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'en:mental retardation, autosomal dominant 28'
(id=7888024 ; fe=en:mental retardation, autosomal dominant 28 ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=4077 creation date=2017-07-13 touchdate=2025-07-25 11:30:56.000)
≈ 73 relations sortantes

  1. en:mental retardation, autosomal dominant 28 -- r_associated #0: 44 / 1 -> en:autosomal dominant inheritance
    n1=en:mental retardation, autosomal dominant 28 | n2=en:autosomal dominant inheritance | rel=r_associated | relid=0 | w=44
  2. en:mental retardation, autosomal dominant 28 -- r_associated #0: 44 / 1 -> en:intellectual disability, mild to severe
    n1=en:mental retardation, autosomal dominant 28 | n2=en:intellectual disability, mild to severe | rel=r_associated | relid=0 | w=44
  3. en:mental retardation, autosomal dominant 28 -- r_associated #0: 44 / 1 -> en:seizures (less common)
    n1=en:mental retardation, autosomal dominant 28 | n2=en:seizures (less common) | rel=r_associated | relid=0 | w=44
  4. en:mental retardation, autosomal dominant 28 -- r_associated #0: 40 / 0.909 -> en:joint laxity
    n1=en:mental retardation, autosomal dominant 28 | n2=en:joint laxity | rel=r_associated | relid=0 | w=40
  5. en:mental retardation, autosomal dominant 28 -- r_associated #0: 40 / 0.909 -> en:motor stereotypy
    n1=en:mental retardation, autosomal dominant 28 | n2=en:motor stereotypy | rel=r_associated | relid=0 | w=40
  6. en:mental retardation, autosomal dominant 28 -- r_associated #0: 39 / 0.886 -> en:adnp, 4-bp del, 2496taaa
    n1=en:mental retardation, autosomal dominant 28 | n2=en:adnp, 4-bp del, 2496taaa | rel=r_associated | relid=0 | w=39
  7. en:mental retardation, autosomal dominant 28 -- r_associated #0: 36 / 0.818 -> en:congenital heart defects (less common)
    n1=en:mental retardation, autosomal dominant 28 | n2=en:congenital heart defects (less common) | rel=r_associated | relid=0 | w=36
  8. en:mental retardation, autosomal dominant 28 -- r_associated #0: 36 / 0.818 -> en:variable extraneurologic features
    n1=en:mental retardation, autosomal dominant 28 | n2=en:variable extraneurologic features | rel=r_associated | relid=0 | w=36
  9. en:mental retardation, autosomal dominant 28 -- r_associated #0: 36 / 0.818 -> en:wide nasal bridge
    n1=en:mental retardation, autosomal dominant 28 | n2=en:wide nasal bridge | rel=r_associated | relid=0 | w=36
  10. en:mental retardation, autosomal dominant 28 -- r_associated #0: 35 / 0.795 -> en:adnp, ser404ter
    n1=en:mental retardation, autosomal dominant 28 | n2=en:adnp, ser404ter | rel=r_associated | relid=0 | w=35
  11. en:mental retardation, autosomal dominant 28 -- r_associated #0: 35 / 0.795 -> en:global developmental delay
    n1=en:mental retardation, autosomal dominant 28 | n2=en:global developmental delay | rel=r_associated | relid=0 | w=35
  12. en:mental retardation, autosomal dominant 28 -- r_associated #0: 35 / 0.795 -> en:helsmoortel-van der aa syndrome
    n1=en:mental retardation, autosomal dominant 28 | n2=en:helsmoortel-van der aa syndrome | rel=r_associated | relid=0 | w=35
  13. en:mental retardation, autosomal dominant 28 -- r_associated #0: 35 / 0.795 -> en:hyperactivity
    n1=en:mental retardation, autosomal dominant 28 | n2=en:hyperactivity | rel=r_associated | relid=0 | w=35
  14. en:mental retardation, autosomal dominant 28 -- r_associated #0: 35 / 0.795 -> en:short nose
    n1=en:mental retardation, autosomal dominant 28 | n2=en:short nose | rel=r_associated | relid=0 | w=35
  15. en:mental retardation, autosomal dominant 28 -- r_associated #0: 32 / 0.727 -> en:autism spectrum disorder
    n1=en:mental retardation, autosomal dominant 28 | n2=en:autism spectrum disorder | rel=r_associated | relid=0 | w=32
  16. en:mental retardation, autosomal dominant 28 -- r_associated #0: 32 / 0.727 -> en:coloboma of the eyelid
    n1=en:mental retardation, autosomal dominant 28 | n2=en:coloboma of the eyelid | rel=r_associated | relid=0 | w=32
  17. en:mental retardation, autosomal dominant 28 -- r_associated #0: 32 / 0.727 -> en:hypotonia
    n1=en:mental retardation, autosomal dominant 28 | n2=en:hypotonia | rel=r_associated | relid=0 | w=32
  18. en:mental retardation, autosomal dominant 28 -- r_associated #0: 32 / 0.727 -> en:infantile onset
    n1=en:mental retardation, autosomal dominant 28 | n2=en:infantile onset | rel=r_associated | relid=0 | w=32
  19. en:mental retardation, autosomal dominant 28 -- r_associated #0: 31 / 0.705 -> en:adnp-related multiple congenital anomalies, intellectual disability, autism spectrum disorder
    n1=en:mental retardation, autosomal dominant 28 | n2=en:adnp-related multiple congenital anomalies, intellectual disability, autism spectrum disorder | rel=r_associated | relid=0 | w=31
  20. en:mental retardation, autosomal dominant 28 -- r_associated #0: 31 / 0.705 -> en:recurrent infections
    n1=en:mental retardation, autosomal dominant 28 | n2=en:recurrent infections | rel=r_associated | relid=0 | w=31
  21. en:mental retardation, autosomal dominant 28 -- r_associated #0: 30 / 0.682 -> en:adnp, 4-bp del, 2491ttaa
    n1=en:mental retardation, autosomal dominant 28 | n2=en:adnp, 4-bp del, 2491ttaa | rel=r_associated | relid=0 | w=30
  22. en:mental retardation, autosomal dominant 28 -- r_associated #0: 30 / 0.682 -> en:feeding problem
    n1=en:mental retardation, autosomal dominant 28 | n2=en:feeding problem | rel=r_associated | relid=0 | w=30
  23. en:mental retardation, autosomal dominant 28 -- r_associated #0: 29 / 0.659 -> en:downward slant of palpebral fissure
