syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:saldino-noonan syndrome | rel=r_associated | relid=0 | w=32
  428. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:sarcosinemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=32
  429. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:short rib-polydactyly syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:short rib-polydactyly syndrome | rel=r_associated | relid=0 | w=32
  430. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:spasmodic torticollis
    n1=en:pseudotrisomy 13 syndrome | n2=en:spasmodic torticollis | rel=r_associated | relid=0 | w=32
  431. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:stevens-johnson syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:stevens-johnson syndrome | rel=r_associated | relid=0 | w=32
  432. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:thalidomide embryopathy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:thalidomide embryopathy syndrome | rel=r_associated | relid=0 | w=32
  433. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:tourette syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:tourette syndrome | rel=r_associated | relid=0 | w=32
  434. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:trichorhinophalangeal syndrome type i
    n1=en:pseudotrisomy 13 syndrome | n2=en:trichorhinophalangeal syndrome type i | rel=r_associated | relid=0 | w=32
  435. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:trisomy 14 mosaicism
    n1=en:pseudotrisomy 13 syndrome | n2=en:trisomy 14 mosaicism | rel=r_associated | relid=0 | w=32
  436. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:twiddler's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:twiddler's syndrome | rel=r_associated | relid=0 | w=32
  437. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:tyrosinemia, type iii
    n1=en:pseudotrisomy 13 syndrome | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=32
  438. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:uv-sensitive syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=32
  439. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:uveitis glaucoma and hyphema syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:uveitis glaucoma and hyphema syndrome | rel=r_associated | relid=0 | w=32
  440. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:weaver syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:weaver syndrome | rel=r_associated | relid=0 | w=32
  441. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:wegener granulomatosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:wegener granulomatosis | rel=r_associated | relid=0 | w=32
  442. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:weill-marchesani syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:weill-marchesani syndrome | rel=r_associated | relid=0 | w=32
  443. en:pseudotrisomy 13 syndrome -- r_associated #0: 32 / 0.744 -> en:wolfram syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:wolfram syndrome | rel=r_associated | relid=0 | w=32
  444. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:1p36 deletion syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:1p36 deletion syndrome | rel=r_associated | relid=0 | w=31
  445. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:21-hydroxylase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=31
  446. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:adenylosuccinate lyase deficiency (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=31
  447. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:al awadi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=31
  448. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:alstrom syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=31
  449. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:aminomethyltransferase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=31
  450. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:amniotic band syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=31
  451. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:aortic arch syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:aortic arch syndrome | rel=r_associated | relid=0 | w=31
  452. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:apl differentiation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:apl differentiation syndrome | rel=r_associated | relid=0 | w=31
  453. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:arterial tortuosity syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=31
  454. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:ataxia with vitamin e deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=31
  455. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:atransferrinemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:atransferrinemia | rel=r_associated | relid=0 | w=31
  456. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:behr syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:behr syndrome | rel=r_associated | relid=0 | w=31
  457. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:calciphylaxis
    n1=en:pseudotrisomy 13 syndrome | n2=en:calciphylaxis | rel=r_associated | relid=0 | w=31
  458. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:cardiofaciocutaneous syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cardiofaciocutaneous syndrome | rel=r_associated | relid=0 | w=31
  459. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:cerebellar mutism
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebellar mutism | rel=r_associated | relid=0 | w=31
  460. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:cervicocranial syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cervicocranial syndrome | rel=r_associated | relid=0 | w=31
  461. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:childhood myocerebrohepatopathy spectrum
    n1=en:pseudotrisomy 13 syndrome | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=31
  462. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:chromosome 2q37 deletion syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chromosome 2q37 deletion syndrome | rel=r_associated | relid=0 | w=31
  463. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:chronic fatigue syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chronic fatigue syndrome | rel=r_associated | relid=0 | w=31
  464. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:codas syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:codas syndrome | rel=r_associated | relid=0 | w=31
  465. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:cohen syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=31
  466. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:complete trisomy 18 syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=31
  467. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:congenital absence of kidney
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital absence of kidney | rel=r_associated | relid=0 | w=31
  468. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:congenital fiber-type disproportion
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital fiber-type disproportion | rel=r_associated | relid=0 | w=31
  469. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:cushing syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cushing syndrome | rel=r_associated | relid=0 | w=31
  470. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:cytokine release syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cytokine release syndrome | rel=r_associated | relid=0 | w=31
  471. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:deafness, autosomal recessive 1a
    n1=en:pseudotrisomy 13 syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=31
  472. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:deafness, autosomal recessive 49
    n1=en:pseudotrisomy 13 syndrome | n2=en:deafness, autosomal recessive 49 | rel=r_associated | relid=0 | w=31
  473. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:dentatorubral-pallidoluysian atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=31
  474. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:desmosterolosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=31
  475. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:diarrhea-associated hemolytic uremic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:diarrhea-associated hemolytic uremic syndrome | rel=r_associated | relid=0 | w=31
  476. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:dihydropyrimidine dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  477. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:dihydrouracil dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:dihydrouracil dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  478. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:donohue syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=31
  479. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:dravet syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dravet syndrome | rel=r_associated | relid=0 | w=31
  480. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:duplicate vagina
    n1=en:pseudotrisomy 13 syndrome | n2=en:duplicate vagina | rel=r_associated | relid=0 | w=31
  481. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:dyggve-melchior-clausen syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dyggve-melchior-clausen syndrome | rel=r_associated | relid=0 | w=31
  482. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:epidermolysis bullosa
    n1=en:pseudotrisomy 13 syndrome | n2=en:epidermolysis bullosa | rel=r_associated | relid=0 | w=31
  483. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:familial atypical hemolytic uremic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial atypical hemolytic uremic syndrome | rel=r_associated | relid=0 | w=31
  484. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:familial mediterranean fever
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial mediterranean fever | rel=r_associated | relid=0 | w=31
  485. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:fetal akinesia deformation sequence
    n1=en:pseudotrisomy 13 syndrome | n2=en:fetal akinesia deformation sequence | rel=r_associated | relid=0 | w=31
  486. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:gerstmann-straussler-scheinker disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=31
  487. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:greig syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:greig syndrome | rel=r_associated | relid=0 | w=31
  488. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:guillain-barre syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:guillain-barre syndrome | rel=r_associated | relid=0 | w=31
  489. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hajdu-cheney syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hajdu-cheney syndrome | rel=r_associated | relid=0 | w=31
  490. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hard skin syndrome parana type
    n1=en:pseudotrisomy 13 syndrome | n2=en:hard skin syndrome parana type | rel=r_associated | relid=0 | w=31
  491. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hemophagocytic lymphohistiocytosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hemophagocytic lymphohistiocytosis | rel=r_associated | relid=0 | w=31
  492. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary factor xi deficiency disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary factor xi deficiency disease | rel=r_associated | relid=0 | w=31
  493. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary spastic paralysis, infantile onset ascending
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=31
  494. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hermansky-pudlak syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hermansky-pudlak syndrome | rel=r_associated | relid=0 | w=31
  495. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:heterotaxy syndrome with asplenia
    n1=en:pseudotrisomy 13 syndrome | n2=en:heterotaxy syndrome with asplenia | rel=r_associated | relid=0 | w=31
  496. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hnsha due to glutathione synthetase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:hnsha due to glutathione synthetase deficiency | rel=r_associated | relid=0 | w=31
  497. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:holoprosencephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=31
  498. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:holoprosencephaly type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly type 1 | rel=r_associated | relid=0 | w=31
  499. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hyperkalemic periodic paralysis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperkalemic periodic paralysis | rel=r_associated | relid=0 | w=31
  500. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hyperprolinemia type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=31
  501. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hypoalphalipoproteinemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypoalphalipoproteinemia | rel=r_associated | relid=0 | w=31
  502. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hypophosphatemic rickets with hypercalciuria, hereditary
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=31
  503. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:hypotonia
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypotonia | rel=r_associated | relid=0 | w=31
  504. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:jacobsen syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=31
  505. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:juvenile x-linked retinoschisis
    n1=en:pseudotrisomy 13 syndrome | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=31
  506. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:kawasaki disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:kawasaki disease | rel=r_associated | relid=0 | w=31
  507. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:kluver-bucy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:kluver-bucy syndrome | rel=r_associated | relid=0 | w=31
  508. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:lateral medullary syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lateral medullary syndrome | rel=r_associated | relid=0 | w=31
  509. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:laurence-moon syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=31
  510. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:leber hereditary optic atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:leber hereditary optic atrophy | rel=r_associated | relid=0 | w=31
  511. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:lennox-gastaut syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lennox-gastaut syndrome | rel=r_associated | relid=0 | w=31
  512. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:leprosy
    n1=en:pseudotrisomy 13 syndrome | n2=en:leprosy | rel=r_associated | relid=0 | w=31
  513. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:lesch-nyhan syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=31
  514. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
    n1=en:pseudotrisomy 13 syndrome | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=31
  515. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:lubs x-linked mental retardation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=31
  516. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:mallory-weiss syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mallory-weiss syndrome | rel=r_associated | relid=0 | w=31
  517. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:mandibuloacral dysplasia with type a lipodystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=31
  518. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:marles greenberg persaud syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=31
  519. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:mayer-rokitansky-kuster-hauser syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mayer-rokitansky-kuster-hauser syndrome | rel=r_associated | relid=0 | w=31
  520. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:meconium aspiration syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:meconium aspiration syndrome | rel=r_associated | relid=0 | w=31
  521. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  522. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:meningeal tuberculosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:meningeal tuberculosis | rel=r_associated | relid=0 | w=31
  523. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:methylene thf reductase deficiency and homocystinuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=31
  524. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:miliaria
    n1=en:pseudotrisomy 13 syndrome | n2=en:miliaria | rel=r_associated | relid=0 | w=31
  525. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:mobius syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=31
  526. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:mowat-wilson syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=31
  527. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:myopathy with exercise intolerance, swedish type
    n1=en:pseudotrisomy 13 syndrome | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=31
  528. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:myopathy, congenital nonprogressive with moebius and robin sequences
    n1=en:pseudotrisomy 13 syndrome | n2=en:myopathy, congenital nonprogressive with moebius and robin sequences | rel=r_associated | relid=0 | w=31
  529. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:n-acetylglutamate synthase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=31
  530. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:neurodegeneration with brain iron accumulation 4
    n1=en:pseudotrisomy 13 syndrome | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=31
  531. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:neuropathy, hereditary sensory and autonomic, type vii
    n1=en:pseudotrisomy 13 syndrome | n2=en:neuropathy, hereditary sensory and autonomic, type vii | rel=r_associated | relid=0 | w=31
  532. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:neutral lipid storage disease with myopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=31
  533. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:non-trisomic autosomal aneuploidy
    n1=en:pseudotrisomy 13 syndrome | n2=en:non-trisomic autosomal aneuploidy | rel=r_associated | relid=0 | w=31
  534. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:noonan syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=31
  535. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:orotic aciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=31
  536. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:overgrowth syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:overgrowth syndrome | rel=r_associated | relid=0 | w=31
  537. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:pain agnosia
    n1=en:pseudotrisomy 13 syndrome | n2=en:pain agnosia | rel=r_associated | relid=0 | w=31
  538. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:pain amplification syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pain amplification syndrome | rel=r_associated | relid=0 | w=31
  539. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:pancreatic lipase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:pancreatic lipase deficiency | rel=r_associated | relid=0 | w=31
  540. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:peeling skin syndrome, acral type
    n1=en:pseudotrisomy 13 syndrome | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=31
  541. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:pena-shokeir syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pena-shokeir syndrome | rel=r_associated | relid=0 | w=31
  542. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:pettigrew syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pettigrew syndrome | rel=r_associated | relid=0 | w=31
  543. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:plague
    n1=en:pseudotrisomy 13 syndrome | n2=en:plague | rel=r_associated | relid=0 | w=31
  544. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:porphyria cutanea tarda
    n1=en:pseudotrisomy 13 syndrome | n2=en:porphyria cutanea tarda | rel=r_associated | relid=0 | w=31
  545. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:postural orthostatic tachycardia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:postural orthostatic tachycardia syndrome | rel=r_associated | relid=0 | w=31
  546. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:prickle1-related progressive myoclonus epilepsy with ataxia
    n1=en:pseudotrisomy 13 syndrome | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=31
  547. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:progressive hemifacial atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:progressive hemifacial atrophy | rel=r_associated | relid=0 | w=31
  548. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:pseudohypoaldosteronism, type 1, recessive form
    n1=en:pseudotrisomy 13 syndrome | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=31
  549. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:pyle metaphyseal dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=31
  550. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:renal coloboma syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:renal coloboma syndrome | rel=r_associated | relid=0 | w=31
  551. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:richards-rundle syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=31
  552. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:sanfilippo syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=31
  553. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:scheie syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:scheie syndrome | rel=r_associated | relid=0 | w=31
  554. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:schwartz-jampel syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:schwartz-jampel syndrome | rel=r_associated | relid=0 | w=31
  555. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:septo-optic dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:septo-optic dysplasia | rel=r_associated | relid=0 | w=31
  556. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:shone syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:shone syndrome | rel=r_associated | relid=0 | w=31
  557. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:shprintzen-goldberg craniosynostosis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:shprintzen-goldberg craniosynostosis syndrome | rel=r_associated | relid=0 | w=31
  558. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:small penis
    n1=en:pseudotrisomy 13 syndrome | n2=en:small penis | rel=r_associated | relid=0 | w=31
  559. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:spinal muscular atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:spinal muscular atrophy | rel=r_associated | relid=0 | w=31
  560. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:stiff skin syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:stiff skin syndrome | rel=r_associated | relid=0 | w=31
  561. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:stokes-adams syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:stokes-adams syndrome | rel=r_associated | relid=0 | w=31
  562. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:sunct syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sunct syndrome | rel=r_associated | relid=0 | w=31
  563. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:susac syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:susac syndrome | rel=r_associated | relid=0 | w=31
  564. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:teething syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:teething syndrome | rel=r_associated | relid=0 | w=31
  565. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:tempi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:tempi syndrome | rel=r_associated | relid=0 | w=31
  566. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:thrombocytopenia 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:thrombocytopenia 2 | rel=r_associated | relid=0 | w=31
  567. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:tooth and nail syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:tooth and nail syndrome | rel=r_associated | relid=0 | w=31
  568. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:transcobalamin ii deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=31
  569. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:transient global amnesia
    n1=en:pseudotrisomy 13 syndrome | n2=en:transient global amnesia | rel=r_associated | relid=0 | w=31
  570. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:treacher collins syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=31
  571. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:trisomy
    n1=en:pseudotrisomy 13 syndrome | n2=en:trisomy | rel=r_associated | relid=0 | w=31
  572. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:tungland bellman syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=31
  573. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:undescended testes
    n1=en:pseudotrisomy 13 syndrome | n2=en:undescended testes | rel=r_associated | relid=0 | w=31
  574. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:van der woude syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:van der woude syndrome | rel=r_associated | relid=0 | w=31
  575. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:wallerian degeneration
    n1=en:pseudotrisomy 13 syndrome | n2=en:wallerian degeneration | rel=r_associated | relid=0 | w=31
  576. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:wiskott-aldrich syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=31
  577. en:pseudotrisomy 13 syndrome -- r_associated #0: 31 / 0.721 -> en:x-linked creatine transporter deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:x-linked creatine transporter deficiency | rel=r_associated | relid=0 | w=31
  578. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:abetalipoproteinemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:abetalipoproteinemia | rel=r_associated | relid=0 | w=30
  579. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:acatalasemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:acatalasemia | rel=r_associated | relid=0 | w=30
  580. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:achondrogenesis
    n1=en:pseudotrisomy 13 syndrome | n2=en:achondrogenesis | rel=r_associated | relid=0 | w=30
  581. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:acromegaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:acromegaly | rel=r_associated | relid=0 | w=30
  582. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:acute intermittent porphyria
    n1=en:pseudotrisomy 13 syndrome | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=30
  583. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:adenine phosphoribosyltransferase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=30
  584. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:adrenal hypoplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:adrenal hypoplasia | rel=r_associated | relid=0 | w=30
  585. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:alagille syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=30
  586. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:allgrove syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=30
  587. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:amaurosis fugax
    n1=en:pseudotrisomy 13 syndrome | n2=en:amaurosis fugax | rel=r_associated | relid=0 | w=30
  588. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:analbuminemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:analbuminemia | rel=r_associated | relid=0 | w=30
  589. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:antley-bixler syndrome, autosomal dominant
    n1=en:pseudotrisomy 13 syndrome | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=30
  590. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:aprosencephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:aprosencephaly | rel=r_associated | relid=0 | w=30
  591. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:argininemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:argininemia | rel=r_associated | relid=0 | w=30
  592. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=30
  593. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:atrial septal defect
    n1=en:pseudotrisomy 13 syndrome | n2=en:atrial septal defect | rel=r_associated | relid=0 | w=30
  594. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:atrioventricular canal structure
    n1=en:pseudotrisomy 13 syndrome | n2=en:atrioventricular canal structure | rel=r_associated | relid=0 | w=30
  595. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal recessive primary microcephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=30
  596. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal recessive spastic paraplegia type 11
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=30
  597. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:barrett esophagus
    n1=en:pseudotrisomy 13 syndrome | n2=en:barrett esophagus | rel=r_associated | relid=0 | w=30
  598. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:basal ganglia disease, biotin-responsive
    n1=en:pseudotrisomy 13 syndrome | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=30
  599. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:behcet syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:behcet syndrome | rel=r_associated | relid=0 | w=30
  600. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:bernard-soulier syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:bernard-soulier syndrome | rel=r_associated | relid=0 | w=30
  601. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:brachydactyly syndrome type b
    n1=en:pseudotrisomy 13 syndrome | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=30
  602. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:brody myopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:brody myopathy | rel=r_associated | relid=0 | w=30
  603. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:cat-eye syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cat-eye syndrome | rel=r_associated | relid=0 | w=30
  604. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:cauda equina syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cauda equina syndrome | rel=r_associated | relid=0 | w=30
  605. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:cayler cardiofacial syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cayler cardiofacial syndrome | rel=r_associated | relid=0 | w=30
  606. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:char syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:char syndrome | rel=r_associated | relid=0 | w=30
  607. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:charge syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:charge syndrome | rel=r_associated | relid=0 | w=30
  608. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:chitty hall baraitser syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=30
  609. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:chronic infantile neurological cutaneous and articular syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chronic infantile neurological cutaneous and articular syndrome | rel=r_associated | relid=0 | w=30
  610. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:cleft lip sequence
    n1=en:pseudotrisomy 13 syndrome | n2=en:cleft lip sequence | rel=r_associated | relid=0 | w=30
  611. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:cogan-reese syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cogan-reese syndrome | rel=r_associated | relid=0 | w=30
  612. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:compartment syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:compartment syndrome | rel=r_associated | relid=0 | w=30
  613. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:complete trisomy 13 syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:complete trisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  614. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:complex regional pain syndrome i
    n1=en:pseudotrisomy 13 syndrome | n2=en:complex regional pain syndrome i | rel=r_associated | relid=0 | w=30
  615. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:congenital cataracts, facial dysmorphism, and neuropathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=30
  616. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:congenital central hypoventilation
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital central hypoventilation | rel=r_associated | relid=0 | w=30
  617. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:congenital disorder of glycosylation type ic
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=30
  618. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:congenital dyserythropoietic anemia, type i
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=30
  619. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:craniofacial dysostosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:craniofacial dysostosis | rel=r_associated | relid=0 | w=30
  620. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:cryptophthalmos syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=30
  621. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:darier disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:darier disease | rel=r_associated | relid=0 | w=30
  622. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:deafness-craniofacial syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=30
  623. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:diffuse cerebral sclerosis of schilder
    n1=en:pseudotrisomy 13 syndrome | n2=en:diffuse cerebral sclerosis of schilder | rel=r_associated | relid=0 | w=30
  624. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:duplicate uterus
    n1=en:pseudotrisomy 13 syndrome | n2=en:duplicate uterus | rel=r_associated | relid=0 | w=30
  625. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:ectromelia
    n1=en:pseudotrisomy 13 syndrome | n2=en:ectromelia | rel=r_associated | relid=0 | w=30
  626. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:escobar syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:escobar syndrome | rel=r_associated | relid=0 | w=30
  627. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:familial partial lipodystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial partial lipodystrophy | rel=r_associated | relid=0 | w=30
  628. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:fetal retinoid syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fetal retinoid syndrome | rel=r_associated | relid=0 | w=30
  629. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:friedreich ataxia
    n1=en:pseudotrisomy 13 syndrome | n2=en:friedreich ataxia | rel=r_associated | relid=0 | w=30
  630. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:frohlich syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:frohlich syndrome | rel=r_associated | relid=0 | w=30
  631. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:frontonasal dysplasia sequence
    n1=en:pseudotrisomy 13 syndrome | n2=en:frontonasal dysplasia sequence | rel=r_associated | relid=0 | w=30
  632. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:frontotemporal dementia
    n1=en:pseudotrisomy 13 syndrome | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=30
  633. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:fuchs endothelial dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:fuchs endothelial dystrophy | rel=r_associated | relid=0 | w=30
  634. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:gilbert syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:gilbert syndrome | rel=r_associated | relid=0 | w=30
  635. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:glutaric acidemia type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:glutaric acidemia type 1 | rel=r_associated | relid=0 | w=30
  636. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:glycogen storage disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=30
  637. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:glycogen storage disease type i
    n1=en:pseudotrisomy 13 syndrome | n2=en:glycogen storage disease type i | rel=r_associated | relid=0 | w=30
  638. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:goldenhar syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=30
  639. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:hallermann syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hallermann syndrome | rel=r_associated | relid=0 | w=30
  640. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:hemophagocytic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hemophagocytic syndrome | rel=r_associated | relid=0 | w=30
  641. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:holt-oram syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=30
  642. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:hyperimmunoglobulin e syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperimmunoglobulin e syndrome | rel=r_associated | relid=0 | w=30
  643. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:hyperphosphatasia with mental retardation
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=30
  644. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:immunodeficiency syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:immunodeficiency syndrome | rel=r_associated | relid=0 | w=30
  645. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:infantile hypophosphatasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=30
  646. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:inspissated bile syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:inspissated bile syndrome | rel=r_associated | relid=0 | w=30
  647. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:intestinal atresia
    n1=en:pseudotrisomy 13 syndrome | n2=en:intestinal atresia | rel=r_associated | relid=0 | w=30
  648. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:isolated hypoplasia of the right ventricle
    n1=en:pseudotrisomy 13 syndrome | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=30
  649. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:jankovic rivera syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=30
  650. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:kartagener syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:kartagener syndrome | rel=r_associated | relid=0 | w=30
  651. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:karyotype analysis normal finding
    n1=en:pseudotrisomy 13 syndrome | n2=en:karyotype analysis normal finding | rel=r_associated | relid=0 | w=30
  652. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:kundrat's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:kundrat's syndrome | rel=r_associated | relid=0 | w=30
  653. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:landau-kleffner syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:landau-kleffner syndrome | rel=r_associated | relid=0 | w=30
  654. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:lateral cleft lip
    n1=en:pseudotrisomy 13 syndrome | n2=en:lateral cleft lip | rel=r_associated | relid=0 | w=30
  655. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:laurin-sandrow syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=30
  656. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:leopard syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=30
  657. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:lysinuric protein intolerance
    n1=en:pseudotrisomy 13 syndrome | n2=en:lysinuric protein intolerance | rel=r_associated | relid=0 | w=30
  658. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:macdermot winter syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=30
  659. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:malsegmentation
    n1=en:pseudotrisomy 13 syndrome | n2=en:malsegmentation | rel=r_associated | relid=0 | w=30
  660. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:melkersson-rosenthal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:melkersson-rosenthal syndrome | rel=r_associated | relid=0 | w=30
  661. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:melorheostosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:melorheostosis | rel=r_associated | relid=0 | w=30
  662. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=30
  663. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:methylcrotonyl-coa carboxylase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=30
  664. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:microphthalmos
    n1=en:pseudotrisomy 13 syndrome | n2=en:microphthalmos | rel=r_associated | relid=0 | w=30
  665. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:mirror polydactyly, vertebral segmentation and limb defect syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mirror polydactyly, vertebral segmentation and limb defect syndrome | rel=r_associated | relid=0 | w=30
  666. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:muscle-eye-brain disease, congenital muscular dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:muscle-eye-brain disease, congenital muscular dystrophy | rel=r_associated | relid=0 | w=30
  667. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:nephrocalcinosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:nephrocalcinosis | rel=r_associated | relid=0 | w=30
  668. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:neural tube defect
    n1=en:pseudotrisomy 13 syndrome | n2=en:neural tube defect | rel=r_associated | relid=0 | w=30
  669. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:neuronal intranuclear inclusion disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:neuronal intranuclear inclusion disease | rel=r_associated | relid=0 | w=30
  670. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:obstructive sleep apnea syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:obstructive sleep apnea syndrome | rel=r_associated | relid=0 | w=30
  671. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:omphalocele
    n1=en:pseudotrisomy 13 syndrome | n2=en:omphalocele | rel=r_associated | relid=0 | w=30
  672. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:optic neuritis
    n1=en:pseudotrisomy 13 syndrome | n2=en:optic neuritis | rel=r_associated | relid=0 | w=30
  673. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:overlap syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:overlap syndrome | rel=r_associated | relid=0 | w=30
  674. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:pallister-killian syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pallister-killian syndrome | rel=r_associated | relid=0 | w=30
  675. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:papillon-lefevre syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=30
  676. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:parinaud syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:parinaud syndrome | rel=r_associated | relid=0 | w=30
  677. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:penta x syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:penta x syndrome | rel=r_associated | relid=0 | w=30
  678. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:perlman syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:perlman syndrome | rel=r_associated | relid=0 | w=30
  679. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:pierre robin syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pierre robin syndrome | rel=r_associated | relid=0 | w=30
  680. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:pityriasis lichenoides
    n1=en:pseudotrisomy 13 syndrome | n2=en:pityriasis lichenoides | rel=r_associated | relid=0 | w=30
  681. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=30
  682. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:polydactyly preaxial type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:polydactyly preaxial type 1 | rel=r_associated | relid=0 | w=30
  683. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:popliteal pterygium syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=30
  684. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:posterior fossa syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:posterior fossa syndrome | rel=r_associated | relid=0 | w=30
  685. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:prader-willi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=30
  686. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:primary progressive aphasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:primary progressive aphasia | rel=r_associated | relid=0 | w=30
  687. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:pseudohypoaldosteronism
    n1=en:pseudotrisomy 13 syndrome | n2=en:pseudohypoaldosteronism | rel=r_associated | relid=0 | w=30
  688. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:rhizomelic dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:rhizomelic dysplasia | rel=r_associated | relid=0 | w=30
  689. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:rozin hertz goodman syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:rozin hertz goodman syndrome | rel=r_associated | relid=0 | w=30
  690. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:schinzel-giedion midface-retraction syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=30
  691. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:sinus histiocytosis with massive lymphadenopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:sinus histiocytosis with massive lymphadenopathy | rel=r_associated | relid=0 | w=30
  692. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:somnolence syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:somnolence syndrome | rel=r_associated | relid=0 | w=30
  693. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:spondyloepiphyseal dysplasia, omani type
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=30
  694. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:syndromic orbital border hypoplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=30
  695. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:thyroid hormone resistance syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:thyroid hormone resistance syndrome | rel=r_associated | relid=0 | w=30
  696. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:tolosa-hunt syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:tolosa-hunt syndrome | rel=r_associated | relid=0 | w=30
  697. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:tyrosinemia type ii
    n1=en:pseudotrisomy 13 syndrome | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=30
  698. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:usher syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:usher syndrome | rel=r_associated | relid=0 | w=30
  699. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:very long-chain acyl-coa dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:very long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=30
  700. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:waardenburg anophthalmia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=30
  701. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:waardenburg syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:waardenburg syndrome | rel=r_associated | relid=0 | w=30
  702. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:whipple disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:whipple disease | rel=r_associated | relid=0 | w=30
  703. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:x-linked dominant hypophosphatemic rickets
    n1=en:pseudotrisomy 13 syndrome | n2=en:x-linked dominant hypophosphatemic rickets | rel=r_associated | relid=0 | w=30
  704. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:xanthinuria, type i
    n1=en:pseudotrisomy 13 syndrome | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=30
  705. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> en:xxxy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:xxxy syndrome | rel=r_associated | relid=0 | w=30
  706. en:pseudotrisomy 13 syndrome -- r_associated #0: 30 / 0.698 -> peste
    (maladie)
    n1=en:pseudotrisomy 13 syndrome | n2=peste
    (maladie)
    | rel=r_associated | relid=0 | w=30
  707. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:22q telomere deletion syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:22q telomere deletion syndrome | rel=r_associated | relid=0 | w=29
  708. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:3-methylglutaconic aciduria type 5
    n1=en:pseudotrisomy 13 syndrome | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=29
  709. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=29
  710. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:abstinence syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:abstinence syndrome | rel=r_associated | relid=0 | w=29
  711. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:acroparesthesia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:acroparesthesia syndrome | rel=r_associated | relid=0 | w=29
  712. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:atypical hemolytic uremic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:atypical hemolytic uremic syndrome | rel=r_associated | relid=0 | w=29
  713. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:autoimmune polyendocrinopathy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:autoimmune polyendocrinopathy syndrome | rel=r_associated | relid=0 | w=29
  714. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal recessive distal osteolysis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=29
  715. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal recessive hypohidrotic ectodermal dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive hypohidrotic ectodermal dysplasia | rel=r_associated | relid=0 | w=29
  716. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal recessive ocular albinism
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=29
  717. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:benign mucous membrane pemphigoid
    n1=en:pseudotrisomy 13 syndrome | n2=en:benign mucous membrane pemphigoid | rel=r_associated | relid=0 | w=29
  718. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:bicornuate uterus
    n1=en:pseudotrisomy 13 syndrome | n2=en:bicornuate uterus | rel=r_associated | relid=0 | w=29
  719. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:burning mouth syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:burning mouth syndrome | rel=r_associated | relid=0 | w=29
  720. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:carnitine palmitoyltransferase ii deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:carnitine palmitoyltransferase ii deficiency | rel=r_associated | relid=0 | w=29
  721. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:cataplexy
    n1=en:pseudotrisomy 13 syndrome | n2=en:cataplexy | rel=r_associated | relid=0 | w=29
  722. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=29
  723. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:chromosome 17, trisomy 17p
    n1=en:pseudotrisomy 13 syndrome | n2=en:chromosome 17, trisomy 17p | rel=r_associated | relid=0 | w=29
  724. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:coffin-lowry syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:coffin-lowry syndrome | rel=r_associated | relid=0 | w=29
  725. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:congenital hand deformities
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital hand deformities | rel=r_associated | relid=0 | w=29
  726. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:congenital pain insensitivity
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=29
  727. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:congenital plasminogen activator inhibitor deficiency type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=29
  728. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:congenital sucrase-isomaltase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=29
  729. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:cryopyrin-associated periodic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cryopyrin-associated periodic syndrome | rel=r_associated | relid=0 | w=29
  730. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:cystathionine beta-synthase deficiency disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=29
  731. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:deafness, progressive, with stapes fixation
    n1=en:pseudotrisomy 13 syndrome | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=29
  732. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:deep scrotal raphe
    n1=en:pseudotrisomy 13 syndrome | n2=en:deep scrotal raphe | rel=r_associated | relid=0 | w=29
  733. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:deficiency of fructokinase
    n1=en:pseudotrisomy 13 syndrome | n2=en:deficiency of fructokinase | rel=r_associated | relid=0 | w=29
  734. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:dialyzer first use syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dialyzer first use syndrome | rel=r_associated | relid=0 | w=29
  735. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:diencephalic syndrome of infancy
    n1=en:pseudotrisomy 13 syndrome | n2=en:diencephalic syndrome of infancy | rel=r_associated | relid=0 | w=29
  736. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:diethylstilbestrol syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:diethylstilbestrol syndrome | rel=r_associated | relid=0 | w=29
  737. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:donnai-barrow syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=29
  738. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:dubin-johnson syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=29
  739. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:dyschromatosis symmetrica hereditaria
    n1=en:pseudotrisomy 13 syndrome | n2=en:dyschromatosis symmetrica hereditaria | rel=r_associated | relid=0 | w=29
  740. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:ear, patella, short stature syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=29
  741. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:ehlers-danlos syndrome, arthrochalasia type
    n1=en:pseudotrisomy 13 syndrome | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=29
  742. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:ehlers-danlos syndrome, type vi
    n1=en:pseudotrisomy 13 syndrome | n2=en:ehlers-danlos syndrome, type vi | rel=r_associated | relid=0 | w=29
  743. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:factor v leiden
    n1=en:pseudotrisomy 13 syndrome | n2=en:factor v leiden | rel=r_associated | relid=0 | w=29
  744. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:freeman-sheldon syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=29
  745. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:fucosidosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:fucosidosis | rel=r_associated | relid=0 | w=29
  746. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:gangrenous stomatitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:gangrenous stomatitis | rel=r_associated | relid=0 | w=29
  747. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:generalized arterial calcification of infancy 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:generalized arterial calcification of infancy 1 | rel=r_associated | relid=0 | w=29
  748. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:glutamate-cysteine ligase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=29
  749. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:hand polydactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:hand polydactyly | rel=r_associated | relid=0 | w=29
  750. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:hereditary orotic aciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=29
  751. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:hexadactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:hexadactyly | rel=r_associated | relid=0 | w=29
  752. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:homocystinuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:homocystinuria | rel=r_associated | relid=0 | w=29
  753. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:horner syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:horner syndrome | rel=r_associated | relid=0 | w=29
  754. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:hydrops fetalis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hydrops fetalis | rel=r_associated | relid=0 | w=29
  755. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:hyperprolinemia type 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=29
  756. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:hypoplastic left heart syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypoplastic left heart syndrome | rel=r_associated | relid=0 | w=29
  757. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:immunodeficiency with hyper-igm type 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:immunodeficiency with hyper-igm type 2 | rel=r_associated | relid=0 | w=29
  758. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:infantile neuroaxonal dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:infantile neuroaxonal dystrophy | rel=r_associated | relid=0 | w=29
  759. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:intestinal epithelial dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=29
  760. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:klippel-feil syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=29
  761. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:kshv inflammatory cytokine syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:kshv inflammatory cytokine syndrome | rel=r_associated | relid=0 | w=29
  762. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:lactase deficiency, congenital
    n1=en:pseudotrisomy 13 syndrome | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=29
  763. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:lecithin acyltransferase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=29
  764. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:leptospirosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:leptospirosis | rel=r_associated | relid=0 | w=29
  765. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:leukodystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=29
  766. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:lipase hypersecretion syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lipase hypersecretion syndrome | rel=r_associated | relid=0 | w=29
  767. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:pseudotrisomy 13 syndrome | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=29
  768. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:lupus anticoagulant disorder
    n1=en:pseudotrisomy 13 syndrome | n2=en:lupus anticoagulant disorder | rel=r_associated | relid=0 | w=29
  769. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:maroteaux-lamy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=29
  770. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:melas syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:melas syndrome | rel=r_associated | relid=0 | w=29
  771. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:menkes disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:menkes disease | rel=r_associated | relid=0 | w=29
  772. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:mesoaxial polydactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:mesoaxial polydactyly | rel=r_associated | relid=0 | w=29
  773. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=29
  774. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:microcephaly cervical spine fusion anomalies
    n1=en:pseudotrisomy 13 syndrome | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=29
  775. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:multicentric osteolysis, nodulosis, and arthropathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:multicentric osteolysis, nodulosis, and arthropathy | rel=r_associated | relid=0 | w=29
  776. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:myopathy, early-onset, with fatal cardiomyopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=29
  777. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:naxos disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:naxos disease | rel=r_associated | relid=0 | w=29
  778. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:neuromyelitis optica
    n1=en:pseudotrisomy 13 syndrome | n2=en:neuromyelitis optica | rel=r_associated | relid=0 | w=29
  779. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:oculo-respiratory syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:oculo-respiratory syndrome | rel=r_associated | relid=0 | w=29
  780. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:olivopontocerebellar atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:olivopontocerebellar atrophy | rel=r_associated | relid=0 | w=29
  781. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:ossification of posterior longitudinal ligament
    n1=en:pseudotrisomy 13 syndrome | n2=en:ossification of posterior longitudinal ligament | rel=r_associated | relid=0 | w=29
  782. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:paroxysmal extreme pain disorder
    n1=en:pseudotrisomy 13 syndrome | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=29
  783. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:plummer-vinson syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:plummer-vinson syndrome | rel=r_associated | relid=0 | w=29
  784. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:polymicrogyria
    n1=en:pseudotrisomy 13 syndrome | n2=en:polymicrogyria | rel=r_associated | relid=0 | w=29
  785. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:pseudotumor cerebri
    n1=en:pseudotrisomy 13 syndrome | n2=en:pseudotumor cerebri | rel=r_associated | relid=0 | w=29
  786. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:purine-nucleoside phosphorylase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=29
  787. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:pyramidal tract dysfunction
    n1=en:pseudotrisomy 13 syndrome | n2=en:pyramidal tract dysfunction | rel=r_associated | relid=0 | w=29
  788. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:pyruvate carboxylase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=29
  789. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:sitosterolemia with xanthomatosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=29
  790. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:sjogren-larsson syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=29
  791. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:spondylocarpotarsal synostosis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=29
  792. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:sulfite oxidase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=29
  793. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:takotsubo cardiomyopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:takotsubo cardiomyopathy | rel=r_associated | relid=0 | w=29
  794. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:thoracic outlet syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:thoracic outlet syndrome | rel=r_associated | relid=0 | w=29
  795. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:thyroid dyshormonogenesis 4
    n1=en:pseudotrisomy 13 syndrome | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=29
  796. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:toxic shock syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:toxic shock syndrome | rel=r_associated | relid=0 | w=29
  797. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:trichohepatoenteric syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=29
  798. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:trichorhinophalangeal syndrome type ii
    n1=en:pseudotrisomy 13 syndrome | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=29
  799. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:urea cycle metabolism disorder
    n1=en:pseudotrisomy 13 syndrome | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=29
  800. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:warsaw breakage syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=29
  801. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> en:wildervanck's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:wildervanck's syndrome | rel=r_associated | relid=0 | w=29
  802. en:pseudotrisomy 13 syndrome -- r_associated #0: 29 / 0.674 -> syndrome de Marfan
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=29
  803. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:absent olfactory tracts and bulbs
    n1=en:pseudotrisomy 13 syndrome | n2=en:absent olfactory tracts and bulbs | rel=r_associated | relid=0 | w=28
  804. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:acrocallosal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=28
  805. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:acyl-coa dehydrogenase, short-chain deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:acyl-coa dehydrogenase, short-chain deficiency | rel=r_associated | relid=0 | w=28
  806. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:aicardi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=28
  807. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:albinotic fundus
    n1=en:pseudotrisomy 13 syndrome | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=28
  808. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:alkaptonuria
    n1=en:pseudotrisomy 13 syndrome | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=28
  809. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:alpha thalassemia x-linked mental retardation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:alpha thalassemia x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=28
  810. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=28
  811. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:aniridia
    n1=en:pseudotrisomy 13 syndrome | n2=en:aniridia | rel=r_associated | relid=0 | w=28
  812. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:antithrombin iii deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:antithrombin iii deficiency | rel=r_associated | relid=0 | w=28
  813. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:aortic coarctation
    n1=en:pseudotrisomy 13 syndrome | n2=en:aortic coarctation | rel=r_associated | relid=0 | w=28
  814. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:arnold-chiari malformation
    n1=en:pseudotrisomy 13 syndrome | n2=en:arnold-chiari malformation | rel=r_associated | relid=0 | w=28
  815. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=28
  816. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:ateliotic dwarfism without insulinopenia
    n1=en:pseudotrisomy 13 syndrome | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=28
  817. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:atrophic muscular disorder
    n1=en:pseudotrisomy 13 syndrome | n2=en:atrophic muscular disorder | rel=r_associated | relid=0 | w=28
  818. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:auditory perceptual disorder
    n1=en:pseudotrisomy 13 syndrome | n2=en:auditory perceptual disorder | rel=r_associated | relid=0 | w=28
  819. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal recessive scid
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=28
  820. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:bonnevie-ullrich syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:bonnevie-ullrich syndrome | rel=r_associated | relid=0 | w=28
  821. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:brown-sequard syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:brown-sequard syndrome | rel=r_associated | relid=0 | w=28
  822. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:campomelic dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:campomelic dysplasia | rel=r_associated | relid=0 | w=28
  823. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:carnitine palmitoyltransferase i deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:carnitine palmitoyltransferase i deficiency | rel=r_associated | relid=0 | w=28
  824. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:cebocephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:cebocephaly | rel=r_associated | relid=0 | w=28
  825. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:cleft lip/palate-ectodermal dysplasia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=28
  826. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:combined malonic and methylmalonic aciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=28
  827. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:complex regional pain syndrome ii
    n1=en:pseudotrisomy 13 syndrome | n2=en:complex regional pain syndrome ii | rel=r_associated | relid=0 | w=28
  828. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=28
  829. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:congenital cortical hyperostosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital cortical hyperostosis | rel=r_associated | relid=0 | w=28
  830. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:congenital dyserythropoietic anemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital dyserythropoietic anemia | rel=r_associated | relid=0 | w=28
  831. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:congenital structural myopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital structural myopathy | rel=r_associated | relid=0 | w=28
  832. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:conn syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:conn syndrome | rel=r_associated | relid=0 | w=28
  833. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:craniosynostosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=28
  834. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:crigler-najjar syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=28
  835. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:d-bifunctional protein deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:d-bifunctional protein deficiency | rel=r_associated | relid=0 | w=28
  836. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:double cortex syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:double cortex syndrome | rel=r_associated | relid=0 | w=28
  837. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:drug hypersensitivity syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:drug hypersensitivity syndrome | rel=r_associated | relid=0 | w=28
  838. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:duane syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:duane syndrome | rel=r_associated | relid=0 | w=28
  839. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:dumping syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dumping syndrome | rel=r_associated | relid=0 | w=28
  840. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:ectodermal dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=28
  841. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:empty sella syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=28
  842. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:encephalopathy due to sulfite oxidase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=28
  843. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:erythrokeratodermia variabilis
    n1=en:pseudotrisomy 13 syndrome | n2=en:erythrokeratodermia variabilis | rel=r_associated | relid=0 | w=28
  844. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:ethanolaminosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=28
  845. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:fatty acid hydroxylase-associated neurodegeneration
    n1=en:pseudotrisomy 13 syndrome | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=28
  846. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:felty syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:felty syndrome | rel=r_associated | relid=0 | w=28
  847. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:fetal methotrexate syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fetal methotrexate syndrome | rel=r_associated | relid=0 | w=28
  848. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:fragile x syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=28
  849. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:frontonasal dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:frontonasal dysplasia | rel=r_associated | relid=0 | w=28
  850. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:gamma-glutamyltransferase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=28
  851. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:glanzmann thrombasthenia
    n1=en:pseudotrisomy 13 syndrome | n2=en:glanzmann thrombasthenia | rel=r_associated | relid=0 | w=28
  852. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:gray platelet syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:gray platelet syndrome | rel=r_associated | relid=0 | w=28
  853. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:hemochromatosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hemochromatosis | rel=r_associated | relid=0 | w=28
  854. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:hepatolenticular degeneration
    n1=en:pseudotrisomy 13 syndrome | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=28
  855. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary angioedema
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=28
  856. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary persistence of fetal hemoglobin
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary persistence of fetal hemoglobin | rel=r_associated | relid=0 | w=28
  857. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:hunter syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hunter syndrome | rel=r_associated | relid=0 | w=28
  858. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:hyperpipecolatemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperpipecolatemia | rel=r_associated | relid=0 | w=28
  859. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:hyperviscosity syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyperviscosity syndrome | rel=r_associated | relid=0 | w=28
  860. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:hypokalemia, familial
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=28
  861. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:hypospadias-mental retardation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=28
  862. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma
    n1=en:pseudotrisomy 13 syndrome | n2=en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma | rel=r_associated | relid=0 | w=28
  863. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:imperforate vagina
    n1=en:pseudotrisomy 13 syndrome | n2=en:imperforate vagina | rel=r_associated | relid=0 | w=28
  864. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:infantile convulsions and paroxysmal choreoathetosis, familial
    n1=en:pseudotrisomy 13 syndrome | n2=en:infantile convulsions and paroxysmal choreoathetosis, familial | rel=r_associated | relid=0 | w=28
  865. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:isovaleric acidemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=28
  866. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:jervell and lange nielsen syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=28
  867. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:joubert syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=28
  868. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:kaufman-mckusick syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:kaufman-mckusick syndrome | rel=r_associated | relid=0 | w=28
  869. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:korsakoff syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:korsakoff syndrome | rel=r_associated | relid=0 | w=28
  870. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:leber congenital amaurosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:leber congenital amaurosis | rel=r_associated | relid=0 | w=28
  871. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:lethal congenital contracture syndrome 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=28
  872. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:lethal congenital contracture syndrome type 3
    n1=en:pseudotrisomy 13 syndrome | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=28
  873. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:liddle syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=28
  874. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:loeys-dietz syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=28
  875. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:majeed syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=28
  876. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:malabsorption syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:malabsorption syndrome | rel=r_associated | relid=0 | w=28
  877. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:malakoplakia
    n1=en:pseudotrisomy 13 syndrome | n2=en:malakoplakia | rel=r_associated | relid=0 | w=28
