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'en:norrie disease'
(id=9097890 ; fe=en:norrie disease ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=2527 creation date=2017-10-27 touchdate=2025-03-23 09:02:35.000)
≈ 77 relations sortantes

  1. en:norrie disease -- r_associated #0: 35 / 1 -> microphtalmie oligophrénique
    n1=en:norrie disease | n2=microphtalmie oligophrénique | rel=r_associated | relid=0 | w=35
  2. en:norrie disease -- r_associated #0: 31 / 0.886 -> atrophie héréditaire des globes oculaires
    n1=en:norrie disease | n2=atrophie héréditaire des globes oculaires | rel=r_associated | relid=0 | w=31
  3. en:norrie disease -- r_associated #0: 31 / 0.886 -> en:norrie syndrome
    n1=en:norrie disease | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=31
  4. en:norrie disease -- r_associated #0: 30 / 0.857 -> maladie de Norrie
    n1=en:norrie disease | n2=maladie de Norrie | rel=r_associated | relid=0 | w=30
  5. en:norrie disease -- r_associated #0: 30 / 0.857 -> Norrie
    n1=en:norrie disease | n2=Norrie | rel=r_associated | relid=0 | w=30
  6. en:norrie disease -- r_associated #0: 29 / 0.829 -> maladie de norrie
    n1=en:norrie disease | n2=maladie de norrie | rel=r_associated | relid=0 | w=29
  7. en:norrie disease -- r_associated #0: 27 / 0.771 -> maladie
    n1=en:norrie disease | n2=maladie | rel=r_associated | relid=0 | w=27
  8. en:norrie disease -- r_associated #0: 20 / 0.571 -> coeur triatrial
    n1=en:norrie disease | n2=coeur triatrial | rel=r_associated | relid=0 | w=20
  9. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:acrodysostosis 1
    n1=en:norrie disease | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
  10. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:aniridia and intellectual disability syndrome
    n1=en:norrie disease | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  11. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome
    n1=en:norrie disease | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=20
  12. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ataxia-telangiectasisa-like disorder 1
    n1=en:norrie disease | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
  13. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:carbonic anhydrase i deficiency
    n1=en:norrie disease | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
  14. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:cataract glaucoma syndrome
    n1=en:norrie disease | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=20
  15. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:chitayat meunier hodgkinson syndrome
    n1=en:norrie disease | n2=en:chitayat meunier hodgkinson syndrome | rel=r_associated | relid=0 | w=20
  16. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:chromosome xp22.3 microdeletion syndrome
    n1=en:norrie disease | n2=en:chromosome xp22.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20
  17. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:congenital cataract with ataxia and deafness syndrome
    n1=en:norrie disease | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20
  18. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:congenital disorder of glycosylation type 1s
    n1=en:norrie disease | n2=en:congenital disorder of glycosylation type 1s | rel=r_associated | relid=0 | w=20
  19. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:cor triatriatum
    n1=en:norrie disease | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=20
  20. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:cortical dysplasia-focal epilepsy syndrome
    n1=en:norrie disease | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
  21. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:deafness and myopia syndrome
    n1=en:norrie disease | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20
  22. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:disorder of eye co-occurrent and due to marfan syndrome
    n1=en:norrie disease | n2=en:disorder of eye co-occurrent and due to marfan syndrome | rel=r_associated | relid=0 | w=20
  23. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ectodermal dysplasia with blindness syndrome
    n1=en:norrie disease | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
  24. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:eiken type chondrodysplasia
    n1=en:norrie disease | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
  25. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:emanuel syndrome