    n1=en:mental retardation, autosomal dominant 28 | n2=en:downward slant of palpebral fissure | rel=r_associated | relid=0 | w=29
  24. en:mental retardation, autosomal dominant 28 -- r_associated #0: 29 / 0.659 -> en:small hand
    n1=en:mental retardation, autosomal dominant 28 | n2=en:small hand | rel=r_associated | relid=0 | w=29
  25. en:mental retardation, autosomal dominant 28 -- r_associated #0: 29 / 0.659 -> en:thin upper lips
    n1=en:mental retardation, autosomal dominant 28 | n2=en:thin upper lips | rel=r_associated | relid=0 | w=29
  26. en:mental retardation, autosomal dominant 28 -- r_associated #0: 28 / 0.636 -> en:adnp, 1-bp del, 2808c
    n1=en:mental retardation, autosomal dominant 28 | n2=en:adnp, 1-bp del, 2808c | rel=r_associated | relid=0 | w=28
  27. en:mental retardation, autosomal dominant 28 -- r_associated #0: 28 / 0.636 -> en:adnp, tyr719ter
    n1=en:mental retardation, autosomal dominant 28 | n2=en:adnp, tyr719ter | rel=r_associated | relid=0 | w=28
  28. en:mental retardation, autosomal dominant 28 -- r_associated #0: 28 / 0.636 -> en:caused by mutation in the activity-dependent neuroprotector homeobox gene (adnp, 611386.0001)
    n1=en:mental retardation, autosomal dominant 28 | n2=en:caused by mutation in the activity-dependent neuroprotector homeobox gene (adnp, 611386.0001) | rel=r_associated | relid=0 | w=28
  29. en:mental retardation, autosomal dominant 28 -- r_associated #0: 28 / 0.636 -> en:obsessive compulsive behavior
    n1=en:mental retardation, autosomal dominant 28 | n2=en:obsessive compulsive behavior | rel=r_associated | relid=0 | w=28
  30. en:mental retardation, autosomal dominant 28 -- r_associated #0: 27 / 0.614 -> en:obesity
    n1=en:mental retardation, autosomal dominant 28 | n2=en:obesity | rel=r_associated | relid=0 | w=27
  31. en:mental retardation, autosomal dominant 28 -- r_associated #0: 27 / 0.614 -> en:prominent forehead
    n1=en:mental retardation, autosomal dominant 28 | n2=en:prominent forehead | rel=r_associated | relid=0 | w=27
  32. en:mental retardation, autosomal dominant 28 -- r_associated #0: 27 / 0.614 -> en:short stature
    n1=en:mental retardation, autosomal dominant 28 | n2=en:short stature | rel=r_associated | relid=0 | w=27
  33. en:mental retardation, autosomal dominant 28 -- r_associated #0: 27 / 0.614 -> en:smooth philtrum
    n1=en:mental retardation, autosomal dominant 28 | n2=en:smooth philtrum | rel=r_associated | relid=0 | w=27
  34. en:mental retardation, autosomal dominant 28 -- r_associated #0: 25 / 0.568 -> en:mental
    n1=en:mental retardation, autosomal dominant 28 | n2=en:mental | rel=r_associated | relid=0 | w=25
  35. en:mental retardation, autosomal dominant 28 -- r_associated #0: 21 / 0.477 -> obésité
    n1=en:mental retardation, autosomal dominant 28 | n2=obésité | rel=r_associated | relid=0 | w=21
  36. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> Bec de lièvre
    n1=en:mental retardation, autosomal dominant 28 | n2=Bec de lièvre | rel=r_associated | relid=0 | w=20
  37. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> bec de lièvre
    n1=en:mental retardation, autosomal dominant 28 | n2=bec de lièvre | rel=r_associated | relid=0 | w=20
  38. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:adnp, 1-bp ins, t
    n1=en:mental retardation, autosomal dominant 28 | n2=en:adnp, 1-bp ins, t | rel=r_associated | relid=0 | w=20
  39. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:adnp, 2-bp del, tt
    n1=en:mental retardation, autosomal dominant 28 | n2=en:adnp, 2-bp del, tt | rel=r_associated | relid=0 | w=20
  40. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:adnp, 4-bp del, ttta
    n1=en:mental retardation, autosomal dominant 28 | n2=en:adnp, 4-bp del, ttta | rel=r_associated | relid=0 | w=20
  41. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:and hypogonadotropic hypogonadism
    n1=en:mental retardation, autosomal dominant 28 | n2=en:and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=20
  42. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:and proeminent incisors
    n1=en:mental retardation, autosomal dominant 28 | n2=en:and proeminent incisors | rel=r_associated | relid=0 | w=20
  43. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:and teething delay
    n1=en:mental retardation, autosomal dominant 28 | n2=en:and teething delay | rel=r_associated | relid=0 | w=20
  44. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:autosomal dominant congenital deafness with onychodystrophy
    n1=en:mental retardation, autosomal dominant 28 | n2=en:autosomal dominant congenital deafness with onychodystrophy | rel=r_associated | relid=0 | w=20
  45. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:cleft lip
    n1=en:mental retardation, autosomal dominant 28 | n2=en:cleft lip | rel=r_associated | relid=0 | w=20
  46. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:cranioectodermal dysplasia
    n1=en:mental retardation, autosomal dominant 28 | n2=en:cranioectodermal dysplasia | rel=r_associated | relid=0 | w=20
  47. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
    n1=en:mental retardation, autosomal dominant 28 | n2=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | rel=r_associated | relid=0 | w=20
  48. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:harelip
    n1=en:mental retardation, autosomal dominant 28 | n2=en:harelip | rel=r_associated | relid=0 | w=20
  49. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:hernia
    n1=en:mental retardation, autosomal dominant 28 | n2=en:hernia | rel=r_associated | relid=0 | w=20
  50. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:hyperextensibility
