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'en:genetic diseases, x-linked'
(id=6818700 ; fe=en:genetic diseases, x-linked ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=19812 creation date=2017-06-25 touchdate=2025-08-27 16:38:57.000)
≈ 389 relations sortantes

  1. en:genetic diseases, x-linked -- r_associated #0: 43 / 1 -> en:hydrocephalus with cerebellar agenesis
    n1=en:genetic diseases, x-linked | n2=en:hydrocephalus with cerebellar agenesis | rel=r_associated | relid=0 | w=43
  2. en:genetic diseases, x-linked -- r_associated #0: 42 / 0.977 -> en:ataxia telangiectasia syndrome
    n1=en:genetic diseases, x-linked | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=42
  3. en:genetic diseases, x-linked -- r_associated #0: 42 / 0.977 -> en:fragile x syndrome
    n1=en:genetic diseases, x-linked | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=42
  4. en:genetic diseases, x-linked -- r_associated #0: 42 / 0.977 -> en:nasodigitoacoustic syndrome
    n1=en:genetic diseases, x-linked | n2=en:nasodigitoacoustic syndrome | rel=r_associated | relid=0 | w=42
  5. en:genetic diseases, x-linked -- r_associated #0: 42 / 0.977 -> en:osteogenesis imperfecta
    n1=en:genetic diseases, x-linked | n2=en:osteogenesis imperfecta | rel=r_associated | relid=0 | w=42
  6. en:genetic diseases, x-linked -- r_associated #0: 41 / 0.953 -> en:adrenal hypoplasia, congenital, with precocious puberty
    n1=en:genetic diseases, x-linked | n2=en:adrenal hypoplasia, congenital, with precocious puberty | rel=r_associated | relid=0 | w=41
  7. en:genetic diseases, x-linked -- r_associated #0: 41 / 0.953 -> en:cherubism
    n1=en:genetic diseases, x-linked | n2=en:cherubism | rel=r_associated | relid=0 | w=41
  8. en:genetic diseases, x-linked -- r_associated #0: 41 / 0.953 -> en:ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema
    n1=en:genetic diseases, x-linked | n2=en:ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema | rel=r_associated | relid=0 | w=41
  9. en:genetic diseases, x-linked -- r_associated #0: 41 / 0.953 -> en:mental retardation, skeletal dysplasia, and abducens palsy
    n1=en:genetic diseases, x-linked | n2=en:mental retardation, skeletal dysplasia, and abducens palsy | rel=r_associated | relid=0 | w=41
  10. en:genetic diseases, x-linked -- r_associated #0: 41 / 0.953 -> en:microphthalmia, isolated, with coloboma 1
    n1=en:genetic diseases, x-linked | n2=en:microphthalmia, isolated, with coloboma 1 | rel=r_associated | relid=0 | w=41
  11. en:genetic diseases, x-linked -- r_associated #0: 41 / 0.953 -> en:ovarian dysgenesis 2
    n1=en:genetic diseases, x-linked | n2=en:ovarian dysgenesis 2 | rel=r_associated | relid=0 | w=41
  12. en:genetic diseases, x-linked -- r_associated #0: 40 / 0.93 -> en:alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
    n1=en:genetic diseases, x-linked | n2=en:alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis | rel=r_associated | relid=0 | w=40
  13. en:genetic diseases, x-linked -- r_associated #0: 40 / 0.93 -> en:coxoauricular syndrome
    n1=en:genetic diseases, x-linked | n2=en:coxoauricular syndrome | rel=r_associated | relid=0 | w=40
  14. en:genetic diseases, x-linked -- r_associated #0: 40 / 0.93 -> en:ehlers-danlos syndrome type 5
    n1=en:genetic diseases, x-linked | n2=en:ehlers-danlos syndrome type 5 | rel=r_associated | relid=0 | w=40
  15. en:genetic diseases, x-linked -- r_associated #0: 40 / 0.93 -> en:microcephaly microcornea syndrome seemanova type
    n1=en:genetic diseases, x-linked | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=40
  16. en:genetic diseases, x-linked -- r_associated #0: 40 / 0.93 -> en:protoporphyria, erythropoietic, x-linked dominant
    n1=en:genetic diseases, x-linked | n2=en:protoporphyria, erythropoietic, x-linked dominant | rel=r_associated | relid=0 | w=40
  17. en:genetic diseases, x-linked -- r_associated #0: 39 / 0.907 -> en:epidemiologic
    n1=en:genetic diseases, x-linked | n2=en:epidemiologic | rel=r_associated | relid=0 | w=39
  18. en:genetic diseases, x-linked -- r_associated #0: 39 / 0.907 -> en:thrombocytopenia, x-linked, intermittent
    n1=en:genetic diseases, x-linked | n2=en:thrombocytopenia, x-linked, intermittent | rel=r_associated | relid=0 | w=39
  19. en:genetic diseases, x-linked -- r_associated #0: 38 / 0.884 -> en:congenital keratoglobus
    n1=en:genetic diseases, x-linked | n2=en:congenital keratoglobus | rel=r_associated | relid=0 | w=38
  20. en:genetic diseases, x-linked -- r_associated #0: 38 / 0.884 -> en:mental retardation, x-linked
    n1=en:genetic diseases, x-linked | n2=en:mental retardation, x-linked | rel=r_associated | relid=0 | w=38
  21. en:genetic diseases, x-linked -- r_associated #0: 38 / 0.884 -> en:spastic paraplegia 16, x-linked (disorder)
    n1=en:genetic diseases, x-linked | n2=en:spastic paraplegia 16, x-linked (disorder) | rel=r_associated | relid=0 | w=38
  22. en:genetic diseases, x-linked -- r_associated #0: 37 / 0.86 -> en:angioma serpiginosum
    n1=en:genetic diseases, x-linked | n2=en:angioma serpiginosum | rel=r_associated | relid=0 | w=37
  23. en:genetic diseases, x-linked -- r_associated #0: 37 / 0.86 -> en:arthrogryposis multiplex congenita, distal, x-linked
    n1=en:genetic diseases, x-linked | n2=en:arthrogryposis multiplex congenita, distal, x-linked | rel=r_associated | relid=0 | w=37
  24. en:genetic diseases, x-linked -- r_associated #0: 37 / 0.86 -> en:deafness, x-linked 3
    n1=en:genetic diseases, x-linked | n2=en:deafness, x-linked 3 | rel=r_associated | relid=0 | w=37
  25. en:genetic diseases, x-linked -- r_associated #0: 37 / 0.86 -> en:embryologic
    n1=en:genetic diseases, x-linked | n2=en:embryologic | rel=r_associated | relid=0 | w=37
  26. en:genetic diseases, x-linked -- r_associated #0: 37 / 0.86 -> en:fetal akinesia syndrome, x-linked
    n1=en:genetic diseases, x-linked | n2=en:fetal akinesia syndrome, x-linked | rel=r_associated | relid=0 | w=37
  27. en:genetic diseases, x-linked -- r_associated #0: 37 / 0.86 -> en:physiopathological
    n1=en:genetic diseases, x-linked | n2=en:physiopathological | rel=r_associated | relid=0 | w=37
  28. en:genetic diseases, x-linked -- r_associated #0: 37 / 0.86 -> en:sketetal dysplasia coarse facies mental retardation
    n1=en:genetic diseases, x-linked | n2=en:sketetal dysplasia coarse facies mental retardation | rel=r_associated | relid=0 | w=37
  29. en:genetic diseases, x-linked -- r_associated #0: 37 / 0.86 -> en:skin diseases, genetic
    n1=en:genetic diseases, x-linked | n2=en:skin diseases, genetic | rel=r_associated | relid=0 | w=37
  30. en:genetic diseases, x-linked -- r_associated #0: 37 / 0.86 -> en:spinocerebellar ataxia, x-linked 3
    n1=en:genetic diseases, x-linked | n2=en:spinocerebellar ataxia, x-linked 3 | rel=r_associated | relid=0 | w=37
  31. en:genetic diseases, x-linked -- r_associated #0: 36 / 0.837 -> en:alpha-1 antitrypsin deficiency
    n1=en:genetic diseases, x-linked | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=36
  32. en:genetic diseases, x-linked -- r_associated #0: 36 / 0.837 -> en:myopathy, reducing body, x-linked, early-onset, severe
    n1=en:genetic diseases, x-linked | n2=en:myopathy, reducing body, x-linked, early-onset, severe | rel=r_associated | relid=0 | w=36
  33. en:genetic diseases, x-linked -- r_associated #0: 36 / 0.837 -> en:panhypopituitarism - x-linked
    n1=en:genetic diseases, x-linked | n2=en:panhypopituitarism - x-linked | rel=r_associated | relid=0 | w=36
  34. en:genetic diseases, x-linked -- r_associated #0: 36 / 0.837 -> en:reticuloendothelial hyperplasia
    n1=en:genetic diseases, x-linked | n2=en:reticuloendothelial hyperplasia | rel=r_associated | relid=0 | w=36
  35. en:genetic diseases, x-linked -- r_associated #0: 36 / 0.837 -> en:thrombocytopenia 1 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:thrombocytopenia 1 (disorder) | rel=r_associated | relid=0 | w=36
  36. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:aicardi syndrome
    n1=en:genetic diseases, x-linked | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=35
  37. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:anemia, sideroblastic, and spinocerebellar ataxia
    n1=en:genetic diseases, x-linked | n2=en:anemia, sideroblastic, and spinocerebellar ataxia | rel=r_associated | relid=0 | w=35
  38. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:anhidrotic ectodermal dysplasia 1
    n1=en:genetic diseases, x-linked | n2=en:anhidrotic ectodermal dysplasia 1 | rel=r_associated | relid=0 | w=35
  39. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:aspects of radionuclide imaging
    n1=en:genetic diseases, x-linked | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=35
  40. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:camurati-engelmann syndrome
    n1=en:genetic diseases, x-linked | n2=en:camurati-engelmann syndrome | rel=r_associated | relid=0 | w=35
  41. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:cone-rod dystrophy, x-linked, 2
    n1=en:genetic diseases, x-linked | n2=en:cone-rod dystrophy, x-linked, 2 | rel=r_associated | relid=0 | w=35
  42. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:deafness, x-linked 4 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:deafness, x-linked 4 (disorder) | rel=r_associated | relid=0 | w=35
  43. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:exposure as collected domain
    n1=en:genetic diseases, x-linked | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=35
  44. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:glycogen storage disease type ixd
    n1=en:genetic diseases, x-linked | n2=en:glycogen storage disease type ixd | rel=r_associated | relid=0 | w=35
  45. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:hereditary autoinflammatory diseases
    n1=en:genetic diseases, x-linked | n2=en:hereditary autoinflammatory diseases | rel=r_associated | relid=0 | w=35
  46. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:hereditary hemolytic anemia
    n1=en:genetic diseases, x-linked | n2=en:hereditary hemolytic anemia | rel=r_associated | relid=0 | w=35
  47. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:hereditary neoplastic syndrome
    n1=en:genetic diseases, x-linked | n2=en:hereditary neoplastic syndrome | rel=r_associated | relid=0 | w=35
  48. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:heterotaxy, visceral, 1, x-linked
    n1=en:genetic diseases, x-linked | n2=en:heterotaxy, visceral, 1, x-linked | rel=r_associated | relid=0 | w=35
  49. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:insulin-dependent diabetes mellitus secretory diarrhea syndrome
    n1=en:genetic diseases, x-linked | n2=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | rel=r_associated | relid=0 | w=35
  50. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:juvenile x-linked retinoschisis
    n1=en:genetic diseases, x-linked | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=35
  51. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:loeys-dietz syndrome
    n1=en:genetic diseases, x-linked | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=35
  52. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:martin-probst deafness-mental retardation syndrome
    n1=en:genetic diseases, x-linked | n2=en:martin-probst deafness-mental retardation syndrome | rel=r_associated | relid=0 | w=35
  53. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:nance-horan syndrome
    n1=en:genetic diseases, x-linked | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=35
  54. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:nemo mutation with immunodeficiency
    n1=en:genetic diseases, x-linked | n2=en:nemo mutation with immunodeficiency | rel=r_associated | relid=0 | w=35
  55. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:nutritional management
    n1=en:genetic diseases, x-linked | n2=en:nutritional management | rel=r_associated | relid=0 | w=35
  56. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:nystagmus 5, infantile periodic alternating
    n1=en:genetic diseases, x-linked | n2=en:nystagmus 5, infantile periodic alternating | rel=r_associated | relid=0 | w=35
  57. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:oculocerebrorenal syndrome
    n1=en:genetic diseases, x-linked | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=35
  58. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:prostate cancer, hereditary, x-linked 2
    n1=en:genetic diseases, x-linked | n2=en:prostate cancer, hereditary, x-linked 2 | rel=r_associated | relid=0 | w=35
  59. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:psychology qualifier
    n1=en:genetic diseases, x-linked | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=35
  60. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:radial ray deficiency, x-linked
    n1=en:genetic diseases, x-linked | n2=en:radial ray deficiency, x-linked | rel=r_associated | relid=0 | w=35
  61. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:sex chromosome aberrations
    n1=en:genetic diseases, x-linked | n2=en:sex chromosome aberrations | rel=r_associated | relid=0 | w=35
  62. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:surfactant metabolism dysfunction, pulmonary, 4
    n1=en:genetic diseases, x-linked | n2=en:surfactant metabolism dysfunction, pulmonary, 4 | rel=r_associated | relid=0 | w=35
  63. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:testicular germ cell tumor 1
    n1=en:genetic diseases, x-linked | n2=en:testicular germ cell tumor 1 | rel=r_associated | relid=0 | w=35
  64. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:thrombophilia, x-linked, due to factor ix defect
    n1=en:genetic diseases, x-linked | n2=en:thrombophilia, x-linked, due to factor ix defect | rel=r_associated | relid=0 | w=35
  65. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:thyroxine-binding globulin deficiency
    n1=en:genetic diseases, x-linked | n2=en:thyroxine-binding globulin deficiency | rel=r_associated | relid=0 | w=35
  66. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:torticollis, keloids, cryptorchidism, and renal dysplasia (disorder)
    n1=en:genetic diseases, x-linked | n2=en:torticollis, keloids, cryptorchidism, and renal dysplasia (disorder) | rel=r_associated | relid=0 | w=35
  67. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:veterinary aspects
    n1=en:genetic diseases, x-linked | n2=en:veterinary aspects | rel=r_associated | relid=0 | w=35
  68. en:genetic diseases, x-linked -- r_associated #0: 35 / 0.814 -> en:x-linked agammaglobulinemia with growth hormone deficiency
    n1=en:genetic diseases, x-linked | n2=en:x-linked agammaglobulinemia with growth hormone deficiency | rel=r_associated | relid=0 | w=35
  69. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:agammaglobulinemia, x-linked, type 2 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:agammaglobulinemia, x-linked, type 2 (disorder) | rel=r_associated | relid=0 | w=34
  70. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:alagille syndrome
    n1=en:genetic diseases, x-linked | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=34
  71. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:androgen insensitivity syndrome
    n1=en:genetic diseases, x-linked | n2=en:androgen insensitivity syndrome | rel=r_associated | relid=0 | w=34
  72. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:aneurysm, intracranial berry, 5
    n1=en:genetic diseases, x-linked | n2=en:aneurysm, intracranial berry, 5 | rel=r_associated | relid=0 | w=34
  73. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:brunner syndrome
    n1=en:genetic diseases, x-linked | n2=en:brunner syndrome | rel=r_associated | relid=0 | w=34
  74. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:chondrodysplasia punctata, x-linked dominant type
    n1=en:genetic diseases, x-linked | n2=en:chondrodysplasia punctata, x-linked dominant type | rel=r_associated | relid=0 | w=34
  75. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:chromosome xq28 duplication syndrome
    n1=en:genetic diseases, x-linked | n2=en:chromosome xq28 duplication syndrome | rel=r_associated | relid=0 | w=34
  76. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:congenital adrenal hyperplasia
    n1=en:genetic diseases, x-linked | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=34
  77. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:congenital myasthenic syndrome
    n1=en:genetic diseases, x-linked | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=34
  78. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:dyskeratosis congenita
    n1=en:genetic diseases, x-linked | n2=en:dyskeratosis congenita | rel=r_associated | relid=0 | w=34
  79. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:epidermodysplasia verruciformis, x-linked
    n1=en:genetic diseases, x-linked | n2=en:epidermodysplasia verruciformis, x-linked | rel=r_associated | relid=0 | w=34
  80. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:genes, x-linked
    n1=en:genetic diseases, x-linked | n2=en:genes, x-linked | rel=r_associated | relid=0 | w=34
  81. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:glycogen storage disease type viii
    n1=en:genetic diseases, x-linked | n2=en:glycogen storage disease type viii | rel=r_associated | relid=0 | w=34
  82. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:hypoparathyroidism - x-linked
    n1=en:genetic diseases, x-linked | n2=en:hypoparathyroidism - x-linked | rel=r_associated | relid=0 | w=34
  83. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:in blood
    n1=en:genetic diseases, x-linked | n2=en:in blood | rel=r_associated | relid=0 | w=34
  84. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:keratosis follicularis spinulosa decalvans, x-linked
    n1=en:genetic diseases, x-linked | n2=en:keratosis follicularis spinulosa decalvans, x-linked | rel=r_associated | relid=0 | w=34
  85. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:leukoencephalopathy with metaphyseal chondrodysplasia
    n1=en:genetic diseases, x-linked | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia | rel=r_associated | relid=0 | w=34
  86. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:mental retardation, x-linked, syndromic, christianson type
    n1=en:genetic diseases, x-linked | n2=en:mental retardation, x-linked, syndromic, christianson type | rel=r_associated | relid=0 | w=34
  87. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:mental retardation, x-linked, syndromic, turner type
    n1=en:genetic diseases, x-linked | n2=en:mental retardation, x-linked, syndromic, turner type | rel=r_associated | relid=0 | w=34
  88. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:microbiological
    n1=en:genetic diseases, x-linked | n2=en:microbiological | rel=r_associated | relid=0 | w=34
  89. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:muscular dystrophy
    n1=en:genetic diseases, x-linked | n2=en:muscular dystrophy | rel=r_associated | relid=0 | w=34
  90. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:night blindness, congenital stationary
    n1=en:genetic diseases, x-linked | n2=en:night blindness, congenital stationary | rel=r_associated | relid=0 | w=34
  91. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:ornithine carbamoyltransferase deficiency disease
    n1=en:genetic diseases, x-linked | n2=en:ornithine carbamoyltransferase deficiency disease | rel=r_associated | relid=0 | w=34
  92. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:parasitology
    n1=en:genetic diseases, x-linked | n2=en:parasitology | rel=r_associated | relid=0 | w=34
  93. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:parkinson disease 12
    n1=en:genetic diseases, x-linked | n2=en:parkinson disease 12 | rel=r_associated | relid=0 | w=34
  94. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:pelger-huet anomaly
    n1=en:genetic diseases, x-linked | n2=en:pelger-huet anomaly | rel=r_associated | relid=0 | w=34
  95. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:radiotherapeutic
    n1=en:genetic diseases, x-linked | n2=en:radiotherapeutic | rel=r_associated | relid=0 | w=34
  96. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:rehabilitation aspects
    n1=en:genetic diseases, x-linked | n2=en:rehabilitation aspects | rel=r_associated | relid=0 | w=34
  97. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:rolandic epilepsy, mental retardation, and speech dyspraxia, x-linked
    n1=en:genetic diseases, x-linked | n2=en:rolandic epilepsy, mental retardation, and speech dyspraxia, x-linked | rel=r_associated | relid=0 | w=34
