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'en:genetic diseases, inborn'
(id=6913426 ; fe=en:genetic diseases, inborn ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=18078 creation date=2017-06-25 touchdate=2025-08-27 16:39:02.000)
≈ 209 relations sortantes

  1. en:genetic diseases, inborn -- r_associated #0: 43 / 1 -> en:microbiological
    n1=en:genetic diseases, inborn | n2=en:microbiological | rel=r_associated | relid=0 | w=43
  2. en:genetic diseases, inborn -- r_associated #0: 43 / 1 -> en:viruses
    n1=en:genetic diseases, inborn | n2=en:viruses | rel=r_associated | relid=0 | w=43
  3. en:genetic diseases, inborn -- r_associated #0: 42 / 0.977 -> en:fetal disorder
    n1=en:genetic diseases, inborn | n2=en:fetal disorder | rel=r_associated | relid=0 | w=42
  4. en:genetic diseases, inborn -- r_associated #0: 40 / 0.93 -> en:pycnodysostosis
    n1=en:genetic diseases, inborn | n2=en:pycnodysostosis | rel=r_associated | relid=0 | w=40
  5. en:genetic diseases, inborn -- r_associated #0: 38 / 0.884 -> en:cherubism
    n1=en:genetic diseases, inborn | n2=en:cherubism | rel=r_associated | relid=0 | w=38
  6. en:genetic diseases, inborn -- r_associated #0: 37 / 0.86 -> en:werner syndrome
    n1=en:genetic diseases, inborn | n2=en:werner syndrome | rel=r_associated | relid=0 | w=37
  7. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:acth deficiency, isolated
    n1=en:genetic diseases, inborn | n2=en:acth deficiency, isolated | rel=r_associated | relid=0 | w=35
  8. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:aspects of mortality statistics
    n1=en:genetic diseases, inborn | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=35
  9. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:ataxia telangiectasia syndrome
    n1=en:genetic diseases, inborn | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=35
  10. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:autoimmune lymphoproliferative syndrome
    n1=en:genetic diseases, inborn | n2=en:autoimmune lymphoproliferative syndrome | rel=r_associated | relid=0 | w=35
  11. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:congenital hypoplastic anemia
    n1=en:genetic diseases, inborn | n2=en:congenital hypoplastic anemia | rel=r_associated | relid=0 | w=35
  12. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:donohue syndrome
    n1=en:genetic diseases, inborn | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=35
  13. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:genetic disorder
    n1=en:genetic diseases, inborn | n2=en:genetic disorder | rel=r_associated | relid=0 | w=35
  14. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:hajdu-cheney syndrome
    n1=en:genetic diseases, inborn | n2=en:hajdu-cheney syndrome | rel=r_associated | relid=0 | w=35
  15. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:parotidomegaly, hereditary bilateral
    n1=en:genetic diseases, inborn | n2=en:parotidomegaly, hereditary bilateral | rel=r_associated | relid=0 | w=35
  16. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:pelger-huet anomaly
    n1=en:genetic diseases, inborn | n2=en:pelger-huet anomaly | rel=r_associated | relid=0 | w=35
  17. en:genetic diseases, inborn -- r_associated #0: 35 / 0.814 -> en:pulmonary alveolar microlithiasis
    n1=en:genetic diseases, inborn | n2=en:pulmonary alveolar microlithiasis | rel=r_associated | relid=0 | w=35
  18. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:autosomal recessive polycystic kidney disease
    n1=en:genetic diseases, inborn | n2=en:autosomal recessive polycystic kidney disease | rel=r_associated | relid=0 | w=34
  19. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:blood coagulation disorders, inherited
    n1=en:genetic diseases, inborn | n2=en:blood coagulation disorders, inherited | rel=r_associated | relid=0 | w=34
  20. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:corticosteroid-binding globulin deficiency
    n1=en:genetic diseases, inborn | n2=en:corticosteroid-binding globulin deficiency | rel=r_associated | relid=0 | w=34
  21. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:cryoglobulinemia, familial mixed
    n1=en:genetic diseases, inborn | n2=en:cryoglobulinemia, familial mixed | rel=r_associated | relid=0 | w=34
  22. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:etiology aspects
    n1=en:genetic diseases, inborn | n2=en:etiology aspects | rel=r_associated | relid=0 | w=34
  23. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:genetic diseases, x-linked
    n1=en:genetic diseases, inborn | n2=en:genetic diseases, x-linked | rel=r_associated | relid=0 | w=34
  24. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:hereditary myopathy with early respiratory failure
    n1=en:genetic diseases, inborn | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=34
  25. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:hypoprolactinemia
    n1=en:genetic diseases, inborn | n2=en:hypoprolactinemia | rel=r_associated | relid=0 | w=34
  26. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:in blood
    n1=en:genetic diseases, inborn | n2=en:in blood | rel=r_associated | relid=0 | w=34
  27. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:loeys-dietz syndrome
    n1=en:genetic diseases, inborn | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=34
  28. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:neutropenia, nonimmune chronic idiopathic, adult
    n1=en:genetic diseases, inborn | n2=en:neutropenia, nonimmune chronic idiopathic, adult | rel=r_associated | relid=0 | w=34
  29. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:parasitology
    n1=en:genetic diseases, inborn | n2=en:parasitology | rel=r_associated | relid=0 | w=34
  30. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:rh deficiency syndrome
    n1=en:genetic diseases, inborn | n2=en:rh deficiency syndrome | rel=r_associated | relid=0 | w=34
  31. en:genetic diseases, inborn -- r_associated #0: 34 / 0.791 -> en:taxonomic
    n1=en:genetic diseases, inborn | n2=en:taxonomic | rel=r_associated | relid=0 | w=34
  32. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:alagille syndrome
    n1=en:genetic diseases, inborn | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=32
  33. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:congenital pain insensitivity
    n1=en:genetic diseases, inborn | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=32
  34. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:defects, single-gene
    n1=en:genetic diseases, inborn | n2=en:defects, single-gene | rel=r_associated | relid=0 | w=32
  35. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:frasier syndrome
    n1=en:genetic diseases, inborn | n2=en:frasier syndrome | rel=r_associated | relid=0 | w=32
  36. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:genetic aspects
    n1=en:genetic diseases, inborn | n2=en:genetic aspects | rel=r_associated | relid=0 | w=32
  37. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:heredodegenerative disorders, nervous system
    n1=en:genetic diseases, inborn | n2=en:heredodegenerative disorders, nervous system | rel=r_associated | relid=0 | w=32
  38. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:historical aspects qualifier
    n1=en:genetic diseases, inborn | n2=en:historical aspects qualifier | rel=r_associated | relid=0 | w=32
  39. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:in urine
    n1=en:genetic diseases, inborn | n2=en:in urine | rel=r_associated | relid=0 | w=32
  40. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:physiopathological
    n1=en:genetic diseases, inborn | n2=en:physiopathological | rel=r_associated | relid=0 | w=32
  41. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:radiotherapeutic
    n1=en:genetic diseases, inborn | n2=en:radiotherapeutic | rel=r_associated | relid=0 | w=32
  42. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> en:surgical aspects
    n1=en:genetic diseases, inborn | n2=en:surgical aspects | rel=r_associated | relid=0 | w=32
  43. en:genetic diseases, inborn -- r_associated #0: 32 / 0.744 -> génopathies
    n1=en:genetic diseases, inborn | n2=génopathies | rel=r_associated | relid=0 | w=32
  44. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:adrenocortical hypofunction, chronic primary congenital
    n1=en:genetic diseases, inborn | n2=en:adrenocortical hypofunction, chronic primary congenital | rel=r_associated | relid=0 | w=31
  45. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:aspects of radionuclide imaging
    n1=en:genetic diseases, inborn | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=31
  46. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:ataxic cerebral palsy
    n1=en:genetic diseases, inborn | n2=en:ataxic cerebral palsy | rel=r_associated | relid=0 | w=31
  47. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:atrial standstill
    n1=en:genetic diseases, inborn | n2=en:atrial standstill | rel=r_associated | relid=0 | w=31
  48. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:brugada syndrome ventricular arrhythmia by ecg finding
    n1=en:genetic diseases, inborn | n2=en:brugada syndrome ventricular arrhythmia by ecg finding | rel=r_associated | relid=0 | w=31
  49. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:chemically induced
    n1=en:genetic diseases, inborn | n2=en:chemically induced | rel=r_associated | relid=0 | w=31
  50. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:congenital myasthenic syndrome
    n1=en:genetic diseases, inborn | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=31
  51. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:genetic diseases, y-linked
    n1=en:genetic diseases, inborn | n2=en:genetic diseases, y-linked | rel=r_associated | relid=0 | w=31
  52. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:hereditary angioedema
    n1=en:genetic diseases, inborn | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=31
  53. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:histiocytosis, familial lipochrome
    n1=en:genetic diseases, inborn | n2=en:histiocytosis, familial lipochrome | rel=r_associated | relid=0 | w=31
  54. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:kallmann syndrome
    n1=en:genetic diseases, inborn | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=31
  55. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:platelet glycoprotein iv deficiency
    n1=en:genetic diseases, inborn | n2=en:platelet glycoprotein iv deficiency | rel=r_associated | relid=0 | w=31
  56. en:genetic diseases, inborn -- r_associated #0: 31 / 0.721 -> en:veterinary aspects
    n1=en:genetic diseases, inborn | n2=en:veterinary aspects | rel=r_associated | relid=0 | w=31
  57. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:complement factor i (c3 inactivator) deficiency
    n1=en:genetic diseases, inborn | n2=en:complement factor i (c3 inactivator) deficiency | rel=r_associated | relid=0 | w=30
  58. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:congenital hepatic fibrosis
    n1=en:genetic diseases, inborn | n2=en:congenital hepatic fibrosis | rel=r_associated | relid=0 | w=30
  59. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:epistaxis, hereditary
    n1=en:genetic diseases, inborn | n2=en:epistaxis, hereditary | rel=r_associated | relid=0 | w=30
  60. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:exposure as collected domain
    n1=en:genetic diseases, inborn | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=30
  61. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:genetic disorders screening