  878. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:mcdonough syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mcdonough syndrome | rel=r_associated | relid=0 | w=28
  879. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:meckel-gruber syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:meckel-gruber syndrome | rel=r_associated | relid=0 | w=28
  880. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:mehes syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mehes syndrome | rel=r_associated | relid=0 | w=28
  881. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:melnick-fraser syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=28
  882. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:monilethrix
    n1=en:pseudotrisomy 13 syndrome | n2=en:monilethrix | rel=r_associated | relid=0 | w=28
  883. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:monosomy 13q syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:monosomy 13q syndrome | rel=r_associated | relid=0 | w=28
  884. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:morquio syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=28
  885. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:multicentric osteolysis nodulosis arthropathy spectrum
    n1=en:pseudotrisomy 13 syndrome | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=28
  886. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:myotonic disorder
    n1=en:pseudotrisomy 13 syndrome | n2=en:myotonic disorder | rel=r_associated | relid=0 | w=28
  887. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:nadh dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:nadh dehydrogenase deficiency | rel=r_associated | relid=0 | w=28
  888. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:neuroacanthocytosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=28
  889. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:neurotoxicity syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:neurotoxicity syndrome | rel=r_associated | relid=0 | w=28
  890. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:niemann-pick disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=28
  891. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:osteochondrodysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:osteochondrodysplasia | rel=r_associated | relid=0 | w=28
  892. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:otocephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:otocephaly | rel=r_associated | relid=0 | w=28
  893. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:otoonychoperoneal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=28
  894. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:otopalatodigital syndrome type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:otopalatodigital syndrome type 1 | rel=r_associated | relid=0 | w=28
  895. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:palmar-plantar erythodysthesia
    n1=en:pseudotrisomy 13 syndrome | n2=en:palmar-plantar erythodysthesia | rel=r_associated | relid=0 | w=28
  896. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:pelizaeus merzbacher like disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=28
  897. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:pentalogy of cantrell
    n1=en:pseudotrisomy 13 syndrome | n2=en:pentalogy of cantrell | rel=r_associated | relid=0 | w=28
  898. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:periodic fever syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:periodic fever syndrome | rel=r_associated | relid=0 | w=28
  899. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:persistent mullerian duct syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=28
  900. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:pityriasis rubra pilaris
    n1=en:pseudotrisomy 13 syndrome | n2=en:pityriasis rubra pilaris | rel=r_associated | relid=0 | w=28
  901. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:polydactyly of toes
    n1=en:pseudotrisomy 13 syndrome | n2=en:polydactyly of toes | rel=r_associated | relid=0 | w=28
  902. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:polymyalgia rheumatica
    n1=en:pseudotrisomy 13 syndrome | n2=en:polymyalgia rheumatica | rel=r_associated | relid=0 | w=28
  903. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:post-pericardiotomy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:post-pericardiotomy syndrome | rel=r_associated | relid=0 | w=28
  904. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:potocki-shaffer syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=28
  905. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:potter syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:potter syndrome | rel=r_associated | relid=0 | w=28
  906. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:prader-willi habitus, osteopenia, and camptodactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=28
  907. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:primary carnitine deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:primary carnitine deficiency | rel=r_associated | relid=0 | w=28
  908. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:pseudoxanthoma elasticum
    n1=en:pseudotrisomy 13 syndrome | n2=en:pseudoxanthoma elasticum | rel=r_associated | relid=0 | w=28
  909. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:retinitis punctata albescens (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=28
  910. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:rna polymerase iii-related leukodystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=28
  911. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:sandifer's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sandifer's syndrome | rel=r_associated | relid=0 | w=28
  912. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:sick euthyroid syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sick euthyroid syndrome | rel=r_associated | relid=0 | w=28
  913. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:sick sinus syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sick sinus syndrome | rel=r_associated | relid=0 | w=28
  914. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:sjogren syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sjogren syndrome | rel=r_associated | relid=0 | w=28
  915. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:smith-magenis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=28
  916. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:status epilepticus
    n1=en:pseudotrisomy 13 syndrome | n2=en:status epilepticus | rel=r_associated | relid=0 | w=28
  917. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:stein-leventhal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:stein-leventhal syndrome | rel=r_associated | relid=0 | w=28
  918. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:steinfeld syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=28
  919. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:stiff person syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:stiff person syndrome | rel=r_associated | relid=0 | w=28
  920. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:substance withdrawal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:substance withdrawal syndrome | rel=r_associated | relid=0 | w=28
  921. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:sunset syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sunset syndrome | rel=r_associated | relid=0 | w=28
  922. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:syndrome of apparent mineralocorticoid excess
    n1=en:pseudotrisomy 13 syndrome | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=28
  923. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:tangier disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:tangier disease | rel=r_associated | relid=0 | w=28
  924. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:tethered spinal cord syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:tethered spinal cord syndrome | rel=r_associated | relid=0 | w=28
  925. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:tetra-amelia autosomal recessive
    n1=en:pseudotrisomy 13 syndrome | n2=en:tetra-amelia autosomal recessive | rel=r_associated | relid=0 | w=28
  926. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:tracheobronchomegaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:tracheobronchomegaly | rel=r_associated | relid=0 | w=28
  927. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:upward slant of palpebral fissure
    n1=en:pseudotrisomy 13 syndrome | n2=en:upward slant of palpebral fissure | rel=r_associated | relid=0 | w=28
  928. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:vascular access steal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:vascular access steal syndrome | rel=r_associated | relid=0 | w=28
  929. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:ventricular septal defect
    n1=en:pseudotrisomy 13 syndrome | n2=en:ventricular septal defect | rel=r_associated | relid=0 | w=28
  930. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:vertebral artery syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:vertebral artery syndrome | rel=r_associated | relid=0 | w=28
  931. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:vitelliform macular dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=28
  932. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:walker-warburg syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=28
  933. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:werner syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:werner syndrome | rel=r_associated | relid=0 | w=28
  934. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:wolff-parkinson-white syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:wolff-parkinson-white syndrome | rel=r_associated | relid=0 | w=28
  935. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:xxyy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:xxyy syndrome | rel=r_associated | relid=0 | w=28
  936. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:yellow nail syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=28
  937. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> en:zellweger syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=28
  938. en:pseudotrisomy 13 syndrome -- r_associated #0: 28 / 0.651 -> maladie de Marfan
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Marfan | rel=r_associated | relid=0 | w=28
  939. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:3-methylglutaconic aciduria type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:3-methylglutaconic aciduria type 1 | rel=r_associated | relid=0 | w=27
  940. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:acute respiratory distress syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:acute respiratory distress syndrome | rel=r_associated | relid=0 | w=27
  941. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:adrenal gland hyperplasia ii
    n1=en:pseudotrisomy 13 syndrome | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=27
  942. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:anencephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:anencephaly | rel=r_associated | relid=0 | w=27
  943. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:angelman syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=27
  944. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:arakawa syndrome ii
    n1=en:pseudotrisomy 13 syndrome | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=27
  945. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:autoinflammatory syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:autoinflammatory syndrome | rel=r_associated | relid=0 | w=27
  946. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:autosomal dominant optic atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=27
  947. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:beare-stevenson cutis gyrata syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=27
  948. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:behrens baumann dust syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=27
  949. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:berardinelli-seip congenital lipodystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:berardinelli-seip congenital lipodystrophy | rel=r_associated | relid=0 | w=27
  950. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:beta-aminoisobutyricaciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:beta-aminoisobutyricaciduria | rel=r_associated | relid=0 | w=27
  951. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:biotinidase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=27
  952. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:blau syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:blau syndrome | rel=r_associated | relid=0 | w=27
  953. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:camurati-engelmann syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:camurati-engelmann syndrome | rel=r_associated | relid=0 | w=27
  954. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:chorea
    n1=en:pseudotrisomy 13 syndrome | n2=en:chorea | rel=r_associated | relid=0 | w=27
  955. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:complete trisomy 21 syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:complete trisomy 21 syndrome | rel=r_associated | relid=0 | w=27
  956. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:congenital
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital | rel=r_associated | relid=0 | w=27
  957. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:congenital cerebellar hypoplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital cerebellar hypoplasia | rel=r_associated | relid=0 | w=27
  958. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:congenital malformation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital malformation syndrome | rel=r_associated | relid=0 | w=27
  959. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=27
  960. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:congenital pancreatic enterokinase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=27
  961. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:cranio-orbito-ocular dysraphia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cranio-orbito-ocular dysraphia syndrome | rel=r_associated | relid=0 | w=27
  962. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:craniofrontonasal dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:craniofrontonasal dysplasia | rel=r_associated | relid=0 | w=27
  963. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:crest syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:crest syndrome | rel=r_associated | relid=0 | w=27
  964. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:crisponi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=27
  965. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:cystinosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:cystinosis | rel=r_associated | relid=0 | w=27
  966. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:dandy-walker malformation
    n1=en:pseudotrisomy 13 syndrome | n2=en:dandy-walker malformation | rel=r_associated | relid=0 | w=27
  967. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:dentinogenesis imperfecta
    n1=en:pseudotrisomy 13 syndrome | n2=en:dentinogenesis imperfecta | rel=r_associated | relid=0 | w=27
  968. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:dicarboxylicaminoaciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=27
  969. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:ehlers-danlos syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=27
  970. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:erythropoietic protoporphyria
    n1=en:pseudotrisomy 13 syndrome | n2=en:erythropoietic protoporphyria | rel=r_associated | relid=0 | w=27
  971. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:familial hypertrophic cardiomyopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial hypertrophic cardiomyopathy | rel=r_associated | relid=0 | w=27
  972. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:glycine dehydrogenase (decarboxylating) deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=27
  973. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:glycogen storage disease type x
    n1=en:pseudotrisomy 13 syndrome | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=27
  974. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:hartnup disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:hartnup disease | rel=r_associated | relid=0 | w=27
  975. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:hemolytic anemia due to pyruvate kinase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=27
  976. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:hemorrhagic fever with renal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hemorrhagic fever with renal syndrome | rel=r_associated | relid=0 | w=27
  977. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary hyperbilirubinemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary hyperbilirubinemia | rel=r_associated | relid=0 | w=27
  978. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:heterotaxy syndrome with polysplenia
    n1=en:pseudotrisomy 13 syndrome | n2=en:heterotaxy syndrome with polysplenia | rel=r_associated | relid=0 | w=27
  979. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:holoprosencephaly (100%)
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly (100%) | rel=r_associated | relid=0 | w=27
  980. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=27
  981. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:hurler-scheie syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hurler-scheie syndrome | rel=r_associated | relid=0 | w=27
  982. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:hyaline membrane syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hyaline membrane syndrome | rel=r_associated | relid=0 | w=27
  983. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:hydrocephalus
    n1=en:pseudotrisomy 13 syndrome | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=27
  984. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:hypomyelination and congenital cataract
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=27
  985. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:ichthyosis--cheek--eyebrow syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:ichthyosis--cheek--eyebrow syndrome | rel=r_associated | relid=0 | w=27
  986. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:iridocorneal endothelial syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:iridocorneal endothelial syndrome | rel=r_associated | relid=0 | w=27
  987. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:irritable bowel syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:irritable bowel syndrome | rel=r_associated | relid=0 | w=27
  988. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:kearns-sayre syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:kearns-sayre syndrome | rel=r_associated | relid=0 | w=27
  989. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:lipoprotein glomerulopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:lipoprotein glomerulopathy | rel=r_associated | relid=0 | w=27
  990. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:lysosomal storage disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=27
  991. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:microcephaly deafness syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=27
  992. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=27
  993. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:molybdenum cofactor deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:molybdenum cofactor deficiency | rel=r_associated | relid=0 | w=27
  994. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:nonaka myopathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=27
  995. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:ochronosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:ochronosis | rel=r_associated | relid=0 | w=27
  996. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:oculocerebrorenal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=27
  997. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:opitz g/bbb syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:opitz g/bbb syndrome | rel=r_associated | relid=0 | w=27
  998. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:orbital separation diminished
    n1=en:pseudotrisomy 13 syndrome | n2=en:orbital separation diminished | rel=r_associated | relid=0 | w=27
  999. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:orofaciodigital syndrome type 6
    n1=en:pseudotrisomy 13 syndrome | n2=en:orofaciodigital syndrome type 6 | rel=r_associated | relid=0 | w=27
  1000. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:pallister-hall syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pallister-hall syndrome | rel=r_associated | relid=0 | w=27
  1001. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:pantothenate kinase-associated neurodegeneration
    n1=en:pseudotrisomy 13 syndrome | n2=en:pantothenate kinase-associated neurodegeneration | rel=r_associated | relid=0 | w=27
  1002. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:peritoneal panniculitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:peritoneal panniculitis | rel=r_associated | relid=0 | w=27
  1003. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:persistent fetal circulation
    n1=en:pseudotrisomy 13 syndrome | n2=en:persistent fetal circulation | rel=r_associated | relid=0 | w=27
  1004. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:polydactyly, postaxial
    n1=en:pseudotrisomy 13 syndrome | n2=en:polydactyly, postaxial | rel=r_associated | relid=0 | w=27
  1005. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:posteriorly rotated ear
    n1=en:pseudotrisomy 13 syndrome | n2=en:posteriorly rotated ear | rel=r_associated | relid=0 | w=27
  1006. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:prekallikrein deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:prekallikrein deficiency | rel=r_associated | relid=0 | w=27
  1007. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:premenstrual syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:premenstrual syndrome | rel=r_associated | relid=0 | w=27
  1008. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:primary hypertrophic osteoarthropathy
    n1=en:pseudotrisomy 13 syndrome | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=27
  1009. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:progeria
    n1=en:pseudotrisomy 13 syndrome | n2=en:progeria | rel=r_associated | relid=0 | w=27
  1010. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:progressive familial intrahepatic cholestasis
    n1=en:pseudotrisomy 13 syndrome | n2=en:progressive familial intrahepatic cholestasis | rel=r_associated | relid=0 | w=27
  1011. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:prune belly syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=27
  1012. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:radial polydactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:radial polydactyly | rel=r_associated | relid=0 | w=27
  1013. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:reversible posterior leukoencephalopathy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:reversible posterior leukoencephalopathy syndrome | rel=r_associated | relid=0 | w=27
  1014. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:scleredema adultorum
    n1=en:pseudotrisomy 13 syndrome | n2=en:scleredema adultorum | rel=r_associated | relid=0 | w=27
  1015. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:semilobar holoprosencephalies
    n1=en:pseudotrisomy 13 syndrome | n2=en:semilobar holoprosencephalies | rel=r_associated | relid=0 | w=27
  1016. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:severe steroid 21-hydroxylase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=27
  1017. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:short stature homeobox deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:short stature homeobox deficiency | rel=r_associated | relid=0 | w=27
  1018. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:short-rib thoracic dysplasia 6 with or without polydactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:short-rib thoracic dysplasia 6 with or without polydactyly | rel=r_associated | relid=0 | w=27
  1019. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:shprintzen omphalocele syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=27
  1020. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:smith-lemli-opitz syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=27
  1021. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:smith-mccort dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=27
  1022. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:sonoda syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=27
  1023. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:sotos syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=27
  1024. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:spinal muscular atrophy with respiratory distress 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=27
  1025. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:spondyloenchondrodysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=27
  1026. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:staphylococcal scalded skin syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:staphylococcal scalded skin syndrome | rel=r_associated | relid=0 | w=27
  1027. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:sudden infant death with dysgenesis of the testes syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=27
  1028. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:superior mesenteric artery syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:superior mesenteric artery syndrome | rel=r_associated | relid=0 | w=27
  1029. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:sweet syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sweet syndrome | rel=r_associated | relid=0 | w=27
  1030. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:systemic inflammatory response syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:systemic inflammatory response syndrome | rel=r_associated | relid=0 | w=27
  1031. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:thomas syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=27
  1032. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:torch syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:torch syndrome | rel=r_associated | relid=0 | w=27
  1033. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:townes-brocks syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:townes-brocks syndrome | rel=r_associated | relid=0 | w=27
  1034. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:trigger finger disorder
    n1=en:pseudotrisomy 13 syndrome | n2=en:trigger finger disorder | rel=r_associated | relid=0 | w=27
  1035. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:true hermaphroditism
    n1=en:pseudotrisomy 13 syndrome | n2=en:true hermaphroditism | rel=r_associated | relid=0 | w=27
  1036. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:uveomeningoencephalitic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:uveomeningoencephalitic syndrome | rel=r_associated | relid=0 | w=27
  1037. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:von hippel-lindau syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:von hippel-lindau syndrome | rel=r_associated | relid=0 | w=27
  1038. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:xxxy and xxxxy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:xxxy and xxxxy syndrome | rel=r_associated | relid=0 | w=27
  1039. en:pseudotrisomy 13 syndrome -- r_associated #0: 27 / 0.628 -> en:zollinger ellison syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:zollinger ellison syndrome | rel=r_associated | relid=0 | w=27
  1040. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:11 pairs of ribs
    n1=en:pseudotrisomy 13 syndrome | n2=en:11 pairs of ribs | rel=r_associated | relid=0 | w=26
  1041. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=26
  1042. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:achard syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:achard syndrome | rel=r_associated | relid=0 | w=26
  1043. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:achromatopsia
    n1=en:pseudotrisomy 13 syndrome | n2=en:achromatopsia | rel=r_associated | relid=0 | w=26
  1044. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:acid phosphatase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=26
  1045. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:acrocephalosyndactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:acrocephalosyndactyly | rel=r_associated | relid=0 | w=26
  1046. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:acute coronary syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:acute coronary syndrome | rel=r_associated | relid=0 | w=26
  1047. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:agnosia
    n1=en:pseudotrisomy 13 syndrome | n2=en:agnosia | rel=r_associated | relid=0 | w=26
  1048. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:alice in wonderland syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:alice in wonderland syndrome | rel=r_associated | relid=0 | w=26
  1049. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:arginine:glycine amidinotransferase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=26
  1050. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal recessive ichthyosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive ichthyosis | rel=r_associated | relid=0 | w=26
  1051. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal recessive inheritance
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=26
  1052. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:brain iron accumulation type i syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:brain iron accumulation type i syndrome | rel=r_associated | relid=0 | w=26
  1053. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:carpal tunnel syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:carpal tunnel syndrome | rel=r_associated | relid=0 | w=26
  1054. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:cebocephaly (36%)
    n1=en:pseudotrisomy 13 syndrome | n2=en:cebocephaly (36%) | rel=r_associated | relid=0 | w=26
  1055. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:cerebellar ataxia ectodermal dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=26
  1056. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:childhood hypophosphatasia (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  1057. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:chondrodysplasia punctata syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=26
  1058. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:choroideremia
    n1=en:pseudotrisomy 13 syndrome | n2=en:choroideremia | rel=r_associated | relid=0 | w=26
  1059. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:chromosome 13
    n1=en:pseudotrisomy 13 syndrome | n2=en:chromosome 13 | rel=r_associated | relid=0 | w=26
  1060. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:cleft hand with polydactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:cleft hand with polydactyly | rel=r_associated | relid=0 | w=26
  1061. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:cockayne syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cockayne syndrome | rel=r_associated | relid=0 | w=26
  1062. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:congenital bowing of long bone
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=26
  1063. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:congenital disorder of deglycosylation
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital disorder of deglycosylation | rel=r_associated | relid=0 | w=26
  1064. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:congenital insensitivity to pain with anhidrosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital insensitivity to pain with anhidrosis | rel=r_associated | relid=0 | w=26
  1065. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:congenital transferrin deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=26
  1066. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:deafness, sensorineural, and male infertility
    n1=en:pseudotrisomy 13 syndrome | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=26
  1067. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:diffuse idiopathic skeletal hyperostosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:diffuse idiopathic skeletal hyperostosis | rel=r_associated | relid=0 | w=26
  1068. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:ectodermal dysplasia/ skin fragility syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=26
  1069. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:eisenmenger syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:eisenmenger syndrome | rel=r_associated | relid=0 | w=26
  1070. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:evans syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:evans syndrome | rel=r_associated | relid=0 | w=26
  1071. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:familial c3b inhibitor deficiency syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=26
  1072. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:familial dysautonomia
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial dysautonomia | rel=r_associated | relid=0 | w=26
  1073. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:farber lipogranulomatosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=26
  1074. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:fetal valproate syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fetal valproate syndrome | rel=r_associated | relid=0 | w=26
  1075. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:fox-fordyce disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:fox-fordyce disease | rel=r_associated | relid=0 | w=26
  1076. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:fryns macrocephaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=26
  1077. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:giacci familial neurogenic acroosteolysis
    n1=en:pseudotrisomy 13 syndrome | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=26
  1078. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:gitelman syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:gitelman syndrome | rel=r_associated | relid=0 | w=26
  1079. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:grob's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:grob's syndrome | rel=r_associated | relid=0 | w=26
  1080. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:hair tourniquet
    n1=en:pseudotrisomy 13 syndrome | n2=en:hair tourniquet | rel=r_associated | relid=0 | w=26
  1081. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:hellp syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hellp syndrome | rel=r_associated | relid=0 | w=26
  1082. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:hepatorenal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hepatorenal syndrome | rel=r_associated | relid=0 | w=26
  1083. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary factor xii deficiency disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:hereditary factor xii deficiency disease | rel=r_associated | relid=0 | w=26
  1084. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:heterotaxy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=26
  1085. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:histidinemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:histidinemia | rel=r_associated | relid=0 | w=26
  1086. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:hnsha due to diphosphoglycerate mutase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=26
  1087. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:hnsha due to glucose phosphate isomerase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:hnsha due to glucose phosphate isomerase deficiency | rel=r_associated | relid=0 | w=26
  1088. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:holoprosencephaly type 4
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly type 4 | rel=r_associated | relid=0 | w=26
  1089. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:hymenolepiasis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hymenolepiasis | rel=r_associated | relid=0 | w=26
  1090. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:hypereosinophilic syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypereosinophilic syndrome | rel=r_associated | relid=0 | w=26
  1091. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:i-cell disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:i-cell disease | rel=r_associated | relid=0 | w=26
  1092. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:idiopathic hypersomnolence
    n1=en:pseudotrisomy 13 syndrome | n2=en:idiopathic hypersomnolence | rel=r_associated | relid=0 | w=26
  1093. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:infantile globoid cell leukodystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=26
  1094. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:isolated hyperchlorhidrosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=26
  1095. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:kuskokwim disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=26
  1096. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:leukotriene c4 synthase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=26
  1097. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:li-fraumeni syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=26
  1098. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:loffler syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:loffler syndrome | rel=r_associated | relid=0 | w=26
  1099. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:long qt syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:long qt syndrome | rel=r_associated | relid=0 | w=26
  1100. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:low set ears
    n1=en:pseudotrisomy 13 syndrome | n2=en:low set ears | rel=r_associated | relid=0 | w=26
  1101. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:lymphedema-distichiasis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lymphedema-distichiasis syndrome | rel=r_associated | relid=0 | w=26
  1102. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:macular corneal dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=26
  1103. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:mannosidosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:mannosidosis | rel=r_associated | relid=0 | w=26
  1104. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:marfan syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=26
  1105. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:maternal uniparental disomy chromosome 14 syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:maternal uniparental disomy chromosome 14 syndrome | rel=r_associated | relid=0 | w=26
  1106. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:medial cleft lip and palate (59%)
    n1=en:pseudotrisomy 13 syndrome | n2=en:medial cleft lip and palate (59%) | rel=r_associated | relid=0 | w=26
  1107. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:membranous cranial ossification, delayed
    n1=en:pseudotrisomy 13 syndrome | n2=en:membranous cranial ossification, delayed | rel=r_associated | relid=0 | w=26
  1108. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:merrf syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:merrf syndrome | rel=r_associated | relid=0 | w=26
  1109. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:methionine adenosyltransferase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=26
  1110. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:methylmalonic acidemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:methylmalonic acidemia | rel=r_associated | relid=0 | w=26
  1111. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:microcephalic primordial dwarfism toriello type
    n1=en:pseudotrisomy 13 syndrome | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=26
  1112. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:microcephaly-capillary malformation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  1113. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:moderate steroid 21-hydroxylase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=26
  1114. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:mucopolysaccharidosis type i
    n1=en:pseudotrisomy 13 syndrome | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=26
  1115. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:mullerian inhibiting factor deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:mullerian inhibiting factor deficiency | rel=r_associated | relid=0 | w=26
  1116. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:multiple system atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:multiple system atrophy | rel=r_associated | relid=0 | w=26
  1117. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:muscular dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:muscular dystrophy | rel=r_associated | relid=0 | w=26
  1118. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:nelson syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:nelson syndrome | rel=r_associated | relid=0 | w=26
  1119. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:neonatal progeroid syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=26
  1120. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:orofaciodigital syndrome type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:orofaciodigital syndrome type 1 | rel=r_associated | relid=0 | w=26
  1121. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=26
  1122. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:pelizaeus-merzbacher disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=26
  1123. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:peters-plus syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=26
  1124. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:pituitary stalk interruption syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pituitary stalk interruption syndrome | rel=r_associated | relid=0 | w=26
  1125. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:poland syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:poland syndrome | rel=r_associated | relid=0 | w=26
  1126. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:pontocerebellar hypoplasia type 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=26
  1127. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:presentey anomaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=26
  1128. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:prosopagnosia
    n1=en:pseudotrisomy 13 syndrome | n2=en:prosopagnosia | rel=r_associated | relid=0 | w=26
  1129. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:pseudohermaphroditism
    n1=en:pseudotrisomy 13 syndrome | n2=en:pseudohermaphroditism | rel=r_associated | relid=0 | w=26
  1130. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:radial aplasia-thrombocytopenia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:radial aplasia-thrombocytopenia syndrome | rel=r_associated | relid=0 | w=26
  1131. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:restless leg syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:restless leg syndrome | rel=r_associated | relid=0 | w=26
  1132. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:rett syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:rett syndrome | rel=r_associated | relid=0 | w=26
  1133. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:saito kuba tsuruta syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=26
  1134. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:sea-blue histiocyte syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sea-blue histiocyte syndrome | rel=r_associated | relid=0 | w=26
  1135. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:seckel syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:seckel syndrome | rel=r_associated | relid=0 | w=26
  1136. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:selective antibody deficiency with normal immunoglobulins
    n1=en:pseudotrisomy 13 syndrome | n2=en:selective antibody deficiency with normal immunoglobulins | rel=r_associated | relid=0 | w=26
  1137. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:spastic ataxia, charlevoix-saguenay type
    n1=en:pseudotrisomy 13 syndrome | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=26
  1138. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:spondylo-ocular syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=26
  1139. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:spondyloepimetaphyseal dysplasia with joint laxity type 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | rel=r_associated | relid=0 | w=26
  1140. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:temporomandibular joint dysfunction syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:temporomandibular joint dysfunction syndrome | rel=r_associated | relid=0 | w=26
  1141. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:thyroid dysgenesis
    n1=en:pseudotrisomy 13 syndrome | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=26
  1142. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:tracheobronchomalacia
    n1=en:pseudotrisomy 13 syndrome | n2=en:tracheobronchomalacia | rel=r_associated | relid=0 | w=26
  1143. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:trichothiodystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:trichothiodystrophy | rel=r_associated | relid=0 | w=26
  1144. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:triploidy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:triploidy syndrome | rel=r_associated | relid=0 | w=26
  1145. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:valinemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:valinemia | rel=r_associated | relid=0 | w=26
  1146. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:wandering spleen
    n1=en:pseudotrisomy 13 syndrome | n2=en:wandering spleen | rel=r_associated | relid=0 | w=26
  1147. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:west syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:west syndrome | rel=r_associated | relid=0 | w=26
  1148. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:wolf-hirschhorn syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=26
  1149. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:x-linked bulbar-muscular atrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:x-linked bulbar-muscular atrophy | rel=r_associated | relid=0 | w=26
  1150. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> en:xyy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:xyy syndrome | rel=r_associated | relid=0 | w=26
  1151. en:pseudotrisomy 13 syndrome -- r_associated #0: 26 / 0.605 -> syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome | rel=r_associated | relid=0 | w=26
  1152. en:pseudotrisomy 13 syndrome -- r_associated #0: 25 / 0.581 -> paralysies périodiques familiales
    n1=en:pseudotrisomy 13 syndrome | n2=paralysies périodiques familiales | rel=r_associated | relid=0 | w=25
  1153. en:pseudotrisomy 13 syndrome -- r_associated #0: 22 / 0.512 -> syndrome de Walker-Warburg
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=22
  1154. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> acidémie glutarique de type 1
    n1=en:pseudotrisomy 13 syndrome | n2=acidémie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  1155. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> acidurie glutarique de type 1
    n1=en:pseudotrisomy 13 syndrome | n2=acidurie glutarique de type 1 | rel=r_associated | relid=0 | w=20
  1156. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> acrodermatite entéropathique
    n1=en:pseudotrisomy 13 syndrome | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
  1157. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> acromégalie
    n1=en:pseudotrisomy 13 syndrome | n2=acromégalie | rel=r_associated | relid=0 | w=20
  1158. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> acromegaly
    n1=en:pseudotrisomy 13 syndrome | n2=acromegaly | rel=r_associated | relid=0 | w=20
  1159. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> agnosie
    n1=en:pseudotrisomy 13 syndrome | n2=agnosie | rel=r_associated | relid=0 | w=20
  1160. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> aïnhum
    n1=en:pseudotrisomy 13 syndrome | n2=aïnhum | rel=r_associated | relid=0 | w=20
  1161. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ainhum
    n1=en:pseudotrisomy 13 syndrome | n2=ainhum | rel=r_associated | relid=0 | w=20
  1162. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> albinisme
    n1=en:pseudotrisomy 13 syndrome | n2=albinisme | rel=r_associated | relid=0 | w=20
  1163. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> albinisme oculocutané de type mutant jaune
    n1=en:pseudotrisomy 13 syndrome | n2=albinisme oculocutané de type mutant jaune | rel=r_associated | relid=0 | w=20
  1164. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> anasarque foetal
    n1=en:pseudotrisomy 13 syndrome | n2=anasarque foetal | rel=r_associated | relid=0 | w=20
  1165. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> anasarque foeto-placentaire
    n1=en:pseudotrisomy 13 syndrome | n2=anasarque foeto-placentaire | rel=r_associated | relid=0 | w=20
  1166. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> anasarque foetoplacentaire
    n1=en:pseudotrisomy 13 syndrome | n2=anasarque foetoplacentaire | rel=r_associated | relid=0 | w=20
  1167. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> anencéphalie
    n1=en:pseudotrisomy 13 syndrome | n2=anencéphalie | rel=r_associated | relid=0 | w=20
  1168. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> aniridie, ataxie cérébelleuse et déficience mentale
    n1=en:pseudotrisomy 13 syndrome | n2=aniridie, ataxie cérébelleuse et déficience mentale | rel=r_associated | relid=0 | w=20
  1169. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> aniridie, microcornée et cataracte régressive
    n1=en:pseudotrisomy 13 syndrome | n2=aniridie, microcornée et cataracte régressive | rel=r_associated | relid=0 | w=20
  1170. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> anomalie d'Ebstein
    n1=en:pseudotrisomy 13 syndrome | n2=anomalie d'Ebstein | rel=r_associated | relid=0 | w=20
  1171. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> anomalie du septum auriculaire
    n1=en:pseudotrisomy 13 syndrome | n2=anomalie du septum auriculaire | rel=r_associated | relid=0 | w=20
  1172. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> anti-sida
    n1=en:pseudotrisomy 13 syndrome | n2=anti-sida | rel=r_associated | relid=0 | w=20
  1173. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> antisida
    n1=en:pseudotrisomy 13 syndrome | n2=antisida | rel=r_associated | relid=0 | w=20
  1174. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> aphasie primaire progressive
    n1=en:pseudotrisomy 13 syndrome | n2=aphasie primaire progressive | rel=r_associated | relid=0 | w=20
  1175. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> aphasie progressive primaire
    n1=en:pseudotrisomy 13 syndrome | n2=aphasie progressive primaire | rel=r_associated | relid=0 | w=20
  1176. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> aphasies primaires progressives
    n1=en:pseudotrisomy 13 syndrome | n2=aphasies primaires progressives | rel=r_associated | relid=0 | w=20
  1177. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> aplasie de la paroi abdominale
    n1=en:pseudotrisomy 13 syndrome | n2=aplasie de la paroi abdominale | rel=r_associated | relid=0 | w=20
  1178. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> arachnodactylie
    n1=en:pseudotrisomy 13 syndrome | n2=arachnodactylie | rel=r_associated | relid=0 | w=20
  1179. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> arthrogrypose
    n1=en:pseudotrisomy 13 syndrome | n2=arthrogrypose | rel=r_associated | relid=0 | w=20
  1180. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né
    n1=en:pseudotrisomy 13 syndrome | n2=association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né | rel=r_associated | relid=0 | w=20
  1181. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> atélectasie congestive
    n1=en:pseudotrisomy 13 syndrome | n2=atélectasie congestive | rel=r_associated | relid=0 | w=20
  1182. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> atransferrinémie
    n1=en:pseudotrisomy 13 syndrome | n2=atransferrinémie | rel=r_associated | relid=0 | w=20
  1183. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique autosomique dominante
    n1=en:pseudotrisomy 13 syndrome | n2=atrophie optique autosomique dominante | rel=r_associated | relid=0 | w=20
  1184. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> brides amniotiques (syndrome des)
    n1=en:pseudotrisomy 13 syndrome | n2=brides amniotiques (syndrome des) | rel=r_associated | relid=0 | w=20
  1185. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> cataplexie
    n1=en:pseudotrisomy 13 syndrome | n2=cataplexie | rel=r_associated | relid=0 | w=20
  1186. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> choc au poumon
    n1=en:pseudotrisomy 13 syndrome | n2=choc au poumon | rel=r_associated | relid=0 | w=20
  1187. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> choc toxique
    n1=en:pseudotrisomy 13 syndrome | n2=choc toxique | rel=r_associated | relid=0 | w=20
  1188. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> choc toxique staphylococcique
    n1=en:pseudotrisomy 13 syndrome | n2=choc toxique staphylococcique | rel=r_associated | relid=0 | w=20
  1189. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> cholestase intrahépatique progressive familiale de type 1
    n1=en:pseudotrisomy 13 syndrome | n2=cholestase intrahépatique progressive familiale de type 1 | rel=r_associated | relid=0 | w=20
  1190. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> chondrodysplasia punctata
    n1=en:pseudotrisomy 13 syndrome | n2=chondrodysplasia punctata | rel=r_associated | relid=0 | w=20
  1191. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> chromosome 13
    n1=en:pseudotrisomy 13 syndrome | n2=chromosome 13 | rel=r_associated | relid=0 | w=20
  1192. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> coarctation aortique
    n1=en:pseudotrisomy 13 syndrome | n2=coarctation aortique | rel=r_associated | relid=0 | w=20
  1193. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> coeur triatrial
    n1=en:pseudotrisomy 13 syndrome | n2=coeur triatrial | rel=r_associated | relid=0 | w=20
  1194. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> communication interauriculaire
    n1=en:pseudotrisomy 13 syndrome | n2=communication interauriculaire | rel=r_associated | relid=0 | w=20
  1195. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> communication interventriculaire
    n1=en:pseudotrisomy 13 syndrome | n2=communication interventriculaire | rel=r_associated | relid=0 | w=20
  1196. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> congénital
    n1=en:pseudotrisomy 13 syndrome | n2=congénital | rel=r_associated | relid=0 | w=20
  1197. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> congenital
    n1=en:pseudotrisomy 13 syndrome | n2=congenital | rel=r_associated | relid=0 | w=20
  1198. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> congénitale
    n1=en:pseudotrisomy 13 syndrome | n2=congénitale | rel=r_associated | relid=0 | w=20
  1199. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> contractures congénitales et arachnodactylie
    n1=en:pseudotrisomy 13 syndrome | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20
  1200. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> crânio-sténose
    n1=en:pseudotrisomy 13 syndrome | n2=crânio-sténose | rel=r_associated | relid=0 | w=20
  1201. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> craniosténose
    n1=en:pseudotrisomy 13 syndrome | n2=craniosténose | rel=r_associated | relid=0 | w=20
  1202. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> crâniosténose
    n1=en:pseudotrisomy 13 syndrome | n2=crâniosténose | rel=r_associated | relid=0 | w=20
  1203. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> craniosynostose
    n1=en:pseudotrisomy 13 syndrome | n2=craniosynostose | rel=r_associated | relid=0 | w=20
  1204. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> crâniosynostose
    n1=en:pseudotrisomy 13 syndrome | n2=crâniosynostose | rel=r_associated | relid=0 | w=20
  1205. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> crosse aortique(syndrome de la)
    n1=en:pseudotrisomy 13 syndrome | n2=crosse aortique(syndrome de la) | rel=r_associated | relid=0 | w=20
  1206. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> cysticercose
    n1=en:pseudotrisomy 13 syndrome | n2=cysticercose | rel=r_associated | relid=0 | w=20
  1207. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> cysticercose cérébrale
    n1=en:pseudotrisomy 13 syndrome | n2=cysticercose cérébrale | rel=r_associated | relid=0 | w=20
  1208. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> cysticercose du système nerveux central
    n1=en:pseudotrisomy 13 syndrome | n2=cysticercose du système nerveux central | rel=r_associated | relid=0 | w=20
  1209. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> cysticercose neurologique
    n1=en:pseudotrisomy 13 syndrome | n2=cysticercose neurologique | rel=r_associated | relid=0 | w=20
  1210. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> cysticercoses
    n1=en:pseudotrisomy 13 syndrome | n2=cysticercoses | rel=r_associated | relid=0 | w=20
  1211. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> déficit en céto-acide décarboxylase
    n1=en:pseudotrisomy 13 syndrome | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
  1212. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> déficit en cytochrome oxydase
    n1=en:pseudotrisomy 13 syndrome | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
  1213. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> déficit en cytochrome-c oxydase
    n1=en:pseudotrisomy 13 syndrome | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
  1214. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> déficit en neuraminidase
    n1=en:pseudotrisomy 13 syndrome | n2=déficit en neuraminidase | rel=r_associated | relid=0 | w=20
  1215. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> déficit en prolidase
    n1=en:pseudotrisomy 13 syndrome | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
  1216. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> déficit en protéine trifonctionnelle mitochondriale
    n1=en:pseudotrisomy 13 syndrome | n2=déficit en protéine trifonctionnelle mitochondriale | rel=r_associated | relid=0 | w=20
  1217. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> déficit en pyruvate carboxylase
    n1=en:pseudotrisomy 13 syndrome | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20
  1218. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> déficit en semialdéhyde succinique-déshydrogénase
    n1=en:pseudotrisomy 13 syndrome | n2=déficit en semialdéhyde succinique-déshydrogénase | rel=r_associated | relid=0 | w=20
  1219. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> déficit en sulfite-oxydase
    n1=en:pseudotrisomy 13 syndrome | n2=déficit en sulfite-oxydase | rel=r_associated | relid=0 | w=20
  1220. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dégénérescence wallérienne
    n1=en:pseudotrisomy 13 syndrome | n2=dégénérescence wallérienne | rel=r_associated | relid=0 | w=20
  1221. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> démence fronto-temporale
    n1=en:pseudotrisomy 13 syndrome | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=20
  1222. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> démence frontotemporale
    n1=en:pseudotrisomy 13 syndrome | n2=démence frontotemporale | rel=r_associated | relid=0 | w=20
  1223. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dentine opalescente héréditaire
    n1=en:pseudotrisomy 13 syndrome | n2=dentine opalescente héréditaire | rel=r_associated | relid=0 | w=20
  1224. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dentinogénèse imparfaite
    n1=en:pseudotrisomy 13 syndrome | n2=dentinogénèse imparfaite | rel=r_associated | relid=0 | w=20
  1225. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> DentinoGenesis Imperfecta
    n1=en:pseudotrisomy 13 syndrome | n2=DentinoGenesis Imperfecta | rel=r_associated | relid=0 | w=20
  1226. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dentinogenesis imperfecta
    n1=en:pseudotrisomy 13 syndrome | n2=dentinogenesis imperfecta | rel=r_associated | relid=0 | w=20
  1227. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> détresse respiratoire
    n1=en:pseudotrisomy 13 syndrome | n2=détresse respiratoire | rel=r_associated | relid=0 | w=20
  1228. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dextrocardie
    n1=en:pseudotrisomy 13 syndrome | n2=dextrocardie | rel=r_associated | relid=0 | w=20
  1229. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> distomatoses pulmonaires
    n1=en:pseudotrisomy 13 syndrome | n2=distomatoses pulmonaires | rel=r_associated | relid=0 | w=20
  1230. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dumping syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=dumping syndrome | rel=r_associated | relid=0 | w=20
  1231. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysérythropoïèse congénitale
    n1=en:pseudotrisomy 13 syndrome | n2=dysérythropoïèse congénitale | rel=r_associated | relid=0 | w=20
  1232. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysostose craniofaciale
    n1=en:pseudotrisomy 13 syndrome | n2=dysostose craniofaciale | rel=r_associated | relid=0 | w=20
  1233. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysostose fronto-nasale acromélique
    n1=en:pseudotrisomy 13 syndrome | n2=dysostose fronto-nasale acromélique | rel=r_associated | relid=0 | w=20
  1234. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysplasie campomélique
    n1=en:pseudotrisomy 13 syndrome | n2=dysplasie campomélique | rel=r_associated | relid=0 | w=20
  1235. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysplasie cléido-crânienne
    n1=en:pseudotrisomy 13 syndrome | n2=dysplasie cléido-crânienne | rel=r_associated | relid=0 | w=20
  1236. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysplasie cléidocrânienne
    n1=en:pseudotrisomy 13 syndrome | n2=dysplasie cléidocrânienne | rel=r_associated | relid=0 | w=20
  1237. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysplasie craniodiaphysaire
    n1=en:pseudotrisomy 13 syndrome | n2=dysplasie craniodiaphysaire | rel=r_associated | relid=0 | w=20
  1238. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique
    n1=en:pseudotrisomy 13 syndrome | n2=dysplasie ectodermique | rel=r_associated | relid=0 | w=20
  1239. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental
    n1=en:pseudotrisomy 13 syndrome | n2=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | rel=r_associated | relid=0 | w=20
  1240. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysplasie ectodermique, ectrodactylie et dystrophie maculaire
    n1=en:pseudotrisomy 13 syndrome | n2=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | rel=r_associated | relid=0 | w=20
  1241. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysplasie fronto-nasale acromélique
    n1=en:pseudotrisomy 13 syndrome | n2=dysplasie fronto-nasale acromélique | rel=r_associated | relid=0 | w=20
  1242. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dysplasie frontonasale
    n1=en:pseudotrisomy 13 syndrome | n2=dysplasie frontonasale | rel=r_associated | relid=0 | w=20
  1243. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dystrophie neuro-axonale infantile
    n1=en:pseudotrisomy 13 syndrome | n2=dystrophie neuro-axonale infantile | rel=r_associated | relid=0 | w=20
  1244. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dystrophie neuroaxonale
    n1=en:pseudotrisomy 13 syndrome | n2=dystrophie neuroaxonale | rel=r_associated | relid=0 | w=20
  1245. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dystrophie neuroaxonale de Seitelberger
    n1=en:pseudotrisomy 13 syndrome | n2=dystrophie neuroaxonale de Seitelberger | rel=r_associated | relid=0 | w=20
  1246. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dystrophie neuroaxonale infantile
    n1=en:pseudotrisomy 13 syndrome | n2=dystrophie neuroaxonale infantile | rel=r_associated | relid=0 | w=20
  1247. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dystrophie orbitaire congénitale
    n1=en:pseudotrisomy 13 syndrome | n2=dystrophie orbitaire congénitale | rel=r_associated | relid=0 | w=20
  1248. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> dystrophies neuroaxonales
    n1=en:pseudotrisomy 13 syndrome | n2=dystrophies neuroaxonales | rel=r_associated | relid=0 | w=20
  1249. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie)
    n1=en:pseudotrisomy 13 syndrome | n2=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | rel=r_associated | relid=0 | w=20
  1250. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ectrodactylie
    n1=en:pseudotrisomy 13 syndrome | n2=ectrodactylie | rel=r_associated | relid=0 | w=20
  1251. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:10p13-p14 deletion syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:10p13-p14 deletion syndrome | rel=r_associated | relid=0 | w=20
  1252. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:acrodysostosis 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
  1253. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:acrorenal mandibular syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20
  1254. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
    n1=en:pseudotrisomy 13 syndrome | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20
  1255. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:adducted thumbs and arthrogryposis syndrome christian type
    n1=en:pseudotrisomy 13 syndrome | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=20
  1256. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:adenocutanemucous syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:adenocutanemucous syndrome | rel=r_associated | relid=0 | w=20
  1257. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:adrenal cytomegaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:adrenal cytomegaly | rel=r_associated | relid=0 | w=20
  1258. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:AIDS
    n1=en:pseudotrisomy 13 syndrome | n2=en:AIDS | rel=r_associated | relid=0 | w=20
  1259. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:AIDS awareness
    n1=en:pseudotrisomy 13 syndrome | n2=en:AIDS awareness | rel=r_associated | relid=0 | w=20
  1260. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Alice in Wonderland syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Alice in Wonderland syndrome | rel=r_associated | relid=0 | w=20
  1261. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Alice in wonderland Syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Alice in wonderland Syndrome | rel=r_associated | relid=0 | w=20
  1262. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:alligator skin
    n1=en:pseudotrisomy 13 syndrome | n2=en:alligator skin | rel=r_associated | relid=0 | w=20
  1263. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:alveolar proteinosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:alveolar proteinosis | rel=r_associated | relid=0 | w=20
  1264. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:anal imperforation
    n1=en:pseudotrisomy 13 syndrome | n2=en:anal imperforation | rel=r_associated | relid=0 | w=20
  1265. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:anasarca
    n1=en:pseudotrisomy 13 syndrome | n2=en:anasarca | rel=r_associated | relid=0 | w=20
  1266. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:anauxetic dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20
  1267. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:and mental retardation
    n1=en:pseudotrisomy 13 syndrome | n2=en:and mental retardation | rel=r_associated | relid=0 | w=20
  1268. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:and proeminent incisors
    n1=en:pseudotrisomy 13 syndrome | n2=en:and proeminent incisors | rel=r_associated | relid=0 | w=20
  1269. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Angelman syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Angelman syndrome | rel=r_associated | relid=0 | w=20
  1270. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:anterior plagiocephalies, synostotic
    n1=en:pseudotrisomy 13 syndrome | n2=en:anterior plagiocephalies, synostotic | rel=r_associated | relid=0 | w=20
  1271. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:anti-AIDS
    n1=en:pseudotrisomy 13 syndrome | n2=en:anti-AIDS | rel=r_associated | relid=0 | w=20
  1272. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:arachnodactily
    n1=en:pseudotrisomy 13 syndrome | n2=en:arachnodactily | rel=r_associated | relid=0 | w=20
  1273. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:arachnodactyly
    n1=en:pseudotrisomy 13 syndrome | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20
  1274. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:arhinia, choanal atresia, and microphthalmia
    n1=en:pseudotrisomy 13 syndrome | n2=en:arhinia, choanal atresia, and microphthalmia | rel=r_associated | relid=0 | w=20
  1275. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:arnold chiari malformation
    n1=en:pseudotrisomy 13 syndrome | n2=en:arnold chiari malformation | rel=r_associated | relid=0 | w=20
  1276. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:arnold-chiari deformity
    n1=en:pseudotrisomy 13 syndrome | n2=en:arnold-chiari deformity | rel=r_associated | relid=0 | w=20
  1277. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:ataxia-telangiectasisa-like disorder 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
  1278. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:autoimmune polyglandular syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:autoimmune polyglandular syndrome | rel=r_associated | relid=0 | w=20
  1279. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal dominant congenital deafness with onychodystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal dominant congenital deafness with onychodystrophy | rel=r_associated | relid=0 | w=20
  1280. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal recessive spastic paraplegia type 39
    n1=en:pseudotrisomy 13 syndrome | n2=en:autosomal recessive spastic paraplegia type 39 | rel=r_associated | relid=0 | w=20
  1281. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:bamforth syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20
  1282. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:bestrophinopathy, autosomal recessive
    n1=en:pseudotrisomy 13 syndrome | n2=en:bestrophinopathy, autosomal recessive | rel=r_associated | relid=0 | w=20
  1283. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:black death
    n1=en:pseudotrisomy 13 syndrome | n2=en:black death | rel=r_associated | relid=0 | w=20
  1284. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Black death
    n1=en:pseudotrisomy 13 syndrome | n2=en:Black death | rel=r_associated | relid=0 | w=20
  1285. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:black plague
    n1=en:pseudotrisomy 13 syndrome | n2=en:black plague | rel=r_associated | relid=0 | w=20
  1286. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:brachioskeletogenital syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:brachioskeletogenital syndrome | rel=r_associated | relid=0 | w=20
  1287. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:braddock syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=20
  1288. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:brain calcification rajab type
    n1=en:pseudotrisomy 13 syndrome | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20
  1289. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:brain malformation, congenital heart disease, postaxial polydactyly syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:brain malformation, congenital heart disease, postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=20
  1290. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:branched-chain ketoaciduria
    n1=en:pseudotrisomy 13 syndrome | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
  1291. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:carbonic anhydrase i deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
  1292. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cardio-facio-cutaneous syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cardio-facio-cutaneous syndrome | rel=r_associated | relid=0 | w=20
  1293. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cataplexia
    n1=en:pseudotrisomy 13 syndrome | n2=en:cataplexia | rel=r_associated | relid=0 | w=20
  1294. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cataplexis
    n1=en:pseudotrisomy 13 syndrome | n2=en:cataplexis | rel=r_associated | relid=0 | w=20
  1295. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:CDA
    n1=en:pseudotrisomy 13 syndrome | n2=en:CDA | rel=r_associated | relid=0 | w=20
  1296. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cerebral gigantism
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
  1297. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cerebral tuberculosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebral tuberculosis | rel=r_associated | relid=0 | w=20
  1298. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cerebral ventriculomegaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:cerebral ventriculomegaly | rel=r_associated | relid=0 | w=20
  1299. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cervical hypertrichosis and peripheral neuropathy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20
  1300. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:child's sudden death
    n1=en:pseudotrisomy 13 syndrome | n2=en:child's sudden death | rel=r_associated | relid=0 | w=20
  1301. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:chondrodystrophia punctata
    n1=en:pseudotrisomy 13 syndrome | n2=en:chondrodystrophia punctata | rel=r_associated | relid=0 | w=20
  1302. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:chromosome 16p12.1 deletion syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:chromosome 16p12.1 deletion syndrome | rel=r_associated | relid=0 | w=20
  1303. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:classical maple syrup urine disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
  1304. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cleft lip and palate
    n1=en:pseudotrisomy 13 syndrome | n2=en:cleft lip and palate | rel=r_associated | relid=0 | w=20
  1305. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:coloboma and anal atresia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:coloboma and anal atresia syndrome | rel=r_associated | relid=0 | w=20
  1306. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:congenital analbuminemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20
  1307. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:congenital cataract with ataxia and deafness syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20
  1308. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 1h
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital disorder of glycosylation type 1h | rel=r_associated | relid=0 | w=20
  1309. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 2e
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital disorder of glycosylation type 2e | rel=r_associated | relid=0 | w=20
  1310. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type id
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital disorder of glycosylation type id | rel=r_associated | relid=0 | w=20
  1311. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type ie
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital disorder of glycosylation type ie | rel=r_associated | relid=0 | w=20
  1312. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation, type if
    n1=en:pseudotrisomy 13 syndrome | n2=en:congenital disorder of glycosylation, type if | rel=r_associated | relid=0 | w=20
  1313. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cooper jabs syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20
  1314. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cortical dysplasia-focal epilepsy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
  1315. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cot death
    n1=en:pseudotrisomy 13 syndrome | n2=en:cot death | rel=r_associated | relid=0 | w=20
  1316. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:craniofacial ulnar renal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:craniofacial ulnar renal syndrome | rel=r_associated | relid=0 | w=20
  1317. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:crib death
    n1=en:pseudotrisomy 13 syndrome | n2=en:crib death | rel=r_associated | relid=0 | w=20
  1318. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cutaneous photosensitivity and lethal colitis syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20
  1319. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cysticercal disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:cysticercal disease | rel=r_associated | relid=0 | w=20