  98. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:simpson-golabi-behmel syndrome, type 2 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:simpson-golabi-behmel syndrome, type 2 (disorder) | rel=r_associated | relid=0 | w=34
  99. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:spastic paraplegia 2, x-linked (disorder)
    n1=en:genetic diseases, x-linked | n2=en:spastic paraplegia 2, x-linked (disorder) | rel=r_associated | relid=0 | w=34
  100. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:taxonomic
    n1=en:genetic diseases, x-linked | n2=en:taxonomic | rel=r_associated | relid=0 | w=34
  101. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:x-linked hypogammaglobulinemia
    n1=en:genetic diseases, x-linked | n2=en:x-linked hypogammaglobulinemia | rel=r_associated | relid=0 | w=34
  102. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> en:xiap deficiency
    n1=en:genetic diseases, x-linked | n2=en:xiap deficiency | rel=r_associated | relid=0 | w=34
  103. en:genetic diseases, x-linked -- r_associated #0: 34 / 0.791 -> maladies liées à l'x
    n1=en:genetic diseases, x-linked | n2=maladies liées à l'x | rel=r_associated | relid=0 | w=34
  104. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:anemia, x-linked, without thrombocytopenia
    n1=en:genetic diseases, x-linked | n2=en:anemia, x-linked, without thrombocytopenia | rel=r_associated | relid=0 | w=32
  105. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:barth syndrome
    n1=en:genetic diseases, x-linked | n2=en:barth syndrome | rel=r_associated | relid=0 | w=32
  106. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:cadasil syndrome
    n1=en:genetic diseases, x-linked | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=32
  107. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:cardiac valvular dysplasia, x-linked
    n1=en:genetic diseases, x-linked | n2=en:cardiac valvular dysplasia, x-linked | rel=r_associated | relid=0 | w=32
  108. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:cataract, congenital, with microcornea or slight microphthalmia
    n1=en:genetic diseases, x-linked | n2=en:cataract, congenital, with microcornea or slight microphthalmia | rel=r_associated | relid=0 | w=32
  109. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:choroideremia
    n1=en:genetic diseases, x-linked | n2=en:choroideremia | rel=r_associated | relid=0 | w=32
  110. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:congenital hypoplastic anemia
    n1=en:genetic diseases, x-linked | n2=en:congenital hypoplastic anemia | rel=r_associated | relid=0 | w=32
  111. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:congenital pain insensitivity
    n1=en:genetic diseases, x-linked | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=32
  112. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:enzymology
    n1=en:genetic diseases, x-linked | n2=en:enzymology | rel=r_associated | relid=0 | w=32
  113. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:epilepsy, female-restricted, with mental retardation (disorder)
    n1=en:genetic diseases, x-linked | n2=en:epilepsy, female-restricted, with mental retardation (disorder) | rel=r_associated | relid=0 | w=32
  114. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:genetic diseases, inborn
    n1=en:genetic diseases, x-linked | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  115. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:historical aspects qualifier
    n1=en:genetic diseases, x-linked | n2=en:historical aspects qualifier | rel=r_associated | relid=0 | w=32
  116. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:hyperimmunoglobulin m syndrome
    n1=en:genetic diseases, x-linked | n2=en:hyperimmunoglobulin m syndrome | rel=r_associated | relid=0 | w=32
  117. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:hypertrichosis, congenital generalized
    n1=en:genetic diseases, x-linked | n2=en:hypertrichosis, congenital generalized | rel=r_associated | relid=0 | w=32
  118. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:immunodeficiency, x-linked, with deficiency of 115,000 dalton surface glycoprotein
    n1=en:genetic diseases, x-linked | n2=en:immunodeficiency, x-linked, with deficiency of 115,000 dalton surface glycoprotein | rel=r_associated | relid=0 | w=32
  119. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:liver glycogenosis, x-linked, type ii
    n1=en:genetic diseases, x-linked | n2=en:liver glycogenosis, x-linked, type ii | rel=r_associated | relid=0 | w=32
  120. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:mental retardation, x-linked, syndromic 12
    n1=en:genetic diseases, x-linked | n2=en:mental retardation, x-linked, syndromic 12 | rel=r_associated | relid=0 | w=32
  121. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:midline defects, x-linked
    n1=en:genetic diseases, x-linked | n2=en:midline defects, x-linked | rel=r_associated | relid=0 | w=32
  122. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:modifier, x-linked, for neurofunctional defects
    n1=en:genetic diseases, x-linked | n2=en:modifier, x-linked, for neurofunctional defects | rel=r_associated | relid=0 | w=32
  123. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:muscular dystrophy, progressive pectorodorsal
    n1=en:genetic diseases, x-linked | n2=en:muscular dystrophy, progressive pectorodorsal | rel=r_associated | relid=0 | w=32
  124. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:myopia 1, x-linked
    n1=en:genetic diseases, x-linked | n2=en:myopia 1, x-linked | rel=r_associated | relid=0 | w=32
  125. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:myopia 13
    n1=en:genetic diseases, x-linked | n2=en:myopia 13 | rel=r_associated | relid=0 | w=32
  126. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:neural tube defects x-linked
    n1=en:genetic diseases, x-linked | n2=en:neural tube defects x-linked | rel=r_associated | relid=0 | w=32
  127. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:neutropenia, severe congenital, x-linked
    n1=en:genetic diseases, x-linked | n2=en:neutropenia, severe congenital, x-linked | rel=r_associated | relid=0 | w=32
  128. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:optic atrophy 2 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:optic atrophy 2 (disorder) | rel=r_associated | relid=0 | w=32
  129. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:retinitis pigmentosa 34 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:retinitis pigmentosa 34 (disorder) | rel=r_associated | relid=0 | w=32
  130. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:spinal muscular atrophy, distal, x-linked 3
    n1=en:genetic diseases, x-linked | n2=en:spinal muscular atrophy, distal, x-linked 3 | rel=r_associated | relid=0 | w=32
  131. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia, x-linked 1
    n1=en:genetic diseases, x-linked | n2=en:spinocerebellar ataxia, x-linked 1 | rel=r_associated | relid=0 | w=32
  132. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis
    n1=en:genetic diseases, x-linked | n2=en:thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis | rel=r_associated | relid=0 | w=32
  133. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:wells jankovic syndrome
    n1=en:genetic diseases, x-linked | n2=en:wells jankovic syndrome | rel=r_associated | relid=0 | w=32
  134. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:x inactivation, familial skewed, 2
    n1=en:genetic diseases, x-linked | n2=en:x inactivation, familial skewed, 2 | rel=r_associated | relid=0 | w=32
  135. en:genetic diseases, x-linked -- r_associated #0: 32 / 0.744 -> en:yellow nail syndrome
    n1=en:genetic diseases, x-linked | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=32
  136. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:alpha-thalassemia myelodysplasia syndrome
    n1=en:genetic diseases, x-linked | n2=en:alpha-thalassemia myelodysplasia syndrome | rel=r_associated | relid=0 | w=31
  137. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:anencephaly and spina bifida x-linked
    n1=en:genetic diseases, x-linked | n2=en:anencephaly and spina bifida x-linked | rel=r_associated | relid=0 | w=31
  138. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:cardiomyopathy, dilated, 3a
    n1=en:genetic diseases, x-linked | n2=en:cardiomyopathy, dilated, 3a | rel=r_associated | relid=0 | w=31
  139. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:cleft palate with ankyloglossia
    n1=en:genetic diseases, x-linked | n2=en:cleft palate with ankyloglossia | rel=r_associated | relid=0 | w=31
  140. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:congenital heart defects, x-linked
    n1=en:genetic diseases, x-linked | n2=en:congenital heart defects, x-linked | rel=r_associated | relid=0 | w=31
  141. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:craniofacioskeletal syndrome
    n1=en:genetic diseases, x-linked | n2=en:craniofacioskeletal syndrome | rel=r_associated | relid=0 | w=31
  142. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:deafness, high-frequency sensorineural, x-linked
    n1=en:genetic diseases, x-linked | n2=en:deafness, high-frequency sensorineural, x-linked | rel=r_associated | relid=0 | w=31
  143. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:dyserythropoietic anemia with thrombocytopenia
    n1=en:genetic diseases, x-linked | n2=en:dyserythropoietic anemia with thrombocytopenia | rel=r_associated | relid=0 | w=31
  144. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:emery-dreifuss muscular dystrophy
    n1=en:genetic diseases, x-linked | n2=en:emery-dreifuss muscular dystrophy | rel=r_associated | relid=0 | w=31
  145. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:exudative vitreoretinopathy, familial, x-linked recessive
    n1=en:genetic diseases, x-linked | n2=en:exudative vitreoretinopathy, familial, x-linked recessive | rel=r_associated | relid=0 | w=31
  146. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:hereditary angioedema
    n1=en:genetic diseases, x-linked | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=31
  147. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:hereditary sideroblastic anemia
    n1=en:genetic diseases, x-linked | n2=en:hereditary sideroblastic anemia | rel=r_associated | relid=0 | w=31
  148. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:hypohidrotic ectodermal dysplasia with immune deficiency
    n1=en:genetic diseases, x-linked | n2=en:hypohidrotic ectodermal dysplasia with immune deficiency | rel=r_associated | relid=0 | w=31
  149. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:hypospadias 2, x-linked
    n1=en:genetic diseases, x-linked | n2=en:hypospadias 2, x-linked | rel=r_associated | relid=0 | w=31
  150. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:masa syndrome (disorder)
    n1=en:genetic diseases, x-linked | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=31
  151. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:mental retardation, x-linked, syndromic, zdhhc9-related
    n1=en:genetic diseases, x-linked | n2=en:mental retardation, x-linked, syndromic, zdhhc9-related | rel=r_associated | relid=0 | w=31
  152. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:neuropathy, hereditary sensory, x-linked
    n1=en:genetic diseases, x-linked | n2=en:neuropathy, hereditary sensory, x-linked | rel=r_associated | relid=0 | w=31
  153. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:orofaciodigital syndromes
    n1=en:genetic diseases, x-linked | n2=en:orofaciodigital syndromes | rel=r_associated | relid=0 | w=31
  154. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:phosphoglycerate kinase 1 deficiency
    n1=en:genetic diseases, x-linked | n2=en:phosphoglycerate kinase 1 deficiency | rel=r_associated | relid=0 | w=31
  155. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:properdin deficiency, x-linked
    n1=en:genetic diseases, x-linked | n2=en:properdin deficiency, x-linked | rel=r_associated | relid=0 | w=31
  156. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:proud syndrome
    n1=en:genetic diseases, x-linked | n2=en:proud syndrome | rel=r_associated | relid=0 | w=31
  157. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:retinitis pigmentosa 3
    n1=en:genetic diseases, x-linked | n2=en:retinitis pigmentosa 3 | rel=r_associated | relid=0 | w=31
  158. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness
    n1=en:genetic diseases, x-linked | n2=en:retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness | rel=r_associated | relid=0 | w=31
  159. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:short stature, idiopathic, x-linked
    n1=en:genetic diseases, x-linked | n2=en:short stature, idiopathic, x-linked | rel=r_associated | relid=0 | w=31
  160. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:spondyloepimetaphyseal dysplasia, x-linked
    n1=en:genetic diseases, x-linked | n2=en:spondyloepimetaphyseal dysplasia, x-linked | rel=r_associated | relid=0 | w=31
  161. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:thrombocytosis, familial x-linked
    n1=en:genetic diseases, x-linked | n2=en:thrombocytosis, familial x-linked | rel=r_associated | relid=0 | w=31
  162. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:tooth agenesis, selective, x-linked, 1
    n1=en:genetic diseases, x-linked | n2=en:tooth agenesis, selective, x-linked, 1 | rel=r_associated | relid=0 | w=31
  163. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:x-linked agammaglobulinemia
    n1=en:genetic diseases, x-linked | n2=en:x-linked agammaglobulinemia | rel=r_associated | relid=0 | w=31
  164. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:x-linked dystonia parkinsonism
    n1=en:genetic diseases, x-linked | n2=en:x-linked dystonia parkinsonism | rel=r_associated | relid=0 | w=31
  165. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:x-linked infantile nystagmus
    n1=en:genetic diseases, x-linked | n2=en:x-linked infantile nystagmus | rel=r_associated | relid=0 | w=31
  166. en:genetic diseases, x-linked -- r_associated #0: 31 / 0.721 -> en:x-linked recessive nephrolithiasis with renal failure
    n1=en:genetic diseases, x-linked | n2=en:x-linked recessive nephrolithiasis with renal failure | rel=r_associated | relid=0 | w=31
  167. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:alzheimer disease 16
    n1=en:genetic diseases, x-linked | n2=en:alzheimer disease 16 | rel=r_associated | relid=0 | w=30
  168. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:arthrogryposis, x-linked, type v
    n1=en:genetic diseases, x-linked | n2=en:arthrogryposis, x-linked, type v | rel=r_associated | relid=0 | w=30
  169. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:atypical mycobacteriosis, familial, x-linked 1 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:atypical mycobacteriosis, familial, x-linked 1 (disorder) | rel=r_associated | relid=0 | w=30
  170. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:atypical mycobacteriosis, familial, x-linked 2
    n1=en:genetic diseases, x-linked | n2=en:atypical mycobacteriosis, familial, x-linked 2 | rel=r_associated | relid=0 | w=30
  171. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:bornholm eye disease
    n1=en:genetic diseases, x-linked | n2=en:bornholm eye disease | rel=r_associated | relid=0 | w=30
  172. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:chromosome disorder
    n1=en:genetic diseases, x-linked | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=30
  173. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:cone-rod dystrophy, x-linked, 1
    n1=en:genetic diseases, x-linked | n2=en:cone-rod dystrophy, x-linked, 1 | rel=r_associated | relid=0 | w=30
  174. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:cone-rod dystrophy, x-linked, 3
    n1=en:genetic diseases, x-linked | n2=en:cone-rod dystrophy, x-linked, 3 | rel=r_associated | relid=0 | w=30
  175. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:ethnologic
    n1=en:genetic diseases, x-linked | n2=en:ethnologic | rel=r_associated | relid=0 | w=30
  176. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:eye diseases, hereditary
    n1=en:genetic diseases, x-linked | n2=en:eye diseases, hereditary | rel=r_associated | relid=0 | w=30
  177. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:hajdu-cheney syndrome
    n1=en:genetic diseases, x-linked | n2=en:hajdu-cheney syndrome | rel=r_associated | relid=0 | w=30
  178. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:hemophilia b
    n1=en:genetic diseases, x-linked | n2=en:hemophilia b | rel=r_associated | relid=0 | w=30
  179. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:heredodegenerative disorders, nervous system
    n1=en:genetic diseases, x-linked | n2=en:heredodegenerative disorders, nervous system | rel=r_associated | relid=0 | w=30
  180. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:hyperthyroxinemia, familial dysalbuminemic
    n1=en:genetic diseases, x-linked | n2=en:hyperthyroxinemia, familial dysalbuminemic | rel=r_associated | relid=0 | w=30
  181. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:hypospadias 1, x-linked
    n1=en:genetic diseases, x-linked | n2=en:hypospadias 1, x-linked | rel=r_associated | relid=0 | w=30
  182. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:joubert syndrome 10 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:joubert syndrome 10 (disorder) | rel=r_associated | relid=0 | w=30
  183. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:leigh syndrome, x-linked
    n1=en:genetic diseases, x-linked | n2=en:leigh syndrome, x-linked | rel=r_associated | relid=0 | w=30
  184. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:multiple pterygium syndrome, x-linked
    n1=en:genetic diseases, x-linked | n2=en:multiple pterygium syndrome, x-linked | rel=r_associated | relid=0 | w=30
  185. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:myopathy, reducing body, x-linked, childhood-onset
    n1=en:genetic diseases, x-linked | n2=en:myopathy, reducing body, x-linked, childhood-onset | rel=r_associated | relid=0 | w=30
  186. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:nephrogenic syndrome of inappropriate antidiuresis
    n1=en:genetic diseases, x-linked | n2=en:nephrogenic syndrome of inappropriate antidiuresis | rel=r_associated | relid=0 | w=30
  187. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:norrie syndrome
    n1=en:genetic diseases, x-linked | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=30
  188. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:ocular albinism, type ii
    n1=en:genetic diseases, x-linked | n2=en:ocular albinism, type ii | rel=r_associated | relid=0 | w=30
  189. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:pelizaeus-merzbacher disease
    n1=en:genetic diseases, x-linked | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=30
  190. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:pharmacotherapeutic
    n1=en:genetic diseases, x-linked | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=30
  191. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:premature ovarian failure 2a
    n1=en:genetic diseases, x-linked | n2=en:premature ovarian failure 2a | rel=r_associated | relid=0 | w=30
  192. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:properdin deficiency, type iii
    n1=en:genetic diseases, x-linked | n2=en:properdin deficiency, type iii | rel=r_associated | relid=0 | w=30
  193. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:use of ultrasonography
    n1=en:genetic diseases, x-linked | n2=en:use of ultrasonography | rel=r_associated | relid=0 | w=30
  194. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:viruses
    n1=en:genetic diseases, x-linked | n2=en:viruses | rel=r_associated | relid=0 | w=30
  195. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:werner syndrome
    n1=en:genetic diseases, x-linked | n2=en:werner syndrome | rel=r_associated | relid=0 | w=30
  196. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:wiskott-aldrich syndrome
    n1=en:genetic diseases, x-linked | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=30
  197. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:x-linked ichthyosis
    n1=en:genetic diseases, x-linked | n2=en:x-linked ichthyosis | rel=r_associated | relid=0 | w=30
  198. en:genetic diseases, x-linked -- r_associated #0: 30 / 0.698 -> en:x-linked severe combined immunodeficiency
    n1=en:genetic diseases, x-linked | n2=en:x-linked severe combined immunodeficiency | rel=r_associated | relid=0 | w=30
  199. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:angiokeratoma corporis diffusum