    n1=en:genetic diseases, inborn | n2=en:genetic disorders screening | rel=r_associated | relid=0 | w=30
  62. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:hereditary autoinflammatory diseases
    n1=en:genetic diseases, inborn | n2=en:hereditary autoinflammatory diseases | rel=r_associated | relid=0 | w=30
  63. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:immunology aspects
    n1=en:genetic diseases, inborn | n2=en:immunology aspects | rel=r_associated | relid=0 | w=30
  64. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:kartagener syndrome
    n1=en:genetic diseases, inborn | n2=en:kartagener syndrome | rel=r_associated | relid=0 | w=30
  65. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:lennox-gastaut syndrome
    n1=en:genetic diseases, inborn | n2=en:lennox-gastaut syndrome | rel=r_associated | relid=0 | w=30
  66. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:nail-patella syndrome
    n1=en:genetic diseases, inborn | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=30
  67. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:osteogenesis imperfecta
    n1=en:genetic diseases, inborn | n2=en:osteogenesis imperfecta | rel=r_associated | relid=0 | w=30
  68. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:pharmacotherapeutic
    n1=en:genetic diseases, inborn | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=30
  69. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:roentgenographic
    n1=en:genetic diseases, inborn | n2=en:roentgenographic | rel=r_associated | relid=0 | w=30
  70. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> en:skin diseases, genetic
    n1=en:genetic diseases, inborn | n2=en:skin diseases, genetic | rel=r_associated | relid=0 | w=30
  71. en:genetic diseases, inborn -- r_associated #0: 30 / 0.698 -> syndrome de Marfan
    n1=en:genetic diseases, inborn | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=30
  72. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:cadasil syndrome
    n1=en:genetic diseases, inborn | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=29
  73. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:camurati-engelmann syndrome
    n1=en:genetic diseases, inborn | n2=en:camurati-engelmann syndrome | rel=r_associated | relid=0 | w=29
  74. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:chromosome disorder
    n1=en:genetic diseases, inborn | n2=en:chromosome disorder | rel=r_associated | relid=0 | w=29
  75. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:complication aspects
    n1=en:genetic diseases, inborn | n2=en:complication aspects | rel=r_associated | relid=0 | w=29
  76. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:congenital adrenal hyperplasia
    n1=en:genetic diseases, inborn | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=29
  77. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:congenital metabolic disorder
    n1=en:genetic diseases, inborn | n2=en:congenital metabolic disorder | rel=r_associated | relid=0 | w=29
  78. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:congenital, hereditary, and neonatal diseases and abnormalities
    n1=en:genetic diseases, inborn | n2=en:congenital, hereditary, and neonatal diseases and abnormalities | rel=r_associated | relid=0 | w=29
  79. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:dwarfism
    n1=en:genetic diseases, inborn | n2=en:dwarfism | rel=r_associated | relid=0 | w=29
  80. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:ethnologic
    n1=en:genetic diseases, inborn | n2=en:ethnologic | rel=r_associated | relid=0 | w=29
  81. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:in cerebrospinal fluid
    n1=en:genetic diseases, inborn | n2=en:in cerebrospinal fluid | rel=r_associated | relid=0 | w=29
  82. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:neonatal disorder
    n1=en:genetic diseases, inborn | n2=en:neonatal disorder | rel=r_associated | relid=0 | w=29
  83. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:nursing therapy
    n1=en:genetic diseases, inborn | n2=en:nursing therapy | rel=r_associated | relid=0 | w=29
  84. en:genetic diseases, inborn -- r_associated #0: 29 / 0.674 -> en:pathological aspects
    n1=en:genetic diseases, inborn | n2=en:pathological aspects | rel=r_associated | relid=0 | w=29
  85. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:cirrhosis, familial
    n1=en:genetic diseases, inborn | n2=en:cirrhosis, familial | rel=r_associated | relid=0 | w=28
  86. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:diagnosis aspect
    n1=en:genetic diseases, inborn | n2=en:diagnosis aspect | rel=r_associated | relid=0 | w=28
  87. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:embryologic
    n1=en:genetic diseases, inborn | n2=en:embryologic | rel=r_associated | relid=0 | w=28
  88. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:epidemiologic
    n1=en:genetic diseases, inborn | n2=en:epidemiologic | rel=r_associated | relid=0 | w=28
  89. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:familial hypertrophic cardiomyopathy
    n1=en:genetic diseases, inborn | n2=en:familial hypertrophic cardiomyopathy | rel=r_associated | relid=0 | w=28
  90. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:hemoglobinopathy
    n1=en:genetic diseases, inborn | n2=en:hemoglobinopathy | rel=r_associated | relid=0 | w=28
  91. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:hereditary hemolytic anemia
    n1=en:genetic diseases, inborn | n2=en:hereditary hemolytic anemia | rel=r_associated | relid=0 | w=28
  92. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:hyperthyroxinemia, familial dysalbuminemic
    n1=en:genetic diseases, inborn | n2=en:hyperthyroxinemia, familial dysalbuminemic | rel=r_associated | relid=0 | w=28
  93. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:medical genetics
    n1=en:genetic diseases, inborn | n2=en:medical genetics | rel=r_associated | relid=0 | w=28
  94. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:muscular dystrophy
    n1=en:genetic diseases, inborn | n2=en:muscular dystrophy | rel=r_associated | relid=0 | w=28
  95. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:nutritional management
    n1=en:genetic diseases, inborn | n2=en:nutritional management | rel=r_associated | relid=0 | w=28
  96. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> en:yellow nail syndrome
    n1=en:genetic diseases, inborn | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=28
  97. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> maladie génétique
    n1=en:genetic diseases, inborn | n2=maladie génétique | rel=r_associated | relid=0 | w=28
  98. en:genetic diseases, inborn -- r_associated #0: 28 / 0.651 -> maladies génétiques congénitales
    n1=en:genetic diseases, inborn | n2=maladies génétiques congénitales | rel=r_associated | relid=0 | w=28
  99. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> en:alpha-2-deficient collagen disease
    n1=en:genetic diseases, inborn | n2=en:alpha-2-deficient collagen disease | rel=r_associated | relid=0 | w=27
  100. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> en:charge syndrome
    n1=en:genetic diseases, inborn | n2=en:charge syndrome | rel=r_associated | relid=0 | w=27
  101. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> en:cystic fibrosis
    n1=en:genetic diseases, inborn | n2=en:cystic fibrosis | rel=r_associated | relid=0 | w=27
  102. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> en:desquamative interstitial pneumonia
    n1=en:genetic diseases, inborn | n2=en:desquamative interstitial pneumonia | rel=r_associated | relid=0 | w=27
  103. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> en:eye diseases, hereditary
    n1=en:genetic diseases, inborn | n2=en:eye diseases, hereditary | rel=r_associated | relid=0 | w=27
  104. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> en:hyperimmunoglobulin m syndrome
    n1=en:genetic diseases, inborn | n2=en:hyperimmunoglobulin m syndrome | rel=r_associated | relid=0 | w=27
  105. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> en:marfan syndrome
    n1=en:genetic diseases, inborn | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=27
  106. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> en:primary hypertrophic osteoarthropathy
    n1=en:genetic diseases, inborn | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=27
  107. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> en:therapeutic aspects
    n1=en:genetic diseases, inborn | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=27
  108. en:genetic diseases, inborn -- r_associated #0: 27 / 0.628 -> maladie héréditaire
    n1=en:genetic diseases, inborn | n2=maladie héréditaire | rel=r_associated | relid=0 | w=27
  109. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:alpha-1 antitrypsin deficiency
    n1=en:genetic diseases, inborn | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=26
  110. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:congenital abnormality
    n1=en:genetic diseases, inborn | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=26
  111. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:costello syndrome
    n1=en:genetic diseases, inborn | n2=en:costello syndrome | rel=r_associated | relid=0 | w=26
  112. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:enzymology
    n1=en:genetic diseases, inborn | n2=en:enzymology | rel=r_associated | relid=0 | w=26
  113. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:hereditary neoplastic syndrome
    n1=en:genetic diseases, inborn | n2=en:hereditary neoplastic syndrome | rel=r_associated | relid=0 | w=26
  114. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:metabolic aspects
    n1=en:genetic diseases, inborn | n2=en:metabolic aspects | rel=r_associated | relid=0 | w=26
  115. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:osteochondrodysplasia
    n1=en:genetic diseases, inborn | n2=en:osteochondrodysplasia | rel=r_associated | relid=0 | w=26
  116. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:psychology qualifier
    n1=en:genetic diseases, inborn | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=26
  117. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:rehabilitation aspects
    n1=en:genetic diseases, inborn | n2=en:rehabilitation aspects | rel=r_associated | relid=0 | w=26
  118. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> en:use of ultrasonography
    n1=en:genetic diseases, inborn | n2=en:use of ultrasonography | rel=r_associated | relid=0 | w=26
  119. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> maladie de Marfan
    n1=en:genetic diseases, inborn | n2=maladie de Marfan | rel=r_associated | relid=0 | w=26
  120. en:genetic diseases, inborn -- r_associated #0: 26 / 0.605 -> maladie génétique congénitale
    n1=en:genetic diseases, inborn | n2=maladie génétique congénitale | rel=r_associated | relid=0 | w=26
  121. en:genetic diseases, inborn -- r_associated #0: 25 / 0.581 -> en:genetic
    n1=en:genetic diseases, inborn | n2=en:genetic | rel=r_associated | relid=0 | w=25
  122. en:genetic diseases, inborn -- r_associated #0: 24 / 0.558 -> anomalie congénitale
    n1=en:genetic diseases, inborn | n2=anomalie congénitale | rel=r_associated | relid=0 | w=24
  123. en:genetic diseases, inborn -- r_associated #0: 22 / 0.512 -> anomalie héréditaire
    n1=en:genetic diseases, inborn | n2=anomalie héréditaire | rel=r_associated | relid=0 | w=22
  124. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> angiofibromatose hépatique
    n1=en:genetic diseases, inborn | n2=angiofibromatose hépatique | rel=r_associated | relid=0 | w=20