  1320. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:cysticercosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:cysticercosis | rel=r_associated | relid=0 | w=20
  1321. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:dactylolysis spontanea
    n1=en:pseudotrisomy 13 syndrome | n2=en:dactylolysis spontanea | rel=r_associated | relid=0 | w=20
  1322. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:deafness and myopia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20
  1323. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Degos's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Degos's syndrome | rel=r_associated | relid=0 | w=20
  1324. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  1325. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Dercum's disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Dercum's disease | rel=r_associated | relid=0 | w=20
  1326. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Devergie's disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Devergie's disease | rel=r_associated | relid=0 | w=20
  1327. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:diaphanospondylodysostosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=20
  1328. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:disease aids
    n1=en:pseudotrisomy 13 syndrome | n2=en:disease aids | rel=r_associated | relid=0 | w=20
  1329. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Diskinson's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Diskinson's syndrome | rel=r_associated | relid=0 | w=20
  1330. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Down syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Down syndrome | rel=r_associated | relid=0 | w=20
  1331. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Duane's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Duane's syndrome | rel=r_associated | relid=0 | w=20
  1332. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:dumping stomach
    n1=en:pseudotrisomy 13 syndrome | n2=en:dumping stomach | rel=r_associated | relid=0 | w=20
  1333. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:dysequilibrium syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dysequilibrium syndrome | rel=r_associated | relid=0 | w=20
  1334. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:dysmorphism, pectus carinatum, joint laxity syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:dysmorphism, pectus carinatum, joint laxity syndrome | rel=r_associated | relid=0 | w=20
  1335. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:ectodermal dysplasia with blindness syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
  1336. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type
    n1=en:pseudotrisomy 13 syndrome | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=20
  1337. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:eiken type chondrodysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
  1338. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:erythermalgia
    n1=en:pseudotrisomy 13 syndrome | n2=en:erythermalgia | rel=r_associated | relid=0 | w=20
  1339. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:exomphalos
    n1=en:pseudotrisomy 13 syndrome | n2=en:exomphalos | rel=r_associated | relid=0 | w=20
  1340. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:familial median cleft of upper and lower lip
    n1=en:pseudotrisomy 13 syndrome | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20
  1341. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:fara chlupackova syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fara chlupackova syndrome | rel=r_associated | relid=0 | w=20
  1342. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:fish skin disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:fish skin disease | rel=r_associated | relid=0 | w=20
  1343. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:fountain syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20
  1344. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:fragile X syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
  1345. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:generalized peeling skin syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20
  1346. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:gigantism and hyperplastic visceromegaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:gigantism and hyperplastic visceromegaly | rel=r_associated | relid=0 | w=20
  1347. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Gitelman syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Gitelman syndrome | rel=r_associated | relid=0 | w=20
  1348. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:glutaric aciduria, type 1
    n1=en:pseudotrisomy 13 syndrome | n2=en:glutaric aciduria, type 1 | rel=r_associated | relid=0 | w=20
  1349. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | rel=r_associated | relid=0 | w=20
  1350. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Goltz syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Goltz syndrome | rel=r_associated | relid=0 | w=20
  1351. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Gray platelet syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Gray platelet syndrome | rel=r_associated | relid=0 | w=20
  1352. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Guillain-Barre syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Guillain-Barre syndrome | rel=r_associated | relid=0 | w=20
  1353. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:halal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:halal syndrome | rel=r_associated | relid=0 | w=20
  1354. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:hall riggs syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
  1355. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:hand and foot deformity
    n1=en:pseudotrisomy 13 syndrome | n2=en:hand and foot deformity | rel=r_associated | relid=0 | w=20
  1356. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:heart defects limb shortening
    n1=en:pseudotrisomy 13 syndrome | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20
  1357. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Hebra's pityriasis
    n1=en:pseudotrisomy 13 syndrome | n2=en:Hebra's pityriasis | rel=r_associated | relid=0 | w=20
  1358. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:heterotaxy
    n1=en:pseudotrisomy 13 syndrome | n2=en:heterotaxy | rel=r_associated | relid=0 | w=20
  1359. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:histidinaemia
    n1=en:pseudotrisomy 13 syndrome | n2=en:histidinaemia | rel=r_associated | relid=0 | w=20
  1360. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:holoprosencephaly 2 (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly 2 (disorder) | rel=r_associated | relid=0 | w=20
  1361. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:holoprosencephaly 4 (disorder)
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly 4 (disorder) | rel=r_associated | relid=0 | w=20
  1362. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:holoprosencephaly 5
    n1=en:pseudotrisomy 13 syndrome | n2=en:holoprosencephaly 5 | rel=r_associated | relid=0 | w=20
  1363. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Hurler syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Hurler syndrome | rel=r_associated | relid=0 | w=20
  1364. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:hydrencephalus
    n1=en:pseudotrisomy 13 syndrome | n2=en:hydrencephalus | rel=r_associated | relid=0 | w=20
  1365. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:hypertrichosis and acromegaloid facial appearance syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypertrichosis and acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=20
  1366. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:hypomandibular faciocranial dysostosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20
  1367. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:hypophosphatasia infantile
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypophosphatasia infantile | rel=r_associated | relid=0 | w=20
  1368. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:hypothalamic hamartoblastoma
    n1=en:pseudotrisomy 13 syndrome | n2=en:hypothalamic hamartoblastoma | rel=r_associated | relid=0 | w=20
  1369. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:I-cell disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:I-cell disease | rel=r_associated | relid=0 | w=20
  1370. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:immune deficiency syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:immune deficiency syndrome | rel=r_associated | relid=0 | w=20
  1371. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:insulin growth factor i deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
  1372. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:insulin receptor mutation - associated insulin resistance syndromes
    n1=en:pseudotrisomy 13 syndrome | n2=en:insulin receptor mutation - associated insulin resistance syndromes | rel=r_associated | relid=0 | w=20
  1373. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:kallman syndrome with heart disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=20
  1374. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Kawasaki disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Kawasaki disease | rel=r_associated | relid=0 | w=20
  1375. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Kawasaki's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Kawasaki's syndrome | rel=r_associated | relid=0 | w=20
  1376. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:kenny-caffey syndrome type 2
    n1=en:pseudotrisomy 13 syndrome | n2=en:kenny-caffey syndrome type 2 | rel=r_associated | relid=0 | w=20
  1377. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Klinefelter syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20
  1378. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Köbberling's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Köbberling's syndrome | rel=r_associated | relid=0 | w=20
  1379. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Korsakoff syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Korsakoff syndrome | rel=r_associated | relid=0 | w=20
  1380. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:late-onset junctional epidermolysis bullosa
    n1=en:pseudotrisomy 13 syndrome | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20
  1381. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:lazar-house
    n1=en:pseudotrisomy 13 syndrome | n2=en:lazar-house | rel=r_associated | relid=0 | w=20
  1382. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:leprosarium
    n1=en:pseudotrisomy 13 syndrome | n2=en:leprosarium | rel=r_associated | relid=0 | w=20
  1383. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Leriche syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Leriche syndrome | rel=r_associated | relid=0 | w=20
  1384. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:lethal larsen-like syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=20
  1385. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:lethal neonatal rigidity and multifocal seizure syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
  1386. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:leucinosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  1387. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20
  1388. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  1389. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:macroglossia
    n1=en:pseudotrisomy 13 syndrome | n2=en:macroglossia | rel=r_associated | relid=0 | w=20
  1390. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:manouvrier syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=20
  1391. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:maple-tree syrup disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
  1392. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Marburg virus disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Marburg virus disease | rel=r_associated | relid=0 | w=20
  1393. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Marfan's disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20
  1394. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Marfan's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20
  1395. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:maternal diabetes and deafness syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:maternal diabetes and deafness syndrome | rel=r_associated | relid=0 | w=20
  1396. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | rel=r_associated | relid=0 | w=20
  1397. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:mental retardation, autosomal dominant 9
    n1=en:pseudotrisomy 13 syndrome | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
  1398. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:mental retardation, autosomal recessive 34
    n1=en:pseudotrisomy 13 syndrome | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
  1399. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20
  1400. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:microcephaly albinism digital anomalies syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
  1401. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:mitochondrial dna depletion syndrome 12
    n1=en:pseudotrisomy 13 syndrome | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
  1402. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:moyamoya disease with early onset achalasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
  1403. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:mucocutaneous lymph node syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mucocutaneous lymph node syndrome | rel=r_associated | relid=0 | w=20
  1404. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:mucolipidosis type iii gamma
    n1=en:pseudotrisomy 13 syndrome | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
  1405. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:mucopolysaccharidosis i
    n1=en:pseudotrisomy 13 syndrome | n2=en:mucopolysaccharidosis i | rel=r_associated | relid=0 | w=20
  1406. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:mullerian-renal-cervical spine syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:mullerian-renal-cervical spine syndrome | rel=r_associated | relid=0 | w=20
  1407. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:multiple vascular disruption syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:multiple vascular disruption syndrome | rel=r_associated | relid=0 | w=20
  1408. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:myitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:myitis | rel=r_associated | relid=0 | w=20
  1409. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:nablus mask-like facial syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:nablus mask-like facial syndrome | rel=r_associated | relid=0 | w=20
  1410. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:najjar syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=20
  1411. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Nathalie syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  1412. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:neurological cysticercosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:neurological cysticercosis | rel=r_associated | relid=0 | w=20
  1413. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Niemann-Pick disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Niemann-Pick disease | rel=r_associated | relid=0 | w=20
  1414. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:noma
    n1=en:pseudotrisomy 13 syndrome | n2=en:noma | rel=r_associated | relid=0 | w=20
  1415. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:oculocutaneous albinism type 6
    n1=en:pseudotrisomy 13 syndrome | n2=en:oculocutaneous albinism type 6 | rel=r_associated | relid=0 | w=20
  1416. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:oculorespiratory syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:oculorespiratory syndrome | rel=r_associated | relid=0 | w=20
  1417. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:odontogenesis imperfecta
    n1=en:pseudotrisomy 13 syndrome | n2=en:odontogenesis imperfecta | rel=r_associated | relid=0 | w=20
  1418. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:ombilical hernia
    n1=en:pseudotrisomy 13 syndrome | n2=en:ombilical hernia | rel=r_associated | relid=0 | w=20
  1419. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:onychoosteodysostosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:onychoosteodysostosis | rel=r_associated | relid=0 | w=20
  1420. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:ophthalmoneuritis
    n1=en:pseudotrisomy 13 syndrome | n2=en:ophthalmoneuritis | rel=r_associated | relid=0 | w=20
  1421. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20
  1422. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:pelviscapular dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20
  1423. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:persistent mullerian derivative with lymphangiectasia and polydactyly syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:persistent mullerian derivative with lymphangiectasia and polydactyly syndrome | rel=r_associated | relid=0 | w=20
  1424. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Pick's disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Pick's disease | rel=r_associated | relid=0 | w=20
  1425. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:pili torti onychodysplasia syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20
  1426. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:plasma kallikrein deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
  1427. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Plummer-Vinson syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Plummer-Vinson syndrome | rel=r_associated | relid=0 | w=20
  1428. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Prader-Willi syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
  1429. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:primary immunodeficiency syndrome due to p14 deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20
  1430. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:pulmonary shunting
    n1=en:pseudotrisomy 13 syndrome | n2=en:pulmonary shunting | rel=r_associated | relid=0 | w=20
  1431. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:renal dysplasia - limb defects syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=20
  1432. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:respiratory distress
    n1=en:pseudotrisomy 13 syndrome | n2=en:respiratory distress | rel=r_associated | relid=0 | w=20
  1433. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:robinow-like syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20
  1434. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:sacral agenesis
    n1=en:pseudotrisomy 13 syndrome | n2=en:sacral agenesis | rel=r_associated | relid=0 | w=20
  1435. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:sarcitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:sarcitis | rel=r_associated | relid=0 | w=20
  1436. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:schock lung
    n1=en:pseudotrisomy 13 syndrome | n2=en:schock lung | rel=r_associated | relid=0 | w=20
  1437. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Seitelberger's disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Seitelberger's disease | rel=r_associated | relid=0 | w=20
  1438. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Seitelberger's neuroaxonal dystrophy
    n1=en:pseudotrisomy 13 syndrome | n2=en:Seitelberger's neuroaxonal dystrophy | rel=r_associated | relid=0 | w=20
  1439. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Sheehan's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Sheehan's syndrome | rel=r_associated | relid=0 | w=20
  1440. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:short stature syndrome, brussels type
    n1=en:pseudotrisomy 13 syndrome | n2=en:short stature syndrome, brussels type | rel=r_associated | relid=0 | w=20
  1441. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:SIDS
    n1=en:pseudotrisomy 13 syndrome | n2=en:SIDS | rel=r_associated | relid=0 | w=20
  1442. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:sids
    n1=en:pseudotrisomy 13 syndrome | n2=en:sids | rel=r_associated | relid=0 | w=20
  1443. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:single central incisor syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:single central incisor syndrome | rel=r_associated | relid=0 | w=20
  1444. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:situs inversus
    n1=en:pseudotrisomy 13 syndrome | n2=en:situs inversus | rel=r_associated | relid=0 | w=20
  1445. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:situs inversus viscerum
    n1=en:pseudotrisomy 13 syndrome | n2=en:situs inversus viscerum | rel=r_associated | relid=0 | w=20
  1446. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:situs mutatus
    n1=en:pseudotrisomy 13 syndrome | n2=en:situs mutatus | rel=r_associated | relid=0 | w=20
  1447. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Soto's syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
  1448. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Sotos' syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
  1449. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:sotos' syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
  1450. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:split-hand/foot malformation 3
    n1=en:pseudotrisomy 13 syndrome | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20
  1451. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:spondyloepiphyseal dysplasia tarda kohn type
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20
  1452. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=20
  1453. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Stein-Leventhal syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Stein-Leventhal syndrome | rel=r_associated | relid=0 | w=20
  1454. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Stevens-Johnson syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Stevens-Johnson syndrome | rel=r_associated | relid=0 | w=20
  1455. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Stokes-Adams syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Stokes-Adams syndrome | rel=r_associated | relid=0 | w=20
  1456. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:sudden infant death
    n1=en:pseudotrisomy 13 syndrome | n2=en:sudden infant death | rel=r_associated | relid=0 | w=20
  1457. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Tay-Sachs disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20
  1458. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:thiamin-responsive maple syrup urine disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
  1459. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:tissue kallikrein deficiency
    n1=en:pseudotrisomy 13 syndrome | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
  1460. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Townes-Brocks syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Townes-Brocks syndrome | rel=r_associated | relid=0 | w=20
  1461. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Toxic Shock Syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Toxic Shock Syndrome | rel=r_associated | relid=0 | w=20
  1462. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:trichorhinophalangeal syndrome type II
    n1=en:pseudotrisomy 13 syndrome | n2=en:trichorhinophalangeal syndrome type II | rel=r_associated | relid=0 | w=20
  1463. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Triple a syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Triple a syndrome | rel=r_associated | relid=0 | w=20
  1464. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:triple a syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:triple a syndrome | rel=r_associated | relid=0 | w=20
  1465. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:trisomy xq28 syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:trisomy xq28 syndrome | rel=r_associated | relid=0 | w=20
  1466. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculosis of meninges (cerebral)(spinal)
    n1=en:pseudotrisomy 13 syndrome | n2=en:tuberculosis of meninges (cerebral)(spinal) | rel=r_associated | relid=0 | w=20
  1467. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculosis, meningeal
    n1=en:pseudotrisomy 13 syndrome | n2=en:tuberculosis, meningeal | rel=r_associated | relid=0 | w=20
  1468. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculous hypertrophic pachymeningitides
    n1=en:pseudotrisomy 13 syndrome | n2=en:tuberculous hypertrophic pachymeningitides | rel=r_associated | relid=0 | w=20
  1469. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculous leptomeningitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:tuberculous leptomeningitis | rel=r_associated | relid=0 | w=20
  1470. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:tuberculous meningitis
    n1=en:pseudotrisomy 13 syndrome | n2=en:tuberculous meningitis | rel=r_associated | relid=0 | w=20
  1471. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:type a 14
    n1=en:pseudotrisomy 13 syndrome | n2=en:type a 14 | rel=r_associated | relid=0 | w=20
  1472. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Umbilical hernia
    n1=en:pseudotrisomy 13 syndrome | n2=en:Umbilical hernia | rel=r_associated | relid=0 | w=20
  1473. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:umbilical hernia
    n1=en:pseudotrisomy 13 syndrome | n2=en:umbilical hernia | rel=r_associated | relid=0 | w=20
  1474. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:ventriculomeglia
    n1=en:pseudotrisomy 13 syndrome | n2=en:ventriculomeglia | rel=r_associated | relid=0 | w=20
  1475. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Waterhouse-Friderichsen syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Waterhouse-Friderichsen syndrome | rel=r_associated | relid=0 | w=20
  1476. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Wegener granulomatosis
    n1=en:pseudotrisomy 13 syndrome | n2=en:Wegener granulomatosis | rel=r_associated | relid=0 | w=20
  1477. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Whipple disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Whipple disease | rel=r_associated | relid=0 | w=20
  1478. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Williams syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20
  1479. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:wilms tumor 1 gene syndromes
    n1=en:pseudotrisomy 13 syndrome | n2=en:wilms tumor 1 gene syndromes | rel=r_associated | relid=0 | w=20
  1480. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:wolman's disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:wolman's disease | rel=r_associated | relid=0 | w=20
  1481. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Wolman's disease
    n1=en:pseudotrisomy 13 syndrome | n2=en:Wolman's disease | rel=r_associated | relid=0 | w=20
  1482. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability seemanova type
    n1=en:pseudotrisomy 13 syndrome | n2=en:x-linked intellectual disability seemanova type | rel=r_associated | relid=0 | w=20
  1483. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability stoll type
    n1=en:pseudotrisomy 13 syndrome | n2=en:x-linked intellectual disability stoll type | rel=r_associated | relid=0 | w=20
  1484. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:yemenite deaf-blind hypopigmentation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20
  1485. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:Zellweger syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:Zellweger syndrome | rel=r_associated | relid=0 | w=20
  1486. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> en:zellweger-like syndrome without peroxisomal anomaly
    n1=en:pseudotrisomy 13 syndrome | n2=en:zellweger-like syndrome without peroxisomal anomaly | rel=r_associated | relid=0 | w=20
  1487. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> érythermalgie
    n1=en:pseudotrisomy 13 syndrome | n2=érythermalgie | rel=r_associated | relid=0 | w=20
  1488. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> erythromelalgia
    n1=en:pseudotrisomy 13 syndrome | n2=erythromelalgia | rel=r_associated | relid=0 | w=20
  1489. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> érythromélalgie
    n1=en:pseudotrisomy 13 syndrome | n2=érythromélalgie | rel=r_associated | relid=0 | w=20
  1490. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> examen non précisé, méningite tuberculeuse
    n1=en:pseudotrisomy 13 syndrome | n2=examen non précisé, méningite tuberculeuse | rel=r_associated | relid=0 | w=20
  1491. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> exomphale
    n1=en:pseudotrisomy 13 syndrome | n2=exomphale | rel=r_associated | relid=0 | w=20
  1492. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> exomphale congénitale
    n1=en:pseudotrisomy 13 syndrome | n2=exomphale congénitale | rel=r_associated | relid=0 | w=20
  1493. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> fucosidose
    n1=en:pseudotrisomy 13 syndrome | n2=fucosidose | rel=r_associated | relid=0 | w=20
  1494. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> gigantisme cérébral
    n1=en:pseudotrisomy 13 syndrome | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
  1495. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Goltz
    n1=en:pseudotrisomy 13 syndrome | n2=Goltz | rel=r_associated | relid=0 | w=20
  1496. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale
    n1=en:pseudotrisomy 13 syndrome | n2=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | rel=r_associated | relid=0 | w=20
  1497. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hémicéphalie
    n1=en:pseudotrisomy 13 syndrome | n2=hémicéphalie | rel=r_associated | relid=0 | w=20
  1498. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hérédité autosomale récessive
    n1=en:pseudotrisomy 13 syndrome | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
  1499. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hernie ombilicale
    n1=en:pseudotrisomy 13 syndrome | n2=hernie ombilicale | rel=r_associated | relid=0 | w=20
  1500. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hernie ombilicale congénitale
    n1=en:pseudotrisomy 13 syndrome | n2=hernie ombilicale congénitale | rel=r_associated | relid=0 | w=20
  1501. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hernies ombilicales
    n1=en:pseudotrisomy 13 syndrome | n2=hernies ombilicales | rel=r_associated | relid=0 | w=20
  1502. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hétérotaxie
    n1=en:pseudotrisomy 13 syndrome | n2=hétérotaxie | rel=r_associated | relid=0 | w=20
  1503. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> histidinémie
    n1=en:pseudotrisomy 13 syndrome | n2=histidinémie | rel=r_associated | relid=0 | w=20
  1504. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> histiocytose sinusale hémophagocytaire
    n1=en:pseudotrisomy 13 syndrome | n2=histiocytose sinusale hémophagocytaire | rel=r_associated | relid=0 | w=20
  1505. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie
    n1=en:pseudotrisomy 13 syndrome | n2=holoprosencéphalie | rel=r_associated | relid=0 | w=20
  1506. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie de type 2
    n1=en:pseudotrisomy 13 syndrome | n2=holoprosencéphalie de type 2 | rel=r_associated | relid=0 | w=20
  1507. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie de type 3
    n1=en:pseudotrisomy 13 syndrome | n2=holoprosencéphalie de type 3 | rel=r_associated | relid=0 | w=20
  1508. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie de type 4
    n1=en:pseudotrisomy 13 syndrome | n2=holoprosencéphalie de type 4 | rel=r_associated | relid=0 | w=20
  1509. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> holoprosencéphalie familiale alobaire de type 1
    n1=en:pseudotrisomy 13 syndrome | n2=holoprosencéphalie familiale alobaire de type 1 | rel=r_associated | relid=0 | w=20
  1510. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hydrocéphalie
    n1=en:pseudotrisomy 13 syndrome | n2=hydrocéphalie | rel=r_associated | relid=0 | w=20
  1511. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hydrops foetoplacentaire
    n1=en:pseudotrisomy 13 syndrome | n2=hydrops foetoplacentaire | rel=r_associated | relid=0 | w=20
  1512. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hyperoxalurie primaire
    n1=en:pseudotrisomy 13 syndrome | n2=hyperoxalurie primaire | rel=r_associated | relid=0 | w=20
  1513. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hyperoxalurie primitive
    n1=en:pseudotrisomy 13 syndrome | n2=hyperoxalurie primitive | rel=r_associated | relid=0 | w=20
  1514. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hyperplasie congénitale des surrénales
    n1=en:pseudotrisomy 13 syndrome | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20
  1515. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypertrophie staturale avec macroglossie et omphalocèle
    n1=en:pseudotrisomy 13 syndrome | n2=hypertrophie staturale avec macroglossie et omphalocèle | rel=r_associated | relid=0 | w=20
  1516. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypophosphatasie foetale
    n1=en:pseudotrisomy 13 syndrome | n2=hypophosphatasie foetale | rel=r_associated | relid=0 | w=20
  1517. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypophosphatasie infantile
    n1=en:pseudotrisomy 13 syndrome | n2=hypophosphatasie infantile | rel=r_associated | relid=0 | w=20
  1518. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypoplasie dermique en aires
    n1=en:pseudotrisomy 13 syndrome | n2=hypoplasie dermique en aires | rel=r_associated | relid=0 | w=20
  1519. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypoplasie dermique focale
    n1=en:pseudotrisomy 13 syndrome | n2=hypoplasie dermique focale | rel=r_associated | relid=0 | w=20
  1520. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypothyroïdie (manifestations neuromusculaires dans l')
    n1=en:pseudotrisomy 13 syndrome | n2=hypothyroïdie (manifestations neuromusculaires dans l') | rel=r_associated | relid=0 | w=20
  1521. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypotonie
    n1=en:pseudotrisomy 13 syndrome | n2=hypotonie | rel=r_associated | relid=0 | w=20
  1522. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypotonie musculaire
    n1=en:pseudotrisomy 13 syndrome | n2=hypotonie musculaire | rel=r_associated | relid=0 | w=20
  1523. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Hypotonie musculaire
    n1=en:pseudotrisomy 13 syndrome | n2=Hypotonie musculaire | rel=r_associated | relid=0 | w=20
  1524. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypotonie, obésité et incisives proéminentes
    n1=en:pseudotrisomy 13 syndrome | n2=hypotonie, obésité et incisives proéminentes | rel=r_associated | relid=0 | w=20
  1525. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> hypoxémie
    n1=en:pseudotrisomy 13 syndrome | n2=hypoxémie | rel=r_associated | relid=0 | w=20
  1526. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ichthyose
    n1=en:pseudotrisomy 13 syndrome | n2=ichthyose | rel=r_associated | relid=0 | w=20
  1527. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ichtyose
    n1=en:pseudotrisomy 13 syndrome | n2=ichtyose | rel=r_associated | relid=0 | w=20
  1528. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ichtyose folliculaire, atrichie et photophobie
    n1=en:pseudotrisomy 13 syndrome | n2=ichtyose folliculaire, atrichie et photophobie | rel=r_associated | relid=0 | w=20
  1529. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ichtyose, affection neurologique spastique, et oligophrénie
    n1=en:pseudotrisomy 13 syndrome | n2=ichtyose, affection neurologique spastique, et oligophrénie | rel=r_associated | relid=0 | w=20
  1530. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ictère nucléaire
    n1=en:pseudotrisomy 13 syndrome | n2=ictère nucléaire | rel=r_associated | relid=0 | w=20
  1531. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> idiotie spastique amaurotique axonale
    n1=en:pseudotrisomy 13 syndrome | n2=idiotie spastique amaurotique axonale | rel=r_associated | relid=0 | w=20
  1532. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> imperforation anale
    n1=en:pseudotrisomy 13 syndrome | n2=imperforation anale | rel=r_associated | relid=0 | w=20
  1533. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> imperforation de l'anus
    n1=en:pseudotrisomy 13 syndrome | n2=imperforation de l'anus | rel=r_associated | relid=0 | w=20
  1534. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> inflammation musculaire
    n1=en:pseudotrisomy 13 syndrome | n2=inflammation musculaire | rel=r_associated | relid=0 | w=20
  1535. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> insensibilité congénitale à la douleur de type III
    n1=en:pseudotrisomy 13 syndrome | n2=insensibilité congénitale à la douleur de type III | rel=r_associated | relid=0 | w=20
  1536. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> insuffisance pulmonaire post-traumatique
    n1=en:pseudotrisomy 13 syndrome | n2=insuffisance pulmonaire post-traumatique | rel=r_associated | relid=0 | w=20
  1537. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> insuffisance respiratoire, problème respiratoire
    n1=en:pseudotrisomy 13 syndrome | n2=insuffisance respiratoire, problème respiratoire | rel=r_associated | relid=0 | w=20
  1538. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> intolérance au fructose
    n1=en:pseudotrisomy 13 syndrome | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
  1539. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Kawasaki (maladie de)
    n1=en:pseudotrisomy 13 syndrome | n2=Kawasaki (maladie de) | rel=r_associated | relid=0 | w=20
  1540. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> lèpre
    n1=en:pseudotrisomy 13 syndrome | n2=lèpre | rel=r_associated | relid=0 | w=20
  1541. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> léproserie
    n1=en:pseudotrisomy 13 syndrome | n2=léproserie | rel=r_associated | relid=0 | w=20
  1542. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> leprosy
    n1=en:pseudotrisomy 13 syndrome | n2=leprosy | rel=r_associated | relid=0 | w=20
  1543. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> leptoméningite tuberculeuse
    n1=en:pseudotrisomy 13 syndrome | n2=leptoméningite tuberculeuse | rel=r_associated | relid=0 | w=20
  1544. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> leucinose
    n1=en:pseudotrisomy 13 syndrome | n2=leucinose | rel=r_associated | relid=0 | w=20
  1545. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> lévocardie
    n1=en:pseudotrisomy 13 syndrome | n2=lévocardie | rel=r_associated | relid=0 | w=20
  1546. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> lipodystrophie partielle familiale
    n1=en:pseudotrisomy 13 syndrome | n2=lipodystrophie partielle familiale | rel=r_associated | relid=0 | w=20
  1547. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> lissencéphalie
    n1=en:pseudotrisomy 13 syndrome | n2=lissencéphalie | rel=r_associated | relid=0 | w=20
  1548. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> macroglossie
    n1=en:pseudotrisomy 13 syndrome | n2=macroglossie | rel=r_associated | relid=0 | w=20
  1549. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> macrosomie foetale
    n1=en:pseudotrisomy 13 syndrome | n2=macrosomie foetale | rel=r_associated | relid=0 | w=20
  1550. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie à virus de Marburg
    n1=en:pseudotrisomy 13 syndrome | n2=maladie à virus de Marburg | rel=r_associated | relid=0 | w=20
  1551. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Dercum
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Dercum | rel=r_associated | relid=0 | w=20
  1552. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de dercum
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de dercum | rel=r_associated | relid=0 | w=20
  1553. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de dubin-johnson
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de dubin-johnson | rel=r_associated | relid=0 | w=20
  1554. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de hurler
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de hurler | rel=r_associated | relid=0 | w=20
  1555. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Hurler
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Hurler | rel=r_associated | relid=0 | w=20
  1556. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Kawasaki
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Kawasaki | rel=r_associated | relid=0 | w=20
  1557. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de marfan
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de marfan | rel=r_associated | relid=0 | w=20
  1558. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Niemann-Pick
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Niemann-Pick | rel=r_associated | relid=0 | w=20
  1559. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Perthes
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Perthes | rel=r_associated | relid=0 | w=20
  1560. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Roger
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Roger | rel=r_associated | relid=0 | w=20
  1561. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de roger
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de roger | rel=r_associated | relid=0 | w=20
  1562. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de seitelberger
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de seitelberger | rel=r_associated | relid=0 | w=20
  1563. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Seitelberger
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Seitelberger | rel=r_associated | relid=0 | w=20
  1564. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Tay-Sachs
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
  1565. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de tay-sachs
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20
  1566. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Tay-sachs
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20
  1567. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Maladie de Whipple
    n1=en:pseudotrisomy 13 syndrome | n2=Maladie de Whipple | rel=r_associated | relid=0 | w=20
  1568. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Whipple
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Whipple | rel=r_associated | relid=0 | w=20
  1569. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de whipple
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de whipple | rel=r_associated | relid=0 | w=20
  1570. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de wolman
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de wolman | rel=r_associated | relid=0 | w=20
  1571. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Maladie de Wolman
    n1=en:pseudotrisomy 13 syndrome | n2=Maladie de Wolman | rel=r_associated | relid=0 | w=20
  1572. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie de Wolman
    n1=en:pseudotrisomy 13 syndrome | n2=maladie de Wolman | rel=r_associated | relid=0 | w=20
  1573. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie des épiphyses ponctuées
    n1=en:pseudotrisomy 13 syndrome | n2=maladie des épiphyses ponctuées | rel=r_associated | relid=0 | w=20
  1574. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:pseudotrisomy 13 syndrome | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
  1575. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie des urines avec odeur de sirop erable
    n1=en:pseudotrisomy 13 syndrome | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
  1576. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie du cri du chat
    n1=en:pseudotrisomy 13 syndrome | n2=maladie du cri du chat | rel=r_associated | relid=0 | w=20
  1577. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie du sirop d'érable
    n1=en:pseudotrisomy 13 syndrome | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
  1578. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladie lysosomique de surcharge
    n1=en:pseudotrisomy 13 syndrome | n2=maladie lysosomique de surcharge | rel=r_associated | relid=0 | w=20
  1579. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> maladies des bandes amniotiques
    n1=en:pseudotrisomy 13 syndrome | n2=maladies des bandes amniotiques | rel=r_associated | relid=0 | w=20
  1580. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> malformation d'Arnold-Chiari
    n1=en:pseudotrisomy 13 syndrome | n2=malformation d'Arnold-Chiari | rel=r_associated | relid=0 | w=20
  1581. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> malformation d'arnold-chiari
    n1=en:pseudotrisomy 13 syndrome | n2=malformation d'arnold-chiari | rel=r_associated | relid=0 | w=20
  1582. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Malformation d'Arnold-Chiari
    n1=en:pseudotrisomy 13 syndrome | n2=Malformation d'Arnold-Chiari | rel=r_associated | relid=0 | w=20
  1583. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> méningite tuberculeuse
    n1=en:pseudotrisomy 13 syndrome | n2=méningite tuberculeuse | rel=r_associated | relid=0 | w=20
  1584. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> méningite tuberculeuse examen non précisé
    n1=en:pseudotrisomy 13 syndrome | n2=méningite tuberculeuse examen non précisé | rel=r_associated | relid=0 | w=20
  1585. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> mésentérique supérieure (syndrome de l'artère)
    n1=en:pseudotrisomy 13 syndrome | n2=mésentérique supérieure (syndrome de l'artère) | rel=r_associated | relid=0 | w=20
  1586. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> mort subite du nourrisson
    n1=en:pseudotrisomy 13 syndrome | n2=mort subite du nourrisson | rel=r_associated | relid=0 | w=20
  1587. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> mucolipidose II
    n1=en:pseudotrisomy 13 syndrome | n2=mucolipidose II | rel=r_associated | relid=0 | w=20
  1588. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> mucolipidose type ii
    n1=en:pseudotrisomy 13 syndrome | n2=mucolipidose type ii | rel=r_associated | relid=0 | w=20
  1589. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> mucolipidose type II
    n1=en:pseudotrisomy 13 syndrome | n2=mucolipidose type II | rel=r_associated | relid=0 | w=20
  1590. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> myocardiopathie de tako-tsubo
    n1=en:pseudotrisomy 13 syndrome | n2=myocardiopathie de tako-tsubo | rel=r_associated | relid=0 | w=20
  1591. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> myokymie
    n1=en:pseudotrisomy 13 syndrome | n2=myokymie | rel=r_associated | relid=0 | w=20
  1592. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> myosite
    n1=en:pseudotrisomy 13 syndrome | n2=myosite | rel=r_associated | relid=0 | w=20
  1593. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> myosites
    n1=en:pseudotrisomy 13 syndrome | n2=myosites | rel=r_associated | relid=0 | w=20
  1594. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> néphrocalcinose
    n1=en:pseudotrisomy 13 syndrome | n2=néphrocalcinose | rel=r_associated | relid=0 | w=20
  1595. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> neuro-acanthocytose
    n1=en:pseudotrisomy 13 syndrome | n2=neuro-acanthocytose | rel=r_associated | relid=0 | w=20
  1596. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> neurocysticercose
    n1=en:pseudotrisomy 13 syndrome | n2=neurocysticercose | rel=r_associated | relid=0 | w=20
  1597. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> neuropathie optique
    n1=en:pseudotrisomy 13 syndrome | n2=neuropathie optique | rel=r_associated | relid=0 | w=20
  1598. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> nevrilème
    n1=en:pseudotrisomy 13 syndrome | n2=nevrilème | rel=r_associated | relid=0 | w=20
  1599. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> névrite optique
    n1=en:pseudotrisomy 13 syndrome | n2=névrite optique | rel=r_associated | relid=0 | w=20
  1600. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> noma
    n1=en:pseudotrisomy 13 syndrome | n2=noma | rel=r_associated | relid=0 | w=20
  1601. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> nystagmus congénital isolé
    n1=en:pseudotrisomy 13 syndrome | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  1602. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> odontogénèse imparfaite
    n1=en:pseudotrisomy 13 syndrome | n2=odontogénèse imparfaite | rel=r_associated | relid=0 | w=20
  1603. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> oedème du poumon non cardiogénique
    n1=en:pseudotrisomy 13 syndrome | n2=oedème du poumon non cardiogénique | rel=r_associated | relid=0 | w=20
  1604. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> oedème pulmonaire non cardiogénique
    n1=en:pseudotrisomy 13 syndrome | n2=oedème pulmonaire non cardiogénique | rel=r_associated | relid=0 | w=20
  1605. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> omphalocèle
    n1=en:pseudotrisomy 13 syndrome | n2=omphalocèle | rel=r_associated | relid=0 | w=20
  1606. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> omphalocèles
    n1=en:pseudotrisomy 13 syndrome | n2=omphalocèles | rel=r_associated | relid=0 | w=20
  1607. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ongles jaunes (syndrome des)
    n1=en:pseudotrisomy 13 syndrome | n2=ongles jaunes (syndrome des) | rel=r_associated | relid=0 | w=20
  1608. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> onycho-ostéodysostose
    n1=en:pseudotrisomy 13 syndrome | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20
  1609. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> onycho-patellaire (syndrome)
    n1=en:pseudotrisomy 13 syndrome | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20
  1610. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose
    n1=en:pseudotrisomy 13 syndrome | n2=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | rel=r_associated | relid=0 | w=20
  1611. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ophtalmorhino-stomatoxérose
    n1=en:pseudotrisomy 13 syndrome | n2=ophtalmorhino-stomatoxérose | rel=r_associated | relid=0 | w=20
  1612. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasie
    n1=en:pseudotrisomy 13 syndrome | n2=ostéochondrodysplasie | rel=r_associated | relid=0 | w=20
  1613. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasies
    n1=en:pseudotrisomy 13 syndrome | n2=ostéochondrodysplasies | rel=r_associated | relid=0 | w=20
  1614. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ostéopétrose avec acidose rénale tubulaire
    n1=en:pseudotrisomy 13 syndrome | n2=ostéopétrose avec acidose rénale tubulaire | rel=r_associated | relid=0 | w=20
  1615. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ostéopoecilie
    n1=en:pseudotrisomy 13 syndrome | n2=ostéopoecilie | rel=r_associated | relid=0 | w=20
  1616. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> otocéphale
    n1=en:pseudotrisomy 13 syndrome | n2=otocéphale | rel=r_associated | relid=0 | w=20
  1617. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> otocéphalie
    n1=en:pseudotrisomy 13 syndrome | n2=otocéphalie | rel=r_associated | relid=0 | w=20
  1618. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> oxalose
    n1=en:pseudotrisomy 13 syndrome | n2=oxalose | rel=r_associated | relid=0 | w=20
  1619. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> oxalose primitive
    n1=en:pseudotrisomy 13 syndrome | n2=oxalose primitive | rel=r_associated | relid=0 | w=20
  1620. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> oxaloses
    n1=en:pseudotrisomy 13 syndrome | n2=oxaloses | rel=r_associated | relid=0 | w=20
  1621. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> pachyméningite hypertrophique tuberculeuse
    n1=en:pseudotrisomy 13 syndrome | n2=pachyméningite hypertrophique tuberculeuse | rel=r_associated | relid=0 | w=20
  1622. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> pachyonychie congénitale de Jadassohn-Lewandowsky
    n1=en:pseudotrisomy 13 syndrome | n2=pachyonychie congénitale de Jadassohn-Lewandowsky | rel=r_associated | relid=0 | w=20
  1623. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> panencéphalite subaiguë sclérosante
    n1=en:pseudotrisomy 13 syndrome | n2=panencéphalite subaiguë sclérosante | rel=r_associated | relid=0 | w=20
  1624. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> panuvéite
    n1=en:pseudotrisomy 13 syndrome | n2=panuvéite | rel=r_associated | relid=0 | w=20
  1625. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> papulose atrophiante maligne de Degos
    n1=en:pseudotrisomy 13 syndrome | n2=papulose atrophiante maligne de Degos | rel=r_associated | relid=0 | w=20
  1626. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> paragangliome (mise en évidence scintigraphique du)
    n1=en:pseudotrisomy 13 syndrome | n2=paragangliome (mise en évidence scintigraphique du) | rel=r_associated | relid=0 | w=20
  1627. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> paragonimiase
    n1=en:pseudotrisomy 13 syndrome | n2=paragonimiase | rel=r_associated | relid=0 | w=20
  1628. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> paragonimose
    n1=en:pseudotrisomy 13 syndrome | n2=paragonimose | rel=r_associated | relid=0 | w=20
  1629. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> paralysie périodique familiale
    n1=en:pseudotrisomy 13 syndrome | n2=paralysie périodique familiale | rel=r_associated | relid=0 | w=20
  1630. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> paralysie supranucléaire progressive
    n1=en:pseudotrisomy 13 syndrome | n2=paralysie supranucléaire progressive | rel=r_associated | relid=0 | w=20
  1631. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> pemphigoïde bénigne des muqueuses
    n1=en:pseudotrisomy 13 syndrome | n2=pemphigoïde bénigne des muqueuses | rel=r_associated | relid=0 | w=20
  1632. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> peste
    n1=en:pseudotrisomy 13 syndrome | n2=peste | rel=r_associated | relid=0 | w=20
  1633. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> peste noire
    n1=en:pseudotrisomy 13 syndrome | n2=peste noire | rel=r_associated | relid=0 | w=20
  1634. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> phacomatose congenitale
    n1=en:pseudotrisomy 13 syndrome | n2=phacomatose congenitale | rel=r_associated | relid=0 | w=20
  1635. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> piébaldisme
    n1=en:pseudotrisomy 13 syndrome | n2=piébaldisme | rel=r_associated | relid=0 | w=20
  1636. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> piebaldisme
    n1=en:pseudotrisomy 13 syndrome | n2=piebaldisme | rel=r_associated | relid=0 | w=20
  1637. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> pityriasis rubra pilaire
    n1=en:pseudotrisomy 13 syndrome | n2=pityriasis rubra pilaire | rel=r_associated | relid=0 | w=20
  1638. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Pityriasis rubra pilaire
    n1=en:pseudotrisomy 13 syndrome | n2=Pityriasis rubra pilaire | rel=r_associated | relid=0 | w=20
  1639. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Plummer-Vinson (syndrome de)
    n1=en:pseudotrisomy 13 syndrome | n2=Plummer-Vinson (syndrome de) | rel=r_associated | relid=0 | w=20
  1640. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> porphyrie cutanée tardive
    n1=en:pseudotrisomy 13 syndrome | n2=porphyrie cutanée tardive | rel=r_associated | relid=0 | w=20
  1641. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> porphyrie érythropoïétique
    n1=en:pseudotrisomy 13 syndrome | n2=porphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
  1642. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> poumon de choc
    n1=en:pseudotrisomy 13 syndrome | n2=poumon de choc | rel=r_associated | relid=0 | w=20
  1643. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> poumon de choc traumatique
    n1=en:pseudotrisomy 13 syndrome | n2=poumon de choc traumatique | rel=r_associated | relid=0 | w=20
  1644. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> poumon du vietnam
    n1=en:pseudotrisomy 13 syndrome | n2=poumon du vietnam | rel=r_associated | relid=0 | w=20
  1645. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> présentation sacro-iliaque droite antérieure
    n1=en:pseudotrisomy 13 syndrome | n2=présentation sacro-iliaque droite antérieure | rel=r_associated | relid=0 | w=20
  1646. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> progeria
    n1=en:pseudotrisomy 13 syndrome | n2=progeria | rel=r_associated | relid=0 | w=20
  1647. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> progéria
    n1=en:pseudotrisomy 13 syndrome | n2=progéria | rel=r_associated | relid=0 | w=20
  1648. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> protéinose alvéolaire
    n1=en:pseudotrisomy 13 syndrome | n2=protéinose alvéolaire | rel=r_associated | relid=0 | w=20
  1649. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> protéinose alvéolaire pulmonaire
    n1=en:pseudotrisomy 13 syndrome | n2=protéinose alvéolaire pulmonaire | rel=r_associated | relid=0 | w=20
  1650. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> protoproporphyrie érythropoïétique
    n1=en:pseudotrisomy 13 syndrome | n2=protoproporphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
  1651. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> psychose de korsakoff
    n1=en:pseudotrisomy 13 syndrome | n2=psychose de korsakoff | rel=r_associated | relid=0 | w=20
  1652. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> queue de cheval (syndrome de la)
    n1=en:pseudotrisomy 13 syndrome | n2=queue de cheval (syndrome de la) | rel=r_associated | relid=0 | w=20
  1653. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> rétention des chylomicrons (maladie de la)
    n1=en:pseudotrisomy 13 syndrome | n2=rétention des chylomicrons (maladie de la) | rel=r_associated | relid=0 | w=20
  1654. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> S.I.D.A.
    n1=en:pseudotrisomy 13 syndrome | n2=S.I.D.A. | rel=r_associated | relid=0 | w=20
  1655. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Sars
    n1=en:pseudotrisomy 13 syndrome | n2=Sars | rel=r_associated | relid=0 | w=20
  1656. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> scléromyxoedème d'Arndt-Gottron
    n1=en:pseudotrisomy 13 syndrome | n2=scléromyxoedème d'Arndt-Gottron | rel=r_associated | relid=0 | w=20
  1657. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Seitelberger
    n1=en:pseudotrisomy 13 syndrome | n2=Seitelberger | rel=r_associated | relid=0 | w=20
  1658. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Seitelberger (dystrophie neuroaxonale de)
    n1=en:pseudotrisomy 13 syndrome | n2=Seitelberger (dystrophie neuroaxonale de) | rel=r_associated | relid=0 | w=20
  1659. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Seitelberger (maladie de)
    n1=en:pseudotrisomy 13 syndrome | n2=Seitelberger (maladie de) | rel=r_associated | relid=0 | w=20
  1660. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> septo-optic dysplasia
    n1=en:pseudotrisomy 13 syndrome | n2=septo-optic dysplasia | rel=r_associated | relid=0 | w=20
  1661. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> sicca syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=sicca syndrome | rel=r_associated | relid=0 | w=20
  1662. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> SIDA
    n1=en:pseudotrisomy 13 syndrome | n2=SIDA | rel=r_associated | relid=0 | w=20
  1663. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Silver-Russell (syndrome de)
    n1=en:pseudotrisomy 13 syndrome | n2=Silver-Russell (syndrome de) | rel=r_associated | relid=0 | w=20
  1664. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> sirop d'érable (urine à odeur de)
    n1=en:pseudotrisomy 13 syndrome | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
  1665. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> situs inversus
    n1=en:pseudotrisomy 13 syndrome | n2=situs inversus | rel=r_associated | relid=0 | w=20
  1666. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Sotos (syndrome de)
    n1=en:pseudotrisomy 13 syndrome | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
  1667. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> souffrance respiratoire
    n1=en:pseudotrisomy 13 syndrome | n2=souffrance respiratoire | rel=r_associated | relid=0 | w=20
  1668. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> SRAS
    n1=en:pseudotrisomy 13 syndrome | n2=SRAS | rel=r_associated | relid=0 | w=20
  1669. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome adéno-cutanéo-muqueux
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome adéno-cutanéo-muqueux | rel=r_associated | relid=0 | w=20
  1670. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome adénocutanéomuqueux
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome adénocutanéomuqueux | rel=r_associated | relid=0 | w=20
  1671. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome cardio-facio-cutané
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome cardio-facio-cutané | rel=r_associated | relid=0 | w=20
  1672. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome cérébro-oculo-faciosquelettique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome cérébro-oculo-faciosquelettique | rel=r_associated | relid=0 | w=20
  1673. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Adair-Dighton
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome d'Adair-Dighton | rel=r_associated | relid=0 | w=20
  1674. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Alice au pays des merveilles
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome d'Alice au pays des merveilles | rel=r_associated | relid=0 | w=20
  1675. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Alport
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome d'Alport | rel=r_associated | relid=0 | w=20
  1676. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'alport
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome d'alport | rel=r_associated | relid=0 | w=20
  1677. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'angelman
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome d'angelman | rel=r_associated | relid=0 | w=20
  1678. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Angelman
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  1679. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Syndrome d'Angelman
    n1=en:pseudotrisomy 13 syndrome | n2=Syndrome d'Angelman | rel=r_associated | relid=0 | w=20
  1680. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'immunodéficience acquise
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome d'immunodéficience acquise | rel=r_associated | relid=0 | w=20
  1681. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de bile épaisse
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de bile épaisse | rel=r_associated | relid=0 | w=20
  1682. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de bride amniotique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de bride amniotique | rel=r_associated | relid=0 | w=20
  1683. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de chasse
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de chasse | rel=r_associated | relid=0 | w=20
  1684. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de détresse respiratoire
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de détresse respiratoire | rel=r_associated | relid=0 | w=20
  1685. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de détresse respiratoire aiguë
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de détresse respiratoire aiguë | rel=r_associated | relid=0 | w=20
  1686. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de détresse respiratoire aigüe
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de détresse respiratoire aigüe | rel=r_associated | relid=0 | w=20
  1687. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de détresse respiratoire aiguë
    n1=en:pseudotrisomy 13 syndrome | n2=Syndrome de détresse respiratoire aiguë | rel=r_associated | relid=0 | w=20
  1688. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de douleur extrême paroxystique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de douleur extrême paroxystique | rel=r_associated | relid=0 | w=20
  1689. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de duane
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de duane | rel=r_associated | relid=0 | w=20
  1690. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Duane
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Duane | rel=r_associated | relid=0 | w=20
  1691. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Dubin-Johnson
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Dubin-Johnson | rel=r_associated | relid=0 | w=20
  1692. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de dubin-johnson
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de dubin-johnson | rel=r_associated | relid=0 | w=20
  1693. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de fragilité du chromosome X
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
  1694. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de goltz
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de goltz | rel=r_associated | relid=0 | w=20
  1695. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Goltz
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Goltz | rel=r_associated | relid=0 | w=20
  1696. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Jacobsen
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Jacobsen | rel=r_associated | relid=0 | w=20
  1697. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de jadassohn-lewandowsky
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de jadassohn-lewandowsky | rel=r_associated | relid=0 | w=20
  1698. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Jadassohn-Lewandowsky
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Jadassohn-Lewandowsky | rel=r_associated | relid=0 | w=20
  1699. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Joubert-Boltshauser (syndrome de)
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Joubert-Boltshauser (syndrome de) | rel=r_associated | relid=0 | w=20
  1700. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de kawasaki
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de kawasaki | rel=r_associated | relid=0 | w=20
  1701. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Kawasaki
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Kawasaki | rel=r_associated | relid=0 | w=20
  1702. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Kelly-Paterson
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Kelly-Paterson | rel=r_associated | relid=0 | w=20
  1703. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de l'arc aortique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de l'arc aortique | rel=r_associated | relid=0 | w=20
  1704. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de l'immunodéficience acquise
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de l'immunodéficience acquise | rel=r_associated | relid=0 | w=20
  1705. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de la crosse aortique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de la crosse aortique | rel=r_associated | relid=0 | w=20
  1706. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de la mort subite du nourrisson
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de la mort subite du nourrisson | rel=r_associated | relid=0 | w=20
  1707. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de la queue de cheval
    n1=en:pseudotrisomy 13 syndrome | n2=Syndrome de la queue de cheval | rel=r_associated | relid=0 | w=20
  1708. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de la queue de cheval
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de la queue de cheval | rel=r_associated | relid=0 | w=20
  1709. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Laurence-Moon
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20
  1710. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de malabsorption
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de malabsorption | rel=r_associated | relid=0 | w=20
  1711. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de marfan
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20
  1712. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de Marfan
    n1=en:pseudotrisomy 13 syndrome | n2=Syndrome de Marfan | rel=r_associated | relid=0 | w=20
  1713. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Martin-Bell
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
  1714. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de membrane hyaline
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de membrane hyaline | rel=r_associated | relid=0 | w=20
  1715. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de plummer-vinson
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de plummer-vinson | rel=r_associated | relid=0 | w=20
  1716. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de Plummer-Vinson
    n1=en:pseudotrisomy 13 syndrome | n2=Syndrome de Plummer-Vinson | rel=r_associated | relid=0 | w=20
  1717. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Plummer-Vinson
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Plummer-Vinson | rel=r_associated | relid=0 | w=20
  1718. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de réaction inflammatoire généralisée
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de réaction inflammatoire généralisée | rel=r_associated | relid=0 | w=20
  1719. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de rett
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de rett | rel=r_associated | relid=0 | w=20
  1720. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de Rett
    n1=en:pseudotrisomy 13 syndrome | n2=Syndrome de Rett | rel=r_associated | relid=0 | w=20
  1721. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Rett
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Rett | rel=r_associated | relid=0 | w=20
  1722. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Sheehan
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Sheehan | rel=r_associated | relid=0 | w=20
  1723. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Shy-Drager
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Shy-Drager | rel=r_associated | relid=0 | w=20
  1724. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de shy-drager
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de shy-drager | rel=r_associated | relid=0 | w=20
  1725. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Syndrome de Shy-Drager
    n1=en:pseudotrisomy 13 syndrome | n2=Syndrome de Shy-Drager | rel=r_associated | relid=0 | w=20
  1726. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de silver-russell
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de silver-russell | rel=r_associated | relid=0 | w=20
  1727. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Silver-Russell
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Silver-Russell | rel=r_associated | relid=0 | w=20
  1728. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de soto
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
  1729. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Sotos
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
  1730. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de sotos
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
  1731. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Stilling-Türk-Duane
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Stilling-Türk-Duane | rel=r_associated | relid=0 | w=20
  1732. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de synostose spondylo-carpo-tarsale
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de synostose spondylo-carpo-tarsale | rel=r_associated | relid=0 | w=20
  1733. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de türk-stilling-duane
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de türk-stilling-duane | rel=r_associated | relid=0 | w=20
  1734. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Türk-Stilling-Duane
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome de Türk-Stilling-Duane | rel=r_associated | relid=0 | w=20
  1735. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome des brides amniotiques
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome des brides amniotiques | rel=r_associated | relid=0 | w=20
  1736. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome des yeux de chat
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome des yeux de chat | rel=r_associated | relid=0 | w=20
  1737. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome du bébé gris
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome du bébé gris | rel=r_associated | relid=0 | w=20
  1738. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome du canal tarsien
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome du canal tarsien | rel=r_associated | relid=0 | w=20
  1739. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome du choc toxique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome du choc toxique | rel=r_associated | relid=0 | w=20
  1740. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome du grêle court
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome du grêle court | rel=r_associated | relid=0 | w=20
  1741. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome du tunnel tarsien
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome du tunnel tarsien | rel=r_associated | relid=0 | w=20
  1742. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome gris du nourrisson
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome gris du nourrisson | rel=r_associated | relid=0 | w=20
  1743. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome hémolytique et urémique atypique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome hémolytique et urémique atypique | rel=r_associated | relid=0 | w=20
  1744. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome hétérotaxique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome hétérotaxique | rel=r_associated | relid=0 | w=20
  1745. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome inflammatoire aigu systémique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome inflammatoire aigu systémique | rel=r_associated | relid=0 | w=20
  1746. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome lympho-cutanéo-muqueux
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome lympho-cutanéo-muqueux | rel=r_associated | relid=0 | w=20
  1747. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome métabolique
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome métabolique | rel=r_associated | relid=0 | w=20
  1748. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome sec
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome sec | rel=r_associated | relid=0 | w=20
  1749. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome TORCH
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome TORCH | rel=r_associated | relid=0 | w=20
  1750. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome torch
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome torch | rel=r_associated | relid=0 | w=20
  1751. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type 2
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome tricho-rhino-phalangien de type 2 | rel=r_associated | relid=0 | w=20
  1752. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type II
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome tricho-rhino-phalangien de type II | rel=r_associated | relid=0 | w=20
  1753. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> syndrome tricho-rhino-phalangien de type ii
    n1=en:pseudotrisomy 13 syndrome | n2=syndrome tricho-rhino-phalangien de type ii | rel=r_associated | relid=0 | w=20
  1754. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> toxémie staphylococcique
    n1=en:pseudotrisomy 13 syndrome | n2=toxémie staphylococcique | rel=r_associated | relid=0 | w=20
  1755. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> trachéo-bronchomégalie
    n1=en:pseudotrisomy 13 syndrome | n2=trachéo-bronchomégalie | rel=r_associated | relid=0 | w=20
  1756. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> trichothiodystrophie
    n1=en:pseudotrisomy 13 syndrome | n2=trichothiodystrophie | rel=r_associated | relid=0 | w=20
  1757. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> tuberculose des méninges
    n1=en:pseudotrisomy 13 syndrome | n2=tuberculose des méninges | rel=r_associated | relid=0 | w=20
  1758. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> tuberculose méningée
    n1=en:pseudotrisomy 13 syndrome | n2=tuberculose méningée | rel=r_associated | relid=0 | w=20
  1759. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> tunnel tarsien (syndrome du)
    n1=en:pseudotrisomy 13 syndrome | n2=tunnel tarsien (syndrome du) | rel=r_associated | relid=0 | w=20
  1760. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Türk-Stilling-Duane (syndrome de)
    n1=en:pseudotrisomy 13 syndrome | n2=Türk-Stilling-Duane (syndrome de) | rel=r_associated | relid=0 | w=20
  1761. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> van Bogaert (xanthomatose cérébrotendineuse de)
    n1=en:pseudotrisomy 13 syndrome | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20
  1762. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> varicelle congénitale
    n1=en:pseudotrisomy 13 syndrome | n2=varicelle congénitale | rel=r_associated | relid=0 | w=20
  1763. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> ventriculomégalie cérébrale