    n1=en:genetic diseases, x-linked | n2=en:angiokeratoma corporis diffusum | rel=r_associated | relid=0 | w=29
  200. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:aspects of mortality statistics
    n1=en:genetic diseases, x-linked | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=29
  201. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:blood coagulation disorders, inherited
    n1=en:genetic diseases, x-linked | n2=en:blood coagulation disorders, inherited | rel=r_associated | relid=0 | w=29
  202. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia
    n1=en:genetic diseases, x-linked | n2=en:brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia | rel=r_associated | relid=0 | w=29
  203. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:chemically induced
    n1=en:genetic diseases, x-linked | n2=en:chemically induced | rel=r_associated | relid=0 | w=29
  204. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:chromosome xp11.23-p11.22 duplication syndrome
    n1=en:genetic diseases, x-linked | n2=en:chromosome xp11.23-p11.22 duplication syndrome | rel=r_associated | relid=0 | w=29
  205. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:chromosomes, human, x
    n1=en:genetic diseases, x-linked | n2=en:chromosomes, human, x | rel=r_associated | relid=0 | w=29
  206. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:chronic granulomatous disease
    n1=en:genetic diseases, x-linked | n2=en:chronic granulomatous disease | rel=r_associated | relid=0 | w=29
  207. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:dent's disease
    n1=en:genetic diseases, x-linked | n2=en:dent's disease | rel=r_associated | relid=0 | w=29
  208. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:diagnosis aspect
    n1=en:genetic diseases, x-linked | n2=en:diagnosis aspect | rel=r_associated | relid=0 | w=29
  209. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:glycogen storage disease type iib
    n1=en:genetic diseases, x-linked | n2=en:glycogen storage disease type iib | rel=r_associated | relid=0 | w=29
  210. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:hereditary macular epidermolysis bullosa
    n1=en:genetic diseases, x-linked | n2=en:hereditary macular epidermolysis bullosa | rel=r_associated | relid=0 | w=29
  211. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:hydrocephalus, x-linked, with congenital idiopathic intestinal pseudoobstruction
    n1=en:genetic diseases, x-linked | n2=en:hydrocephalus, x-linked, with congenital idiopathic intestinal pseudoobstruction | rel=r_associated | relid=0 | w=29
  212. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:hyperekplexia and epilepsy
    n1=en:genetic diseases, x-linked | n2=en:hyperekplexia and epilepsy | rel=r_associated | relid=0 | w=29
  213. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:kartagener syndrome
    n1=en:genetic diseases, x-linked | n2=en:kartagener syndrome | rel=r_associated | relid=0 | w=29
  214. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:metabolic aspects
    n1=en:genetic diseases, x-linked | n2=en:metabolic aspects | rel=r_associated | relid=0 | w=29
  215. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:myopathy, x-linked, with excessive autophagy (disorder)
    n1=en:genetic diseases, x-linked | n2=en:myopathy, x-linked, with excessive autophagy (disorder) | rel=r_associated | relid=0 | w=29
  216. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:nail-patella syndrome
    n1=en:genetic diseases, x-linked | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=29
  217. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:nursing therapy
    n1=en:genetic diseases, x-linked | n2=en:nursing therapy | rel=r_associated | relid=0 | w=29
  218. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:ophthalmoplegia, external, and myopia (disorder)
    n1=en:genetic diseases, x-linked | n2=en:ophthalmoplegia, external, and myopia (disorder) | rel=r_associated | relid=0 | w=29
  219. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:pigmentary disorder, reticulate, with systemic manifestations
    n1=en:genetic diseases, x-linked | n2=en:pigmentary disorder, reticulate, with systemic manifestations | rel=r_associated | relid=0 | w=29
  220. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:radiation sensitivity of natural killer activity
    n1=en:genetic diseases, x-linked | n2=en:radiation sensitivity of natural killer activity | rel=r_associated | relid=0 | w=29
  221. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:retinitis pigmentosa 6 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:retinitis pigmentosa 6 (disorder) | rel=r_associated | relid=0 | w=29
  222. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:roentgenographic
    n1=en:genetic diseases, x-linked | n2=en:roentgenographic | rel=r_associated | relid=0 | w=29
  223. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:sex chromosome disorders of sex development
    n1=en:genetic diseases, x-linked | n2=en:sex chromosome disorders of sex development | rel=r_associated | relid=0 | w=29
  224. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:vacterl association with hydrocephalus
    n1=en:genetic diseases, x-linked | n2=en:vacterl association with hydrocephalus | rel=r_associated | relid=0 | w=29
  225. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:vesicoureteral reflux, x-linked
    n1=en:genetic diseases, x-linked | n2=en:vesicoureteral reflux, x-linked | rel=r_associated | relid=0 | w=29
  226. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:waisman syndrome
    n1=en:genetic diseases, x-linked | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=29
  227. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:x chromosome-linked pyridoxine refractory sideroblastic anemia
    n1=en:genetic diseases, x-linked | n2=en:x chromosome-linked pyridoxine refractory sideroblastic anemia | rel=r_associated | relid=0 | w=29
  228. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> en:x-linked hydrocephalus syndrome
    n1=en:genetic diseases, x-linked | n2=en:x-linked hydrocephalus syndrome | rel=r_associated | relid=0 | w=29
  229. en:genetic diseases, x-linked -- r_associated #0: 29 / 0.674 -> maladies génétiques liées au chromosome x
    n1=en:genetic diseases, x-linked | n2=maladies génétiques liées au chromosome x | rel=r_associated | relid=0 | w=29
  230. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:aarskog syndrome
    n1=en:genetic diseases, x-linked | n2=en:aarskog syndrome | rel=r_associated | relid=0 | w=28
  231. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:autosomal recessive polycystic kidney disease
    n1=en:genetic diseases, x-linked | n2=en:autosomal recessive polycystic kidney disease | rel=r_associated | relid=0 | w=28
  232. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:cleft palate, x-linked
    n1=en:genetic diseases, x-linked | n2=en:cleft palate, x-linked | rel=r_associated | relid=0 | w=28
  233. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:cone dystrophy, x-linked, 1
    n1=en:genetic diseases, x-linked | n2=en:cone dystrophy, x-linked, 1 | rel=r_associated | relid=0 | w=28
  234. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:cone dystrophy, x-linked, with tapetal-like sheen
    n1=en:genetic diseases, x-linked | n2=en:cone dystrophy, x-linked, with tapetal-like sheen | rel=r_associated | relid=0 | w=28
  235. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:congenital hemidysplasia with ichthyosiform erythroderma and limb defects
    n1=en:genetic diseases, x-linked | n2=en:congenital hemidysplasia with ichthyosiform erythroderma and limb defects | rel=r_associated | relid=0 | w=28
  236. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:deafness, x-linked 1 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:deafness, x-linked 1 (disorder) | rel=r_associated | relid=0 | w=28
  237. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:deafness, x-linked 5 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:deafness, x-linked 5 (disorder) | rel=r_associated | relid=0 | w=28
  238. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:dent disease 2
    n1=en:genetic diseases, x-linked | n2=en:dent disease 2 | rel=r_associated | relid=0 | w=28
  239. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:epilepsy, x-linked, with variable learning disabilities and behavior disorders
    n1=en:genetic diseases, x-linked | n2=en:epilepsy, x-linked, with variable learning disabilities and behavior disorders | rel=r_associated | relid=0 | w=28
  240. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:familial hypertrophic cardiomyopathy
    n1=en:genetic diseases, x-linked | n2=en:familial hypertrophic cardiomyopathy | rel=r_associated | relid=0 | w=28
  241. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:genetic aspects
    n1=en:genetic diseases, x-linked | n2=en:genetic aspects | rel=r_associated | relid=0 | w=28
  242. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:glycogen storage disease, type ixa2
    n1=en:genetic diseases, x-linked | n2=en:glycogen storage disease, type ixa2 | rel=r_associated | relid=0 | w=28
  243. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:heterotopia, periventricular nodular, with frontometaphyseal dysplasia
    n1=en:genetic diseases, x-linked | n2=en:heterotopia, periventricular nodular, with frontometaphyseal dysplasia | rel=r_associated | relid=0 | w=28
  244. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:hodgkin disease, x-linked pseudoautosomal
    n1=en:genetic diseases, x-linked | n2=en:hodgkin disease, x-linked pseudoautosomal | rel=r_associated | relid=0 | w=28
  245. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:ichthyosis, x-linked, complicated
    n1=en:genetic diseases, x-linked | n2=en:ichthyosis, x-linked, complicated | rel=r_associated | relid=0 | w=28
  246. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:immunology aspects
    n1=en:genetic diseases, x-linked | n2=en:immunology aspects | rel=r_associated | relid=0 | w=28
  247. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:major affective disorder 2
    n1=en:genetic diseases, x-linked | n2=en:major affective disorder 2 | rel=r_associated | relid=0 | w=28
  248. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:marfan syndrome
    n1=en:genetic diseases, x-linked | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=28
  249. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> en:radius absent anogenital anomalies
    n1=en:genetic diseases, x-linked | n2=en:radius absent anogenital anomalies | rel=r_associated | relid=0 | w=28
  250. en:genetic diseases, x-linked -- r_associated #0: 28 / 0.651 -> maladies liées au chromosome x
    n1=en:genetic diseases, x-linked | n2=maladies liées au chromosome x | rel=r_associated | relid=0 | w=28
  251. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:abruzzo erickson syndrome
    n1=en:genetic diseases, x-linked | n2=en:abruzzo erickson syndrome | rel=r_associated | relid=0 | w=27
  252. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:complication aspects
    n1=en:genetic diseases, x-linked | n2=en:complication aspects | rel=r_associated | relid=0 | w=27
  253. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:congenital absence of parathyroid gland
    n1=en:genetic diseases, x-linked | n2=en:congenital absence of parathyroid gland | rel=r_associated | relid=0 | w=27
  254. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:congenital metabolic disorder
    n1=en:genetic diseases, x-linked | n2=en:congenital metabolic disorder | rel=r_associated | relid=0 | w=27
  255. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:corpus callosum, partial agenesis of, x-linked
    n1=en:genetic diseases, x-linked | n2=en:corpus callosum, partial agenesis of, x-linked | rel=r_associated | relid=0 | w=27
  256. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:cystic fibrosis
    n1=en:genetic diseases, x-linked | n2=en:cystic fibrosis | rel=r_associated | relid=0 | w=27
  257. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:dent disease 1
    n1=en:genetic diseases, x-linked | n2=en:dent disease 1 | rel=r_associated | relid=0 | w=27
  258. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:episodic muscle weakness, x-linked
    n1=en:genetic diseases, x-linked | n2=en:episodic muscle weakness, x-linked | rel=r_associated | relid=0 | w=27
  259. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:etiology aspects
    n1=en:genetic diseases, x-linked | n2=en:etiology aspects | rel=r_associated | relid=0 | w=27
  260. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:focal dermal hypoplasia
    n1=en:genetic diseases, x-linked | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=27
  261. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:genetic diseases, y-linked
    n1=en:genetic diseases, x-linked | n2=en:genetic diseases, y-linked | rel=r_associated | relid=0 | w=27
  262. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:heterotopia, periventricular, ehlers-danlos variant
    n1=en:genetic diseases, x-linked | n2=en:heterotopia, periventricular, ehlers-danlos variant | rel=r_associated | relid=0 | w=27
  263. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:hyper-igm immunodeficiency syndrome, type 1
    n1=en:genetic diseases, x-linked | n2=en:hyper-igm immunodeficiency syndrome, type 1 | rel=r_associated | relid=0 | w=27
  264. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:in cerebrospinal fluid
    n1=en:genetic diseases, x-linked | n2=en:in cerebrospinal fluid | rel=r_associated | relid=0 | w=27
  265. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:in urine
    n1=en:genetic diseases, x-linked | n2=en:in urine | rel=r_associated | relid=0 | w=27
  266. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:isolated noncompaction of the ventricular myocardium
    n1=en:genetic diseases, x-linked | n2=en:isolated noncompaction of the ventricular myocardium | rel=r_associated | relid=0 | w=27
  267. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:kallmann syndrome
    n1=en:genetic diseases, x-linked | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=27
  268. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:macular dystrophy, x-linked
    n1=en:genetic diseases, x-linked | n2=en:macular dystrophy, x-linked | rel=r_associated | relid=0 | w=27
  269. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:membranoproliferative glomerulonephritis, x-linked
    n1=en:genetic diseases, x-linked | n2=en:membranoproliferative glomerulonephritis, x-linked | rel=r_associated | relid=0 | w=27
  270. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:microphthalmia, syndromic 7
    n1=en:genetic diseases, x-linked | n2=en:microphthalmia, syndromic 7 | rel=r_associated | relid=0 | w=27
  271. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:opitz g/bbb syndrome
    n1=en:genetic diseases, x-linked | n2=en:opitz g/bbb syndrome | rel=r_associated | relid=0 | w=27
  272. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:pathological aspects
    n1=en:genetic diseases, x-linked | n2=en:pathological aspects | rel=r_associated | relid=0 | w=27
  273. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:prevention & control
    n1=en:genetic diseases, x-linked | n2=en:prevention & control | rel=r_associated | relid=0 | w=27
  274. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:ptosis, hereditary congenital 2
    n1=en:genetic diseases, x-linked | n2=en:ptosis, hereditary congenital 2 | rel=r_associated | relid=0 | w=27
  275. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:pycnodysostosis
    n1=en:genetic diseases, x-linked | n2=en:pycnodysostosis | rel=r_associated | relid=0 | w=27
  276. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:sex chromosome disorders
    n1=en:genetic diseases, x-linked | n2=en:sex chromosome disorders | rel=r_associated | relid=0 | w=27
  277. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:simpson golabi behmel syndrome type 1
    n1=en:genetic diseases, x-linked | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=27
  278. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:spastic paraplegia 34, x-linked (disorder)
    n1=en:genetic diseases, x-linked | n2=en:spastic paraplegia 34, x-linked (disorder) | rel=r_associated | relid=0 | w=27
  279. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:spina bifida, x-linked
    n1=en:genetic diseases, x-linked | n2=en:spina bifida, x-linked | rel=r_associated | relid=0 | w=27
  280. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia, x-linked 5
    n1=en:genetic diseases, x-linked | n2=en:spinocerebellar ataxia, x-linked 5 | rel=r_associated | relid=0 | w=27
  281. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:split-hand/foot malformation 2
    n1=en:genetic diseases, x-linked | n2=en:split-hand/foot malformation 2 | rel=r_associated | relid=0 | w=27
  282. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:spondylometaphyseal dysplasia, x-linked
    n1=en:genetic diseases, x-linked | n2=en:spondylometaphyseal dysplasia, x-linked | rel=r_associated | relid=0 | w=27
  283. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:terminal osseous dysplasia and pigmentary defects
    n1=en:genetic diseases, x-linked | n2=en:terminal osseous dysplasia and pigmentary defects | rel=r_associated | relid=0 | w=27
  284. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:therapeutic aspects
    n1=en:genetic diseases, x-linked | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=27
  285. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:vasquez hurst sotos syndrome
    n1=en:genetic diseases, x-linked | n2=en:vasquez hurst sotos syndrome | rel=r_associated | relid=0 | w=27
  286. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:von willebrand disease, x-linked form
    n1=en:genetic diseases, x-linked | n2=en:von willebrand disease, x-linked form | rel=r_associated | relid=0 | w=27
  287. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:x-linked bulbar-muscular atrophy
    n1=en:genetic diseases, x-linked | n2=en:x-linked bulbar-muscular atrophy | rel=r_associated | relid=0 | w=27
  288. en:genetic diseases, x-linked -- r_associated #0: 27 / 0.628 -> en:x-linked tetra-amelia
    n1=en:genetic diseases, x-linked | n2=en:x-linked tetra-amelia | rel=r_associated | relid=0 | w=27
  289. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:achromatopsia incomplete, x-linked
    n1=en:genetic diseases, x-linked | n2=en:achromatopsia incomplete, x-linked | rel=r_associated | relid=0 | w=26
  290. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:anemia, nonspherocytic hemolytic, due to g6pd deficiency
    n1=en:genetic diseases, x-linked | n2=en:anemia, nonspherocytic hemolytic, due to g6pd deficiency | rel=r_associated | relid=0 | w=26
  291. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:ataxia, fatal x-linked, with deafness and loss of vision
    n1=en:genetic diseases, x-linked | n2=en:ataxia, fatal x-linked, with deafness and loss of vision | rel=r_associated | relid=0 | w=26
  292. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:autoimmune lymphoproliferative syndrome
    n1=en:genetic diseases, x-linked | n2=en:autoimmune lymphoproliferative syndrome | rel=r_associated | relid=0 | w=26
  293. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:branchial arch syndrome x-linked
    n1=en:genetic diseases, x-linked | n2=en:branchial arch syndrome x-linked | rel=r_associated | relid=0 | w=26
  294. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:brugada syndrome ventricular arrhythmia by ecg finding
    n1=en:genetic diseases, x-linked | n2=en:brugada syndrome ventricular arrhythmia by ecg finding | rel=r_associated | relid=0 | w=26
  295. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:charge syndrome
    n1=en:genetic diseases, x-linked | n2=en:charge syndrome | rel=r_associated | relid=0 | w=26
  296. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:congenital alopecia
    n1=en:genetic diseases, x-linked | n2=en:congenital alopecia | rel=r_associated | relid=0 | w=26
  297. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:congenital idiopathic intestinal pseudoobstruction
    n1=en:genetic diseases, x-linked | n2=en:congenital idiopathic intestinal pseudoobstruction | rel=r_associated | relid=0 | w=26
  298. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:costello syndrome
    n1=en:genetic diseases, x-linked | n2=en:costello syndrome | rel=r_associated | relid=0 | w=26
  299. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:donohue syndrome