  125. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> anomalie chromosomique
    n1=en:genetic diseases, inborn | n2=anomalie chromosomique | rel=r_associated | relid=0 | w=20
  126. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> anomalie cytogénétique
    n1=en:genetic diseases, inborn | n2=anomalie cytogénétique | rel=r_associated | relid=0 | w=20
  127. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> anomalie du développement
    n1=en:genetic diseases, inborn | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
  128. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> anormalité des chromosomes
    n1=en:genetic diseases, inborn | n2=anormalité des chromosomes | rel=r_associated | relid=0 | w=20
  129. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> arachnodactylie
    n1=en:genetic diseases, inborn | n2=arachnodactylie | rel=r_associated | relid=0 | w=20
  130. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> arrêt auriculaire
    n1=en:genetic diseases, inborn | n2=arrêt auriculaire | rel=r_associated | relid=0 | w=20
  131. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> chérubisme
    n1=en:genetic diseases, inborn | n2=chérubisme | rel=r_associated | relid=0 | w=20
  132. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> déficience congénitale
    n1=en:genetic diseases, inborn | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
  133. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> déformation congénitale
    n1=en:genetic diseases, inborn | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
  134. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> difformité congénitale
    n1=en:genetic diseases, inborn | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
  135. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:arachnodactily
    n1=en:genetic diseases, inborn | n2=en:arachnodactily | rel=r_associated | relid=0 | w=20
  136. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:arachnodactyly
    n1=en:genetic diseases, inborn | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20
  137. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:auricular standstill
    n1=en:genetic diseases, inborn | n2=en:auricular standstill | rel=r_associated | relid=0 | w=20
  138. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:birth defect
    n1=en:genetic diseases, inborn | n2=en:birth defect | rel=r_associated | relid=0 | w=20
  139. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:brittle bone disease
    n1=en:genetic diseases, inborn | n2=en:brittle bone disease | rel=r_associated | relid=0 | w=20
  140. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:chromosomal aberration
    n1=en:genetic diseases, inborn | n2=en:chromosomal aberration | rel=r_associated | relid=0 | w=20
  141. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:chromosomal abnormality
    n1=en:genetic diseases, inborn | n2=en:chromosomal abnormality | rel=r_associated | relid=0 | w=20
  142. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:congenital anomaly
    n1=en:genetic diseases, inborn | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
  143. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:congenital defect
    n1=en:genetic diseases, inborn | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
  144. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:congenital malformation
    n1=en:genetic diseases, inborn | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
  145. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:developmental fault
    n1=en:genetic diseases, inborn | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
  146. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:Donohue syndrome
    n1=en:genetic diseases, inborn | n2=en:Donohue syndrome | rel=r_associated | relid=0 | w=20
  147. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:Eddowes's disease
    n1=en:genetic diseases, inborn | n2=en:Eddowes's disease | rel=r_associated | relid=0 | w=20
  148. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:genetic condition
    n1=en:genetic diseases, inborn | n2=en:genetic condition | rel=r_associated | relid=0 | w=20
  149. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:genetic disease
    n1=en:genetic diseases, inborn | n2=en:genetic disease | rel=r_associated | relid=0 | w=20
  150. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:genetic illness
    n1=en:genetic diseases, inborn | n2=en:genetic illness | rel=r_associated | relid=0 | w=20
  151. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:hemoglobin related disease
    n1=en:genetic diseases, inborn | n2=en:hemoglobin related disease | rel=r_associated | relid=0 | w=20
  152. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:hereditary disease
    n1=en:genetic diseases, inborn | n2=en:hereditary disease | rel=r_associated | relid=0 | w=20
  153. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:Lennox Gastaut's syndrome
    n1=en:genetic diseases, inborn | n2=en:Lennox Gastaut's syndrome | rel=r_associated | relid=0 | w=20
  154. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:major physical defect
    n1=en:genetic diseases, inborn | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
  155. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:Marfan's disease
    n1=en:genetic diseases, inborn | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20
  156. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:marfan's syndrome
    n1=en:genetic diseases, inborn | n2=en:marfan's syndrome | rel=r_associated | relid=0 | w=20
  157. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:Marfan's syndrome
    n1=en:genetic diseases, inborn | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20
  158. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:OI
    n1=en:genetic diseases, inborn | n2=en:OI | rel=r_associated | relid=0 | w=20
  159. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:onychoosteodysostosis
    n1=en:genetic diseases, inborn | n2=en:onychoosteodysostosis | rel=r_associated | relid=0 | w=20
  160. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:Osteogenesis imperfecta
    n1=en:genetic diseases, inborn | n2=en:Osteogenesis imperfecta | rel=r_associated | relid=0 | w=20
  161. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:osteopsathyrosis
    n1=en:genetic diseases, inborn | n2=en:osteopsathyrosis | rel=r_associated | relid=0 | w=20
  162. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:physical defect
    n1=en:genetic diseases, inborn | n2=en:physical defect | rel=r_associated | relid=0 | w=20
  163. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:teratosis
    n1=en:genetic diseases, inborn | n2=en:teratosis | rel=r_associated | relid=0 | w=20
  164. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> en:yellow nail
    n1=en:genetic diseases, inborn | n2=en:yellow nail | rel=r_associated | relid=0 | w=20
  165. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> enzymologie
    n1=en:genetic diseases, inborn | n2=enzymologie | rel=r_associated | relid=0 | w=20
  166. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> enzymology
    n1=en:genetic diseases, inborn | n2=enzymology | rel=r_associated | relid=0 | w=20
  167. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> épidémiologique
    n1=en:genetic diseases, inborn | n2=épidémiologique | rel=r_associated | relid=0 | w=20
  168. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> fibrose hépatique congénitale
    n1=en:genetic diseases, inborn | n2=fibrose hépatique congénitale | rel=r_associated | relid=0 | w=20
  169. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> fibrose kystique
    n1=en:genetic diseases, inborn | n2=fibrose kystique | rel=r_associated | relid=0 | w=20
  170. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> hémoglobinopathie
    n1=en:genetic diseases, inborn | n2=hémoglobinopathie | rel=r_associated | relid=0 | w=20
  171. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> hyperplasie congénitale des surrénales
    n1=en:genetic diseases, inborn | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20
  172. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> Lennox-Gastaut (syndrome de)
    n1=en:genetic diseases, inborn | n2=Lennox-Gastaut (syndrome de) | rel=r_associated | relid=0 | w=20
  173. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> maladie congénitale
    n1=en:genetic diseases, inborn | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
  174. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> maladie de l'homme de verre
    n1=en:genetic diseases, inborn | n2=maladie de l'homme de verre | rel=r_associated | relid=0 | w=20
  175. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> maladie de marfan
    n1=en:genetic diseases, inborn | n2=maladie de marfan | rel=r_associated | relid=0 | w=20
  176. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> maladie des os de verre
    n1=en:genetic diseases, inborn | n2=maladie des os de verre | rel=r_associated | relid=0 | w=20
  177. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> malformation
    n1=en:genetic diseases, inborn | n2=malformation | rel=r_associated | relid=0 | w=20
  178. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> malformation congénitale
    n1=en:genetic diseases, inborn | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
  179. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> Meyenburg (complexe de von)
    n1=en:genetic diseases, inborn | n2=Meyenburg (complexe de von) | rel=r_associated | relid=0 | w=20
  180. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> microbiologique
    n1=en:genetic diseases, inborn | n2=microbiologique | rel=r_associated | relid=0 | w=20
  181. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> microlithiase alvéolaire pulmonaire
    n1=en:genetic diseases, inborn | n2=microlithiase alvéolaire pulmonaire | rel=r_associated | relid=0 | w=20
  182. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> mucoviscidose
    n1=en:genetic diseases, inborn | n2=mucoviscidose | rel=r_associated | relid=0 | w=20
  183. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> ongles jaunes (syndrome des)
    n1=en:genetic diseases, inborn | n2=ongles jaunes (syndrome des) | rel=r_associated | relid=0 | w=20
  184. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> onycho-ostéodysostose
    n1=en:genetic diseases, inborn | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20
  185. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> onycho-patellaire (syndrome)
    n1=en:genetic diseases, inborn | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20
  186. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasie
    n1=en:genetic diseases, inborn | n2=ostéochondrodysplasie | rel=r_associated | relid=0 | w=20
  187. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> ostéochondrodysplasies
    n1=en:genetic diseases, inborn | n2=ostéochondrodysplasies | rel=r_associated | relid=0 | w=20
  188. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> ostéogénèse imparfaite
    n1=en:genetic diseases, inborn | n2=ostéogénèse imparfaite | rel=r_associated | relid=0 | w=20
  189. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> ostéogenèse imparfaite
    n1=en:genetic diseases, inborn | n2=ostéogenèse imparfaite | rel=r_associated | relid=0 | w=20
  190. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> Ostéogenèse imparfaite
    n1=en:genetic diseases, inborn | n2=Ostéogenèse imparfaite | rel=r_associated | relid=0 | w=20
  191. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> osteogenesis imperfecta
