Javascript doit fonctionner ! Activez-le et rechargez cette page.
Le Rézo de JeuxDeMots
• Types de relations
• Types de noeuds
• Consolider
le terme
  Options  
             

  Filtrage type relations : +   - (ex: 4, 12, 18, 36, 444, 555, 777)
  Filtrage valeur :          min   max
  Filtrage type noeuds :   +   - (ex: 4, 6, 8, 9, 10, 12, 18, 36, 444, 555, 777)

  Présentation de sortie :   (ex: -rien-, cloud, nicecloud)
 

'en:genee-wiedemann syndrome'
(id=6836761 ; fe=en:genee-wiedemann syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=11115 creation date=2017-06-25 touchdate=2025-08-21 12:08:27.000)
≈ 197 relations sortantes

  1. en:genee-wiedemann syndrome -- r_associated #0: 43 / 1 -> en:autosomal recessive inheritance
    n1=en:genee-wiedemann syndrome | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=43
  2. en:genee-wiedemann syndrome -- r_associated #0: 43 / 1 -> en:syndactyly
    n1=en:genee-wiedemann syndrome | n2=en:syndactyly | rel=r_associated | relid=0 | w=43
  3. en:genee-wiedemann syndrome -- r_associated #0: 43 / 1 -> en:trisomy 10p
    n1=en:genee-wiedemann syndrome | n2=en:trisomy 10p | rel=r_associated | relid=0 | w=43
  4. en:genee-wiedemann syndrome -- r_associated #0: 38 / 0.884 -> en:congenital dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:congenital dysplasia | rel=r_associated | relid=0 | w=38
  5. en:genee-wiedemann syndrome -- r_associated #0: 38 / 0.884 -> en:greig syndrome
    n1=en:genee-wiedemann syndrome | n2=en:greig syndrome | rel=r_associated | relid=0 | w=38
  6. en:genee-wiedemann syndrome -- r_associated #0: 38 / 0.884 -> en:osteodysplasia
    n1=en:genee-wiedemann syndrome | n2=en:osteodysplasia | rel=r_associated | relid=0 | w=38
  7. en:genee-wiedemann syndrome -- r_associated #0: 37 / 0.86 -> en:kniest-stickler dysplasia group
    n1=en:genee-wiedemann syndrome | n2=en:kniest-stickler dysplasia group | rel=r_associated | relid=0 | w=37
  8. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:congenital
    n1=en:genee-wiedemann syndrome | n2=en:congenital | rel=r_associated | relid=0 | w=35
  9. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:defects of tubular bones and spine
    n1=en:genee-wiedemann syndrome | n2=en:defects of tubular bones and spine | rel=r_associated | relid=0 | w=35
  10. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:dhodh, gly202asp
    n1=en:genee-wiedemann syndrome | n2=en:dhodh, gly202asp | rel=r_associated | relid=0 | w=35
  11. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:disorganized development of cartilaginous and fibrous components of the skeleton
    n1=en:genee-wiedemann syndrome | n2=en:disorganized development of cartilaginous and fibrous components of the skeleton | rel=r_associated | relid=0 | w=35
  12. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:idiopathic osteolyses
    n1=en:genee-wiedemann syndrome | n2=en:idiopathic osteolyses | rel=r_associated | relid=0 | w=35
  13. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:miller-mckusick-malvaux-syndrome (3m syndrome)
    n1=en:genee-wiedemann syndrome | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=35
  14. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:multicentric osteolysis nodulosis arthropathy spectrum
    n1=en:genee-wiedemann syndrome | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=35
  15. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:multiple dislocations with dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:multiple dislocations with dysplasia | rel=r_associated | relid=0 | w=35
  16. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:multiple synostosis syndrome
    n1=en:genee-wiedemann syndrome | n2=en:multiple synostosis syndrome | rel=r_associated | relid=0 | w=35
  17. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:radioulnar synostosis
    n1=en:genee-wiedemann syndrome | n2=en:radioulnar synostosis | rel=r_associated | relid=0 | w=35
  18. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:rib defects
    n1=en:genee-wiedemann syndrome | n2=en:rib defects | rel=r_associated | relid=0 | w=35
  19. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:spondyloepiphyseal dysplasia, congenita
    n1=en:genee-wiedemann syndrome | n2=en:spondyloepiphyseal dysplasia, congenita | rel=r_associated | relid=0 | w=35
  20. en:genee-wiedemann syndrome -- r_associated #0: 35 / 0.814 -> en:townes-brocks syndrome
    n1=en:genee-wiedemann syndrome | n2=en:townes-brocks syndrome | rel=r_associated | relid=0 | w=35
  21. en:genee-wiedemann syndrome -- r_associated #0: 34 / 0.791 -> en:acrocallosal syndrome
    n1=en:genee-wiedemann syndrome | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=34
  22. en:genee-wiedemann syndrome -- r_associated #0: 34 / 0.791 -> en:chitty hall baraitser syndrome
    n1=en:genee-wiedemann syndrome | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=34
  23. en:genee-wiedemann syndrome -- r_associated #0: 34 / 0.791 -> en:chromosome 11p deletion syndrome
    n1=en:genee-wiedemann syndrome | n2=en:chromosome 11p deletion syndrome | rel=r_associated | relid=0 | w=34
  24. en:genee-wiedemann syndrome -- r_associated #0: 34 / 0.791 -> en:congenital hypoplasia of penis
    n1=en:genee-wiedemann syndrome | n2=en:congenital hypoplasia of penis | rel=r_associated | relid=0 | w=34
  25. en:genee-wiedemann syndrome -- r_associated #0: 34 / 0.791 -> en:defects of the tubular (and flat) bones and/or axial skeleton
    n1=en:genee-wiedemann syndrome | n2=en:defects of the tubular (and flat) bones and/or axial skeleton | rel=r_associated | relid=0 | w=34
  26. en:genee-wiedemann syndrome -- r_associated #0: 34 / 0.791 -> en:dhodh, gly152arg
    n1=en:genee-wiedemann syndrome | n2=en:dhodh, gly152arg | rel=r_associated | relid=0 | w=34
  27. en:genee-wiedemann syndrome -- r_associated #0: 34 / 0.791 -> en:dysplasia with increased bone density
    n1=en:genee-wiedemann syndrome | n2=en:dysplasia with increased bone density | rel=r_associated | relid=0 | w=34
  28. en:genee-wiedemann syndrome -- r_associated #0: 34 / 0.791 -> en:ophthalmomandibulomelic dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:ophthalmomandibulomelic dysplasia | rel=r_associated | relid=0 | w=34
  29. en:genee-wiedemann syndrome -- r_associated #0: 34 / 0.791 -> en:rudiger syndrome 1
    n1=en:genee-wiedemann syndrome | n2=en:rudiger syndrome 1 | rel=r_associated | relid=0 | w=34
  30. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:acromesomelic dysplasia syndrome
    n1=en:genee-wiedemann syndrome | n2=en:acromesomelic dysplasia syndrome | rel=r_associated | relid=0 | w=32
  31. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:atelosteogenesis, type 1
    n1=en:genee-wiedemann syndrome | n2=en:atelosteogenesis, type 1 | rel=r_associated | relid=0 | w=32
  32. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the dihydroorotate dehydrogenase gene (dhodh, 126064.0001)
    n1=en:genee-wiedemann syndrome | n2=en:caused by mutation in the dihydroorotate dehydrogenase gene (dhodh, 126064.0001) | rel=r_associated | relid=0 | w=32
  33. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:coffin-lowry syndrome
    n1=en:genee-wiedemann syndrome | n2=en:coffin-lowry syndrome | rel=r_associated | relid=0 | w=32
  34. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:dhodh, arg135cys
    n1=en:genee-wiedemann syndrome | n2=en:dhodh, arg135cys | rel=r_associated | relid=0 | w=32
  35. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:dysplasia with defective mineralization
    n1=en:genee-wiedemann syndrome | n2=en:dysplasia with defective mineralization | rel=r_associated | relid=0 | w=32
  36. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:ehlers-danlos syndrome
    n1=en:genee-wiedemann syndrome | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=32
  37. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:epiphyseal dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:epiphyseal dysplasia | rel=r_associated | relid=0 | w=32
  38. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:gurrieri sammito bellussi syndrome
    n1=en:genee-wiedemann syndrome | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=32
  39. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:hypochondroplasia
    n1=en:genee-wiedemann syndrome | n2=en:hypochondroplasia | rel=r_associated | relid=0 | w=32
  40. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:in-curving forearms
    n1=en:genee-wiedemann syndrome | n2=en:in-curving forearms | rel=r_associated | relid=0 | w=32
  41. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:melnick-needles syndrome
    n1=en:genee-wiedemann syndrome | n2=en:melnick-needles syndrome | rel=r_associated | relid=0 | w=32
  42. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:micrognathism
    n1=en:genee-wiedemann syndrome | n2=en:micrognathism | rel=r_associated | relid=0 | w=32
  43. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:most case are sporadic
    n1=en:genee-wiedemann syndrome | n2=en:most case are sporadic | rel=r_associated | relid=0 | w=32
  44. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:osteoplastic dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:osteoplastic dysplasia | rel=r_associated | relid=0 | w=32
  45. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:pectus excavatum
    n1=en:genee-wiedemann syndrome | n2=en:pectus excavatum | rel=r_associated | relid=0 | w=32
  46. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:short rib dysplasia group (with or without polydactyly)
    n1=en:genee-wiedemann syndrome | n2=en:short rib dysplasia group (with or without polydactyly) | rel=r_associated | relid=0 | w=32
  47. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:stickler syndrome
    n1=en:genee-wiedemann syndrome | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=32
  48. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:supernumerary vertebra