    n1=en:mental retardation, autosomal dominant 28 | n2=en:hyperextensibility | rel=r_associated | relid=0 | w=20
  51. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:keratoconus posticus
    n1=en:mental retardation, autosomal dominant 28 | n2=en:keratoconus posticus | rel=r_associated | relid=0 | w=20
  52. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:macrosomia
    n1=en:mental retardation, autosomal dominant 28 | n2=en:macrosomia | rel=r_associated | relid=0 | w=20
  53. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:multicore disease with mental retardation
    n1=en:mental retardation, autosomal dominant 28 | n2=en:multicore disease with mental retardation | rel=r_associated | relid=0 | w=20
  54. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:obeseness
    n1=en:mental retardation, autosomal dominant 28 | n2=en:obeseness | rel=r_associated | relid=0 | w=20
  55. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:obesitas
    n1=en:mental retardation, autosomal dominant 28 | n2=en:obesitas | rel=r_associated | relid=0 | w=20
  56. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:ocular depression
    n1=en:mental retardation, autosomal dominant 28 | n2=en:ocular depression | rel=r_associated | relid=0 | w=20
  57. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:ophthalmoplegia
    n1=en:mental retardation, autosomal dominant 28 | n2=en:ophthalmoplegia | rel=r_associated | relid=0 | w=20
  58. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> en:palate-blepharophimosis
    n1=en:mental retardation, autosomal dominant 28 | n2=en:palate-blepharophimosis | rel=r_associated | relid=0 | w=20
  59. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> Fenn (diagramme de)
    n1=en:mental retardation, autosomal dominant 28 | n2=Fenn (diagramme de) | rel=r_associated | relid=0 | w=20
  60. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> fente labiale
    n1=en:mental retardation, autosomal dominant 28 | n2=fente labiale | rel=r_associated | relid=0 | w=20
  61. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> fente labiopalatine et blépharophimosis
    n1=en:mental retardation, autosomal dominant 28 | n2=fente labiopalatine et blépharophimosis | rel=r_associated | relid=0 | w=20
  62. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> hypothyroïdie (manifestations neuromusculaires dans l')
    n1=en:mental retardation, autosomal dominant 28 | n2=hypothyroïdie (manifestations neuromusculaires dans l') | rel=r_associated | relid=0 | w=20
  63. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> hypotonie
    n1=en:mental retardation, autosomal dominant 28 | n2=hypotonie | rel=r_associated | relid=0 | w=20
  64. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> hypotonie musculaire
    n1=en:mental retardation, autosomal dominant 28 | n2=hypotonie musculaire | rel=r_associated | relid=0 | w=20
  65. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> Hypotonie musculaire
    n1=en:mental retardation, autosomal dominant 28 | n2=Hypotonie musculaire | rel=r_associated | relid=0 | w=20
  66. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> hypotonie, obésité et incisives proéminentes
    n1=en:mental retardation, autosomal dominant 28 | n2=hypotonie, obésité et incisives proéminentes | rel=r_associated | relid=0 | w=20
  67. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> kératocône postérieur-fente labiale-petite taille
    n1=en:mental retardation, autosomal dominant 28 | n2=kératocône postérieur-fente labiale-petite taille | rel=r_associated | relid=0 | w=20
  68. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> macrosomie, obésité, macrocéphalie et anomalies oculaires
    n1=en:mental retardation, autosomal dominant 28 | n2=macrosomie, obésité, macrocéphalie et anomalies oculaires | rel=r_associated | relid=0 | w=20
  69. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> MOMO (syndrome)
    n1=en:mental retardation, autosomal dominant 28 | n2=MOMO (syndrome) | rel=r_associated | relid=0 | w=20
  70. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique
    n1=en:mental retardation, autosomal dominant 28 | n2=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | rel=r_associated | relid=0 | w=20
  71. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose
    n1=en:mental retardation, autosomal dominant 28 | n2=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | rel=r_associated | relid=0 | w=20
  72. en:mental retardation, autosomal dominant 28 -- r_associated #0: 20 / 0.455 -> petite taille, hyperextensibilité, hernie et dépression oculaire
    n1=en:mental retardation, autosomal dominant 28 | n2=petite taille, hyperextensibilité, hernie et dépression oculaire | rel=r_associated | relid=0 | w=20
  73. en:mental retardation, autosomal dominant 28 -- r_associated #0: 1 / 0.023 -> en:disease or syndrome
    n1=en:mental retardation, autosomal dominant 28 | n2=en:disease or syndrome | rel=r_associated | relid=0 | w=1
≈ 163 relations entrantes

  1. en:obesity --- r_associated #0: 279 --> en:mental retardation, autosomal dominant 28
    n1=en:obesity | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=279
  2. obésité --- r_associated #0: 278 --> en:mental retardation, autosomal dominant 28
    n1=obésité | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=278
  3. en:hypotonia --- r_associated #0: 86 --> en:mental retardation, autosomal dominant 28
    n1=en:hypotonia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=86
  4. hypotonie --- r_associated #0: 85 --> en:mental retardation, autosomal dominant 28