    n1=en:genetic diseases, inborn | n2=osteogenesis imperfecta | rel=r_associated | relid=0 | w=20
  192. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> osteogenesis imperfecta forme oculaire
    n1=en:genetic diseases, inborn | n2=osteogenesis imperfecta forme oculaire | rel=r_associated | relid=0 | w=20
  193. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> osteogenesis imperfecta progressivement déformante avec sclères normales
    n1=en:genetic diseases, inborn | n2=osteogenesis imperfecta progressivement déformante avec sclères normales | rel=r_associated | relid=0 | w=20
  194. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> ostéopsathyrose
    n1=en:genetic diseases, inborn | n2=ostéopsathyrose | rel=r_associated | relid=0 | w=20
  195. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> parasitologie
    n1=en:genetic diseases, inborn | n2=parasitologie | rel=r_associated | relid=0 | w=20
  196. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> pathologie congénitale
    n1=en:genetic diseases, inborn | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
  197. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> radiographique
    n1=en:genetic diseases, inborn | n2=radiographique | rel=r_associated | relid=0 | w=20
  198. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> syndrome de Lennox-Gastaut
    n1=en:genetic diseases, inborn | n2=syndrome de Lennox-Gastaut | rel=r_associated | relid=0 | w=20
  199. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> syndrome de lennox-gastaut
    n1=en:genetic diseases, inborn | n2=syndrome de lennox-gastaut | rel=r_associated | relid=0 | w=20
  200. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> syndrome de Lobstein-van der Hoeve
    n1=en:genetic diseases, inborn | n2=syndrome de Lobstein-van der Hoeve | rel=r_associated | relid=0 | w=20
  201. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> syndrome de marfan
    n1=en:genetic diseases, inborn | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20
  202. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> syndrome lymphoprolifératif auto-immun
    n1=en:genetic diseases, inborn | n2=syndrome lymphoprolifératif auto-immun | rel=r_associated | relid=0 | w=20
  203. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> syndrome lymphoprolifératif avec auto-immunité
    n1=en:genetic diseases, inborn | n2=syndrome lymphoprolifératif avec auto-immunité | rel=r_associated | relid=0 | w=20
  204. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> syndrome lymphoprolifératif avec autoimmunité
    n1=en:genetic diseases, inborn | n2=syndrome lymphoprolifératif avec autoimmunité | rel=r_associated | relid=0 | w=20
  205. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> tare congénitale
    n1=en:genetic diseases, inborn | n2=tare congénitale | rel=r_associated | relid=0 | w=20
  206. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> trouble chromosomique
    n1=en:genetic diseases, inborn | n2=trouble chromosomique | rel=r_associated | relid=0 | w=20
  207. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> une anomalie congénitale
    n1=en:genetic diseases, inborn | n2=une anomalie congénitale | rel=r_associated | relid=0 | w=20
  208. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> vice de conformation
    n1=en:genetic diseases, inborn | n2=vice de conformation | rel=r_associated | relid=0 | w=20
  209. en:genetic diseases, inborn -- r_associated #0: 20 / 0.465 -> yellow nail syndrome
    n1=en:genetic diseases, inborn | n2=yellow nail syndrome | rel=r_associated | relid=0 | w=20
≈ 325 relations entrantes

  1. anomalie congénitale --- r_associated #0: 424 --> en:genetic diseases, inborn
    n1=anomalie congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=424
  2. en:congenital abnormality --- r_associated #0: 422 --> en:genetic diseases, inborn
    n1=en:congenital abnormality | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=422
  3. maladie héréditaire --- r_associated #0: 391 --> en:genetic diseases, inborn
    n1=maladie héréditaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=391
  4. en:hereditary disease --- r_associated #0: 390 --> en:genetic diseases, inborn
    n1=en:hereditary disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=390
  5. maladie génétique --- r_associated #0: 386 --> en:genetic diseases, inborn
    n1=maladie génétique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=386
  6. malformation congénitale --- r_associated #0: 356 --> en:genetic diseases, inborn
    n1=malformation congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=356
  7. en:genetic disease --- r_associated #0: 355 --> en:genetic diseases, inborn
    n1=en:genetic disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=355
  8. en:congenital anomaly --- r_associated #0: 353 --> en:genetic diseases, inborn
    n1=en:congenital anomaly | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=353
  9. anormalité des chromosomes --- r_associated #0: 324 --> en:genetic diseases, inborn
    n1=anormalité des chromosomes | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=324
  10. en:chromosome disorder --- r_associated #0: 320 --> en:genetic diseases, inborn
    n1=en:chromosome disorder | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=320
  11. en:congenital defect --- r_associated #0: 310 --> en:genetic diseases, inborn
    n1=en:congenital defect | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=310
  12. en:genetic disorder --- r_associated #0: 305 --> en:genetic diseases, inborn
    n1=en:genetic disorder | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=305
  13. déformation congénitale --- r_associated #0: 296 --> en:genetic diseases, inborn
    n1=déformation congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=296
  14. déficience congénitale --- r_associated #0: 295 --> en:genetic diseases, inborn
    n1=déficience congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=295
  15. en:marfan syndrome --- r_associated #0: 285 --> en:genetic diseases, inborn
    n1=en:marfan syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=285
  16. anomalie héréditaire --- r_associated #0: 281 --> en:genetic diseases, inborn
    n1=anomalie héréditaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=281
  17. maladie de Marfan --- r_associated #0: 281 --> en:genetic diseases, inborn
    n1=maladie de Marfan | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=281
  18. syndrome de Marfan --- r_associated #0: 281 --> en:genetic diseases, inborn
    n1=syndrome de Marfan | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=281
  19. arachnodactylie --- r_associated #0: 274 --> en:genetic diseases, inborn
    n1=arachnodactylie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=274
  20. en:arachnodactyly --- r_associated #0: 250 --> en:genetic diseases, inborn
    n1=en:arachnodactyly | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=250
  21. syndrome lymphoprolifératif avec auto-immunité --- r_associated #0: 250 --> en:genetic diseases, inborn
    n1=syndrome lymphoprolifératif avec auto-immunité | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=250
  22. en:autoimmune lymphoproliferative syndrome --- r_associated #0: 249 --> en:genetic diseases, inborn
    n1=en:autoimmune lymphoproliferative syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=249
  23. syndrome lymphoprolifératif avec autoimmunité --- r_associated #0: 249 --> en:genetic diseases, inborn
    n1=syndrome lymphoprolifératif avec autoimmunité | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=249
  24. syndrome lymphoprolifératif auto-immun --- r_associated #0: 245 --> en:genetic diseases, inborn
    n1=syndrome lymphoprolifératif auto-immun | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=245
  25. trouble chromosomique --- r_associated #0: 220 --> en:genetic diseases, inborn
    n1=trouble chromosomique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=220
  26. en:genetic condition --- r_associated #0: 210 --> en:genetic diseases, inborn
    n1=en:genetic condition | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=210
  27. en:enzymology --- r_associated #0: 204 --> en:genetic diseases, inborn
    n1=en:enzymology | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=204
  28. difformité congénitale --- r_associated #0: 200 --> en:genetic diseases, inborn
    n1=difformité congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=200
  29. enzymologie --- r_associated #0: 200 --> en:genetic diseases, inborn
    n1=enzymologie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=200
  30. maladie congénitale --- r_associated #0: 190 --> en:genetic diseases, inborn
    n1=maladie congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=190
  31. pathologie congénitale --- r_associated #0: 185 --> en:genetic diseases, inborn
    n1=pathologie congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=185
  32. anomalie chromosomique --- r_associated #0: 170 --> en:genetic diseases, inborn
    n1=anomalie chromosomique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=170
  33. en:parasitology --- r_associated #0: 162 --> en:genetic diseases, inborn
    n1=en:parasitology | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=162
  34. parasitologie --- r_associated #0: 160 --> en:genetic diseases, inborn
    n1=parasitologie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=160
  35. maladie des os de verre --- r_associated #0: 156 --> en:genetic diseases, inborn
    n1=maladie des os de verre | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=156
  36. ostéogénèse imparfaite --- r_associated #0: 156 --> en:genetic diseases, inborn
    n1=ostéogénèse imparfaite | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=156
  37. en:osteogenesis imperfecta --- r_associated #0: 155 --> en:genetic diseases, inborn
    n1=en:osteogenesis imperfecta | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=155
  38. enzymology --- r_associated #0: 155 --> en:genetic diseases, inborn
    n1=enzymology | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=155
  39. ostéogenèse imparfaite --- r_associated #0: 155 --> en:genetic diseases, inborn
    n1=ostéogenèse imparfaite | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=155
  40. en:Osteogenesis imperfecta --- r_associated #0: 145 --> en:genetic diseases, inborn
    n1=en:Osteogenesis imperfecta | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=145
  41. en:brittle bone disease --- r_associated #0: 145 --> en:genetic diseases, inborn
    n1=en:brittle bone disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=145
  42. en:OI --- r_associated #0: 140 --> en:genetic diseases, inborn
    n1=en:OI | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=140
  43. en:congenital malformation --- r_associated #0: 130 --> en:genetic diseases, inborn
    n1=en:congenital malformation | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=130
  44. en:birth defect --- r_associated #0: 120 --> en:genetic diseases, inborn
    n1=en:birth defect | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=120
  45. en:genetic illness --- r_associated #0: 110 --> en:genetic diseases, inborn
    n1=en:genetic illness | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=110
  46. en:yellow nail syndrome --- r_associated #0: 100 --> en:genetic diseases, inborn
    n1=en:yellow nail syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=100
  47. yellow nail syndrome --- r_associated #0: 98 --> en:genetic diseases, inborn
    n1=yellow nail syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=98
  48. hémoglobinopathie --- r_associated #0: 97 --> en:genetic diseases, inborn