    n1=en:pseudotrisomy 13 syndrome | n2=ventriculomégalie cérébrale | rel=r_associated | relid=0 | w=20
  1764. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Walker-Warburg (syndrome de)
    n1=en:pseudotrisomy 13 syndrome | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20
  1765. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> wallérienne (dégénérescence)
    n1=en:pseudotrisomy 13 syndrome | n2=wallérienne (dégénérescence) | rel=r_associated | relid=0 | w=20
  1766. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Warburg
    n1=en:pseudotrisomy 13 syndrome | n2=Warburg | rel=r_associated | relid=0 | w=20
  1767. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Whipple (maladie de)
    n1=en:pseudotrisomy 13 syndrome | n2=Whipple (maladie de) | rel=r_associated | relid=0 | w=20
  1768. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Wolman (maladie de)
    n1=en:pseudotrisomy 13 syndrome | n2=Wolman (maladie de) | rel=r_associated | relid=0 | w=20
  1769. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> xanthomatose cérébro-tendineuse
    n1=en:pseudotrisomy 13 syndrome | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20
  1770. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse
    n1=en:pseudotrisomy 13 syndrome | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20
  1771. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse de Van Bogaert
    n1=en:pseudotrisomy 13 syndrome | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20
  1772. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> xeroderma pigmentosum
    n1=en:pseudotrisomy 13 syndrome | n2=xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  1773. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> Xeroderma pigmentosum
    n1=en:pseudotrisomy 13 syndrome | n2=Xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  1774. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> xérodermite pigmentaire
    n1=en:pseudotrisomy 13 syndrome | n2=xérodermite pigmentaire | rel=r_associated | relid=0 | w=20
  1775. en:pseudotrisomy 13 syndrome -- r_associated #0: 20 / 0.465 -> yellow nail syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=yellow nail syndrome | rel=r_associated | relid=0 | w=20
≈ 2494 relations entrantes

  1. en:maple syrup urine disease --- r_associated #0: 696 --> en:pseudotrisomy 13 syndrome
    n1=en:maple syrup urine disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=696
  2. maladie du sirop d'érable --- r_associated #0: 604.37 --> en:pseudotrisomy 13 syndrome
    n1=maladie du sirop d'érable | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=604.37
  3. leucinose --- r_associated #0: 599.18 --> en:pseudotrisomy 13 syndrome
    n1=leucinose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=599.18
  4. en:branched-chain ketoaciduria --- r_associated #0: 520 --> en:pseudotrisomy 13 syndrome
    n1=en:branched-chain ketoaciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=520
  5. peste
    (maladie)
     --- r_associated #0: 499 --> en:pseudotrisomy 13 syndrome
    n1=peste
    (maladie)
    | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=499
  6. en:plague --- r_associated #0: 495 --> en:pseudotrisomy 13 syndrome
    n1=en:plague | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=495
  7. en:SIDS --- r_associated #0: 355 --> en:pseudotrisomy 13 syndrome
    n1=en:SIDS | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=355
  8. en:cot death --- r_associated #0: 355 --> en:pseudotrisomy 13 syndrome
    n1=en:cot death | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=355
  9. mort subite du nourrisson --- r_associated #0: 355 --> en:pseudotrisomy 13 syndrome
    n1=mort subite du nourrisson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=355
  10. en:sudden infant death syndrome --- r_associated #0: 351 --> en:pseudotrisomy 13 syndrome
    n1=en:sudden infant death syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=351
  11. syndrome de la mort subite du nourrisson --- r_associated #0: 345 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de la mort subite du nourrisson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=345
  12. omphalocèle --- r_associated #0: 323 --> en:pseudotrisomy 13 syndrome
    n1=omphalocèle | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=323
  13. en:omphalocele --- r_associated #0: 319 --> en:pseudotrisomy 13 syndrome
    n1=en:omphalocele | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=319
  14. atélectasie congestive --- r_associated #0: 315 --> en:pseudotrisomy 13 syndrome
    n1=atélectasie congestive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=315
  15. exomphale --- r_associated #0: 315 --> en:pseudotrisomy 13 syndrome
    n1=exomphale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=315
  16. hernie ombilicale congénitale --- r_associated #0: 315 --> en:pseudotrisomy 13 syndrome
    n1=hernie ombilicale congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=315
  17. syndrome du choc toxique --- r_associated #0: 315 --> en:pseudotrisomy 13 syndrome
    n1=syndrome du choc toxique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=315
  18. en:toxic shock syndrome --- r_associated #0: 314 --> en:pseudotrisomy 13 syndrome
    n1=en:toxic shock syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=314
  19. omphalocèles --- r_associated #0: 311 --> en:pseudotrisomy 13 syndrome
    n1=omphalocèles | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=311
  20. choc au poumon --- r_associated #0: 310 --> en:pseudotrisomy 13 syndrome
    n1=choc au poumon | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=310
  21. exomphale congénitale --- r_associated #0: 310 --> en:pseudotrisomy 13 syndrome
    n1=exomphale congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=310
  22. poumon du vietnam --- r_associated #0: 310 --> en:pseudotrisomy 13 syndrome
    n1=poumon du vietnam | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=310
  23. insuffisance pulmonaire post-traumatique --- r_associated #0: 306 --> en:pseudotrisomy 13 syndrome
    n1=insuffisance pulmonaire post-traumatique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=306
  24. hernie ombilicale --- r_associated #0: 305 --> en:pseudotrisomy 13 syndrome
    n1=hernie ombilicale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=305
  25. oedème du poumon non cardiogénique --- r_associated #0: 304 --> en:pseudotrisomy 13 syndrome
    n1=oedème du poumon non cardiogénique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=304
  26. oedème pulmonaire non cardiogénique --- r_associated #0: 301 --> en:pseudotrisomy 13 syndrome
    n1=oedème pulmonaire non cardiogénique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=301
  27. en:umbilical hernia --- r_associated #0: 300 --> en:pseudotrisomy 13 syndrome
    n1=en:umbilical hernia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=300
  28. poumon de choc traumatique --- r_associated #0: 300 --> en:pseudotrisomy 13 syndrome
    n1=poumon de choc traumatique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=300
  29. hernies ombilicales --- r_associated #0: 296 --> en:pseudotrisomy 13 syndrome
    n1=hernies ombilicales | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=296
  30. en:Toxic Shock Syndrome --- r_associated #0: 295 --> en:pseudotrisomy 13 syndrome
    n1=en:Toxic Shock Syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=295
  31. en:acute respiratory distress syndrome --- r_associated #0: 288 --> en:pseudotrisomy 13 syndrome
    n1=en:acute respiratory distress syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=288
  32. en:marfan syndrome --- r_associated #0: 285 --> en:pseudotrisomy 13 syndrome
    n1=en:marfan syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=285
  33. en:craniosynostosis --- r_associated #0: 284 --> en:pseudotrisomy 13 syndrome
    n1=en:craniosynostosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=284
  34. crâniosynostose --- r_associated #0: 281 --> en:pseudotrisomy 13 syndrome
    n1=crâniosynostose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=281
  35. maladie de Marfan --- r_associated #0: 281 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Marfan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=281
  36. syndrome de Marfan --- r_associated #0: 281 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Marfan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=281
  37. craniosynostose --- r_associated #0: 280 --> en:pseudotrisomy 13 syndrome
    n1=craniosynostose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=280
  38. crâniosténose --- r_associated #0: 280 --> en:pseudotrisomy 13 syndrome
    n1=crâniosténose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=280
  39. Sars --- r_associated #0: 279 --> en:pseudotrisomy 13 syndrome
    n1=Sars | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=279
  40. crânio-sténose --- r_associated #0: 276 --> en:pseudotrisomy 13 syndrome
    n1=crânio-sténose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=276
  41. arachnodactylie --- r_associated #0: 274 --> en:pseudotrisomy 13 syndrome
    n1=arachnodactylie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=274
  42. en:langer-giedion syndrome --- r_associated #0: 273 --> en:pseudotrisomy 13 syndrome
    n1=en:langer-giedion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=273
  43. syndrome de détresse respiratoire aigüe --- r_associated #0: 273 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de détresse respiratoire aigüe | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=273
  44. en:crib death --- r_associated #0: 265 --> en:pseudotrisomy 13 syndrome
    n1=en:crib death | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=265
  45. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 265 --> en:pseudotrisomy 13 syndrome
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=265
  46. atrophie optique autosomique dominante --- r_associated #0: 264 --> en:pseudotrisomy 13 syndrome
    n1=atrophie optique autosomique dominante | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=264
  47. poumon de choc --- r_associated #0: 264 --> en:pseudotrisomy 13 syndrome
    n1=poumon de choc | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=264
  48. en:classical maple syrup urine disease --- r_associated #0: 260 --> en:pseudotrisomy 13 syndrome
    n1=en:classical maple syrup urine disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=260
  49. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 260 --> en:pseudotrisomy 13 syndrome
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=260
  50. maladie des urines avec odeur de sirop erable --- r_associated #0: 260 --> en:pseudotrisomy 13 syndrome
    n1=maladie des urines avec odeur de sirop erable | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=260
  51. méningite tuberculeuse --- r_associated #0: 256 --> en:pseudotrisomy 13 syndrome
    n1=méningite tuberculeuse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=256
  52. déficit en céto-acide décarboxylase --- r_associated #0: 255 --> en:pseudotrisomy 13 syndrome
    n1=déficit en céto-acide décarboxylase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=255
  53. en:meningeal tuberculosis --- r_associated #0: 255 --> en:pseudotrisomy 13 syndrome
    n1=en:meningeal tuberculosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=255
  54. en:tuberculosis of meninges (cerebral)(spinal) --- r_associated #0: 255 --> en:pseudotrisomy 13 syndrome
    n1=en:tuberculosis of meninges (cerebral)(spinal) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=255
  55. examen non précisé, méningite tuberculeuse --- r_associated #0: 255 --> en:pseudotrisomy 13 syndrome
    n1=examen non précisé, méningite tuberculeuse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=255
  56. leptoméningite tuberculeuse --- r_associated #0: 255 --> en:pseudotrisomy 13 syndrome
    n1=leptoméningite tuberculeuse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=255
  57. syndrome de détresse respiratoire aiguë --- r_associated #0: 255 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de détresse respiratoire aiguë | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=255
  58. tuberculose des méninges --- r_associated #0: 255 --> en:pseudotrisomy 13 syndrome
    n1=tuberculose des méninges | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=255
  59. tuberculose méningée --- r_associated #0: 255 --> en:pseudotrisomy 13 syndrome
    n1=tuberculose méningée | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=255
  60. en:arachnodactyly --- r_associated #0: 250 --> en:pseudotrisomy 13 syndrome
    n1=en:arachnodactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=250
  61. en:tuberculosis, meningeal --- r_associated #0: 250 --> en:pseudotrisomy 13 syndrome
    n1=en:tuberculosis, meningeal | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=250
  62. en:tuberculous hypertrophic pachymeningitides --- r_associated #0: 250 --> en:pseudotrisomy 13 syndrome
    n1=en:tuberculous hypertrophic pachymeningitides | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=250
  63. en:tuberculous leptomeningitis --- r_associated #0: 250 --> en:pseudotrisomy 13 syndrome
    n1=en:tuberculous leptomeningitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=250
  64. syndrome de chasse --- r_associated #0: 250 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de chasse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=250
  65. en:dumping syndrome --- r_associated #0: 246 --> en:pseudotrisomy 13 syndrome
    n1=en:dumping syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=246
  66. pachyméningite hypertrophique tuberculeuse --- r_associated #0: 245 --> en:pseudotrisomy 13 syndrome
    n1=pachyméningite hypertrophique tuberculeuse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=245
  67. en:acromelic frontonasal dysostosis --- r_associated #0: 243 --> en:pseudotrisomy 13 syndrome
    n1=en:acromelic frontonasal dysostosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=243
  68. dysostose fronto-nasale acromélique --- r_associated #0: 242 --> en:pseudotrisomy 13 syndrome
    n1=dysostose fronto-nasale acromélique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=242
  69. dysplasie fronto-nasale acromélique --- r_associated #0: 240 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie fronto-nasale acromélique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=240
  70. en:anterior plagiocephalies, synostotic --- r_associated #0: 237 --> en:pseudotrisomy 13 syndrome
    n1=en:anterior plagiocephalies, synostotic | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=237
  71. Warburg --- r_associated #0: 210 --> en:pseudotrisomy 13 syndrome
    n1=Warburg | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=210
  72. en:primary progressive aphasia --- r_associated #0: 210 --> en:pseudotrisomy 13 syndrome
    n1=en:primary progressive aphasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=210
  73. méningite tuberculeuse examen non précisé --- r_associated #0: 210 --> en:pseudotrisomy 13 syndrome
    n1=méningite tuberculeuse examen non précisé | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=210
  74. aphasie primaire progressive --- r_associated #0: 209 --> en:pseudotrisomy 13 syndrome
    n1=aphasie primaire progressive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=209
  75. en:gray baby syndrome --- r_associated #0: 207 --> en:pseudotrisomy 13 syndrome
    n1=en:gray baby syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=207
  76. aphasies primaires progressives --- r_associated #0: 206 --> en:pseudotrisomy 13 syndrome
    n1=aphasies primaires progressives | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=206
  77. syndrome du bébé gris --- r_associated #0: 205 --> en:pseudotrisomy 13 syndrome
    n1=syndrome du bébé gris | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=205
  78. en:sotos syndrome --- r_associated #0: 204 --> en:pseudotrisomy 13 syndrome
    n1=en:sotos syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=204
  79. gigantisme cérébral --- r_associated #0: 201 --> en:pseudotrisomy 13 syndrome
    n1=gigantisme cérébral | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=201
  80. hypoxémie --- r_associated #0: 201 --> en:pseudotrisomy 13 syndrome
    n1=hypoxémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=201
  81. syndrome de soto --- r_associated #0: 200 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de soto | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=200
  82. syndrome gris du nourrisson --- r_associated #0: 200 --> en:pseudotrisomy 13 syndrome
    n1=syndrome gris du nourrisson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=200
  83. syndrome de Sotos --- r_associated #0: 195 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Sotos | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=195
  84. hypoplasie dermique en aires --- r_associated #0: 192 --> en:pseudotrisomy 13 syndrome
    n1=hypoplasie dermique en aires | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=192
  85. Goltz --- r_associated #0: 190 --> en:pseudotrisomy 13 syndrome
    n1=Goltz | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=190
  86. en:focal dermal hypoplasia --- r_associated #0: 190 --> en:pseudotrisomy 13 syndrome
    n1=en:focal dermal hypoplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=190
  87. en:sotos' syndrome --- r_associated #0: 190 --> en:pseudotrisomy 13 syndrome
    n1=en:sotos' syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=190
  88. hypoplasie dermique focale --- r_associated #0: 190 --> en:pseudotrisomy 13 syndrome
    n1=hypoplasie dermique focale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=190
  89. syndrome de Goltz --- r_associated #0: 190 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Goltz | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=190
  90. craniosténose --- r_associated #0: 185 --> en:pseudotrisomy 13 syndrome
    n1=craniosténose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=185
  91. en:Plummer-Vinson syndrome --- r_associated #0: 180 --> en:pseudotrisomy 13 syndrome
    n1=en:Plummer-Vinson syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=180
  92. en:walker-warburg syndrome --- r_associated #0: 180 --> en:pseudotrisomy 13 syndrome
    n1=en:walker-warburg syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=180
  93. en:plummer-vinson syndrome --- r_associated #0: 178 --> en:pseudotrisomy 13 syndrome
    n1=en:plummer-vinson syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=178
  94. syndrome de Walker-Warburg --- r_associated #0: 178 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Walker-Warburg | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=178
  95. aphasie progressive primaire --- r_associated #0: 175 --> en:pseudotrisomy 13 syndrome
    n1=aphasie progressive primaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=175
  96. en:pyruvate carboxylase deficiency --- r_associated #0: 175 --> en:pseudotrisomy 13 syndrome
    n1=en:pyruvate carboxylase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=175
  97. en:xeroderma pigmentosum --- r_associated #0: 175 --> en:pseudotrisomy 13 syndrome
    n1=en:xeroderma pigmentosum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=175
  98. xeroderma pigmentosum --- r_associated #0: 174 --> en:pseudotrisomy 13 syndrome
    n1=xeroderma pigmentosum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=174
  99. en:zellweger syndrome --- r_associated #0: 172 --> en:pseudotrisomy 13 syndrome
    n1=en:zellweger syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=172
  100. déficit en pyruvate carboxylase --- r_associated #0: 171 --> en:pseudotrisomy 13 syndrome
    n1=déficit en pyruvate carboxylase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=171
  101. en:Zellweger syndrome --- r_associated #0: 170 --> en:pseudotrisomy 13 syndrome
    n1=en:Zellweger syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=170
  102. paralysies périodiques familiales --- r_associated #0: 168 --> en:pseudotrisomy 13 syndrome
    n1=paralysies périodiques familiales | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=168
  103. en:familial periodic paralysis --- r_associated #0: 167 --> en:pseudotrisomy 13 syndrome
    n1=en:familial periodic paralysis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=167
  104. paralysie périodique familiale --- r_associated #0: 165 --> en:pseudotrisomy 13 syndrome
    n1=paralysie périodique familiale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=165
  105. syndrome d'Alport --- r_associated #0: 161 --> en:pseudotrisomy 13 syndrome
    n1=syndrome d'Alport | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=161
  106. en:Diskinson's syndrome --- r_associated #0: 160 --> en:pseudotrisomy 13 syndrome
    n1=en:Diskinson's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=160
  107. en:wolman disease --- r_associated #0: 157 --> en:pseudotrisomy 13 syndrome
    n1=en:wolman disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=157
  108. en:arthrogryposis --- r_associated #0: 156 --> en:pseudotrisomy 13 syndrome
    n1=en:arthrogryposis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=156
  109. maladie de Wolman --- r_associated #0: 156 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Wolman | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=156
  110. arthrogrypose --- r_associated #0: 155 --> en:pseudotrisomy 13 syndrome
    n1=arthrogrypose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=155
  111. hyperoxalurie primaire --- r_associated #0: 151 --> en:pseudotrisomy 13 syndrome
    n1=hyperoxalurie primaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=151
  112. malformation d'Arnold-Chiari --- r_associated #0: 151 --> en:pseudotrisomy 13 syndrome
    n1=malformation d'Arnold-Chiari | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=151
  113. oxaloses --- r_associated #0: 151 --> en:pseudotrisomy 13 syndrome
    n1=oxaloses | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=151
  114. hyperoxalurie primitive --- r_associated #0: 150 --> en:pseudotrisomy 13 syndrome
    n1=hyperoxalurie primitive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=150
  115. en:primary hyperoxaluria --- r_associated #0: 147 --> en:pseudotrisomy 13 syndrome
    n1=en:primary hyperoxaluria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=147
  116. oxalose primitive --- r_associated #0: 146 --> en:pseudotrisomy 13 syndrome
    n1=oxalose primitive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=146
  117. en:arnold chiari malformation --- r_associated #0: 145 --> en:pseudotrisomy 13 syndrome
    n1=en:arnold chiari malformation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=145
  118. syndrome de Türk-Stilling-Duane --- r_associated #0: 145 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Türk-Stilling-Duane | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=145
  119. en:duane syndrome --- r_associated #0: 144 --> en:pseudotrisomy 13 syndrome
    n1=en:duane syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=144
  120. hypophosphatasie infantile --- r_associated #0: 143 --> en:pseudotrisomy 13 syndrome
    n1=hypophosphatasie infantile | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=143
  121. en:arnold-chiari malformation --- r_associated #0: 142 --> en:pseudotrisomy 13 syndrome
    n1=en:arnold-chiari malformation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=142
  122. ostéochondrodysplasies --- r_associated #0: 141 --> en:pseudotrisomy 13 syndrome
    n1=ostéochondrodysplasies | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=141
  123. syndrome de Duane --- r_associated #0: 141 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Duane | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=141
  124. oxalose --- r_associated #0: 140 --> en:pseudotrisomy 13 syndrome
    n1=oxalose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=140
  125. en:infantile hypophosphatasia --- r_associated #0: 139 --> en:pseudotrisomy 13 syndrome
    n1=en:infantile hypophosphatasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=139
  126. hypophosphatasie foetale --- r_associated #0: 139 --> en:pseudotrisomy 13 syndrome
    n1=hypophosphatasie foetale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=139
  127. en:osteochondrodysplasia --- r_associated #0: 137 --> en:pseudotrisomy 13 syndrome
    n1=en:osteochondrodysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=137
  128. en:angelman syndrome --- r_associated #0: 132 --> en:pseudotrisomy 13 syndrome
    n1=en:angelman syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=132
  129. syndrome de duane --- r_associated #0: 131 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de duane | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=131
  130. syndrome d'Angelman --- r_associated #0: 130 --> en:pseudotrisomy 13 syndrome
    n1=syndrome d'Angelman | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=130
  131. démence frontotemporale --- r_associated #0: 115 --> en:pseudotrisomy 13 syndrome
    n1=démence frontotemporale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=115
  132. en:cytochrome-c oxidase deficiency --- r_associated #0: 114 --> en:pseudotrisomy 13 syndrome
    n1=en:cytochrome-c oxidase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=114
  133. aïnhum --- r_associated #0: 113 --> en:pseudotrisomy 13 syndrome
    n1=aïnhum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=113
  134. déficit en cytochrome oxydase --- r_associated #0: 112 --> en:pseudotrisomy 13 syndrome
    n1=déficit en cytochrome oxydase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=112
  135. démence fronto-temporale --- r_associated #0: 112 --> en:pseudotrisomy 13 syndrome
    n1=démence fronto-temporale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=112
  136. en:ainhum --- r_associated #0: 111 --> en:pseudotrisomy 13 syndrome
    n1=en:ainhum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=111
  137. en:yellow nail syndrome --- r_associated #0: 109 --> en:pseudotrisomy 13 syndrome
    n1=en:yellow nail syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=109
  138. ainhum --- r_associated #0: 107 --> en:pseudotrisomy 13 syndrome
    n1=ainhum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=107
  139. otocéphalie --- r_associated #0: 106 --> en:pseudotrisomy 13 syndrome
    n1=otocéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=106
  140. yellow nail syndrome --- r_associated #0: 106 --> en:pseudotrisomy 13 syndrome
    n1=yellow nail syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=106
  141. en:pulmonary shunting --- r_associated #0: 105 --> en:pseudotrisomy 13 syndrome
    n1=en:pulmonary shunting | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=105
  142. en:otocephaly --- r_associated #0: 103 --> en:pseudotrisomy 13 syndrome
    n1=en:otocephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=103
  143. en:kawasaki disease --- r_associated #0: 101 --> en:pseudotrisomy 13 syndrome
    n1=en:kawasaki disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=101
  144. syndrome de Plummer-Vinson --- r_associated #0: 101 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Plummer-Vinson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=101
  145. anencéphalie --- r_associated #0: 100 --> en:pseudotrisomy 13 syndrome
    n1=anencéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=100
  146. en:frontotemporal dementia --- r_associated #0: 100 --> en:pseudotrisomy 13 syndrome
    n1=en:frontotemporal dementia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=100
  147. en:progressive supranuclear palsy --- r_associated #0: 100 --> en:pseudotrisomy 13 syndrome
    n1=en:progressive supranuclear palsy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=100
  148. syndrome de Rett --- r_associated #0: 100 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Rett | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=100
  149. en:anencephaly --- r_associated #0: 99 --> en:pseudotrisomy 13 syndrome
    n1=en:anencephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=99
  150. maladie de Kawasaki --- r_associated #0: 99 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Kawasaki | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=99
  151. en:rett syndrome --- r_associated #0: 98 --> en:pseudotrisomy 13 syndrome
    n1=en:rett syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=98
  152. lissencéphalie --- r_associated #0: 98 --> en:pseudotrisomy 13 syndrome
    n1=lissencéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=98
  153. en:lissencephaly --- r_associated #0: 97 --> en:pseudotrisomy 13 syndrome
    n1=en:lissencephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=97
  154. paralysie supranucléaire progressive --- r_associated #0: 97 --> en:pseudotrisomy 13 syndrome
    n1=paralysie supranucléaire progressive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=97
  155. syndrome adéno-cutanéo-muqueux --- r_associated #0: 97 --> en:pseudotrisomy 13 syndrome
    n1=syndrome adéno-cutanéo-muqueux | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=97
  156. syndrome adénocutanéomuqueux --- r_associated #0: 97 --> en:pseudotrisomy 13 syndrome
    n1=syndrome adénocutanéomuqueux | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=97
  157. en:piebaldism --- r_associated #0: 96 --> en:pseudotrisomy 13 syndrome
    n1=en:piebaldism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=96
  158. syndrome des brides amniotiques --- r_associated #0: 96 --> en:pseudotrisomy 13 syndrome
    n1=syndrome des brides amniotiques | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=96
  159. déficit en cytochrome-c oxydase --- r_associated #0: 95 --> en:pseudotrisomy 13 syndrome
    n1=déficit en cytochrome-c oxydase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=95
  160. en:amniotic band syndrome --- r_associated #0: 95 --> en:pseudotrisomy 13 syndrome
    n1=en:amniotic band syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=95
  161. hyperplasie congénitale des surrénales --- r_associated #0: 95 --> en:pseudotrisomy 13 syndrome
    n1=hyperplasie congénitale des surrénales | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=95
  162. piebaldisme --- r_associated #0: 95 --> en:pseudotrisomy 13 syndrome
    n1=piebaldisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=95
  163. piébaldisme --- r_associated #0: 95 --> en:pseudotrisomy 13 syndrome
    n1=piébaldisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=95
  164. sicca syndrome --- r_associated #0: 95 --> en:pseudotrisomy 13 syndrome
    n1=sicca syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=95
  165. syndrome de Kawasaki --- r_associated #0: 95 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Kawasaki | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=95
  166. syndrome lympho-cutanéo-muqueux --- r_associated #0: 95 --> en:pseudotrisomy 13 syndrome
    n1=syndrome lympho-cutanéo-muqueux | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=95
  167. en:congenital adrenal hyperplasia --- r_associated #0: 94 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital adrenal hyperplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=94
  168. en:sicca syndrome --- r_associated #0: 94 --> en:pseudotrisomy 13 syndrome
    n1=en:sicca syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=94
  169. en:alice in wonderland syndrome --- r_associated #0: 92 --> en:pseudotrisomy 13 syndrome
    n1=en:alice in wonderland syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=92
  170. dystrophie neuroaxonale de Seitelberger --- r_associated #0: 91 --> en:pseudotrisomy 13 syndrome
    n1=dystrophie neuroaxonale de Seitelberger | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=91
  171. maladies des bandes amniotiques --- r_associated #0: 91 --> en:pseudotrisomy 13 syndrome
    n1=maladies des bandes amniotiques | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=91
  172. en:Alice in Wonderland syndrome --- r_associated #0: 90 --> en:pseudotrisomy 13 syndrome
    n1=en:Alice in Wonderland syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=90
  173. en:Angelman syndrome --- r_associated #0: 90 --> en:pseudotrisomy 13 syndrome
    n1=en:Angelman syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=90
  174. en:Umbilical hernia --- r_associated #0: 90 --> en:pseudotrisomy 13 syndrome
    n1=en:Umbilical hernia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=90
  175. en:jacobsen syndrome --- r_associated #0: 90 --> en:pseudotrisomy 13 syndrome
    n1=en:jacobsen syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=90
  176. en:septo-optic dysplasia --- r_associated #0: 90 --> en:pseudotrisomy 13 syndrome
    n1=en:septo-optic dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=90
  177. progeria --- r_associated #0: 90 --> en:pseudotrisomy 13 syndrome
    n1=progeria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=90
  178. protéinose alvéolaire --- r_associated #0: 90 --> en:pseudotrisomy 13 syndrome
    n1=protéinose alvéolaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=90
  179. protéinose alvéolaire pulmonaire --- r_associated #0: 90 --> en:pseudotrisomy 13 syndrome
    n1=protéinose alvéolaire pulmonaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=90
  180. syndrome de l'immunodéficience acquise --- r_associated #0: 90 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de l'immunodéficience acquise | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=90
  181. dumping syndrome --- r_associated #0: 89 --> en:pseudotrisomy 13 syndrome
    n1=dumping syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=89
  182. en:progeria --- r_associated #0: 89 --> en:pseudotrisomy 13 syndrome
    n1=en:progeria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=89
  183. septo-optic dysplasia --- r_associated #0: 89 --> en:pseudotrisomy 13 syndrome
    n1=septo-optic dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=89
  184. dystrophie neuro-axonale infantile --- r_associated #0: 87 --> en:pseudotrisomy 13 syndrome
    n1=dystrophie neuro-axonale infantile | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=87
  185. dystrophie neuroaxonale --- r_associated #0: 87 --> en:pseudotrisomy 13 syndrome
    n1=dystrophie neuroaxonale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=87
  186. dystrophie neuroaxonale infantile --- r_associated #0: 87 --> en:pseudotrisomy 13 syndrome
    n1=dystrophie neuroaxonale infantile | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=87
  187. idiotie spastique amaurotique axonale --- r_associated #0: 87 --> en:pseudotrisomy 13 syndrome
    n1=idiotie spastique amaurotique axonale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=87
  188. en:acquired immunodeficiency syndrome --- r_associated #0: 86 --> en:pseudotrisomy 13 syndrome
    n1=en:acquired immunodeficiency syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=86
  189. en:pulmonary alveolar proteinosis --- r_associated #0: 86 --> en:pseudotrisomy 13 syndrome
    n1=en:pulmonary alveolar proteinosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=86
  190. syndrome de Jacobsen --- r_associated #0: 86 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Jacobsen | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=86
  191. syndrome de bride amniotique --- r_associated #0: 86 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de bride amniotique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=86
  192. syndrome d'immunodéficience acquise --- r_associated #0: 85 --> en:pseudotrisomy 13 syndrome
    n1=syndrome d'immunodéficience acquise | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=85
  193. dentinogenesis imperfecta --- r_associated #0: 83 --> en:pseudotrisomy 13 syndrome
    n1=dentinogenesis imperfecta | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=83
  194. en:ventriculomeglia --- r_associated #0: 83 --> en:pseudotrisomy 13 syndrome
    n1=en:ventriculomeglia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=83
  195. hydrocéphalie --- r_associated #0: 83 --> en:pseudotrisomy 13 syndrome
    n1=hydrocéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=83
  196. syndrome tricho-rhino-phalangien de type ii --- r_associated #0: 82 --> en:pseudotrisomy 13 syndrome
    n1=syndrome tricho-rhino-phalangien de type ii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=82
  197. en:cerebral ventriculomegaly --- r_associated #0: 81 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebral ventriculomegaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=81
  198. en:dentinogenesis imperfecta --- r_associated #0: 81 --> en:pseudotrisomy 13 syndrome
    n1=en:dentinogenesis imperfecta | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=81
  199. progéria --- r_associated #0: 81 --> en:pseudotrisomy 13 syndrome
    n1=progéria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=81
  200. syndrome tricho-rhino-phalangien de type 2 --- r_associated #0: 81 --> en:pseudotrisomy 13 syndrome
    n1=syndrome tricho-rhino-phalangien de type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=81
  201. en:cerebral tuberculosis --- r_associated #0: 80 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebral tuberculosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=80
  202. syndrome d'Alice au pays des merveilles --- r_associated #0: 80 --> en:pseudotrisomy 13 syndrome
    n1=syndrome d'Alice au pays des merveilles | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=80
  203. syndrome du canal tarsien --- r_associated #0: 78 --> en:pseudotrisomy 13 syndrome
    n1=syndrome du canal tarsien | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=78
  204. syndrome de türk-stilling-duane --- r_associated #0: 77 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de türk-stilling-duane | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=77
  205. ventriculomégalie cérébrale --- r_associated #0: 77 --> en:pseudotrisomy 13 syndrome
    n1=ventriculomégalie cérébrale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=77
  206. Seitelberger --- r_associated #0: 76 --> en:pseudotrisomy 13 syndrome
    n1=Seitelberger | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=76
  207. albinisme --- r_associated #0: 76 --> en:pseudotrisomy 13 syndrome
    n1=albinisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=76
  208. Malformation d'Arnold-Chiari --- r_associated #0: 75 --> en:pseudotrisomy 13 syndrome
    n1=Malformation d'Arnold-Chiari | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=75
  209. dystrophies neuroaxonales --- r_associated #0: 75 --> en:pseudotrisomy 13 syndrome
    n1=dystrophies neuroaxonales | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=75
  210. en:trichorhinophalangeal syndrome type ii --- r_associated #0: 75 --> en:pseudotrisomy 13 syndrome
    n1=en:trichorhinophalangeal syndrome type ii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=75
  211. en:fragile x syndrome --- r_associated #0: 74 --> en:pseudotrisomy 13 syndrome
    n1=en:fragile x syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=74
  212. en:tarsal tunnel syndrome --- r_associated #0: 74 --> en:pseudotrisomy 13 syndrome
    n1=en:tarsal tunnel syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=74
  213. syndrome de Kelly-Paterson --- r_associated #0: 74 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Kelly-Paterson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=74
  214. en:albinism --- r_associated #0: 73 --> en:pseudotrisomy 13 syndrome
    n1=en:albinism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=73
  215. en:torch syndrome --- r_associated #0: 72 --> en:pseudotrisomy 13 syndrome
    n1=en:torch syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=72
  216. syndrome TORCH --- r_associated #0: 71 --> en:pseudotrisomy 13 syndrome
    n1=syndrome TORCH | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=71
  217. SIDA --- r_associated #0: 70 --> en:pseudotrisomy 13 syndrome
    n1=SIDA | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=70
  218. anasarque foetal --- r_associated #0: 70 --> en:pseudotrisomy 13 syndrome
    n1=anasarque foetal | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=70
  219. en:fragile X syndrome --- r_associated #0: 70 --> en:pseudotrisomy 13 syndrome
    n1=en:fragile X syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=70
  220. maladie de Seitelberger --- r_associated #0: 70 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Seitelberger | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=70
  221. détresse respiratoire --- r_associated #0: 69 --> en:pseudotrisomy 13 syndrome
    n1=détresse respiratoire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=69
  222. en:atrial septal defect --- r_associated #0: 69 --> en:pseudotrisomy 13 syndrome
    n1=en:atrial septal defect | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=69
  223. en:hydrops fetalis --- r_associated #0: 69 --> en:pseudotrisomy 13 syndrome
    n1=en:hydrops fetalis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=69
  224. malformation d'arnold-chiari --- r_associated #0: 69 --> en:pseudotrisomy 13 syndrome
    n1=malformation d'arnold-chiari | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=69
  225. anomalie du septum auriculaire --- r_associated #0: 68 --> en:pseudotrisomy 13 syndrome
    n1=anomalie du septum auriculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=68
  226. chromosome 13 --- r_associated #0: 68 --> en:pseudotrisomy 13 syndrome
    n1=chromosome 13 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=68
  227. en:russell-silver syndrome --- r_associated #0: 68 --> en:pseudotrisomy 13 syndrome
    n1=en:russell-silver syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=68
  228. en:chromosome 13 --- r_associated #0: 67 --> en:pseudotrisomy 13 syndrome
    n1=en:chromosome 13 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=67
  229. syndrome torch --- r_associated #0: 67 --> en:pseudotrisomy 13 syndrome
    n1=syndrome torch | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=67
  230. en:korsakoff syndrome --- r_associated #0: 66 --> en:pseudotrisomy 13 syndrome
    n1=en:korsakoff syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=66
  231. en:respiratory distress syndrome --- r_associated #0: 66 --> en:pseudotrisomy 13 syndrome
    n1=en:respiratory distress syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=66
  232. Syndrome d'Angelman --- r_associated #0: 65 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome d'Angelman | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=65
  233. Syndrome de Rett --- r_associated #0: 65 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Rett | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=65
  234. association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né --- r_associated #0: 65 --> en:pseudotrisomy 13 syndrome
    n1=association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=65
  235. en:Klinefelter syndrome --- r_associated #0: 65 --> en:pseudotrisomy 13 syndrome
    n1=en:Klinefelter syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=65
  236. en:Korsakoff syndrome --- r_associated #0: 65 --> en:pseudotrisomy 13 syndrome
    n1=en:Korsakoff syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=65
  237. syndrome de Silver-Russell --- r_associated #0: 65 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Silver-Russell | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=65
  238. syndrome de détresse respiratoire --- r_associated #0: 65 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de détresse respiratoire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=65
  239. syndrome de fragilité du chromosome X --- r_associated #0: 65 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de fragilité du chromosome X | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=65
  240. anti-sida --- r_associated #0: 63 --> en:pseudotrisomy 13 syndrome
    n1=anti-sida | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=63
  241. en:Kawasaki disease --- r_associated #0: 62 --> en:pseudotrisomy 13 syndrome
    n1=en:Kawasaki disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=62
  242. en:klinefelter syndrome --- r_associated #0: 62 --> en:pseudotrisomy 13 syndrome
    n1=en:klinefelter syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=62
  243. algodystrophies --- r_associated #0: 61 --> en:pseudotrisomy 13 syndrome
    n1=algodystrophies | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=61
  244. DentinoGenesis Imperfecta --- r_associated #0: 60 --> en:pseudotrisomy 13 syndrome
    n1=DentinoGenesis Imperfecta | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=60
  245. congénitale --- r_associated #0: 60 --> en:pseudotrisomy 13 syndrome
    n1=congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=60
  246. en:AIDS --- r_associated #0: 60 --> en:pseudotrisomy 13 syndrome
    n1=en:AIDS | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=60
  247. en:Sotos' syndrome --- r_associated #0: 60 --> en:pseudotrisomy 13 syndrome
    n1=en:Sotos' syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=60
  248. antisida --- r_associated #0: 59 --> en:pseudotrisomy 13 syndrome
    n1=antisida | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=59
  249. syndrome de rett --- r_associated #0: 59 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de rett | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=59
  250. syndrome d'angelman --- r_associated #0: 57 --> en:pseudotrisomy 13 syndrome
    n1=syndrome d'angelman | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=57
  251. syndrome de silver-russell --- r_associated #0: 57 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de silver-russell | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=57
  252. acromégalie --- r_associated #0: 56 --> en:pseudotrisomy 13 syndrome
    n1=acromégalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=56
  253. en:congenital --- r_associated #0: 56 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=56
  254. situs inversus --- r_associated #0: 56 --> en:pseudotrisomy 13 syndrome
    n1=situs inversus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=56
  255. trachéo-bronchomégalie --- r_associated #0: 56 --> en:pseudotrisomy 13 syndrome
    n1=trachéo-bronchomégalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=56
  256. Xeroderma pigmentosum --- r_associated #0: 55 --> en:pseudotrisomy 13 syndrome
    n1=Xeroderma pigmentosum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=55
  257. dystrophies neuro-axonales --- r_associated #0: 55 --> en:pseudotrisomy 13 syndrome
    n1=dystrophies neuro-axonales | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=55
  258. en:acromegaly --- r_associated #0: 55 --> en:pseudotrisomy 13 syndrome
    n1=en:acromegaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=55
  259. en:immune deficiency syndrome --- r_associated #0: 55 --> en:pseudotrisomy 13 syndrome
    n1=en:immune deficiency syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=55
  260. en:infantile neuroaxonal dystrophy --- r_associated #0: 55 --> en:pseudotrisomy 13 syndrome
    n1=en:infantile neuroaxonal dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=55
  261. en:mucocutaneous lymph node syndrome --- r_associated #0: 55 --> en:pseudotrisomy 13 syndrome
    n1=en:mucocutaneous lymph node syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=55
  262. en:situs inversus --- r_associated #0: 55 --> en:pseudotrisomy 13 syndrome
    n1=en:situs inversus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=55
  263. en:tracheobronchomegaly --- r_associated #0: 55 --> en:pseudotrisomy 13 syndrome
    n1=en:tracheobronchomegaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=55
  264. hypertrophie staturale avec macroglossie et omphalocèle --- r_associated #0: 55 --> en:pseudotrisomy 13 syndrome
    n1=hypertrophie staturale avec macroglossie et omphalocèle | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=55
  265. congénital --- r_associated #0: 54 --> en:pseudotrisomy 13 syndrome
    n1=congénital | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=54
  266. en:guillain-barre syndrome --- r_associated #0: 54 --> en:pseudotrisomy 13 syndrome
    n1=en:guillain-barre syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=54
  267. en:alport syndrome --- r_associated #0: 53 --> en:pseudotrisomy 13 syndrome
    n1=en:alport syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=53
  268. en:down syndrome --- r_associated #0: 53 --> en:pseudotrisomy 13 syndrome
    n1=en:down syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=53
  269. hydrops foetoplacentaire --- r_associated #0: 53 --> en:pseudotrisomy 13 syndrome
    n1=hydrops foetoplacentaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=53
  270. psychose de korsakoff --- r_associated #0: 53 --> en:pseudotrisomy 13 syndrome
    n1=psychose de korsakoff | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=53
  271. peste --- r_associated #0: 52 --> en:pseudotrisomy 13 syndrome
    n1=peste | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=52
  272. dentine opalescente héréditaire --- r_associated #0: 51 --> en:pseudotrisomy 13 syndrome
    n1=dentine opalescente héréditaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=51
  273. syndrome d'alport --- r_associated #0: 51 --> en:pseudotrisomy 13 syndrome
    n1=syndrome d'alport | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=51
  274. syndrome tricho-rhino-phalangien de type II --- r_associated #0: 51 --> en:pseudotrisomy 13 syndrome
    n1=syndrome tricho-rhino-phalangien de type II | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=51
  275. xanthomatose cérébro-tendineuse --- r_associated #0: 51 --> en:pseudotrisomy 13 syndrome
    n1=xanthomatose cérébro-tendineuse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=51
  276. xanthomatose cérébrotendineuse --- r_associated #0: 51 --> en:pseudotrisomy 13 syndrome
    n1=xanthomatose cérébrotendineuse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=51
  277. Syndrome de la queue de cheval --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de la queue de cheval | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  278. acrodermatite entéropathique --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=acrodermatite entéropathique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  279. cœur triatrial --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=cœur triatrial | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  280. en:Down syndrome --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=en:Down syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  281. en:Guillain-Barre syndrome --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=en:Guillain-Barre syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  282. en:Wolman's disease --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=en:Wolman's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  283. en:disease aids --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=en:disease aids | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  284. en:hydrencephalus --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=en:hydrencephalus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  285. en:macroglossia --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=en:macroglossia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  286. en:respiratory distress --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=en:respiratory distress | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  287. hydrops fœtoplacentaire --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=hydrops fœtoplacentaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  288. macrosomie fœtale --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=macrosomie fœtale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  289. queue de cheval (syndrome de la) --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=queue de cheval (syndrome de la) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  290. syndrome de goltz --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de goltz | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  291. xérodermite pigmentaire --- r_associated #0: 50 --> en:pseudotrisomy 13 syndrome
    n1=xérodermite pigmentaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=50
  292. en:cerebrotendinous xanthomatosis --- r_associated #0: 49 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebrotendinous xanthomatosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=49
  293. en:prader-willi syndrome --- r_associated #0: 49 --> en:pseudotrisomy 13 syndrome
    n1=en:prader-willi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=49
  294. en:schock lung --- r_associated #0: 49 --> en:pseudotrisomy 13 syndrome
    n1=en:schock lung | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=49
  295. maladie de wolman --- r_associated #0: 49 --> en:pseudotrisomy 13 syndrome
    n1=maladie de wolman | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=49
  296. otocéphale --- r_associated #0: 49 --> en:pseudotrisomy 13 syndrome
    n1=otocéphale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=49
  297. syndrome du tunnel tarsien --- r_associated #0: 49 --> en:pseudotrisomy 13 syndrome
    n1=syndrome du tunnel tarsien | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=49
  298. Türk-Stilling-Duane (syndrome de) --- r_associated #0: 48 --> en:pseudotrisomy 13 syndrome
    n1=Türk-Stilling-Duane (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=48
  299. acromegaly --- r_associated #0: 48 --> en:pseudotrisomy 13 syndrome
    n1=acromegaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=48
  300. anasarque foeto-placentaire --- r_associated #0: 48 --> en:pseudotrisomy 13 syndrome
    n1=anasarque foeto-placentaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=48
  301. en:acrodermatitis enteropathica --- r_associated #0: 48 --> en:pseudotrisomy 13 syndrome
    n1=en:acrodermatitis enteropathica | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=48
  302. syndrome des yeux de chat --- r_associated #0: 48 --> en:pseudotrisomy 13 syndrome
    n1=syndrome des yeux de chat | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=48
  303. coeur triatrial --- r_associated #0: 47 --> en:pseudotrisomy 13 syndrome
    n1=coeur triatrial | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=47
  304. en:optic neuritis --- r_associated #0: 47 --> en:pseudotrisomy 13 syndrome
    n1=en:optic neuritis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=47
  305. en:williams syndrome --- r_associated #0: 47 --> en:pseudotrisomy 13 syndrome
    n1=en:williams syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=47
  306. syndrome de marfan --- r_associated #0: 47 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de marfan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=47
  307. tunnel tarsien (syndrome du) --- r_associated #0: 47 --> en:pseudotrisomy 13 syndrome
    n1=tunnel tarsien (syndrome du) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=47
  308. congenital --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=congenital | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  309. en:AIDS awareness --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=en:AIDS awareness | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  310. en:cardio-facio-cutaneous syndrome --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=en:cardio-facio-cutaneous syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  311. en:cat-eye syndrome --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=en:cat-eye syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  312. en:cauda equina syndrome --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=en:cauda equina syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  313. en:stokes-adams syndrome --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=en:stokes-adams syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  314. macrosomie foetale --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=macrosomie foetale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  315. pityriasis rubra pilaire --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=pityriasis rubra pilaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  316. rétention des chylomicrons (maladie de la) --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=rétention des chylomicrons (maladie de la) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  317. syndrome de la queue de cheval --- r_associated #0: 46 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de la queue de cheval | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=46
  318. anasarque foetoplacentaire --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=anasarque foetoplacentaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  319. en:Prader-Willi syndrome --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=en:Prader-Willi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  320. en:Soto's syndrome --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=en:Soto's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  321. en:Triple a syndrome --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=en:Triple a syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  322. en:pityriasis rubra pilaris --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=en:pityriasis rubra pilaris | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  323. intolérance au fructose --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=intolérance au fructose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  324. maladie de Dercum --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Dercum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  325. nevrilème --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=nevrilème | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  326. scléromyxœdème d'Arndt-Gottron --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=scléromyxœdème d'Arndt-Gottron | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  327. xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 45 --> en:pseudotrisomy 13 syndrome
    n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=45
  328. S.I.D.A. --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=S.I.D.A. | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  329. dysostose craniofaciale --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=dysostose craniofaciale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  330. en:Williams syndrome --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=en:Williams syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  331. en:adenocutanemucous syndrome --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=en:adenocutanemucous syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  332. en:heterotaxy syndrome --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=en:heterotaxy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  333. maladie de Roger --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Roger | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  334. névrite optique --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=névrite optique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  335. sirop d'érable (urine à odeur de) --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=sirop d'érable (urine à odeur de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  336. syndrome de kawasaki --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de kawasaki | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  337. syndrome du grêle court --- r_associated #0: 44 --> en:pseudotrisomy 13 syndrome
    n1=syndrome du grêle court | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=44
  338. Syndrome de détresse respiratoire aiguë --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de détresse respiratoire aiguë | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  339. déficit en semialdéhyde succinique-déshydrogénase --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=déficit en semialdéhyde succinique-déshydrogénase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  340. en:atrophoderma vermiculatum --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:atrophoderma vermiculatum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  341. en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  342. en:autosomal recessive scid --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive scid | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  343. en:cardiofaciocutaneous syndrome --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:cardiofaciocutaneous syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  344. en:craniofacial ulnar renal syndrome --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:craniofacial ulnar renal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  345. en:ellis-van creveld syndrome --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:ellis-van creveld syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  346. en:hereditary angioedema --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary angioedema | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  347. en:hereditary spastic paralysis, infantile onset ascending --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary spastic paralysis, infantile onset ascending | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  348. en:laron syndrome --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:laron syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  349. en:ophthalmoneuritis --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:ophthalmoneuritis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  350. en:orofacial cleft 1 --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:orofacial cleft 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  351. en:trichorhinophalangeal syndrome type II --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:trichorhinophalangeal syndrome type II | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  352. en:vitelliform macular dystrophy --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:vitelliform macular dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  353. en:x-linked bulbar-muscular atrophy --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=en:x-linked bulbar-muscular atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  354. syndrome d'Adair-Dighton --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=syndrome d'Adair-Dighton | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  355. syndrome de l'arc aortique --- r_associated #0: 43 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de l'arc aortique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=43
  356. Syndrome de Plummer-Vinson --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Plummer-Vinson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  357. en:Stokes-Adams syndrome --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:Stokes-Adams syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  358. en:adrenal cytomegaly --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:adrenal cytomegaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  359. en:aortic arch syndrome --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:aortic arch syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  360. en:chylomicron retention disease --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:chylomicron retention disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  361. en:complete trisomy 18 syndrome --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:complete trisomy 18 syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  362. en:cranio-orbito-ocular dysraphia syndrome --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:cranio-orbito-ocular dysraphia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  363. en:familial renal iminoglycinuria --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:familial renal iminoglycinuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  364. en:farber lipogranulomatosis --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:farber lipogranulomatosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  365. en:hand polydactyly --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:hand polydactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  366. en:hereditary fructose intolerance --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary fructose intolerance | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  367. en:hereditary orotic aciduria --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary orotic aciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  368. en:malignant atrophic papulosis --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:malignant atrophic papulosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  369. en:opitz g/bbb syndrome --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:opitz g/bbb syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  370. en:saito kuba tsuruta syndrome --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:saito kuba tsuruta syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  371. en:triple a syndrome --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=en:triple a syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  372. imperforation de l'anus --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=imperforation de l'anus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  373. maladie de marfan --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=maladie de marfan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  374. phacomatose congenitale --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=phacomatose congenitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  375. scléromyxoedème d'Arndt-Gottron --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=scléromyxoedème d'Arndt-Gottron | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  376. syndrome de la crosse aortique --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de la crosse aortique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  377. syndrome de sotos --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de sotos | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  378. syndrome hétérotaxique --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=syndrome hétérotaxique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  379. trichothiodystrophie --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=trichothiodystrophie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  380. varicelle congénitale --- r_associated #0: 42 --> en:pseudotrisomy 13 syndrome
    n1=varicelle congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=42
  381. Seitelberger (maladie de) --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=Seitelberger (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  382. Syndrome de Shy-Drager --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Shy-Drager | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  383. déficit en protéine trifonctionnelle mitochondriale --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=déficit en protéine trifonctionnelle mitochondriale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  384. en:Kawasaki's syndrome --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:Kawasaki's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  385. en:Marfan's syndrome --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:Marfan's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  386. en:adiposis dolorosa --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:adiposis dolorosa | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  387. en:alpha thalassemia x-linked mental retardation syndrome --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:alpha thalassemia x-linked mental retardation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  388. en:alveolar proteinosis --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:alveolar proteinosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  389. en:childhood hypophosphatasia (disorder) --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  390. en:drug hypersensitivity syndrome --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:drug hypersensitivity syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  391. en:epiphyseal dysplasia, multiple, 4 --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:epiphyseal dysplasia, multiple, 4 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  392. en:holmes-adie syndrome --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:holmes-adie syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  393. en:melnick-fraser syndrome --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:melnick-fraser syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  394. en:rna polymerase iii-related leukodystrophy --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:rna polymerase iii-related leukodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  395. en:split-hand/foot malformation 3 --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:split-hand/foot malformation 3 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  396. en:stein-leventhal syndrome --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:stein-leventhal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  397. en:tissue kallikrein deficiency --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:tissue kallikrein deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  398. en:trichothiodystrophy --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:trichothiodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  399. en:ventricular septal defect --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:ventricular septal defect | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  400. en:xanthinuria, type i --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:xanthinuria, type i | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  401. en:xxxy and xxxxy syndrome --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=en:xxxy and xxxxy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  402. hypotonie musculaire --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=hypotonie musculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  403. hérédité autosomale récessive --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=hérédité autosomale récessive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  404. imperforation anale --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=imperforation anale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  405. syndrome cérébro-oculo-faciosquelettique --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=syndrome cérébro-oculo-faciosquelettique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  406. syndrome sec --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=syndrome sec | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  407. toxémie staphylococcique --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=toxémie staphylococcique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  408. van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 41 --> en:pseudotrisomy 13 syndrome
    n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=41
  409. Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=Walker-Warburg (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  410. anasarque fœtoplacentaire --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=anasarque fœtoplacentaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  411. dysostose crânio-faciale --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=dysostose crânio-faciale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  412. dysplasie cléido-crânienne --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie cléido-crânienne | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  413. dysplasie cléidocrânienne --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie cléidocrânienne | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  414. dysplasie olfacto-génitale --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie olfacto-génitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  415. en:21-hydroxylase deficiency --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:21-hydroxylase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  416. en:arnold-chiari deformity --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:arnold-chiari deformity | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  417. en:black death --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:black death | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  418. en:black plague --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:black plague | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  419. en:cerebrooculofacioskeletal syndrome --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebrooculofacioskeletal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  420. en:ectodermal dysplasia --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:ectodermal dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  421. en:feingold syndrome --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:feingold syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  422. en:hypotonia --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:hypotonia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  423. en:sacral agenesis --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:sacral agenesis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  424. en:scleromyxedema --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:scleromyxedema | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  425. en:short bowel syndrome --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:short bowel syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  426. en:transcobalamin ii deficiency --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:transcobalamin ii deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  427. en:tuberculous meningitis --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=en:tuberculous meningitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  428. hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  429. hypotonie --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=hypotonie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  430. onycho-ostéodysostose --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=onycho-ostéodysostose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  431. ophtalmorhino-stomatoxérose --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=ophtalmorhino-stomatoxérose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  432. peste noire --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=peste noire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  433. syndrome métabolique --- r_associated #0: 40 --> en:pseudotrisomy 13 syndrome
    n1=syndrome métabolique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=40
  434. dysplasie ectodermique --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie ectodermique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  435. en:Devergie's disease --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:Devergie's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  436. en:Gray platelet syndrome --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:Gray platelet syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  437. en:autosomal recessive inheritance --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive inheritance | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  438. en:bernard-soulier syndrome --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:bernard-soulier syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  439. en:congenital varicella syndrome --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital varicella syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  440. en:deafness, sensorineural, and male infertility --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:deafness, sensorineural, and male infertility | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  441. en:dumping stomach --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:dumping stomach | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  442. en:dysmorphism, pectus carinatum, joint laxity syndrome --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:dysmorphism, pectus carinatum, joint laxity syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  443. en:imperforate anus --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:imperforate anus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  444. en:kernicterus --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:kernicterus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  445. en:macrophage activation syndrome --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:macrophage activation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  446. en:mannosidosis --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:mannosidosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  447. en:mitochondrial trifunctional protein deficiency --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:mitochondrial trifunctional protein deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  448. en:najjar syndrome --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:najjar syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  449. en:prolonged electroretinal response suppression --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:prolonged electroretinal response suppression | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  450. en:succinic semialdehyde dehydrogenase deficiency --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  451. holoprosencéphalie de type 3 --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=holoprosencéphalie de type 3 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  452. maladie de whipple --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=maladie de whipple | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  453. syndrome de Shy-Drager --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Shy-Drager | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  454. syndrome de shy-drager --- r_associated #0: 39 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de shy-drager | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=39