    n1=en:genee-wiedemann syndrome | n2=en:supernumerary vertebra | rel=r_associated | relid=0 | w=32
  49. en:genee-wiedemann syndrome -- r_associated #0: 32 / 0.744 -> en:symphalangism-brachydactyly syndrome
    n1=en:genee-wiedemann syndrome | n2=en:symphalangism-brachydactyly syndrome | rel=r_associated | relid=0 | w=32
  50. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:dhodh, arg346trp
    n1=en:genee-wiedemann syndrome | n2=en:dhodh, arg346trp | rel=r_associated | relid=0 | w=31
  51. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:diastrophic dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:diastrophic dysplasia | rel=r_associated | relid=0 | w=31
  52. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:downward slant of palpebral fissure
    n1=en:genee-wiedemann syndrome | n2=en:downward slant of palpebral fissure | rel=r_associated | relid=0 | w=31
  53. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:dysplasia with decreased bone density
    n1=en:genee-wiedemann syndrome | n2=en:dysplasia with decreased bone density | rel=r_associated | relid=0 | w=31
  54. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:mesomelic dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:mesomelic dysplasia | rel=r_associated | relid=0 | w=31
  55. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:metatropic dwarfism
    n1=en:genee-wiedemann syndrome | n2=en:metatropic dwarfism | rel=r_associated | relid=0 | w=31
  56. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:nager syndrome
    n1=en:genee-wiedemann syndrome | n2=en:nager syndrome | rel=r_associated | relid=0 | w=31
  57. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:orofaciodigital syndrome type 1
    n1=en:genee-wiedemann syndrome | n2=en:orofaciodigital syndrome type 1 | rel=r_associated | relid=0 | w=31
  58. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:thumb hypoplasia
    n1=en:genee-wiedemann syndrome | n2=en:thumb hypoplasia | rel=r_associated | relid=0 | w=31
  59. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:treacher collins syndrome
    n1=en:genee-wiedemann syndrome | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=31
  60. en:genee-wiedemann syndrome -- r_associated #0: 31 / 0.721 -> en:undescended testes
    n1=en:genee-wiedemann syndrome | n2=en:undescended testes | rel=r_associated | relid=0 | w=31
  61. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:achondrogenesis
    n1=en:genee-wiedemann syndrome | n2=en:achondrogenesis | rel=r_associated | relid=0 | w=30
  62. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:aminopterin syndrome sine aminopterin
    n1=en:genee-wiedemann syndrome | n2=en:aminopterin syndrome sine aminopterin | rel=r_associated | relid=0 | w=30
  63. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:beals auriculo-osteodysplasia syndrome
    n1=en:genee-wiedemann syndrome | n2=en:beals auriculo-osteodysplasia syndrome | rel=r_associated | relid=0 | w=30
  64. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:brachyolmia type 3
    n1=en:genee-wiedemann syndrome | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=30
  65. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:dhodh, 1-bp del, 611t
    n1=en:genee-wiedemann syndrome | n2=en:dhodh, 1-bp del, 611t | rel=r_associated | relid=0 | w=30
  66. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:dhodh, arg244trp
    n1=en:genee-wiedemann syndrome | n2=en:dhodh, arg244trp | rel=r_associated | relid=0 | w=30
  67. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:dysostosis multiplex group
    n1=en:genee-wiedemann syndrome | n2=en:dysostosis multiplex group | rel=r_associated | relid=0 | w=30
  68. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:fg syndrome
    n1=en:genee-wiedemann syndrome | n2=en:fg syndrome | rel=r_associated | relid=0 | w=30
  69. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:mental retardation mietens weber type
    n1=en:genee-wiedemann syndrome | n2=en:mental retardation mietens weber type | rel=r_associated | relid=0 | w=30
  70. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:oculo-dento-digital syndrome
    n1=en:genee-wiedemann syndrome | n2=en:oculo-dento-digital syndrome | rel=r_associated | relid=0 | w=30
  71. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:osteodysplastic primordial dwarfism
    n1=en:genee-wiedemann syndrome | n2=en:osteodysplastic primordial dwarfism | rel=r_associated | relid=0 | w=30
  72. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:peg-shaped teeth
    n1=en:genee-wiedemann syndrome | n2=en:peg-shaped teeth | rel=r_associated | relid=0 | w=30
  73. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:postnatal growth retardation
    n1=en:genee-wiedemann syndrome | n2=en:postnatal growth retardation | rel=r_associated | relid=0 | w=30
  74. en:genee-wiedemann syndrome -- r_associated #0: 30 / 0.698 -> en:trichorhinophalangeal syndrome
    n1=en:genee-wiedemann syndrome | n2=en:trichorhinophalangeal syndrome | rel=r_associated | relid=0 | w=30
  75. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:camurati-engelmann syndrome
    n1=en:genee-wiedemann syndrome | n2=en:camurati-engelmann syndrome | rel=r_associated | relid=0 | w=29
  76. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:dhodh, gly202ala
    n1=en:genee-wiedemann syndrome | n2=en:dhodh, gly202ala | rel=r_associated | relid=0 | w=29
  77. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:dysostosis
    n1=en:genee-wiedemann syndrome | n2=en:dysostosis | rel=r_associated | relid=0 | w=29
  78. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:heide syndrome
    n1=en:genee-wiedemann syndrome | n2=en:heide syndrome | rel=r_associated | relid=0 | w=29
  79. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:larsen syndrome
    n1=en:genee-wiedemann syndrome | n2=en:larsen syndrome | rel=r_associated | relid=0 | w=29
  80. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:leri's pleonosteosis syndrome
    n1=en:genee-wiedemann syndrome | n2=en:leri's pleonosteosis syndrome | rel=r_associated | relid=0 | w=29
  81. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:low set ears
    n1=en:genee-wiedemann syndrome | n2=en:low set ears | rel=r_associated | relid=0 | w=29
  82. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:malar flattening
    n1=en:genee-wiedemann syndrome | n2=en:malar flattening | rel=r_associated | relid=0 | w=29
  83. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:multiple congenital anomalies
    n1=en:genee-wiedemann syndrome | n2=en:multiple congenital anomalies | rel=r_associated | relid=0 | w=29
  84. en:genee-wiedemann syndrome -- r_associated #0: 29 / 0.674 -> en:pyloric stenosis
    n1=en:genee-wiedemann syndrome | n2=en:pyloric stenosis | rel=r_associated | relid=0 | w=29
  85. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> en:accessory nipple
    n1=en:genee-wiedemann syndrome | n2=en:accessory nipple | rel=r_associated | relid=0 | w=28
  86. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal recessive distal osteolysis syndrome
    n1=en:genee-wiedemann syndrome | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=28
  87. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> en:chondrodysplasia
    n1=en:genee-wiedemann syndrome | n2=en:chondrodysplasia | rel=r_associated | relid=0 | w=28
  88. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> en:cleft palate
    n1=en:genee-wiedemann syndrome | n2=en:cleft palate | rel=r_associated | relid=0 | w=28
  89. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> en:coloboma of the eyelid
    n1=en:genee-wiedemann syndrome | n2=en:coloboma of the eyelid | rel=r_associated | relid=0 | w=28
  90. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> en:conductive hearing loss
    n1=en:genee-wiedemann syndrome | n2=en:conductive hearing loss | rel=r_associated | relid=0 | w=28
  91. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> en:metaphyseal chondrodysplasia
    n1=en:genee-wiedemann syndrome | n2=en:metaphyseal chondrodysplasia | rel=r_associated | relid=0 | w=28
  92. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> en:radial hypoplasia
    n1=en:genee-wiedemann syndrome | n2=en:radial hypoplasia | rel=r_associated | relid=0 | w=28
  93. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> en:skeleton dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:skeleton dysplasia | rel=r_associated | relid=0 | w=28
  94. en:genee-wiedemann syndrome -- r_associated #0: 28 / 0.651 -> Miller
    n1=en:genee-wiedemann syndrome | n2=Miller | rel=r_associated | relid=0 | w=28
  95. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:autosomal recessive and dominant pedigrees described
    n1=en:genee-wiedemann syndrome | n2=en:autosomal recessive and dominant pedigrees described | rel=r_associated | relid=0 | w=27
  96. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:baller-gerold syndrome
    n1=en:genee-wiedemann syndrome | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=27
  97. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:cherubism with gingival fibromatosis
    n1=en:genee-wiedemann syndrome | n2=en:cherubism with gingival fibromatosis | rel=r_associated | relid=0 | w=27
  98. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:choanal atresia
    n1=en:genee-wiedemann syndrome | n2=en:choanal atresia | rel=r_associated | relid=0 | w=27
  99. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:congenital abnormality
    n1=en:genee-wiedemann syndrome | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=27
  100. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:cupped ears (finding)
    n1=en:genee-wiedemann syndrome | n2=en:cupped ears (finding) | rel=r_associated | relid=0 | w=27
  101. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:developmental dysplasia of hip
    n1=en:genee-wiedemann syndrome | n2=en:developmental dysplasia of hip | rel=r_associated | relid=0 | w=27