    n1=hémoglobinopathie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=97
  49. en:hemoglobinopathy --- r_associated #0: 96 --> en:genetic diseases, inborn
    n1=en:hemoglobinopathy | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=96
  50. hyperplasie congénitale des surrénales --- r_associated #0: 95 --> en:genetic diseases, inborn
    n1=hyperplasie congénitale des surrénales | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=95
  51. en:congenital adrenal hyperplasia --- r_associated #0: 94 --> en:genetic diseases, inborn
    n1=en:congenital adrenal hyperplasia | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=94
  52. tare congénitale --- r_associated #0: 80 --> en:genetic diseases, inborn
    n1=tare congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=80
  53. en:chromosomal abnormality --- r_associated #0: 75 --> en:genetic diseases, inborn
    n1=en:chromosomal abnormality | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=75
  54. arrêt auriculaire --- r_associated #0: 74 --> en:genetic diseases, inborn
    n1=arrêt auriculaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=74
  55. en:atrial standstill --- r_associated #0: 71 --> en:genetic diseases, inborn
    n1=en:atrial standstill | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=71
  56. osteogenesis imperfecta --- r_associated #0: 67 --> en:genetic diseases, inborn
    n1=osteogenesis imperfecta | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=67
  57. ostéochondrodysplasies --- r_associated #0: 61 --> en:genetic diseases, inborn
    n1=ostéochondrodysplasies | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=61
  58. anomalie cytogénétique --- r_associated #0: 60 --> en:genetic diseases, inborn
    n1=anomalie cytogénétique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=60
  59. en:osteochondrodysplasia --- r_associated #0: 60 --> en:genetic diseases, inborn
    n1=en:osteochondrodysplasia | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=60
  60. vice de conformation --- r_associated #0: 52 --> en:genetic diseases, inborn
    n1=vice de conformation | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=52
  61. Ostéogenèse imparfaite --- r_associated #0: 50 --> en:genetic diseases, inborn
    n1=Ostéogenèse imparfaite | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=50
  62. en:major physical defect --- r_associated #0: 50 --> en:genetic diseases, inborn
    n1=en:major physical defect | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=50
  63. maladie de l'homme de verre --- r_associated #0: 50 --> en:genetic diseases, inborn
    n1=maladie de l'homme de verre | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=50
  64. en:teratosis --- r_associated #0: 49 --> en:genetic diseases, inborn
    n1=en:teratosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=49
  65. syndrome de marfan --- r_associated #0: 49 --> en:genetic diseases, inborn
    n1=syndrome de marfan | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=49
  66. en:physical defect --- r_associated #0: 46 --> en:genetic diseases, inborn
    n1=en:physical defect | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=46
  67. en:Marfan's syndrome --- r_associated #0: 44 --> en:genetic diseases, inborn
    n1=en:Marfan's syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=44
  68. maladie de marfan --- r_associated #0: 44 --> en:genetic diseases, inborn
    n1=maladie de marfan | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=44
  69. en:platelet glycoprotein iv deficiency --- r_associated #0: 43 --> en:genetic diseases, inborn
    n1=en:platelet glycoprotein iv deficiency | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=43
  70. anomalie du développement --- r_associated #0: 42 --> en:genetic diseases, inborn
    n1=anomalie du développement | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=42
  71. génopathies --- r_associated #0: 42 --> en:genetic diseases, inborn
    n1=génopathies | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=42
  72. dysplasie olfacto-génitale --- r_associated #0: 40 --> en:genetic diseases, inborn
    n1=dysplasie olfacto-génitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=40
  73. en:genetic diseases, y-linked --- r_associated #0: 40 --> en:genetic diseases, inborn
    n1=en:genetic diseases, y-linked | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=40
  74. syndrome de Lennox-Gastaut --- r_associated #0: 40 --> en:genetic diseases, inborn
    n1=syndrome de Lennox-Gastaut | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=40
  75. en:hemoglobin related disease --- r_associated #0: 39 --> en:genetic diseases, inborn
    n1=en:hemoglobin related disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=39
  76. ongles jaunes (syndrome des) --- r_associated #0: 39 --> en:genetic diseases, inborn
    n1=ongles jaunes (syndrome des) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=39
  77. onycho-patellaire (syndrome) --- r_associated #0: 39 --> en:genetic diseases, inborn
    n1=onycho-patellaire (syndrome) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=39
  78. osteogenesis imperfecta forme oculaire --- r_associated #0: 39 --> en:genetic diseases, inborn
    n1=osteogenesis imperfecta forme oculaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=39
  79. en:Lennox Gastaut's syndrome --- r_associated #0: 38 --> en:genetic diseases, inborn
    n1=en:Lennox Gastaut's syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=38
  80. en:familial hypertrophic cardiomyopathy --- r_associated #0: 37 --> en:genetic diseases, inborn
    n1=en:familial hypertrophic cardiomyopathy | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=37
  81. osteogenesis imperfecta progressivement déformante avec sclères normales --- r_associated #0: 37 --> en:genetic diseases, inborn
    n1=osteogenesis imperfecta progressivement déformante avec sclères normales | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=37
  82. en:epistaxis, hereditary --- r_associated #0: 36 --> en:genetic diseases, inborn
    n1=en:epistaxis, hereditary | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=36
  83. en:kallmann syndrome --- r_associated #0: 36 --> en:genetic diseases, inborn
    n1=en:kallmann syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=36
  84. en:nail-patella syndrome --- r_associated #0: 36 --> en:genetic diseases, inborn
    n1=en:nail-patella syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=36
  85. fibrose hépatique congénitale --- r_associated #0: 36 --> en:genetic diseases, inborn
    n1=fibrose hépatique congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=36
  86. fibrose kystique --- r_associated #0: 36 --> en:genetic diseases, inborn
    n1=fibrose kystique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=36
  87. syndrome de lennox-gastaut --- r_associated #0: 36 --> en:genetic diseases, inborn
    n1=syndrome de lennox-gastaut | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=36
  88. dysplasie olfactogénitale --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=dysplasie olfactogénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  89. en:cirrhosis, familial --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:cirrhosis, familial | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  90. en:congenital hypoplastic anemia --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:congenital hypoplastic anemia | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  91. en:costello syndrome --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:costello syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  92. en:donohue syndrome --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:donohue syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  93. en:etiology aspects --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:etiology aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  94. en:eye diseases, hereditary --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:eye diseases, hereditary | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  95. en:hajdu-cheney syndrome --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:hajdu-cheney syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  96. en:hereditary neoplastic syndrome --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:hereditary neoplastic syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  97. en:lennox-gastaut syndrome --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:lennox-gastaut syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  98. en:parotidomegaly, hereditary bilateral --- r_associated #0: 35 --> en:genetic diseases, inborn
    n1=en:parotidomegaly, hereditary bilateral | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=35
  99. Syndrome de Marfan --- r_associated #0: 34 --> en:genetic diseases, inborn
    n1=Syndrome de Marfan | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=34
  100. en:alpha-1 antitrypsin deficiency --- r_associated #0: 34 --> en:genetic diseases, inborn
    n1=en:alpha-1 antitrypsin deficiency | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=34
  101. en:congenital, hereditary, and neonatal diseases and abnormalities --- r_associated #0: 34 --> en:genetic diseases, inborn
    n1=en:congenital, hereditary, and neonatal diseases and abnormalities | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=34
  102. en:cystic fibrosis --- r_associated #0: 34 --> en:genetic diseases, inborn
    n1=en:cystic fibrosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=34
  103. en:exposure as collected domain --- r_associated #0: 34 --> en:genetic diseases, inborn
    n1=en:exposure as collected domain | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=34
  104. en:hereditary angioedema --- r_associated #0: 34 --> en:genetic diseases, inborn
    n1=en:hereditary angioedema | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=34
  105. en:therapeutic aspects --- r_associated #0: 34 --> en:genetic diseases, inborn
    n1=en:therapeutic aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=34
  106. onycho-ostéodysostose --- r_associated #0: 34 --> en:genetic diseases, inborn
    n1=onycho-ostéodysostose | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=34
  107. ostéochondrodysplasie --- r_associated #0: 34 --> en:genetic diseases, inborn
    n1=ostéochondrodysplasie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=34
  108. syndrome de Lobstein-van der Hoeve --- r_associated #0: 33 --> en:genetic diseases, inborn
    n1=syndrome de Lobstein-van der Hoeve | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=33
  109. Meyenburg (complexe de von) --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=Meyenburg (complexe de von) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  110. en:complication aspects --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=en:complication aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  111. en:congenital hepatic fibrosis --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=en:congenital hepatic fibrosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  112. en:corticosteroid-binding globulin deficiency --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=en:corticosteroid-binding globulin deficiency | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  113. en:genetic diseases, x-linked --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=en:genetic diseases, x-linked | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  114. en:hyperimmunoglobulin m syndrome --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=en:hyperimmunoglobulin m syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  115. en:neutropenia, nonimmune chronic idiopathic, adult --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=en:neutropenia, nonimmune chronic idiopathic, adult | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  116. en:pulmonary alveolar microlithiasis --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=en:pulmonary alveolar microlithiasis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  117. en:roentgenographic --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=en:roentgenographic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  118. en:skin diseases, genetic --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=en:skin diseases, genetic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  119. maladies génétiques congénitales --- r_associated #0: 32 --> en:genetic diseases, inborn