  455. Hypotonie musculaire --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=Hypotonie musculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  456. Pityriasis rubra pilaire --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=Pityriasis rubra pilaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  457. ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  458. en:17q21 microdeletion syndrome --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:17q21 microdeletion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  459. en:Duane's syndrome --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:Duane's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  460. en:Goltz syndrome --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:Goltz syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  461. en:cerebral gigantism --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebral gigantism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  462. en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  463. en:cleidocranial dysplasia --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:cleidocranial dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  464. en:congenital leptin deficiency --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital leptin deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  465. en:deletion 18p syndrome --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:deletion 18p syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  466. en:lubs x-linked mental retardation syndrome --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:lubs x-linked mental retardation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  467. en:nail-patella syndrome --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:nail-patella syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  468. en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  469. en:pachyonychia congenita --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:pachyonychia congenita | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  470. en:periodic fever syndrome --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:periodic fever syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  471. en:perthes disease --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:perthes disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  472. en:potocki-shaffer syndrome --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:potocki-shaffer syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  473. en:supernumerary structure --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=en:supernumerary structure | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  474. maladie à virus de Marburg --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=maladie à virus de Marburg | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  475. neuropathie optique --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=neuropathie optique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  476. ostéochondrodysplasie --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=ostéochondrodysplasie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  477. panencéphalite subaiguë sclérosante --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=panencéphalite subaiguë sclérosante | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  478. syndrome de Jadassohn-Lewandowsky --- r_associated #0: 38 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Jadassohn-Lewandowsky | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=38
  479. Syndrome de Marfan --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Marfan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  480. dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  481. en:bardet-biedl syndrome --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:bardet-biedl syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  482. en:cogan-reese syndrome --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:cogan-reese syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  483. en:dysequilibrium syndrome --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:dysequilibrium syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  484. en:exomphalos --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:exomphalos | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  485. en:gigantism and hyperplastic visceromegaly --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:gigantism and hyperplastic visceromegaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  486. en:holoprosencephaly --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  487. en:hyperimmunoglobulin e syndrome --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperimmunoglobulin e syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  488. en:sandifer's syndrome --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:sandifer's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  489. en:shy-drager syndrome --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:shy-drager syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  490. en:sly syndrome --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:sly syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  491. en:surfactant protein deficiency --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=en:surfactant protein deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  492. holoprosencéphalie --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=holoprosencéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  493. hétérotaxie --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=hétérotaxie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  494. syndrome de Stilling-Türk-Duane --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Stilling-Türk-Duane | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  495. syndrome inflammatoire aigu systémique --- r_associated #0: 37 --> en:pseudotrisomy 13 syndrome
    n1=syndrome inflammatoire aigu systémique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=37
  496. déficit en prolidase --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=déficit en prolidase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  497. en:benign mucous membrane pemphigoid --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:benign mucous membrane pemphigoid | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  498. en:churg-strauss syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:churg-strauss syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  499. en:complex regional pain syndrome ii --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:complex regional pain syndrome ii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  500. en:congenital disorder of glycosylation type 2e --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital disorder of glycosylation type 2e | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  501. en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:dyskeratosis congenita, autosomal recessive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  502. en:glycogen storage disease --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:glycogen storage disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  503. en:gray platelet syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:gray platelet syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  504. en:kallmann syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:kallmann syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  505. en:laurence-moon syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:laurence-moon syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  506. en:lethal larsen-like syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:lethal larsen-like syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  507. en:lethal neonatal rigidity and multifocal seizure syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  508. en:maple-tree syrup disease --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:maple-tree syrup disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  509. en:metabolic syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:metabolic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  510. en:papillon-lefevre syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:papillon-lefevre syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  511. en:sarcosinemia --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:sarcosinemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  512. en:situs inversus viscerum --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:situs inversus viscerum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  513. en:situs mutatus --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:situs mutatus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  514. en:somnolence syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:somnolence syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  515. en:systemic inflammatory response syndrome --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=en:systemic inflammatory response syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  516. holoprosencéphalie de type 2 --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=holoprosencéphalie de type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  517. ichtyose folliculaire, atrichie et photophobie --- r_associated #0: 36 --> en:pseudotrisomy 13 syndrome
    n1=ichtyose folliculaire, atrichie et photophobie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=36
  518. Whipple (maladie de) --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=Whipple (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  519. Wolman (maladie de) --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=Wolman (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  520. acidurie glutarique de type 1 --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=acidurie glutarique de type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  521. acidémie glutarique de type 1 --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=acidémie glutarique de type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  522. chondrodysplasia punctata --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=chondrodysplasia punctata | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  523. cysticercose --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=cysticercose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  524. cysticercose cérébrale --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=cysticercose cérébrale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  525. cysticercose du système nerveux central --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=cysticercose du système nerveux central | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  526. cysticercose neurologique --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=cysticercose neurologique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  527. cysticercoses --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=cysticercoses | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  528. distomatoses pulmonaires --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=distomatoses pulmonaires | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  529. en:Hurler syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:Hurler syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  530. en:Niemann-Pick disease --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:Niemann-Pick disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  531. en:Pick's disease --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:Pick's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  532. en:Whipple disease --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:Whipple disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  533. en:acrodermatitis --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:acrodermatitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  534. en:acrodysostosis 1 --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:acrodysostosis 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  535. en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  536. en:arterial tortuosity syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:arterial tortuosity syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  537. en:atrioventricular canal structure --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:atrioventricular canal structure | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  538. en:atrophic muscular disorder --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:atrophic muscular disorder | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  539. en:autosomal recessive hypohidrotic ectodermal dysplasia --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive hypohidrotic ectodermal dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  540. en:autosomal recessive spastic paraplegia type 11 --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive spastic paraplegia type 11 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  541. en:barth syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:barth syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  542. en:behcet syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:behcet syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  543. en:bestrophinopathy, autosomal recessive --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:bestrophinopathy, autosomal recessive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  544. en:bietti crystalline corneoretinal dystrophy --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:bietti crystalline corneoretinal dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  545. en:bile acid synthesis defect --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:bile acid synthesis defect | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  546. en:biotinidase deficiency --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:biotinidase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  547. en:blepharophimosis, ptosis, and epicanthus inversus (disorder) --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:blepharophimosis, ptosis, and epicanthus inversus (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  548. en:brown-vialetto-van laere syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:brown-vialetto-van laere syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  549. en:calciphylaxis --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:calciphylaxis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  550. en:chondrodysplasia punctata --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:chondrodysplasia punctata | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  551. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  552. en:congenital disorder of glycosylation type 1h --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital disorder of glycosylation type 1h | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  553. en:cor triatriatum --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:cor triatriatum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  554. en:craniofacial dysostosis --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:craniofacial dysostosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  555. en:cryptophthalmos syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:cryptophthalmos syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  556. en:cysticercosis --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:cysticercosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  557. en:dihydropyrimidine dehydrogenase deficiency --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:dihydropyrimidine dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  558. en:donohue syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:donohue syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  559. en:double cortex syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:double cortex syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  560. en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:ectodermal dysplasia with blindness syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  561. en:ethanolaminosis --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:ethanolaminosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  562. en:factor v leiden --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:factor v leiden | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  563. en:familial erythrocytosis due to diphosphoglycerate mutase deficiency --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  564. en:fetal retinoid syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:fetal retinoid syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  565. en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  566. en:glutaric acidemia type 1 --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:glutaric acidemia type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  567. en:glutaric aciduria, type 1 --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:glutaric aciduria, type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  568. en:halal syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:halal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  569. en:hereditary coproporphyria --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary coproporphyria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  570. en:hereditary factor x deficiency disease --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary factor x deficiency disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  571. en:high molecular weight kininogen deficiency --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:high molecular weight kininogen deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  572. en:hurler syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:hurler syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  573. en:hyaline membrane syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:hyaline membrane syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  574. en:hydrocephalus --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:hydrocephalus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  575. en:hypermanganesemia with dystonia polycythemia and cirrhosis --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:hypermanganesemia with dystonia polycythemia and cirrhosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  576. en:hypomagnesemia 1, intestinal --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:hypomagnesemia 1, intestinal | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  577. en:isolated hypoplasia of the right ventricle --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:isolated hypoplasia of the right ventricle | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  578. en:karyotype analysis normal finding --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:karyotype analysis normal finding | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  579. en:leigh disease --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:leigh disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  580. en:li-fraumeni syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:li-fraumeni syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  581. en:liddle syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:liddle syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  582. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  583. en:malabsorption syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:malabsorption syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  584. en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  585. en:mental retardation, autosomal recessive 34 --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:mental retardation, autosomal recessive 34 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  586. en:methionine adenosyltransferase deficiency --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:methionine adenosyltransferase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  587. en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:microcephaly albinism digital anomalies syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  588. en:mitochondrial dna depletion syndrome 12 --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:mitochondrial dna depletion syndrome 12 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  589. en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  590. en:n-acetylglutamate synthase deficiency --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:n-acetylglutamate synthase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  591. en:nablus mask-like facial syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:nablus mask-like facial syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  592. en:neurocysticercosis --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:neurocysticercosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  593. en:neutral lipid storage disease with myopathy --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:neutral lipid storage disease with myopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  594. en:niemann-pick disease --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:niemann-pick disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  595. en:oculocutaneous albinism type 4 --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:oculocutaneous albinism type 4 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  596. en:oeis complex --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:oeis complex | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  597. en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  598. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  599. en:pick's disease --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:pick's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  600. en:polydactyly, postaxial --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:polydactyly, postaxial | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  601. en:progressive familial intrahepatic cholestasis --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:progressive familial intrahepatic cholestasis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  602. en:pseudoachondroplasia --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:pseudoachondroplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  603. en:renal dysplasia - limb defects syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:renal dysplasia - limb defects syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  604. en:sanfilippo syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:sanfilippo syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  605. en:spondylo-ocular syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:spondylo-ocular syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  606. en:stevens-johnson syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:stevens-johnson syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  607. en:transposition of great vessels --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:transposition of great vessels | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  608. en:trisomy 14 mosaicism --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:trisomy 14 mosaicism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  609. en:urocanase deficiency --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:urocanase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  610. en:wellesley carman french syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:wellesley carman french syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  611. en:wernicke-korsakoff syndrome --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:wernicke-korsakoff syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  612. en:whipple disease --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=en:whipple disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  613. hypothyroïdie (manifestations neuromusculaires dans l') --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=hypothyroïdie (manifestations neuromusculaires dans l') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  614. hypotonie, obésité et incisives proéminentes --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=hypotonie, obésité et incisives proéminentes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  615. ichtyose, affection neurologique spastique, et oligophrénie --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=ichtyose, affection neurologique spastique, et oligophrénie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  616. maladie de Hurler --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Hurler | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  617. maladie de Perthes --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Perthes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  618. maladie de Whipple --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Whipple | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  619. maladie des épiphyses ponctuées --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=maladie des épiphyses ponctuées | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  620. mésentérique supérieure (syndrome de l'artère) --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=mésentérique supérieure (syndrome de l'artère) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  621. neuro-acanthocytose --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=neuro-acanthocytose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  622. neurocysticercose --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=neurocysticercose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  623. onycho-patellaire (syndrome) --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=onycho-patellaire (syndrome) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  624. syndrome de jadassohn-lewandowsky --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de jadassohn-lewandowsky | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  625. syndrome de plummer-vinson --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de plummer-vinson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  626. trachéobronchomégalie --- r_associated #0: 35 --> en:pseudotrisomy 13 syndrome
    n1=trachéobronchomégalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=35
  627. cataplexie --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=cataplexie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  628. dysplasie frontonasale --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie frontonasale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  629. ectrodactylie --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=ectrodactylie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  630. en:3-methylglutaconic aciduria type 5 --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:3-methylglutaconic aciduria type 5 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  631. en:Black death --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:Black death | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  632. en:Marfan's disease --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:Marfan's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  633. en:acrocallosal syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:acrocallosal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  634. en:acyl-coa dehydrogenase, short-chain deficiency --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:acyl-coa dehydrogenase, short-chain deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  635. en:alagille syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:alagille syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  636. en:allan-herndon-dudley syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:allan-herndon-dudley syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  637. en:anemia, hypochromic microcytic, with iron overload --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:anemia, hypochromic microcytic, with iron overload | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  638. en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  639. en:autosomal recessive primary microcephaly --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive primary microcephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  640. en:beta-methylcrotonylglycinuria --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:beta-methylcrotonylglycinuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  641. en:blau syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:blau syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  642. en:brody myopathy --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:brody myopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  643. en:carnitine palmitoyltransferase i deficiency --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:carnitine palmitoyltransferase i deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  644. en:cataplexy --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:cataplexy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  645. en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  646. en:child's sudden death --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:child's sudden death | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  647. en:childhood myocerebrohepatopathy spectrum --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:childhood myocerebrohepatopathy spectrum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  648. en:choroideremia --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:choroideremia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  649. en:congenital cortical hyperostosis --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital cortical hyperostosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  650. en:congenital disorder of glycosylation type ie --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital disorder of glycosylation type ie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  651. en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  652. en:corpus callosum agenesis --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:corpus callosum agenesis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  653. en:craniofrontonasal dysplasia --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:craniofrontonasal dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  654. en:cri du chat syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:cri du chat syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  655. en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  656. en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:dentatorubral-pallidoluysian atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  657. en:digeorge syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:digeorge syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  658. en:ebstein anomaly --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:ebstein anomaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  659. en:ehlers-danlos syndrome, type vi --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:ehlers-danlos syndrome, type vi | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  660. en:episodic pain syndrome, familial, 3 --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:episodic pain syndrome, familial, 3 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  661. en:escobar syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:escobar syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  662. en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  663. en:fibromyalgia --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:fibromyalgia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  664. en:fibular hypoplasia and complex brachydactyly --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:fibular hypoplasia and complex brachydactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  665. en:fronto-facio-nasal dysplasia --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:fronto-facio-nasal dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  666. en:frontonasal dysplasia --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:frontonasal dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  667. en:generalized arterial calcification of infancy 1 --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:generalized arterial calcification of infancy 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  668. en:glutamate formiminotransferase deficiency --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:glutamate formiminotransferase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  669. en:hartnup disease --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:hartnup disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  670. en:heterotaxy --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:heterotaxy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  671. en:holoprosencephaly 2 (disorder) --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly 2 (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  672. en:holoprosencephaly 4 (disorder) --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly 4 (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  673. en:holoprosencephaly with fetal akinesia-hypokinesia sequence --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  674. en:hyperviscosity syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperviscosity syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  675. en:isovaleric acidemia --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:isovaleric acidemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  676. en:jackson-weiss syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:jackson-weiss syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  677. en:leri-weill dyschondrosteosis --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:leri-weill dyschondrosteosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  678. en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  679. en:lysosomal storage disease --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:lysosomal storage disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  680. en:mallory-weiss syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:mallory-weiss syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  681. en:manouvrier syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:manouvrier syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  682. en:marburg virus disease --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:marburg virus disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  683. en:maxillonasal dysplasia, binder type --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:maxillonasal dysplasia, binder type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  684. en:meckel-gruber syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:meckel-gruber syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  685. en:meconium plug syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:meconium plug syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  686. en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  687. en:moyamoya disease with early onset achalasia --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:moyamoya disease with early onset achalasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  688. en:neurodegeneration due to cerebral folate transport deficiency --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:neurodegeneration due to cerebral folate transport deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  689. en:neuronal intranuclear inclusion disease --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:neuronal intranuclear inclusion disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  690. en:non-trisomic autosomal aneuploidy --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:non-trisomic autosomal aneuploidy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  691. en:nonaka myopathy --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:nonaka myopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  692. en:obstructive sleep apnea syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:obstructive sleep apnea syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  693. en:ossification of posterior longitudinal ligament --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:ossification of posterior longitudinal ligament | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  694. en:overgrowth syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:overgrowth syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  695. en:paragonimiasis --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:paragonimiasis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  696. en:peeling skin syndrome, acral type --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:peeling skin syndrome, acral type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  697. en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  698. en:pili torti onychodysplasia syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:pili torti onychodysplasia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  699. en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  700. en:presentey anomaly --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:presentey anomaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  701. en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  702. en:rapadilino syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:rapadilino syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  703. en:reversible posterior leukoencephalopathy syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:reversible posterior leukoencephalopathy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  704. en:robinow syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:robinow syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  705. en:rozin hertz goodman syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:rozin hertz goodman syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  706. en:saldino-noonan syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:saldino-noonan syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  707. en:subacute sclerosing panencephalitis --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:subacute sclerosing panencephalitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  708. en:synpolydactyly --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:synpolydactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  709. en:triploidy syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:triploidy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  710. en:upward slant of palpebral fissure --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:upward slant of palpebral fissure | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  711. en:urea cycle metabolism disorder --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:urea cycle metabolism disorder | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  712. en:uveomeningoencephalitic syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:uveomeningoencephalitic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  713. en:warsaw breakage syndrome --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:warsaw breakage syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  714. en:x-linked dominant hypophosphatemic rickets --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=en:x-linked dominant hypophosphatemic rickets | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  715. maladie de Niemann-Pick --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Niemann-Pick | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  716. myocardiopathie de tako-tsubo --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=myocardiopathie de tako-tsubo | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  717. nystagmus congénital isolé --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=nystagmus congénital isolé | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  718. pachyonychie congénitale de Jadassohn-Lewandowsky --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=pachyonychie congénitale de Jadassohn-Lewandowsky | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  719. syndrome de Laurence-Moon --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Laurence-Moon | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  720. syndrome sapho --- r_associated #0: 34 --> en:pseudotrisomy 13 syndrome
    n1=syndrome sapho | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=34
  721. Silver-Russell (syndrome de) --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=Silver-Russell (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  722. anasarque --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=anasarque | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  723. dentinogénèse imparfaite --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=dentinogénèse imparfaite | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  724. dystrophie orbitaire congénitale --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=dystrophie orbitaire congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  725. en:familial partial lipodystrophy --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=en:familial partial lipodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  726. en:hypophosphatasia infantile --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=en:hypophosphatasia infantile | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  727. en:myositis --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=en:myositis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  728. en:neurological cysticercosis --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=en:neurological cysticercosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  729. en:prolidase deficiency --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=en:prolidase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  730. en:takotsubo cardiomyopathy --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=en:takotsubo cardiomyopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  731. ongles jaunes (syndrome des) --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=ongles jaunes (syndrome des) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  732. ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  733. papulose atrophiante maligne de Degos --- r_associated #0: 33 --> en:pseudotrisomy 13 syndrome
    n1=papulose atrophiante maligne de Degos | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=33
  734. agnosie --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=agnosie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  735. dysostose crâniofaciale --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=dysostose crâniofaciale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  736. dysplasie craniodiaphysaire --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie craniodiaphysaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  737. dysplasie ectodermique, ectrodactylie et dystrophie maculaire --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  738. en:10p13-p14 deletion syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:10p13-p14 deletion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  739. en:2-hydroxyglutaric aciduria --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:2-hydroxyglutaric aciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  740. en:3-methylglutaconic aciduria type 3 --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:3-methylglutaconic aciduria type 3 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  741. en:3-methylglutaconic aciduria type iv --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:3-methylglutaconic aciduria type iv | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  742. en:achondrogenesis --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:achondrogenesis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  743. en:acid phosphatase deficiency --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:acid phosphatase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  744. en:agnosia --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:agnosia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  745. en:alpha, alpha-trehalase deficiency --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:alpha, alpha-trehalase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  746. en:amelogenesis imperfecta and gingival hyperplasia syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:amelogenesis imperfecta and gingival hyperplasia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  747. en:apl differentiation syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:apl differentiation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  748. en:arakawa syndrome ii --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:arakawa syndrome ii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  749. en:arginine:glycine amidinotransferase deficiency --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:arginine:glycine amidinotransferase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  750. en:ataxia with vitamin e deficiency --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:ataxia with vitamin e deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  751. en:autoimmune polyglandular syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:autoimmune polyglandular syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  752. en:caroli disease --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:caroli disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  753. en:cataplexia --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:cataplexia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  754. en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  755. en:chromosome 2q37 deletion syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:chromosome 2q37 deletion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  756. en:congenital hypoplasia of kidney --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital hypoplasia of kidney | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  757. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  758. en:craniodiaphyseal dysplasia --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:craniodiaphyseal dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  759. en:cushing syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:cushing syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  760. en:darier disease --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:darier disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  761. en:dravet syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:dravet syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  762. en:empty sella syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:empty sella syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  763. en:endocrine syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:endocrine syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  764. en:enterokinase deficiency --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:enterokinase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  765. en:erythropoietic protoporphyria --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:erythropoietic protoporphyria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  766. en:familial dysautonomia --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:familial dysautonomia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  767. en:fragile x tremor/ataxia syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:fragile x tremor/ataxia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  768. en:fryns macrocephaly --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:fryns macrocephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  769. en:giacci familial neurogenic acroosteolysis --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:giacci familial neurogenic acroosteolysis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  770. en:gitelman syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:gitelman syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  771. en:glanzmann thrombasthenia --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:glanzmann thrombasthenia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  772. en:hall riggs syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:hall riggs syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  773. en:heart defects limb shortening --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:heart defects limb shortening | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  774. en:hereditary factor xii deficiency disease --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary factor xii deficiency disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  775. en:hunter syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:hunter syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  776. en:ichthyosis --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:ichthyosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  777. en:jervell and lange nielsen syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:jervell and lange nielsen syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  778. en:kabuki syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:kabuki syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  779. en:kleine-levin syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:kleine-levin syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  780. en:leukotriene c4 synthase deficiency --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:leukotriene c4 synthase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  781. en:levocardia --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:levocardia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  782. en:macular corneal dystrophy --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:macular corneal dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  783. en:maroteaux-lamy syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:maroteaux-lamy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  784. en:maternal diabetes and deafness syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:maternal diabetes and deafness syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  785. en:medial cleft lip and palate (59%) --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:medial cleft lip and palate (59%) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  786. en:melas syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:melas syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  787. en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  788. en:mitochondrial neurogastrointestingal encephalopathy --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:mitochondrial neurogastrointestingal encephalopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  789. en:myhre syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:myhre syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  790. en:neuroacanthocytosis --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:neuroacanthocytosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  791. en:norrie syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:norrie syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  792. en:northern epilepsy syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:northern epilepsy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  793. en:odontohypophosphatasia (disorder) --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:odontohypophosphatasia (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  794. en:ombilical hernia --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:ombilical hernia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  795. en:osteopetrosis with renal tubular acidosis --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:osteopetrosis with renal tubular acidosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  796. en:pain agnosia --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:pain agnosia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  797. en:pelizaeus-merzbacher disease --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:pelizaeus-merzbacher disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  798. en:phenylketonuria ii --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:phenylketonuria ii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  799. en:pontocerebellar hypoplasia type 2 --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:pontocerebellar hypoplasia type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  800. en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  801. en:progressive bulbar palsy --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:progressive bulbar palsy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  802. en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:purine-nucleoside phosphorylase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  803. en:restless leg syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:restless leg syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  804. en:scheie syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:scheie syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  805. en:severe early childhood onset retinal dystrophy --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:severe early childhood onset retinal dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  806. en:short stature syndrome, brussels type --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:short stature syndrome, brussels type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  807. en:sick euthyroid syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:sick euthyroid syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  808. en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  809. en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  810. en:sudden unexplained infant death --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:sudden unexplained infant death | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  811. en:thyroid hormone resistance syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:thyroid hormone resistance syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  812. en:tolosa-hunt syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:tolosa-hunt syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  813. en:treacher collins syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:treacher collins syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  814. en:vertebral artery syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:vertebral artery syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  815. en:wegener granulomatosis --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:wegener granulomatosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  816. en:wilms tumor 1 gene syndromes --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:wilms tumor 1 gene syndromes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  817. en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  818. histiocytose sinusale hémophagocytaire --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=histiocytose sinusale hémophagocytaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  819. holoprosencéphalie de type 4 --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=holoprosencéphalie de type 4 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  820. holoprosencéphalie familiale alobaire de type 1 --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  821. ichtyose --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=ichtyose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  822. insensibilité congénitale à la douleur de type III --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=insensibilité congénitale à la douleur de type III | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  823. macroglossie --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=macroglossie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  824. maladie de seitelberger --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=maladie de seitelberger | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  825. ostéopétrose avec acidose rénale tubulaire --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=ostéopétrose avec acidose rénale tubulaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  826. protoproporphyrie érythropoïétique --- r_associated #0: 32 --> en:pseudotrisomy 13 syndrome
    n1=protoproporphyrie érythropoïétique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=32
  827. Plummer-Vinson (syndrome de) --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=Plummer-Vinson (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  828. Sotos (syndrome de) --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=Sotos (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  829. anomalie d'Ebstein --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=anomalie d'Ebstein | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  830. dysplasie campomélique --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie campomélique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  831. dysérythropoïèse congénitale --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=dysérythropoïèse congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  832. déficit en neuraminidase --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=déficit en neuraminidase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  833. en:achard syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:achard syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  834. en:al awadi syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:al awadi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  835. en:aminoacylase 1 deficiency --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:aminoacylase 1 deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  836. en:anhidrotic ectodermal dysplasia 1 --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:anhidrotic ectodermal dysplasia 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  837. en:argininosuccinic aciduria --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:argininosuccinic aciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  838. en:arrhythmogenic right ventricular dysplasia --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:arrhythmogenic right ventricular dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  839. en:ateliotic dwarfism without insulinopenia --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:ateliotic dwarfism without insulinopenia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  840. en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive idiopathic familial dystonia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  841. en:autosomal recessive spastic paraplegia type 39 --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive spastic paraplegia type 39 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  842. en:behr syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:behr syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  843. en:brachioskeletogenital syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:brachioskeletogenital syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  844. en:braddock syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:braddock syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  845. en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  846. en:chondrodysplasia punctata syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:chondrodysplasia punctata syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  847. en:chronic infantile neurological cutaneous and articular syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:chronic infantile neurological cutaneous and articular syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  848. en:cockayne syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:cockayne syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  849. en:codas syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:codas syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  850. en:cohen syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:cohen syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  851. en:compartment syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:compartment syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  852. en:congenital analbuminemia --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital analbuminemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  853. en:congenital disorder of glycosylation type ig --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital disorder of glycosylation type ig | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  854. en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital dyserythropoietic anemia, type ii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  855. en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  856. en:crisponi syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:crisponi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  857. en:cutis laxa, autosomal recessive --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:cutis laxa, autosomal recessive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  858. en:deafness, autosomal recessive 49 --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:deafness, autosomal recessive 49 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  859. en:deletion 18q syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:deletion 18q syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  860. en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  861. en:desmosterolosis --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:desmosterolosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  862. en:donnai-barrow syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:donnai-barrow syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  863. en:dyschromatosis symmetrica hereditaria --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:dyschromatosis symmetrica hereditaria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  864. en:dysfunctional elimination syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:dysfunctional elimination syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  865. en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  866. en:ectrodactyly --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:ectrodactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  867. en:familial acantholysis --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:familial acantholysis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  868. en:familial hypoaldosteronism --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:familial hypoaldosteronism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  869. en:fara chlupackova syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:fara chlupackova syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  870. en:fucosidosis --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:fucosidosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  871. en:gamma-glutamyltransferase deficiency --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:gamma-glutamyltransferase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  872. en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  873. en:goldenhar syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:goldenhar syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  874. en:grob's syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:grob's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  875. en:heritable pulmonary arterial hypertension --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:heritable pulmonary arterial hypertension | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  876. en:histidinemia --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:histidinemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  877. en:holocarboxylase synthetase deficiency --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:holocarboxylase synthetase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  878. en:holoprosencephaly 5 --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly 5 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  879. en:hyperlysinemia --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperlysinemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  880. en:insufficient breast milk syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:insufficient breast milk syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  881. en:interleukin-1 receptor-associated kinase 4 deficiency --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:interleukin-1 receptor-associated kinase 4 deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  882. en:leucinosis --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:leucinosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  883. en:macdermot winter syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:macdermot winter syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  884. en:majeed syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:majeed syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  885. en:meconium aspiration syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:meconium aspiration syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  886. en:membranous cranial ossification, delayed --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:membranous cranial ossification, delayed | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  887. en:microphthalmos --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:microphthalmos | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  888. en:mirror polydactyly, vertebral segmentation and limb defect syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:mirror polydactyly, vertebral segmentation and limb defect syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  889. en:monosomy 13q syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:monosomy 13q syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  890. en:mowat-wilson syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:mowat-wilson syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  891. en:multiple vascular disruption syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:multiple vascular disruption syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  892. en:neuraminidase deficiency --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:neuraminidase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  893. en:neuropathy, hereditary sensory and autonomic, type vii --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:neuropathy, hereditary sensory and autonomic, type vii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  894. en:orofaciodigital syndrome type 6 --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:orofaciodigital syndrome type 6 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  895. en:panuveitis --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:panuveitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  896. en:peritoneal panniculitis --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:peritoneal panniculitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  897. en:primary carnitine deficiency --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:primary carnitine deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  898. en:propionic acidemia --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:propionic acidemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  899. en:pseudocholinesterase deficiency --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:pseudocholinesterase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  900. en:robinow-like syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:robinow-like syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  901. en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  902. en:sheehan syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:sheehan syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  903. en:short rib-polydactyly syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:short rib-polydactyly syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  904. en:short-rib thoracic dysplasia 6 with or without polydactyly --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:short-rib thoracic dysplasia 6 with or without polydactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  905. en:shprintzen omphalocele syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:shprintzen omphalocele syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  906. en:shprintzen-goldberg craniosynostosis syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:shprintzen-goldberg craniosynostosis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  907. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:simpson golabi behmel syndrome type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  908. en:single central incisor syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:single central incisor syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  909. en:spondyloepimetaphyseal dysplasia with joint laxity type 2 --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  910. en:superior mesenteric artery syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:superior mesenteric artery syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  911. en:syndrome of apparent mineralocorticoid excess --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:syndrome of apparent mineralocorticoid excess | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  912. en:townes-brocks syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:townes-brocks syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  913. en:twiddler's syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:twiddler's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  914. en:von hippel-lindau syndrome --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:von hippel-lindau syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  915. en:wallerian degeneration --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=en:wallerian degeneration | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  916. fucosidose --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=fucosidose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  917. histidinémie --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=histidinémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  918. ichthyose --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=ichthyose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  919. ictère nucléaire --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=ictère nucléaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  920. lipodystrophie partielle familiale --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=lipodystrophie partielle familiale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  921. lévocardie --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=lévocardie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  922. maladie lysosomique de surcharge --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=maladie lysosomique de surcharge | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  923. malformation d'Ebstein --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=malformation d'Ebstein | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  924. mucolipidose II --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=mucolipidose II | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  925. myokymie --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=myokymie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  926. myosite --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=myosite | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  927. myosites --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=myosites | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  928. noma --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=noma | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  929. néphrocalcinose --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=néphrocalcinose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  930. ostéopoecilie --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=ostéopoecilie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  931. panuvéite --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=panuvéite | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  932. paragonimiase --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=paragonimiase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  933. paragonimose --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=paragonimose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  934. pemphigoïde bénigne des muqueuses --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=pemphigoïde bénigne des muqueuses | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  935. syndrome de Martin-Bell --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Martin-Bell | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  936. syndrome de malabsorption --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de malabsorption | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  937. wallérienne (dégénérescence) --- r_associated #0: 31 --> en:pseudotrisomy 13 syndrome
    n1=wallérienne (dégénérescence) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=31