    n1=en:norrie disease | n2=en:emanuel syndrome | rel=r_associated | relid=0 | w=20
  26. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:eye involvement begins at birth, neurologic involvement begins later
    n1=en:norrie disease | n2=en:eye involvement begins at birth, neurologic involvement begins later | rel=r_associated | relid=0 | w=20
  27. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:fried syndrome
    n1=en:norrie disease | n2=en:fried syndrome | rel=r_associated | relid=0 | w=20
  28. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:glaucoma and sleep apnea syndrome
    n1=en:norrie disease | n2=en:glaucoma and sleep apnea syndrome | rel=r_associated | relid=0 | w=20
  29. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome
    n1=en:norrie disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20
  30. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:lethal neonatal rigidity and multifocal seizure syndrome
    n1=en:norrie disease | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
  31. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome
    n1=en:norrie disease | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20
  32. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
    n1=en:norrie disease | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
  33. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:mental retardation spasticity ectrodactyly
    n1=en:norrie disease | n2=en:mental retardation spasticity ectrodactyly | rel=r_associated | relid=0 | w=20
  34. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:mental retardation, autosomal dominant 9
    n1=en:norrie disease | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
  35. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:mental retardation, autosomal recessive 34
    n1=en:norrie disease | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
  36. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:microcephaly and chorioretinopathy, autosomal recessive, type 1
    n1=en:norrie disease | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=20
  37. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:mitochondrial dna depletion syndrome 12
    n1=en:norrie disease | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
  38. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:mucolipidosis type iii gamma
    n1=en:norrie disease | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
  39. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, 1-bp del
    n1=en:norrie disease | n2=en:ndp, 1-bp del | rel=r_associated | relid=0 | w=20
  40. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, ala105thr
    n1=en:norrie disease | n2=en:ndp, ala105thr | rel=r_associated | relid=0 | w=20
  41. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, arg90pro
    n1=en:norrie disease | n2=en:ndp, arg90pro | rel=r_associated | relid=0 | w=20
  42. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, cys128ter
    n1=en:norrie disease | n2=en:ndp, cys128ter | rel=r_associated | relid=0 | w=20
  43. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, cys69ser
    n1=en:norrie disease | n2=en:ndp, cys69ser | rel=r_associated | relid=0 | w=20
  44. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, cys96trp
    n1=en:norrie disease | n2=en:ndp, cys96trp | rel=r_associated | relid=0 | w=20
  45. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, cys96tyr
    n1=en:norrie disease | n2=en:ndp, cys96tyr | rel=r_associated | relid=0 | w=20
  46. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, leu13arg
    n1=en:norrie disease | n2=en:ndp, leu13arg | rel=r_associated | relid=0 | w=20
  47. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, leu61phe
    n1=en:norrie disease | n2=en:ndp, leu61phe | rel=r_associated | relid=0 | w=20
  48. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, met1val
    n1=en:norrie disease | n2=en:ndp, met1val | rel=r_associated | relid=0 | w=20
  49. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, ser101phe
    n1=en:norrie disease | n2=en:ndp, ser101phe | rel=r_associated | relid=0 | w=20
  50. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, ser73ter
    n1=en:norrie disease | n2=en:ndp, ser73ter | rel=r_associated | relid=0 | w=20
  51. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, ser75cys
    n1=en:norrie disease | n2=en:ndp, ser75cys | rel=r_associated | relid=0 | w=20
  52. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, tyr44cys
    n1=en:norrie disease | n2=en:ndp, tyr44cys | rel=r_associated | relid=0 | w=20
  53. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, val45glu
