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'méningé (syndrome)'
(id=16870823 ; fe=méningé (syndrome) ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=49075 creation date=2021-07-25 touchdate=2026-04-23 22:14:01.000)
≈ 5964 relations sortantes

  1. méningé (syndrome) -- r_associated #0: 83 / 1 -> chirurgie
    n1=méningé (syndrome) | n2=chirurgie | rel=r_associated | relid=0 | w=83
  2. méningé (syndrome) -- r_associated #0: 68 / 0.819 -> méningé
    n1=méningé (syndrome) | n2=méningé | rel=r_associated | relid=0 | w=68
  3. méningé (syndrome) -- r_associated #0: 57 / 0.687 -> syndrome
    n1=méningé (syndrome) | n2=syndrome | rel=r_associated | relid=0 | w=57
  4. méningé (syndrome) -- r_associated #0: 47 / 0.566 -> méninge
    n1=méningé (syndrome) | n2=méninge | rel=r_associated | relid=0 | w=47
  5. méningé (syndrome) -- r_associated #0: 46 / 0.554 -> médecine
    n1=méningé (syndrome) | n2=médecine | rel=r_associated | relid=0 | w=46
  6. méningé (syndrome) -- r_associated #0: 45 / 0.542 -> méningite
    n1=méningé (syndrome) | n2=méningite | rel=r_associated | relid=0 | w=45
  7. méningé (syndrome) -- r_associated #0: 42 / 0.506 -> en:meningeal syndrome
    n1=méningé (syndrome) | n2=en:meningeal syndrome | rel=r_associated | relid=0 | w=42
  8. méningé (syndrome) -- r_associated #0: 42 / 0.506 -> spécialités médicales
    n1=méningé (syndrome) | n2=spécialités médicales | rel=r_associated | relid=0 | w=42
  9. méningé (syndrome) -- r_associated #0: 40 / 0.482 -> Brudzi?ski (signe de)
    n1=méningé (syndrome) | n2=Brudzi?ski (signe de) | rel=r_associated | relid=0 | w=40
  10. méningé (syndrome) -- r_associated #0: 40 / 0.482 -> en:meninges
    n1=méningé (syndrome) | n2=en:meninges | rel=r_associated | relid=0 | w=40
  11. méningé (syndrome) -- r_associated #0: 40 / 0.482 -> maladies
    n1=méningé (syndrome) | n2=maladies | rel=r_associated | relid=0 | w=40
  12. méningé (syndrome) -- r_associated #0: 40 / 0.482 -> médecine spécialisée
    n1=méningé (syndrome) | n2=médecine spécialisée | rel=r_associated | relid=0 | w=40
  13. méningé (syndrome) -- r_associated #0: 39 / 0.47 -> anatomie
    n1=méningé (syndrome) | n2=anatomie | rel=r_associated | relid=0 | w=39
  14. méningé (syndrome) -- r_associated #0: 39 / 0.47 -> cancer
    n1=méningé (syndrome) | n2=cancer | rel=r_associated | relid=0 | w=39
  15. méningé (syndrome) -- r_associated #0: 39 / 0.47 -> cancérologie
    n1=méningé (syndrome) | n2=cancérologie | rel=r_associated | relid=0 | w=39
  16. méningé (syndrome) -- r_associated #0: 39 / 0.47 -> tumeurs
    n1=méningé (syndrome) | n2=tumeurs | rel=r_associated | relid=0 | w=39
  17. méningé (syndrome) -- r_associated #0: 37 / 0.446 -> carcinologie
    n1=méningé (syndrome) | n2=carcinologie | rel=r_associated | relid=0 | w=37
  18. méningé (syndrome) -- r_associated #0: 37 / 0.446 -> en:angiomatous meningioma
    n1=méningé (syndrome) | n2=en:angiomatous meningioma | rel=r_associated | relid=0 | w=37
  19. méningé (syndrome) -- r_associated #0: 37 / 0.446 -> oncologie
    n1=méningé (syndrome) | n2=oncologie | rel=r_associated | relid=0 | w=37
  20. méningé (syndrome) -- r_associated #0: 36 / 0.434 -> méningiome
    n1=méningé (syndrome) | n2=méningiome | rel=r_associated | relid=0 | w=36
  21. méningé (syndrome) -- r_associated #0: 35 / 0.422 -> Kernig (signe de)
    n1=méningé (syndrome) | n2=Kernig (signe de) | rel=r_associated | relid=0 | w=35
  22. méningé (syndrome) -- r_associated #0: 35 / 0.422 -> méninge arachnoïdienne
    n1=méningé (syndrome) | n2=méninge arachnoïdienne | rel=r_associated | relid=0 | w=35
  23. méningé (syndrome) -- r_associated #0: 35 / 0.422 -> méningite cérébrospinale épidémique
    n1=méningé (syndrome) | n2=méningite cérébrospinale épidémique | rel=r_associated | relid=0 | w=35
  24. méningé (syndrome) -- r_associated #0: 34 / 0.41 -> méninges
    n1=méningé (syndrome) | n2=méninges | rel=r_associated | relid=0 | w=34
  25. méningé (syndrome) -- r_associated #0: 32 / 0.386 -> en:meningioma
    n1=méningé (syndrome) | n2=en:meningioma | rel=r_associated | relid=0 | w=32
  26. méningé (syndrome) -- r_associated #0: 32 / 0.386 -> méningiomes
    n1=méningé (syndrome) | n2=méningiomes | rel=r_associated | relid=0 | w=32
  27. méningé (syndrome) -- r_associated #0: 32 / 0.386 -> processus pathologique