    n1=hypotonie | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=85
  5. hypotonie, obésité et incisives proéminentes --- r_associated #0: 67 --> en:mental retardation, autosomal dominant 28
    n1=hypotonie, obésité et incisives proéminentes | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=67
  6. hypotonie musculaire --- r_associated #0: 51 --> en:mental retardation, autosomal dominant 28
    n1=hypotonie musculaire | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=51
  7. MOMO (syndrome) --- r_associated #0: 50 --> en:mental retardation, autosomal dominant 28
    n1=MOMO (syndrome) | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=50
  8. en:obeseness --- r_associated #0: 50 --> en:mental retardation, autosomal dominant 28
    n1=en:obeseness | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=50
  9. kératocône postérieur-fente labiale-petite taille --- r_associated #0: 50 --> en:mental retardation, autosomal dominant 28
    n1=kératocône postérieur-fente labiale-petite taille | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=50
  10. en:keratoconus posticus --- r_associated #0: 49 --> en:mental retardation, autosomal dominant 28
    n1=en:keratoconus posticus | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=49
  11. fente labiopalatine et blépharophimosis --- r_associated #0: 49 --> en:mental retardation, autosomal dominant 28
    n1=fente labiopalatine et blépharophimosis | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=49
  12. en:macrosomia --- r_associated #0: 48 --> en:mental retardation, autosomal dominant 28
    n1=en:macrosomia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=48
  13. bec de lièvre --- r_associated #0: 47 --> en:mental retardation, autosomal dominant 28
    n1=bec de lièvre | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=47
  14. en:cleft lip --- r_associated #0: 45 --> en:mental retardation, autosomal dominant 28
    n1=en:cleft lip | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=45
  15. hypothyroïdie (manifestations neuromusculaires dans l') --- r_associated #0: 43 --> en:mental retardation, autosomal dominant 28
    n1=hypothyroïdie (manifestations neuromusculaires dans l') | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=43
  16. en:helsmoortel-van der aa syndrome --- r_associated #0: 42 --> en:mental retardation, autosomal dominant 28
    n1=en:helsmoortel-van der aa syndrome | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=42
  17. en:short stature --- r_associated #0: 42 --> en:mental retardation, autosomal dominant 28
    n1=en:short stature | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=42
  18. fente labiale --- r_associated #0: 42 --> en:mental retardation, autosomal dominant 28
    n1=fente labiale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=42
  19. en:feeding problem --- r_associated #0: 41 --> en:mental retardation, autosomal dominant 28
    n1=en:feeding problem | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=41
  20. en:harelip --- r_associated #0: 40 --> en:mental retardation, autosomal dominant 28
    n1=en:harelip | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=40
  21. macrosomie, obésité, macrocéphalie et anomalies oculaires --- r_associated #0: 40 --> en:mental retardation, autosomal dominant 28
    n1=macrosomie, obésité, macrocéphalie et anomalies oculaires | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=40
  22. myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique --- r_associated #0: 40 --> en:mental retardation, autosomal dominant 28
    n1=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=40
  23. petite taille, hyperextensibilité, hernie et dépression oculaire --- r_associated #0: 40 --> en:mental retardation, autosomal dominant 28
    n1=petite taille, hyperextensibilité, hernie et dépression oculaire | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=40
  24. Hypotonie musculaire --- r_associated #0: 39 --> en:mental retardation, autosomal dominant 28
    n1=Hypotonie musculaire | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=39
  25. Fenn (diagramme de) --- r_associated #0: 36 --> en:mental retardation, autosomal dominant 28
    n1=Fenn (diagramme de) | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=36
  26. en:autosomal dominant congenital deafness with onychodystrophy --- r_associated #0: 36 --> en:mental retardation, autosomal dominant 28
    n1=en:autosomal dominant congenital deafness with onychodystrophy | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=36
  27. en:adnp-related multiple congenital anomalies, intellectual disability, autism spectrum disorder --- r_associated #0: 35 --> en:mental retardation, autosomal dominant 28
    n1=en:adnp-related multiple congenital anomalies, intellectual disability, autism spectrum disorder | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=35
  28. en:adnp, 2-bp del, tt --- r_associated #0: 34 --> en:mental retardation, autosomal dominant 28
    n1=en:adnp, 2-bp del, tt | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=34
  29. ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose --- r_associated #0: 33 --> en:mental retardation, autosomal dominant 28
    n1=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=33
  30. en:adnp, 1-bp ins, t --- r_associated #0: 31 --> en:mental retardation, autosomal dominant 28
    n1=en:adnp, 1-bp ins, t | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=31
  31. en:prominent forehead --- r_associated #0: 31 --> en:mental retardation, autosomal dominant 28
    n1=en:prominent forehead | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=31
  32. en:wide nasal bridge --- r_associated #0: 31 --> en:mental retardation, autosomal dominant 28
    n1=en:wide nasal bridge | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=31
  33. en:caused by mutation in the activity-dependent neuroprotector homeobox gene (adnp, 611386.0001) --- r_associated #0: 30 --> en:mental retardation, autosomal dominant 28
    n1=en:caused by mutation in the activity-dependent neuroprotector homeobox gene (adnp, 611386.0001) | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=30
  34. en:hernia --- r_associated #0: 30 --> en:mental retardation, autosomal dominant 28
    n1=en:hernia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=30
  35. en:joint laxity --- r_associated #0: 30 --> en:mental retardation, autosomal dominant 28
    n1=en:joint laxity | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=30
  36. en:thin upper lips --- r_associated #0: 30 --> en:mental retardation, autosomal dominant 28
    n1=en:thin upper lips | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=30
  37. en:adnp, ser404ter --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 28
    n1=en:adnp, ser404ter | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=29
  38. en:autosomal dominant inheritance --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 28
    n1=en:autosomal dominant inheritance | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=29
  39. en:coloboma of the eyelid --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 28
    n1=en:coloboma of the eyelid | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=29
  40. en:cranioectodermal dysplasia --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 28
    n1=en:cranioectodermal dysplasia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=29
  41. en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 28
    n1=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=29
  42. en:ophthalmoplegia --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 28
    n1=en:ophthalmoplegia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=29
  43. macrocéphalie --- r_associated #0: 29 --> en:mental retardation, autosomal dominant 28
    n1=macrocéphalie | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=29
  44. Bec de lièvre --- r_associated #0: 28 --> en:mental retardation, autosomal dominant 28
    n1=Bec de lièvre | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=28
  45. en:adnp, 4-bp del, 2491ttaa --- r_associated #0: 28 --> en:mental retardation, autosomal dominant 28
    n1=en:adnp, 4-bp del, 2491ttaa | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=28
  46. en:and hypogonadotropic hypogonadism --- r_associated #0: 28 --> en:mental retardation, autosomal dominant 28
    n1=en:and hypogonadotropic hypogonadism | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=28
  47. en:hyperextensibility --- r_associated #0: 28 --> en:mental retardation, autosomal dominant 28
    n1=en:hyperextensibility | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=28
  48. en:small hand --- r_associated #0: 28 --> en:mental retardation, autosomal dominant 28
    n1=en:small hand | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=28
  49. en:smooth philtrum --- r_associated #0: 28 --> en:mental retardation, autosomal dominant 28
    n1=en:smooth philtrum | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=28
  50. en:variable extraneurologic features --- r_associated #0: 28 --> en:mental retardation, autosomal dominant 28
    n1=en:variable extraneurologic features | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=28
  51. en:adnp, 1-bp del, 2808c --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 28
    n1=en:adnp, 1-bp del, 2808c | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=27
  52. en:adnp, 4-bp del, 2496taaa --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 28
    n1=en:adnp, 4-bp del, 2496taaa | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=27
  53. en:adnp, 4-bp del, ttta --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 28
    n1=en:adnp, 4-bp del, ttta | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=27
  54. en:and proeminent incisors --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 28
    n1=en:and proeminent incisors | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=27
  55. en:intellectual disability, mild to severe --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 28
    n1=en:intellectual disability, mild to severe | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=27
  56. en:obesitas --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 28
    n1=en:obesitas | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=27
  57. en:ocular depression --- r_associated #0: 27 --> en:mental retardation, autosomal dominant 28
    n1=en:ocular depression | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=27
  58. en:adnp, tyr719ter --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 28
    n1=en:adnp, tyr719ter | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=26
  59. en:and teething delay --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 28
    n1=en:and teething delay | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=26
  60. en:hyperactivity --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 28
    n1=en:hyperactivity | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=26
  61. en:multicore disease with mental retardation --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 28
    n1=en:multicore disease with mental retardation | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=26
  62. en:palate-blepharophimosis --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 28
    n1=en:palate-blepharophimosis | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=26
  63. en:seizures (less common) --- r_associated #0: 26 --> en:mental retardation, autosomal dominant 28
    n1=en:seizures (less common) | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=26
  64. en:infantile onset --- r_associated #0: 25 --> en:mental retardation, autosomal dominant 28
    n1=en:infantile onset | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=25
  65. en:short nose --- r_associated #0: 25 --> en:mental retardation, autosomal dominant 28
    n1=en:short nose | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=25
  66. kératocône posticus --- r_associated #0: 25 --> en:mental retardation, autosomal dominant 28
    n1=kératocône posticus | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=25
  67. en:pinguefying --- r_associated #0: 24 --> en:mental retardation, autosomal dominant 28
    n1=en:pinguefying | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=24
  68. bébé bronzé (syndrome du) --- r_associated #0: 23 --> en:mental retardation, autosomal dominant 28
    n1=bébé bronzé (syndrome du) | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=23
  69. en:macrocephaly --- r_associated #0: 23 --> en:mental retardation, autosomal dominant 28
    n1=en:macrocephaly | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=23
  70. en:motor stereotypy --- r_associated #0: 23 --> en:mental retardation, autosomal dominant 28
    n1=en:motor stereotypy | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=23
  71. en:Rieger anomaly --- r_associated #0: 22 --> en:mental retardation, autosomal dominant 28
    n1=en:Rieger anomaly | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=22
  72. en:cleft palate --- r_associated #0: 22 --> en:mental retardation, autosomal dominant 28
    n1=en:cleft palate | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=22
  73. en:congenital heart defects (less common) --- r_associated #0: 22 --> en:mental retardation, autosomal dominant 28
    n1=en:congenital heart defects (less common) | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=22
  74. en:global developmental delay --- r_associated #0: 22 --> en:mental retardation, autosomal dominant 28
    n1=en:global developmental delay | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=22
  75. en:labial fissure --- r_associated #0: 22 --> en:mental retardation, autosomal dominant 28
    n1=en:labial fissure | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=22
  76. en:obsessive compulsive behavior --- r_associated #0: 22 --> en:mental retardation, autosomal dominant 28
    n1=en:obsessive compulsive behavior | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=22
  77. en:recurrent infections --- r_associated #0: 22 --> en:mental retardation, autosomal dominant 28
    n1=en:recurrent infections | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=22
  78. insuffisance staturale --- r_associated #0: 22 --> en:mental retardation, autosomal dominant 28
    n1=insuffisance staturale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=22
  79. en:autism spectrum disorder --- r_associated #0: 21 --> en:mental retardation, autosomal dominant 28
    n1=en:autism spectrum disorder | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=21
  80. en:downward slant of palpebral fissure --- r_associated #0: 21 --> en:mental retardation, autosomal dominant 28
    n1=en:downward slant of palpebral fissure | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=21
  81. en:muscular hypotonia --- r_associated #0: 21 --> en:mental retardation, autosomal dominant 28
    n1=en:muscular hypotonia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=21
  82. en:congenital atrophy of thyroid --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=en:congenital atrophy of thyroid | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  83. en:congenital hypothyroidism --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=en:congenital hypothyroidism | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  84. en:neonatal hypothyroidism --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=en:neonatal hypothyroidism | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  85. fente labio-palatine --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=fente labio-palatine | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  86. fente labiopalatine --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=fente labiopalatine | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  87. hypothyroïdie congénitale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypothyroïdie congénitale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  88. hypothyroïdie et psychisme --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypothyroïdie et psychisme | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  89. hypothyroïdie néonatale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypothyroïdie néonatale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  90. hypotonie plasmatique --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotonie plasmatique | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  91. hypotonie sphinctérienne anale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotonie sphinctérienne anale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  92. hypotonie sphinctérienne uréthrale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotonie sphinctérienne uréthrale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  93. hypotonie utérine --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotonie utérine | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  94. hypotonie vésicale --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotonie vésicale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  95. hypotonique --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotonique | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  96. hypotrichose --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotrichose | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  97. hypotrichose avec anodontie et anhidrose de Touraine --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotrichose avec anodontie et anhidrose de Touraine | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  98. hypotrichose congénitale des cils --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotrichose congénitale des cils | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  99. hypotrichose congénitale simple --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotrichose congénitale simple | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  100. hypotrichose héréditaire de Marie Unna --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotrichose héréditaire de Marie Unna | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  101. hypotrichose, atrophodermie folliculaire et épithéliomatose --- r_associated #0: 15 --> en:mental retardation, autosomal dominant 28
    n1=hypotrichose, atrophodermie folliculaire et épithéliomatose | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=15
  102. BEC DE LIEVRE --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=BEC DE LIEVRE | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  103. Hypotonie --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=Hypotonie | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  104. Obésité --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=Obésité | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  105. atonie de l'utérus --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=atonie de l'utérus | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  106. bec de corbin --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=bec de corbin | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  107. bec de cuiller --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=bec de cuiller | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  108. bec de la prostate --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=bec de la prostate | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  109. bec de la rotule --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=bec de la rotule | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  110. bébé collodion --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=bébé collodion | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  111. division palatine --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=division palatine | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  112. en:Fenn's diagram --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:Fenn's diagram | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  113. en:anal sphincter hypotonia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:anal sphincter hypotonia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  114. en:and ocular abnormalities --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:and ocular abnormalities | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  115. en:and ocular abnormalities syndrome --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:and ocular abnormalities syndrome | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  116. en:ataxia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:ataxia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  117. en:bladder hypotonia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:bladder hypotonia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  118. en:bronze baby syndrome --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:bronze baby syndrome | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  119. en:congenital eyelashes hypotrichosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:congenital eyelashes hypotrichosis | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  120. en:hypacusis and athetosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:hypacusis and athetosis | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  121. en:hypothyreosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:hypothyreosis | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  122. en:hypothyroidism and psychism --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:hypothyroidism and psychism | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  123. en:hypotonic --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:hypotonic | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  124. en:hypotrichosis --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:hypotrichosis | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  125. en:hypotrichosis congenita simplex --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:hypotrichosis congenita simplex | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  126. en:hypotrichosis-anodontic syndrome --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:hypotrichosis-anodontic syndrome | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  127. en:labiopalatine cleft --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:labiopalatine cleft | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  128. en:plasma