  102. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:dhodh, arg199cys
    n1=en:genee-wiedemann syndrome | n2=en:dhodh, arg199cys | rel=r_associated | relid=0 | w=27
  103. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:dhodh, gly19glu
    n1=en:genee-wiedemann syndrome | n2=en:dhodh, gly19glu | rel=r_associated | relid=0 | w=27
  104. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:hay-wells syndrome
    n1=en:genee-wiedemann syndrome | n2=en:hay-wells syndrome | rel=r_associated | relid=0 | w=27
  105. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:midgut malrotation
    n1=en:genee-wiedemann syndrome | n2=en:midgut malrotation | rel=r_associated | relid=0 | w=27
  106. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:oculocerebrorenal syndrome
    n1=en:genee-wiedemann syndrome | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=27
  107. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:rhizomelic dysplasia patterson lowry type
    n1=en:genee-wiedemann syndrome | n2=en:rhizomelic dysplasia patterson lowry type | rel=r_associated | relid=0 | w=27
  108. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> en:spondylodysplastic group
    n1=en:genee-wiedemann syndrome | n2=en:spondylodysplastic group | rel=r_associated | relid=0 | w=27
  109. en:genee-wiedemann syndrome -- r_associated #0: 27 / 0.628 -> syndrome
    n1=en:genee-wiedemann syndrome | n2=syndrome | rel=r_associated | relid=0 | w=27
  110. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:absence of fifth digit
    n1=en:genee-wiedemann syndrome | n2=en:absence of fifth digit | rel=r_associated | relid=0 | w=26
  111. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:bent bone dysplasia group
    n1=en:genee-wiedemann syndrome | n2=en:bent bone dysplasia group | rel=r_associated | relid=0 | w=26
  112. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:bone development disorder
    n1=en:genee-wiedemann syndrome | n2=en:bone development disorder | rel=r_associated | relid=0 | w=26
  113. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:chondrodysplasia punctata
    n1=en:genee-wiedemann syndrome | n2=en:chondrodysplasia punctata | rel=r_associated | relid=0 | w=26
  114. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:cleft lip
    n1=en:genee-wiedemann syndrome | n2=en:cleft lip | rel=r_associated | relid=0 | w=26
  115. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:congenital anomaly of the kidney
    n1=en:genee-wiedemann syndrome | n2=en:congenital anomaly of the kidney | rel=r_associated | relid=0 | w=26
  116. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:dysplasias with significant membranous bone involvement
    n1=en:genee-wiedemann syndrome | n2=en:dysplasias with significant membranous bone involvement | rel=r_associated | relid=0 | w=26
  117. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:ectropion
    n1=en:genee-wiedemann syndrome | n2=en:ectropion | rel=r_associated | relid=0 | w=26
  118. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:limb deformities, congenital
    n1=en:genee-wiedemann syndrome | n2=en:limb deformities, congenital | rel=r_associated | relid=0 | w=26
  119. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:otopalatodigital syndrome, type ii
    n1=en:genee-wiedemann syndrome | n2=en:otopalatodigital syndrome, type ii | rel=r_associated | relid=0 | w=26
  120. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:roberts-sc phocomelia syndrome
    n1=en:genee-wiedemann syndrome | n2=en:roberts-sc phocomelia syndrome | rel=r_associated | relid=0 | w=26
  121. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:ruvalcaba syndrome
    n1=en:genee-wiedemann syndrome | n2=en:ruvalcaba syndrome | rel=r_associated | relid=0 | w=26
  122. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:seaver cassidy syndrome
    n1=en:genee-wiedemann syndrome | n2=en:seaver cassidy syndrome | rel=r_associated | relid=0 | w=26
  123. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:steinfeld syndrome
    n1=en:genee-wiedemann syndrome | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=26
  124. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:tarsal-carpal coalition syndrome
    n1=en:genee-wiedemann syndrome | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=26
  125. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:ulnar hypoplasia
    n1=en:genee-wiedemann syndrome | n2=en:ulnar hypoplasia | rel=r_associated | relid=0 | w=26
  126. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> en:weill-marchesani syndrome
    n1=en:genee-wiedemann syndrome | n2=en:weill-marchesani syndrome | rel=r_associated | relid=0 | w=26
  127. en:genee-wiedemann syndrome -- r_associated #0: 26 / 0.605 -> oedème
    n1=en:genee-wiedemann syndrome | n2=oedème | rel=r_associated | relid=0 | w=26
  128. en:genee-wiedemann syndrome -- r_associated #0: 25 / 0.581 -> anomalie congénitale
    n1=en:genee-wiedemann syndrome | n2=anomalie congénitale | rel=r_associated | relid=0 | w=25
  129. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> anomalie du développement
    n1=en:genee-wiedemann syndrome | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
  130. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> chondrodysplasia punctata
    n1=en:genee-wiedemann syndrome | n2=chondrodysplasia punctata | rel=r_associated | relid=0 | w=20
  131. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> congénital
    n1=en:genee-wiedemann syndrome | n2=congénital | rel=r_associated | relid=0 | w=20
  132. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> congenital
    n1=en:genee-wiedemann syndrome | n2=congenital | rel=r_associated | relid=0 | w=20
  133. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> congénitale
    n1=en:genee-wiedemann syndrome | n2=congénitale | rel=r_associated | relid=0 | w=20
  134. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> déficience congénitale
    n1=en:genee-wiedemann syndrome | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
  135. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> déformation congénitale
    n1=en:genee-wiedemann syndrome | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
  136. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> difformité congénitale
    n1=en:genee-wiedemann syndrome | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
  137. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> dysplasie enchondrale
    n1=en:genee-wiedemann syndrome | n2=dysplasie enchondrale | rel=r_associated | relid=0 | w=20
  138. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> dysplasie épiphysaire, microcéphalie et nystagmus
    n1=en:genee-wiedemann syndrome | n2=dysplasie épiphysaire, microcéphalie et nystagmus | rel=r_associated | relid=0 | w=20
  139. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> dysplasie mésomélique
    n1=en:genee-wiedemann syndrome | n2=dysplasie mésomélique | rel=r_associated | relid=0 | w=20
  140. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> dysplasie ophtalmo-mandibulomélique
    n1=en:genee-wiedemann syndrome | n2=dysplasie ophtalmo-mandibulomélique | rel=r_associated | relid=0 | w=20
  141. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:acrorenal mandibular syndrome
    n1=en:genee-wiedemann syndrome | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20
  142. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:adducted thumbs and arthrogryposis syndrome christian type
    n1=en:genee-wiedemann syndrome | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=20
  143. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:arachnodactyly and intellectual disability with facial dysmorphism syndrome
    n1=en:genee-wiedemann syndrome | n2=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | rel=r_associated | relid=0 | w=20
  144. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:birth defect
    n1=en:genee-wiedemann syndrome | n2=en:birth defect | rel=r_associated | relid=0 | w=20
  145. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome
    n1=en:genee-wiedemann syndrome | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=20
  146. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:brain malformation, congenital heart disease, postaxial polydactyly syndrome
    n1=en:genee-wiedemann syndrome | n2=en:brain malformation, congenital heart disease, postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=20
  147. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:congenital anomaly
    n1=en:genee-wiedemann syndrome | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
  148. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:congenital defect
    n1=en:genee-wiedemann syndrome | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
  149. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:congenital malformation
    n1=en:genee-wiedemann syndrome | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
  150. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome
    n1=en:genee-wiedemann syndrome | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=20
  151. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
    n1=en:genee-wiedemann syndrome | n2=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | rel=r_associated | relid=0 | w=20
  152. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:developmental fault
    n1=en:genee-wiedemann syndrome | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
  153. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:fountain syndrome
    n1=en:genee-wiedemann syndrome | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20
  154. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:funnel breast
    n1=en:genee-wiedemann syndrome | n2=en:funnel breast | rel=r_associated | relid=0 | w=20
  155. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:funnel chest