    n1=méningé (syndrome) | n2=processus pathologique | rel=r_associated | relid=0 | w=32
  28. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> cerveau
    n1=méningé (syndrome) | n2=cerveau | rel=r_associated | relid=0 | w=30
  29. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:'globoid multinucleated cells' in brain tissue
    n1=méningé (syndrome) | n2=en:'globoid multinucleated cells' in brain tissue | rel=r_associated | relid=0 | w=30
  30. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:3-4 hz slow sharp waves seen on eeg
    n1=méningé (syndrome) | n2=en:3-4 hz slow sharp waves seen on eeg | rel=r_associated | relid=0 | w=30
  31. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:abnormal corticospinal tract decussation
    n1=méningé (syndrome) | n2=en:abnormal corticospinal tract decussation | rel=r_associated | relid=0 | w=30
  32. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:abnormal gyri (in 1 of 2 patients)
    n1=méningé (syndrome) | n2=en:abnormal gyri (in 1 of 2 patients) | rel=r_associated | relid=0 | w=30
  33. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:abnormal involuntary movement
    n1=méningé (syndrome) | n2=en:abnormal involuntary movement | rel=r_associated | relid=0 | w=30
  34. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:abnormal ocular motility
    n1=méningé (syndrome) | n2=en:abnormal ocular motility | rel=r_associated | relid=0 | w=30
  35. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:abnormal septum pellucidum
    n1=méningé (syndrome) | n2=en:abnormal septum pellucidum | rel=r_associated | relid=0 | w=30
  36. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:abnormal t2-weighted signals in the occipital white and gray matter
    n1=méningé (syndrome) | n2=en:abnormal t2-weighted signals in the occipital white and gray matter | rel=r_associated | relid=0 | w=30
  37. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:abnormality of brainstem morphology
    n1=méningé (syndrome) | n2=en:abnormality of brainstem morphology | rel=r_associated | relid=0 | w=30
  38. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:absence of balloon cells (in type iia)
    n1=méningé (syndrome) | n2=en:absence of balloon cells (in type iia) | rel=r_associated | relid=0 | w=30
  39. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:absence of septum pellucidum
    n1=méningé (syndrome) | n2=en:absence of septum pellucidum | rel=r_associated | relid=0 | w=30
  40. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:absence of transverse pontine fibers
    n1=méningé (syndrome) | n2=en:absence of transverse pontine fibers | rel=r_associated | relid=0 | w=30
  41. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:absence seizures (in some)
    n1=méningé (syndrome) | n2=en:absence seizures (in some) | rel=r_associated | relid=0 | w=30
  42. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:absent cisterna magna
    n1=méningé (syndrome) | n2=en:absent cisterna magna | rel=r_associated | relid=0 | w=30
  43. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:absent pituitary
    n1=méningé (syndrome) | n2=en:absent pituitary | rel=r_associated | relid=0 | w=30
  44. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:acute encephalopathy
    n1=méningé (syndrome) | n2=en:acute encephalopathy | rel=r_associated | relid=0 | w=30
  45. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:agyria (wws)
    n1=méningé (syndrome) | n2=en:agyria (wws) | rel=r_associated | relid=0 | w=30
  46. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:alzheimer's disease
    n1=méningé (syndrome) | n2=en:alzheimer's disease | rel=r_associated | relid=0 | w=30
  47. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:angiographically 'silent'
    n1=méningé (syndrome) | n2=en:angiographically 'silent' | rel=r_associated | relid=0 | w=30
  48. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:anosmia (1 patient)
    n1=méningé (syndrome) | n2=en:anosmia (1 patient) | rel=r_associated | relid=0 | w=30
  49. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:antenatal intracerebral hemorrhage
    n1=méningé (syndrome) | n2=en:antenatal intracerebral hemorrhage | rel=r_associated | relid=0 | w=30