    n1=en:genetic diseases, x-linked | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=26
  300. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:duchenne muscular dystrophy
    n1=en:genetic diseases, x-linked | n2=en:duchenne muscular dystrophy | rel=r_associated | relid=0 | w=26
  301. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:dwarfism
    n1=en:genetic diseases, x-linked | n2=en:dwarfism | rel=r_associated | relid=0 | w=26
  302. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:fg syndrome 5 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:fg syndrome 5 (disorder) | rel=r_associated | relid=0 | w=26
  303. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:frasier syndrome
    n1=en:genetic diseases, x-linked | n2=en:frasier syndrome | rel=r_associated | relid=0 | w=26
  304. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:hemoglobinopathy
    n1=en:genetic diseases, x-linked | n2=en:hemoglobinopathy | rel=r_associated | relid=0 | w=26
  305. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:lennox-gastaut syndrome
    n1=en:genetic diseases, x-linked | n2=en:lennox-gastaut syndrome | rel=r_associated | relid=0 | w=26
  306. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:mental retardation, x-linked, with panhypopituitarism
    n1=en:genetic diseases, x-linked | n2=en:mental retardation, x-linked, with panhypopituitarism | rel=r_associated | relid=0 | w=26
  307. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:mental retardation, x-linked, znf711-related
    n1=en:genetic diseases, x-linked | n2=en:mental retardation, x-linked, znf711-related | rel=r_associated | relid=0 | w=26
  308. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:mitral valve prolapse, familial, x-linked
    n1=en:genetic diseases, x-linked | n2=en:mitral valve prolapse, familial, x-linked | rel=r_associated | relid=0 | w=26
  309. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:osteochondrodysplasia
    n1=en:genetic diseases, x-linked | n2=en:osteochondrodysplasia | rel=r_associated | relid=0 | w=26
  310. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:primary hypertrophic osteoarthropathy
    n1=en:genetic diseases, x-linked | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=26
  311. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:progressive hearing loss stapes fixation
    n1=en:genetic diseases, x-linked | n2=en:progressive hearing loss stapes fixation | rel=r_associated | relid=0 | w=26
  312. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:properdin deficiency, type ii
    n1=en:genetic diseases, x-linked | n2=en:properdin deficiency, type ii | rel=r_associated | relid=0 | w=26
  313. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:russell-silver syndrome, x-linked
    n1=en:genetic diseases, x-linked | n2=en:russell-silver syndrome, x-linked | rel=r_associated | relid=0 | w=26
  314. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:surgical aspects
    n1=en:genetic diseases, x-linked | n2=en:surgical aspects | rel=r_associated | relid=0 | w=26
  315. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:wieacker-wolff syndrome
    n1=en:genetic diseases, x-linked | n2=en:wieacker-wolff syndrome | rel=r_associated | relid=0 | w=26
  316. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:x inactivation, familial skewed, 1 (disorder)
    n1=en:genetic diseases, x-linked | n2=en:x inactivation, familial skewed, 1 (disorder) | rel=r_associated | relid=0 | w=26
  317. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:x-linked adrenal hypoplasia congenita
    n1=en:genetic diseases, x-linked | n2=en:x-linked adrenal hypoplasia congenita | rel=r_associated | relid=0 | w=26
  318. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> en:x-linked chondrodysplasia punctata 1
    n1=en:genetic diseases, x-linked | n2=en:x-linked chondrodysplasia punctata 1 | rel=r_associated | relid=0 | w=26
  319. en:genetic diseases, x-linked -- r_associated #0: 26 / 0.605 -> maladies portées par le chromosome x
    n1=en:genetic diseases, x-linked | n2=maladies portées par le chromosome x | rel=r_associated | relid=0 | w=26
  320. en:genetic diseases, x-linked -- r_associated #0: 25 / 0.581 -> en:genetic
    n1=en:genetic diseases, x-linked | n2=en:genetic | rel=r_associated | relid=0 | w=25
  321. en:genetic diseases, x-linked -- r_associated #0: 25 / 0.581 -> maladie de Marfan
    n1=en:genetic diseases, x-linked | n2=maladie de Marfan | rel=r_associated | relid=0 | w=25
  322. en:genetic diseases, x-linked -- r_associated #0: 23 / 0.535 -> syndrome de Marfan
    n1=en:genetic diseases, x-linked | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=23
  323. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> anomalie chromosomique
    n1=en:genetic diseases, x-linked | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
  324. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> anomalie cytogénétique
    n1=en:genetic diseases, x-linked | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
  325. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> anormalité des chromosomes
    n1=en:genetic diseases, x-linked | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
  326. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> arachnodactylie
    n1=en:genetic diseases, x-linked | n2=arachnodactylie | rel=r_associated | relid=0 | w=20
  327. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> autres anomalies de la densité et de la structure osseuses
    n1=en:genetic diseases, x-linked | n2=autres anomalies de la densité et de la structure osseuses | rel=r_associated | relid=0 | w=20
  328. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> chérubisme
    n1=en:genetic diseases, x-linked | n2=chérubisme | rel=r_associated | relid=0 | w=20
  329. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> dyskératose congénitale
    n1=en:genetic diseases, x-linked | n2=dyskératose congénitale | rel=r_associated | relid=0 | w=20
  330. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> dyskératose congénitale de Zinsser-Cole-Engman
    n1=en:genetic diseases, x-linked | n2=dyskératose congénitale de Zinsser-Cole-Engman | rel=r_associated | relid=0 | w=20
  331. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> dystrophie musculaire d'Emery-Dreifuss
    n1=en:genetic diseases, x-linked | n2=dystrophie musculaire d'Emery-Dreifuss | rel=r_associated | relid=0 | w=20
  332. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> dystrophie musculaire d'emery-dreifuss
    n1=en:genetic diseases, x-linked | n2=dystrophie musculaire d'emery-dreifuss | rel=r_associated | relid=0 | w=20
  333. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:arachnodactyly
    n1=en:genetic diseases, x-linked | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20
  334. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:blue sclera syndrome
    n1=en:genetic diseases, x-linked | n2=en:blue sclera syndrome | rel=r_associated | relid=0 | w=20
  335. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:brittle bone disease
    n1=en:genetic diseases, x-linked | n2=en:brittle bone disease | rel=r_associated | relid=0 | w=20
  336. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:brittle-bone disease
    n1=en:genetic diseases, x-linked | n2=en:brittle-bone disease | rel=r_associated | relid=0 | w=20
  337. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:chromosomal abnormality
    n1=en:genetic diseases, x-linked | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
  338. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:Donohue syndrome
    n1=en:genetic diseases, x-linked | n2=en:Donohue syndrome | rel=r_associated | relid=0 | w=20
  339. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:fragile X syndrome
    n1=en:genetic diseases, x-linked | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
  340. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:Goltz syndrome
    n1=en:genetic diseases, x-linked | n2=en:Goltz syndrome | rel=r_associated | relid=0 | w=20
  341. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:hemoglobin related disease
    n1=en:genetic diseases, x-linked | n2=en:hemoglobin related disease | rel=r_associated | relid=0 | w=20
  342. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:hemophilia B
    n1=en:genetic diseases, x-linked | n2=en:hemophilia B | rel=r_associated | relid=0 | w=20
  343. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:Marfan's disease
    n1=en:genetic diseases, x-linked | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20
  344. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:marfan's syndrome
    n1=en:genetic diseases, x-linked | n2=en:marfan's syndrome | rel=r_associated | relid=0 | w=20
  345. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:Marfan's syndrome
    n1=en:genetic diseases, x-linked | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20
  346. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:Martin-Bell's syndrome
    n1=en:genetic diseases, x-linked | n2=en:Martin-Bell's syndrome | rel=r_associated | relid=0 | w=20
  347. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:muscular dystrophy, emery-dreifuss
    n1=en:genetic diseases, x-linked | n2=en:muscular dystrophy, emery-dreifuss | rel=r_associated | relid=0 | w=20
  348. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:OI
    n1=en:genetic diseases, x-linked | n2=en:OI | rel=r_associated | relid=0 | w=20
  349. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:Osteogenesis imperfecta
    n1=en:genetic diseases, x-linked | n2=en:Osteogenesis imperfecta | rel=r_associated | relid=0 | w=20
  350. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:osteopsathyrosis
    n1=en:genetic diseases, x-linked | n2=en:osteopsathyrosis | rel=r_associated | relid=0 | w=20
  351. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:x-linked thrombocytopenia with beta-thalassemia
    n1=en:genetic diseases, x-linked | n2=en:x-linked thrombocytopenia with beta-thalassemia | rel=r_associated | relid=0 | w=20
  352. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> en:yellow nail
    n1=en:genetic diseases, x-linked | n2=en:yellow nail | rel=r_associated | relid=0 | w=20
  353. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> enzymologie
    n1=en:genetic diseases, x-linked | n2=enzymologie | rel=r_associated | relid=0 | w=20
  354. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> enzymology
    n1=en:genetic diseases, x-linked | n2=enzymology | rel=r_associated | relid=0 | w=20
  355. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> épidémiologique
    n1=en:genetic diseases, x-linked | n2=épidémiologique | rel=r_associated | relid=0 | w=20
  356. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> Goltz
    n1=en:genetic diseases, x-linked | n2=Goltz | rel=r_associated | relid=0 | w=20
  357. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> Goltz (syndrome de)
    n1=en:genetic diseases, x-linked | n2=Goltz (syndrome de) | rel=r_associated | relid=0 | w=20
  358. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> hémoglobinopathie
    n1=en:genetic diseases, x-linked | n2=hémoglobinopathie | rel=r_associated | relid=0 | w=20
  359. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> hyperplasie congénitale des surrénales
    n1=en:genetic diseases, x-linked | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20
  360. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> hypoplasie dermique en aires
    n1=en:genetic diseases, x-linked | n2=hypoplasie dermique en aires | rel=r_associated | relid=0 | w=20
  361. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> hypoplasie dermique focale
    n1=en:genetic diseases, x-linked | n2=hypoplasie dermique focale | rel=r_associated | relid=0 | w=20
  362. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> maladie de l'homme de verre
    n1=en:genetic diseases, x-linked | n2=maladie de l'homme de verre | rel=r_associated | relid=0 | w=20
  363. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> maladie de marfan
    n1=en:genetic diseases, x-linked | n2=maladie de marfan | rel=r_associated | relid=0 | w=20
  364. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> maladie des os de verre
    n1=en:genetic diseases, x-linked | n2=maladie des os de verre | rel=r_associated | relid=0 | w=20
  365. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> Marfan (maladie de)
    n1=en:genetic diseases, x-linked | n2=Marfan (maladie de) | rel=r_associated | relid=0 | w=20
  366. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> microbiologique
    n1=en:genetic diseases, x-linked | n2=microbiologique | rel=r_associated | relid=0 | w=20
  367. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> ongles jaunes (syndrome des)
    n1=en:genetic diseases, x-linked | n2=ongles jaunes (syndrome des) | rel=r_associated | relid=0 | w=20
  368. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> onycho-ostéodysostose
    n1=en:genetic diseases, x-linked | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20
  369. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> onycho-patellaire (syndrome)
    n1=en:genetic diseases, x-linked | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20
  370. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasie
    n1=en:genetic diseases, x-linked | n2=ostéochondrodysplasie | rel=r_associated | relid=0 | w=20
  371. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasies
    n1=en:genetic diseases, x-linked | n2=ostéochondrodysplasies | rel=r_associated | relid=0 | w=20
  372. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> ostéogénèse imparfaite
    n1=en:genetic diseases, x-linked | n2=ostéogénèse imparfaite | rel=r_associated | relid=0 | w=20
  373. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> ostéogenèse imparfaite
    n1=en:genetic diseases, x-linked | n2=ostéogenèse imparfaite | rel=r_associated | relid=0 | w=20
  374. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> Ostéogenèse imparfaite
    n1=en:genetic diseases, x-linked | n2=Ostéogenèse imparfaite | rel=r_associated | relid=0 | w=20
  375. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> osteogenesis imperfecta
    n1=en:genetic diseases, x-linked | n2=osteogenesis imperfecta | rel=r_associated | relid=0 | w=20
  376. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> osteogenesis imperfecta forme oculaire
    n1=en:genetic diseases, x-linked | n2=osteogenesis imperfecta forme oculaire | rel=r_associated | relid=0 | w=20
  377. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> osteogenesis imperfecta progressivement déformante avec sclères normales
    n1=en:genetic diseases, x-linked | n2=osteogenesis imperfecta progressivement déformante avec sclères normales | rel=r_associated | relid=0 | w=20
  378. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> ostéopsathyrose
    n1=en:genetic diseases, x-linked | n2=ostéopsathyrose | rel=r_associated | relid=0 | w=20
  379. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> parasitologie
    n1=en:genetic diseases, x-linked | n2=parasitologie | rel=r_associated | relid=0 | w=20
  380. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> radiographique
    n1=en:genetic diseases, x-linked | n2=radiographique | rel=r_associated | relid=0 | w=20
  381. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> syndrome de fragilité du chromosome X
    n1=en:genetic diseases, x-linked | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
  382. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> syndrome de goltz
    n1=en:genetic diseases, x-linked | n2=syndrome de goltz | rel=r_associated | relid=0 | w=20
  383. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> syndrome de Goltz
    n1=en:genetic diseases, x-linked | n2=syndrome de Goltz | rel=r_associated | relid=0 | w=20
  384. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> syndrome de Lobstein-van der Hoeve
    n1=en:genetic diseases, x-linked | n2=syndrome de Lobstein-van der Hoeve | rel=r_associated | relid=0 | w=20
  385. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> syndrome de marfan
    n1=en:genetic diseases, x-linked | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20
  386. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> syndrome de Martin-Bell
    n1=en:genetic diseases, x-linked | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
  387. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> trouble chromosomique
    n1=en:genetic diseases, x-linked | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
  388. en:genetic diseases, x-linked -- r_associated #0: 20 / 0.465 -> yellow nail syndrome
    n1=en:genetic diseases, x-linked | n2=yellow nail syndrome | rel=r_associated | relid=0 | w=20
  389. en:genetic diseases, x-linked -- r_associated #0: 2 / 0.047 -> en:disease or syndrome
    n1=en:genetic diseases, x-linked | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=2
≈ 490 relations entrantes

  1. syndrome de Goltz --- r_associated #0: 399 --> en:genetic diseases, x-linked
    n1=syndrome de Goltz | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=399
  2. hypoplasie dermique focale --- r_associated #0: 398 --> en:genetic diseases, x-linked
    n1=hypoplasie dermique focale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=398
  3. Goltz --- r_associated #0: 394 --> en:genetic diseases, x-linked
    n1=Goltz | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=394
  4. hypoplasie dermique en aires --- r_associated #0: 392 --> en:genetic diseases, x-linked
    n1=hypoplasie dermique en aires | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=392
  5. en:focal dermal hypoplasia --- r_associated #0: 390 --> en:genetic diseases, x-linked
    n1=en:focal dermal hypoplasia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=390
  6. anormalité des chromosomes --- r_associated #0: 323 --> en:genetic diseases, x-linked
    n1=anormalité des chromosomes | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=323
  7. en:chromosome disorder --- r_associated #0: 320 --> en:genetic diseases, x-linked
    n1=en:chromosome disorder | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=320
  8. en:marfan syndrome --- r_associated #0: 285 --> en:genetic diseases, x-linked
    n1=en:marfan syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=285
  9. maladie de Marfan --- r_associated #0: 281 --> en:genetic diseases, x-linked
    n1=maladie de Marfan | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=281
  10. syndrome de Marfan --- r_associated #0: 281 --> en:genetic diseases, x-linked
    n1=syndrome de Marfan | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=281
  11. arachnodactylie --- r_associated #0: 259 --> en:genetic diseases, x-linked
    n1=arachnodactylie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=259
  12. trouble chromosomique --- r_associated #0: 250 --> en:genetic diseases, x-linked
    n1=trouble chromosomique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=250
  13. anomalie chromosomique --- r_associated #0: 249 --> en:genetic diseases, x-linked
    n1=anomalie chromosomique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=249
  14. en:arachnodactyly --- r_associated #0: 239 --> en:genetic diseases, x-linked
    n1=en:arachnodactyly | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=239
  15. en:enzymology --- r_associated #0: 201 --> en:genetic diseases, x-linked
    n1=en:enzymology | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=201
  16. enzymologie --- r_associated #0: 200 --> en:genetic diseases, x-linked
    n1=enzymologie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=200
  17. en:chromosomal abnormality --- r_associated #0: 180 --> en:genetic diseases, x-linked
    n1=en:chromosomal abnormality | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=180
  18. ostéogénèse imparfaite --- r_associated #0: 165 --> en:genetic diseases, x-linked
    n1=ostéogénèse imparfaite | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=165
  19. ostéogenèse imparfaite --- r_associated #0: 164 --> en:genetic diseases, x-linked
    n1=ostéogenèse imparfaite | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=164
  20. en:parasitology --- r_associated #0: 161 --> en:genetic diseases, x-linked
    n1=en:parasitology | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=161
  21. maladie des os de verre --- r_associated #0: 161 --> en:genetic diseases, x-linked
    n1=maladie des os de verre | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=161
  22. en:osteogenesis imperfecta --- r_associated #0: 160 --> en:genetic diseases, x-linked
    n1=en:osteogenesis imperfecta | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=160