    n1=en:genee-wiedemann syndrome | n2=en:funnel chest | rel=r_associated | relid=0 | w=20
  156. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:gracile bone dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=20
  157. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:heart defects limb shortening
    n1=en:genee-wiedemann syndrome | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20
  158. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:koilosternia
    n1=en:genee-wiedemann syndrome | n2=en:koilosternia | rel=r_associated | relid=0 | w=20
  159. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:kosztolanyi syndrome
    n1=en:genee-wiedemann syndrome | n2=en:kosztolanyi syndrome | rel=r_associated | relid=0 | w=20
  160. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:major physical defect
    n1=en:genee-wiedemann syndrome | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
  161. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome
    n1=en:genee-wiedemann syndrome | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20
  162. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:microcephaly albinism digital anomalies syndrome
    n1=en:genee-wiedemann syndrome | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
  163. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:micrognathia
    n1=en:genee-wiedemann syndrome | n2=en:micrognathia | rel=r_associated | relid=0 | w=20
  164. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:morava mehes syndrome
    n1=en:genee-wiedemann syndrome | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=20
  165. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:pelviscapular dysplasia
    n1=en:genee-wiedemann syndrome | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20
  166. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:physical defect
    n1=en:genee-wiedemann syndrome | n2=en:physical defect | rel=r_associated | relid=0 | w=20
  167. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:polydactyly, preaxial ii (disorder)
    n1=en:genee-wiedemann syndrome | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=20
  168. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:pterygium colli mental retardation digital anomalies
    n1=en:genee-wiedemann syndrome | n2=en:pterygium colli mental retardation digital anomalies | rel=r_associated | relid=0 | w=20
  169. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:pyloric obstruction
    n1=en:genee-wiedemann syndrome | n2=en:pyloric obstruction | rel=r_associated | relid=0 | w=20
  170. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:renal dysplasia - limb defects syndrome
    n1=en:genee-wiedemann syndrome | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=20
  171. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:scholte syndrome
    n1=en:genee-wiedemann syndrome | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20
  172. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:split-hand/foot malformation 3
    n1=en:genee-wiedemann syndrome | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20
  173. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:teratosis
    n1=en:genee-wiedemann syndrome | n2=en:teratosis | rel=r_associated | relid=0 | w=20
  174. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:Townes-Brocks syndrome
    n1=en:genee-wiedemann syndrome | n2=en:Townes-Brocks syndrome | rel=r_associated | relid=0 | w=20
  175. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:trichterbrust
    n1=en:genee-wiedemann syndrome | n2=en:trichterbrust | rel=r_associated | relid=0 | w=20
  176. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:trigonocephaly with bifid nose and acral anomaly syndrome
    n1=en:genee-wiedemann syndrome | n2=en:trigonocephaly with bifid nose and acral anomaly syndrome | rel=r_associated | relid=0 | w=20
  177. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability stevenson type
    n1=en:genee-wiedemann syndrome | n2=en:x-linked intellectual disability stevenson type | rel=r_associated | relid=0 | w=20
  178. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> hérédité autosomale récessive
    n1=en:genee-wiedemann syndrome | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
  179. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> hypochondroplasie
    n1=en:genee-wiedemann syndrome | n2=hypochondroplasie | rel=r_associated | relid=0 | w=20
  180. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> maladie congénitale
    n1=en:genee-wiedemann syndrome | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
  181. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> Maladie congénitale
    n1=en:genee-wiedemann syndrome | n2=Maladie congénitale | rel=r_associated | relid=0 | w=20
  182. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> maladie des épiphyses ponctuées
    n1=en:genee-wiedemann syndrome | n2=maladie des épiphyses ponctuées | rel=r_associated | relid=0 | w=20
  183. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> malformation
    n1=en:genee-wiedemann syndrome | n2=malformation | rel=r_associated | relid=0 | w=20
  184. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> malformation congénitale
    n1=en:genee-wiedemann syndrome | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
  185. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> micrognathie
    n1=en:genee-wiedemann syndrome | n2=micrognathie | rel=r_associated | relid=0 | w=20
  186. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> micrognathisme
    n1=en:genee-wiedemann syndrome | n2=micrognathisme | rel=r_associated | relid=0 | w=20
  187. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> nanisme mésomélique
    n1=en:genee-wiedemann syndrome | n2=nanisme mésomélique | rel=r_associated | relid=0 | w=20
  188. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> nanisme métatropique
    n1=en:genee-wiedemann syndrome | n2=nanisme métatropique | rel=r_associated | relid=0 | w=20
  189. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> nystagmus congénital isolé
    n1=en:genee-wiedemann syndrome | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  190. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> pathologie congénitale
    n1=en:genee-wiedemann syndrome | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
  191. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> pectus excavatum
    n1=en:genee-wiedemann syndrome | n2=pectus excavatum | rel=r_associated | relid=0 | w=20
  192. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> sténose du pylore
    n1=en:genee-wiedemann syndrome | n2=sténose du pylore | rel=r_associated | relid=0 | w=20
  193. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> sténose pylorique
    n1=en:genee-wiedemann syndrome | n2=sténose pylorique | rel=r_associated | relid=0 | w=20
  194. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Lowry-Wood
    n1=en:genee-wiedemann syndrome | n2=syndrome de Lowry-Wood | rel=r_associated | relid=0 | w=20
  195. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> tare congénitale
    n1=en:genee-wiedemann syndrome | n2=tare congénitale | rel=r_associated | relid=0 | w=20
  196. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> thorax en entonnoir
    n1=en:genee-wiedemann syndrome | n2=thorax en entonnoir | rel=r_associated | relid=0 | w=20
  197. en:genee-wiedemann syndrome -- r_associated #0: 20 / 0.465 -> vice de conformation
    n1=en:genee-wiedemann syndrome | n2=vice de conformation | rel=r_associated | relid=0 | w=20
≈ 254 relations entrantes

  1. anomalie congénitale --- r_associated #0: 424 --> en:genee-wiedemann syndrome
    n1=anomalie congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=424
  2. en:congenital abnormality --- r_associated #0: 421 --> en:genee-wiedemann syndrome
    n1=en:congenital abnormality | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=421
  3. malformation congénitale --- r_associated #0: 356 --> en:genee-wiedemann syndrome
    n1=malformation congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=356
  4. en:congenital anomaly --- r_associated #0: 353 --> en:genee-wiedemann syndrome
    n1=en:congenital anomaly | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=353
  5. en:congenital defect --- r_associated #0: 310 --> en:genee-wiedemann syndrome
    n1=en:congenital defect | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=310
  6. micrognathie --- r_associated #0: 308 --> en:genee-wiedemann syndrome
    n1=micrognathie | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=308
  7. micrognathisme --- r_associated #0: 306 --> en:genee-wiedemann syndrome
    n1=micrognathisme | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=306
  8. en:micrognathism --- r_associated #0: 300 --> en:genee-wiedemann syndrome
    n1=en:micrognathism | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=300
  9. déformation congénitale --- r_associated #0: 296 --> en:genee-wiedemann syndrome
    n1=déformation congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=296
  10. déficience congénitale --- r_associated #0: 295 --> en:genee-wiedemann syndrome
    n1=déficience congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=295
  11. difformité congénitale --- r_associated #0: 205 --> en:genee-wiedemann syndrome
    n1=difformité congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=205
  12. maladie congénitale --- r_associated #0: 204 --> en:genee-wiedemann syndrome
    n1=maladie congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=204
  13. pathologie congénitale --- r_associated #0: 195 --> en:genee-wiedemann syndrome
    n1=pathologie congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=195
  14. en:congenital malformation --- r_associated #0: 130 --> en:genee-wiedemann syndrome
    n1=en:congenital malformation | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=130