  50. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:aplasia/hypoplasia of the corpus callosum
    n1=méningé (syndrome) | n2=en:aplasia/hypoplasia of the corpus callosum | rel=r_associated | relid=0 | w=30
  51. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:arachnoid cysts (1 patient)
    n1=méningé (syndrome) | n2=en:arachnoid cysts (1 patient) | rel=r_associated | relid=0 | w=30
  52. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:arachnoid cysts of the cerebellopontine angle (reported in 1 family)
    n1=méningé (syndrome) | n2=en:arachnoid cysts of the cerebellopontine angle (reported in 1 family) | rel=r_associated | relid=0 | w=30
  53. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:areflexia
    n1=méningé (syndrome) | n2=en:areflexia | rel=r_associated | relid=0 | w=30
  54. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:arnold-chiari malformation
    n1=méningé (syndrome) | n2=en:arnold-chiari malformation | rel=r_associated | relid=0 | w=30
  55. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:asymmetry at onset (74%)
    n1=méningé (syndrome) | n2=en:asymmetry at onset (74%) | rel=r_associated | relid=0 | w=30
  56. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ataxia, mild
    n1=méningé (syndrome) | n2=en:ataxia, mild | rel=r_associated | relid=0 | w=30
  57. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ataxias, truncal
    n1=méningé (syndrome) | n2=en:ataxias, truncal | rel=r_associated | relid=0 | w=30
  58. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ataxic gait (in some patients)
    n1=méningé (syndrome) | n2=en:ataxic gait (in some patients) | rel=r_associated | relid=0 | w=30
  59. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:atrophy of pyramids
    n1=méningé (syndrome) | n2=en:atrophy of pyramids | rel=r_associated | relid=0 | w=30
  60. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:atypical absence, atonic/tonic, or tonic-clonic seizures
    n1=méningé (syndrome) | n2=en:atypical absence, atonic/tonic, or tonic-clonic seizures | rel=r_associated | relid=0 | w=30
  61. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:auditory auras
    n1=méningé (syndrome) | n2=en:auditory auras | rel=r_associated | relid=0 | w=30
  62. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:aura may occur
    n1=méningé (syndrome) | n2=en:aura may occur | rel=r_associated | relid=0 | w=30
  63. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:autonomic dysfunction (in patients with hsan2d)
    n1=méningé (syndrome) | n2=en:autonomic dysfunction (in patients with hsan2d) | rel=r_associated | relid=0 | w=30
  64. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:autonomic dysregulation
    n1=méningé (syndrome) | n2=en:autonomic dysregulation | rel=r_associated | relid=0 | w=30
  65. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:axonal loss and gliosis in the corticospinal tracts
    n1=méningé (syndrome) | n2=en:axonal loss and gliosis in the corticospinal tracts | rel=r_associated | relid=0 | w=30
  66. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:axonal spheroids
    n1=méningé (syndrome) | n2=en:axonal spheroids | rel=r_associated | relid=0 | w=30
  67. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:back pain
    n1=méningé (syndrome) | n2=en:back pain | rel=r_associated | relid=0 | w=30
  68. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:blood supply aspects
    n1=méningé (syndrome) | n2=en:blood supply aspects | rel=r_associated | relid=0 | w=30
  69. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:borderline intelligence
    n1=méningé (syndrome) | n2=en:borderline intelligence | rel=r_associated | relid=0 | w=30
  70. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:brain circuit
    n1=méningé (syndrome) | n2=en:brain circuit | rel=r_associated | relid=0 | w=30
  71. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:brain edema
    n1=méningé (syndrome) | n2=en:brain edema | rel=r_associated | relid=0 | w=30
  72. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:brain mri shows arrest in myelination
    n1=méningé (syndrome) | n2=en:brain mri shows arrest in myelination | rel=r_associated | relid=0 | w=30
  73. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:brain stem atrophy
    n1=méningé (syndrome) | n2=en:brain stem atrophy | rel=r_associated | relid=0 | w=30
  74. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:brief involuntary movements of upper extremities
    n1=méningé (syndrome) | n2=en:brief involuntary movements of upper extremities | rel=r_associated | relid=0 | w=30
  75. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:brisk reflexes
    n1=méningé (syndrome) | n2=en:brisk reflexes | rel=r_associated | relid=0 | w=30
  76. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:bulbar and upper limb symptoms more severe than lower limb symptoms
    n1=méningé (syndrome) | n2=en:bulbar and upper limb symptoms more severe than lower limb symptoms | rel=r_associated | relid=0 | w=30
  77. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:burning or tingling of plantar surface of foot (in some patients)
    n1=méningé (syndrome) | n2=en:burning or tingling of plantar surface of foot (in some patients) | rel=r_associated | relid=0 | w=30
  78. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:calcification in the pons and cerebellum
    n1=méningé (syndrome) | n2=en:calcification in the pons and cerebellum | rel=r_associated | relid=0 | w=30
  79. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:calcification of the falx
    n1=méningé (syndrome) | n2=en:calcification of the falx | rel=r_associated | relid=0 | w=30
  80. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cataplexy often triggered by strong emotions
    n1=méningé (syndrome) | n2=en:cataplexy often triggered by strong emotions | rel=r_associated | relid=0 | w=30
  81. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:caudate atrophy
    n1=méningé (syndrome) | n2=en:caudate atrophy | rel=r_associated | relid=0 | w=30
  82. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:central nervous system demyelination
    n1=méningé (syndrome) | n2=en:central nervous system demyelination | rel=r_associated | relid=0 | w=30
  83. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cerebellar ataxia (in 1 of 3 families)
    n1=méningé (syndrome) | n2=en:cerebellar ataxia (in 1 of 3 families) | rel=r_associated | relid=0 | w=30
  84. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cerebellar ataxia, mild, late-onset
    n1=méningé (syndrome) | n2=en:cerebellar ataxia, mild, late-onset | rel=r_associated | relid=0 | w=30
  85. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cerebellar atrophy (1 patient)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy (1 patient) | rel=r_associated | relid=0 | w=30
  86. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cerebellar atrophy, progressive (1 patient)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, progressive (1 patient) | rel=r_associated | relid=0 | w=30
  87. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cerebellar hypoplasia (male)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (male) | rel=r_associated | relid=0 | w=30
  88. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cerebellar medulloblastoma (rare)
    n1=méningé (syndrome) | n2=en:cerebellar medulloblastoma (rare) | rel=r_associated | relid=0 | w=30
  89. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cerebellar vermis atrophy
    n1=méningé (syndrome) | n2=en:cerebellar vermis atrophy | rel=r_associated | relid=0 | w=30
  90. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:chiari i malformation on mri (some)
    n1=méningé (syndrome) | n2=en:chiari i malformation on mri (some) | rel=r_associated | relid=0 | w=30
  91. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:childhood grade i meningioma
    n1=méningé (syndrome) | n2=en:childhood grade i meningioma | rel=r_associated | relid=0 | w=30
  92. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:choreoathetosis (2 patients)
    n1=méningé (syndrome) | n2=en:choreoathetosis (2 patients) | rel=r_associated | relid=0 | w=30
  93. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:clonus
    n1=méningé (syndrome) | n2=en:clonus | rel=r_associated | relid=0 | w=30
  94. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:clumsiness (82%)
    n1=méningé (syndrome) | n2=en:clumsiness (82%) | rel=r_associated | relid=0 | w=30
  95. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cobblestone lissencephaly (1 patient)
    n1=méningé (syndrome) | n2=en:cobblestone lissencephaly (1 patient) | rel=r_associated | relid=0 | w=30
  96. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cobblestone lissencephaly, type ii
    n1=méningé (syndrome) | n2=en:cobblestone lissencephaly, type ii | rel=r_associated | relid=0 | w=30
  97. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cobblestone lissencephaly, type ii (wws)
    n1=méningé (syndrome) | n2=en:cobblestone lissencephaly, type ii (wws) | rel=r_associated | relid=0 | w=30
  98. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:complex motor behavior such as sleep walking
    n1=méningé (syndrome) | n2=en:complex motor behavior such as sleep walking | rel=r_associated | relid=0 | w=30
  99. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:congenital anomaly of brain
    n1=méningé (syndrome) | n2=en:congenital anomaly of brain | rel=r_associated | relid=0 | w=30
  100. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:congenital hypotonia, axial or generalized
    n1=méningé (syndrome) | n2=en:congenital hypotonia, axial or generalized | rel=r_associated | relid=0 | w=30
  101. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cortical dysplasia, focal (1 patient)
    n1=méningé (syndrome) | n2=en:cortical dysplasia, focal (1 patient) | rel=r_associated | relid=0 | w=30
  102. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cranial nerve palsy
    n1=méningé (syndrome) | n2=en:cranial nerve palsy | rel=r_associated | relid=0 | w=30
  103. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cystic cavitation of the white matter
    n1=méningé (syndrome) | n2=en:cystic cavitation of the white matter | rel=r_associated | relid=0 | w=30
  104. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:cysts tend to enlarge with age
    n1=méningé (syndrome) | n2=en:cysts tend to enlarge with age | rel=r_associated | relid=0 | w=30
  105. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:dandy-walker malformation
    n1=méningé (syndrome) | n2=en:dandy-walker malformation | rel=r_associated | relid=0 | w=30
  106. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:decreased core body temperature
    n1=méningé (syndrome) | n2=en:decreased core body temperature | rel=r_associated | relid=0 | w=30
  107. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:decreased myelination seen on mri
    n1=méningé (syndrome) | n2=en:decreased myelination seen on mri | rel=r_associated | relid=0 | w=30
  108. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:decreased pyramidal cells
    n1=méningé (syndrome) | n2=en:decreased pyramidal cells | rel=r_associated | relid=0 | w=30
  109. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:deficit in basic reading
    n1=méningé (syndrome) | n2=en:deficit in basic reading | rel=r_associated | relid=0 | w=30
  110. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:delayed myelinization (in some patients)
    n1=méningé (syndrome) | n2=en:delayed myelinization (in some patients) | rel=r_associated | relid=0 | w=30
  111. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:delayed psychomotor development, variable
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, variable | rel=r_associated | relid=0 | w=30
  112. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:delayed speech development, severe
    n1=méningé (syndrome) | n2=en:delayed speech development, severe | rel=r_associated | relid=0 | w=30
  113. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:dementia of frontal lobe type
    n1=méningé (syndrome) | n2=en:dementia of frontal lobe type | rel=r_associated | relid=0 | w=30
  114. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:depression
    n1=méningé (syndrome) | n2=en:depression | rel=r_associated | relid=0 | w=30
  115. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:development varies from normal to retarded
    n1=méningé (syndrome) | n2=en:development varies from normal to retarded | rel=r_associated | relid=0 | w=30
  116. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:developmental delay (1 patient)
    n1=méningé (syndrome) | n2=en:developmental delay (1 patient) | rel=r_associated | relid=0 | w=30
  117. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:developmental delay (100%)
    n1=méningé (syndrome) | n2=en:developmental delay (100%) | rel=r_associated | relid=0 | w=30
  118. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:developmental delay, mild
    n1=méningé (syndrome) | n2=en:developmental delay, mild | rel=r_associated | relid=0 | w=30
  119. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:difficulties with fine motor skills and coordination
    n1=méningé (syndrome) | n2=en:difficulties with fine motor skills and coordination | rel=r_associated | relid=0 | w=30
  120. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:difficulty standing
    n1=méningé (syndrome) | n2=en:difficulty standing | rel=r_associated | relid=0 | w=30
  121. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:difficulty writing
    n1=méningé (syndrome) | n2=en:difficulty writing | rel=r_associated | relid=0 | w=30
  122. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:disdiadochokinesia
    n1=méningé (syndrome) | n2=en:disdiadochokinesia | rel=r_associated | relid=0 | w=30
  123. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:disorganized eeg
    n1=méningé (syndrome) | n2=en:disorganized eeg | rel=r_associated | relid=0 | w=30
  124. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:disturbance of consciousness
    n1=méningé (syndrome) | n2=en:disturbance of consciousness | rel=r_associated | relid=0 | w=30
  125. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:disturbed gait
    n1=méningé (syndrome) | n2=en:disturbed gait | rel=r_associated | relid=0 | w=30
  126. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:diurnal fluctuations of symptoms (in a subset of patients)
    n1=méningé (syndrome) | n2=en:diurnal fluctuations of symptoms (in a subset of patients) | rel=r_associated | relid=0 | w=30
  127. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:drooling
    n1=méningé (syndrome) | n2=en:drooling | rel=r_associated | relid=0 | w=30
  128. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:dysarthria
    n1=méningé (syndrome) | n2=en:dysarthria | rel=r_associated | relid=0 | w=30
  129. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:dysdiadochokinesis (63%)
    n1=méningé (syndrome) | n2=en:dysdiadochokinesis (63%) | rel=r_associated | relid=0 | w=30
  130. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:dysgenesis of the anterior commissure (in some)
    n1=méningé (syndrome) | n2=en:dysgenesis of the anterior commissure (in some) | rel=r_associated | relid=0 | w=30
  131. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:dyskinesia
    n1=méningé (syndrome) | n2=en:dyskinesia | rel=r_associated | relid=0 | w=30
  132. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:dysmetria (1 patient)
    n1=méningé (syndrome) | n2=en:dysmetria (1 patient) | rel=r_associated | relid=0 | w=30
  133. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:dysplastic c-shaped inferior olivary nuclei
    n1=méningé (syndrome) | n2=en:dysplastic c-shaped inferior olivary nuclei | rel=r_associated | relid=0 | w=30
  134. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:dystonic writer's cramp
    n1=méningé (syndrome) | n2=en:dystonic writer's cramp | rel=r_associated | relid=0 | w=30
  135. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:earlier sleep-offset time (earlier awakening)
    n1=méningé (syndrome) | n2=en:earlier sleep-offset time (earlier awakening) | rel=r_associated | relid=0 | w=30
  136. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:eeg abnormalities in 20-50% impaired language development
    n1=méningé (syndrome) | n2=en:eeg abnormalities in 20-50% impaired language development | rel=r_associated | relid=0 | w=30
  137. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:eeg is slowed with polyspike wave discharges
    n1=méningé (syndrome) | n2=en:eeg is slowed with polyspike wave discharges | rel=r_associated | relid=0 | w=30
  138. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:eeg may be normal at first
    n1=méningé (syndrome) | n2=en:eeg may be normal at first | rel=r_associated | relid=0 | w=30
  139. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:eeg shows epileptiform activity
    n1=méningé (syndrome) | n2=en:eeg shows epileptiform activity | rel=r_associated | relid=0 | w=30