  23. enzymology --- r_associated #0: 160 --> en:genetic diseases, x-linked
    n1=enzymology | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=160
  24. parasitologie --- r_associated #0: 160 --> en:genetic diseases, x-linked
    n1=parasitologie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=160
  25. en:Osteogenesis imperfecta --- r_associated #0: 150 --> en:genetic diseases, x-linked
    n1=en:Osteogenesis imperfecta | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=150
  26. en:brittle bone disease --- r_associated #0: 145 --> en:genetic diseases, x-linked
    n1=en:brittle bone disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=145
  27. ostéochondrodysplasies --- r_associated #0: 141 --> en:genetic diseases, x-linked
    n1=ostéochondrodysplasies | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=141
  28. en:OI --- r_associated #0: 140 --> en:genetic diseases, x-linked
    n1=en:OI | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=140
  29. en:osteochondrodysplasia --- r_associated #0: 138 --> en:genetic diseases, x-linked
    n1=en:osteochondrodysplasia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=138
  30. en:yellow nail syndrome --- r_associated #0: 100 --> en:genetic diseases, x-linked
    n1=en:yellow nail syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=100
  31. chérubisme --- r_associated #0: 97 --> en:genetic diseases, x-linked
    n1=chérubisme | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=97
  32. hémoglobinopathie --- r_associated #0: 97 --> en:genetic diseases, x-linked
    n1=hémoglobinopathie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=97
  33. yellow nail syndrome --- r_associated #0: 97 --> en:genetic diseases, x-linked
    n1=yellow nail syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=97
  34. hyperplasie congénitale des surrénales --- r_associated #0: 95 --> en:genetic diseases, x-linked
    n1=hyperplasie congénitale des surrénales | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=95
  35. en:congenital adrenal hyperplasia --- r_associated #0: 94 --> en:genetic diseases, x-linked
    n1=en:congenital adrenal hyperplasia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=94
  36. en:hemoglobinopathy --- r_associated #0: 94 --> en:genetic diseases, x-linked
    n1=en:hemoglobinopathy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=94
  37. en:cherubism --- r_associated #0: 93 --> en:genetic diseases, x-linked
    n1=en:cherubism | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=93
  38. en:fragile x syndrome --- r_associated #0: 78 --> en:genetic diseases, x-linked
    n1=en:fragile x syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=78
  39. en:fragile X syndrome --- r_associated #0: 75 --> en:genetic diseases, x-linked
    n1=en:fragile X syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=75
  40. dystrophie musculaire d'Emery-Dreifuss --- r_associated #0: 71 --> en:genetic diseases, x-linked
    n1=dystrophie musculaire d'Emery-Dreifuss | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=71
  41. en:muscular dystrophy, emery-dreifuss --- r_associated #0: 71 --> en:genetic diseases, x-linked
    n1=en:muscular dystrophy, emery-dreifuss | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=71
  42. syndrome de fragilité du chromosome X --- r_associated #0: 70 --> en:genetic diseases, x-linked
    n1=syndrome de fragilité du chromosome X | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=70
  43. en:emery-dreifuss muscular dystrophy --- r_associated #0: 68 --> en:genetic diseases, x-linked
    n1=en:emery-dreifuss muscular dystrophy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=68
  44. osteogenesis imperfecta --- r_associated #0: 66 --> en:genetic diseases, x-linked
    n1=osteogenesis imperfecta | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=66
  45. anomalie cytogénétique --- r_associated #0: 60 --> en:genetic diseases, x-linked
    n1=anomalie cytogénétique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=60
  46. Ostéogenèse imparfaite --- r_associated #0: 50 --> en:genetic diseases, x-linked
    n1=Ostéogenèse imparfaite | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=50
  47. maladie de l'homme de verre --- r_associated #0: 50 --> en:genetic diseases, x-linked
    n1=maladie de l'homme de verre | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=50
  48. maladie de marfan --- r_associated #0: 49 --> en:genetic diseases, x-linked
    n1=maladie de marfan | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=49
  49. dystrophie musculaire d'emery-dreifuss --- r_associated #0: 47 --> en:genetic diseases, x-linked
    n1=dystrophie musculaire d'emery-dreifuss | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=47
  50. en:Marfan's syndrome --- r_associated #0: 46 --> en:genetic diseases, x-linked
    n1=en:Marfan's syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=46
  51. en:mental retardation, x-linked, syndromic, zdhhc9-related --- r_associated #0: 43 --> en:genetic diseases, x-linked
    n1=en:mental retardation, x-linked, syndromic, zdhhc9-related | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=43
  52. en:orofaciodigital syndromes --- r_associated #0: 43 --> en:genetic diseases, x-linked
    n1=en:orofaciodigital syndromes | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=43
  53. maladies liées à l'x --- r_associated #0: 43 --> en:genetic diseases, x-linked
    n1=maladies liées à l'x | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=43
  54. en:microphthalmia, isolated, with coloboma 1 --- r_associated #0: 42 --> en:genetic diseases, x-linked
    n1=en:microphthalmia, isolated, with coloboma 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=42
  55. en:protoporphyria, erythropoietic, x-linked dominant --- r_associated #0: 42 --> en:genetic diseases, x-linked
    n1=en:protoporphyria, erythropoietic, x-linked dominant | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=42
  56. microbiologique --- r_associated #0: 42 --> en:genetic diseases, x-linked
    n1=microbiologique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=42
  57. syndrome de marfan --- r_associated #0: 42 --> en:genetic diseases, x-linked
    n1=syndrome de marfan | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=42
  58. en:hypoparathyroidism - x-linked --- r_associated #0: 41 --> en:genetic diseases, x-linked
    n1=en:hypoparathyroidism - x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=41
  59. en:immunology aspects --- r_associated #0: 41 --> en:genetic diseases, x-linked
    n1=en:immunology aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=41
  60. en:microbiological --- r_associated #0: 41 --> en:genetic diseases, x-linked
    n1=en:microbiological | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=41
  61. en:ophthalmoplegia, external, and myopia (disorder) --- r_associated #0: 41 --> en:genetic diseases, x-linked
    n1=en:ophthalmoplegia, external, and myopia (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=41
  62. en:properdin deficiency, type ii --- r_associated #0: 41 --> en:genetic diseases, x-linked
    n1=en:properdin deficiency, type ii | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=41
  63. syndrome de goltz --- r_associated #0: 41 --> en:genetic diseases, x-linked
    n1=syndrome de goltz | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=41
  64. dysplasie olfacto-génitale --- r_associated #0: 40 --> en:genetic diseases, x-linked
    n1=dysplasie olfacto-génitale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=40
  65. en:angiokeratoma corporis diffusum --- r_associated #0: 40 --> en:genetic diseases, x-linked
    n1=en:angiokeratoma corporis diffusum | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=40
  66. en:brugada syndrome ventricular arrhythmia by ecg finding --- r_associated #0: 40 --> en:genetic diseases, x-linked
    n1=en:brugada syndrome ventricular arrhythmia by ecg finding | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=40
  67. en:hodgkin disease, x-linked pseudoautosomal --- r_associated #0: 40 --> en:genetic diseases, x-linked
    n1=en:hodgkin disease, x-linked pseudoautosomal | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=40
  68. en:nail-patella syndrome --- r_associated #0: 40 --> en:genetic diseases, x-linked
    n1=en:nail-patella syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=40
  69. en:x-linked agammaglobulinemia --- r_associated #0: 40 --> en:genetic diseases, x-linked
    n1=en:x-linked agammaglobulinemia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=40
  70. onycho-patellaire (syndrome) --- r_associated #0: 40 --> en:genetic diseases, x-linked
    n1=onycho-patellaire (syndrome) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=40
  71. osteogenesis imperfecta forme oculaire --- r_associated #0: 40 --> en:genetic diseases, x-linked
    n1=osteogenesis imperfecta forme oculaire | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=40
  72. syndrome de Lobstein-van der Hoeve --- r_associated #0: 40 --> en:genetic diseases, x-linked
    n1=syndrome de Lobstein-van der Hoeve | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=40
  73. en:Marfan's disease --- r_associated #0: 38 --> en:genetic diseases, x-linked
    n1=en:Marfan's disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=38
  74. en:complication aspects --- r_associated #0: 38 --> en:genetic diseases, x-linked
    n1=en:complication aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=38
  75. en:hyperekplexia and epilepsy --- r_associated #0: 38 --> en:genetic diseases, x-linked
    n1=en:hyperekplexia and epilepsy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=38
  76. en:spastic paraplegia 34, x-linked (disorder) --- r_associated #0: 38 --> en:genetic diseases, x-linked
    n1=en:spastic paraplegia 34, x-linked (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=38
  77. en:cone-rod dystrophy, x-linked, 1 --- r_associated #0: 37 --> en:genetic diseases, x-linked
    n1=en:cone-rod dystrophy, x-linked, 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=37
  78. en:hemoglobin related disease --- r_associated #0: 37 --> en:genetic diseases, x-linked
    n1=en:hemoglobin related disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=37
  79. ostéochondrodysplasie --- r_associated #0: 37 --> en:genetic diseases, x-linked
    n1=ostéochondrodysplasie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=37
  80. en:kallmann syndrome --- r_associated #0: 36 --> en:genetic diseases, x-linked
    n1=en:kallmann syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=36
  81. en:masa syndrome (disorder) --- r_associated #0: 36 --> en:genetic diseases, x-linked
    n1=en:masa syndrome (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=36
  82. en:x inactivation, familial skewed, 1 (disorder) --- r_associated #0: 36 --> en:genetic diseases, x-linked
    n1=en:x inactivation, familial skewed, 1 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=36
  83. osteogenesis imperfecta progressivement déformante avec sclères normales --- r_associated #0: 36 --> en:genetic diseases, x-linked
    n1=osteogenesis imperfecta progressivement déformante avec sclères normales | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=36
  84. épidémiologique --- r_associated #0: 36 --> en:genetic diseases, x-linked
    n1=épidémiologique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=36
  85. dysplasie olfactogénitale --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=dysplasie olfactogénitale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  86. en:agammaglobulinemia, x-linked, type 2 (disorder) --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:agammaglobulinemia, x-linked, type 2 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  87. en:aneurysm, intracranial berry, 5 --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:aneurysm, intracranial berry, 5 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  88. en:brunner syndrome --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:brunner syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  89. en:chemically induced --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:chemically induced | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  90. en:congenital hemidysplasia with ichthyosiform erythroderma and limb defects --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:congenital hemidysplasia with ichthyosiform erythroderma and limb defects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  91. en:epidermodysplasia verruciformis, x-linked --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:epidermodysplasia verruciformis, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  92. en:epilepsy, x-linked, with variable learning disabilities and behavior disorders --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:epilepsy, x-linked, with variable learning disabilities and behavior disorders | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  93. en:fetal akinesia syndrome, x-linked --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:fetal akinesia syndrome, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  94. en:hemophilia B --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:hemophilia B | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  95. en:hemophilia b --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:hemophilia b | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  96. en:joubert syndrome 10 (disorder) --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:joubert syndrome 10 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  97. en:leukoencephalopathy with metaphyseal chondrodysplasia --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:leukoencephalopathy with metaphyseal chondrodysplasia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  98. en:macular dystrophy, x-linked --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:macular dystrophy, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  99. en:mental retardation, x-linked, with panhypopituitarism --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:mental retardation, x-linked, with panhypopituitarism | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  100. en:nance-horan syndrome --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:nance-horan syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  101. en:opitz g/bbb syndrome --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:opitz g/bbb syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  102. en:radial ray deficiency, x-linked --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:radial ray deficiency, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  103. en:sex chromosome disorders of sex development --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:sex chromosome disorders of sex development | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  104. en:thrombocytosis, familial x-linked --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:thrombocytosis, familial x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  105. en:vesicoureteral reflux, x-linked --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:vesicoureteral reflux, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  106. en:wiskott-aldrich syndrome --- r_associated #0: 35 --> en:genetic diseases, x-linked
    n1=en:wiskott-aldrich syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=35
  107. en:aarskog syndrome --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:aarskog syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  108. en:alagille syndrome --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:alagille syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  109. en:congenital alopecia --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:congenital alopecia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  110. en:deafness, x-linked 1 (disorder) --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:deafness, x-linked 1 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  111. en:genetic diseases, inborn --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:genetic diseases, inborn | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  112. en:hereditary angioedema --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:hereditary angioedema | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  113. en:hypospadias 1, x-linked --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:hypospadias 1, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  114. en:midline defects, x-linked --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:midline defects, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  115. en:modifier, x-linked, for neurofunctional defects --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:modifier, x-linked, for neurofunctional defects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  116. en:muscular dystrophy, progressive pectorodorsal --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:muscular dystrophy, progressive pectorodorsal | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  117. en:premature ovarian failure 2a --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:premature ovarian failure 2a | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  118. en:proud syndrome --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:proud syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  119. en:retinitis pigmentosa 6 (disorder) --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:retinitis pigmentosa 6 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  120. en:retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  121. en:spinocerebellar ataxia, x-linked 5 --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:spinocerebellar ataxia, x-linked 5 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  122. en:testicular germ cell tumor 1 --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:testicular germ cell tumor 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  123. en:x-linked adrenal hypoplasia congenita --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=en:x-linked adrenal hypoplasia congenita | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  124. onycho-ostéodysostose --- r_associated #0: 34 --> en:genetic diseases, x-linked
    n1=onycho-ostéodysostose | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  125. Syndrome de Marfan --- r_associated #0: 33 --> en:genetic diseases, x-linked
    n1=Syndrome de Marfan | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=33
  126. en:Goltz syndrome --- r_associated #0: 33 --> en:genetic diseases, x-linked
    n1=en:Goltz syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=33
  127. ongles jaunes (syndrome des) --- r_associated #0: 33 --> en:genetic diseases, x-linked
    n1=ongles jaunes (syndrome des) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=33