  15. en:birth defect --- r_associated #0: 120 --> en:genee-wiedemann syndrome
    n1=en:birth defect | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=120
  16. en:pyloric stenosis --- r_associated #0: 99 --> en:genee-wiedemann syndrome
    n1=en:pyloric stenosis | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=99
  17. sténose du pylore --- r_associated #0: 95 --> en:genee-wiedemann syndrome
    n1=sténose du pylore | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=95
  18. sténose pylorique --- r_associated #0: 95 --> en:genee-wiedemann syndrome
    n1=sténose pylorique | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=95
  19. en:pectus excavatum --- r_associated #0: 85 --> en:genee-wiedemann syndrome
    n1=en:pectus excavatum | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=85
  20. tare congénitale --- r_associated #0: 85 --> en:genee-wiedemann syndrome
    n1=tare congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=85
  21. pectus excavatum --- r_associated #0: 83 --> en:genee-wiedemann syndrome
    n1=pectus excavatum | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=83
  22. en:pyloric obstruction --- r_associated #0: 75 --> en:genee-wiedemann syndrome
    n1=en:pyloric obstruction | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=75
  23. congénitale --- r_associated #0: 65 --> en:genee-wiedemann syndrome
    n1=congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=65
  24. en:congenital --- r_associated #0: 64 --> en:genee-wiedemann syndrome
    n1=en:congenital | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=64
  25. thorax en entonnoir --- r_associated #0: 61 --> en:genee-wiedemann syndrome
    n1=thorax en entonnoir | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=61
  26. en:funnel chest --- r_associated #0: 58 --> en:genee-wiedemann syndrome
    n1=en:funnel chest | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=58
  27. congenital --- r_associated #0: 56 --> en:genee-wiedemann syndrome
    n1=congenital | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=56
  28. vice de conformation --- r_associated #0: 56 --> en:genee-wiedemann syndrome
    n1=vice de conformation | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=56
  29. congénital --- r_associated #0: 55 --> en:genee-wiedemann syndrome
    n1=congénital | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=55
  30. en:funnel breast --- r_associated #0: 54 --> en:genee-wiedemann syndrome
    n1=en:funnel breast | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=54
  31. dysplasie ophtalmo-mandibulomélique --- r_associated #0: 50 --> en:genee-wiedemann syndrome
    n1=dysplasie ophtalmo-mandibulomélique | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=50
  32. en:chondrodysplasia --- r_associated #0: 50 --> en:genee-wiedemann syndrome
    n1=en:chondrodysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=50
  33. en:major physical defect --- r_associated #0: 50 --> en:genee-wiedemann syndrome
    n1=en:major physical defect | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=50
  34. en:physical defect --- r_associated #0: 50 --> en:genee-wiedemann syndrome
    n1=en:physical defect | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=50
  35. dysplasie enchondrale --- r_associated #0: 49 --> en:genee-wiedemann syndrome
    n1=dysplasie enchondrale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=49
  36. en:chondrodysplasia punctata --- r_associated #0: 49 --> en:genee-wiedemann syndrome
    n1=en:chondrodysplasia punctata | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=49
  37. en:ophthalmomandibulomelic dysplasia --- r_associated #0: 47 --> en:genee-wiedemann syndrome
    n1=en:ophthalmomandibulomelic dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=47
  38. chondrodysplasia punctata --- r_associated #0: 46 --> en:genee-wiedemann syndrome
    n1=chondrodysplasia punctata | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=46
  39. œdème --- r_associated #0: 45 --> en:genee-wiedemann syndrome
    n1=œdème | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=45
  40. oedème --- r_associated #0: 45 --> en:genee-wiedemann syndrome
    n1=oedème | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=45
  41. œdème --- r_associated #0: 45 --> en:genee-wiedemann syndrome
    n1=œdème | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=45
  42. en:treacher collins syndrome --- r_associated #0: 43 --> en:genee-wiedemann syndrome
    n1=en:treacher collins syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=43
  43. anomalie du développement --- r_associated #0: 42 --> en:genee-wiedemann syndrome
    n1=anomalie du développement | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=42
  44. en:skeleton dysplasia --- r_associated #0: 42 --> en:genee-wiedemann syndrome
    n1=en:skeleton dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=42
  45. en:beals auriculo-osteodysplasia syndrome --- r_associated #0: 41 --> en:genee-wiedemann syndrome
    n1=en:beals auriculo-osteodysplasia syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=41
  46. en:steinfeld syndrome --- r_associated #0: 41 --> en:genee-wiedemann syndrome
    n1=en:steinfeld syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=41
  47. en:teratosis --- r_associated #0: 41 --> en:genee-wiedemann syndrome
    n1=en:teratosis | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=41
  48. en:arachnodactyly and intellectual disability with facial dysmorphism syndrome --- r_associated #0: 40 --> en:genee-wiedemann syndrome
    n1=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=40
  49. en:dhodh, arg346trp --- r_associated #0: 39 --> en:genee-wiedemann syndrome
    n1=en:dhodh, arg346trp | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=39
  50. en:malar flattening --- r_associated #0: 39 --> en:genee-wiedemann syndrome
    n1=en:malar flattening | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=39
  51. en:dhodh, arg199cys --- r_associated #0: 38 --> en:genee-wiedemann syndrome
    n1=en:dhodh, arg199cys | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=38
  52. maladie des épiphyses ponctuées --- r_associated #0: 38 --> en:genee-wiedemann syndrome
    n1=maladie des épiphyses ponctuées | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=38
  53. en:acrorenal mandibular syndrome --- r_associated #0: 37 --> en:genee-wiedemann syndrome
    n1=en:acrorenal mandibular syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=37
  54. nystagmus congénital isolé --- r_associated #0: 37 --> en:genee-wiedemann syndrome
    n1=nystagmus congénital isolé | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=37
  55. en:tarsal-carpal coalition syndrome --- r_associated #0: 36 --> en:genee-wiedemann syndrome
    n1=en:tarsal-carpal coalition syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=36
  56. en:accessory nipple --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:accessory nipple | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  57. en:autosomal recessive inheritance --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:autosomal recessive inheritance | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  58. en:brachyolmia type 3 --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:brachyolmia type 3 | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  59. en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  60. en:dhodh, gly152arg --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:dhodh, gly152arg | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  61. en:heart defects limb shortening --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:heart defects limb shortening | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  62. en:leri's pleonosteosis syndrome --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:leri's pleonosteosis syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  63. en:mental retardation mietens weber type --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:mental retardation mietens weber type | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  64. en:morava mehes syndrome --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:morava mehes syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  65. en:pterygium colli mental retardation digital anomalies --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:pterygium colli mental retardation digital anomalies | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  66. en:spondyloepiphyseal dysplasia, congenita --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:spondyloepiphyseal dysplasia, congenita | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  67. en:x-linked intellectual disability stevenson type --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=en:x-linked intellectual disability stevenson type | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  68. hérédité autosomale récessive --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=hérédité autosomale récessive | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  69. nanisme métatropique --- r_associated #0: 35 --> en:genee-wiedemann syndrome
    n1=nanisme métatropique | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  70. Miller --- r_associated #0: 34 --> en:genee-wiedemann syndrome
    n1=Miller | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=34
  71. en:chitty hall baraitser syndrome --- r_associated #0: 34 --> en:genee-wiedemann syndrome
    n1=en:chitty hall baraitser syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=34
  72. en:micrognathia --- r_associated #0: 34 --> en:genee-wiedemann syndrome
    n1=en:micrognathia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=34
  73. en:peg-shaped teeth --- r_associated #0: 34 --> en:genee-wiedemann syndrome
    n1=en:peg-shaped teeth | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=34