  938. Seitelberger (dystrophie neuroaxonale de) --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=Seitelberger (dystrophie neuroaxonale de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  939. Weir Mitchell --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=Weir Mitchell | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  940. coarctation aortique --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=coarctation aortique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  941. communication interventriculaire --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=communication interventriculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  942. dégénérescence wallérienne --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=dégénérescence wallérienne | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  943. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  944. en:Alice in wonderland Syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:Alice in wonderland Syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  945. en:Dercum's disease --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:Dercum's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  946. en:I-cell disease --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:I-cell disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  947. en:Köbberling's syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:Köbberling's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  948. en:Sheehan's syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:Sheehan's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  949. en:Tay-Sachs disease --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:Tay-Sachs disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  950. en:Townes-Brocks syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:Townes-Brocks syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  951. en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:adenine phosphoribosyltransferase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  952. en:allgrove syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:allgrove syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  953. en:alligator skin --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:alligator skin | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  954. en:aniridia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:aniridia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  955. en:anti-AIDS --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:anti-AIDS | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  956. en:aortic coarctation --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:aortic coarctation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  957. en:autosomal dominant optic atrophy --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal dominant optic atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  958. en:capgras syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:capgras syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  959. en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  960. en:combined lipase deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:combined lipase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  961. en:complete trisomy 13 syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:complete trisomy 13 syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  962. en:complete trisomy 21 syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:complete trisomy 21 syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  963. en:congenital absence of kidney --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital absence of kidney | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  964. en:congenital bilateral aplasia of the vas deferens --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital bilateral aplasia of the vas deferens | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  965. en:congenital bowing of long bone --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital bowing of long bone | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  966. en:congenital central hypoventilation --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital central hypoventilation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  967. en:congenital disorder of glycosylation, type if --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital disorder of glycosylation, type if | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  968. en:congenital fiber-type disproportion --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital fiber-type disproportion | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  969. en:conn syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:conn syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  970. en:corpus callosum agenesis neuronopathy --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:corpus callosum agenesis neuronopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  971. en:cryopyrin-associated periodic syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:cryopyrin-associated periodic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  972. en:cystathionine beta-synthase deficiency disease --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:cystathionine beta-synthase deficiency disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  973. en:d-glyceric aciduria --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:d-glyceric aciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  974. en:deafness, progressive, with stapes fixation --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:deafness, progressive, with stapes fixation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  975. en:dry eye syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:dry eye syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  976. en:dubin-johnson syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:dubin-johnson syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  977. en:ectromelia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:ectromelia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  978. en:eisenmenger syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:eisenmenger syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  979. en:erythermalgia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:erythermalgia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  980. en:erythromelalgia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:erythromelalgia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  981. en:familial hypertrophic cardiomyopathy --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:familial hypertrophic cardiomyopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  982. en:felty syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:felty syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  983. en:fibromuscular dysplasia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:fibromuscular dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  984. en:fisher syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:fisher syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  985. en:fountain syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:fountain syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  986. en:frohlich syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:frohlich syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  987. en:fructose-1,6-bisphosphatase deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:fructose-1,6-bisphosphatase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  988. en:glutathione synthetase deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:glutathione synthetase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  989. en:greig syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:greig syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  990. en:griscelli syndrome type 2 --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:griscelli syndrome type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  991. en:hand and foot deformity --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:hand and foot deformity | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  992. en:hereditary mucosal leukokeratosis --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary mucosal leukokeratosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  993. en:holoprosencephaly (100%) --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly (100%) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  994. en:homocystinuria --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:homocystinuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  995. en:horner syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:horner syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  996. en:hyperpipecolatemia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperpipecolatemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  997. en:hypomyelination and congenital cataract --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:hypomyelination and congenital cataract | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  998. en:hypoplastic left heart syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:hypoplastic left heart syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  999. en:i-cell disease --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:i-cell disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1000. en:ichthyosis--cheek--eyebrow syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:ichthyosis--cheek--eyebrow syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1001. en:intestinal atresia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:intestinal atresia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1002. en:isolated hyperchlorhidrosis --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:isolated hyperchlorhidrosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1003. en:kallman syndrome with heart disease --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:kallman syndrome with heart disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1004. en:kniest dysplasia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:kniest dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1005. en:landau-kleffner syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:landau-kleffner syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1006. en:leprosy --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:leprosy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1007. en:leptospirosis --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:leptospirosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1008. en:leriche syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:leriche syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1009. en:lig4 syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:lig4 syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1010. en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1011. en:marles greenberg persaud syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:marles greenberg persaud syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1012. en:melkersson-rosenthal syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:melkersson-rosenthal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1013. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1014. en:menkes disease --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:menkes disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1015. en:microcephalic primordial dwarfism toriello type --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:microcephalic primordial dwarfism toriello type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1016. en:microcephaly cervical spine fusion anomalies --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:microcephaly cervical spine fusion anomalies | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1017. en:microcephaly, amish type (disorder) --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:microcephaly, amish type (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1018. en:miller-dieker syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:miller-dieker syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1019. en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1020. en:mucopolysaccharidosis i --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:mucopolysaccharidosis i | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1021. en:mucopolysaccharidosis type i --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:mucopolysaccharidosis type i | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1022. en:mullerian inhibiting factor deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:mullerian inhibiting factor deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1023. en:muscle-eye-brain disease, congenital muscular dystrophy --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:muscle-eye-brain disease, congenital muscular dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1024. en:myopathy with exercise intolerance, swedish type --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:myopathy with exercise intolerance, swedish type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1025. en:nadh dehydrogenase deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:nadh dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1026. en:netherton syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:netherton syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1027. en:neural tube defect --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:neural tube defect | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1028. en:north american indian childhood cirrhosis --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:north american indian childhood cirrhosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1029. en:odontogenesis imperfecta --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:odontogenesis imperfecta | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1030. en:orotic aciduria --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:orotic aciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1031. en:osteopoikilosis --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:osteopoikilosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1032. en:pelviscapular dysplasia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:pelviscapular dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1033. en:plasma kallikrein deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:plasma kallikrein deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1034. en:poland syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:poland syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1035. en:polydactyly --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:polydactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1036. en:prekallikrein deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:prekallikrein deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1037. en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1038. en:pyle metaphyseal dysplasia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:pyle metaphyseal dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1039. en:pyruvate dehydrogenase deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:pyruvate dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1040. en:retinitis punctata albescens (disorder) --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:retinitis punctata albescens (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1041. en:sids --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:sids | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1042. en:sjogren-larsson syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:sjogren-larsson syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1043. en:spinocerebellar ataxia, autosomal recessive 2 --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:spinocerebellar ataxia, autosomal recessive 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1044. en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:spondylocarpotarsal synostosis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1045. en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1046. en:staphylococcal scalded skin syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:staphylococcal scalded skin syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1047. en:sudden infant death with dysgenesis of the testes syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:sudden infant death with dysgenesis of the testes syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1048. en:sulfite oxidase deficiency --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:sulfite oxidase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1049. en:tay-sachs disease --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:tay-sachs disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1050. en:togaviridae infection --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:togaviridae infection | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1051. en:tracheobronchomalacia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:tracheobronchomalacia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1052. en:trisomy xq28 syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:trisomy xq28 syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1053. en:tungland bellman syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:tungland bellman syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1054. en:tyrosinemia, type iii --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:tyrosinemia, type iii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1055. en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1056. en:verloes bourguignon syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:verloes bourguignon syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1057. en:werdnig-hoffmann disease --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:werdnig-hoffmann disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1058. en:werner syndrome --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=en:werner syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1059. erythromelalgia --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=erythromelalgia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1060. inflammation musculaire --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=inflammation musculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1061. leprosy --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=leprosy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1062. lèpre --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=lèpre | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1063. léproserie --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=léproserie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1064. maladie de Tay-Sachs --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Tay-Sachs | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1065. maladie de Tay-sachs --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Tay-sachs | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1066. maladie de hurler --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=maladie de hurler | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1067. maladie de tay-sachs --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=maladie de tay-sachs | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1068. mucolipidose type II --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=mucolipidose type II | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1069. mucolipidose type ii --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=mucolipidose type ii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1070. odontogénèse imparfaite --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=odontogénèse imparfaite | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1071. présentation sacro-iliaque droite antérieure --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=présentation sacro-iliaque droite antérieure | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1072. syndrome cardio-facio-cutané --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=syndrome cardio-facio-cutané | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1073. syndrome de Dubin-Johnson --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Dubin-Johnson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1074. syndrome de dubin-johnson --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de dubin-johnson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1075. syndrome de synostose spondylo-carpo-tarsale --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de synostose spondylo-carpo-tarsale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1076. syndrome hémolytique et urémique atypique --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=syndrome hémolytique et urémique atypique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1077. tonus musculaire diminué --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=tonus musculaire diminué | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1078. érythermalgie --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=érythermalgie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1079. érythromélalgie --- r_associated #0: 30 --> en:pseudotrisomy 13 syndrome
    n1=érythromélalgie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=30
  1080. Maladie de Whipple --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=Maladie de Whipple | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1081. aplasie de la paroi abdominale --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=aplasie de la paroi abdominale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1082. brides amniotiques (syndrome des) --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=brides amniotiques (syndrome des) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1083. en:1p36 deletion syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:1p36 deletion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1084. en:CDA --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:CDA | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1085. en:Degos's syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:Degos's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1086. en:Hebra's pityriasis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:Hebra's pityriasis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1087. en:Leriche syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:Leriche syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1088. en:Stevens-Johnson syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:Stevens-Johnson syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1089. en:Waterhouse-Friderichsen syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:Waterhouse-Friderichsen syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1090. en:aagenaes syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:aagenaes syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1091. en:adherence syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:adherence syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1092. en:aicardi syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:aicardi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1093. en:albright's hereditary osteodystrophy --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:albright's hereditary osteodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1094. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1095. en:alstrom syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:alstrom syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1096. en:amaurosis fugax --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:amaurosis fugax | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1097. en:and mental retardation --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:and mental retardation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1098. en:arachnodactily --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:arachnodactily | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1099. en:autoimmune polyendocrinopathy syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:autoimmune polyendocrinopathy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1100. en:autosomal dominant congenital deafness with onychodystrophy --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal dominant congenital deafness with onychodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1101. en:baller-gerold syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:baller-gerold syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1102. en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:beare-stevenson cutis gyrata syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1103. en:becker generalized myotonia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:becker generalized myotonia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1104. en:berardinelli-seip congenital lipodystrophy --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:berardinelli-seip congenital lipodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1105. en:brown-sequard syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:brown-sequard syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1106. en:burning mouth syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:burning mouth syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1107. en:cadasil syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:cadasil syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1108. en:campomelic dysplasia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:campomelic dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1109. en:cardiorenal syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:cardiorenal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1110. en:carnosinemia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:carnosinemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1111. en:cataplexis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:cataplexis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1112. en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1113. en:chromosome 15q11-q13 duplication syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:chromosome 15q11-q13 duplication syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1114. en:chromosome 16p11.2 deletion syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:chromosome 16p11.2 deletion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1115. en:chromosome 16p12.1 deletion syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:chromosome 16p12.1 deletion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1116. en:coloboma and anal atresia syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:coloboma and anal atresia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1117. en:congenital dyserythropoietic anemia, type i --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital dyserythropoietic anemia, type i | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1118. en:congenital malformation syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital malformation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1119. en:congenital structural myopathy --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital structural myopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1120. en:cooper jabs syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:cooper jabs syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1121. en:cranioectodermal dysplasia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:cranioectodermal dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1122. en:cystinosis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:cystinosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1123. en:cytokine release syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:cytokine release syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1124. en:deafness, autosomal recessive 28 --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:deafness, autosomal recessive 28 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1125. en:deafness-craniofacial syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:deafness-craniofacial syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1126. en:diethylstilbestrol syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:diethylstilbestrol syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1127. en:ear, patella, short stature syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:ear, patella, short stature syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1128. en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1129. en:ehlers-danlos syndrome, arthrochalasia type --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:ehlers-danlos syndrome, arthrochalasia type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1130. en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1131. en:factor v and factor viii, combined deficiency of --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:factor v and factor viii, combined deficiency of | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1132. en:fanconi syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:fanconi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1133. en:fatal familial insomnia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:fatal familial insomnia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1134. en:fetal alcohol syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:fetal alcohol syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1135. en:gangrenous stomatitis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:gangrenous stomatitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1136. en:generalized peeling skin syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:generalized peeling skin syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1137. en:gurrieri sammito bellussi syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:gurrieri sammito bellussi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1138. en:harrod doman keele syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:harrod doman keele syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1139. en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1140. en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1141. en:heterotaxy syndrome with asplenia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:heterotaxy syndrome with asplenia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1142. en:heterotaxy syndrome with polysplenia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:heterotaxy syndrome with polysplenia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1143. en:histidinaemia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:histidinaemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1144. en:hnsha due to pyrimidine-5'-nucleotidase deficiency --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1145. en:holoprosencephaly type 5 --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly type 5 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1146. en:holt-oram syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:holt-oram syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1147. en:hyperphosphatasia with mental retardation --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperphosphatasia with mental retardation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1148. en:hypokalemic periodic paralysis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:hypokalemic periodic paralysis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1149. en:immunodeficiency with hyper-igm type 2 --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:immunodeficiency with hyper-igm type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1150. en:immunoglobulin a deficiency 1 --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:immunoglobulin a deficiency 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1151. en:infantile uterus --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:infantile uterus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1152. en:inspissated bile syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:inspissated bile syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1153. en:isaacs syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:isaacs syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1154. en:leprosarium --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:leprosarium | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1155. en:lesch-nyhan syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:lesch-nyhan syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1156. en:long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:long-chain acyl-coa dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1157. en:low set ears --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:low set ears | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1158. en:machado-joseph disease --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:machado-joseph disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1159. en:mayer-rokitansky-kuster-hauser syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:mayer-rokitansky-kuster-hauser syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1160. en:mcdonough syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:mcdonough syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1161. en:melorheostosis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:melorheostosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1162. en:methylmalonic acidemia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:methylmalonic acidemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1163. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1164. en:migrating partial seizures in infancy --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:migrating partial seizures in infancy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1165. en:morm syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:morm syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1166. en:mullerian-renal-cervical spine syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:mullerian-renal-cervical spine syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1167. en:multicentric osteolysis, nodulosis, and arthropathy --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:multicentric osteolysis, nodulosis, and arthropathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1168. en:naxos disease --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:naxos disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1169. en:neonatal progeroid syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:neonatal progeroid syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1170. en:neoplastic syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:neoplastic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1171. en:nephrocalcinosis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:nephrocalcinosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1172. en:orbital separation diminished --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:orbital separation diminished | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1173. en:pallister-killian syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:pallister-killian syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1174. en:paraneoplastic syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:paraneoplastic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1175. en:parinaud syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:parinaud syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1176. en:pearson marrow-pancreas syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:pearson marrow-pancreas syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1177. en:pentosuria --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:pentosuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1178. en:pierre robin syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:pierre robin syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1179. en:primary hypertrophic osteoarthropathy --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:primary hypertrophic osteoarthropathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1180. en:progressive hemifacial atrophy --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:progressive hemifacial atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1181. en:rhizomelic dysplasia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:rhizomelic dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1182. en:roberts syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:roberts syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1183. en:schwartz-jampel syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:schwartz-jampel syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1184. en:seckel syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:seckel syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1185. en:sex ratio - 2.3 males-to-1 female --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:sex ratio - 2.3 males-to-1 female | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1186. en:sitosterolemia with xanthomatosis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:sitosterolemia with xanthomatosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1187. en:spasmodic torticollis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:spasmodic torticollis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1188. en:spondyloenchondrodysplasia with immune dysregulation --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1189. en:stargardt disease --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:stargardt disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1190. en:thyroid dyshormonogenesis 4 --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:thyroid dyshormonogenesis 4 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1191. en:trichinosis --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:trichinosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1192. en:true hermaphroditism --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:true hermaphroditism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1193. en:tyrosinemia type ii --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:tyrosinemia type ii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1194. en:usher syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:usher syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1195. en:vacterl association --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:vacterl association | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1196. en:valinemia --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:valinemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1197. en:variegate porphyria --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:variegate porphyria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1198. en:waardenburg anophthalmia syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:waardenburg anophthalmia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1199. en:waardenburg syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:waardenburg syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1200. en:wolfram syndrome --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:wolfram syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1201. en:x-linked creatine transporter deficiency --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:x-linked creatine transporter deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1202. en:x-linked intellectual disability seemanova type --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=en:x-linked intellectual disability seemanova type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1203. maladie de dubin-johnson --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=maladie de dubin-johnson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1204. maladie du cri du chat --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=maladie du cri du chat | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1205. souffrance respiratoire --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=souffrance respiratoire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1206. syndrome de bile épaisse --- r_associated #0: 29 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de bile épaisse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=29
  1207. Kawasaki (maladie de) --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=Kawasaki (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1208. Maladie de Wolman --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=Maladie de Wolman | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1209. albinisme oculocutané de type mutant jaune --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=albinisme oculocutané de type mutant jaune | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1210. aniridie, microcornée et cataracte régressive --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=aniridie, microcornée et cataracte régressive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1211. en:5-oxoprolinase deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:5-oxoprolinase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1212. en:Marburg virus disease --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:Marburg virus disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1213. en:Seitelberger's disease --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:Seitelberger's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1214. en:Stein-Leventhal syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:Stein-Leventhal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1215. en:abetalipoproteinemia --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:abetalipoproteinemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1216. en:absent olfactory tracts and bulbs --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:absent olfactory tracts and bulbs | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1217. en:acatalasemia --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:acatalasemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1218. en:acrorenal mandibular syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:acrorenal mandibular syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1219. en:alpha-fetoprotein deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:alpha-fetoprotein deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1220. en:anauxetic dysplasia --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:anauxetic dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1221. en:and proeminent incisors --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:and proeminent incisors | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1222. en:ataxia-telangiectasisa-like disorder 1 --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1223. en:auditory perceptual disorder --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:auditory perceptual disorder | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1224. en:autoinflammatory syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:autoinflammatory syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1225. en:bamforth syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:bamforth syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1226. en:barrett esophagus --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:barrett esophagus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1227. en:bonnevie-ullrich syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:bonnevie-ullrich syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1228. en:bothnia retinal dystrophy --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:bothnia retinal dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1229. en:bowen-conradi syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:bowen-conradi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1230. en:brachydactyly syndrome type b --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:brachydactyly syndrome type b | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1231. en:carbonic anhydrase i deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:carbonic anhydrase i deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1232. en:chondrodystrophia punctata --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:chondrodystrophia punctata | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1233. en:chromosome 17, trisomy 17p --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:chromosome 17, trisomy 17p | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1234. en:cleft lip and palate --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:cleft lip and palate | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1235. en:coffin-lowry syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:coffin-lowry syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1236. en:combined malonic and methylmalonic aciduria --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:combined malonic and methylmalonic aciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1237. en:complex regional pain syndrome i --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:complex regional pain syndrome i | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1238. en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1239. en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1240. en:congenital insensitivity to pain with anhidrosis --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital insensitivity to pain with anhidrosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1241. en:congenital transferrin deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital transferrin deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1242. en:crane-heise syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:crane-heise syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1243. en:crigler-najjar syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:crigler-najjar syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1244. en:deafness, congenital, with inner ear agenesis, microtia, and microdontia --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1245. en:dicarboxylicaminoaciduria --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:dicarboxylicaminoaciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1246. en:diencephalic syndrome of infancy --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:diencephalic syndrome of infancy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1247. en:diffuse idiopathic skeletal hyperostosis --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:diffuse idiopathic skeletal hyperostosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1248. en:dihydrouracil dehydrogenase deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:dihydrouracil dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1249. en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1250. en:familial atypical hemolytic uremic syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:familial atypical hemolytic uremic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1251. en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1252. en:fetal macrosomia --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:fetal macrosomia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1253. en:fibrodysplasia ossificans progressiva --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:fibrodysplasia ossificans progressiva | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1254. en:giant axonal neuropathy --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:giant axonal neuropathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1255. en:glycogen storage disease type x --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:glycogen storage disease type x | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1256. en:gynatresia --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:gynatresia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1257. en:hard skin syndrome parana type --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hard skin syndrome parana type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1258. en:hepatorenal syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hepatorenal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1259. en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1260. en:hereditary persistence of fetal hemoglobin --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary persistence of fetal hemoglobin | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1261. en:hexadactyly --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hexadactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1262. en:hnsha due to aldolase a deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hnsha due to aldolase a deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1263. en:hnsha due to glutathione synthetase deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hnsha due to glutathione synthetase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1264. en:hyperprolinemia type 1 --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperprolinemia type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1265. en:hyperprolinemia type 2 --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperprolinemia type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1266. en:hypokalemia, familial --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hypokalemia, familial | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1267. en:hypothalamic hamartoblastoma --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:hypothalamic hamartoblastoma | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1268. en:insulin receptor mutation - associated insulin resistance syndromes --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:insulin receptor mutation - associated insulin resistance syndromes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1269. en:jankovic rivera syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:jankovic rivera syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1270. en:juvenile x-linked retinoschisis --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:juvenile x-linked retinoschisis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1271. en:kenny-caffey syndrome type 2 --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:kenny-caffey syndrome type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1272. en:klippel-feil syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:klippel-feil syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1273. en:late-onset junctional epidermolysis bullosa --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:late-onset junctional epidermolysis bullosa | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1274. en:lazar-house --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:lazar-house | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1275. en:lennox-gastaut syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:lennox-gastaut syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1276. en:lethal congenital contracture syndrome 1 --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:lethal congenital contracture syndrome 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1277. en:lethal multiple pterygium syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:lethal multiple pterygium syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1278. en:lobar holoprosencephalies --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:lobar holoprosencephalies | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1279. en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1280. en:mental retardation, autosomal dominant 9 --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:mental retardation, autosomal dominant 9 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1281. en:microcephaly deafness syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:microcephaly deafness syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1282. en:mobius syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:mobius syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1283. en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1284. en:multiple malformation syndrome with facial-limb defects as major feature --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:multiple malformation syndrome with facial-limb defects as major feature | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1285. en:myokymia --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:myokymia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1286. en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1287. en:neuromyelitis optica --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:neuromyelitis optica | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1288. en:noonan syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:noonan syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1289. en:overlap syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:overlap syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1290. en:pain amplification syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:pain amplification syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1291. en:paroxysmal extreme pain disorder --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:paroxysmal extreme pain disorder | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1292. en:pelizaeus merzbacher like disease --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:pelizaeus merzbacher like disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1293. en:perinatal blood aspiration syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:perinatal blood aspiration syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1294. en:persistent fetal circulation --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:persistent fetal circulation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1295. en:persistent mullerian duct syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:persistent mullerian duct syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1296. en:peters-plus syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:peters-plus syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1297. en:polymicrogyria --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:polymicrogyria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1298. en:porokeratosis --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:porokeratosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1299. en:porphobilinogen synthase deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:porphobilinogen synthase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1300. en:posteriorly rotated ear --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:posteriorly rotated ear | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1301. en:primary immunodeficiency syndrome due to p14 deficiency --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1302. en:prosopagnosia --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:prosopagnosia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1303. en:prune belly syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:prune belly syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1304. en:pseudotumor cerebri --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:pseudotumor cerebri | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1305. en:rieger syndrome type 1 --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:rieger syndrome type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1306. en:sarcitis --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:sarcitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1307. en:sinus histiocytosis with massive lymphadenopathy --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:sinus histiocytosis with massive lymphadenopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1308. en:smith-mccort dysplasia --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:smith-mccort dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1309. en:spastic paraplegia 15, autosomal recessive --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:spastic paraplegia 15, autosomal recessive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1310. en:spondyloepiphyseal dysplasia, omani type --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:spondyloepiphyseal dysplasia, omani type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1311. en:status epilepticus --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:status epilepticus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1312. en:steinfeld syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:steinfeld syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1313. en:stickler syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:stickler syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1314. en:sudden infant death --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:sudden infant death | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1315. en:sunct syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:sunct syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1316. en:sweet syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:sweet syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1317. en:tempi syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:tempi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1318. en:temporomandibular joint dysfunction syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:temporomandibular joint dysfunction syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1319. en:thomas syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:thomas syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1320. en:thrombocytopenia 2 --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:thrombocytopenia 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1321. en:trigger finger disorder --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:trigger finger disorder | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1322. en:tubulointerstitial nephritis and uveitis --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:tubulointerstitial nephritis and uveitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1323. en:waterhouse-friderichsen syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:waterhouse-friderichsen syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1324. en:wolf-hirschhorn syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:wolf-hirschhorn syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1325. en:wolff-parkinson-white syndrome --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=en:wolff-parkinson-white syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1326. maladie de roger --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=maladie de roger | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1327. syndrome de Joubert-Boltshauser (syndrome de) --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Joubert-Boltshauser (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1328. syndrome de Sheehan --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Sheehan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1329. syndrome de douleur extrême paroxystique --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de douleur extrême paroxystique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1330. syndrome de membrane hyaline --- r_associated #0: 28 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de membrane hyaline | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=28
  1331. aniridie, ataxie cérébelleuse et déficience mentale --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=aniridie, ataxie cérébelleuse et déficience mentale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1332. choc toxique --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=choc toxique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1333. choc toxique staphylococcique --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=choc toxique staphylococcique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1334. cholestase intrahépatique progressive familiale de type 1 --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=cholestase intrahépatique progressive familiale de type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1335. en:Gitelman syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:Gitelman syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1336. en:Nathalie syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:Nathalie syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1337. en:Wegener granulomatosis --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:Wegener granulomatosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1338. en:abstinence syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:abstinence syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1339. en:acquired hyperostosis syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:acquired hyperostosis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1340. en:acute coronary syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:acute coronary syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1341. en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1342. en:alpha-1 antitrypsin deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:alpha-1 antitrypsin deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1343. en:aminomethyltransferase deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:aminomethyltransferase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1344. en:andersen syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:andersen syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1345. en:aprosencephaly --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:aprosencephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1346. en:arhinia, choanal atresia, and microphthalmia --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:arhinia, choanal atresia, and microphthalmia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1347. en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1348. en:ataxia telangiectasia syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:ataxia telangiectasia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1349. en:basilar artery syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:basilar artery syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1350. en:bicornuate uterus --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:bicornuate uterus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1351. en:brain iron accumulation type i syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:brain iron accumulation type i syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1352. en:carbohydrate-deficient glycoprotein syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:carbohydrate-deficient glycoprotein syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1353. en:cartilage hair hypoplasia --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:cartilage hair hypoplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1354. en:chitty hall baraitser syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:chitty hall baraitser syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1355. en:chronic fatigue syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:chronic fatigue syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1356. en:congenital alpha-2-antiplasmin deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1357. en:congenital disorder of deglycosylation --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital disorder of deglycosylation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1358. en:congenital dyserythropoietic anemia --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital dyserythropoietic anemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1359. en:cyclopia (5%) --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:cyclopia (5%) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1360. en:cystathioninuria --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:cystathioninuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1361. en:de toni-debre-fanconi syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:de toni-debre-fanconi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1362. en:deficiency of glucosyltransferase 1 --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:deficiency of glucosyltransferase 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1363. en:diaphanospondylodysostosis --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:diaphanospondylodysostosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1364. en:drug- and toxin-induced pulmonary arterial hypertension --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:drug- and toxin-induced pulmonary arterial hypertension | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1365. en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1366. en:fetal akinesia deformation sequence --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:fetal akinesia deformation sequence | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1367. en:fetal hydantoin syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:fetal hydantoin syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1368. en:fetal valproate syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:fetal valproate syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1369. en:fox-fordyce disease --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:fox-fordyce disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1370. en:genoa syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:genoa syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1371. en:geroderma osteodysplastica --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:geroderma osteodysplastica | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1372. en:gerstmann-straussler-scheinker disease --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:gerstmann-straussler-scheinker disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1373. en:glucose-6-phosphate dehydrogenase deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1374. en:glutamate-cysteine ligase deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:glutamate-cysteine ligase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1375. en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1376. en:gracile syndrome (disorder) --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:gracile syndrome (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1377. en:growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1378. en:hair tourniquet --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hair tourniquet | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1379. en:hallermann syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hallermann syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1380. en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:haspeslagh fryns muelenaere syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1381. en:hemophagocytic lymphohistiocytosis --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hemophagocytic lymphohistiocytosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1382. en:hereditary hyperbilirubinemia --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary hyperbilirubinemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1383. en:hmg-coa lyase deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hmg-coa lyase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1384. en:hypereosinophilic syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hypereosinophilic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1385. en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1386. en:hypertrichosis and acromegaloid facial appearance syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hypertrichosis and acromegaloid facial appearance syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1387. en:hypohidrotic ectodermal dysplasia with immune deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hypohidrotic ectodermal dysplasia with immune deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1388. en:hypomandibular faciocranial dysostosis --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hypomandibular faciocranial dysostosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1389. en:hypoplastic tibia and postaxial polydactyly syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hypoplastic tibia and postaxial polydactyly syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1390. en:hypospadias-mental retardation syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:hypospadias-mental retardation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1391. en:idiopathic cd4-positive t-lymphocytopenia --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:idiopathic cd4-positive t-lymphocytopenia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1392. en:idiopathic hypersomnolence --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:idiopathic hypersomnolence | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1393. en:imperforate vagina --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:imperforate vagina | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1394. en:infantile convulsions and paroxysmal choreoathetosis, familial --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:infantile convulsions and paroxysmal choreoathetosis, familial | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1395. en:infantile globoid cell leukodystrophy --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:infantile globoid cell leukodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1396. en:kartagener syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:kartagener syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1397. en:knobloch syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:knobloch syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1398. en:kundrat's syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:kundrat's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1399. en:kuskokwim disease --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:kuskokwim disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1400. en:lethal congenital contracture syndrome 2 --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:lethal congenital contracture syndrome 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1401. en:lethal congenital contracture syndrome type 3 --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:lethal congenital contracture syndrome type 3 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1402. en:lipase hypersecretion syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:lipase hypersecretion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1403. en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1404. en:loeys-dietz syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:loeys-dietz syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1405. en:malignant hyperthermia syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:malignant hyperthermia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1406. en:marshall syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:marshall syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1407. en:maternal uniparental disomy chromosome 14 syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:maternal uniparental disomy chromosome 14 syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1408. en:meesmann corneal dystrophy --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:meesmann corneal dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1409. en:mehes syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:mehes syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1410. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1411. en:mevalonate kinase deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:mevalonate kinase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1412. en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1413. en:mitochondrial dna depletion syndrome 2 (myopathic type) --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:mitochondrial dna depletion syndrome 2 (myopathic type) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1414. en:mucolipidosis type iii gamma --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:mucolipidosis type iii gamma | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1415. en:multiple sulfatase deficiency disease --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:multiple sulfatase deficiency disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1416. en:muscle amp deaminase deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:muscle amp deaminase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1417. en:neuroleptic malignant syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:neuroleptic malignant syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1418. en:olivopontocerebellar atrophy --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:olivopontocerebellar atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1419. en:onychoosteodysostosis --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:onychoosteodysostosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1420. en:otoonychoperoneal syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:otoonychoperoneal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1421. en:pentalogy of cantrell --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:pentalogy of cantrell | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1422. en:perlman syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:perlman syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1423. en:pettigrew syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:pettigrew syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1424. en:poems syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:poems syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1425. en:polydactyly preaxial type 1 --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:polydactyly preaxial type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1426. en:pyramidal tract dysfunction --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:pyramidal tract dysfunction | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1427. en:radial polydactyly --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:radial polydactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1428. en:richards-rundle syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:richards-rundle syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1429. en:schinzel-giedion midface-retraction syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:schinzel-giedion midface-retraction syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1430. en:sonoda syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:sonoda syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1431. en:spondyloenchondrodysplasia --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:spondyloenchondrodysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1432. en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1433. en:sudden unexplained death in childhood --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:sudden unexplained death in childhood | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1434. en:sunset syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:sunset syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1435. en:tetra-amelia autosomal recessive --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:tetra-amelia autosomal recessive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1436. en:thyroid dysgenesis --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:thyroid dysgenesis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1437. en:tourette syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:tourette syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1438. en:trichohepatoenteric syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:trichohepatoenteric syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1439. en:tricuspid valve atresia --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:tricuspid valve atresia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1440. en:uveitis glaucoma and hyphema syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:uveitis glaucoma and hyphema syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1441. en:very long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:very long-chain acyl-coa dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1442. en:wandering spleen --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:wandering spleen | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1443. en:wolman's disease --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:wolman's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1444. en:x-linked intellectual disability stoll type --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:x-linked intellectual disability stoll type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1445. en:xerophthalmia --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:xerophthalmia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1446. en:xxxy syndrome --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:xxxy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1447. en:zellweger-like syndrome without peroxisomal anomaly --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=en:zellweger-like syndrome without peroxisomal anomaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1448. maladie de dercum --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=maladie de dercum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1449. paragangliome (mise en évidence scintigraphique du) --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=paragangliome (mise en évidence scintigraphique du) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1450. selle turcique vide --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=selle turcique vide | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1451. syndrome de réaction inflammatoire généralisée --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de réaction inflammatoire généralisée | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1452. triskélion --- r_associated #0: 27 --> en:pseudotrisomy 13 syndrome
    n1=triskélion | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=27
  1453. SRAS --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=SRAS | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1454. atransferrinémie --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=atransferrinémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1455. communication inter-auriculaire --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=communication inter-auriculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1456. communication interauriculaire --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=communication interauriculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1457. contractures congénitales et arachnodactylie --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=contractures congénitales et arachnodactylie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1458. crosse aortique(syndrome de la) --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=crosse aortique(syndrome de la) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1459. dextrocardie --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=dextrocardie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1460. déficit en sulfite-oxydase --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=déficit en sulfite-oxydase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1461. en:22q telomere deletion syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:22q telomere deletion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1462. en:3-methylglutaconic aciduria type 1 --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:3-methylglutaconic aciduria type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1463. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:5 alpha steroid reductase 2 deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1464. en:Seitelberger's neuroaxonal dystrophy --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:Seitelberger's neuroaxonal dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1465. en:achromatopsia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:achromatopsia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1466. en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1467. en:alkaptonuria --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:alkaptonuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1468. en:anal imperforation --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:anal imperforation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1469. en:anasarca --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:anasarca | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1470. en:argininemia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:argininemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1471. en:atransferrinemia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:atransferrinemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1472. en:atypical hemolytic uremic syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:atypical hemolytic uremic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1473. en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive distal osteolysis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1474. en:autosomal recessive ocular albinism --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive ocular albinism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1475. en:autosomal recessive sideroblastic anemia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive sideroblastic anemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1476. en:behrens baumann dust syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:behrens baumann dust syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1477. en:brain calcification rajab type --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:brain calcification rajab type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1478. en:brain malformation, congenital heart disease, postaxial polydactyly syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:brain malformation, congenital heart disease, postaxial polydactyly syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1479. en:capillary leak syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:capillary leak syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1480. en:cebocephaly --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:cebocephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1481. en:cerebellar ataxia, cayman type --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebellar ataxia, cayman type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1482. en:char syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:char syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1483. en:charcot-marie-tooth disease type 4 --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:charcot-marie-tooth disease type 4 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1484. en:charge syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:charge syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1485. en:chediak-higashi syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:chediak-higashi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1486. en:chilblains --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:chilblains | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1487. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1488. en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:chromosome 17q21.31 deletion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1489. en:citrin deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:citrin deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1490. en:classical phenylketonuria --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:classical phenylketonuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1491. en:congenital cerebellar hypoplasia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital cerebellar hypoplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1492. en:congenital disorder of glycosylation type ia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital disorder of glycosylation type ia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1493. en:congenital disorder of glycosylation type ic --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital disorder of glycosylation type ic | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1494. en:congenital disorder of glycosylation type id --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital disorder of glycosylation type id | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1495. en:congenital pain insensitivity --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital pain insensitivity | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1496. en:congenital pancreatic enterokinase deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital pancreatic enterokinase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1497. en:connexin 26 gene anomaly --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:connexin 26 gene anomaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1498. en:cortical dysplasia-focal epilepsy syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1499. en:cutis laxa --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:cutis laxa | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1500. en:cysticercal disease --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:cysticercal disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1501. en:dactylolysis spontanea --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:dactylolysis spontanea | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1502. en:de sanctis-cacchione syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:de sanctis-cacchione syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1503. en:deafness and myopia syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:deafness and myopia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1504. en:deafness, autosomal recessive 1a --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:deafness, autosomal recessive 1a | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1505. en:deficiency of fructokinase --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:deficiency of fructokinase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1506. en:dextrocardia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:dextrocardia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1507. en:eiken type chondrodysplasia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:eiken type chondrodysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1508. en:erythrokeratodermia variabilis --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:erythrokeratodermia variabilis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1509. en:erythropoietic porphyria --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:erythropoietic porphyria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1510. en:exfoliation syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:exfoliation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1511. en:familial alobar holoprosencephaly --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:familial alobar holoprosencephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1512. en:familial juvenile nephronophthisis --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:familial juvenile nephronophthisis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1513. en:familial median cleft of upper and lower lip --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:familial median cleft of upper and lower lip | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1514. en:fish skin disease --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:fish skin disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1515. en:genu varum --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:genu varum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1516. en:gyrate atrophy --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:gyrate atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1517. en:hantavirus pulmonary syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hantavirus pulmonary syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1518. en:hemorrhagic fever with renal syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hemorrhagic fever with renal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1519. en:hepatolenticular degeneration --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hepatolenticular degeneration | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1520. en:hereditary factor xi deficiency disease --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary factor xi deficiency disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1521. en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1522. en:hermansky-pudlak syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hermansky-pudlak syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1523. en:hnsha due to glutathione reductase deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hnsha due to glutathione reductase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1524. en:holoprosencephaly type 4 --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly type 4 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1525. en:hydroa vacciniforme --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hydroa vacciniforme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1526. en:hymenolepiasis --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hymenolepiasis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1527. en:hypophosphatasia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hypophosphatasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1528. en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1529. en:insulin growth factor i deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:insulin growth factor i deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1530. en:intestinal epithelial dysplasia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:intestinal epithelial dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1531. en:irritable bowel syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:irritable bowel syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1532. en:kearns-sayre syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:kearns-sayre syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1533. en:kimura disease --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:kimura disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1534. en:klippel-trenaunay-weber syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:klippel-trenaunay-weber syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1535. en:kshv inflammatory cytokine syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:kshv inflammatory cytokine syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1536. en:lafora disease --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:lafora disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1537. en:lateral cleft lip --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:lateral cleft lip | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1538. en:laurin-sandrow syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:laurin-sandrow syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1539. en:leopard syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:leopard syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1540. en:lupus anticoagulant disorder --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:lupus anticoagulant disorder | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1541. en:lymphedema-distichiasis syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:lymphedema-distichiasis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1542. en:malformations of cortical development --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:malformations of cortical development | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1543. en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1544. en:menopausal syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:menopausal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1545. en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1546. en:microcephaly-capillary malformation syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1547. en:mixed connective tissue disease --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:mixed connective tissue disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1548. en:moderate steroid 21-hydroxylase deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1549. en:monilethrix --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:monilethrix | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1550. en:morquio syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:morquio syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1551. en:multiple acyl-coa dehydrogenase deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:multiple acyl-coa dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1552. en:muscular dystrophy --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:muscular dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1553. en:myitis --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:myitis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1554. en:myopathy, congenital nonprogressive with moebius and robin sequences --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:myopathy, congenital nonprogressive with moebius and robin sequences | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1555. en:myotonic disorder --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:myotonic disorder | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1556. en:nathalie syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:nathalie syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1557. en:nelson syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:nelson syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1558. en:neurotoxicity syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:neurotoxicity syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1559. en:noma --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:noma | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1560. en:oculo-respiratory syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:oculo-respiratory syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1561. en:oculocerebrorenal syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:oculocerebrorenal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1562. en:oculocutaneous albinism type 6 --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:oculocutaneous albinism type 6 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1563. en:oculorespiratory syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:oculorespiratory syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1564. en:orofaciodigital syndrome type 1 --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:orofaciodigital syndrome type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1565. en:palmar-plantar erythodysthesia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:palmar-plantar erythodysthesia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1566. en:pantothenate kinase-associated neurodegeneration --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:pantothenate kinase-associated neurodegeneration | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1567. en:pena-shokeir syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:pena-shokeir syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1568. en:penta x syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:penta x syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1569. en:persistent mullerian derivative with lymphangiectasia and polydactyly syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:persistent mullerian derivative with lymphangiectasia and polydactyly syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1570. en:pituitary stalk interruption syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:pituitary stalk interruption syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1571. en:polydactyly of toes --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:polydactyly of toes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1572. en:porphyria cutanea tarda --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:porphyria cutanea tarda | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1573. en:potocki-lupski syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:potocki-lupski syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1574. en:potter syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:potter syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1575. en:primary fanconi syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:primary fanconi syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1576. en:progressive muscular atrophy --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:progressive muscular atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1577. en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1578. en:radial aplasia-thrombocytopenia syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:radial aplasia-thrombocytopenia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1579. en:radiation sickness syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:radiation sickness syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1580. en:reardon hall slaney syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:reardon hall slaney syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1581. en:renal coloboma syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:renal coloboma syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1582. en:renal tubulopathy with encephalopathy and liver failure syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:renal tubulopathy with encephalopathy and liver failure syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1583. en:retinoschisis --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:retinoschisis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1584. en:scimitar syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:scimitar syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1585. en:selective antibody deficiency with normal immunoglobulins --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:selective antibody deficiency with normal immunoglobulins | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1586. en:short stature homeobox deficiency --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:short stature homeobox deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1587. en:sick sinus syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:sick sinus syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1588. en:simple syndactyly of toes, first web space --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:simple syndactyly of toes, first web space | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1589. en:small penis --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:small penis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1590. en:smith-magenis syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:smith-magenis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1591. en:spinocerebellar ataxia with epilepsy --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:spinocerebellar ataxia with epilepsy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1592. en:spondyloepimetaphyseal dysplasia, sponastrime type --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:spondyloepimetaphyseal dysplasia, sponastrime type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1593. en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1594. en:stiff skin syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:stiff skin syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1595. en:syndromic orbital border hypoplasia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:syndromic orbital border hypoplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1596. en:thalidomide embryopathy syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:thalidomide embryopathy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1597. en:thanatophoric dysplasia --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:thanatophoric dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1598. en:thoracic outlet syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:thoracic outlet syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1599. en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1600. en:trichorhinophalangeal syndrome type i --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:trichorhinophalangeal syndrome type i | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1601. en:type a 14 --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:type a 14 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1602. en:type ii acrocephalopolysyndactyly --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:type ii acrocephalopolysyndactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1603. en:wildervanck's syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:wildervanck's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1604. en:wiskott-aldrich syndrome --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=en:wiskott-aldrich syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1605. hémicéphalie --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=hémicéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1606. insuffisance respiratoire, problème respiratoire --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=insuffisance respiratoire, problème respiratoire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1607. porphyrie cutanée tardive --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=porphyrie cutanée tardive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1608. porphyrie érythropoïétique --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=porphyrie érythropoïétique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1609. syndrome de la selle turcique vide --- r_associated #0: 26 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de la selle turcique vide | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  1610. FMD --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=FMD | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1611. Hölmgren (triade de) --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=Hölmgren (triade de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1612. acatalasémie --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=acatalasémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1613. acrodermatitis enteropathica --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=acrodermatitis enteropathica | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1614. albinisme avec pigmentation minime --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=albinisme avec pigmentation minime | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1615. dysplasie olfactogénitale --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie olfactogénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1616. en:Stargardt disease --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:Stargardt disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1617. en:achenbach syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:achenbach syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1618. en:acute respiratory distress --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:acute respiratory distress | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1619. en:antithrombin iii deficiency --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:antithrombin iii deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1620. en:cleft hand with polydactyly --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:cleft hand with polydactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1621. en:congenital myasthenic syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital myasthenic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1622. en:dicheirus --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:dicheirus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1623. en:dyggve-melchior-clausen syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:dyggve-melchior-clausen syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1624. en:fraser syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:fraser syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1625. en:fuchs endothelial dystrophy --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:fuchs endothelial dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1626. en:hansenarium --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:hansenarium | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1627. en:hematomphalus --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:hematomphalus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1628. en:hemivertebra --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:hemivertebra | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1629. en:hnsha due to diphosphoglycerate mutase deficiency --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1630. en:hnsha due to glucose phosphate isomerase deficiency --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:hnsha due to glucose phosphate isomerase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1631. en:holoprosencephaly type 1 --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1632. en:hyperkalemic periodic paralysis --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperkalemic periodic paralysis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1633. en:incontinentia pigmenti --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:incontinentia pigmenti | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1634. en:joubert syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:joubert syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1635. en:kluver-bucy syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:kluver-bucy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1636. en:lecithin acyltransferase deficiency --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:lecithin acyltransferase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1637. en:leprosary --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:leprosary | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1638. en:leukodystrophy --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:leukodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1639. en:loffler syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:loffler syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1640. en:medium-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:medium-chain acyl-coa dehydrogenase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1641. en:microcephaly --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:microcephaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1642. en:muenke syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:muenke syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1643. en:ochronosis --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:ochronosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1644. en:otopalatodigital syndrome type 1 --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:otopalatodigital syndrome type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1645. en:pelger-huet anomaly --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:pelger-huet anomaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1646. en:pinta --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:pinta | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1647. en:post-pericardiotomy syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:post-pericardiotomy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1648. en:premenstrual syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:premenstrual syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1649. en:proteus syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:proteus syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1650. en:renal cysts and diabetes syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:renal cysts and diabetes syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1651. en:shone syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:shone syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1652. en:sjogren syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:sjogren syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1653. en:smith-lemli-opitz syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:smith-lemli-opitz syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1654. en:spinal muscular atrophy --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:spinal muscular atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1655. en:superior vena cava syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:superior vena cava syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1656. en:tooth and nail syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:tooth and nail syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1657. en:toxemia --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:toxemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1658. en:umbilical hiatus --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:umbilical hiatus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1659. en:vascular access steal syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:vascular access steal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1660. en:xerophtalmy --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:xerophtalmy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1661. en:xxyy syndrome --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:xxyy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1662. en:zinc-deficiency type --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=en:zinc-deficiency type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1663. granulomatose éosinophilique avec polyangéite --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=granulomatose éosinophilique avec polyangéite | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1664. hypogonadisme avec anosmie --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=hypogonadisme avec anosmie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1665. pemphigus bénin des muqueuses --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=pemphigus bénin des muqueuses | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1666. xanthique (lithiase) --- r_associated #0: 25 --> en:pseudotrisomy 13 syndrome
    n1=xanthique (lithiase) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=25
  1667. Jacobsen (syndrome de) --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=Jacobsen (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1668. S.I.D.A --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=S.I.D.A | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1669. TPN ou NADP --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=TPN ou NADP | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1670. anasarque f?toplacentaire --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=anasarque f?toplacentaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1671. cholestases intrahépatiques progressives familiales --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=cholestases intrahépatiques progressives familiales | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1672. en:11 pairs of ribs --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:11 pairs of ribs | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1673. en:FPLD --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:FPLD | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1674. en:Laurence-Moon's syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:Laurence-Moon's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1675. en:Martin-Bell's syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:Martin-Bell's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1676. en:acroparesthesia syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:acroparesthesia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1677. en:adrenal hypoplasia --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:adrenal hypoplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1678. en:albinotic fundus --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:albinotic fundus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1679. en:amelogenesis imperfecta - recessive - rough --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:amelogenesis imperfecta - recessive - rough | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1680. en:anaerosis --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:anaerosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1681. en:antiphospholipid syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:antiphospholipid syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1682. en:aspartylglycosaminuria --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:aspartylglycosaminuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1683. en:autosomal recessive asexual dwarfism --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive asexual dwarfism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1684. en:beta-aminoisobutyricaciduria --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:beta-aminoisobutyricaciduria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1685. en:carpal tunnel syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:carpal tunnel syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1686. en:cleft lip sequence --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:cleft lip sequence | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1687. en:coffin-siris syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:coffin-siris syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1688. en:cysticercus disease --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:cysticercus disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1689. en:d-bifunctional protein deficiency --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:d-bifunctional protein deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1690. en:deep scrotal raphe --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:deep scrotal raphe | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1691. en:erythropoietic uroporphyria --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:erythropoietic uroporphyria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1692. en:evans syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:evans syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1693. en:freeman-sheldon syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:freeman-sheldon syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1694. en:friedreich ataxia --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:friedreich ataxia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1695. en:gastric antral vascular ectasia --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:gastric antral vascular ectasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1696. en:hemochromatosis --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:hemochromatosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1697. en:hemophagocytic syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:hemophagocytic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1698. en:hereditary benign intraepithelial dyskeratosis --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary benign intraepithelial dyskeratosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1699. en:holoprosencephaly type 2 --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:holoprosencephaly type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1700. en:hyperglycerolemia --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperglycerolemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1701. en:hypoplastic right heart syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:hypoplastic right heart syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1702. en:ichthyosis vera --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:ichthyosis vera | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1703. en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1704. en:immunodeficiency syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:immunodeficiency syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1705. en:leber congenital amaurosis --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:leber congenital amaurosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1706. en:left ventricular non-compaction syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:left ventricular non-compaction syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1707. en:leper colony --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:leper colony | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1708. en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1709. en:multiple system atrophy --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:multiple system atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1710. en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1711. en:muscular hypotonia --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:muscular hypotonia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1712. en:oxalosis --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:oxalosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1713. en:popliteal pterygium syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:popliteal pterygium syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1714. en:postural orthostatic tachycardia syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:postural orthostatic tachycardia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1715. en:pre-excitation syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:pre-excitation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1716. en:pseudohermaphroditism --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:pseudohermaphroditism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1717. en:pseudohypoaldosteronism --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:pseudohypoaldosteronism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1718. en:pseudoxanthoma elasticum --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:pseudoxanthoma elasticum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1719. en:reye syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:reye syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1720. en:stiff person syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:stiff person syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1721. en:subclavian steal syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:subclavian steal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1722. en:syringomyelia --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:syringomyelia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1723. en:trisomy --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:trisomy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1724. en:uniparental disomy --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:uniparental disomy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1725. en:uv-sensitive syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:uv-sensitive syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1726. en:west syndrome --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=en:west syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1727. lichen ruber acuminatus --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=lichen ruber acuminatus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1728. mucopolysaccharidose de type I --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=mucopolysaccharidose de type I | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1729. porphyrie (anesthésie chez un patient atteint de) --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=porphyrie (anesthésie chez un patient atteint de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1730. syndrome de Williams --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Williams | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1731. trisomie --- r_associated #0: 24 --> en:pseudotrisomy 13 syndrome
    n1=trisomie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24
  1732. Duane (syndrome de) --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=Duane (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1733. Goltz (syndrome de) --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=Goltz (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1734. Marfan (maladie de) --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=Marfan (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1735. albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1736. déficit congénital en mégacaryocytes --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=déficit congénital en mégacaryocytes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1737. déficit en biotinidase --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=déficit en biotinidase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1738. en:Donohue syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:Donohue syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1739. en:Hurler's disease --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:Hurler's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1740. en:allanson pantzar mcleod syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:allanson pantzar mcleod syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1741. en:bartter syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:bartter syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1742. en:carnitine palmitoyltransferase ii deficiency --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:carnitine palmitoyltransferase ii deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1743. en:cayler cardiofacial syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:cayler cardiofacial syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1744. en:cebocephaly (36%) --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:cebocephaly (36%) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1745. en:cerebellar mutism --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:cerebellar mutism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1746. en:crest syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:crest syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1747. en:cystinuria --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:cystinuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1748. en:diarrhea-associated hemolytic uremic syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:diarrhea-associated hemolytic uremic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1749. en:dubowitz syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:dubowitz syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1750. en:duplicate uterus --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:duplicate uterus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1751. en:duplicate vagina --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:duplicate vagina | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1752. en:epidermolysis bullosa --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:epidermolysis bullosa | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1753. en:familial mediterranean fever --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:familial mediterranean fever | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1754. en:fryns syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:fryns syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1755. en:gasping syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:gasping syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1756. en:glycogen storage disease type i --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:glycogen storage disease type i | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1757. en:hurler-scheie syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:hurler-scheie syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1758. en:hydrops foetalis --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:hydrops foetalis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1759. en:hypoalphalipoproteinemia --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:hypoalphalipoproteinemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1760. en:hypopituitarism --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:hypopituitarism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1761. en:jeune syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:jeune syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1762. en:lateral medullary syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:lateral medullary syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1763. en:long qt syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:long qt syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1764. en:lysinuric protein intolerance --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:lysinuric protein intolerance | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1765. en:marfan's syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:marfan's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1766. en:molybdenum cofactor deficiency --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:molybdenum cofactor deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1767. en:mulibrey nanism --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:mulibrey nanism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1768. en:ophthalmoplegia --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:ophthalmoplegia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1769. en:pallister-hall syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:pallister-hall syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1770. en:phosphoenolpyruvate carboxykinase deficiency --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:phosphoenolpyruvate carboxykinase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1771. en:red man syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:red man syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1772. en:reiter syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:reiter syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1773. en:sea-blue histiocyte syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:sea-blue histiocyte syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1774. en:susac syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:susac syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1775. en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1776. en:teething syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:teething syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1777. en:turner syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:turner syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1778. en:weaver syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:weaver syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1779. en:weill-marchesani syndrome --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:weill-marchesani syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1780. en:yellow nail --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=en:yellow nail | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1781. fibromyalgie --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=fibromyalgie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1782. glycogénose --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=glycogénose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1783. microdélétion 5q35 --- r_associated #0: 23 --> en:pseudotrisomy 13 syndrome
    n1=microdélétion 5q35 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=23
  1784. DUGV --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=DUGV | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1785. acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1786. adénite sinusale cytophagique --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=adénite sinusale cytophagique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1787. aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1788. chondrodysplasie léthale avec brièveté des côtes --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=chondrodysplasie léthale avec brièveté des côtes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1789. en:Hurler's syndome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:Hurler's syndome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1790. en:Laron syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:Laron syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1791. en:acrocephalosyndactyly --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:acrocephalosyndactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1792. en:aids --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:aids | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1793. en:alper syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:alper syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1794. en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:antley-bixler syndrome, autosomal dominant | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1795. en:autoinflammation, lipodystrophy and dermatosis syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:autoinflammation, lipodystrophy and dermatosis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1796. en:autosomal recessive ichthyosis --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:autosomal recessive ichthyosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1797. en:congenital hand deformities --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital hand deformities | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1798. en:dandy-walker malformation --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:dandy-walker malformation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1799. en:dialyzer first use syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:dialyzer first use syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1800. en:diffuse cerebral sclerosis of schilder --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:diffuse cerebral sclerosis of schilder | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1801. en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:familial c3b inhibitor deficiency syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1802. en:fetal methotrexate syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:fetal methotrexate syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1803. en:fetal warfarin syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:fetal warfarin syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1804. en:gastroschisis --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:gastroschisis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1805. en:glycine encephalopathy --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:glycine encephalopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1806. en:goodpasture syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:goodpasture syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1807. en:hajdu-cheney syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:hajdu-cheney syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1808. en:lactase deficiency, congenital --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:lactase deficiency, congenital | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1809. en:leber hereditary optic atrophy --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:leber hereditary optic atrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1810. en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:lipoid proteinosis of urbach and wiethe | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1811. en:malakoplakia --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:malakoplakia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1812. en:malsegmentation --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:malsegmentation | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1813. en:mansonelliasis --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:mansonelliasis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1814. en:moyamoya disease --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:moyamoya disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1815. en:nephrogenic fibrosing dermopathy --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:nephrogenic fibrosing dermopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1816. en:organic brain syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:organic brain syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1817. en:proctatresia --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:proctatresia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1818. en:semilobar holoprosencephalies --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:semilobar holoprosencephalies | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1819. en:sitosterolemia --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:sitosterolemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1820. en:swyer james syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:swyer james syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1821. en:tethered spinal cord syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:tethered spinal cord syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1822. en:tyrosinemia type II --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:tyrosinemia type II | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1823. en:undescended testes --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:undescended testes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1824. en:van der woude syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:van der woude syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1825. en:xyy syndrome --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=en:xyy syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1826. psychose de Korsakoff --- r_associated #0: 22 --> en:pseudotrisomy 13 syndrome
    n1=psychose de Korsakoff | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=22
  1827. Maladie de Tay-Sachs --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=Maladie de Tay-Sachs | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1828. acidurie argininosuccinique --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=acidurie argininosuccinique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1829. acidémie isovalérique --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=acidémie isovalérique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1830. adipose douloureuse de Dercum --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=adipose douloureuse de Dercum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1831. alcaptonurie --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=alcaptonurie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1832. aniridie --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=aniridie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1833. argininémie --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=argininémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1834. calciphylaxie --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=calciphylaxie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1835. choroïdérémie --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=choroïdérémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1836. coproporphyrie héréditaire --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=coproporphyrie héréditaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1837. cétoacidurie à chaînes ramifiées --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=cétoacidurie à chaînes ramifiées | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1838. déficit enzymatique partiel de la surrénale --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=déficit enzymatique partiel de la surrénale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1839. en:Angelman's syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:Angelman's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1840. en:Dubin-Johnson's syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:Dubin-Johnson's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1841. en:Dubin-Sprinz disease --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:Dubin-Sprinz disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1842. en:Feingold syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:Feingold syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1843. en:Fox-Fordyce disease --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:Fox-Fordyce disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1844. en:Günther's disease --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:Günther's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1845. en:Leroy's i-cell disease --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:Leroy's i-cell disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1846. en:acute intermittent porphyria --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:acute intermittent porphyria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1847. en:adrenal gland hyperplasia ii --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:adrenal gland hyperplasia ii | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1848. en:amyoplasia congenita --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:amyoplasia congenita | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1849. en:analbuminemia --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:analbuminemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1850. en:basal ganglia disease, biotin-responsive --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:basal ganglia disease, biotin-responsive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1851. en:bloom syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:bloom syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1852. en:camurati-engelmann syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:camurati-engelmann syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1853. en:central sleep apnea syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:central sleep apnea syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1854. en:cervicocranial syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:cervicocranial syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1855. en:chorea --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:chorea | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1856. en:congenital abnormality --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital abnormality | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1857. en:congenital porphyria --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital porphyria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1858. en:craniostenosis --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:craniostenosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1859. en:diffuse infiltrative lymphocytosis syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:diffuse infiltrative lymphocytosis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1860. en:ehlers-danlos syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:ehlers-danlos syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1861. en:encephalocele --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:encephalocele | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1862. en:exumbilication --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:exumbilication | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1863. en:frasier syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:frasier syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1864. en:frontonasal dysplasia sequence --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:frontonasal dysplasia sequence | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1865. en:gargoylism --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:gargoylism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1866. en:gilbert syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:gilbert syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1867. en:glutaric aciduria type 1 --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:glutaric aciduria type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1868. en:hellp syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:hellp syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1869. en:hypoxaemia --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:hypoxaemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1870. en:iridocorneal endothelial syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:iridocorneal endothelial syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1871. en:kaufman-mckusick syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:kaufman-mckusick syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1872. en:lipoprotein glomerulopathy --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:lipoprotein glomerulopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1873. en:megaloglossia --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:megaloglossia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1874. en:merrf syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:merrf syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1875. en:mesoaxial polydactyly --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:mesoaxial polydactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1876. en:miliaria --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:miliaria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1877. en:mmih syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:mmih syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1878. en:nephrotic syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:nephrotic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1879. en:nystagmus --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:nystagmus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1880. en:obesity --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:obesity | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1881. en:osteopoecilia --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:osteopoecilia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1882. en:pancreatic lipase deficiency --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:pancreatic lipase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1883. en:pemphigoid gestationis --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:pemphigoid gestationis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1884. en:piriformis muscle syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:piriformis muscle syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1885. en:pityriasis lichenoides --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:pityriasis lichenoides | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1886. en:polymyalgia rheumatica --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:polymyalgia rheumatica | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1887. en:posterior fossa syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:posterior fossa syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1888. en:scleredema adultorum --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:scleredema adultorum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1889. en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:severe steroid 21-hydroxylase deficiency | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1890. en:tangier disease --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:tangier disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1891. en:transient global amnesia --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:transient global amnesia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1892. en:zollinger ellison syndrome --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=en:zollinger ellison syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1893. hypopituitarisme --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=hypopituitarisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1894. idiosyncrasie au fructose --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=idiosyncrasie au fructose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1895. mannosidose --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=mannosidose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1896. mucopolysaccharidose de type 1 --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=mucopolysaccharidose de type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1897. semialdéhyde succinique-déshydrogénase (déficit en) --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=semialdéhyde succinique-déshydrogénase (déficit en) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1898. syndrome de Churg-Strauss --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Churg-Strauss | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1899. syndrome de Prader-Willi --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Prader-Willi | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1900. syndrome de Zellweger --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Zellweger | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1901. syndrome de sevrage --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de sevrage | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1902. syndrome des ongles jaunes --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=syndrome des ongles jaunes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1903. xérophtalmie --- r_associated #0: 21 --> en:pseudotrisomy 13 syndrome
    n1=xérophtalmie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
  1904. ARTHROGRYPOSE --- r_associated #0: 20 --> en:pseudotrisomy 13 syndrome
    n1=ARTHROGRYPOSE | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=20
  1905. dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie olfactogénitale de De Morsier | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=20
  1906. leptospirose --- r_associated #0: 20 --> en:pseudotrisomy 13 syndrome
    n1=leptospirose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=20
  1907. syndrome --- r_associated #0: 20 --> en:pseudotrisomy 13 syndrome
    n1=syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=20
  1908. syndrome de Warburg --- r_associated #0: 16 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Warburg | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=16
  1909. triploïdie --- r_associated #0: 16 --> en:pseudotrisomy 13 syndrome
    n1=triploïdie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=16
  1910. trisomie 21 --- r_associated #0: 16 --> en:pseudotrisomy 13 syndrome
    n1=trisomie 21 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=16
  1911. Albert (position d') --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Albert (position d') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1912. Anomalie d'Ebstein --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Anomalie d'Ebstein | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1913. Arthrogrypose --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Arthrogrypose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1914. Détresse respiratoire --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Détresse respiratoire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1915. Fuchs (syndrome de) --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Fuchs (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1916. Giessen (test de) --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Giessen (test de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1917. His (faisceau de) --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=His (faisceau de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1918. Hyperplasie congénitale des surrénales --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Hyperplasie congénitale des surrénales | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1919. Intolérance au fructose --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Intolérance au fructose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1920. Kallman --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Kallman | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1921. Maladie de Marfan --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Maladie de Marfan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1922. Maladie de Niemann-Pick --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Maladie de Niemann-Pick | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1923. Noma --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Noma | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1924. Syndrome d'immunodéficience acquise --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome d'immunodéficience acquise | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1925. Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Walker-Warburg | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1926. Syndrome de sevrage --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de sevrage | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1927. acidoses lactiques (classification selon Cohen et Woods) --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=acidoses lactiques (classification selon Cohen et Woods) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1928. agglutinines froides (neuropathie à) --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=agglutinines froides (neuropathie à) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1929. cysticercoïde (larve) --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=cysticercoïde (larve) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1930. dysembryome (bénin, malin) --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=dysembryome (bénin, malin) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1931. dégénérescence wallerienne --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=dégénérescence wallerienne | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1932. démence (sémiologie) --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=démence (sémiologie) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1933. en:congenital atrophy of thyroid --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital atrophy of thyroid | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1934. en:congenital hypothyroidism --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital hypothyroidism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1935. en:neonatal hypothyroidism --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=en:neonatal hypothyroidism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1936. goltz --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=goltz | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1937. hydrocèle (cure chirurgicale d') --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hydrocèle (cure chirurgicale d') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1938. hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1939. hypophosphatasie --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypophosphatasie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1940. hypothyroïdie congénitale --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypothyroïdie congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1941. hypothyroïdie et psychisme --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypothyroïdie et psychisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1942. hypothyroïdie néonatale --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypothyroïdie néonatale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1943. hypotonie plasmatique --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotonie plasmatique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1944. hypotonie sphinctérienne anale --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotonie sphinctérienne anale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1945. hypotonie sphinctérienne uréthrale --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotonie sphinctérienne uréthrale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1946. hypotonie utérine --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotonie utérine | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1947. hypotonie vésicale --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotonie vésicale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1948. hypotonique --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotonique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1949. hypotrichose --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotrichose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1950. hypotrichose avec anodontie et anhidrose de Touraine --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotrichose avec anodontie et anhidrose de Touraine | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1951. hypotrichose congénitale des cils --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotrichose congénitale des cils | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1952. hypotrichose congénitale simple --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotrichose congénitale simple | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1953. hypotrichose héréditaire de Marie Unna --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotrichose héréditaire de Marie Unna | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1954. hypotrichose, atrophodermie folliculaire et épithéliomatose --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=hypotrichose, atrophodermie folliculaire et épithéliomatose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1955. iceberg (signe de l') --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=iceberg (signe de l') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1956. maladie à virus de marburg --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=maladie à virus de marburg | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1957. obésité --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=obésité | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1958. osteopœcilie --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=osteopœcilie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1959. snm --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=snm | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1960. syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Kallman-de Morsier | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1961. syndrome de Korsakoff --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Korsakoff | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1962. syndrome de Plummer-VInson --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Plummer-VInson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1963. syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de de Morsier-Kallmann | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1964. syndrome malin neuroleptique --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=syndrome malin neuroleptique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1965. triple arthrodèse --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=triple arthrodèse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1966. triple opération à la française --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=triple opération à la française | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1967. triptans --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=triptans | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1968. triquétrum --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=triquétrum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1969. triradialis sulcus de Turner --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=triradialis sulcus de Turner | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1970. tris --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=tris | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1971. trismus --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=trismus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1972. trisomie du bras court du chromosome 3 --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=trisomie du bras court du chromosome 3 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1973. xérophthalmie --- r_associated #0: 15 --> en:pseudotrisomy 13 syndrome
    n1=xérophthalmie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=15
  1974. aprosencéphalie --- r_associated #0: 11 --> en:pseudotrisomy 13 syndrome
    n1=aprosencéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=11
  1975. dysautonomie familiale --- r_associated #0: 11 --> en:pseudotrisomy 13 syndrome
    n1=dysautonomie familiale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=11
  1976. insomnie familiale fatale --- r_associated #0: 11 --> en:pseudotrisomy 13 syndrome
    n1=insomnie familiale fatale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=11
  1977. lepréchaunisme --- r_associated #0: 11 --> en:pseudotrisomy 13 syndrome
    n1=lepréchaunisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=11
  1978. maladie de Fox-Fordyce --- r_associated #0: 11 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Fox-Fordyce | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=11