  128. en:aicardi syndrome --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:aicardi syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  129. en:alpha-1 antitrypsin deficiency --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:alpha-1 antitrypsin deficiency | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  130. en:cadasil syndrome --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:cadasil syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  131. en:charge syndrome --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:charge syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  132. en:choroideremia --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:choroideremia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  133. en:chromosome xq28 duplication syndrome --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:chromosome xq28 duplication syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  134. en:deafness, high-frequency sensorineural, x-linked --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:deafness, high-frequency sensorineural, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  135. en:duchenne muscular dystrophy --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:duchenne muscular dystrophy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  136. en:epidemiologic --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:epidemiologic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  137. en:genetic diseases, y-linked --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:genetic diseases, y-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  138. en:hypohidrotic ectodermal dysplasia with immune deficiency --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:hypohidrotic ectodermal dysplasia with immune deficiency | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  139. en:mental retardation, x-linked, syndromic, turner type --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:mental retardation, x-linked, syndromic, turner type | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  140. en:panhypopituitarism - x-linked --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:panhypopituitarism - x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  141. en:pigmentary disorder, reticulate, with systemic manifestations --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:pigmentary disorder, reticulate, with systemic manifestations | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  142. en:prostate cancer, hereditary, x-linked 2 --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:prostate cancer, hereditary, x-linked 2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  143. en:retinitis pigmentosa 34 (disorder) --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:retinitis pigmentosa 34 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  144. en:therapeutic aspects --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:therapeutic aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  145. en:torticollis, keloids, cryptorchidism, and renal dysplasia (disorder) --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:torticollis, keloids, cryptorchidism, and renal dysplasia (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  146. en:x-linked dystonia parkinsonism --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:x-linked dystonia parkinsonism | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  147. en:x-linked hypogammaglobulinemia --- r_associated #0: 32 --> en:genetic diseases, x-linked
    n1=en:x-linked hypogammaglobulinemia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=32
  148. dyskératose congénitale de Zinsser-Cole-Engman --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=dyskératose congénitale de Zinsser-Cole-Engman | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  149. en:achromatopsia incomplete, x-linked --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:achromatopsia incomplete, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  150. en:androgen insensitivity syndrome --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:androgen insensitivity syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  151. en:aspects of radionuclide imaging --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:aspects of radionuclide imaging | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  152. en:ataxia, fatal x-linked, with deafness and loss of vision --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:ataxia, fatal x-linked, with deafness and loss of vision | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  153. en:blood coagulation disorders, inherited --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:blood coagulation disorders, inherited | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  154. en:cardiac valvular dysplasia, x-linked --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:cardiac valvular dysplasia, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  155. en:chondrodysplasia punctata, x-linked dominant type --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:chondrodysplasia punctata, x-linked dominant type | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  156. en:cone dystrophy, x-linked, with tapetal-like sheen --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:cone dystrophy, x-linked, with tapetal-like sheen | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  157. en:costello syndrome --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:costello syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  158. en:craniofacioskeletal syndrome --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:craniofacioskeletal syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  159. en:exposure as collected domain --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:exposure as collected domain | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  160. en:fg syndrome 5 (disorder) --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:fg syndrome 5 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  161. en:mental retardation, x-linked, syndromic 12 --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:mental retardation, x-linked, syndromic 12 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  162. en:mitral valve prolapse, familial, x-linked --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:mitral valve prolapse, familial, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  163. en:myopia 1, x-linked --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:myopia 1, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  164. en:psychology qualifier --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:psychology qualifier | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  165. en:pycnodysostosis --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:pycnodysostosis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  166. en:short stature, idiopathic, x-linked --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:short stature, idiopathic, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  167. en:simpson-golabi-behmel syndrome, type 2 (disorder) --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:simpson-golabi-behmel syndrome, type 2 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  168. en:spinocerebellar ataxia, x-linked 1 --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:spinocerebellar ataxia, x-linked 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  169. en:von willebrand disease, x-linked form --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:von willebrand disease, x-linked form | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  170. en:x-linked agammaglobulinemia with growth hormone deficiency --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:x-linked agammaglobulinemia with growth hormone deficiency | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  171. en:x-linked chondrodysplasia punctata 1 --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:x-linked chondrodysplasia punctata 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  172. en:x-linked ichthyosis --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:x-linked ichthyosis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  173. en:x-linked severe combined immunodeficiency --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=en:x-linked severe combined immunodeficiency | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  174. ostéopsathyrose --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=ostéopsathyrose | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  175. syndrome de Martin-Bell --- r_associated #0: 31 --> en:genetic diseases, x-linked
    n1=syndrome de Martin-Bell | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=31
  176. autres anomalies de la densité et de la structure osseuses --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=autres anomalies de la densité et de la structure osseuses | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  177. en:adrenal hypoplasia, congenital, with precocious puberty --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:adrenal hypoplasia, congenital, with precocious puberty | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  178. en:alpha-thalassemia myelodysplasia syndrome --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:alpha-thalassemia myelodysplasia syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  179. en:anemia, sideroblastic, and spinocerebellar ataxia --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:anemia, sideroblastic, and spinocerebellar ataxia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  180. en:brittle-bone disease --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:brittle-bone disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  181. en:chromosome xp11.23-p11.22 duplication syndrome --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:chromosome xp11.23-p11.22 duplication syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  182. en:cleft palate with ankyloglossia --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:cleft palate with ankyloglossia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  183. en:congenital heart defects, x-linked --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:congenital heart defects, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  184. en:congenital hypoplastic anemia --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:congenital hypoplastic anemia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  185. en:congenital metabolic disorder --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:congenital metabolic disorder | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  186. en:deafness, x-linked 5 (disorder) --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:deafness, x-linked 5 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  187. en:dent disease 2 --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:dent disease 2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  188. en:epilepsy, female-restricted, with mental retardation (disorder) --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:epilepsy, female-restricted, with mental retardation (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  189. en:ethnologic --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:ethnologic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  190. en:eye diseases, hereditary --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:eye diseases, hereditary | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  191. en:hereditary hemolytic anemia --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:hereditary hemolytic anemia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  192. en:hydrocephalus, x-linked, with congenital idiopathic intestinal pseudoobstruction --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:hydrocephalus, x-linked, with congenital idiopathic intestinal pseudoobstruction | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  193. en:insulin-dependent diabetes mellitus secretory diarrhea syndrome --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  194. en:keratosis follicularis spinulosa decalvans, x-linked --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:keratosis follicularis spinulosa decalvans, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  195. en:lennox-gastaut syndrome --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:lennox-gastaut syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  196. en:metabolic aspects --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:metabolic aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  197. en:microcephaly microcornea syndrome seemanova type --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:microcephaly microcornea syndrome seemanova type | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  198. en:multiple pterygium syndrome, x-linked --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:multiple pterygium syndrome, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  199. en:muscular dystrophy --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:muscular dystrophy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  200. en:myopathy, reducing body, x-linked, childhood-onset --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:myopathy, reducing body, x-linked, childhood-onset | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  201. en:norrie syndrome --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:norrie syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  202. en:pelizaeus-merzbacher disease --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:pelizaeus-merzbacher disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  203. en:russell-silver syndrome, x-linked --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:russell-silver syndrome, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  204. en:sex chromosome disorders --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:sex chromosome disorders | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  205. en:werner syndrome --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:werner syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  206. en:x inactivation, familial skewed, 2 --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:x inactivation, familial skewed, 2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  207. en:x-linked infantile nystagmus --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:x-linked infantile nystagmus | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  208. en:x-linked recessive nephrolithiasis with renal failure --- r_associated #0: 30 --> en:genetic diseases, x-linked
    n1=en:x-linked recessive nephrolithiasis with renal failure | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=30
  209. en:anhidrotic ectodermal dysplasia 1 --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:anhidrotic ectodermal dysplasia 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  210. en:ataxia telangiectasia syndrome --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:ataxia telangiectasia syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  211. en:atypical mycobacteriosis, familial, x-linked 1 (disorder) --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:atypical mycobacteriosis, familial, x-linked 1 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  212. en:autosomal recessive polycystic kidney disease --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:autosomal recessive polycystic kidney disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  213. en:blue sclera syndrome --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:blue sclera syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  214. en:chronic granulomatous disease --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:chronic granulomatous disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  215. en:cleft palate, x-linked --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:cleft palate, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  216. en:cone-rod dystrophy, x-linked, 2 --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:cone-rod dystrophy, x-linked, 2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  217. en:congenital absence of parathyroid gland --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:congenital absence of parathyroid gland | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  218. en:congenital keratoglobus --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:congenital keratoglobus | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  219. en:congenital pain insensitivity --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:congenital pain insensitivity | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  220. en:coxoauricular syndrome --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:coxoauricular syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  221. en:deafness, x-linked 3 --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:deafness, x-linked 3 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  222. en:deafness, x-linked 4 (disorder) --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:deafness, x-linked 4 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  223. en:dent disease 1 --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:dent disease 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  224. en:etiology aspects --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:etiology aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  225. en:exudative vitreoretinopathy, familial, x-linked recessive --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:exudative vitreoretinopathy, familial, x-linked recessive | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  226. en:hereditary neoplastic syndrome --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:hereditary neoplastic syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  227. en:hyperthyroxinemia, familial dysalbuminemic --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:hyperthyroxinemia, familial dysalbuminemic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  228. en:hypospadias 2, x-linked --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:hypospadias 2, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  229. en:ichthyosis, x-linked, complicated --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:ichthyosis, x-linked, complicated | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  230. en:membranoproliferative glomerulonephritis, x-linked --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:membranoproliferative glomerulonephritis, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  231. en:mental retardation, x-linked --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:mental retardation, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  232. en:mental retardation, x-linked, znf711-related --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:mental retardation, x-linked, znf711-related | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  233. en:myopathy, reducing body, x-linked, early-onset, severe --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:myopathy, reducing body, x-linked, early-onset, severe | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  234. en:myopathy, x-linked, with excessive autophagy (disorder) --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:myopathy, x-linked, with excessive autophagy (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  235. en:nursing therapy --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:nursing therapy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  236. en:nystagmus 5, infantile periodic alternating --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:nystagmus 5, infantile periodic alternating | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  237. en:ocular albinism, type ii --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:ocular albinism, type ii | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  238. en:parkinson disease 12 --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:parkinson disease 12 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  239. en:pharmacotherapeutic --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:pharmacotherapeutic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  240. en:progressive hearing loss stapes fixation --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:progressive hearing loss stapes fixation | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  241. en:ptosis, hereditary congenital 2 --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:ptosis, hereditary congenital 2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  242. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:simpson golabi behmel syndrome type 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  243. en:sketetal dysplasia coarse facies mental retardation --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:sketetal dysplasia coarse facies mental retardation | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  244. en:spondyloepimetaphyseal dysplasia, x-linked --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:spondyloepimetaphyseal dysplasia, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  245. en:taxonomic --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:taxonomic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  246. en:viruses --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:viruses | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  247. en:x-linked bulbar-muscular atrophy --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:x-linked bulbar-muscular atrophy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  248. en:x-linked thrombocytopenia with beta-thalassemia --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:x-linked thrombocytopenia with beta-thalassemia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  249. en:yellow nail --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=en:yellow nail | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  250. hémophilie B --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=hémophilie B | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  251. maladies portées par le chromosome x --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=maladies portées par le chromosome x | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  252. radiographique --- r_associated #0: 29 --> en:genetic diseases, x-linked