  74. en:polydactyly, preaxial ii (disorder) --- r_associated #0: 34 --> en:genee-wiedemann syndrome
    n1=en:polydactyly, preaxial ii (disorder) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=34
  75. en:symphalangism-brachydactyly syndrome --- r_associated #0: 34 --> en:genee-wiedemann syndrome
    n1=en:symphalangism-brachydactyly syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=34
  76. dysplasie épiphysaire, microcéphalie et nystagmus --- r_associated #0: 33 --> en:genee-wiedemann syndrome
    n1=dysplasie épiphysaire, microcéphalie et nystagmus | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=33
  77. en:metatropic dwarfism --- r_associated #0: 33 --> en:genee-wiedemann syndrome
    n1=en:metatropic dwarfism | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=33
  78. nanisme mésomélique --- r_associated #0: 33 --> en:genee-wiedemann syndrome
    n1=nanisme mésomélique | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=33
  79. en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:autosomal recessive distal osteolysis syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  80. en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  81. en:conductive hearing loss --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:conductive hearing loss | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  82. en:dysplasia with decreased bone density --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:dysplasia with decreased bone density | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  83. en:fg syndrome --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:fg syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  84. en:fountain syndrome --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:fountain syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  85. en:gracile bone dysplasia --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:gracile bone dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  86. en:gurrieri sammito bellussi syndrome --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:gurrieri sammito bellussi syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  87. en:hay-wells syndrome --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:hay-wells syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  88. en:limb deformities, congenital --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:limb deformities, congenital | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  89. en:mesomelic dysplasia --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:mesomelic dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  90. en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  91. en:osteodysplastic primordial dwarfism --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:osteodysplastic primordial dwarfism | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  92. en:renal dysplasia - limb defects syndrome --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:renal dysplasia - limb defects syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  93. en:spondylodysplastic group --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:spondylodysplastic group | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  94. en:townes-brocks syndrome --- r_associated #0: 32 --> en:genee-wiedemann syndrome
    n1=en:townes-brocks syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=32
  95. Maladie congénitale --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=Maladie congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  96. en:aminopterin syndrome sine aminopterin --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=en:aminopterin syndrome sine aminopterin | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  97. en:coffin-lowry syndrome --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=en:coffin-lowry syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  98. en:epiphyseal dysplasia --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=en:epiphyseal dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  99. en:greig syndrome --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=en:greig syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  100. en:melnick-needles syndrome --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=en:melnick-needles syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  101. en:multiple dislocations with dysplasia --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=en:multiple dislocations with dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  102. en:radioulnar synostosis --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=en:radioulnar synostosis | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  103. hypochondroplasie --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=hypochondroplasie | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  104. syndrome de Lowry-Wood --- r_associated #0: 31 --> en:genee-wiedemann syndrome
    n1=syndrome de Lowry-Wood | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=31
  105. en:Townes-Brocks syndrome --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:Townes-Brocks syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  106. en:bone development disorder --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:bone development disorder | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  107. en:brain malformation, congenital heart disease, postaxial polydactyly syndrome --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:brain malformation, congenital heart disease, postaxial polydactyly syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  108. en:cherubism with gingival fibromatosis --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:cherubism with gingival fibromatosis | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  109. en:chromosome 11p deletion syndrome --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:chromosome 11p deletion syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  110. en:developmental dysplasia of hip --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:developmental dysplasia of hip | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  111. en:developmental fault --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:developmental fault | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  112. en:dhodh, arg244trp --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:dhodh, arg244trp | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  113. en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:microcephaly albinism digital anomalies syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  114. en:osteoplastic dysplasia --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:osteoplastic dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  115. en:split-hand/foot malformation 3 --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:split-hand/foot malformation 3 | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  116. en:trichorhinophalangeal syndrome --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:trichorhinophalangeal syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  117. en:trichterbrust --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=en:trichterbrust | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  118. malformation --- r_associated #0: 30 --> en:genee-wiedemann syndrome
    n1=malformation | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=30
  119. en:achondrogenesis --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:achondrogenesis | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  120. en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  121. en:dhodh, 1-bp del, 611t --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:dhodh, 1-bp del, 611t | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  122. en:dhodh, arg135cys --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:dhodh, arg135cys | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  123. en:hypochondroplasia --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:hypochondroplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  124. en:pelviscapular dysplasia --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:pelviscapular dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  125. en:rhizomelic dysplasia patterson lowry type --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:rhizomelic dysplasia patterson lowry type | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  126. en:scholte syndrome --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:scholte syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  127. en:short rib dysplasia group (with or without polydactyly) --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:short rib dysplasia group (with or without polydactyly) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  128. en:trigonocephaly with bifid nose and acral anomaly syndrome --- r_associated #0: 29 --> en:genee-wiedemann syndrome
    n1=en:trigonocephaly with bifid nose and acral anomaly syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  129. en:baller-gerold syndrome --- r_associated #0: 28 --> en:genee-wiedemann syndrome
    n1=en:baller-gerold syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=28
  130. en:disorganized development of cartilaginous and fibrous components of the skeleton --- r_associated #0: 28 --> en:genee-wiedemann syndrome
    n1=en:disorganized development of cartilaginous and fibrous components of the skeleton | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=28
  131. en:heide syndrome --- r_associated #0: 28 --> en:genee-wiedemann syndrome
    n1=en:heide syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=28
  132. en:kniest-stickler dysplasia group --- r_associated #0: 28 --> en:genee-wiedemann syndrome
    n1=en:kniest-stickler dysplasia group | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=28