    n1=maladies génétiques congénitales | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=32
  120. chérubisme --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=chérubisme | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  121. en:Marfan's disease --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=en:Marfan's disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  122. en:adrenocortical hypofunction, chronic primary congenital --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=en:adrenocortical hypofunction, chronic primary congenital | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  123. en:brugada syndrome ventricular arrhythmia by ecg finding --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=en:brugada syndrome ventricular arrhythmia by ecg finding | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  124. en:cherubism --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=en:cherubism | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  125. en:cryoglobulinemia, familial mixed --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=en:cryoglobulinemia, familial mixed | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  126. en:defects, single-gene --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=en:defects, single-gene | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  127. en:microbiological --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=en:microbiological | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  128. en:pycnodysostosis --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=en:pycnodysostosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  129. maladie génétique congénitale --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=maladie génétique congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  130. microbiologique --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=microbiologique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  131. microlithiase alvéolaire pulmonaire --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=microlithiase alvéolaire pulmonaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  132. mucoviscidose --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=mucoviscidose | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  133. ostéopsathyrose --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=ostéopsathyrose | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  134. épidémiologique --- r_associated #0: 31 --> en:genetic diseases, inborn
    n1=épidémiologique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=31
  135. en:aspects of mortality statistics --- r_associated #0: 30 --> en:genetic diseases, inborn
    n1=en:aspects of mortality statistics | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=30
  136. en:complement factor i (c3 inactivator) deficiency --- r_associated #0: 30 --> en:genetic diseases, inborn
    n1=en:complement factor i (c3 inactivator) deficiency | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=30
  137. en:developmental fault --- r_associated #0: 30 --> en:genetic diseases, inborn
    n1=en:developmental fault | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=30
  138. en:immunology aspects --- r_associated #0: 30 --> en:genetic diseases, inborn
    n1=en:immunology aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=30
  139. en:neonatal disorder --- r_associated #0: 30 --> en:genetic diseases, inborn
    n1=en:neonatal disorder | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=30
  140. en:rh deficiency syndrome --- r_associated #0: 30 --> en:genetic diseases, inborn
    n1=en:rh deficiency syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=30
  141. radiographique --- r_associated #0: 30 --> en:genetic diseases, inborn
    n1=radiographique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=30
  142. Lennox-Gastaut (syndrome de) --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=Lennox-Gastaut (syndrome de) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  143. en:Donohue syndrome --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=en:Donohue syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  144. en:alpha-2-deficient collagen disease --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=en:alpha-2-deficient collagen disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  145. en:ataxia telangiectasia syndrome --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=en:ataxia telangiectasia syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  146. en:chromosomal aberration --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=en:chromosomal aberration | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  147. en:ethnologic --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=en:ethnologic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  148. en:hereditary myopathy with early respiratory failure --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=en:hereditary myopathy with early respiratory failure | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  149. en:onychoosteodysostosis --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=en:onychoosteodysostosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  150. en:psychology qualifier --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=en:psychology qualifier | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  151. malformation --- r_associated #0: 29 --> en:genetic diseases, inborn
    n1=malformation | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=29
  152. en:auricular standstill --- r_associated #0: 28 --> en:genetic diseases, inborn
    n1=en:auricular standstill | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=28
  153. en:congenital metabolic disorder --- r_associated #0: 28 --> en:genetic diseases, inborn
    n1=en:congenital metabolic disorder | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=28
  154. en:pelger-huet anomaly --- r_associated #0: 28 --> en:genetic diseases, inborn
    n1=en:pelger-huet anomaly | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=28
  155. en:pharmacotherapeutic --- r_associated #0: 28 --> en:genetic diseases, inborn
    n1=en:pharmacotherapeutic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=28
  156. une anomalie congénitale --- r_associated #0: 28 --> en:genetic diseases, inborn
    n1=une anomalie congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=28
  157. Maladie congénitale --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=Maladie congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  158. angiofibromatose hépatique --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=angiofibromatose hépatique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  159. en:Eddowes's disease --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:Eddowes's disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  160. en:arachnodactily --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:arachnodactily | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  161. en:aspects of radionuclide imaging --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:aspects of radionuclide imaging | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  162. en:blood coagulation disorders, inherited --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:blood coagulation disorders, inherited | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  163. en:cadasil syndrome --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:cadasil syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  164. en:charge syndrome --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:charge syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  165. en:chemically induced --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:chemically induced | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  166. en:epidemiologic --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:epidemiologic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  167. en:heredodegenerative disorders, nervous system --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:heredodegenerative disorders, nervous system | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  168. en:hypoprolactinemia --- r_associated #0: 27 --> en:genetic diseases, inborn
    n1=en:hypoprolactinemia | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=27
  169. en:alagille syndrome --- r_associated #0: 26 --> en:genetic diseases, inborn
    n1=en:alagille syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=26
  170. en:hereditary hemolytic anemia --- r_associated #0: 26 --> en:genetic diseases, inborn
    n1=en:hereditary hemolytic anemia | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=26
  171. en:loeys-dietz syndrome --- r_associated #0: 26 --> en:genetic diseases, inborn
    n1=en:loeys-dietz syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=26
  172. en:marfan's syndrome --- r_associated #0: 26 --> en:genetic diseases, inborn
    n1=en:marfan's syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=26
  173. en:osteopsathyrosis --- r_associated #0: 26 --> en:genetic diseases, inborn
    n1=en:osteopsathyrosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=26
  174. en:yellow nail --- r_associated #0: 26 --> en:genetic diseases, inborn
    n1=en:yellow nail | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=26
  175. en:angiofibromatosis --- r_associated #0: 25 --> en:genetic diseases, inborn
    n1=en:angiofibromatosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=25
  176. en:hereditary illness --- r_associated #0: 25 --> en:genetic diseases, inborn
    n1=en:hereditary illness | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=25
  177. en:inherited disease --- r_associated #0: 25 --> en:genetic diseases, inborn
    n1=en:inherited disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=25
  178. en:mucoviscidosis --- r_associated #0: 25 --> en:genetic diseases, inborn
    n1=en:mucoviscidosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=25
  179. fibroscopie bronchique (intubation sous) --- r_associated #0: 25 --> en:genetic diseases, inborn
    n1=fibroscopie bronchique (intubation sous) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=25
  180. hypogonadisme avec anosmie --- r_associated #0: 25 --> en:genetic diseases, inborn
    n1=hypogonadisme avec anosmie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=25
  181. Maladie héréditaire --- r_associated #0: 24 --> en:genetic diseases, inborn
    n1=Maladie héréditaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=24
  182. Marfan (maladie de) --- r_associated #0: 24 --> en:genetic diseases, inborn
    n1=Marfan (maladie de) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=24
  183. en:brittle-bone disease --- r_associated #0: 24 --> en:genetic diseases, inborn