hypotonia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:plasma hypotonia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  129. en:sphincteric hypotony --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:sphincteric hypotony | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  130. en:uterine hypotonia --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=en:uterine hypotonia | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  131. fente cérébrale de Bichat --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente cérébrale de Bichat | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  132. fente de Larrey --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente de Larrey | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  133. fente de la glotte --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente de la glotte | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  134. fente foetale --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente foetale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  135. fente hypophysaire --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente hypophysaire | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  136. fente interaryténoïdienne --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente interaryténoïdienne | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  137. fente interfessière --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente interfessière | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  138. fente labiopalatine et kystes muqueux de la lèvre inférieure --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente labiopalatine et kystes muqueux de la lèvre inférieure | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  139. fente labiopalatine, ectropion et dents coniques --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente labiopalatine, ectropion et dents coniques | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  140. fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  141. fente palatine --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fente palatine | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  142. fissure palatine --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fissure palatine | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  143. fénotérol --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=fénotérol | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  144. inertie utérine --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=inertie utérine | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  145. macrosomie --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=macrosomie | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  146. polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  147. syndrome de Treft-Sanborn-Carey --- r_associated #0: 10 --> en:mental retardation, autosomal dominant 28
    n1=syndrome de Treft-Sanborn-Carey | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=10
  148. Fente labiale --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=Fente labiale | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  149. Hypotonique --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=Hypotonique | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  150. Macrocéphalie --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=Macrocéphalie | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  151. atrophie congénitale de la thyroïde --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=atrophie congénitale de la thyroïde | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  152. bec de perroquet --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=bec de perroquet | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  153. bec du cuboïde --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=bec du cuboïde | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  154. bec du sphénoïde --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=bec du sphénoïde | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  155. bec scléral --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=bec scléral | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  156. bécégite --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=bécégite | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  157. crétinismes --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=crétinismes | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  158. en:congenital goiter --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=en:congenital goiter | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  159. goitre congénital --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=goitre congénital | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  160. hypothyroïdisme congénital --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=hypothyroïdisme congénital | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  161. infantilisme type brissaud --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=infantilisme type brissaud | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  162. nanisme hypothyroïdien --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=nanisme hypothyroïdien | n2=en:mental retardation, autosomal dominant 28 | rel=r_associated | relid=0 | w=5
  163. syndrome d'insuffisance thyroïdienne congénitale --- r_associated #0: 5 --> en:mental retardation, autosomal dominant 28
    n1=syndrome d'insuffisance thyroïdienne congénitale | n2=en:mental retardation, autosomal dominant 28 | 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