  133. en:kosztolanyi syndrome --- r_associated #0: 28 --> en:genee-wiedemann syndrome
    n1=en:kosztolanyi syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=28
  134. dysplasie mésomélique --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=dysplasie mésomélique | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  135. en:acrocallosal syndrome --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:acrocallosal syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  136. en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  137. en:bent bone dysplasia group --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:bent bone dysplasia group | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  138. en:congenital dysplasia --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:congenital dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  139. en:dhodh, gly202ala --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:dhodh, gly202ala | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  140. en:dhodh, gly202asp --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:dhodh, gly202asp | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  141. en:dysostosis --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:dysostosis | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  142. en:dysplasias with significant membranous bone involvement --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:dysplasias with significant membranous bone involvement | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  143. en:idiopathic osteolyses --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:idiopathic osteolyses | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  144. en:koilosternia --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:koilosternia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  145. en:larsen syndrome --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:larsen syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  146. en:low set ears --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:low set ears | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  147. en:osteodysplasia --- r_associated #0: 27 --> en:genee-wiedemann syndrome
    n1=en:osteodysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=27
  148. en:acromesomelic dysplasia syndrome --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:acromesomelic dysplasia syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  149. en:congenital hypoplasia of penis --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:congenital hypoplasia of penis | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  150. en:defects of the tubular (and flat) bones and/or axial skeleton --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:defects of the tubular (and flat) bones and/or axial skeleton | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  151. en:defects of tubular bones and spine --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:defects of tubular bones and spine | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  152. en:dhodh, gly19glu --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:dhodh, gly19glu | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  153. en:dysplasia with defective mineralization --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:dysplasia with defective mineralization | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  154. en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  155. en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  156. en:multiple synostosis syndrome --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:multiple synostosis syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  157. en:nager syndrome --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:nager syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  158. en:oculo-dento-digital syndrome --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:oculo-dento-digital syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  159. en:seaver cassidy syndrome --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:seaver cassidy syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  160. en:trisomy 10p --- r_associated #0: 26 --> en:genee-wiedemann syndrome
    n1=en:trisomy 10p | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=26
  161. en:mesomelis dwarfism --- r_associated #0: 25 --> en:genee-wiedemann syndrome
    n1=en:mesomelis dwarfism | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=25
  162. en:microcephaly --- r_associated #0: 25 --> en:genee-wiedemann syndrome
    n1=en:microcephaly | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=25
  163. en:pectus recurvatum --- r_associated #0: 24 --> en:genee-wiedemann syndrome
    n1=en:pectus recurvatum | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=24
  164. en:and nystagmus --- r_associated #0: 23 --> en:genee-wiedemann syndrome
    n1=en:and nystagmus | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=23
  165. en:dysostegenesis --- r_associated #0: 22 --> en:genee-wiedemann syndrome
    n1=en:dysostegenesis | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=22
  166. en:nystagmus --- r_associated #0: 22 --> en:genee-wiedemann syndrome
    n1=en:nystagmus | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=22
  167. contractures congénitales et arachnodactylie --- r_associated #0: 21 --> en:genee-wiedemann syndrome
    n1=contractures congénitales et arachnodactylie | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=21
  168. cuvette sternale --- r_associated #0: 21 --> en:genee-wiedemann syndrome
    n1=cuvette sternale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=21
  169. dysostose --- r_associated #0: 21 --> en:genee-wiedemann syndrome
    n1=dysostose | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=21
  170. en:developmental anomaly --- r_associated #0: 21 --> en:genee-wiedemann syndrome
    n1=en:developmental anomaly | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=21
  171. une anomalie congénitale --- r_associated #0: 21 --> en:genee-wiedemann syndrome
    n1=une anomalie congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=21
  172. en:absence of fifth digit --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:absence of fifth digit | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  173. en:atelosteogenesis, type 1 --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:atelosteogenesis, type 1 | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  174. en:autosomal recessive and dominant pedigrees described --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:autosomal recessive and dominant pedigrees described | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  175. en:camurati-engelmann syndrome --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:camurati-engelmann syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  176. en:caused by mutation in the dihydroorotate dehydrogenase gene (dhodh, 126064.0001) --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:caused by mutation in the dihydroorotate dehydrogenase gene (dhodh, 126064.0001) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  177. en:choanal atresia --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:choanal atresia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  178. en:cleft lip --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:cleft lip | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  179. en:cleft palate --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:cleft palate | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  180. en:coloboma of the eyelid --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:coloboma of the eyelid | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  181. en:congenital anomaly of the kidney --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:congenital anomaly of the kidney | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  182. en:cupped ears (finding) --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:cupped ears (finding) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  183. en:diastrophic dysplasia --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:diastrophic dysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  184. en:downward slant of palpebral fissure --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:downward slant of palpebral fissure | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  185. en:dysostosis multiplex group --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:dysostosis multiplex group | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  186. en:dysplasia with increased bone density --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:dysplasia with increased bone density | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  187. en:ectropion --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:ectropion | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  188. en:ehlers-danlos syndrome --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:ehlers-danlos syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  189. en:in-curving forearms --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:in-curving forearms | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  190. en:metaphyseal chondrodysplasia --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:metaphyseal chondrodysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  191. en:midgut malrotation --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:midgut malrotation | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  192. en:most case are sporadic --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:most case are sporadic | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  193. en:multiple congenital anomalies --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:multiple congenital anomalies | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  194. en:oculocerebrorenal syndrome --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:oculocerebrorenal syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  195. en:orofaciodigital syndrome type 1 --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:orofaciodigital syndrome type 1 | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  196. en:otopalatodigital syndrome, type ii --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:otopalatodigital syndrome, type ii | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  197. en:postnatal growth retardation --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:postnatal growth retardation | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  198. en:radial hypoplasia --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:radial hypoplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  199. en:rib defects --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:rib defects | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  200. en:roberts-sc phocomelia syndrome --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:roberts-sc phocomelia syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  201. en:rudiger syndrome 1 --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:rudiger syndrome 1 | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  202. en:ruvalcaba syndrome --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:ruvalcaba syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  203. en:stickler syndrome --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:stickler syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  204. en:supernumerary vertebra --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:supernumerary vertebra | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  205. en:syndactyly --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:syndactyly | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  206. en:thumb hypoplasia --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:thumb hypoplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  207. en:ulnar hypoplasia --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:ulnar hypoplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  208. en:undescended testes --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:undescended testes | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  209. en:weill-marchesani syndrome --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=en:weill-marchesani syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  210. syndrome --- r_associated #0: 20 --> en:genee-wiedemann syndrome
    n1=syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=20
  211. Malformation congénitale --- r_associated #0: 15 --> en:genee-wiedemann syndrome
    n1=Malformation congénitale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=15
  212. chondrodysplasia --- r_associated #0: 15 --> en:genee-wiedemann syndrome
    n1=chondrodysplasia | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=15
  213. malentendant (enfant) --- r_associated #0: 15 --> en:genee-wiedemann syndrome
    n1=malentendant (enfant) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=15
  214. CONGÉNITALE --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=CONGÉNITALE | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  215. DYSOSTOSE --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=DYSOSTOSE | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  216. Malformation --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=Malformation | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  217. Micrognathie --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=Micrognathie | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  218. Oedème --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=Oedème | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  219. achondrogénèses --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=achondrogénèses | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  220. chondrodysplasie --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=chondrodysplasie | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  221. chondrodysplasie ponctuée --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=chondrodysplasie ponctuée | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  222. chondrodystrophie --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=chondrodystrophie | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  223. en:achondroplasia hyperplastic --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=en:achondroplasia hyperplastic | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  224. en:cacomorphosis --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=en:cacomorphosis | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  225. en:contractural arachnodactyly --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=en:contractural arachnodactyly | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  226. en:edema --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=en:edema | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  227. en:eds --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=en:eds | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  228. en:ehlers danlos syndrome --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=en:ehlers danlos syndrome | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  229. en:hypoacousic child --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=en:hypoacousic child | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  230. microcéphalie-hernie hiatale-syndrome néphrotique --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=microcéphalie-hernie hiatale-syndrome néphrotique | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  231. micrognatisme --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=micrognatisme | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  232. microgéodes phalangiennes (syndrome des) --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=microgéodes phalangiennes (syndrome des) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  233. nanisme diastrophique --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=nanisme diastrophique | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  234. nystagmus --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=nystagmus | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  235. nystagmus héréditaire vertical --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=nystagmus héréditaire vertical | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  236. nystagmus lié au sexe --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=nystagmus lié au sexe | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  237. nystagmus myoclonies --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=nystagmus myoclonies | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  238. pectinés (organes) --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=pectinés (organes) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  239. syndrome cataracte, microcéphalie, arrêt de croissance et cyphoscoliose --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=syndrome cataracte, microcéphalie, arrêt de croissance et cyphoscoliose | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  240. syndrome de Townes-Brocks --- r_associated #0: 10 --> en:genee-wiedemann syndrome
    n1=syndrome de Townes-Brocks | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  241. Lowry-Wood (syndrome de) --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=Lowry-Wood (syndrome de) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  242. malf ormation dysraphique --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malf ormation dysraphique | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  243. malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malformation kystique adénomatoïde du poumon | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  244. malformation luxante de la hanche --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malformation luxante de la hanche | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  245. malformation mamelonnaire --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malformation mamelonnaire | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  246. malformation mammaire --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malformation mammaire | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  247. malformation ombilicale --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malformation ombilicale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  248. malformation utérine --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malformation utérine | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  249. malformation vaginale --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malformation vaginale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  250. malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malformation vasculaire cérébrale du nourrisson | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  251. malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=malformations de la charnière occipitocervicale | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  252. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=nystagmus (zone de moindre) | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  253. syndrome d'Ehlers-Danlos --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=syndrome d'Ehlers-Danlos | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
  254. syndrome de Stickler --- r_associated #0: 5 --> en:genee-wiedemann syndrome
    n1=syndrome de Stickler | n2=en:genee-wiedemann syndrome | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr