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'en:hereditary oculoleptomeningeal amyloid angiopathy'
(id=6799587 ; fe=en:hereditary oculoleptomeningeal amyloid angiopathy ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=33656.5 creation date=2017-06-25 touchdate=2025-09-28 00:40:15.000)
≈ 668 relations sortantes

  1. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 39 / 1 -> en:disease of capillaries
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:disease of capillaries | rel=r_associated | relid=0 | w=39
  2. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 38 / 0.974 -> en:decreased and nonspecific blood pressure disorders and shock
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:decreased and nonspecific blood pressure disorders and shock | rel=r_associated | relid=0 | w=38
  3. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 35 / 0.897 -> amyloïdose de type vii
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=amyloïdose de type vii | rel=r_associated | relid=0 | w=35
  4. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 35 / 0.897 -> en:angiomatosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:angiomatosis | rel=r_associated | relid=0 | w=35
  5. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 35 / 0.897 -> en:eyelid vascular disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:eyelid vascular disorder | rel=r_associated | relid=0 | w=35
  6. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 35 / 0.897 -> en:hypotension
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hypotension | rel=r_associated | relid=0 | w=35
  7. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 35 / 0.897 -> en:ocular vascular disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ocular vascular disorder | rel=r_associated | relid=0 | w=35
  8. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 35 / 0.897 -> en:veno-occlusive disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:veno-occlusive disease | rel=r_associated | relid=0 | w=35
  9. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 34 / 0.872 -> en:hyperemia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperemia | rel=r_associated | relid=0 | w=34
  10. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 34 / 0.872 -> en:penile vascular disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:penile vascular disorder | rel=r_associated | relid=0 | w=34
  11. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 34 / 0.872 -> en:scimitar syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:scimitar syndrome | rel=r_associated | relid=0 | w=34
  12. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 34 / 0.872 -> en:telangiectasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:telangiectasia | rel=r_associated | relid=0 | w=34
  13. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 32 / 0.821 -> en:hand-arm vibration syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hand-arm vibration syndrome | rel=r_associated | relid=0 | w=32
  14. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 32 / 0.821 -> en:liver veno-occlusive disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:liver veno-occlusive disease | rel=r_associated | relid=0 | w=32
  15. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 32 / 0.821 -> en:varicose vein
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:varicose vein | rel=r_associated | relid=0 | w=32
  16. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 32 / 0.821 -> en:vasodilation
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vasodilation | rel=r_associated | relid=0 | w=32
  17. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 31 / 0.795 -> en:aorta disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:aorta disease | rel=r_associated | relid=0 | w=31
  18. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 31 / 0.795 -> en:optic neuropathy, ischemic
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:optic neuropathy, ischemic | rel=r_associated | relid=0 | w=31
  19. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 31 / 0.795 -> en:vascular system injuries
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular system injuries | rel=r_associated | relid=0 | w=31
  20. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 31 / 0.795 -> en:vasculitis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vasculitis | rel=r_associated | relid=0 | w=31
  21. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:amyloid angiopathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:amyloid angiopathy | rel=r_associated | relid=0 | w=30
  22. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:aneurysms and artery dissections
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:aneurysms and artery dissections | rel=r_associated | relid=0 | w=30
  23. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:arterial and arteriolar disorders
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:arterial and arteriolar disorders | rel=r_associated | relid=0 | w=30
  24. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:autosomal dominant muscular dystrophy not predominantly limb girdle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant muscular dystrophy not predominantly limb girdle | rel=r_associated | relid=0 | w=30
  25. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:blood vessel perforation
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:blood vessel perforation | rel=r_associated | relid=0 | w=30
  26. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:cerebellar ataxia ectodermal dysplasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=30
  27. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:char syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:char syndrome | rel=r_associated | relid=0 | w=30
  28. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:charcot-marie-tooth disease type 2d
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:charcot-marie-tooth disease type 2d | rel=r_associated | relid=0 | w=30
  29. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:cleidocranial dysplasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=30
  30. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:disorders of meninges, nec in mdr
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:disorders of meninges, nec in mdr | rel=r_associated | relid=0 | w=30
  31. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:dominant beta-thalassemia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dominant beta-thalassemia | rel=r_associated | relid=0 | w=30
  32. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:dystrophia myotonica 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dystrophia myotonica 2 | rel=r_associated | relid=0 | w=30
  33. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:epidural abscess
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:epidural abscess | rel=r_associated | relid=0 | w=30
  34. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:familial digital arthropathy and brachydactyly syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial digital arthropathy and brachydactyly syndrome | rel=r_associated | relid=0 | w=30
  35. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:familial osteochondritis dissecans
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial osteochondritis dissecans | rel=r_associated | relid=0 | w=30
  36. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:fatty acid hydroxylase-associated neurodegeneration
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=30
  37. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:feingold syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=30
  38. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:frontotemporal dementia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=30
  39. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:hereditary cerebellar atrophy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary cerebellar atrophy | rel=r_associated | relid=0 | w=30
  40. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:hereditary motor neuron disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary motor neuron disease | rel=r_associated | relid=0 | w=30
  41. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:hyaline dystrophy of bruch's membrane
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyaline dystrophy of bruch's membrane | rel=r_associated | relid=0 | w=30
  42. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:hypoplasia of spinal vessel
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hypoplasia of spinal vessel | rel=r_associated | relid=0 | w=30
  43. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:iris coloboma with ptosis, hypertelorism, and mental retardation
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:iris coloboma with ptosis, hypertelorism, and mental retardation | rel=r_associated | relid=0 | w=30
  44. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:kbg syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=30
  45. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:late effect of injury to peripheral blood vessel
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:late effect of injury to peripheral blood vessel | rel=r_associated | relid=0 | w=30
  46. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:lymphatic vessel diseases
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:lymphatic vessel diseases | rel=r_associated | relid=0 | w=30
  47. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:lynch syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:lynch syndrome | rel=r_associated | relid=0 | w=30
  48. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:megalencephalic leukoencephalopathy with subcortical cysts
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=30
  49. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:nemaline myopathy 3
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:nemaline myopathy 3 | rel=r_associated | relid=0 | w=30
  50. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:noonan syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=30
  51. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:parietal foramina
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:parietal foramina | rel=r_associated | relid=0 | w=30
  52. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:paroxysmal extreme pain disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=30
  53. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:peripheral resistance to thyroid hormone
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:peripheral resistance to thyroid hormone | rel=r_associated | relid=0 | w=30
  54. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:pseudocholinesterase deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=30
  55. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:pseudohypoaldosteronism, type 1, dominant form
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:pseudohypoaldosteronism, type 1, dominant form | rel=r_associated | relid=0 | w=30
  56. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:reis-bucklers' corneal dystrophy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:reis-bucklers' corneal dystrophy | rel=r_associated | relid=0 | w=30
  57. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:roch leri mesosomatous lipomatosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:roch leri mesosomatous lipomatosis | rel=r_associated | relid=0 | w=30
  58. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:rud syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:rud syndrome | rel=r_associated | relid=0 | w=30
  59. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:spinocerebellar ataxia 28
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia 28 | rel=r_associated | relid=0 | w=30
  60. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:spinocerebellar ataxia 29
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia 29 | rel=r_associated | relid=0 | w=30
  61. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:spinocerebellar ataxia type 6 (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia type 6 (disorder) | rel=r_associated | relid=0 | w=30
  62. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:spondyloperipheral dysplasia short ulna
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spondyloperipheral dysplasia short ulna | rel=r_associated | relid=0 | w=30
  63. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:varicocele
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:varicocele | rel=r_associated | relid=0 | w=30
  64. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:vascular fistula
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular fistula | rel=r_associated | relid=0 | w=30
  65. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:vascular hemostatic disorders
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular hemostatic disorders | rel=r_associated | relid=0 | w=30
  66. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:vascular inflammations
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular inflammations | rel=r_associated | relid=0 | w=30
  67. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:vascular insufficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular insufficiency | rel=r_associated | relid=0 | w=30
  68. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:venous insufficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:venous insufficiency | rel=r_associated | relid=0 | w=30
  69. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 30 / 0.769 -> en:wnt4 mullerian aplasia and ovarian dysfunction
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:wnt4 mullerian aplasia and ovarian dysfunction | rel=r_associated | relid=0 | w=30
  70. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:acromicric dysplasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=29
  71. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:arterial occlusive diseases
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:arterial occlusive diseases | rel=r_associated | relid=0 | w=29
  72. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:beare-stevenson cutis gyrata syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=29
  73. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:beckwith-wiedemann syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=29
  74. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:cadasil syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=29
  75. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:cerebrovascular disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebrovascular disorder | rel=r_associated | relid=0 | w=29
  76. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:charcot-marie-tooth disease, axonal, type 2b (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | rel=r_associated | relid=0 | w=29
  77. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:colitis, ischemic
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:colitis, ischemic | rel=r_associated | relid=0 | w=29
  78. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:congenital dyserythropoietic anemia, type iii
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:congenital dyserythropoietic anemia, type iii | rel=r_associated | relid=0 | w=29
  79. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:congenitally corrected transposition of the great arteries
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:congenitally corrected transposition of the great arteries | rel=r_associated | relid=0 | w=29
  80. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:falx laceration
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:falx laceration | rel=r_associated | relid=0 | w=29
  81. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:familial encephalopathy with neuroserpin inclusion bodies
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=29
  82. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:game friedman paradice syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:game friedman paradice syndrome | rel=r_associated | relid=0 | w=29
  83. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:hawkinsinuria
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hawkinsinuria | rel=r_associated | relid=0 | w=29
  84. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:hereditary angioedema
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=29
  85. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:hereditary cystatin c amyloid angiopathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=29
  86. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=29
  87. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:hyperinsulinism due to deficiency of glucokinase
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperinsulinism due to deficiency of glucokinase | rel=r_associated | relid=0 | w=29
  88. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:hypertension
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hypertension | rel=r_associated | relid=0 | w=29
  89. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:isaacs syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=29
  90. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:isolated hypoplasia of the right ventricle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=29
  91. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:jervell and lange nielsen syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=29
  92. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  93. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=29
  94. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:mousa al din al nassar syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:mousa al din al nassar syndrome | rel=r_associated | relid=0 | w=29
  95. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:multiple endocrine neoplasia type 2b
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:multiple endocrine neoplasia type 2b | rel=r_associated | relid=0 | w=29
  96. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:osteogenesis imperfecta, levin type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:osteogenesis imperfecta, levin type | rel=r_associated | relid=0 | w=29
  97. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:periventricular heterotopia, x-linked
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:periventricular heterotopia, x-linked | rel=r_associated | relid=0 | w=29
  98. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:pitt-hopkins syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:pitt-hopkins syndrome | rel=r_associated | relid=0 | w=29
  99. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:reticulate acropigmentation of kitamura
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:reticulate acropigmentation of kitamura | rel=r_associated | relid=0 | w=29
  100. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:splenic infarction
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:splenic infarction | rel=r_associated | relid=0 | w=29
  101. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:strudwick syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:strudwick syndrome | rel=r_associated | relid=0 | w=29
  102. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:syndromic orbital border hypoplasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=29
  103. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:vascular neoplasm
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular neoplasm | rel=r_associated | relid=0 | w=29
  104. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:vasoplegia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vasoplegia | rel=r_associated | relid=0 | w=29
  105. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> en:vitreoretinochoroidopathy (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vitreoretinochoroidopathy (disorder) | rel=r_associated | relid=0 | w=29
  106. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 29 / 0.744 -> syndrome de Walker-Warburg
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=29
  107. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:acrocallosal syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=28
  108. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:advanced sleep-phase syndrome, familial
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:advanced sleep-phase syndrome, familial | rel=r_associated | relid=0 | w=28
  109. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:allan-herndon-dudley syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=28
  110. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:alpha-fetoprotein, hereditary persistence of
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:alpha-fetoprotein, hereditary persistence of | rel=r_associated | relid=0 | w=28
  111. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:aplasia of lacrimal and salivary glands
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=28
  112. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:arteriovenous hemangioma
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:arteriovenous hemangioma | rel=r_associated | relid=0 | w=28
  113. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:ataxia telangiectasia syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=28
  114. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:autosomal dominant excess of transthyretin
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant excess of transthyretin | rel=r_associated | relid=0 | w=28
  115. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:autosomal dominant ichthyosis vulgaris
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant ichthyosis vulgaris | rel=r_associated | relid=0 | w=28
  116. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:autosomal dominant idiopathic familial dystonia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=28
  117. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:autosomal dominant pterygium of conjunctiva
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=28
  118. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:charcot-marie-tooth disease, axonal, type 2l (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | rel=r_associated | relid=0 | w=28
  119. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:chromosome 3q29 deletion syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:chromosome 3q29 deletion syndrome | rel=r_associated | relid=0 | w=28
  120. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:compartment syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:compartment syndrome | rel=r_associated | relid=0 | w=28
  121. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:crisponi syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=28
  122. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:dystonia 12
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=28
  123. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:embolism
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:embolism | rel=r_associated | relid=0 | w=28
  124. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:embolism and thrombosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:embolism and thrombosis | rel=r_associated | relid=0 | w=28
  125. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:familial amyloid neuropathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial amyloid neuropathy | rel=r_associated | relid=0 | w=28
  126. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:goniodysgenesis-mental retardation-short stature syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=28
  127. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:heritable pulmonary arterial hypertension due to bmpr2 mutation
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | rel=r_associated | relid=0 | w=28
  128. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | rel=r_associated | relid=0 | w=28
  129. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:hypomagnesemia 1, intestinal
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=28
  130. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:keratosis palmoplantaris papulosa
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:keratosis palmoplantaris papulosa | rel=r_associated | relid=0 | w=28
  131. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:lamellar ichthyosis, autosomal dominant form
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:lamellar ichthyosis, autosomal dominant form | rel=r_associated | relid=0 | w=28
  132. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:leukotriene c4 synthase deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=28
  133. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:liver vascular disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:liver vascular disorder | rel=r_associated | relid=0 | w=28
  134. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:meningeal melanosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:meningeal melanosis | rel=r_associated | relid=0 | w=28
  135. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:nevoid basal cell carcinoma syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:nevoid basal cell carcinoma syndrome | rel=r_associated | relid=0 | w=28
  136. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:pathologic arteriovenous shunt
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:pathologic arteriovenous shunt | rel=r_associated | relid=0 | w=28
  137. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:portal hypertension
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:portal hypertension | rel=r_associated | relid=0 | w=28
  138. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:schindler disease, type i
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:schindler disease, type i | rel=r_associated | relid=0 | w=28
  139. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:spinocerebellar ataxia type 4
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia type 4 | rel=r_associated | relid=0 | w=28
  140. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:stricture of artery
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:stricture of artery | rel=r_associated | relid=0 | w=28
  141. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:vascular disorder of extremity
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular disorder of extremity | rel=r_associated | relid=0 | w=28
  142. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:vascular disorders nec
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular disorders nec | rel=r_associated | relid=0 | w=28
  143. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:vascular disorders, general and nec
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular disorders, general and nec | rel=r_associated | relid=0 | w=28
  144. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:vascular hypertensive disorders
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular hypertensive disorders | rel=r_associated | relid=0 | w=28
  145. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:venous and venular disorders
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:venous and venular disorders | rel=r_associated | relid=0 | w=28
  146. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:vitelliform macular dystrophy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=28
  147. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> en:walker-warburg syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=28
  148. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 28 / 0.718 -> maladie de Marfan
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie de Marfan | rel=r_associated | relid=0 | w=28
  149. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:alagille syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=27
  150. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:autosomal dominant analbuminemia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant analbuminemia | rel=r_associated | relid=0 | w=27
  151. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:benign autosomal dominant osteopetrosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:benign autosomal dominant osteopetrosis | rel=r_associated | relid=0 | w=27
  152. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:blau syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:blau syndrome | rel=r_associated | relid=0 | w=27
  153. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:blood pressure disorders
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:blood pressure disorders | rel=r_associated | relid=0 | w=27
  154. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=27
  155. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:chromosome 22q11.2 microduplication syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:chromosome 22q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=27
  156. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:cochleosaccular degeneration of the inner ear and progressive cataracts
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=27
  157. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:congenital nephrogenic diabetes insipidus
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=27
  158. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:corneal dystrophy, congenital stromal
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:corneal dystrophy, congenital stromal | rel=r_associated | relid=0 | w=27
  159. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:dominant autosomal hereditary disorder, complete penetrance
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dominant autosomal hereditary disorder, complete penetrance | rel=r_associated | relid=0 | w=27
  160. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:epidural lipomatosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:epidural lipomatosis | rel=r_associated | relid=0 | w=27
  161. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:epiphyseal dysplasia, multiple, 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:epiphyseal dysplasia, multiple, 1 | rel=r_associated | relid=0 | w=27
  162. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:esophageal varices
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:esophageal varices | rel=r_associated | relid=0 | w=27
  163. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=27
  164. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:glomuvenous malformations
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:glomuvenous malformations | rel=r_associated | relid=0 | w=27
  165. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:hypotrichosis simplex of scalp
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hypotrichosis simplex of scalp | rel=r_associated | relid=0 | w=27
  166. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | rel=r_associated | relid=0 | w=27
  167. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:knobloch syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=27
  168. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:leigh disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:leigh disease | rel=r_associated | relid=0 | w=27
  169. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:li-fraumeni syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=27
  170. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:masa syndrome (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=27
  171. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:microcephaly cervical spine fusion anomalies
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=27
  172. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:mohr-tranebjaerg syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=27
  173. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:multiple endocrine neoplasia type 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:multiple endocrine neoplasia type 1 | rel=r_associated | relid=0 | w=27
  174. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:neurofibromatosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:neurofibromatosis | rel=r_associated | relid=0 | w=27
  175. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:nicolaides baraitser syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=27
  176. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:ohdo syndrome, maat-kievit-brunner type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=27
  177. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:peripheral vascular disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:peripheral vascular disorder | rel=r_associated | relid=0 | w=27
  178. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:pontocerebellar hypoplasia type 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=27
  179. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:reperfusion injury
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:reperfusion injury | rel=r_associated | relid=0 | w=27
  180. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:simpson golabi behmel syndrome type 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=27
  181. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:spinocerebellar ataxia 31 (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia 31 (disorder) | rel=r_associated | relid=0 | w=27
  182. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:split-hand-foot malformation with long bone deficiency 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:split-hand-foot malformation with long bone deficiency 1 | rel=r_associated | relid=0 | w=27
  183. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:sting-associated vasculopathy with onset in infancy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:sting-associated vasculopathy with onset in infancy | rel=r_associated | relid=0 | w=27
  184. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:syndactyly, type i
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:syndactyly, type i | rel=r_associated | relid=0 | w=27
  185. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:synpolydactyly
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=27
  186. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:tarsal-carpal coalition syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=27
  187. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:ulna metaphyseal dysplasia syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ulna metaphyseal dysplasia syndrome | rel=r_associated | relid=0 | w=27
  188. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:vein disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vein disorder | rel=r_associated | relid=0 | w=27
  189. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 27 / 0.692 -> en:von hippel-lindau syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:von hippel-lindau syndrome | rel=r_associated | relid=0 | w=27
  190. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:2-hydroxyglutaric aciduria
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=26
  191. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=26
  192. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:angiodysplasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:angiodysplasia | rel=r_associated | relid=0 | w=26
  193. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:autosomal dominant oculocutaneous albinism
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant oculocutaneous albinism | rel=r_associated | relid=0 | w=26
  194. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:autosomal recessive idiopathic familial dystonia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=26
  195. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:bannayan syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:bannayan syndrome | rel=r_associated | relid=0 | w=26
  196. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:blood vessel occlusion
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:blood vessel occlusion | rel=r_associated | relid=0 | w=26
  197. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:capillary leak syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:capillary leak syndrome | rel=r_associated | relid=0 | w=26
  198. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:cerebellar ataxia, cayman type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=26
  199. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:cerebral hemorrhage with amyloidosis, hereditary, dutch type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=26
  200. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:cerebral lipidosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebral lipidosis | rel=r_associated | relid=0 | w=26
  201. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:chromosome 17q21.31 deletion syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=26
  202. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:cole disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cole disease | rel=r_associated | relid=0 | w=26
  203. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | rel=r_associated | relid=0 | w=26
  204. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:congenital reticular ichthyosiform erythroderma
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:congenital reticular ichthyosiform erythroderma | rel=r_associated | relid=0 | w=26
  205. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:dentatorubral-pallidoluysian atrophy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=26
  206. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:diabetic vascular disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:diabetic vascular disorder | rel=r_associated | relid=0 | w=26
  207. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:dyskeratosis congenita, autosomal dominant
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dyskeratosis congenita, autosomal dominant | rel=r_associated | relid=0 | w=26
  208. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:epilepsy, myoclonic, benign adult familial, type 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=26
  209. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:familial hypercalciuric hypocalcemia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial hypercalciuric hypocalcemia | rel=r_associated | relid=0 | w=26
  210. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:familial isolated arrhythmogenic right ventricular dysplasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial isolated arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=26
  211. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:fatal familial insomnia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=26
  212. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:folinic acid responsive seizure syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:folinic acid responsive seizure syndrome | rel=r_associated | relid=0 | w=26
  213. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:gerstmann-straussler-scheinker disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=26
  214. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:hereditary cerebellar degeneration
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary cerebellar degeneration | rel=r_associated | relid=0 | w=26
  215. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:hereditary motor and sensory neuropathy type i
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary motor and sensory neuropathy type i | rel=r_associated | relid=0 | w=26
  216. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:hereditary stomatocytosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary stomatocytosis | rel=r_associated | relid=0 | w=26
  217. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:hyperpigmentation, familial progressive
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperpigmentation, familial progressive | rel=r_associated | relid=0 | w=26
  218. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:hypoplastic tibia and postaxial polydactyly syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=26
  219. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=26
  220. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:liddle syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=26
  221. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:lissencephaly, x-linked, 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:lissencephaly, x-linked, 2 | rel=r_associated | relid=0 | w=26
  222. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:myopathy, distal, tateyama type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:myopathy, distal, tateyama type | rel=r_associated | relid=0 | w=26
  223. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:oculodental syndrome rutherfurd syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26
  224. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:prehypertension
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:prehypertension | rel=r_associated | relid=0 | w=26
  225. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:short stature with valvular heart disease and characteristic facies syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:short stature with valvular heart disease and characteristic facies syndrome | rel=r_associated | relid=0 | w=26
  226. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:sotos syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=26
  227. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:spinal vascular disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinal vascular disorder | rel=r_associated | relid=0 | w=26
  228. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:syndrome, branchio-oculo-facial
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=26
  229. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:vascular disease of abdomen
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular disease of abdomen | rel=r_associated | relid=0 | w=26
  230. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 26 / 0.667 -> en:wells jankovic syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:wells jankovic syndrome | rel=r_associated | relid=0 | w=26
  231. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:angiofibroma
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:angiofibroma | rel=r_associated | relid=0 | w=25
  232. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:arthrogryposis, distal, type 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:arthrogryposis, distal, type 1 | rel=r_associated | relid=0 | w=25
  233. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:autosomal dominant deficiency of plasminogen
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant deficiency of plasminogen | rel=r_associated | relid=0 | w=25
  234. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:brachyolmia type 3
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=25
  235. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:carotid artery disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:carotid artery disorder | rel=r_associated | relid=0 | w=25
  236. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=25
  237. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=25
  238. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:congenital cataracts, facial dysmorphism, and neuropathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=25
  239. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:crouzon syndrome with acanthosis nigricans (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25
  240. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:familial benign neonatal epilepsy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=25
  241. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:familial partial lipodystrophy, type 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial partial lipodystrophy, type 2 | rel=r_associated | relid=0 | w=25
  242. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:geniospasm 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=25
  243. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:hereditary
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary | rel=r_associated | relid=0 | w=25
  244. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:hereditary cutaneous vascular syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary cutaneous vascular syndrome | rel=r_associated | relid=0 | w=25
  245. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:hereditary gastrogenic lactose intolerance
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary gastrogenic lactose intolerance | rel=r_associated | relid=0 | w=25
  246. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:hereditary papillary renal cell carcinoma
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary papillary renal cell carcinoma | rel=r_associated | relid=0 | w=25
  247. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:hyperparathyroidism-jaw tumor syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperparathyroidism-jaw tumor syndrome | rel=r_associated | relid=0 | w=25
  248. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:hypomyelination and congenital cataract
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=25
  249. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:laurin-sandrow syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=25
  250. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:macdermot winter syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=25
  251. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:melnick-fraser syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=25
  252. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:meningeal cyst
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:meningeal cyst | rel=r_associated | relid=0 | w=25
  253. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:mesomelic dwarfism reinhardt pfeiffer type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:mesomelic dwarfism reinhardt pfeiffer type | rel=r_associated | relid=0 | w=25
  254. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:microcephaly microcornea syndrome seemanova type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=25
  255. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:microcornea with glaucoma and absent frontal sinus syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=25
  256. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:multiple epiphyseal dysplasia type 5
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:multiple epiphyseal dysplasia type 5 | rel=r_associated | relid=0 | w=25
  257. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:myopathy, distal 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:myopathy, distal 2 | rel=r_associated | relid=0 | w=25
  258. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:neurodegeneration with brain iron accumulation 4
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=25
  259. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:neurofibromatosis type 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:neurofibromatosis type 1 | rel=r_associated | relid=0 | w=25
  260. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:neurofibromatosis type 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:neurofibromatosis type 2 | rel=r_associated | relid=0 | w=25
  261. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:neuropathy, hereditary thermosensitive
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:neuropathy, hereditary thermosensitive | rel=r_associated | relid=0 | w=25
  262. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:perinatal falx laceration
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:perinatal falx laceration | rel=r_associated | relid=0 | w=25
  263. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:pituitary thyroid hormone resistance
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:pituitary thyroid hormone resistance | rel=r_associated | relid=0 | w=25
  264. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:port-wine stain in rubinstein-taybi syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:port-wine stain in rubinstein-taybi syndrome | rel=r_associated | relid=0 | w=25
  265. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:sebastian syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:sebastian syndrome | rel=r_associated | relid=0 | w=25
  266. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=25
  267. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:spinocerebellar ataxia 36
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia 36 | rel=r_associated | relid=0 | w=25
  268. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:spinocerebellar ataxia type 5
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia type 5 | rel=r_associated | relid=0 | w=25
  269. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:spondylocostal dysostosis 4, autosomal dominant
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=25
  270. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=25
  271. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> en:x-linked lissencephaly
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:x-linked lissencephaly | rel=r_associated | relid=0 | w=25
  272. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 25 / 0.641 -> trouble vasculaire périphérique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=trouble vasculaire périphérique | rel=r_associated | relid=0 | w=25
  273. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:ataxia with vitamin e deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=24
  274. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:autosomal dominant charcot-marie-tooth disease type 2a1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant charcot-marie-tooth disease type 2a1 | rel=r_associated | relid=0 | w=24
  275. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:autosomal dominant hyperinsulinism due to sur1 deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant hyperinsulinism due to sur1 deficiency | rel=r_associated | relid=0 | w=24
  276. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:autosomal dominant optic atrophy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=24
  277. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:behavioral variant of frontotemporal dementia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=24
  278. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:brachydactyly, type a1 (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:brachydactyly, type a1 (disorder) | rel=r_associated | relid=0 | w=24
  279. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:brachymesophalangy 2 and 5
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:brachymesophalangy 2 and 5 | rel=r_associated | relid=0 | w=24
  280. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:budd-chiari syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:budd-chiari syndrome | rel=r_associated | relid=0 | w=24
  281. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:capillary malformation-arteriovenous malformation (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:capillary malformation-arteriovenous malformation (disorder) | rel=r_associated | relid=0 | w=24
  282. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:centronuclear myopathy 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:centronuclear myopathy 1 | rel=r_associated | relid=0 | w=24
  283. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:collateral
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:collateral | rel=r_associated | relid=0 | w=24
  284. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:deafness-craniofacial syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=24
  285. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:disorder of central nervous system due to xeroderma pigmentosum
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:disorder of central nervous system due to xeroderma pigmentosum | rel=r_associated | relid=0 | w=24
  286. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:dominant autosomal hereditary disorder, incomplete penetrance
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dominant autosomal hereditary disorder, incomplete penetrance | rel=r_associated | relid=0 | w=24
  287. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:ectodermal dysplasia with natal teeth, turnpenny type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ectodermal dysplasia with natal teeth, turnpenny type | rel=r_associated | relid=0 | w=24
  288. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:episodic ataxia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=24
  289. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:familial creutzfeldt-jakob
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=24
  290. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:frontotemporal dementia, chromosome 3-linked
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=24
  291. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:glycogen storage disease type iib
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:glycogen storage disease type iib | rel=r_associated | relid=0 | w=24
  292. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:great vessel neoplasm
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:great vessel neoplasm | rel=r_associated | relid=0 | w=24
  293. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:hand foot uterus syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hand foot uterus syndrome | rel=r_associated | relid=0 | w=24
  294. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:hereditary breast and ovarian cancer syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary breast and ovarian cancer syndrome | rel=r_associated | relid=0 | w=24
  295. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:hereditary myopathy with early respiratory failure
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=24
  296. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:hereditary optic atrophy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary optic atrophy | rel=r_associated | relid=0 | w=24
  297. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:hyperinsulinemic hypoglycemia, familial, 6
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperinsulinemic hypoglycemia, familial, 6 | rel=r_associated | relid=0 | w=24
  298. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:intracranial granuloma
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:intracranial granuloma | rel=r_associated | relid=0 | w=24
  299. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | rel=r_associated | relid=0 | w=24
  300. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:jackson-weiss syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=24
  301. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:keratoacanthoma familial
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:keratoacanthoma familial | rel=r_associated | relid=0 | w=24
  302. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:may-hegglin anomaly
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:may-hegglin anomaly | rel=r_associated | relid=0 | w=24
  303. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:menkes disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:menkes disease | rel=r_associated | relid=0 | w=24
  304. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:metaphyseal dysplasia, braun-tinschert type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:metaphyseal dysplasia, braun-tinschert type | rel=r_associated | relid=0 | w=24
  305. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:microcephaly, amish type (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=24
  306. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:microphthalmia, syndromic 3
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=24
  307. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | rel=r_associated | relid=0 | w=24
  308. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:neuropathy, hereditary motor and sensory, okinawa type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:neuropathy, hereditary motor and sensory, okinawa type | rel=r_associated | relid=0 | w=24
  309. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:perinatal tentorial laceration
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:perinatal tentorial laceration | rel=r_associated | relid=0 | w=24
  310. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:pituitary adenoma, familial isolated (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=24
  311. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:polydactyly, preaxial ii (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=24
  312. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:sonoda syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=24
  313. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:spinocerebellar ataxia 1s
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia 1s | rel=r_associated | relid=0 | w=24
  314. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:steinfeld syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=24
  315. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:thomas syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=24
  316. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:type i acrocephalosyndactyly
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:type i acrocephalosyndactyly | rel=r_associated | relid=0 | w=24
  317. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:vascular dilation or proliferation
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular dilation or proliferation | rel=r_associated | relid=0 | w=24
  318. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 24 / 0.615 -> en:waisman syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=24
  319. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:aicardi syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=23
  320. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=23
  321. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:autosomal dominant mutilating keratoderma
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant mutilating keratoderma | rel=r_associated | relid=0 | w=23
  322. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:autosomal dominant variant form of albumin
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant variant form of albumin | rel=r_associated | relid=0 | w=23
  323. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:behr syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:behr syndrome | rel=r_associated | relid=0 | w=23
  324. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:brown-vialetto-van laere syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=23
  325. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:cap myopathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cap myopathy | rel=r_associated | relid=0 | w=23
  326. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:charcot-marie-tooth disease, type 2j
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:charcot-marie-tooth disease, type 2j | rel=r_associated | relid=0 | w=23
  327. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:choreoathetosis/spasticity, episodic
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=23
  328. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:dysplasia, saddan
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dysplasia, saddan | rel=r_associated | relid=0 | w=23
  329. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:encephalopathy due to sulfite oxidase deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=23
  330. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:familial hemiplegic migraine
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=23
  331. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:familial spontaneous pneumothorax
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial spontaneous pneumothorax | rel=r_associated | relid=0 | w=23
  332. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:hereditary diffuse gastric adenocarcinoma
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary diffuse gastric adenocarcinoma | rel=r_associated | relid=0 | w=23
  333. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:hereditary mucosal leukokeratosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=23
  334. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:hnsha due to triosephosphate isomerase deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hnsha due to triosephosphate isomerase deficiency | rel=r_associated | relid=0 | w=23
  335. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:hydrocephalus with cerebellar agenesis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hydrocephalus with cerebellar agenesis | rel=r_associated | relid=0 | w=23
  336. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:hyperferritinemia, hereditary, with congenital cataracts
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=23
  337. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:hyperinsulinemic hypoglycemia, familial, 7
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperinsulinemic hypoglycemia, familial, 7 | rel=r_associated | relid=0 | w=23
  338. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:microcephaly deafness syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=23
  339. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:neurofibromatosis, type 1-like syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:neurofibromatosis, type 1-like syndrome | rel=r_associated | relid=0 | w=23
  340. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:prickle1-related progressive myoclonus epilepsy with ataxia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=23
  341. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:pseudomeningocele
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:pseudomeningocele | rel=r_associated | relid=0 | w=23
  342. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:shprintzen omphalocele syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=23
  343. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:spinocerebellar ataxia 8
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia 8 | rel=r_associated | relid=0 | w=23
  344. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:spinocerebellar ataxia type 7
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia type 7 | rel=r_associated | relid=0 | w=23
  345. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:subarachnoid intracranial abscess
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:subarachnoid intracranial abscess | rel=r_associated | relid=0 | w=23
  346. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:syndactyly, type iii
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:syndactyly, type iii | rel=r_associated | relid=0 | w=23
  347. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:treacher collins syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=23
  348. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:tuberculoma of meninges
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:tuberculoma of meninges | rel=r_associated | relid=0 | w=23
  349. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:type v acrocephalosyndactyly
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:type v acrocephalosyndactyly | rel=r_associated | relid=0 | w=23
  350. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> en:waardenburg syndrome type 4
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:waardenburg syndrome type 4 | rel=r_associated | relid=0 | w=23
  351. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 23 / 0.59 -> syndrome de Marfan
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=23
  352. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:aneurysm, infected
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:aneurysm, infected | rel=r_associated | relid=0 | w=22
  353. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:angiomatosis of meninges
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:angiomatosis of meninges | rel=r_associated | relid=0 | w=22
  354. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:autosomal recessive primary microcephaly
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=22
  355. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:bilateral multiple fibroadenoma of breast
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:bilateral multiple fibroadenoma of breast | rel=r_associated | relid=0 | w=22
  356. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:bilateral pheochromocytoma and islet cell adenoma of the pancreas
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | rel=r_associated | relid=0 | w=22
  357. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:cerebral cavernous malformation
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=22
  358. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:cockayne syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cockayne syndrome | rel=r_associated | relid=0 | w=22
  359. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:craniofacial deafness hand syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:craniofacial deafness hand syndrome | rel=r_associated | relid=0 | w=22
  360. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:currarino triad
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:currarino triad | rel=r_associated | relid=0 | w=22
  361. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:dicer1 syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dicer1 syndrome | rel=r_associated | relid=0 | w=22
  362. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:familial non-autoimmune autosomal dominant hyperthyroidism
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:familial non-autoimmune autosomal dominant hyperthyroidism | rel=r_associated | relid=0 | w=22
  363. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:gaze palsy, familial horizontal, with progressive scoliosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=22
  364. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:haspeslagh fryns muelenaere syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=22
  365. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:hereditary sensory autonomic neuropathy, type 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary sensory autonomic neuropathy, type 1 | rel=r_associated | relid=0 | w=22
  366. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:hereditary systemic amyloidosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary systemic amyloidosis | rel=r_associated | relid=0 | w=22
  367. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:leopard syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=22
  368. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=22
  369. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:melanoma astrocytoma syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=22
  370. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:microcephalic primordial dwarfism toriello type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=22
  371. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:moloney syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:moloney syndrome | rel=r_associated | relid=0 | w=22
  372. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:mowat-wilson syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=22
  373. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:muckle-wells syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:muckle-wells syndrome | rel=r_associated | relid=0 | w=22
  374. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:okihiro syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=22
  375. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:potassium aggravated myotonia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:potassium aggravated myotonia | rel=r_associated | relid=0 | w=22
  376. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:spinocerebellar ataxia 10
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia 10 | rel=r_associated | relid=0 | w=22
  377. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:transthyretin related familial amyloid cardiomyopathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:transthyretin related familial amyloid cardiomyopathy | rel=r_associated | relid=0 | w=22
  378. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:tuberous sclerosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=22
  379. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:vascular malformations
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular malformations | rel=r_associated | relid=0 | w=22
  380. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:wellesley carman french syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=22
  381. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 22 / 0.564 -> en:zimmerman laband syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:zimmerman laband syndrome | rel=r_associated | relid=0 | w=22
  382. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:ameloonychohypohidrotic syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ameloonychohypohidrotic syndrome | rel=r_associated | relid=0 | w=21
  383. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:autosomal dominant charcot-marie-tooth disease type 2c
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant charcot-marie-tooth disease type 2c | rel=r_associated | relid=0 | w=21
  384. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:autosomal dominant hyperinsulinism due to kir6.2 deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | rel=r_associated | relid=0 | w=21
  385. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:autosomal dominant progressive nephropathy with hypertension
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant progressive nephropathy with hypertension | rel=r_associated | relid=0 | w=21
  386. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:avascular necrosis of femoral head
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:avascular necrosis of femoral head | rel=r_associated | relid=0 | w=21
  387. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:behrens baumann dust syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=21
  388. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:brachydactyly type a6
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:brachydactyly type a6 | rel=r_associated | relid=0 | w=21
  389. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:brooke-spiegler syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:brooke-spiegler syndrome | rel=r_associated | relid=0 | w=21
  390. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:charcot-marie-tooth disease, axonal, type 2e (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | rel=r_associated | relid=0 | w=21
  391. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:dmd-associated dilated cardiomyopathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dmd-associated dilated cardiomyopathy | rel=r_associated | relid=0 | w=21
  392. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:dopa-responsive dystonia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=21
  393. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:epithelial recurrent erosion dystrophy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:epithelial recurrent erosion dystrophy | rel=r_associated | relid=0 | w=21
  394. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:generalized epilepsy and paroxysmal dyskinesia syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=21
  395. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:hereditary cerebral amyloid angiopathy, icelandic type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=21
  396. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:hereditary dysplasia of blood vessel
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary dysplasia of blood vessel | rel=r_associated | relid=0 | w=21
  397. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:hereditary multiple exostoses
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=21
  398. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:hereditary nonpolyposis colorectal cancer
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary nonpolyposis colorectal cancer | rel=r_associated | relid=0 | w=21
  399. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:hereditary peripheral neuropathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary peripheral neuropathy | rel=r_associated | relid=0 | w=21
  400. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:hyperinsulinism due to hnf4a deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperinsulinism due to hnf4a deficiency | rel=r_associated | relid=0 | w=21
  401. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:marfan syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=21
  402. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:maternally inherited mitochondrial dystonia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:maternally inherited mitochondrial dystonia | rel=r_associated | relid=0 | w=21
  403. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:non-polyposis turcot syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:non-polyposis turcot syndrome | rel=r_associated | relid=0 | w=21
  404. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:piebaldism
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:piebaldism | rel=r_associated | relid=0 | w=21
  405. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=21
  406. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:proteus-like syndrome (disorder)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=21
  407. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:radial hypoplasia, triphalangeal thumbs and hypospadias
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:radial hypoplasia, triphalangeal thumbs and hypospadias | rel=r_associated | relid=0 | w=21
  408. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:retinopathy of prematurity
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:retinopathy of prematurity | rel=r_associated | relid=0 | w=21
  409. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:spinocerebellar ataxia type 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia type 2 | rel=r_associated | relid=0 | w=21
  410. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:tylosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:tylosis | rel=r_associated | relid=0 | w=21
  411. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:ulnar-mammary syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ulnar-mammary syndrome | rel=r_associated | relid=0 | w=21
  412. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 21 / 0.538 -> en:x-linked dystonia parkinsonism
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:x-linked dystonia parkinsonism | rel=r_associated | relid=0 | w=21
  413. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> aclasie diaphysaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=aclasie diaphysaire | rel=r_associated | relid=0 | w=20
  414. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> amyloïdose de type VII
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=amyloïdose de type VII | rel=r_associated | relid=0 | w=20
  415. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> anévrisme
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=anévrisme | rel=r_associated | relid=0 | w=20
  416. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Anévrisme
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Anévrisme | rel=r_associated | relid=0 | w=20
  417. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> anévrysme
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=anévrysme | rel=r_associated | relid=0 | w=20
  418. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> angiofibrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=angiofibrome | rel=r_associated | relid=0 | w=20
  419. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> angiomatose
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=angiomatose | rel=r_associated | relid=0 | w=20
  420. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> arachnodactylie
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=arachnodactylie | rel=r_associated | relid=0 | w=20
  421. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> artério-sclérose
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=artério-sclérose | rel=r_associated | relid=0 | w=20
  422. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> artériosclérose
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=artériosclérose | rel=r_associated | relid=0 | w=20
  423. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> artériosclérose sévère juvénile de Kaitila
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=artériosclérose sévère juvénile de Kaitila | rel=r_associated | relid=0 | w=20
  424. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> atrophie optique autosomique dominante
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=atrophie optique autosomique dominante | rel=r_associated | relid=0 | w=20
  425. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> bloc supra-hépatique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=bloc supra-hépatique | rel=r_associated | relid=0 | w=20
  426. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> cancer colo-rectal héréditaire sans polypose
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=cancer colo-rectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20
  427. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> cancer colorectal héréditaire sans polypose
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=cancer colorectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20
  428. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Cancer colorectal héréditaire sans polypose
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Cancer colorectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20
  429. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> caution financière
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=caution financière | rel=r_associated | relid=0 | w=20
  430. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> chondrodysplasie déformante héréditaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=chondrodysplasie déformante héréditaire | rel=r_associated | relid=0 | w=20
  431. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> chondrodysplasie héréditaire déformante
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=chondrodysplasie héréditaire déformante | rel=r_associated | relid=0 | w=20
  432. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> collatérale
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=collatérale | rel=r_associated | relid=0 | w=20
  433. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> corne cutanée de la paupière
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=corne cutanée de la paupière | rel=r_associated | relid=0 | w=20
  434. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> démence fronto-temporale
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=20
  435. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> démence frontotemporale
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=démence frontotemporale | rel=r_associated | relid=0 | w=20
  436. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> dilatation d'un vaisseau
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=dilatation d'un vaisseau | rel=r_associated | relid=0 | w=20
  437. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> dilatation vasculaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=dilatation vasculaire | rel=r_associated | relid=0 | w=20
  438. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> dysplasie acromicrique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20
  439. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> dysplasie cléido-crânienne
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=dysplasie cléido-crânienne | rel=r_associated | relid=0 | w=20
  440. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> dysplasie cléidocrânienne
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=dysplasie cléidocrânienne | rel=r_associated | relid=0 | w=20
  441. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> dystonie dopasensible
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=dystonie dopasensible | rel=r_associated | relid=0 | w=20
  442. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> embole de tumeur
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=embole de tumeur | rel=r_associated | relid=0 | w=20
  443. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> embole tumoral
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=embole tumoral | rel=r_associated | relid=0 | w=20
  444. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> embolie tumorale
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=embolie tumorale | rel=r_associated | relid=0 | w=20
  445. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> embolisme
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=embolisme | rel=r_associated | relid=0 | w=20
  446. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:17q11.2 microduplication syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=20
  447. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:absence of fingerprints with congenital milia syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:absence of fingerprints with congenital milia syndrome | rel=r_associated | relid=0 | w=20
  448. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:acro-dermato-ungual-lacrimal-tooth syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:acro-dermato-ungual-lacrimal-tooth syndrome | rel=r_associated | relid=0 | w=20
  449. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:aneurysm
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:aneurysm | rel=r_associated | relid=0 | w=20
  450. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:aniridia and intellectual disability syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  451. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=20
  452. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | rel=r_associated | relid=0 | w=20
  453. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:aphalangy and syndactyly with microcephaly syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=20
  454. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:arachnodactily
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:arachnodactily | rel=r_associated | relid=0 | w=20
  455. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:arachnodactyly
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20
  456. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:arrhythmogenic right ventricular dysplasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=20
  457. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:arterial dissection and lentiginosis syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:arterial dissection and lentiginosis syndrome | rel=r_associated | relid=0 | w=20
  458. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:arteriosclerosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:arteriosclerosis | rel=r_associated | relid=0 | w=20
  459. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:atherosclerotic plaque
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:atherosclerotic plaque | rel=r_associated | relid=0 | w=20
  460. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:autosomal dominant beta2-microglobulinic amyloidosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant beta2-microglobulinic amyloidosis | rel=r_associated | relid=0 | w=20
  461. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20
  462. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:autosomal dominant charcot-marie-tooth disease type 2m
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant charcot-marie-tooth disease type 2m | rel=r_associated | relid=0 | w=20
  463. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:autosomal dominant focal dystonia dyt25 type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=20
  464. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:autosomal dominant palmoplantar keratoderma and congenital alopecia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | rel=r_associated | relid=0 | w=20
  465. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:basal cell nævus
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:basal cell nævus | rel=r_associated | relid=0 | w=20
  466. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:basal cell nevus syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:basal cell nevus syndrome | rel=r_associated | relid=0 | w=20
  467. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:bethlem myopathy 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:bethlem myopathy 1 | rel=r_associated | relid=0 | w=20
  468. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=20
  469. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:braddock syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=20
  470. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:brain calcification rajab type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20
  471. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Budd Chiari's disease (or syndrome)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Budd Chiari's disease (or syndrome) | rel=r_associated | relid=0 | w=20
  472. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Budd's syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Budd's syndrome | rel=r_associated | relid=0 | w=20
  473. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:buerger disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:buerger disease | rel=r_associated | relid=0 | w=20
  474. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:cardiac anomaly and heterotaxy syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=20
  475. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:cardiomyopathy and renal anomaly syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cardiomyopathy and renal anomaly syndrome | rel=r_associated | relid=0 | w=20
  476. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:cataract glaucoma syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=20
  477. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:cerebral gigantism
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
  478. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:cerebrospinal fluid otorrhea
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cerebrospinal fluid otorrhea | rel=r_associated | relid=0 | w=20
  479. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:cleidorhizomelic syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cleidorhizomelic syndrome | rel=r_associated | relid=0 | w=20
  480. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:cooper jabs syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20
  481. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:corneal dystrophy, subepithelial mucinous
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:corneal dystrophy, subepithelial mucinous | rel=r_associated | relid=0 | w=20
  482. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=20
  483. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:czech dysplasia, metatarsal type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:czech dysplasia, metatarsal type | rel=r_associated | relid=0 | w=20
  484. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:degenerative and/or vascular disorder of ear
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:degenerative and/or vascular disorder of ear | rel=r_associated | relid=0 | w=20
  485. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:diffuse palmoplantar keratoderma and acrocyanosis syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=20
  486. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:drug-induced toxic (predictable) liver disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:drug-induced toxic (predictable) liver disease | rel=r_associated | relid=0 | w=20
  487. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:dyschondrosteosis and nephritis syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=20
  488. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:ehlers-danlos syndrome vascular-like type
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=20
  489. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:empyema, subdural
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:empyema, subdural | rel=r_associated | relid=0 | w=20
  490. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:encephalomeningocele
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:encephalomeningocele | rel=r_associated | relid=0 | w=20
  491. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:epiphyseal dysplasia, multiple, 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:epiphyseal dysplasia, multiple, 2 | rel=r_associated | relid=0 | w=20
  492. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:fatal congenital nonlysosomal heart glycogenosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:fatal congenital nonlysosomal heart glycogenosis | rel=r_associated | relid=0 | w=20
  493. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Feingold syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Feingold syndrome | rel=r_associated | relid=0 | w=20
  494. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:ferro-cerebro-cutaneous syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:ferro-cerebro-cutaneous syndrome | rel=r_associated | relid=0 | w=20
  495. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:fibrodysplasia ossificans progressiva
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=20
  496. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:focal amyloid
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:focal amyloid | rel=r_associated | relid=0 | w=20
  497. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:gracile bone dysplasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=20
  498. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:halal syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:halal syndrome | rel=r_associated | relid=0 | w=20
  499. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hall riggs syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
  500. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:heart defects limb shortening
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20
  501. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hemorrhoid
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hemorrhoid | rel=r_associated | relid=0 | w=20
  502. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hepatic veino occlusive disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hepatic veino occlusive disease | rel=r_associated | relid=0 | w=20
  503. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20
  504. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hereditary motor and sensory neuropathy type I
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary motor and sensory neuropathy type I | rel=r_associated | relid=0 | w=20
  505. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hereditary multiple ossifying ecchondromata
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary multiple ossifying ecchondromata | rel=r_associated | relid=0 | w=20
  506. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hereditary non polyposis colorectal cancer
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary non polyposis colorectal cancer | rel=r_associated | relid=0 | w=20
  507. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hereditary sensory and autonomic neuropathy type 1b
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary sensory and autonomic neuropathy type 1b | rel=r_associated | relid=0 | w=20
  508. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hyperinsulinism due to hnf1a deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperinsulinism due to hnf1a deficiency | rel=r_associated | relid=0 | w=20
  509. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hyperinsulinism due to insulin receptor deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperinsulinism due to insulin receptor deficiency | rel=r_associated | relid=0 | w=20
  510. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  511. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:hyperuricemia, anemia, renal failure syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperuricemia, anemia, renal failure syndrome | rel=r_associated | relid=0 | w=20
  512. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:insulin growth factor i deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
  513. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:intercalation
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:intercalation | rel=r_associated | relid=0 | w=20
  514. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:juvenile amyotrophic lateral sclerosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:juvenile amyotrophic lateral sclerosis | rel=r_associated | relid=0 | w=20
  515. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:kallman syndrome with heart disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=20
  516. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20
  517. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20
  518. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:localized amyloid deposit
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:localized amyloid deposit | rel=r_associated | relid=0 | w=20
  519. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:localized hereditary amyloidosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:localized hereditary amyloidosis | rel=r_associated | relid=0 | w=20
  520. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Lynch syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Lynch syndrome | rel=r_associated | relid=0 | w=20
  521. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Lynch'syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Lynch'syndrome | rel=r_associated | relid=0 | w=20
  522. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:manouvrier syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=20
  523. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Marfan's disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20
  524. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Marfan's syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20
  525. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:meningeal hemorrhage
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:meningeal hemorrhage | rel=r_associated | relid=0 | w=20
  526. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:meningitis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:meningitis | rel=r_associated | relid=0 | w=20
  527. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:meningo-encephalocele
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:meningo-encephalocele | rel=r_associated | relid=0 | w=20
  528. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20
  529. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:metastatic tumor
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:metastatic tumor | rel=r_associated | relid=0 | w=20
  530. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:microcephaly albinism digital anomalies syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
  531. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Mohr-Tranebjaerg syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Mohr-Tranebjaerg syndrome | rel=r_associated | relid=0 | w=20
  532. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:morava mehes syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=20
  533. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:moyamoya disease with early onset achalasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
  534. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:multiple osteogenic exostoses
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:multiple osteogenic exostoses | rel=r_associated | relid=0 | w=20
  535. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20
  536. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:najjar syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=20
  537. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:phlebectasia
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:phlebectasia | rel=r_associated | relid=0 | w=20
  538. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:phlebectasis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:phlebectasis | rel=r_associated | relid=0 | w=20
  539. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Pitt-Hopkins syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Pitt-Hopkins syndrome | rel=r_associated | relid=0 | w=20
  540. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:piussan lenaerts mathieu syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20
  541. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | rel=r_associated | relid=0 | w=20
  542. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:potocki-shaffer syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=20
  543. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:preaxial deficiency, postaxial polydactyly and hypospadias
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=20
  544. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:primary pigmented nodular adrenocortical disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:primary pigmented nodular adrenocortical disease | rel=r_associated | relid=0 | w=20
  545. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:retinal vascular disorder
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:retinal vascular disorder | rel=r_associated | relid=0 | w=20
  546. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:schulman upshaw syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:schulman upshaw syndrome | rel=r_associated | relid=0 | w=20
  547. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome | rel=r_associated | relid=0 | w=20
  548. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:serous hepatosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:serous hepatosis | rel=r_associated | relid=0 | w=20
  549. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:short fifth metacarpal insulin resistance syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:short fifth metacarpal insulin resistance syndrome | rel=r_associated | relid=0 | w=20
  550. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Soto's syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
  551. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:Sotos' syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
  552. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:sotos' syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
  553. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:spinal cord vascular diseases
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinal cord vascular diseases | rel=r_associated | relid=0 | w=20
  554. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:spinocerebellar ataxia type 32
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia type 32 | rel=r_associated | relid=0 | w=20
  555. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:spinocerebellar ataxia type 37
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:spinocerebellar ataxia type 37 | rel=r_associated | relid=0 | w=20
  556. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:subpial siderosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:subpial siderosis | rel=r_associated | relid=0 | w=20
  557. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:timothy syndrome type 2
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=20
  558. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:tubular renal disease with cardiomyopathy syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=20
  559. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:tumor embolism
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:tumor embolism | rel=r_associated | relid=0 | w=20
  560. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:type a 14
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:type a 14 | rel=r_associated | relid=0 | w=20
  561. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:varicosity
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:varicosity | rel=r_associated | relid=0 | w=20
  562. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:vascular thrombosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vascular thrombosis | rel=r_associated | relid=0 | w=20
  563. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:vasoconstriction
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:vasoconstriction | rel=r_associated | relid=0 | w=20
  564. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:venous varicosity
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:venous varicosity | rel=r_associated | relid=0 | w=20
  565. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:von Recklinghausen's disease
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:von Recklinghausen's disease | rel=r_associated | relid=0 | w=20
  566. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20
  567. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:x-linked intellectual disability with ataxia and apraxia syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=20
  568. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=20
  569. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> encéphalo-méningocèle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=encéphalo-méningocèle | rel=r_associated | relid=0 | w=20
  570. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> encéphaloméningocèle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=encéphaloméningocèle | rel=r_associated | relid=0 | w=20
  571. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> épidurite bactérienne
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=épidurite bactérienne | rel=r_associated | relid=0 | w=20
  572. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> exostosante (maladie)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=exostosante (maladie) | rel=r_associated | relid=0 | w=20
  573. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> exostose héréditaire multiple
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=exostose héréditaire multiple | rel=r_associated | relid=0 | w=20
  574. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> fibroplasie rétrolentale
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=fibroplasie rétrolentale | rel=r_associated | relid=0 | w=20
  575. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> gigantisme cérébral
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
  576. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> goniodysgénésie-retard mental-petite taille (syndrome)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=goniodysgénésie-retard mental-petite taille (syndrome) | rel=r_associated | relid=0 | w=20
  577. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> hémangiomatose
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=hémangiomatose | rel=r_associated | relid=0 | w=20
  578. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> hémorragie méningée
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=hémorragie méningée | rel=r_associated | relid=0 | w=20
  579. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> hémorrhoïde
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=hémorrhoïde | rel=r_associated | relid=0 | w=20
  580. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> hémorroïde
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=hémorroïde | rel=r_associated | relid=0 | w=20
  581. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> hypertension portale
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=hypertension portale | rel=r_associated | relid=0 | w=20
  582. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> lipomatose épidurale
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=lipomatose épidurale | rel=r_associated | relid=0 | w=20
  583. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Lynch (syndrome de)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Lynch (syndrome de) | rel=r_associated | relid=0 | w=20
  584. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie clinique de recklinghausen
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie clinique de recklinghausen | rel=r_associated | relid=0 | w=20
  585. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie de Bessel-Hagen
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie de Bessel-Hagen | rel=r_associated | relid=0 | w=20
  586. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie de Budd-Chiari
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie de Budd-Chiari | rel=r_associated | relid=0 | w=20
  587. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie de marfan
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie de marfan | rel=r_associated | relid=0 | w=20
  588. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie de Recklinghausen
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie de Recklinghausen | rel=r_associated | relid=0 | w=20
  589. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie de von Recklinghausen
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie de von Recklinghausen | rel=r_associated | relid=0 | w=20
  590. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie des exostoses multiples
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie des exostoses multiples | rel=r_associated | relid=0 | w=20
  591. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie exostosante multiple
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie exostosante multiple | rel=r_associated | relid=0 | w=20
  592. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie ostéogénique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie ostéogénique | rel=r_associated | relid=0 | w=20
  593. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie toxique du foie
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie toxique du foie | rel=r_associated | relid=0 | w=20
  594. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie vasculaire périphérique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie vasculaire périphérique | rel=r_associated | relid=0 | w=20
  595. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie veino occlusive du foie
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie veino occlusive du foie | rel=r_associated | relid=0 | w=20
  596. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie veino occlusive foie
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie veino occlusive foie | rel=r_associated | relid=0 | w=20
  597. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie veino-occlusive du foie
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie veino-occlusive du foie | rel=r_associated | relid=0 | w=20
  598. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> maladie véno-occlusive du foie
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=maladie véno-occlusive du foie | rel=r_associated | relid=0 | w=20
  599. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Marfan (maladie de)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Marfan (maladie de) | rel=r_associated | relid=0 | w=20
  600. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> méningite
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=méningite | rel=r_associated | relid=0 | w=20
  601. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Méningite
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Méningite | rel=r_associated | relid=0 | w=20
  602. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> méningo-encéphalocèle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=méningo-encéphalocèle | rel=r_associated | relid=0 | w=20
  603. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> méningoencéphalocèle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=méningoencéphalocèle | rel=r_associated | relid=0 | w=20
  604. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> métastase tumorale
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=métastase tumorale | rel=r_associated | relid=0 | w=20
  605. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> métastase
    (médecine)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=métastase
    (médecine)
    | rel=r_associated | relid=0 | w=20
  606. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> métastase
    (médecine, cancer)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=métastase
    (médecine, cancer)
    | rel=r_associated | relid=0 | w=20
  607. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> microdélétion 5q35
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20
  608. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> migraine hémiplégique familiale
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=migraine hémiplégique familiale | rel=r_associated | relid=0 | w=20
  609. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> naevomatose baso-cellulaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=naevomatose baso-cellulaire | rel=r_associated | relid=0 | w=20
  610. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> naevomatose basocellulaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=naevomatose basocellulaire | rel=r_associated | relid=0 | w=20
  611. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> nævomatose basocellulaire multiple
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=nævomatose basocellulaire multiple | rel=r_associated | relid=0 | w=20
  612. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> néoplasme métastatique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=néoplasme métastatique | rel=r_associated | relid=0 | w=20
  613. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> néoplasme secondaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=néoplasme secondaire | rel=r_associated | relid=0 | w=20
  614. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neurofibromatose
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neurofibromatose | rel=r_associated | relid=0 | w=20
  615. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neurofibromatose de Recklinghausen
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neurofibromatose de Recklinghausen | rel=r_associated | relid=0 | w=20
  616. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neurofibromatose de recklinghausen
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neurofibromatose de recklinghausen | rel=r_associated | relid=0 | w=20
  617. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neurofibromatose de type 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neurofibromatose de type 1 | rel=r_associated | relid=0 | w=20
  618. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neurofibromatose de type périphérique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neurofibromatose de type périphérique | rel=r_associated | relid=0 | w=20
  619. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neurofibromatose de type VI
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neurofibromatose de type VI | rel=r_associated | relid=0 | w=20
  620. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neuropathie héréditaire sensitive et autonome de type 1
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neuropathie héréditaire sensitive et autonome de type 1 | rel=r_associated | relid=0 | w=20
  621. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neuropathie héréditaire sensitive et autonome de type i
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neuropathie héréditaire sensitive et autonome de type i | rel=r_associated | relid=0 | w=20
  622. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neuropathie sensitive héréditaire dominante de type i
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neuropathie sensitive héréditaire dominante de type i | rel=r_associated | relid=0 | w=20
  623. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> neuropathie sensitive héréditaire dominante de type I
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=neuropathie sensitive héréditaire dominante de type I | rel=r_associated | relid=0 | w=20
  624. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> obstruction des veines sus-hépatiques
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=obstruction des veines sus-hépatiques | rel=r_associated | relid=0 | w=20
  625. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> obstruction du débit veineux hépatique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=obstruction du débit veineux hépatique | rel=r_associated | relid=0 | w=20
  626. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> occlusion de la veine hépatique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=occlusion de la veine hépatique | rel=r_associated | relid=0 | w=20
  627. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> piébaldisme
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=piébaldisme | rel=r_associated | relid=0 | w=20
  628. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> piebaldisme
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=piebaldisme | rel=r_associated | relid=0 | w=20
  629. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> plaque d'athérosclérose
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=plaque d'athérosclérose | rel=r_associated | relid=0 | w=20
  630. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> pseudo-méningocèle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=pseudo-méningocèle | rel=r_associated | relid=0 | w=20
  631. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> pseudoméningocèle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=pseudoméningocèle | rel=r_associated | relid=0 | w=20
  632. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Recklinghausen (maladie de von)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Recklinghausen (maladie de von) | rel=r_associated | relid=0 | w=20
  633. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Recklinghausen (neurofibromatose de)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Recklinghausen (neurofibromatose de) | rel=r_associated | relid=0 | w=20
  634. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> rétinopathie du prématuré
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=rétinopathie du prématuré | rel=r_associated | relid=0 | w=20
  635. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> sclérose artérielle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=sclérose artérielle | rel=r_associated | relid=0 | w=20
  636. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> sclérose des artères
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=sclérose des artères | rel=r_associated | relid=0 | w=20
  637. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> sclérose tubéreuse du cerveau
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=sclérose tubéreuse du cerveau | rel=r_associated | relid=0 | w=20
  638. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Sotos (syndrome de)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
  639. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> stomatocytose héréditaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=stomatocytose héréditaire | rel=r_associated | relid=0 | w=20
  640. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome d'Alagille
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome d'Alagille | rel=r_associated | relid=0 | w=20
  641. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome d'alagille
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome d'alagille | rel=r_associated | relid=0 | w=20
  642. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de budd-chiari
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de budd-chiari | rel=r_associated | relid=0 | w=20
  643. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de Budd-Chiari
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de Budd-Chiari | rel=r_associated | relid=0 | w=20
  644. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Syndrome de Budd-Chiari
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Syndrome de Budd-Chiari | rel=r_associated | relid=0 | w=20
  645. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de chiari
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de chiari | rel=r_associated | relid=0 | w=20
  646. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de douleur extrême paroxystique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de douleur extrême paroxystique | rel=r_associated | relid=0 | w=20
  647. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de Gorlin
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de Gorlin | rel=r_associated | relid=0 | w=20
  648. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de Lynch
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de Lynch | rel=r_associated | relid=0 | w=20
  649. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de marfan
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20
  650. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Syndrome de Marfan
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Syndrome de Marfan | rel=r_associated | relid=0 | w=20
  651. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20
  652. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de soto
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
  653. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de Sotos
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
  654. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome de sotos
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
  655. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome héréditaire de cancer du sein et de l'ovaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome héréditaire de cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20
  656. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20
  657. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> télangiectasie
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=télangiectasie | rel=r_associated | relid=0 | w=20
  658. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> tumeur métastasique
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=tumeur métastasique | rel=r_associated | relid=0 | w=20
  659. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> tumeur secondaire
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=tumeur secondaire | rel=r_associated | relid=0 | w=20
  660. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> tylosis
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=tylosis | rel=r_associated | relid=0 | w=20
  661. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> varice
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=varice | rel=r_associated | relid=0 | w=20
  662. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> varicocèle
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=varicocèle | rel=r_associated | relid=0 | w=20
  663. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> vaso-constriction
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=vaso-constriction | rel=r_associated | relid=0 | w=20
  664. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> vasoconstriction
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=vasoconstriction | rel=r_associated | relid=0 | w=20
  665. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> vasodilatation
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=vasodilatation | rel=r_associated | relid=0 | w=20
  666. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> vasoplégie
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=vasoplégie | rel=r_associated | relid=0 | w=20
  667. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> veine variqueuse
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=veine variqueuse | rel=r_associated | relid=0 | w=20
  668. en:hereditary oculoleptomeningeal amyloid angiopathy -- r_associated #0: 20 / 0.513 -> Walker-Warburg (syndrome de)
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20
≈ 809 relations entrantes

  1. en:vasoconstriction --- r_associated #0: 687 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vasoconstriction | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=687
  2. vasoconstriction --- r_associated #0: 686.5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vasoconstriction | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=686.5
  3. en:peripheral vascular disorder --- r_associated #0: 340 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:peripheral vascular disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=340
  4. trouble vasculaire périphérique --- r_associated #0: 338 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=trouble vasculaire périphérique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=338
  5. en:marfan syndrome --- r_associated #0: 285 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:marfan syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=285
  6. maladie de Marfan --- r_associated #0: 281 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie de Marfan | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=281
  7. syndrome de Marfan --- r_associated #0: 281 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Marfan | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=281
  8. arachnodactylie --- r_associated #0: 271 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=arachnodactylie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=271
  9. en:arachnodactyly --- r_associated #0: 250 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:arachnodactyly | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=250
  10. syndrome de soto --- r_associated #0: 210 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de soto | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=210
  11. en:sotos syndrome --- r_associated #0: 202 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:sotos syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=202
  12. gigantisme cérébral --- r_associated #0: 201 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gigantisme cérébral | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=201
  13. syndrome de Sotos --- r_associated #0: 195 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Sotos | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=195
  14. en:sotos' syndrome --- r_associated #0: 190 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:sotos' syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=190
  15. vaso-constriction --- r_associated #0: 182 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vaso-constriction | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=182
  16. en:walker-warburg syndrome --- r_associated #0: 180 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:walker-warburg syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=180
  17. syndrome de Walker-Warburg --- r_associated #0: 178 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Walker-Warburg | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=178
  18. syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire --- r_associated #0: 169 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=169
  19. en:hereditary breast and ovarian cancer syndrome --- r_associated #0: 167 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary breast and ovarian cancer syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=167
  20. syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire --- r_associated #0: 162 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=162
  21. syndrome d'Alagille --- r_associated #0: 159 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome d'Alagille | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=159
  22. syndrome héréditaire de cancer du sein et de l'ovaire --- r_associated #0: 159 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome héréditaire de cancer du sein et de l'ovaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=159
  23. amyloïdose de type VII --- r_associated #0: 145 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=amyloïdose de type VII | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=145
  24. amyloïdose de type vii --- r_associated #0: 142 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=amyloïdose de type vii | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=142
  25. en:liver veno-occlusive disease --- r_associated #0: 139 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:liver veno-occlusive disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=139
  26. en:hereditary sensory autonomic neuropathy, type 1 --- r_associated #0: 136 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary sensory autonomic neuropathy, type 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=136
  27. neuropathie héréditaire sensitive et autonome de type 1 --- r_associated #0: 136 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neuropathie héréditaire sensitive et autonome de type 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=136
  28. neuropathie héréditaire sensitive et autonome de type i --- r_associated #0: 136 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neuropathie héréditaire sensitive et autonome de type i | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=136
  29. aclasie diaphysaire --- r_associated #0: 135 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=aclasie diaphysaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=135
  30. exostose héréditaire multiple --- r_associated #0: 135 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=exostose héréditaire multiple | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=135
  31. maladie veino occlusive du foie --- r_associated #0: 135 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie veino occlusive du foie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=135
  32. neuropathie sensitive héréditaire dominante de type i --- r_associated #0: 135 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neuropathie sensitive héréditaire dominante de type i | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=135
  33. en:hereditary multiple exostoses --- r_associated #0: 133 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary multiple exostoses | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=133
  34. en:tylosis --- r_associated #0: 133 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:tylosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=133
  35. maladie veino-occlusive du foie --- r_associated #0: 131 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie veino-occlusive du foie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=131
  36. chondrodysplasie héréditaire déformante --- r_associated #0: 130 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=chondrodysplasie héréditaire déformante | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=130
  37. maladie exostosante multiple --- r_associated #0: 130 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie exostosante multiple | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=130
  38. maladie veino occlusive foie --- r_associated #0: 130 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie veino occlusive foie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=130
  39. tylosis --- r_associated #0: 130 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=tylosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=130
  40. chondrodysplasie déformante héréditaire --- r_associated #0: 125 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=chondrodysplasie déformante héréditaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=125
  41. en:serous hepatosis --- r_associated #0: 125 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:serous hepatosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=125
  42. maladie véno-occlusive du foie --- r_associated #0: 125 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie véno-occlusive du foie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=125
  43. méningoencéphalocèle --- r_associated #0: 125 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=méningoencéphalocèle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=125
  44. encéphalo-méningocèle --- r_associated #0: 122 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=encéphalo-méningocèle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=122
  45. en:encephalomeningocele --- r_associated #0: 121 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:encephalomeningocele | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=121
  46. méningo-encéphalocèle --- r_associated #0: 121 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=méningo-encéphalocèle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=121
  47. encéphaloméningocèle --- r_associated #0: 120 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=encéphaloméningocèle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=120
  48. maladie ostéogénique --- r_associated #0: 120 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie ostéogénique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=120
  49. atrophie optique autosomique dominante --- r_associated #0: 119 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=atrophie optique autosomique dominante | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=119
  50. en:lynch syndrome --- r_associated #0: 116 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:lynch syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=116
  51. démence frontotemporale --- r_associated #0: 115 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=démence frontotemporale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=115
  52. en:Lynch syndrome --- r_associated #0: 115 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Lynch syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=115
  53. maladie de Bessel-Hagen --- r_associated #0: 115 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie de Bessel-Hagen | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=115
  54. démence fronto-temporale --- r_associated #0: 114 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=démence fronto-temporale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=114
  55. Anévrisme --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Anévrisme | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  56. anévrysme --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=anévrysme | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  57. embole de tumeur --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=embole de tumeur | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  58. en:metastatic tumor --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:metastatic tumor | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  59. maladie des exostoses multiples --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie des exostoses multiples | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  60. métastase tumorale --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=métastase tumorale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  61. métastase
    (médecine, cancer)
     --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=métastase
    (médecine, cancer)
    | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  62. néoplasme métastatique --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=néoplasme métastatique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  63. néoplasme secondaire --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=néoplasme secondaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  64. tumeur métastasique --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=tumeur métastasique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  65. tumeur secondaire --- r_associated #0: 110 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=tumeur secondaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=110
  66. maladie vasculaire périphérique --- r_associated #0: 108 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie vasculaire périphérique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=108
  67. embole tumoral --- r_associated #0: 107 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=embole tumoral | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=107
  68. en:aneurysm --- r_associated #0: 106 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:aneurysm | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=106
  69. en:piebaldism --- r_associated #0: 106 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:piebaldism | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=106
  70. embolie tumorale --- r_associated #0: 105 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=embolie tumorale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=105
  71. neuropathie sensitive héréditaire dominante de type I --- r_associated #0: 105 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neuropathie sensitive héréditaire dominante de type I | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=105
  72. piebaldisme --- r_associated #0: 105 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=piebaldisme | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=105
  73. varicocèle --- r_associated #0: 105 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=varicocèle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=105
  74. en:varicocele --- r_associated #0: 104 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:varicocele | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=104
  75. varice --- r_associated #0: 104 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=varice | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=104
  76. piébaldisme --- r_associated #0: 103 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=piébaldisme | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=103
  77. en:varicose vein --- r_associated #0: 102 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:varicose vein | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=102
  78. en:frontotemporal dementia --- r_associated #0: 100 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:frontotemporal dementia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=100
  79. veine variqueuse --- r_associated #0: 100 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=veine variqueuse | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=100
  80. artério-sclérose --- r_associated #0: 81 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=artério-sclérose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=81
  81. syndrome de Lynch --- r_associated #0: 81 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Lynch | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=81
  82. en:multiple osteogenic exostoses --- r_associated #0: 80 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:multiple osteogenic exostoses | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=80
  83. artériosclérose --- r_associated #0: 77 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=artériosclérose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=77
  84. dilatation d'un vaisseau --- r_associated #0: 76 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=dilatation d'un vaisseau | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=76
  85. en:vasodilation --- r_associated #0: 74 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vasodilation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=74
  86. en:arteriosclerosis --- r_associated #0: 73 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:arteriosclerosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=73
  87. vasodilatation --- r_associated #0: 71 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vasodilatation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=71
  88. hypertension portale --- r_associated #0: 65 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=hypertension portale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=65
  89. en:portal hypertension --- r_associated #0: 64 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:portal hypertension | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=64
  90. dilatation vasculaire --- r_associated #0: 61 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=dilatation vasculaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=61
  91. en:Sotos' syndrome --- r_associated #0: 60 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Sotos' syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=60
  92. naevomatose baso-cellulaire --- r_associated #0: 57 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=naevomatose baso-cellulaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=57
  93. syndrome de Gorlin --- r_associated #0: 56 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Gorlin | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=56
  94. cancer colorectal héréditaire sans polypose --- r_associated #0: 55 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=cancer colorectal héréditaire sans polypose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=55
  95. en:tumor embolism --- r_associated #0: 55 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:tumor embolism | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=55
  96. cancer colo-rectal héréditaire sans polypose --- r_associated #0: 54 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=cancer colo-rectal héréditaire sans polypose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=54
  97. dysplasie cléidocrânienne --- r_associated #0: 53 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=dysplasie cléidocrânienne | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=53
  98. naevomatose basocellulaire --- r_associated #0: 53 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=naevomatose basocellulaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=53
  99. Recklinghausen (neurofibromatose de) --- r_associated #0: 52 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Recklinghausen (neurofibromatose de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=52
  100. en:Marfan's syndrome --- r_associated #0: 51 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Marfan's syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=51
  101. maladie de Budd-Chiari --- r_associated #0: 51 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie de Budd-Chiari | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=51
  102. Cancer colorectal héréditaire sans polypose --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Cancer colorectal héréditaire sans polypose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  103. bloc supra-hépatique --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=bloc supra-hépatique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  104. dysplasie cléido-crânienne --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=dysplasie cléido-crânienne | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  105. embolisme --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=embolisme | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  106. en:intercalation --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:intercalation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  107. en:neurofibromatosis --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:neurofibromatosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  108. en:von Recklinghausen's disease --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:von Recklinghausen's disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  109. maladie toxique du foie --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie toxique du foie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  110. métastase
    (médecine)
     --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=métastase
    (médecine)
    | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  111. obstruction des veines sus-hépatiques --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=obstruction des veines sus-hépatiques | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  112. obstruction du débit veineux hépatique --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=obstruction du débit veineux hépatique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  113. occlusion de la veine hépatique --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=occlusion de la veine hépatique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  114. syndrome de Budd-Chiari --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Budd-Chiari | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  115. syndrome de budd-chiari --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de budd-chiari | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  116. syndrome de chiari --- r_associated #0: 50 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de chiari | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=50
  117. en:hereditary nonpolyposis colorectal cancer --- r_associated #0: 48 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary nonpolyposis colorectal cancer | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=48
  118. syndrome de marfan --- r_associated #0: 48 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de marfan | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=48
  119. en:embolism --- r_associated #0: 46 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:embolism | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=46
  120. maladie de Recklinghausen --- r_associated #0: 46 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie de Recklinghausen | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=46
  121. maladie de von Recklinghausen --- r_associated #0: 46 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie de von Recklinghausen | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=46
  122. neurofibromatose de Recklinghausen --- r_associated #0: 46 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neurofibromatose de Recklinghausen | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=46
  123. neurofibromatose de type 1 --- r_associated #0: 46 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neurofibromatose de type 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=46
  124. en:Marfan's disease --- r_associated #0: 45 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Marfan's disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=45
  125. en:neurofibromatosis type 1 --- r_associated #0: 45 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:neurofibromatosis type 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=45
  126. syndrome de douleur extrême paroxystique --- r_associated #0: 45 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de douleur extrême paroxystique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=45
  127. épidurite bactérienne --- r_associated #0: 45 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=épidurite bactérienne | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=45
  128. syndrome de sotos --- r_associated #0: 44 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de sotos | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=44
  129. en:bannayan syndrome --- r_associated #0: 43 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:bannayan syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=43
  130. en:cadasil syndrome --- r_associated #0: 43 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cadasil syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=43
  131. en:czech dysplasia, metatarsal type --- r_associated #0: 43 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:czech dysplasia, metatarsal type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=43
  132. en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 43 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dentatorubral-pallidoluysian atrophy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=43
  133. en:oculodental syndrome rutherfurd syndrome --- r_associated #0: 43 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=43
  134. en:thomas syndrome --- r_associated #0: 43 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:thomas syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=43
  135. en:x-linked lissencephaly --- r_associated #0: 43 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:x-linked lissencephaly | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=43
  136. en:epidural abscess --- r_associated #0: 42 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:epidural abscess | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=42
  137. en:okihiro syndrome --- r_associated #0: 42 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:okihiro syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=42
  138. en:paroxysmal extreme pain disorder --- r_associated #0: 42 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:paroxysmal extreme pain disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=42
  139. en:preaxial deficiency, postaxial polydactyly and hypospadias --- r_associated #0: 42 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=42
  140. en:venous varicosity --- r_associated #0: 42 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:venous varicosity | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=42
  141. maladie de marfan --- r_associated #0: 42 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie de marfan | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=42
  142. en:dyskeratosis congenita, autosomal dominant --- r_associated #0: 41 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dyskeratosis congenita, autosomal dominant | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=41
  143. en:hereditary dysplasia of blood vessel --- r_associated #0: 41 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary dysplasia of blood vessel | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=41
  144. en:hereditary stomatocytosis --- r_associated #0: 41 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary stomatocytosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=41
  145. maladie clinique de recklinghausen --- r_associated #0: 41 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie clinique de recklinghausen | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=41
  146. rétinopathie du prématuré --- r_associated #0: 41 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=rétinopathie du prématuré | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=41
  147. stomatocytose héréditaire --- r_associated #0: 41 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=stomatocytose héréditaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=41
  148. télangiectasie --- r_associated #0: 41 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=télangiectasie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=41
  149. Syndrome de Marfan --- r_associated #0: 40 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Syndrome de Marfan | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=40
  150. Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Walker-Warburg (syndrome de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=40
  151. angiomatose --- r_associated #0: 40 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=angiomatose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=40
  152. en:brachydactyly type a6 --- r_associated #0: 40 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:brachydactyly type a6 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=40
  153. en:budd-chiari syndrome --- r_associated #0: 40 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:budd-chiari syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=40
  154. en:telangiectasia --- r_associated #0: 40 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:telangiectasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=40
  155. en:corneal dystrophy, congenital stromal --- r_associated #0: 39 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:corneal dystrophy, congenital stromal | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=39
  156. en:hyperinsulinemic hypoglycemia, familial, 7 --- r_associated #0: 39 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperinsulinemic hypoglycemia, familial, 7 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=39
  157. en:nevoid basal cell carcinoma syndrome --- r_associated #0: 39 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:nevoid basal cell carcinoma syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=39
  158. en:retinopathy of prematurity --- r_associated #0: 39 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:retinopathy of prematurity | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=39
  159. en:sebastian syndrome --- r_associated #0: 39 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:sebastian syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=39
  160. en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 39 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=39
  161. exostosante (maladie) --- r_associated #0: 39 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=exostosante (maladie) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=39
  162. en:hyperparathyroidism-jaw tumor syndrome --- r_associated #0: 38 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperparathyroidism-jaw tumor syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=38
  163. en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 38 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=38
  164. en:non-polyposis turcot syndrome --- r_associated #0: 38 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:non-polyposis turcot syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=38
  165. en:penile vascular disorder --- r_associated #0: 38 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:penile vascular disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=38
  166. en:phlebectasia --- r_associated #0: 38 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:phlebectasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=38
  167. sclérose artérielle --- r_associated #0: 38 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=sclérose artérielle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=38
  168. en:Soto's syndrome --- r_associated #0: 37 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Soto's syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=37
  169. en:angiomatosis --- r_associated #0: 37 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:angiomatosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=37
  170. en:basal cell nevus syndrome --- r_associated #0: 37 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:basal cell nevus syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=37
  171. en:gracile bone dysplasia --- r_associated #0: 37 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:gracile bone dysplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=37
  172. en:hereditary non polyposis colorectal cancer --- r_associated #0: 37 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary non polyposis colorectal cancer | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=37
  173. en:isolated hypoplasia of the right ventricle --- r_associated #0: 37 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:isolated hypoplasia of the right ventricle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=37
  174. nævomatose basocellulaire multiple --- r_associated #0: 37 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=nævomatose basocellulaire multiple | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=37
  175. Sotos (syndrome de) --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Sotos (syndrome de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  176. en:amyloid angiopathy --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:amyloid angiopathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  177. en:cleidocranial dysplasia --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cleidocranial dysplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  178. en:iris coloboma with ptosis, hypertelorism, and mental retardation --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:iris coloboma with ptosis, hypertelorism, and mental retardation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  179. en:microphthalmia, syndromic 3 --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microphthalmia, syndromic 3 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  180. en:strudwick syndrome --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:strudwick syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  181. en:subarachnoid intracranial abscess --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:subarachnoid intracranial abscess | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  182. en:syndactyly, type iii --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:syndactyly, type iii | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  183. neurofibromatose de type VI --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neurofibromatose de type VI | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  184. vasoplégie --- r_associated #0: 36 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vasoplégie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=36
  185. Méningite --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Méningite | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  186. angiofibrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=angiofibrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  187. en:acro-dermato-ungual-lacrimal-tooth syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:acro-dermato-ungual-lacrimal-tooth syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  188. en:acrocallosal syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:acrocallosal syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  189. en:autosomal dominant charcot-marie-tooth disease type 2a1 --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant charcot-marie-tooth disease type 2a1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  190. en:autosomal recessive primary microcephaly --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal recessive primary microcephaly | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  191. en:behr syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:behr syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  192. en:cardiomyopathy and renal anomaly syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cardiomyopathy and renal anomaly syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  193. en:cerebral cavernous malformation --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebral cavernous malformation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  194. en:cerebrovascular disorder --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebrovascular disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  195. en:cleidorhizomelic syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cleidorhizomelic syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  196. en:cole disease --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cole disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  197. en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  198. en:craniofacial deafness hand syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:craniofacial deafness hand syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  199. en:crisponi syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:crisponi syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  200. en:diabetic vascular disorder --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:diabetic vascular disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  201. en:dominant autosomal hereditary disorder, incomplete penetrance --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dominant autosomal hereditary disorder, incomplete penetrance | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  202. en:dopa-responsive dystonia --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dopa-responsive dystonia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  203. en:ectodermal dysplasia with natal teeth, turnpenny type --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ectodermal dysplasia with natal teeth, turnpenny type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  204. en:epilepsy, myoclonic, benign adult familial, type 2 --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:epilepsy, myoclonic, benign adult familial, type 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  205. en:familial amyloid neuropathy --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial amyloid neuropathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  206. en:familial benign neonatal epilepsy --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial benign neonatal epilepsy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  207. en:fatal familial insomnia --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:fatal familial insomnia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  208. en:focal amyloid --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:focal amyloid | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  209. en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  210. en:great vessel neoplasm --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:great vessel neoplasm | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  211. en:hall riggs syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hall riggs syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  212. en:hereditary motor neuron disease --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary motor neuron disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  213. en:holoprosencephaly with fetal akinesia-hypokinesia sequence --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  214. en:hyaline dystrophy of bruch's membrane --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyaline dystrophy of bruch's membrane | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  215. en:hydrocephalus with cerebellar agenesis --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hydrocephalus with cerebellar agenesis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  216. en:hyperinsulinemic hypoglycemia, familial, 6 --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperinsulinemic hypoglycemia, familial, 6 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  217. en:insulin growth factor i deficiency --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:insulin growth factor i deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  218. en:jervell and lange nielsen syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:jervell and lange nielsen syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  219. en:keratoacanthoma familial --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:keratoacanthoma familial | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  220. en:lamellar ichthyosis, autosomal dominant form --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:lamellar ichthyosis, autosomal dominant form | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  221. en:leopard syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:leopard syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  222. en:leukotriene c4 synthase deficiency --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:leukotriene c4 synthase deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  223. en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  224. en:lissencephaly, x-linked, 2 --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:lissencephaly, x-linked, 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  225. en:localized hereditary amyloidosis --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:localized hereditary amyloidosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  226. en:melnick-fraser syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:melnick-fraser syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  227. en:meningitis --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:meningitis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  228. en:menkes disease --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:menkes disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  229. en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microcephaly albinism digital anomalies syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  230. en:microcephaly deafness syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microcephaly deafness syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  231. en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  232. en:morava mehes syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:morava mehes syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  233. en:muckle-wells syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:muckle-wells syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  234. en:osteogenesis imperfecta, levin type --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:osteogenesis imperfecta, levin type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  235. en:parietal foramina --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:parietal foramina | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  236. en:piussan lenaerts mathieu syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:piussan lenaerts mathieu syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  237. en:reticulate acropigmentation of kitamura --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:reticulate acropigmentation of kitamura | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  238. en:steinfeld syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:steinfeld syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  239. en:syndrome, branchio-oculo-facial --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:syndrome, branchio-oculo-facial | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  240. en:synpolydactyly --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:synpolydactyly | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  241. en:ulnar-mammary syndrome --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ulnar-mammary syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  242. en:vitelliform macular dystrophy --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vitelliform macular dystrophy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  243. méningite --- r_associated #0: 35 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=méningite | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=35
  244. collatérale --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=collatérale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  245. en:arterial occlusive diseases --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:arterial occlusive diseases | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  246. en:autosomal dominant charcot-marie-tooth disease type 2c --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant charcot-marie-tooth disease type 2c | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  247. en:autosomal dominant mutilating keratoderma --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant mutilating keratoderma | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  248. en:autosomal dominant oculocutaneous albinism --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant oculocutaneous albinism | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  249. en:autosomal dominant progressive nephropathy with hypertension --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant progressive nephropathy with hypertension | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  250. en:avascular necrosis of femoral head --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:avascular necrosis of femoral head | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  251. en:beckwith-wiedemann syndrome --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:beckwith-wiedemann syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  252. en:bethlem myopathy 1 --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:bethlem myopathy 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  253. en:cap myopathy --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cap myopathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  254. en:centronuclear myopathy 1 --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:centronuclear myopathy 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  255. en:cerebral lipidosis --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebral lipidosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  256. en:cerebrospinal fluid otorrhea --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebrospinal fluid otorrhea | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  257. en:charcot-marie-tooth disease, type 2j --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:charcot-marie-tooth disease, type 2j | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  258. en:collateral --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:collateral | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  259. en:congenitally corrected transposition of the great arteries --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:congenitally corrected transposition of the great arteries | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  260. en:crouzon syndrome with acanthosis nigricans (disorder) --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  261. en:degenerative and/or vascular disorder of ear --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:degenerative and/or vascular disorder of ear | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  262. en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dyschondrosteosis and nephritis syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  263. en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ehlers-danlos syndrome vascular-like type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  264. en:episodic ataxia --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:episodic ataxia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  265. en:eyelid vascular disorder --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:eyelid vascular disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  266. en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  267. en:ferro-cerebro-cutaneous syndrome --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ferro-cerebro-cutaneous syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  268. en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  269. en:heart defects limb shortening --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:heart defects limb shortening | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  270. en:hereditary cerebellar degeneration --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary cerebellar degeneration | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  271. en:hereditary gastrogenic lactose intolerance --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary gastrogenic lactose intolerance | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  272. en:hereditary peripheral neuropathy --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary peripheral neuropathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  273. en:melanoma astrocytoma syndrome --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:melanoma astrocytoma syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  274. en:meningeal cyst --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:meningeal cyst | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  275. en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  276. en:najjar syndrome --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:najjar syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  277. en:neuropathy, hereditary motor and sensory, okinawa type --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:neuropathy, hereditary motor and sensory, okinawa type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  278. en:pontocerebellar hypoplasia type 2 --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:pontocerebellar hypoplasia type 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  279. en:potocki-shaffer syndrome --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:potocki-shaffer syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  280. en:sonoda syndrome --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:sonoda syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  281. en:spinocerebellar ataxia 1s --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia 1s | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  282. en:spondyloperipheral dysplasia short ulna --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spondyloperipheral dysplasia short ulna | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  283. en:syndactyly, type i --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:syndactyly, type i | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  284. en:transthyretin related familial amyloid cardiomyopathy --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:transthyretin related familial amyloid cardiomyopathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  285. en:vascular disease of abdomen --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular disease of abdomen | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  286. en:vascular hypertensive disorders --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular hypertensive disorders | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  287. en:von hippel-lindau syndrome --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:von hippel-lindau syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  288. sclérose des artères --- r_associated #0: 34 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=sclérose des artères | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34
  289. en:Lynch'syndrome --- r_associated #0: 33 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Lynch'syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=33
  290. en:angiofibroma --- r_associated #0: 33 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:angiofibroma | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=33
  291. en:cerebral gigantism --- r_associated #0: 33 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebral gigantism | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=33
  292. en:vasoplegia --- r_associated #0: 33 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vasoplegia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=33
  293. dystonie dopasensible --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=dystonie dopasensible | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  294. en:alagille syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:alagille syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  295. en:angiomatosis of meninges --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:angiomatosis of meninges | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  296. en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  297. en:autosomal dominant idiopathic familial dystonia --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant idiopathic familial dystonia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  298. en:autosomal dominant palmoplantar keratoderma and congenital alopecia --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  299. en:blood vessel perforation --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:blood vessel perforation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  300. en:brachydactyly, type a1 (disorder) --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:brachydactyly, type a1 (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  301. en:brachyolmia type 3 --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:brachyolmia type 3 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  302. en:brooke-spiegler syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:brooke-spiegler syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  303. en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  304. en:chromosome 22q11.2 microduplication syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:chromosome 22q11.2 microduplication syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  305. en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  306. en:dicer1 syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dicer1 syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  307. en:disorder of central nervous system due to xeroderma pigmentosum --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:disorder of central nervous system due to xeroderma pigmentosum | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  308. en:epiphyseal dysplasia, multiple, 1 --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:epiphyseal dysplasia, multiple, 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  309. en:epiphyseal dysplasia, multiple, 2 --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:epiphyseal dysplasia, multiple, 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  310. en:familial creutzfeldt-jakob --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial creutzfeldt-jakob | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  311. en:familial non-autoimmune autosomal dominant hyperthyroidism --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial non-autoimmune autosomal dominant hyperthyroidism | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  312. en:gerstmann-straussler-scheinker disease --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:gerstmann-straussler-scheinker disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  313. en:hawkinsinuria --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hawkinsinuria | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  314. en:hepatic veino occlusive disease --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hepatic veino occlusive disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  315. en:hereditary cutaneous vascular syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary cutaneous vascular syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  316. en:hereditary mucosal leukokeratosis --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary mucosal leukokeratosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  317. en:heritable pulmonary arterial hypertension due to bmpr2 mutation --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  318. en:hypoplastic tibia and postaxial polydactyly syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hypoplastic tibia and postaxial polydactyly syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  319. en:microcephaly cervical spine fusion anomalies --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microcephaly cervical spine fusion anomalies | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  320. en:microcornea with glaucoma and absent frontal sinus syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microcornea with glaucoma and absent frontal sinus syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  321. en:mousa al din al nassar syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:mousa al din al nassar syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  322. en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  323. en:perinatal tentorial laceration --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:perinatal tentorial laceration | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  324. en:polydactyly, preaxial ii (disorder) --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:polydactyly, preaxial ii (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  325. en:spondylocostal dysostosis 4, autosomal dominant --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  326. en:tarsal-carpal coalition syndrome --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:tarsal-carpal coalition syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  327. en:tuberculoma of meninges --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:tuberculoma of meninges | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  328. en:type v acrocephalosyndactyly --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:type v acrocephalosyndactyly | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  329. en:vascular malformations --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular malformations | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  330. en:venous insufficiency --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:venous insufficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  331. hémorragie méningée --- r_associated #0: 32 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=hémorragie méningée | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=32
  332. dysplasie acromicrique --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=dysplasie acromicrique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  333. en:aicardi syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:aicardi syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  334. en:aneurysm, infected --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:aneurysm, infected | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  335. en:ataxia telangiectasia syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ataxia telangiectasia syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  336. en:autosomal dominant excess of transthyretin --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant excess of transthyretin | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  337. en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:beare-stevenson cutis gyrata syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  338. en:blood pressure disorders --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:blood pressure disorders | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  339. en:charcot-marie-tooth disease type 2d --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:charcot-marie-tooth disease type 2d | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  340. en:choreoathetosis/spasticity, episodic --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:choreoathetosis/spasticity, episodic | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  341. en:compartment syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:compartment syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  342. en:congenital nephrogenic diabetes insipidus --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:congenital nephrogenic diabetes insipidus | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  343. en:congenital reticular ichthyosiform erythroderma --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:congenital reticular ichthyosiform erythroderma | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  344. en:cooper jabs syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cooper jabs syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  345. en:deafness-craniofacial syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:deafness-craniofacial syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  346. en:diffuse palmoplantar keratoderma and acrocyanosis syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  347. en:empyema, subdural --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:empyema, subdural | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  348. en:game friedman paradice syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:game friedman paradice syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  349. en:glomuvenous malformations --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:glomuvenous malformations | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  350. en:hand foot uterus syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hand foot uterus syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  351. en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:haspeslagh fryns muelenaere syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  352. en:hyperinsulinism due to uncoupling protein 2 deficiency --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  353. en:hypomyelination and congenital cataract --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hypomyelination and congenital cataract | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  354. en:kbg syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:kbg syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  355. en:lymphatic vessel diseases --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:lymphatic vessel diseases | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  356. en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  357. en:meningo-encephalocele --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:meningo-encephalocele | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  358. en:microcephaly microcornea syndrome seemanova type --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microcephaly microcornea syndrome seemanova type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  359. en:mowat-wilson syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:mowat-wilson syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  360. en:multiple endocrine neoplasia type 1 --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:multiple endocrine neoplasia type 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  361. en:myopathy, distal, tateyama type --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:myopathy, distal, tateyama type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  362. en:nemaline myopathy 3 --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:nemaline myopathy 3 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  363. en:nicolaides baraitser syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:nicolaides baraitser syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  364. en:noonan syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:noonan syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  365. en:potassium aggravated myotonia --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:potassium aggravated myotonia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  366. en:pseudocholinesterase deficiency --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:pseudocholinesterase deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  367. en:pseudomeningocele --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:pseudomeningocele | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  368. en:retinal vascular disorder --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:retinal vascular disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  369. en:roch leri mesosomatous lipomatosis --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:roch leri mesosomatous lipomatosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  370. en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  371. en:type i acrocephalosyndactyly --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:type i acrocephalosyndactyly | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  372. en:varicosity --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:varicosity | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  373. en:vascular dilation or proliferation --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular dilation or proliferation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  374. en:vascular disorder of extremity --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular disorder of extremity | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  375. en:vascular inflammations --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular inflammations | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  376. en:wells jankovic syndrome --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:wells jankovic syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  377. en:x-linked dystonia parkinsonism --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:x-linked dystonia parkinsonism | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  378. fibroplasie rétrolentale --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibroplasie rétrolentale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  379. hémangiomatose --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=hémangiomatose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  380. lipomatose épidurale --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=lipomatose épidurale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  381. migraine hémiplégique familiale --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=migraine hémiplégique familiale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  382. neurofibromatose --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neurofibromatose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  383. neurofibromatose de type périphérique --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neurofibromatose de type périphérique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  384. pseudo-méningocèle --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=pseudo-méningocèle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  385. pseudoméningocèle --- r_associated #0: 31 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=pseudoméningocèle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  386. Marfan (maladie de) --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Marfan (maladie de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  387. Syndrome d'Alagille --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Syndrome d'Alagille | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  388. Syndrome de Budd-Chiari --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Syndrome de Budd-Chiari | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  389. Syndrome de Gorlin --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Syndrome de Gorlin | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  390. en:Budd Chiari's disease (or syndrome) --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Budd Chiari's disease (or syndrome) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  391. en:Feingold syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Feingold syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  392. en:acromicric dysplasia --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:acromicric dysplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  393. en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  394. en:ameloonychohypohidrotic syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ameloonychohypohidrotic syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  395. en:arthrogryposis, distal, type 1 --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:arthrogryposis, distal, type 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  396. en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  397. en:autosomal dominant focal dystonia dyt25 type --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  398. en:autosomal dominant variant form of albumin --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant variant form of albumin | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  399. en:bilateral pheochromocytoma and islet cell adenoma of the pancreas --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  400. en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  401. en:congenital dyserythropoietic anemia, type iii --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:congenital dyserythropoietic anemia, type iii | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  402. en:falx laceration --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:falx laceration | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  403. en:familial partial lipodystrophy, type 2 --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial partial lipodystrophy, type 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  404. en:fibrodysplasia ossificans progressiva --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:fibrodysplasia ossificans progressiva | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  405. en:generalized epilepsy and paroxysmal dyskinesia syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:generalized epilepsy and paroxysmal dyskinesia syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  406. en:geniospasm 1 --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:geniospasm 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  407. en:hemorrhoid --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hemorrhoid | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  408. en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  409. en:intracranial granuloma --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:intracranial granuloma | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  410. en:isaacs syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:isaacs syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  411. en:leigh disease --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:leigh disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  412. en:microcephaly, amish type (disorder) --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microcephaly, amish type (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  413. en:mohr-tranebjaerg syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:mohr-tranebjaerg syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  414. en:ocular vascular disorder --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ocular vascular disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  415. en:perinatal falx laceration --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:perinatal falx laceration | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  416. en:periventricular heterotopia, x-linked --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:periventricular heterotopia, x-linked | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  417. en:pitt-hopkins syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:pitt-hopkins syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  418. en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  419. en:short stature with valvular heart disease and characteristic facies syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:short stature with valvular heart disease and characteristic facies syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  420. en:spinocerebellar ataxia 29 --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia 29 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  421. en:spinocerebellar ataxia type 2 --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia type 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  422. en:spinocerebellar ataxia type 37 --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia type 37 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  423. en:split-hand-foot malformation with long bone deficiency 1 --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:split-hand-foot malformation with long bone deficiency 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  424. en:treacher collins syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:treacher collins syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  425. en:tuberous sclerosis --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:tuberous sclerosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  426. en:vascular neoplasm --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular neoplasm | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  427. en:vasculitis --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vasculitis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  428. en:vitreoretinochoroidopathy (disorder) --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vitreoretinochoroidopathy (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  429. en:waisman syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:waisman syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  430. en:wellesley carman french syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:wellesley carman french syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  431. en:x-linked intellectual disability with acromegaly and hyperactivity syndrome --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  432. hémorragie sous-arachnoïdienne --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=hémorragie sous-arachnoïdienne | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  433. hémorrhoïde --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=hémorrhoïde | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  434. hémorroïde --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=hémorroïde | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  435. neurofibromatose de recklinghausen --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neurofibromatose de recklinghausen | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  436. sclérose tubéreuse du cerveau --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=sclérose tubéreuse du cerveau | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  437. syndrome d'alagille --- r_associated #0: 30 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome d'alagille | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30
  438. Recklinghausen (maladie de von) --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Recklinghausen (maladie de von) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  439. anévrisme --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=anévrisme | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  440. artériosclérose sévère juvénile de Kaitila --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=artériosclérose sévère juvénile de Kaitila | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  441. caution financière --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=caution financière | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  442. corne cutanée de la paupière --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=corne cutanée de la paupière | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  443. en:aneurysms and artery dissections --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:aneurysms and artery dissections | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  444. en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  445. en:arachnodactily --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:arachnodactily | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  446. en:autosomal dominant optic atrophy --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant optic atrophy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  447. en:autosomal dominant pterygium of conjunctiva --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant pterygium of conjunctiva | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  448. en:behrens baumann dust syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:behrens baumann dust syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  449. en:blau syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:blau syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  450. en:brain calcification rajab type --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:brain calcification rajab type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  451. en:buerger disease --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:buerger disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  452. en:carotid artery disorder --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:carotid artery disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  453. en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  454. en:colitis, ischemic --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:colitis, ischemic | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  455. en:dominant autosomal hereditary disorder, complete penetrance --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dominant autosomal hereditary disorder, complete penetrance | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  456. en:drug-induced toxic (predictable) liver disease --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:drug-induced toxic (predictable) liver disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  457. en:epidural lipomatosis --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:epidural lipomatosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  458. en:esophageal varices --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:esophageal varices | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  459. en:familial hypercalciuric hypocalcemia --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial hypercalciuric hypocalcemia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  460. en:familial isolated arrhythmogenic right ventricular dysplasia --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial isolated arrhythmogenic right ventricular dysplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  461. en:feingold syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:feingold syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  462. en:glycogen storage disease type iib --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:glycogen storage disease type iib | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  463. en:hereditary angioedema --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary angioedema | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  464. en:hereditary cerebellar atrophy --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary cerebellar atrophy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  465. en:hereditary sensory and autonomic neuropathy type 1b --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary sensory and autonomic neuropathy type 1b | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  466. en:hnsha due to triosephosphate isomerase deficiency --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hnsha due to triosephosphate isomerase deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  467. en:hyperferritinemia, hereditary, with congenital cataracts --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  468. en:hyperinsulinism due to deficiency of glucokinase --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperinsulinism due to deficiency of glucokinase | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  469. en:hyperpigmentation, familial progressive --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperpigmentation, familial progressive | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  470. en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  471. en:hyperuricemia, anemia, renal failure syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperuricemia, anemia, renal failure syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  472. en:hypomagnesemia 1, intestinal --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hypomagnesemia 1, intestinal | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  473. en:hypotension --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hypotension | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  474. en:hypotrichosis simplex of scalp --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hypotrichosis simplex of scalp | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  475. en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  476. en:jackson-weiss syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:jackson-weiss syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  477. en:li-fraumeni syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:li-fraumeni syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  478. en:masa syndrome (disorder) --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:masa syndrome (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  479. en:meningeal hemorrhage --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:meningeal hemorrhage | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  480. en:microcephalic primordial dwarfism toriello type --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microcephalic primordial dwarfism toriello type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  481. en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  482. en:neurofibromatosis type 2 --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:neurofibromatosis type 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  483. en:neuropathy, hereditary thermosensitive --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:neuropathy, hereditary thermosensitive | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  484. en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  485. en:port-wine stain in rubinstein-taybi syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:port-wine stain in rubinstein-taybi syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  486. en:primary pigmented nodular adrenocortical disease --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:primary pigmented nodular adrenocortical disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  487. en:proteus-like syndrome (disorder) --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:proteus-like syndrome (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  488. en:rud syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:rud syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  489. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:simpson golabi behmel syndrome type 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  490. en:spinocerebellar ataxia 10 --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia 10 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  491. en:spinocerebellar ataxia type 4 --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia type 4 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  492. en:spinocerebellar ataxia type 5 --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia type 5 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  493. en:vascular disorders, general and nec --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular disorders, general and nec | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  494. en:vascular hemostatic disorders --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular hemostatic disorders | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  495. en:vein disorder --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vein disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  496. en:wnt4 mullerian aplasia and ovarian dysfunction --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:wnt4 mullerian aplasia and ovarian dysfunction | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  497. en:x-linked intellectual disability with ataxia and apraxia syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  498. en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  499. microdélétion 5q35 --- r_associated #0: 29 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=microdélétion 5q35 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=29
  500. en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  501. en:ataxia with vitamin e deficiency --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ataxia with vitamin e deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  502. en:autosomal dominant analbuminemia --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant analbuminemia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  503. en:autosomal dominant deficiency of plasminogen --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant deficiency of plasminogen | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  504. en:autosomal dominant muscular dystrophy not predominantly limb girdle --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant muscular dystrophy not predominantly limb girdle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  505. en:blood vessel occlusion --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:blood vessel occlusion | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  506. en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  507. en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  508. en:cerebellar ataxia, cayman type --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebellar ataxia, cayman type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  509. en:char syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:char syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  510. en:cochleosaccular degeneration of the inner ear and progressive cataracts --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  511. en:corneal dystrophy, subepithelial mucinous --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:corneal dystrophy, subepithelial mucinous | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  512. en:currarino triad --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:currarino triad | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  513. en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  514. en:epithelial recurrent erosion dystrophy --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:epithelial recurrent erosion dystrophy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  515. en:familial hemiplegic migraine --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial hemiplegic migraine | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  516. en:familial spontaneous pneumothorax --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial spontaneous pneumothorax | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  517. en:fatal congenital nonlysosomal heart glycogenosis --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:fatal congenital nonlysosomal heart glycogenosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  518. en:hand-arm vibration syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hand-arm vibration syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  519. en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  520. en:hereditary cystatin c amyloid angiopathy --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary cystatin c amyloid angiopathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  521. en:hereditary diffuse gastric adenocarcinoma --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary diffuse gastric adenocarcinoma | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  522. en:hereditary multiple ossifying ecchondromata --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary multiple ossifying ecchondromata | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  523. en:hereditary myopathy with early respiratory failure --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary myopathy with early respiratory failure | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  524. en:hereditary optic atrophy --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary optic atrophy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  525. en:hyperinsulinism due to hnf1a deficiency --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperinsulinism due to hnf1a deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  526. en:hypoplasia of spinal vessel --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hypoplasia of spinal vessel | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  527. en:juvenile amyotrophic lateral sclerosis --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:juvenile amyotrophic lateral sclerosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  528. en:keratosis palmoplantaris papulosa --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:keratosis palmoplantaris papulosa | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  529. en:late effect of injury to peripheral blood vessel --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:late effect of injury to peripheral blood vessel | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  530. en:laurin-sandrow syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:laurin-sandrow syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  531. en:liddle syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:liddle syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  532. en:liver vascular disorder --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:liver vascular disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  533. en:manouvrier syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:manouvrier syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  534. en:may-hegglin anomaly --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:may-hegglin anomaly | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  535. en:mesomelic dwarfism reinhardt pfeiffer type --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:mesomelic dwarfism reinhardt pfeiffer type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  536. en:moloney syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:moloney syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  537. en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  538. en:pseudohypoaldosteronism, type 1, dominant form --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:pseudohypoaldosteronism, type 1, dominant form | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  539. en:schulman upshaw syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:schulman upshaw syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  540. en:short fifth metacarpal insulin resistance syndrome --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:short fifth metacarpal insulin resistance syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  541. en:spinocerebellar ataxia 31 (disorder) --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia 31 (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  542. en:spinocerebellar ataxia type 6 (disorder) --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia type 6 (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  543. en:sting-associated vasculopathy with onset in infancy --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:sting-associated vasculopathy with onset in infancy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  544. en:vascular disorders nec --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular disorders nec | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  545. en:venous and venular disorders --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:venous and venular disorders | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  546. en:waardenburg syndrome type 4 --- r_associated #0: 28 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:waardenburg syndrome type 4 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=28
  547. Lynch (syndrome de) --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Lynch (syndrome de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  548. en:Mohr-Tranebjaerg syndrome --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Mohr-Tranebjaerg syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  549. en:Pitt-Hopkins syndrome --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Pitt-Hopkins syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  550. en:advanced sleep-phase syndrome, familial --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:advanced sleep-phase syndrome, familial | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  551. en:aphalangy and syndactyly with microcephaly syndrome --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  552. en:aplasia of lacrimal and salivary glands --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:aplasia of lacrimal and salivary glands | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  553. en:arrhythmogenic right ventricular dysplasia --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:arrhythmogenic right ventricular dysplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  554. en:arteriovenous hemangioma --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:arteriovenous hemangioma | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  555. en:basal cell nævus --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:basal cell nævus | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  556. en:behavioral variant of frontotemporal dementia --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:behavioral variant of frontotemporal dementia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  557. en:benign autosomal dominant osteopetrosis --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:benign autosomal dominant osteopetrosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  558. en:brachymesophalangy 2 and 5 --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:brachymesophalangy 2 and 5 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  559. en:brown-vialetto-van laere syndrome --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:brown-vialetto-van laere syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  560. en:capillary malformation-arteriovenous malformation (disorder) --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:capillary malformation-arteriovenous malformation (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  561. en:cerebral hemorrhage with amyloidosis, hereditary, dutch type --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  562. en:charcot-marie-tooth disease, axonal, type 2b (disorder) --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  563. en:charcot-marie-tooth disease, axonal, type 2e (disorder) --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  564. en:cockayne syndrome --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cockayne syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  565. en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  566. en:halal syndrome --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:halal syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  567. en:hereditary motor and sensory neuropathy type i --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary motor and sensory neuropathy type i | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  568. en:hereditary papillary renal cell carcinoma --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary papillary renal cell carcinoma | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  569. en:hyperemia --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperemia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  570. en:hyperinsulinism due to insulin receptor deficiency --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperinsulinism due to insulin receptor deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  571. en:kallman syndrome with heart disease --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:kallman syndrome with heart disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  572. en:knobloch syndrome --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:knobloch syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  573. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  574. en:localized amyloid deposit --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:localized amyloid deposit | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  575. en:meningeal melanosis --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:meningeal melanosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  576. en:microcephaly-capillary malformation syndrome --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  577. en:myopathy, distal 2 --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:myopathy, distal 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  578. en:ohdo syndrome, maat-kievit-brunner type --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  579. en:phlebectasis --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:phlebectasis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  580. en:spinal cord vascular diseases --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinal cord vascular diseases | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  581. en:spinocerebellar ataxia 28 --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia 28 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  582. en:spinocerebellar ataxia 36 --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia 36 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  583. en:vascular thrombosis --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular thrombosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  584. en:zimmerman laband syndrome --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:zimmerman laband syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  585. métastase --- r_associated #0: 27 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=métastase | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  586. en:17q11.2 microduplication syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:17q11.2 microduplication syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  587. en:2-hydroxyglutaric aciduria --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:2-hydroxyglutaric aciduria | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  588. en:Budd's syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Budd's syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  589. en:absence of fingerprints with congenital milia syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:absence of fingerprints with congenital milia syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  590. en:allan-herndon-dudley syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:allan-herndon-dudley syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  591. en:alpha-fetoprotein, hereditary persistence of --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:alpha-fetoprotein, hereditary persistence of | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  592. en:aniridia and intellectual disability syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:aniridia and intellectual disability syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  593. en:arterial and arteriolar disorders --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:arterial and arteriolar disorders | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  594. en:arterial dissection and lentiginosis syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:arterial dissection and lentiginosis syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  595. en:atherosclerotic plaque --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:atherosclerotic plaque | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  596. en:autosomal dominant beta2-microglobulinic amyloidosis --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant beta2-microglobulinic amyloidosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  597. en:autosomal dominant charcot-marie-tooth disease type 2m --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant charcot-marie-tooth disease type 2m | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  598. en:autosomal dominant hyperinsulinism due to kir6.2 deficiency --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  599. en:autosomal dominant hyperinsulinism due to sur1 deficiency --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant hyperinsulinism due to sur1 deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  600. en:autosomal dominant ichthyosis vulgaris --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal dominant ichthyosis vulgaris | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  601. en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:autosomal recessive idiopathic familial dystonia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  602. en:bilateral multiple fibroadenoma of breast --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:bilateral multiple fibroadenoma of breast | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  603. en:braddock syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:braddock syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  604. en:capillary leak syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:capillary leak syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  605. en:cataract glaucoma syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:cataract glaucoma syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  606. en:charcot-marie-tooth disease, axonal, type 2l (disorder) --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  607. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  608. en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:chromosome 17q21.31 deletion syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  609. en:chromosome 3q29 deletion syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:chromosome 3q29 deletion syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  610. en:disease of capillaries --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:disease of capillaries | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  611. en:dmd-associated dilated cardiomyopathy --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dmd-associated dilated cardiomyopathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  612. en:dominant beta-thalassemia --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dominant beta-thalassemia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  613. en:dysplasia, saddan --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dysplasia, saddan | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  614. en:dystonia 12 --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dystonia 12 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  615. en:dystrophia myotonica 2 --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:dystrophia myotonica 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  616. en:embolism and thrombosis --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:embolism and thrombosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  617. en:familial digital arthropathy and brachydactyly syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial digital arthropathy and brachydactyly syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  618. en:familial encephalopathy with neuroserpin inclusion bodies --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial encephalopathy with neuroserpin inclusion bodies | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  619. en:familial osteochondritis dissecans --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:familial osteochondritis dissecans | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  620. en:folinic acid responsive seizure syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:folinic acid responsive seizure syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  621. en:frontotemporal dementia, chromosome 3-linked --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:frontotemporal dementia, chromosome 3-linked | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  622. en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  623. en:hereditary motor and sensory neuropathy type I --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary motor and sensory neuropathy type I | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  624. en:hereditary systemic amyloidosis --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hereditary systemic amyloidosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  625. en:hyperinsulinism due to hnf4a deficiency --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperinsulinism due to hnf4a deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  626. en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  627. en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  628. en:macdermot winter syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:macdermot winter syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  629. en:maternally inherited mitochondrial dystonia --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:maternally inherited mitochondrial dystonia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  630. en:metaphyseal dysplasia, braun-tinschert type --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:metaphyseal dysplasia, braun-tinschert type | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  631. en:moyamoya disease with early onset achalasia --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:moyamoya disease with early onset achalasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  632. en:multiple endocrine neoplasia type 2b --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:multiple endocrine neoplasia type 2b | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  633. en:multiple epiphyseal dysplasia type 5 --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:multiple epiphyseal dysplasia type 5 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  634. en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  635. en:neurofibromatosis, type 1-like syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:neurofibromatosis, type 1-like syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  636. en:optic neuropathy, ischemic --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:optic neuropathy, ischemic | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  637. en:peripheral resistance to thyroid hormone --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:peripheral resistance to thyroid hormone | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  638. en:pituitary adenoma, familial isolated (disorder) --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:pituitary adenoma, familial isolated (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  639. en:pituitary thyroid hormone resistance --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:pituitary thyroid hormone resistance | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  640. en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  641. en:radial hypoplasia, triphalangeal thumbs and hypospadias --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:radial hypoplasia, triphalangeal thumbs and hypospadias | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  642. en:reis-bucklers' corneal dystrophy --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:reis-bucklers' corneal dystrophy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  643. en:schindler disease, type i --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:schindler disease, type i | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  644. en:shprintzen omphalocele syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:shprintzen omphalocele syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  645. en:spinocerebellar ataxia 8 --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia 8 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  646. en:spinocerebellar ataxia type 32 --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia type 32 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  647. en:spinocerebellar ataxia type 7 --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinocerebellar ataxia type 7 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  648. en:subpial siderosis --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:subpial siderosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  649. en:syndromic orbital border hypoplasia --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:syndromic orbital border hypoplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  650. en:timothy syndrome type 2 --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:timothy syndrome type 2 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  651. en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  652. en:type a 14 --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:type a 14 | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  653. en:ulna metaphyseal dysplasia syndrome --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:ulna metaphyseal dysplasia syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  654. en:vascular insufficiency --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular insufficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  655. goniodysgénésie-retard mental-petite taille (syndrome) --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=goniodysgénésie-retard mental-petite taille (syndrome) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  656. plaque d'athérosclérose --- r_associated #0: 26 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=plaque d'athérosclérose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26
  657. en:Budd-Chiari's disease --- r_associated #0: 25 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Budd-Chiari's disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=25
  658. en:marfan's syndrome --- r_associated #0: 25 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:marfan's syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=25
  659. en:prehypertension --- r_associated #0: 25 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:prehypertension | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=25
  660. en:secondary neoplasm --- r_associated #0: 25 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:secondary neoplasm | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=25
  661. en:vascular fistula --- r_associated #0: 25 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular fistula | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=25
  662. sclérodermie tubéreuse de bourneville --- r_associated #0: 25 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=sclérodermie tubéreuse de bourneville | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=25
  663. syndrome de gorlin --- r_associated #0: 25 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de gorlin | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=25
  664. IPCV --- r_associated #0: 24 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=IPCV | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=24
  665. en:Alagille's syndrome --- r_associated #0: 24 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Alagille's syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=24
  666. en:decreased and nonspecific blood pressure disorders and shock --- r_associated #0: 24 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:decreased and nonspecific blood pressure disorders and shock | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=24
  667. en:hypertension --- r_associated #0: 24 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hypertension | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=24
  668. en:pathologic arteriovenous shunt --- r_associated #0: 24 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:pathologic arteriovenous shunt | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=24
  669. en:retrolental fibroplasia --- r_associated #0: 24 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:retrolental fibroplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=24
  670. en:veno-occlusive disease --- r_associated #0: 24 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:veno-occlusive disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=24
  671. en:aorta disease --- r_associated #0: 23 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:aorta disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=23
  672. en:hepatic veno-occlusive disease --- r_associated #0: 23 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hepatic veno-occlusive disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=23
  673. en:reperfusion injury --- r_associated #0: 23 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:reperfusion injury | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=23
  674. en:scimitar syndrome --- r_associated #0: 23 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:scimitar syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=23
  675. en:stricture of artery --- r_associated #0: 23 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:stricture of artery | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=23
  676. en:Bessel-Hagen's disease --- r_associated #0: 22 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Bessel-Hagen's disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=22
  677. en:Gorlin syndrome --- r_associated #0: 22 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Gorlin syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=22
  678. en:angiodysplasia --- r_associated #0: 22 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:angiodysplasia | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=22
  679. en:disorders of meninges, nec in mdr --- r_associated #0: 22 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:disorders of meninges, nec in mdr | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=22
  680. en:spinal vascular disorder --- r_associated #0: 22 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spinal vascular disorder | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=22
  681. en:splenic infarction --- r_associated #0: 22 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:splenic infarction | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=22
  682. en:vascular system injuries --- r_associated #0: 22 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vascular system injuries | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=22
  683. en:vasoplegy --- r_associated #0: 22 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:vasoplegy | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=22
  684. abcès épidural --- r_associated #0: 21 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=abcès épidural | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=21
  685. tylose --- r_associated #0: 21 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=tylose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=21
  686. varicosité --- r_associated #0: 21 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=varicosité | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=21
  687. syndrome de Warburg --- r_associated #0: 16 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Warburg | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=16
  688. Giessen (test de) --- r_associated #0: 15 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Giessen (test de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=15
  689. Hémorroïde --- r_associated #0: 15 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Hémorroïde | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=15
  690. Maladie de Marfan --- r_associated #0: 15 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Maladie de Marfan | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=15
  691. Syndrome de Lynch --- r_associated #0: 15 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Syndrome de Lynch | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=15
  692. Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Syndrome de Walker-Warburg | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=15
  693. Varicocèle --- r_associated #0: 15 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Varicocèle | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=15
  694. démence (sémiologie) --- r_associated #0: 15 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=démence (sémiologie) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=15
  695. en:tylose --- r_associated #0: 15 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:tylose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=15
  696. fibromyalgie (critères de l' American College of Rheumatology ) --- r_associated #0: 15 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyalgie (critères de l' American College of Rheumatology ) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=15
  697. insomnie familiale fatale --- r_associated #0: 11 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=insomnie familiale fatale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=11
  698. Artériosclérose --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Artériosclérose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  699. Bessel-Hagen (maladie de) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Bessel-Hagen (maladie de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  700. Budd-Chiari (syndrome de) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Budd-Chiari (syndrome de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  701. Embolisme --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Embolisme | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  702. Gorlin (syndrome de) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Gorlin (syndrome de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  703. Hémorragie méningée --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Hémorragie méningée | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  704. Insler et Bernstein (score cervical d') --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Insler et Bernstein (score cervical d') | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  705. MIGP (orientation) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=MIGP (orientation) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  706. Neurofibromatose --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Neurofibromatose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  707. Syndrome de Sotos --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Syndrome de Sotos | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  708. Teissier (spatule de) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Teissier (spatule de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  709. Tylosis --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Tylosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  710. Varice --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Varice | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  711. Varicosité --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Varicosité | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  712. Vasoconstriction --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Vasoconstriction | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  713. Vasodilatation --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Vasodilatation | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  714. absence d'empreintes digitales avec syndrome de milia congénital --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=absence d'empreintes digitales avec syndrome de milia congénital | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  715. angl. HNPCC --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=angl. HNPCC | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  716. collapsus (rein de) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=collapsus (rein de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  717. en:5q microdeletion --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:5q microdeletion | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  718. en:LEOPARD syndrome --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:LEOPARD syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  719. en:Recklinghausen's disease --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Recklinghausen's disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  720. en:Sotos's syndrome --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:Sotos's syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  721. en:angiophakomatosis --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:angiophakomatosis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  722. en:effluent --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:effluent | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  723. en:meningo-encephalocele. --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:meningo-encephalocele. | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  724. en:spider vein --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:spider vein | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  725. en:subarachnoid haemorrhage --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:subarachnoid haemorrhage | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  726. en:subarachnoide haemorrhage --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:subarachnoide haemorrhage | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  727. en:type I --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:type I | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  728. en:type VI --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:type VI | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  729. en:varix --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:varix | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  730. en:venoocclusive disease --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:venoocclusive disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  731. en:von recklinghausen's disease --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:von recklinghausen's disease | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  732. exostose du conduit auditif externe --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=exostose du conduit auditif externe | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  733. exostose ostéocartilagineuse --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=exostose ostéocartilagineuse | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  734. exostose sous-unguéale --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=exostose sous-unguéale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  735. exostosectomie --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=exostosectomie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  736. goniome --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=goniome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  737. goniomètre --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=goniomètre | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  738. gonion --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonion | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  739. gonioscopie --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonioscopie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  740. goniosynéchies --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=goniosynéchies | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  741. goniotomie endoscopique --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=goniotomie endoscopique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  742. gonochorisme --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonochorisme | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  743. gonococcie --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonococcie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  744. gonocoque --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonocoque | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  745. gonocyte --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonocyte | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  746. gonocytome --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonocytome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  747. gonométrie --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonométrie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  748. gonorrhée --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonorrhée | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  749. gonosome --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonosome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  750. gonosomique --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=gonosomique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  751. hypotension --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=hypotension | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  752. nantissement --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=nantissement | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  753. neuropathie sensitivomotrice héréditaire forme I --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=neuropathie sensitivomotrice héréditaire forme I | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  754. paraplégie spastique dans la syphilis congénitale --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=paraplégie spastique dans la syphilis congénitale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  755. reclassement professionnel --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=reclassement professionnel | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  756. souche de référence --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=souche de référence | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  757. souche transduite --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=souche transduite | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  758. syndrome de Feingold --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Feingold | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  759. syndrome de Mohr-Tranebjaerg --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Mohr-Tranebjaerg | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  760. syndrome de Pitt-Hopkins --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de Pitt-Hopkins | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  761. syndrome de warburg --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=syndrome de warburg | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  762. ty (élément) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=ty (élément) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  763. varices digestives (sclérothérapie des) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=varices digestives (sclérothérapie des) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  764. vascularite --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vascularite | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  765. vasculopathie choroïdienne polypoïdale idiopathique --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vasculopathie choroïdienne polypoïdale idiopathique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  766. vasculorénal (syndrome) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vasculorénal (syndrome) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  767. vaseline --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vaseline | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  768. vaseline salicylée --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vaseline salicylée | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  769. vaselinome --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vaselinome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  770. vaso-inhibiteur --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vaso-inhibiteur | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  771. vaso-vasostomie --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vaso-vasostomie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  772. vaso-vésiculectomie --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vaso-vésiculectomie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  773. vaso-épididymostomie --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vaso-épididymostomie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  774. vasodilatateur (traitement) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vasodilatateur (traitement) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  775. vasogénique (choc) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=vasogénique (choc) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  776. von Recklinghausen (maladie de) --- r_associated #0: 10 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=von Recklinghausen (maladie de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=10
  777. fibroplasie rétrocristallinienne --- r_associated #0: 6 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibroplasie rétrocristallinienne | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=6
  778. Alagille (syndrome d') --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Alagille (syndrome d') | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  779. Angiomatose --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Angiomatose | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  780. Hypertension portale --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Hypertension portale | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  781. Stokvis-Talma (syndrome de) --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Stokvis-Talma (syndrome de) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  782. Télangiectasie --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=Télangiectasie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  783. démence d'Alzheimer --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=démence d'Alzheimer | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  784. en:metastasis --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:metastasis | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  785. fibromyalgie associée --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyalgie associée | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  786. fibromyalgie primitive --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyalgie primitive | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  787. fibromyalgie secondaire --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyalgie secondaire | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  788. fibromyoadénome prostatique --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyoadénome prostatique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  789. fibromyome --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  790. fibromyome utérin --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyome utérin | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  791. fibromyopathie ossifiante neurogène --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyopathie ossifiante neurogène | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  792. fibromyosite --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyosite | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  793. fibromyxome trichogénique --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibromyxome trichogénique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  794. fibronectine --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibronectine | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  795. fibroplasie --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibroplasie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  796. fibroplastique --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibroplastique | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  797. fibrosarcome --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibrosarcome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  798. fibrosarcome cutané --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibrosarcome cutané | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  799. fibrosarcome de l'utérus --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibrosarcome de l'utérus | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  800. fibrosarcome du sein --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibrosarcome du sein | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  801. fibrosarcome du système musculosquelettique extraosseux --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=fibrosarcome du système musculosquelettique extraosseux | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  802. ipcv --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=ipcv | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  803. lynestrénol --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=lynestrénol | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  804. lyo-enzyme --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=lyo-enzyme | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  805. lyoglycogène --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=lyoglycogène | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  806. maladie veino-occlusive --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie veino-occlusive | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  807. maladie veino-occlusive foie --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=maladie veino-occlusive foie | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  808. nævique irien (syndrome) --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=nævique irien (syndrome) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=5
  809. varicocèle (cure chirurgicale) --- r_associated #0: 5 --> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=varicocèle (cure chirurgicale) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | 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