    n1=en:brittle-bone disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=24
  184. en:epidemiological --- r_associated #0: 24 --> en:genetic diseases, inborn
    n1=en:epidemiological | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=24
  185. en:cystic fibrosis of the pancreas --- r_associated #0: 23 --> en:genetic diseases, inborn
    n1=en:cystic fibrosis of the pancreas | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=23
  186. ethnologique --- r_associated #0: 23 --> en:genetic diseases, inborn
    n1=ethnologique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=23
  187. en:Adair Dighton's syndrome --- r_associated #0: 22 --> en:genetic diseases, inborn
    n1=en:Adair Dighton's syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=22
  188. en:blue sclera syndrome --- r_associated #0: 22 --> en:genetic diseases, inborn
    n1=en:blue sclera syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=22
  189. syndrome d'Andersen --- r_associated #0: 22 --> en:genetic diseases, inborn
    n1=syndrome d'Andersen | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=22
  190. déficit enzymatique partiel de la surrénale --- r_associated #0: 21 --> en:genetic diseases, inborn
    n1=déficit enzymatique partiel de la surrénale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=21
  191. en:developmental anomaly --- r_associated #0: 21 --> en:genetic diseases, inborn
    n1=en:developmental anomaly | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=21
  192. en:spurway-eddowes syndrome --- r_associated #0: 21 --> en:genetic diseases, inborn
    n1=en:spurway-eddowes syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=21
  193. fragilité osseuse héréditaire --- r_associated #0: 21 --> en:genetic diseases, inborn
    n1=fragilité osseuse héréditaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=21
  194. syndrome des ongles jaunes --- r_associated #0: 21 --> en:genetic diseases, inborn
    n1=syndrome des ongles jaunes | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=21
  195. dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=dysplasie olfactogénitale de De Morsier | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  196. en:acth deficiency, isolated --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:acth deficiency, isolated | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  197. en:ataxic cerebral palsy --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:ataxic cerebral palsy | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  198. en:autosomal recessive polycystic kidney disease --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:autosomal recessive polycystic kidney disease | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  199. en:camurati-engelmann syndrome --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:camurati-engelmann syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  200. en:congenital myasthenic syndrome --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:congenital myasthenic syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  201. en:congenital pain insensitivity --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:congenital pain insensitivity | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  202. en:desquamative interstitial pneumonia --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:desquamative interstitial pneumonia | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  203. en:diagnosis aspect --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:diagnosis aspect | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  204. en:dwarfism --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:dwarfism | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  205. en:embryologic --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:embryologic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  206. en:fetal disorder --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:fetal disorder | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  207. en:frasier syndrome --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:frasier syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  208. en:genetic aspects --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:genetic aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  209. en:genetic disorders screening --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:genetic disorders screening | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  210. en:hereditary autoinflammatory diseases --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:hereditary autoinflammatory diseases | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  211. en:histiocytosis, familial lipochrome --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:histiocytosis, familial lipochrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  212. en:historical aspects qualifier --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:historical aspects qualifier | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  213. en:hyperthyroxinemia, familial dysalbuminemic --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:hyperthyroxinemia, familial dysalbuminemic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  214. en:in blood --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:in blood | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  215. en:in cerebrospinal fluid --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:in cerebrospinal fluid | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  216. en:in urine --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:in urine | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  217. en:kartagener syndrome --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:kartagener syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  218. en:medical genetics --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:medical genetics | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  219. en:metabolic aspects --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:metabolic aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  220. en:muscular dystrophy --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:muscular dystrophy | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  221. en:nursing therapy --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:nursing therapy | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  222. en:nutritional management --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:nutritional management | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  223. en:pathological aspects --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:pathological aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  224. en:physiopathological --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:physiopathological | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  225. en:primary hypertrophic osteoarthropathy --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:primary hypertrophic osteoarthropathy | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  226. en:radiotherapeutic --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:radiotherapeutic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  227. en:rehabilitation aspects --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:rehabilitation aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  228. en:surgical aspects --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:surgical aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  229. en:taxonomic --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:taxonomic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  230. en:use of ultrasonography --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:use of ultrasonography | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  231. en:veterinary aspects --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:veterinary aspects | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  232. en:viruses --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:viruses | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  233. en:werner syndrome --- r_associated #0: 20 --> en:genetic diseases, inborn
    n1=en:werner syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=20
  234. Chernosky (hyperpigmentation familiale progressive de) --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=Chernosky (hyperpigmentation familiale progressive de) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  235. Enzymologie --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=Enzymologie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  236. Hyperplasie congénitale des surrénales --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=Hyperplasie congénitale des surrénales | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  237. Kallman --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=Kallman | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  238. Maladie de Marfan --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=Maladie de Marfan | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  239. Maladie génétique --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=Maladie génétique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  240. Malformation congénitale --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=Malformation congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  241. Parasitologie --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=Parasitologie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  242. fibrose kystique du pancréas --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=fibrose kystique du pancréas | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  243. hémoglobine modifiée (solution d') --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=hémoglobine modifiée (solution d') | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  244. malentendant (enfant) --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=malentendant (enfant) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  245. syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=syndrome de Kallman-de Morsier | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  246. syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:genetic diseases, inborn
    n1=syndrome de de Morsier-Kallmann | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=15
  247. lepréchaunisme --- r_associated #0: 11 --> en:genetic diseases, inborn
    n1=lepréchaunisme | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=11