    n1=radiographique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=29
  253. en:alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  254. en:alzheimer disease 16 --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:alzheimer disease 16 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  255. en:barth syndrome --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:barth syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  256. en:cystic fibrosis --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:cystic fibrosis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  257. en:donohue syndrome --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:donohue syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  258. en:dyskeratosis congenita --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:dyskeratosis congenita | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  259. en:ehlers-danlos syndrome type 5 --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:ehlers-danlos syndrome type 5 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  260. en:episodic muscle weakness, x-linked --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:episodic muscle weakness, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  261. en:hereditary autoinflammatory diseases --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:hereditary autoinflammatory diseases | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  262. en:heredodegenerative disorders, nervous system --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:heredodegenerative disorders, nervous system | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  263. en:heterotopia, periventricular nodular, with frontometaphyseal dysplasia --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:heterotopia, periventricular nodular, with frontometaphyseal dysplasia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  264. en:hyper-igm immunodeficiency syndrome, type 1 --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:hyper-igm immunodeficiency syndrome, type 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  265. en:isolated noncompaction of the ventricular myocardium --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:isolated noncompaction of the ventricular myocardium | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  266. en:juvenile x-linked retinoschisis --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:juvenile x-linked retinoschisis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  267. en:marfan's syndrome --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:marfan's syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  268. en:myopia 13 --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:myopia 13 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  269. en:reticuloendothelial hyperplasia --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:reticuloendothelial hyperplasia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  270. en:retinitis pigmentosa 3 --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:retinitis pigmentosa 3 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  271. en:spinal muscular atrophy, distal, x-linked 3 --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:spinal muscular atrophy, distal, x-linked 3 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  272. en:spondylometaphyseal dysplasia, x-linked --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:spondylometaphyseal dysplasia, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  273. en:thyroxine-binding globulin deficiency --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:thyroxine-binding globulin deficiency | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  274. en:waisman syndrome --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:waisman syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  275. en:wieacker-wolff syndrome --- r_associated #0: 28 --> en:genetic diseases, x-linked
    n1=en:wieacker-wolff syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=28
  276. en:Donohue syndrome --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:Donohue syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  277. en:anemia, nonspherocytic hemolytic, due to g6pd deficiency --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:anemia, nonspherocytic hemolytic, due to g6pd deficiency | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  278. en:anemia, x-linked, without thrombocytopenia --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:anemia, x-linked, without thrombocytopenia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  279. en:angioma serpiginosum --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:angioma serpiginosum | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  280. en:arthrogryposis, x-linked, type v --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:arthrogryposis, x-linked, type v | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  281. en:branchial arch syndrome x-linked --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:branchial arch syndrome x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  282. en:camurati-engelmann syndrome --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:camurati-engelmann syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  283. en:chromosomes, human, x --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:chromosomes, human, x | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  284. en:dent's disease --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:dent's disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  285. en:dwarfism --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:dwarfism | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  286. en:dyserythropoietic anemia with thrombocytopenia --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:dyserythropoietic anemia with thrombocytopenia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  287. en:familial hypertrophic cardiomyopathy --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:familial hypertrophic cardiomyopathy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  288. en:frasier syndrome --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:frasier syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  289. en:genetic aspects --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:genetic aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  290. en:glycogen storage disease type iib --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:glycogen storage disease type iib | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  291. en:glycogen storage disease, type ixa2 --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:glycogen storage disease, type ixa2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  292. en:hereditary sideroblastic anemia --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:hereditary sideroblastic anemia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  293. en:heterotopia, periventricular, ehlers-danlos variant --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:heterotopia, periventricular, ehlers-danlos variant | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  294. en:historical aspects qualifier --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:historical aspects qualifier | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  295. en:hyperimmunoglobulin m syndrome --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:hyperimmunoglobulin m syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  296. en:immunodeficiency, x-linked, with deficiency of 115,000 dalton surface glycoprotein --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:immunodeficiency, x-linked, with deficiency of 115,000 dalton surface glycoprotein | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  297. en:neural tube defects x-linked --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:neural tube defects x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  298. en:oculocerebrorenal syndrome --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:oculocerebrorenal syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  299. en:ornithine carbamoyltransferase deficiency disease --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:ornithine carbamoyltransferase deficiency disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  300. en:osteopsathyrosis --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:osteopsathyrosis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  301. en:pelger-huet anomaly --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:pelger-huet anomaly | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  302. en:properdin deficiency, type iii --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:properdin deficiency, type iii | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  303. en:radius absent anogenital anomalies --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:radius absent anogenital anomalies | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  304. en:roentgenographic --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:roentgenographic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  305. en:sex chromosome aberrations --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:sex chromosome aberrations | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  306. en:split-hand/foot malformation 2 --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:split-hand/foot malformation 2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  307. en:terminal osseous dysplasia and pigmentary defects --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:terminal osseous dysplasia and pigmentary defects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  308. en:thrombophilia, x-linked, due to factor ix defect --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:thrombophilia, x-linked, due to factor ix defect | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  309. en:tooth agenesis, selective, x-linked, 1 --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:tooth agenesis, selective, x-linked, 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  310. en:vasquez hurst sotos syndrome --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:vasquez hurst sotos syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  311. en:wells jankovic syndrome --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:wells jankovic syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  312. en:x-linked tetra-amelia --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=en:x-linked tetra-amelia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  313. maladies liées au chromosome x --- r_associated #0: 27 --> en:genetic diseases, x-linked
    n1=maladies liées au chromosome x | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=27
  314. Goltz (syndrome de) --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=Goltz (syndrome de) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  315. Marfan (maladie de) --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=Marfan (maladie de) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  316. dyskératose congénitale --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=dyskératose congénitale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  317. en:Martin-Bell's syndrome --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:Martin-Bell's syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  318. en:abruzzo erickson syndrome --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:abruzzo erickson syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  319. en:anencephaly and spina bifida x-linked --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:anencephaly and spina bifida x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  320. en:aspects of mortality statistics --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:aspects of mortality statistics | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  321. en:brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  322. en:cardiomyopathy, dilated, 3a --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:cardiomyopathy, dilated, 3a | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  323. en:cone-rod dystrophy, x-linked, 3 --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:cone-rod dystrophy, x-linked, 3 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  324. en:glycogen storage disease type viii --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:glycogen storage disease type viii | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  325. en:hajdu-cheney syndrome --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:hajdu-cheney syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  326. en:hydrocephalus with cerebellar agenesis --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:hydrocephalus with cerebellar agenesis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  327. en:liver glycogenosis, x-linked, type ii --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:liver glycogenosis, x-linked, type ii | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  328. en:major affective disorder 2 --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:major affective disorder 2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  329. en:martin-probst deafness-mental retardation syndrome --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:martin-probst deafness-mental retardation syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  330. en:mental retardation, x-linked, syndromic, christianson type --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:mental retardation, x-linked, syndromic, christianson type | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  331. en:nemo mutation with immunodeficiency --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:nemo mutation with immunodeficiency | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  332. en:neuropathy, hereditary sensory, x-linked --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:neuropathy, hereditary sensory, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  333. en:neutropenia, severe congenital, x-linked --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:neutropenia, severe congenital, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  334. en:ovarian dysgenesis 2 --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:ovarian dysgenesis 2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  335. en:primary hypertrophic osteoarthropathy --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:primary hypertrophic osteoarthropathy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  336. en:rolandic epilepsy, mental retardation, and speech dyspraxia, x-linked --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:rolandic epilepsy, mental retardation, and speech dyspraxia, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  337. en:skin diseases, genetic --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:skin diseases, genetic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  338. en:spina bifida, x-linked --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:spina bifida, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  339. en:thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  340. en:thrombocytopenia, x-linked, intermittent --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:thrombocytopenia, x-linked, intermittent | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  341. en:x chromosome-linked pyridoxine refractory sideroblastic anemia --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:x chromosome-linked pyridoxine refractory sideroblastic anemia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  342. en:x-linked hydrocephalus syndrome --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=en:x-linked hydrocephalus syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  343. maladies génétiques liées au chromosome x --- r_associated #0: 26 --> en:genetic diseases, x-linked
    n1=maladies génétiques liées au chromosome x | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=26
  344. dysimmune (neuropathie) --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=dysimmune (neuropathie) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  345. en:Eddowes's disease --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:Eddowes's disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  346. en:arthrogryposis multiplex congenita, distal, x-linked --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:arthrogryposis multiplex congenita, distal, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  347. en:cone dystrophy, x-linked, 1 --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:cone dystrophy, x-linked, 1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  348. en:hereditary macular epidermolysis bullosa --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:hereditary macular epidermolysis bullosa | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  349. en:heterotaxy, visceral, 1, x-linked --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:heterotaxy, visceral, 1, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  350. en:hypertrichosis, congenital generalized --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:hypertrichosis, congenital generalized | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  351. en:leigh syndrome, x-linked --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:leigh syndrome, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  352. en:mental retardation, skeletal dysplasia, and abducens palsy --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:mental retardation, skeletal dysplasia, and abducens palsy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  353. en:microphthalmia, syndromic 7 --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:microphthalmia, syndromic 7 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  354. en:nephrogenic syndrome of inappropriate antidiuresis --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:nephrogenic syndrome of inappropriate antidiuresis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  355. en:properdin deficiency, x-linked --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:properdin deficiency, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  356. en:radiation sensitivity of natural killer activity --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:radiation sensitivity of natural killer activity | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  357. en:radiotherapeutic --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:radiotherapeutic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  358. en:use of ultrasonography --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:use of ultrasonography | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  359. en:xiap deficiency --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=en:xiap deficiency | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  360. hypogonadisme avec anosmie --- r_associated #0: 25 --> en:genetic diseases, x-linked
    n1=hypogonadisme avec anosmie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=25