    n1=en:norrie disease | n2=en:ndp, val45glu | rel=r_associated | relid=0 | w=20
  54. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ndp, val60glu
    n1=en:norrie disease | n2=en:ndp, val60glu | rel=r_associated | relid=0 | w=20
  55. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:Norrie's disease
    n1=en:norrie disease | n2=en:Norrie's disease | rel=r_associated | relid=0 | w=20
  56. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:pigmented paravenous chorioretinal atrophy
    n1=en:norrie disease | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20
  57. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:plasma kallikrein deficiency
    n1=en:norrie disease | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
  58. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:ppp2r5d-related intellectual disability
    n1=en:norrie disease | n2=en:ppp2r5d-related intellectual disability | rel=r_associated | relid=0 | w=20
  59. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:primary ciliary dyskinesia and retinitis pigmentosa syndrome
    n1=en:norrie disease | n2=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=20
  60. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:robinow-like syndrome
    n1=en:norrie disease | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20
  61. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:scholte syndrome
    n1=en:norrie disease | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20
  62. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:tissue kallikrein deficiency
    n1=en:norrie disease | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
  63. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x- linked recessive
    n1=en:norrie disease | n2=en:x- linked recessive | rel=r_associated | relid=0 | w=20
  64. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability armfield type
    n1=en:norrie disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
  65. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability miles carpenter type
    n1=en:norrie disease | n2=en:x-linked intellectual disability miles carpenter type | rel=r_associated | relid=0 | w=20
  66. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability pai type
    n1=en:norrie disease | n2=en:x-linked intellectual disability pai type | rel=r_associated | relid=0 | w=20
  67. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability seemanova type
    n1=en:norrie disease | n2=en:x-linked intellectual disability seemanova type | rel=r_associated | relid=0 | w=20
  68. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability stevenson type
    n1=en:norrie disease | n2=en:x-linked intellectual disability stevenson type | rel=r_associated | relid=0 | w=20
  69. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability stoll type
    n1=en:norrie disease | n2=en:x-linked intellectual disability stoll type | rel=r_associated | relid=0 | w=20
  70. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability van esch type
    n1=en:norrie disease | n2=en:x-linked intellectual disability van esch type | rel=r_associated | relid=0 | w=20
  71. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
    n1=en:norrie disease | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20
  72. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability with ataxia and apraxia syndrome
    n1=en:norrie disease | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=20
  73. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
    n1=en:norrie disease | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=20
  74. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome
    n1=en:norrie disease | n2=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | rel=r_associated | relid=0 | w=20
  75. en:norrie disease -- r_associated #0: 20 / 0.571 -> en:yemenite deaf-blind hypopigmentation syndrome
    n1=en:norrie disease | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20
  76. en:norrie disease -- r_associated #0: 20 / 0.571 -> Norrie (maladie de)
    n1=en:norrie disease | n2=Norrie (maladie de) | rel=r_associated | relid=0 | w=20
  77. en:norrie disease -- r_associated #0: 20 / 0.571 -> rétinite pigmentaire paraveineuse
    n1=en:norrie disease | n2=rétinite pigmentaire paraveineuse | rel=r_associated | relid=0 | w=20
≈ 79 relations entrantes

  1. cœur triatrial --- r_associated #0: 50 --> en:norrie disease
    n1=cœur triatrial | n2=en:norrie disease | rel=r_associated | relid=0 | w=50
  2. maladie de norrie --- r_associated #0: 50 --> en:norrie disease
    n1=maladie de norrie | n2=en:norrie disease | rel=r_associated | relid=0 | w=50
  3. maladie de Norrie --- r_associated #0: 49 --> en:norrie disease
    n1=maladie de Norrie | n2=en:norrie disease | rel=r_associated | relid=0 | w=49
  4. coeur triatrial --- r_associated #0: 46 --> en:norrie disease
    n1=coeur triatrial | n2=en:norrie disease | rel=r_associated | relid=0 | w=46
  5. rétinite pigmentaire paraveineuse --- r_associated #0: 42 --> en:norrie disease
    n1=rétinite pigmentaire paraveineuse | n2=en:norrie disease | rel=r_associated | relid=0 | w=42
  6. en:aniridia and intellectual disability syndrome --- r_associated #0: 41 --> en:norrie disease
    n1=en:aniridia and intellectual disability syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=41
  7. en:pigmented paravenous chorioretinal atrophy --- r_associated #0: 41 --> en:norrie disease
    n1=en:pigmented paravenous chorioretinal atrophy | n2=en:norrie disease | rel=r_associated | relid=0 | w=41
  8. en:x- linked recessive --- r_associated #0: 41 --> en:norrie disease
    n1=en:x- linked recessive | n2=en:norrie disease | rel=r_associated | relid=0 | w=41
  9. en:x-linked intellectual disability with acromegaly and hyperactivity syndrome --- r_associated #0: 41 --> en:norrie disease
    n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=41
  10. Norrie --- r_associated #0: 40 --> en:norrie disease
    n1=Norrie | n2=en:norrie disease | rel=r_associated | relid=0 | w=40
  11. en:ndp, ser75cys --- r_associated #0: 40 --> en:norrie disease
    n1=en:ndp, ser75cys | n2=en:norrie disease | rel=r_associated | relid=0 | w=40
  12. en:ndp, cys69ser --- r_associated #0: 36 --> en:norrie disease
    n1=en:ndp, cys69ser | n2=en:norrie disease | rel=r_associated | relid=0 | w=36
  13. en:x-linked intellectual disability van esch type --- r_associated #0: 36 --> en:norrie disease
    n1=en:x-linked intellectual disability van esch type | n2=en:norrie disease | rel=r_associated | relid=0 | w=36
  14. en:mental retardation, autosomal dominant 9 --- r_associated #0: 35 --> en:norrie disease
    n1=en:mental retardation, autosomal dominant 9 | n2=en:norrie disease | rel=r_associated | relid=0 | w=35
  15. en:mitochondrial dna depletion syndrome 12 --- r_associated #0: 35 --> en:norrie disease
    n1=en:mitochondrial dna depletion syndrome 12 | n2=en:norrie disease | rel=r_associated | relid=0 | w=35
  16. en:ndp, met1val --- r_associated #0: 35 --> en:norrie disease
    n1=en:ndp, met1val | n2=en:norrie disease | rel=r_associated | relid=0 | w=35
  17. en:ndp, val60glu --- r_associated #0: 35 --> en:norrie disease
    n1=en:ndp, val60glu | n2=en:norrie disease | rel=r_associated | relid=0 | w=35
  18. en:x-linked intellectual disability seemanova type --- r_associated #0: 35 --> en:norrie disease
    n1=en:x-linked intellectual disability seemanova type | n2=en:norrie disease | rel=r_associated | relid=0 | w=35
  19. en:x-linked intellectual disability with ataxia and apraxia syndrome --- r_associated #0: 35 --> en:norrie disease
    n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=35
  20. en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 35 --> en:norrie disease
    n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=35
  21. en:acrodysostosis 1 --- r_associated #0: 34 --> en:norrie disease
    n1=en:acrodysostosis 1 | n2=en:norrie disease | rel=r_associated | relid=0 | w=34
  22. en:carbonic anhydrase i deficiency --- r_associated #0: 34 --> en:norrie disease
    n1=en:carbonic anhydrase i deficiency | n2=en:norrie disease | rel=r_associated | relid=0 | w=34
  23. en:emanuel syndrome --- r_associated #0: 34 --> en:norrie disease
    n1=en:emanuel syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=34
  24. en:microcephaly and chorioretinopathy, autosomal recessive, type 1 --- r_associated #0: 34 --> en:norrie disease
    n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:norrie disease | rel=r_associated | relid=0 | w=34
  25. en:robinow-like syndrome --- r_associated #0: 34 --> en:norrie disease
    n1=en:robinow-like syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=34
  26. en:scholte syndrome --- r_associated #0: 34 --> en:norrie disease
    n1=en:scholte syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=34
  27. en:Norrie's disease --- r_associated #0: 32 --> en:norrie disease
    n1=en:Norrie's disease | n2=en:norrie disease | rel=r_associated | relid=0 | w=32
  28. en:ataxia-telangiectasisa-like disorder 1 --- r_associated #0: 32 --> en:norrie disease
    n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:norrie disease | rel=r_associated | relid=0 | w=32
  29. en:fried syndrome --- r_associated #0: 32 --> en:norrie disease
    n1=en:fried syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=32
  30. en:mucolipidosis type iii gamma --- r_associated #0: 32 --> en:norrie disease
    n1=en:mucolipidosis type iii gamma | n2=en:norrie disease | rel=r_associated | relid=0 | w=32
  31. en:ndp, ala105thr --- r_associated #0: 32 --> en:norrie disease
    n1=en:ndp, ala105thr | n2=en:norrie disease | rel=r_associated | relid=0 | w=32
  32. en:ndp, cys128ter --- r_associated #0: 32 --> en:norrie disease
    n1=en:ndp, cys128ter | n2=en:norrie disease | rel=r_associated | relid=0 | w=32
  33. en:ndp, cys96tyr --- r_associated #0: 32 --> en:norrie disease
    n1=en:ndp, cys96tyr | n2=en:norrie disease | rel=r_associated | relid=0 | w=32
  34. en:x-linked intellectual disability stevenson type --- r_associated #0: 32 --> en:norrie disease
    n1=en:x-linked intellectual disability stevenson type | n2=en:norrie disease | rel=r_associated | relid=0 | w=32
  35. en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome --- r_associated #0: 32 --> en:norrie disease
    n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=32
  36. en:disorder of eye co-occurrent and due to marfan syndrome --- r_associated #0: 31 --> en:norrie disease
    n1=en:disorder of eye co-occurrent and due to marfan syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  37. en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 31 --> en:norrie disease
    n1=en:ectodermal dysplasia with blindness syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  38. en:glaucoma and sleep apnea syndrome --- r_associated #0: 31 --> en:norrie disease
    n1=en:glaucoma and sleep apnea syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  39. en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 31 --> en:norrie disease
    n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  40. en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 31 --> en:norrie disease
    n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  41. en:mental retardation spasticity ectrodactyly --- r_associated #0: 31 --> en:norrie disease
    n1=en:mental retardation spasticity ectrodactyly | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  42. en:ndp, ser73ter --- r_associated #0: 31 --> en:norrie disease
    n1=en:ndp, ser73ter | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  43. en:plasma kallikrein deficiency --- r_associated #0: 31 --> en:norrie disease
    n1=en:plasma kallikrein deficiency | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  44. en:ppp2r5d-related intellectual disability --- r_associated #0: 31 --> en:norrie disease
    n1=en:ppp2r5d-related intellectual disability | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  45. microphtalmie oligophrénique --- r_associated #0: 31 --> en:norrie disease
    n1=microphtalmie oligophrénique | n2=en:norrie disease | rel=r_associated | relid=0 | w=31
  46. en:chromosome xp22.3 microdeletion syndrome --- r_associated #0: 30 --> en:norrie disease
    n1=en:chromosome xp22.3 microdeletion syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=30
  47. en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome --- r_associated #0: 30 --> en:norrie disease
    n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=30
  48. en:ndp, 1-bp del --- r_associated #0: 30 --> en:norrie disease
    n1=en:ndp, 1-bp del | n2=en:norrie disease | rel=r_associated | relid=0 | w=30
  49. en:ndp, ser101phe --- r_associated #0: 30 --> en:norrie disease
    n1=en:ndp, ser101phe | n2=en:norrie disease | rel=r_associated | relid=0 | w=30
  50. en:x-linked intellectual disability stoll type --- r_associated #0: 30 --> en:norrie disease
    n1=en:x-linked intellectual disability stoll type | n2=en:norrie disease | rel=r_associated | relid=0 | w=30
  51. Norrie (maladie de) --- r_associated #0: 29 --> en:norrie disease
    n1=Norrie (maladie de) | n2=en:norrie disease | rel=r_associated | relid=0 | w=29
  52. en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 29 --> en:norrie disease
    n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=29
  53. en:cor triatriatum --- r_associated #0: 29 --> en:norrie disease
    n1=en:cor triatriatum | n2=en:norrie disease | rel=r_associated | relid=0 | w=29
  54. en:deafness and myopia syndrome --- r_associated #0: 29 --> en:norrie disease
    n1=en:deafness and myopia syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=29
  55. en:eye involvement begins at birth, neurologic involvement begins later --- r_associated #0: 29 --> en:norrie disease
    n1=en:eye involvement begins at birth, neurologic involvement begins later | n2=en:norrie disease | rel=r_associated | relid=0 | w=29
  56. en:mental retardation, autosomal recessive 34 --- r_associated #0: 29 --> en:norrie disease
    n1=en:mental retardation, autosomal recessive 34 | n2=en:norrie disease | rel=r_associated | relid=0 | w=29
  57. en:ndp, arg90pro --- r_associated #0: 29 --> en:norrie disease
    n1=en:ndp, arg90pro | n2=en:norrie disease | rel=r_associated | relid=0 | w=29
  58. atrophie héréditaire des globes oculaires --- r_associated #0: 28 --> en:norrie disease
    n1=atrophie héréditaire des globes oculaires | n2=en:norrie disease | rel=r_associated | relid=0 | w=28
  59. en:cataract glaucoma syndrome --- r_associated #0: 28 --> en:norrie disease
    n1=en:cataract glaucoma syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=28
  60. en:cortical dysplasia-focal epilepsy syndrome --- r_associated #0: 28 --> en:norrie disease
    n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=28
  61. en:eiken type chondrodysplasia --- r_associated #0: 28 --> en:norrie disease
    n1=en:eiken type chondrodysplasia | n2=en:norrie disease | rel=r_associated | relid=0 | w=28
  62. en:lethal neonatal rigidity and multifocal seizure syndrome --- r_associated #0: 28 --> en:norrie disease
    n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=28
  63. en:ndp, tyr44cys --- r_associated #0: 28 --> en:norrie disease
    n1=en:ndp, tyr44cys | n2=en:norrie disease | rel=r_associated | relid=0 | w=28
  64. en:ndp, val45glu --- r_associated #0: 28 --> en:norrie disease
    n1=en:ndp, val45glu | n2=en:norrie disease | rel=r_associated | relid=0 | w=28
  65. en:x-linked intellectual disability pai type --- r_associated #0: 28 --> en:norrie disease
    n1=en:x-linked intellectual disability pai type | n2=en:norrie disease | rel=r_associated | relid=0 | w=28
  66. en:chitayat meunier hodgkinson syndrome --- r_associated #0: 27 --> en:norrie disease
    n1=en:chitayat meunier hodgkinson syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=27
  67. en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 27 --> en:norrie disease
    n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=27
  68. en:congenital disorder of glycosylation type 1s --- r_associated #0: 27 --> en:norrie disease
    n1=en:congenital disorder of glycosylation type 1s | n2=en:norrie disease | rel=r_associated | relid=0 | w=27
  69. en:norrie syndrome --- r_associated #0: 27 --> en:norrie disease
    n1=en:norrie syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=27
  70. en:primary ciliary dyskinesia and retinitis pigmentosa syndrome --- r_associated #0: 27 --> en:norrie disease
    n1=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=27
  71. en:x-linked intellectual disability armfield type --- r_associated #0: 27 --> en:norrie disease
    n1=en:x-linked intellectual disability armfield type | n2=en:norrie disease | rel=r_associated | relid=0 | w=27
  72. en:x-linked intellectual disability miles carpenter type --- r_associated #0: 27 --> en:norrie disease
    n1=en:x-linked intellectual disability miles carpenter type | n2=en:norrie disease | rel=r_associated | relid=0 | w=27
  73. en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome --- r_associated #0: 27 --> en:norrie disease
    n1=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=27
  74. en:ndp, cys96trp --- r_associated #0: 26 --> en:norrie disease
    n1=en:ndp, cys96trp | n2=en:norrie disease | rel=r_associated | relid=0 | w=26
  75. en:ndp, leu13arg --- r_associated #0: 26 --> en:norrie disease
    n1=en:ndp, leu13arg | n2=en:norrie disease | rel=r_associated | relid=0 | w=26
  76. en:ndp, leu61phe --- r_associated #0: 26 --> en:norrie disease
    n1=en:ndp, leu61phe | n2=en:norrie disease | rel=r_associated | relid=0 | w=26
  77. en:tissue kallikrein deficiency --- r_associated #0: 26 --> en:norrie disease
    n1=en:tissue kallikrein deficiency | n2=en:norrie disease | rel=r_associated | relid=0 | w=26
  78. maladie --- r_associated #0: 20 --> en:norrie disease
    n1=maladie | n2=en:norrie disease | rel=r_associated | relid=0 | w=20
  79. rétinite pigmentaire liée à la périphérine (pro219leu) --- r_associated #0: 10 --> en:norrie disease
    n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:norrie disease | rel=r_associated | relid=0 | w=10
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