  1979. mongolisme --- r_associated #0: 11 --> en:pseudotrisomy 13 syndrome
    n1=mongolisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=11
  1980. rétinoschisis --- r_associated #0: 11 --> en:pseudotrisomy 13 syndrome
    n1=rétinoschisis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=11
  1981. syndrome de Gitelman --- r_associated #0: 11 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Gitelman | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=11
  1982. Acromégalie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Acromégalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1983. Agnosie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Agnosie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1984. Albinisme --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Albinisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1985. Alice au pays des merveilles (syndrome d') --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Alice au pays des merveilles (syndrome d') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1986. Anencéphalie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Anencéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1987. Angelman (syndrome d') --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Angelman (syndrome d') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1988. CONGÉNITALE --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=CONGÉNITALE | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1989. Cataplexie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Cataplexie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1990. Communication interauriculaire --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Communication interauriculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1991. Craniosynostose --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Craniosynostose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1992. Cysticercose --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Cysticercose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1993. Dercum (maladie de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Dercum (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1994. Dubin-Johnson (syndrome de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Dubin-Johnson (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1995. Dugbe (virus) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Dugbe (virus) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1996. Fibromyalgie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Fibromyalgie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1997. Fucosidose --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Fucosidose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1998. Glycogénose --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Glycogénose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  1999. HELLP syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=HELLP syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2000. HLP3 --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=HLP3 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2001. HPE3 --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=HPE3 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2002. HPE4 --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=HPE4 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2003. Haltia-Santavuori (maladie de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Haltia-Santavuori (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2004. Hernie ombilicale --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Hernie ombilicale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2005. Histidinémie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Histidinémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2006. Hurler (maladie de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Hurler (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2007. Hydrocéphalie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Hydrocéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2008. Hypopituitarisme --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Hypopituitarisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2009. Hypotonie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Hypotonie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2010. Hypoxémie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Hypoxémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2011. Insler et Bernstein (score cervical d') --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Insler et Bernstein (score cervical d') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2012. Laurence-Moon (syndrome de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Laurence-Moon (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2013. Levine-Critchley (syndrome de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Levine-Critchley (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2014. Lisfranc (fracture de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Lisfranc (fracture de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2015. Léproserie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Léproserie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2016. MOMO (syndrome) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=MOMO (syndrome) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2017. Macroglossie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Macroglossie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2018. Maladie de Kawasaki --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Maladie de Kawasaki | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2019. Malformation d'Ebstein --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Malformation d'Ebstein | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2020. Manning (score de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Manning (score de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2021. Mannosidose --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Mannosidose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2022. Marburg (fièvre de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Marburg (fièvre de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2023. Martin-Bell (syndrome de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Martin-Bell (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2024. Mort subite du nourrisson --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Mort subite du nourrisson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2025. Myosite --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Myosite | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2026. Niemann-Pick (maladie de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Niemann-Pick (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2027. PMDS --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=PMDS | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2028. PMI gene --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=PMI gene | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2029. Panum (aire de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Panum (aire de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2030. Peste noire --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Peste noire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2031. Pitt-Rogers-Danks (syndrome de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Pitt-Rogers-Danks (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2032. Progéria --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Progéria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2033. Roger (maladie de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Roger (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2034. Sheehan (syndrome de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Sheehan (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2035. Shy-Drager (syndrome de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Shy-Drager (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2036. Sicard (opération de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Sicard (opération de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2037. Situs inversus --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Situs inversus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2038. Stargardt (maladie de ) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Stargardt (maladie de ) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2039. Stilling-Türk-Duane (syndrome de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Stilling-Türk-Duane (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2040. Syndrome de Churg-Strauss --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Churg-Strauss | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2041. Syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2042. Syndrome de Prader-Willi --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Prader-Willi | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2043. Syndrome de Sheehan --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Sheehan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2044. Syndrome de Sotos --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de Sotos | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2045. Syndrome de détresse respiratoire --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de détresse respiratoire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2046. Syndrome de malabsorption --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome de malabsorption | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2047. Syndrome du choc toxique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome du choc toxique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2048. Syndrome métabolique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome métabolique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2049. Townes-Brocks (syndrome de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Townes-Brocks (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2050. Trichothiodystrophie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Trichothiodystrophie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2051. Trisomie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Trisomie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2052. Wegener (granulomatose de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Wegener (granulomatose de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2053. Yellen-Gomco (clamp de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=Yellen-Gomco (clamp de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2054. a-bêta-lipoprotéinémie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=a-bêta-lipoprotéinémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2055. achondrogénèses --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=achondrogénèses | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2056. achromatopsie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=achromatopsie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2057. alcalose métabolique (classification) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=alcalose métabolique (classification) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2058. allocations --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=allocations | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2059. angl. TBS --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=angl. TBS | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2060. angl. XLSA/A --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=angl. XLSA/A | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2061. aniline (intoxication par l') --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=aniline (intoxication par l') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2062. association de tics vocaux et tics moteurs du syndrome de gilles de la tourette --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=association de tics vocaux et tics moteurs du syndrome de gilles de la tourette | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2063. atonie de l'utérus --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=atonie de l'utérus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2064. chondrodysplasie ponctuée --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=chondrodysplasie ponctuée | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2065. coproantigènes (recherche de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=coproantigènes (recherche de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2066. cornée et tyrosinose de type II --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=cornée et tyrosinose de type II | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2067. cutis laxa --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=cutis laxa | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2068. diabète bronzé --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=diabète bronzé | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2069. distance interpédiculaire (mesure de la) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=distance interpédiculaire (mesure de la) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2070. dysplasie frontométaphysaire --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie frontométaphysaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2071. dysplasie génitale --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie génitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2072. dysplasie iridodentaire --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=dysplasie iridodentaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2073. dystrophie musculaire --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=dystrophie musculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2074. déficit en phosphatases alcalines --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=déficit en phosphatases alcalines | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2075. ectodermitis erosiva pluriorificialis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectodermitis erosiva pluriorificialis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2076. ectodermose --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectodermose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2077. ectodermose érosive pluriorificielle de Fiessinger-Rendu --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectodermose érosive pluriorificielle de Fiessinger-Rendu | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2078. ectoenzyme --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectoenzyme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2079. ectomie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectomie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2080. ectomorphie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectomorphie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2081. ectoparasite --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectoparasite | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2082. ectoparasitose --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectoparasitose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2083. ectopie cardiaque --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectopie cardiaque | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2084. ectopie des procès ciliaires --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectopie des procès ciliaires | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2085. ectopie du cristallin --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ectopie du cristallin | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2086. en:5p minus syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:5p minus syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2087. en:5q microdeletion --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:5q microdeletion | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2088. en:Albert's position --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Albert's position | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2089. en:Albright's hereditary osteodystrophy --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Albright's hereditary osteodystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2090. en:Cogan-Reese syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Cogan-Reese syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2091. en:Crouzon's disease --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Crouzon's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2092. en:Crouzon?s disease --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Crouzon?s disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2093. en:Down's --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Down's | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2094. en:Down's syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Down's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2095. en:FrontoMetaphyseal Dysplasia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:FrontoMetaphyseal Dysplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2096. en:HHH syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:HHH syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2097. en:Holt-Oram syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Holt-Oram syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2098. en:Jadassohn-Lewandowsky syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Jadassohn-Lewandowsky syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2099. en:Korsakoff''s syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Korsakoff''s syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2100. en:Korsakoff's syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Korsakoff's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2101. en:LEOPARD syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:LEOPARD syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2102. en:Lejeune's syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Lejeune's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2103. en:MELAS syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:MELAS syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2104. en:NHSA III --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:NHSA III | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2105. en:PWS --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:PWS | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2106. en:Perthes' disease --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Perthes' disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2107. en:Riley-Day's syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Riley-Day's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2108. en:Schmorl's jaundice --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Schmorl's jaundice | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2109. en:Schridde's disease --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Schridde's disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2110. en:Shy-Drager's syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Shy-Drager's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2111. en:Smith-Magenis syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Smith-Magenis syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2112. en:Sotos's syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Sotos's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2113. en:Stilling-Türk-Duane's syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Stilling-Türk-Duane's syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2114. en:Tay Sachs' disease --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Tay Sachs' disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2115. en:WBS --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:WBS | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2116. en:Williams' syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Williams' syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2117. en:Williams-Beuren syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:Williams-Beuren syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2118. en:abdominal wall aplasia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:abdominal wall aplasia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2119. en:acquired immune deficiency syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:acquired immune deficiency syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2120. en:acromegalia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:acromegalia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2121. en:adactylia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:adactylia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2122. en:alcaptonuria --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:alcaptonuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2123. en:anaesthesia for porphyria --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:anaesthesia for porphyria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2124. en:anal sphincter hypotonia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:anal sphincter hypotonia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2125. en:and oligophrenia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:and oligophrenia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2126. en:and photophobia syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:and photophobia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2127. en:and postaxil polydactylie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:and postaxil polydactylie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2128. en:ataxia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:ataxia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2129. en:atresia ani --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:atresia ani | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2130. en:atrichia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:atrichia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2131. en:bilirubin encephalopathy --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:bilirubin encephalopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2132. en:bladder hypotonia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:bladder hypotonia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2133. en:cancrum oris --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:cancrum oris | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2134. en:cat cry disease --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:cat cry disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2135. en:cat cry syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:cat cry syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2136. en:chromosome 5p deletion syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:chromosome 5p deletion syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2137. en:congenital eyelashes hypotrichosis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital eyelashes hypotrichosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2138. en:congenital insensitivity to pain type III --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital insensitivity to pain type III | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2139. en:contractural arachnodactyly --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:contractural arachnodactyly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2140. en:ectrodactyly and macular dystrophy --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:ectrodactyly and macular dystrophy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2141. en:eds --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:eds | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2142. en:ehlers danlos syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:ehlers danlos syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2143. en:erythroblastosis fetalis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:erythroblastosis fetalis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2144. en:follicularis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:follicularis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2145. en:glycogenosis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:glycogenosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2146. en:green monkey virus disease --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:green monkey virus disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2147. en:hereditary sensory and autonomic neuropathy type III --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hereditary sensory and autonomic neuropathy type III | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2148. en:homogentisuria --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:homogentisuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2149. en:hypacusis and athetosis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hypacusis and athetosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2150. en:hyperornithinemia hyperammoniemia homocitrullinuria --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hyperornithinemia hyperammoniemia homocitrullinuria | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2151. en:hypothyreosis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hypothyreosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2152. en:hypothyroidism and psychism --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hypothyroidism and psychism | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2153. en:hypotonic --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hypotonic | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2154. en:hypotrichosis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hypotrichosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2155. en:hypotrichosis congenita simplex --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hypotrichosis congenita simplex | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2156. en:hypotrichosis-anodontic syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hypotrichosis-anodontic syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2157. en:hypoxemia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:hypoxemia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2158. en:infectious gangrene of the mouth --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:infectious gangrene of the mouth | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2159. en:interatrial septal defect --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:interatrial septal defect | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2160. en:interventricular septal defect --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:interventricular septal defect | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2161. en:intestinal malabsorption --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:intestinal malabsorption | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2162. en:irideremia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:irideremia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2163. en:leper house --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:leper house | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2164. en:minimal pigment type --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:minimal pigment type | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2165. en:nuclear icterus --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:nuclear icterus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2166. en:nuclear jaundice --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:nuclear jaundice | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2167. en:optic neuropathy --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:optic neuropathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2168. en:patterson-kelly syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:patterson-kelly syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2169. en:peripheral neuropathy in cold agglutinin disease --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:peripheral neuropathy in cold agglutinin disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2170. en:phosphatide thesaurismosis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:phosphatide thesaurismosis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2171. en:plasma hypotonia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:plasma hypotonia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2172. en:right sacrum anterior position --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:right sacrum anterior position | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2173. en:secundum defect --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:secundum defect | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2174. en:sign of the iceberg --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:sign of the iceberg | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2175. en:sinus venosus defect --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:sinus venosus defect | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2176. en:spastic neurologic disorder --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:spastic neurologic disorder | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2177. en:sphincteric hypotony --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:sphincteric hypotony | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2178. en:stress cardiomyopathy --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:stress cardiomyopathy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2179. en:substance withdrawal syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:substance withdrawal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2180. en:surgical treatment of hydrocele --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:surgical treatment of hydrocele | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2181. en:trisomy 21 --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:trisomy 21 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2182. en:type 1 --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:type 1 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2183. en:type 2 --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:type 2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2184. en:type 3 --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:type 3 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2185. en:type 4 --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:type 4 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2186. en:uterine hypotonia --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:uterine hypotonia | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2187. en:water on the brain --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:water on the brain | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2188. en:weaning syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:weaning syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2189. en:withdrawal syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:withdrawal syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2190. en:xanthine lithiasis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:xanthine lithiasis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2191. en:xanthonychia syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:xanthonychia syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2192. en:xanthonychie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=en:xanthonychie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2193. encéphalocèle --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=encéphalocèle | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2194. fente nasolabiopalatine --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=fente nasolabiopalatine | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2195. gastroschisis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=gastroschisis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2196. genu varum --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=genu varum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2197. glaucome capsulaire --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=glaucome capsulaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2198. glycogénique (surcharge et infiltration) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=glycogénique (surcharge et infiltration) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2199. hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2200. holocentromère --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=holocentromère | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2201. holocentromérique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=holocentromérique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2202. holocrine --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=holocrine | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2203. holodiastolique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=holodiastolique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2204. holoenzyme --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=holoenzyme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2205. hologamie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hologamie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2206. hologynique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hologynique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2207. holomérocrine --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=holomérocrine | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2208. holophrase --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=holophrase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2209. holoproencéphalie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=holoproencéphalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2210. hydroa vacciniforme --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hydroa vacciniforme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2211. hydrocephalus --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hydrocephalus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2212. hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2213. hypohypophysie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hypohypophysie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2214. hypophosphatasies --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hypophosphatasies | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2215. hypostimulinie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hypostimulinie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2216. hémochromatose primitive --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=hémochromatose primitive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2217. impédance acoustique (symb. Z) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=impédance acoustique (symb. Z) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2218. incontinentia pigmenti --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=incontinentia pigmenti | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2219. inertie utérine --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=inertie utérine | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2220. laparoschisis --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=laparoschisis | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2221. macrosomie, obésité, macrocéphalie et anomalies oculaires --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=macrosomie, obésité, macrocéphalie et anomalies oculaires | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2222. maladie de Duhring --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Duhring | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2223. maladie de Gilles de la Tourette --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Gilles de la Tourette | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2224. maladie de Stargardt --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Stargardt | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2225. maladie de Tangier --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Tangier | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2226. maladie de niemann-pick --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=maladie de niemann-pick | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2227. maladie des tics --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=maladie des tics | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2228. maladie des tics de Gilles de la Tourette --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=maladie des tics de Gilles de la Tourette | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2229. maladies de gilles de la tourette --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=maladies de gilles de la tourette | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2230. mort imminente (expérience de la) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=mort imminente (expérience de la) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2231. nanisme de type Laron --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=nanisme de type Laron | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2232. neuraminidase (déficit en) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=neuraminidase (déficit en) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2233. neuroblastome (mise en évidence scintigraphique du) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=neuroblastome (mise en évidence scintigraphique du) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2234. nystagmus --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=nystagmus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2235. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=nystagmus héréditaire vertical | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2236. nystagmus lié au sexe --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=nystagmus lié au sexe | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2237. nystagmus myoclonies --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=nystagmus myoclonies | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2238. néphritique (syndrome) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=néphritique (syndrome) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2239. omovertébral (os) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=omovertébral (os) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2240. ostéoporose-pseudogliome (syndrome) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=ostéoporose-pseudogliome (syndrome) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2241. paralysie périodique hypokaliémique familiale (maladie de Westphal) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=paralysie périodique hypokaliémique familiale (maladie de Westphal) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2242. paraplégie spastique dans la syphilis congénitale --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=paraplégie spastique dans la syphilis congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2243. pinta --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pinta | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2244. pluripotence --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pluripotence | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2245. pluripotent --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pluripotent | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2246. plurisegmentectomie hépatique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=plurisegmentectomie hépatique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2247. pneumallergène --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pneumallergène | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2248. pneumatisation de l'apophyse unciforme --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pneumatisation de l'apophyse unciforme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2249. pneumatisation du cornet moyen --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pneumatisation du cornet moyen | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2250. pneumatocèle --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pneumatocèle | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2251. pneumatose colique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pneumatose colique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2252. pneumaturie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pneumaturie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2253. pneumectomie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pneumectomie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2254. pneumoarthrographie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pneumoarthrographie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2255. pneumobilie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pneumobilie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2256. polydactylie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=polydactylie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2257. polymyalgia rheumatica --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=polymyalgia rheumatica | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2258. polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2259. poumon (fonctions métaboliques du) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=poumon (fonctions métaboliques du) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2260. profondeur de l'anesthésie (stade de) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=profondeur de l'anesthésie (stade de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2261. prolidase (déficit en) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=prolidase (déficit en) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2262. protéine trifonctionnelle mitochondriale (déficit en) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=protéine trifonctionnelle mitochondriale (déficit en) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2263. pseudo-hypoaldostéronisme --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pseudo-hypoaldostéronisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2264. pseudohypoaldostéronisme --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=pseudohypoaldostéronisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2265. quadriplégie spastique, rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2266. rate aberrante --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rate aberrante | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2267. rate flottante --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rate flottante | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2268. rate vagabonde --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rate vagabonde | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2269. red man syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=red man syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2270. rétention hydrochlorurée sodique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rétention hydrochlorurée sodique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2271. rétention membraneuse --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rétention membraneuse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2272. rétention placentaire --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rétention placentaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2273. rétention placentaire du postabortum --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rétention placentaire du postabortum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2274. rétention sudorale --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rétention sudorale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2275. rétentionniste --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rétentionniste | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2276. rétinite pigmentaire et retard mental --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=rétinite pigmentaire et retard mental | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2277. seitelberger --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=seitelberger | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2278. sel biliaire --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=sel biliaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2279. sirtuine --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=sirtuine | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2280. sisi-test --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=sisi-test | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2281. sismothérapie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=sismothérapie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2282. situs inversus viscerum --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=situs inversus viscerum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2283. situs mutatus --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=situs mutatus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2284. souche de référence --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=souche de référence | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2285. souche transduite --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=souche transduite | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2286. splénoptose --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=splénoptose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2287. stiff skin syndrome --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=stiff skin syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2288. syndrome de Duker-Weiss-Siber --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Duker-Weiss-Siber | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2289. syndrome de Feingold --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Feingold | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2290. syndrome de Gilles de la Tourette --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Gilles de la Tourette | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2291. syndrome de Leriche --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Leriche | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2292. syndrome de Mayer-Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Mayer-Rokitansky-Küster-Hauser | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2293. syndrome de Nathalie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Nathalie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2294. syndrome de Rathbun --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Rathbun | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2295. syndrome de Rokitansky --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Rokitansky | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2296. syndrome de Rokitansky-Küster-Hauser --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Rokitansky-Küster-Hauser | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2297. syndrome de Stein-Leventhal-Cohen --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Stein-Leventhal-Cohen | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2298. syndrome de Stevens-Johnson --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Stevens-Johnson | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2299. syndrome de Townes-Brocks --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Townes-Brocks | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2300. syndrome de Treft-Sanborn-Carey --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Treft-Sanborn-Carey | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2301. syndrome de de Morsier --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de de Morsier | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2302. syndrome de la Tourette --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de la Tourette | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2303. syndrome de sheehan --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de sheehan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2304. syndrome de stress respiratoire de l'adulte --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de stress respiratoire de l'adulte | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2305. syndrome de tourette --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de tourette | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2306. syndrome de warburg --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de warburg | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2307. syndrome de zellweger --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de zellweger | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2308. syndrome des pouces en adduction-arthrogrypose (type Dundar) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome des pouces en adduction-arthrogrypose (type Dundar) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2309. syndrome des tics de Gilles de la Tourette --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome des tics de Gilles de la Tourette | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2310. syndrome du p(17)p11.2p11.2 --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome du p(17)p11.2p11.2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2311. syndrome malin d'un neuroleptique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome malin d'un neuroleptique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2312. syndrome malin de neuroleptiques --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome malin de neuroleptiques | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2313. syndrome malin des neuroleptiques --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=syndrome malin des neuroleptiques | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2314. sélacien venimeux --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=sélacien venimeux | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2315. toxémie --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=toxémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2316. triphosphopyridine-nucléotide --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=triphosphopyridine-nucléotide | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2317. trisomie 9p --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=trisomie 9p | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2318. trouble de gilles de la tourette --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=trouble de gilles de la tourette | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2319. varicelle (complications neurologiques de la) --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=varicelle (complications neurologiques de la) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2320. xanthomatose familiale primitive --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=xanthomatose familiale primitive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2321. état de mal épileptique --- r_associated #0: 10 --> en:pseudotrisomy 13 syndrome
    n1=état de mal épileptique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=10
  2322. dysencéphalie splanchnokystique --- r_associated #0: 6 --> en:pseudotrisomy 13 syndrome
    n1=dysencéphalie splanchnokystique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=6
  2323. trisomie 13 --- r_associated #0: 6 --> en:pseudotrisomy 13 syndrome
    n1=trisomie 13 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=6
  2324. trisomie 18 --- r_associated #0: 6 --> en:pseudotrisomy 13 syndrome
    n1=trisomie 18 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=6
  2325. Acinetobacter --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Acinetobacter | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2326. Adair-Dighton (syndrome d') --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Adair-Dighton (syndrome d') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2327. Anasarque --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Anasarque | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2328. Dumoulin (classification de) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Dumoulin (classification de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2329. Exomphale --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Exomphale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2330. Hypotonique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Hypotonique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2331. Korsakoff (syndrome de) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Korsakoff (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2332. Maladie du cri du chat --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Maladie du cri du chat | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2333. Neurocysticercose --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Neurocysticercose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2334. Neuropathie optique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Neuropathie optique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2335. Onsager (relation d') --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Onsager (relation d') | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2336. Perthes (maladie de) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Perthes (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2337. Peste Noire --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Peste Noire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2338. Syndrome d'Immunodéficience Acquise --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Syndrome d'Immunodéficience Acquise | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2339. Tay-Sachs (maladie de) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Tay-Sachs (maladie de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2340. Williams (syndrome de) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=Williams (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2341. abêtalipoprotéinémie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=abêtalipoprotéinémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2342. acidurie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=acidurie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2343. acidurie 3-hydroxy-3-méthyl-glutarique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=acidurie 3-hydroxy-3-méthyl-glutarique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2344. acidurie 3-méthylglutaconique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=acidurie 3-méthylglutaconique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2345. acidurie 4-hydroxybutyrique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=acidurie 4-hydroxybutyrique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2346. acidurie paradoxale --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=acidurie paradoxale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2347. acineux --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=acineux | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2348. acini --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=acini | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2349. acinus --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=acinus | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2350. acinus hépatique de Rappaport --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=acinus hépatique de Rappaport | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2351. agglutinines irrégulières --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=agglutinines irrégulières | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2352. agglutinogène --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=agglutinogène | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2353. agitation postopératoire --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=agitation postopératoire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2354. aglossie et adactylie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=aglossie et adactylie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2355. aglycone --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=aglycone | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2356. agnosie chromatique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=agnosie chromatique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2357. agnosie d'extensité --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=agnosie d'extensité | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2358. agnosie d'intensité --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=agnosie d'intensité | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2359. agnosie des couleurs --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=agnosie des couleurs | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2360. albinisme avec immunodéficience et troubles hématologiques --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2361. albinisme avec surdité --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=albinisme avec surdité | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2362. amnésie globale transitoire --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=amnésie globale transitoire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2363. anomalie congénitale --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=anomalie congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2364. atrophie congénitale de la thyroïde --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=atrophie congénitale de la thyroïde | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2365. cri du chat (maladie du) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=cri du chat (maladie du) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2366. crétinismes --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=crétinismes | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2367. disomie uniparentale --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=disomie uniparentale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2368. duodénectomie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=duodénectomie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2369. duodénite --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=duodénite | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2370. dysembryome cutané --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysembryome cutané | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2371. dysembryome de l'ovaire --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysembryome de l'ovaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2372. dysembryome testiculaire --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysembryome testiculaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2373. dysembryoplasie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysembryoplasie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2374. dysembryoplasie neuro-épithéliale --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysembryoplasie neuro-épithéliale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2375. dysenterie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysenterie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2376. dysenterie amibienne --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysenterie amibienne | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2377. dysentériforme --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysentériforme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2378. dysentérique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysentérique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2379. dysérythropoïèse --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=dysérythropoïèse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2380. démence d'Alzheimer --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=démence d'Alzheimer | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2381. en:Neuroleptic malignant syndrome --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=en:Neuroleptic malignant syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2382. en:PFIC11 --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=en:PFIC11 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2383. en:Sachs' disease --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=en:Sachs' disease | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2384. en:Seckel syndrome --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=en:Seckel syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2385. en:cat's cry syndrome --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=en:cat's cry syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2386. en:congenital anomaly --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital anomaly | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2387. en:congenital goiter --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=en:congenital goiter | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2388. faisceau de His --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=faisceau de His | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2389. fibrose systémique néphrogénique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=fibrose systémique néphrogénique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2390. fuchsine --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=fuchsine | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2391. fucose --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=fucose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2392. fucosidase --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=fucosidase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2393. fucoside --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=fucoside | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2394. goitre congénital --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=goitre congénital | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2395. histaminergie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histaminergie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2396. histaminergique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histaminergique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2397. histaminique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histaminique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2398. histaminolibération --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histaminolibération | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2399. histaminolytique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histaminolytique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2400. histaminopexie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histaminopexie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2401. histaminurie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histaminurie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2402. histaminémie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histaminémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2403. histidase --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histidase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2404. histidinase --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histidinase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2405. histidine --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histidine | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2406. histidine-ammoniac-lyase --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histidine-ammoniac-lyase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2407. histidine-décarboxylase --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histidine-décarboxylase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2408. histidine-désaminase --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=histidine-désaminase | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2409. hydrocèle de la femme --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hydrocèle de la femme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2410. hydrocèle de la vaginale --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hydrocèle de la vaginale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2411. hydrocèle du canal de Nück --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hydrocèle du canal de Nück | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2412. hydrocèle du cou --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hydrocèle du cou | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2413. hyperostose vertébrale ankylosante --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hyperostose vertébrale ankylosante | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2414. hyperoxalurie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hyperoxalurie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2415. hyperoxalémie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hyperoxalémie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2416. hypothyroïdisme congénital --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hypothyroïdisme congénital | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2417. hypoxanthine-guanine-phosphoribosyl-transferase (déficit en) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hypoxanthine-guanine-phosphoribosyl-transferase (déficit en) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2418. hémochromatose --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=hémochromatose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2419. ichtyophtalmie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=ichtyophtalmie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2420. ichtyosarcotoxisme --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=ichtyosarcotoxisme | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2421. infantilisme type brissaud --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=infantilisme type brissaud | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2422. insectes (allergie aux) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=insectes (allergie aux) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2423. malabsorption (syndrome de) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=malabsorption (syndrome de) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2424. maladie de Duhring-Brocq --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=maladie de Duhring-Brocq | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2425. malformation congénitale --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=malformation congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2426. myopathie primitive progressive --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=myopathie primitive progressive | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2427. mésentérite rétractile --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=mésentérite rétractile | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2428. mésentérite sclérosante --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=mésentérite sclérosante | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2429. nanisme hypothyroïdien --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=nanisme hypothyroïdien | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2430. neurinome bilatéral du nerf cochléaire (VIII) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=neurinome bilatéral du nerf cochléaire (VIII) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2431. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=nystagmus (zone de moindre) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2432. onychodysplasie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=onychodysplasie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2433. onychogryphose --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=onychogryphose | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2434. onycholyse --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=onycholyse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2435. onycholyse candidosique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=onycholyse candidosique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2436. onycholyse semi-lunaire partielle --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=onycholyse semi-lunaire partielle | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2437. onychomadèse --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=onychomadèse | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2438. onychomatricome --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=onychomatricome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2439. opération de Dunn --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=opération de Dunn | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2440. osteopoecilie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=osteopoecilie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2441. paragnathe --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=paragnathe | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2442. pemphigoïde muqueux bénin --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=pemphigoïde muqueux bénin | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2443. porphyrie aigüe intermittente --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=porphyrie aigüe intermittente | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2444. porphyrie cutanée --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=porphyrie cutanée | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2445. porphyrie de Doss --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=porphyrie de Doss | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2446. ptose splénique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=ptose splénique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2447. rate ectopique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=rate ectopique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2448. rate errante --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=rate errante | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2449. sars --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=sars | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2450. semidominance --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=semidominance | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2451. semiquinone --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=semiquinone | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2452. syndrome d'Ehlers-Danlos --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome d'Ehlers-Danlos | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2453. syndrome d'insuffisance thyroïdienne congénitale --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome d'insuffisance thyroïdienne congénitale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2454. syndrome de Dunnigan --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Dunnigan | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2455. syndrome de Fuchs --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Fuchs | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2456. syndrome de Kallmann --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Kallmann | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2457. syndrome de Kaposi-Juliusberg --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Kaposi-Juliusberg | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2458. syndrome de Kearns-Sayre --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Kearns-Sayre | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2459. syndrome de Kleine-Levin --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Kleine-Levin | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2460. syndrome de Klüver-Bucy --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Klüver-Bucy | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2461. syndrome de Reye --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Reye | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2462. syndrome de Stickler --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Stickler | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2463. syndrome de Waterhouse-Friderichsen --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Waterhouse-Friderichsen | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2464. syndrome de Wolff-Parkinson-White --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de Wolff-Parkinson-White | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2465. syndrome de fiessinger-leroy-reiter --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de fiessinger-leroy-reiter | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2466. syndrome de l'angle pontocérébelleux --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de l'angle pontocérébelleux | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2467. syndrome de l'apex orbitaire --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de l'apex orbitaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2468. syndrome de l'apophyse styloïde longue --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de l'apophyse styloïde longue | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2469. syndrome de reiter --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de reiter | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2470. syndrome de syndrome de Joubert-Boltshauser --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome de syndrome de Joubert-Boltshauser | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2471. syndrome olfacto-génital --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndrome olfacto-génital | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2472. syndromes du gène 1 de la tumeur de Wilms --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=syndromes du gène 1 de la tumeur de Wilms | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2473. séminal --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=séminal | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2474. séminifère --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=séminifère | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2475. séminomateux --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=séminomateux | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2476. séminome --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=séminome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2477. séminome de l'ovaire --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=séminome de l'ovaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2478. séminome du médiastin --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=séminome du médiastin | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2479. séminome spermatocytaire --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=séminome spermatocytaire | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2480. sémiochimique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=sémiochimique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2481. sémiologie extrapyramidale --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=sémiologie extrapyramidale | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2482. triplet (CGG) n --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=triplet (CGG) n | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2483. trisomie 17p11.2 --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=trisomie 17p11.2 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2484. trisomie 8 --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=trisomie 8 | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2485. xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthoastrocytome pléomorphe | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2486. xanthochromie --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthochromie | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2487. xanthochromie caroténique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthochromie caroténique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2488. xanthoerythrodermia perstans --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthoerythrodermia perstans | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2489. xanthogranulome juvénile --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthogranulome juvénile | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2490. xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthogranulome nécrobiotique | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2491. xanthogranulome palpébral --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthogranulome palpébral | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2492. xanthohistiocytome --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthohistiocytome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2493. xanthoma disseminatum --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthoma disseminatum | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=5
  2494. xanthomatose --- r_associated #0: 5 --> en:pseudotrisomy 13 syndrome
    n1=xanthomatose | n2=en:pseudotrisomy 13 syndrome | 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