  361. en:arachnodactily --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:arachnodactily | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  362. en:autoimmune lymphoproliferative syndrome --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:autoimmune lymphoproliferative syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  363. en:chromosomal aberration --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:chromosomal aberration | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  364. en:congenital idiopathic intestinal pseudoobstruction --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:congenital idiopathic intestinal pseudoobstruction | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  365. en:ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  366. en:epidemiological --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:epidemiological | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  367. en:in blood --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:in blood | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  368. en:in urine --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:in urine | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  369. en:kartagener syndrome --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:kartagener syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  370. en:night blindness, congenital stationary --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:night blindness, congenital stationary | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  371. en:optic atrophy 2 (disorder) --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:optic atrophy 2 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  372. en:phosphoglycerate kinase 1 deficiency --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:phosphoglycerate kinase 1 deficiency | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  373. en:rehabilitation aspects --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:rehabilitation aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  374. en:spastic paraplegia 16, x-linked (disorder) --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:spastic paraplegia 16, x-linked (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  375. en:vacterl association with hydrocephalus --- r_associated #0: 24 --> en:genetic diseases, x-linked
    n1=en:vacterl association with hydrocephalus | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=24
  376. en:bornholm eye disease --- r_associated #0: 23 --> en:genetic diseases, x-linked
    n1=en:bornholm eye disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=23
  377. en:congenital myasthenic syndrome --- r_associated #0: 23 --> en:genetic diseases, x-linked
    n1=en:congenital myasthenic syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=23
  378. en:embryologic --- r_associated #0: 23 --> en:genetic diseases, x-linked
    n1=en:embryologic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=23
  379. en:loeys-dietz syndrome --- r_associated #0: 23 --> en:genetic diseases, x-linked
    n1=en:loeys-dietz syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=23
  380. en:pathological aspects --- r_associated #0: 23 --> en:genetic diseases, x-linked
    n1=en:pathological aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=23
  381. en:spastic paraplegia 2, x-linked (disorder) --- r_associated #0: 23 --> en:genetic diseases, x-linked
    n1=en:spastic paraplegia 2, x-linked (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=23
  382. en:surgical aspects --- r_associated #0: 23 --> en:genetic diseases, x-linked
    n1=en:surgical aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=23
  383. en:thrombocytopenia 1 (disorder) --- r_associated #0: 23 --> en:genetic diseases, x-linked
    n1=en:thrombocytopenia 1 (disorder) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=23
  384. ethnologique --- r_associated #0: 23 --> en:genetic diseases, x-linked
    n1=ethnologique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=23
  385. en:atypical mycobacteriosis, familial, x-linked 2 --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=en:atypical mycobacteriosis, familial, x-linked 2 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  386. en:corpus callosum, partial agenesis of, x-linked --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=en:corpus callosum, partial agenesis of, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  387. en:diagnosis aspect --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=en:diagnosis aspect | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  388. en:glycogen storage disease type ixd --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=en:glycogen storage disease type ixd | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  389. en:in cerebrospinal fluid --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=en:in cerebrospinal fluid | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  390. en:nutritional management --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=en:nutritional management | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  391. en:onychoosteodysostosis --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=en:onychoosteodysostosis | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  392. en:spurway-eddowes syndrome --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=en:spurway-eddowes syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  393. en:veterinary aspects --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=en:veterinary aspects | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  394. maladie de Bowen --- r_associated #0: 22 --> en:genetic diseases, x-linked
    n1=maladie de Bowen | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=22
  395. alopécie congénitale --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=alopécie congénitale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  396. choroïdérémie --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=choroïdérémie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  397. déficit enzymatique partiel de la surrénale --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=déficit enzymatique partiel de la surrénale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  398. en:Adair Dighton's syndrome --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=en:Adair Dighton's syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  399. en:cataract, congenital, with microcornea or slight microphthalmia --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=en:cataract, congenital, with microcornea or slight microphthalmia | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  400. en:genes, x-linked --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=en:genes, x-linked | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  401. en:nasodigitoacoustic syndrome --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=en:nasodigitoacoustic syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  402. en:physiopathological --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=en:physiopathological | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  403. en:spinocerebellar ataxia, x-linked 3 --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=en:spinocerebellar ataxia, x-linked 3 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  404. en:surfactant metabolism dysfunction, pulmonary, 4 --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=en:surfactant metabolism dysfunction, pulmonary, 4 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  405. fragilité osseuse héréditaire --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=fragilité osseuse héréditaire | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  406. syndrome de Zinsser-Engman-Cole --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=syndrome de Zinsser-Engman-Cole | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  407. syndrome des ongles jaunes --- r_associated #0: 21 --> en:genetic diseases, x-linked
    n1=syndrome des ongles jaunes | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=21
  408. dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:genetic diseases, x-linked
    n1=dysplasie olfactogénitale de De Morsier | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=20
  409. en:prevention & control --- r_associated #0: 20 --> en:genetic diseases, x-linked
    n1=en:prevention & control | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=20
  410. Chernosky (hyperpigmentation familiale progressive de) --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=Chernosky (hyperpigmentation familiale progressive de) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  411. Enzymologie --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=Enzymologie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  412. Hyperplasie congénitale des surrénales --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=Hyperplasie congénitale des surrénales | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  413. Kallman --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=Kallman | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  414. Maladie de Marfan --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=Maladie de Marfan | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  415. Maladies liées à l'X --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=Maladies liées à l'X | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  416. Parasitologie --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=Parasitologie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  417. goltz --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=goltz | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  418. hémoglobine modifiée (solution d') --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=hémoglobine modifiée (solution d') | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  419. syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=syndrome de Kallman-de Morsier | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  420. syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:genetic diseases, x-linked
    n1=syndrome de de Morsier-Kallmann | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=15
  421. lepréchaunisme --- r_associated #0: 11 --> en:genetic diseases, x-linked
    n1=lepréchaunisme | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=11
  422. Anomalie chromosomique --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=Anomalie chromosomique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  423. CX3CL1 --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=CX3CL1 | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  424. Hémoglobinopathie --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=Hémoglobinopathie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  425. Martin-Bell (syndrome de) --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=Martin-Bell (syndrome de) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  426. Paraquat ® (intoxication par le) --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=Paraquat ® (intoxication par le) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  427. Yellen-Gomco (clamp de) --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=Yellen-Gomco (clamp de) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  428. aberration chromosomique --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=aberration chromosomique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  429. dyskaliémie --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=dyskaliémie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  430. dyskèle --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=dyskèle | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  431. dyskératome verruqueux --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=dyskératome verruqueux | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  432. dyskératose --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=dyskératose | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  433. dyskératose acantholytique focale --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=dyskératose acantholytique focale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  434. dyskératose bénigne héréditaire intraépithéliale --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=dyskératose bénigne héréditaire intraépithéliale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  435. dyskératose héréditaire bénigne intraépithéliale --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=dyskératose héréditaire bénigne intraépithéliale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  436. dystrophie musculaire --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=dystrophie musculaire | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  437. en:Bowen's disease --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:Bowen's disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  438. en:Dent's disease --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:Dent's disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  439. en:Zinsser-Cole-Engman's syndrome --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:Zinsser-Cole-Engman's syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  440. en:Zinsser-Cole-Engman?s syndrome --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:Zinsser-Cole-Engman?s syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  441. en:cell free haemoglobin solution --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:cell free haemoglobin solution | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  442. en:chromosomal disorder --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:chromosomal disorder | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  443. en:dysimmune neuropathy --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:dysimmune neuropathy | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  444. en:ethnological --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:ethnological | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  445. en:haemophilia B --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:haemophilia B | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  446. en:modified haemoglobin solution --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:modified haemoglobin solution | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  447. en:ocular form --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:ocular form | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  448. en:progressively deforming --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:progressively deforming | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  449. en:radiographic --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:radiographic | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  450. en:with normal sclerae --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:with normal sclerae | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  451. en:xanthonychia syndrome --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:xanthonychia syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  452. en:xanthonychie --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=en:xanthonychie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  453. maladies liées à l'X --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=maladies liées à l'X | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  454. mucoviscidose --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=mucoviscidose | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  455. nanisme --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=nanisme | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  456. ostéoporose-pseudogliome (syndrome) --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=ostéoporose-pseudogliome (syndrome) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  457. paraplégie spastique dans la syphilis congénitale --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=paraplégie spastique dans la syphilis congénitale | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  458. syndrome de Bridges et Good --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=syndrome de Bridges et Good | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  459. syndrome de de Morsier --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=syndrome de de Morsier | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  460. syndrome de zinsser-engman-cole --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=syndrome de zinsser-engman-cole | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  461. taxinomique --- r_associated #0: 10 --> en:genetic diseases, x-linked
    n1=taxinomique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=10
  462. Bowen (maladie de) --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=Bowen (maladie de) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  463. Lobstein-van der Hoeve (syndrome de) --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=Lobstein-van der Hoeve (syndrome de) | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  464. Maladie de Bowen --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=Maladie de Bowen | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  465. Microbiologique --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=Microbiologique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  466. Onsager (relation d') --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=Onsager (relation d') | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  467. dyskératose congénitale de Scoggins --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=dyskératose congénitale de Scoggins | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  468. dyskératose folliculaire --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=dyskératose folliculaire | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  469. dyskératose folliculaire isolée --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=dyskératose folliculaire isolée | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  470. en:Cole's syndrome --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=en:Cole's syndrome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  471. en:bowen's disease --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=en:bowen's disease | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  472. hémoglobine Portland --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=hémoglobine Portland | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  473. hémoglobine S --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=hémoglobine S | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  474. hémoglobinique a --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=hémoglobinique a | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  475. hémoglobinobilie --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=hémoglobinobilie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  476. hémoglobinogenèse --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=hémoglobinogenèse | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  477. hémoglobinomètre --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=hémoglobinomètre | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  478. hémoglobinomètrie --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=hémoglobinomètrie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  479. hémoglobinémie --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=hémoglobinémie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  480. myopathie primitive progressive --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=myopathie primitive progressive | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  481. onychodysplasie --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=onychodysplasie | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  482. onychogryphose --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=onychogryphose | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  483. onycholyse --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=onycholyse | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  484. onycholyse candidosique --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=onycholyse candidosique | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  485. onycholyse semi-lunaire partielle --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=onycholyse semi-lunaire partielle | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  486. onychomadèse --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=onychomadèse | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  487. onychomatricome --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=onychomatricome | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  488. syndrome lymphoprolifératif avec autoimmunité --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=syndrome lymphoprolifératif avec autoimmunité | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  489. syndrome olfacto-génital --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=syndrome olfacto-génital | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=5
  490. troubles de la coagulation sanguine, héréditaires --- r_associated #0: 5 --> en:genetic diseases, x-linked
    n1=troubles de la coagulation sanguine, héréditaires | n2=en:genetic diseases, x-linked | 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