  248. Anomalie chromosomique --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=Anomalie chromosomique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  249. CX3CL1 --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=CX3CL1 | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  250. Fibrose kystique --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=Fibrose kystique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  251. Hémoglobinopathie --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=Hémoglobinopathie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  252. Malformation --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=Malformation | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  253. Mucoviscidose --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=Mucoviscidose | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  254. Paraquat ® (intoxication par le) --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=Paraquat ® (intoxication par le) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  255. Yellen-Gomco (clamp de) --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=Yellen-Gomco (clamp de) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  256. aberration chromosomique --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=aberration chromosomique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  257. dystrophie musculaire --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=dystrophie musculaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  258. en:CF --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:CF | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  259. en:cacomorphosis --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:cacomorphosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  260. en:cell free haemoglobin solution --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:cell free haemoglobin solution | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  261. en:chromosomal disorder --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:chromosomal disorder | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  262. en:congenital liver fibrosis --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:congenital liver fibrosis | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  263. en:ethnological --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:ethnological | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  264. en:hypoacousic child --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:hypoacousic child | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  265. en:intubation with bronchial fibroscopy --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:intubation with bronchial fibroscopy | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  266. en:modified haemoglobin solution --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:modified haemoglobin solution | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  267. en:ocular form --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:ocular form | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  268. en:progressively deforming --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:progressively deforming | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  269. en:radiographic --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:radiographic | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  270. en:with normal sclerae --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:with normal sclerae | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  271. en:xanthonychia syndrome --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:xanthonychia syndrome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  272. en:xanthonychie --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=en:xanthonychie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  273. fibrose avec rétraction isolée du droit inférieur --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose avec rétraction isolée du droit inférieur | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  274. fibrose cardiaque du nourrisson --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose cardiaque du nourrisson | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  275. fibrose cervico-faciale --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose cervico-faciale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  276. fibrose cervicocéphalique --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose cervicocéphalique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  277. fibrose congénitale des muscles oculaires extrinsèques --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose congénitale des muscles oculaires extrinsèques | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  278. fibrose cutanée --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose cutanée | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  279. fibrose du quadriceps --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose du quadriceps | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  280. fibrose généralisée des muscles oculomoteurs --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose généralisée des muscles oculomoteurs | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  281. fibrose hépatique --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose hépatique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  282. fibrose hépatique-rein polykystique-colobome --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose hépatique-rein polykystique-colobome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  283. fibrose kystique du pancreas --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose kystique du pancreas | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  284. fibrose élastigène --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose élastigène | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  285. fibrose élastique --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=fibrose élastique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  286. microgéodes phalangiennes (syndrome des) --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=microgéodes phalangiennes (syndrome des) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  287. nanisme --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=nanisme | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  288. ostéoporose-pseudogliome (syndrome) --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=ostéoporose-pseudogliome (syndrome) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  289. paraplégie spastique dans la syphilis congénitale --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=paraplégie spastique dans la syphilis congénitale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  290. syndrome de de Morsier --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=syndrome de de Morsier | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  291. taxinomique --- r_associated #0: 10 --> en:genetic diseases, inborn
    n1=taxinomique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=10
  292. Lobstein-van der Hoeve (syndrome de) --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=Lobstein-van der Hoeve (syndrome de) | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  293. Microbiologique --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=Microbiologique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  294. Onsager (relation d') --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=Onsager (relation d') | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  295. Syndrome de Lennox-Gastaut --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=Syndrome de Lennox-Gastaut | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  296. fibroscopie vésicale --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=fibroscopie vésicale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  297. fibrose --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=fibrose | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  298. hémoglobine Portland --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=hémoglobine Portland | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  299. hémoglobine S --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=hémoglobine S | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  300. hémoglobinique a --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=hémoglobinique a | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  301. hémoglobinobilie --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=hémoglobinobilie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  302. hémoglobinogenèse --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=hémoglobinogenèse | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  303. hémoglobinomètre --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=hémoglobinomètre | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  304. hémoglobinomètrie --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=hémoglobinomètrie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  305. hémoglobinémie --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=hémoglobinémie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  306. malf ormation dysraphique --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malf ormation dysraphique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  307. malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malformation kystique adénomatoïde du poumon | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  308. malformation luxante de la hanche --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malformation luxante de la hanche | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  309. malformation mamelonnaire --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malformation mamelonnaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  310. malformation mammaire --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malformation mammaire | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  311. malformation ombilicale --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malformation ombilicale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  312. malformation utérine --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malformation utérine | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  313. malformation vaginale --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malformation vaginale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  314. malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malformation vasculaire cérébrale du nourrisson | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  315. malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=malformations de la charnière occipitocervicale | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  316. myopathie primitive progressive --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=myopathie primitive progressive | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  317. onychodysplasie --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=onychodysplasie | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  318. onychogryphose --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=onychogryphose | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  319. onycholyse --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=onycholyse | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  320. onycholyse candidosique --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=onycholyse candidosique | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  321. onycholyse semi-lunaire partielle --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=onycholyse semi-lunaire partielle | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  322. onychomadèse --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=onychomadèse | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  323. onychomatricome --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=onychomatricome | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  324. syndrome olfacto-génital --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=syndrome olfacto-génital | n2=en:genetic diseases, inborn | rel=r_associated | relid=0 | w=5
  325. troubles de la coagulation sanguine, héréditaires --- r_associated #0: 5 --> en:genetic diseases, inborn
    n1=troubles de la coagulation sanguine, héréditaires | n2=en:genetic diseases, inborn | 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