  140. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:eeg shows slow frequency high amplitude waves with high frequency polyspikes
    n1=méningé (syndrome) | n2=en:eeg shows slow frequency high amplitude waves with high frequency polyspikes | rel=r_associated | relid=0 | w=30
  141. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:eeg shows suppression with ictal burst activities
    n1=méningé (syndrome) | n2=en:eeg shows suppression with ictal burst activities | rel=r_associated | relid=0 | w=30
  142. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:effaced gyral pattern
    n1=méningé (syndrome) | n2=en:effaced gyral pattern | rel=r_associated | relid=0 | w=30
  143. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:elevated interferon levels in cerebrospinal fluid
    n1=méningé (syndrome) | n2=en:elevated interferon levels in cerebrospinal fluid | rel=r_associated | relid=0 | w=30
  144. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials
    n1=méningé (syndrome) | n2=en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials | rel=r_associated | relid=0 | w=30
  145. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:end-position nystagmus
    n1=méningé (syndrome) | n2=en:end-position nystagmus | rel=r_associated | relid=0 | w=30
  146. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:enlarged fourth ventricle, mild
    n1=méningé (syndrome) | n2=en:enlarged fourth ventricle, mild | rel=r_associated | relid=0 | w=30
  147. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:enlarged white matter
    n1=méningé (syndrome) | n2=en:enlarged white matter | rel=r_associated | relid=0 | w=30
  148. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:episodic absence-like spells
    n1=méningé (syndrome) | n2=en:episodic absence-like spells | rel=r_associated | relid=0 | w=30
  149. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:extensor plantar responses (early-on)
    n1=méningé (syndrome) | n2=en:extensor plantar responses (early-on) | rel=r_associated | relid=0 | w=30
  150. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions
    n1=méningé (syndrome) | n2=en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions | rel=r_associated | relid=0 | w=30
  151. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:facial-lingual fasciculations
    n1=méningé (syndrome) | n2=en:facial-lingual fasciculations | rel=r_associated | relid=0 | w=30
  152. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:febrile seizures may occur
    n1=méningé (syndrome) | n2=en:febrile seizures may occur | rel=r_associated | relid=0 | w=30
  153. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:feeding problem
    n1=méningé (syndrome) | n2=en:feeding problem | rel=r_associated | relid=0 | w=30
  154. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:finger dysmetria
    n1=méningé (syndrome) | n2=en:finger dysmetria | rel=r_associated | relid=0 | w=30
  155. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:first dorsal interossei muscle atrophy
    n1=méningé (syndrome) | n2=en:first dorsal interossei muscle atrophy | rel=r_associated | relid=0 | w=30
  156. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:flaccidity, episodic
    n1=méningé (syndrome) | n2=en:flaccidity, episodic | rel=r_associated | relid=0 | w=30
  157. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:focal dyscognitive seizures
    n1=méningé (syndrome) | n2=en:focal dyscognitive seizures | rel=r_associated | relid=0 | w=30
  158. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:focal dystonia (rare)
    n1=méningé (syndrome) | n2=en:focal dystonia (rare) | rel=r_associated | relid=0 | w=30
  159. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:focal dystonias
    n1=méningé (syndrome) | n2=en:focal dystonias | rel=r_associated | relid=0 | w=30
  160. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:focal neurologic deficits (i.e., hemiparesis)
    n1=méningé (syndrome) | n2=en:focal neurologic deficits (i.e., hemiparesis) | rel=r_associated | relid=0 | w=30
  161. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:focal pachygyria
    n1=méningé (syndrome) | n2=en:focal pachygyria | rel=r_associated | relid=0 | w=30
  162. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:four-repeat tau plaques in the striatum
    n1=méningé (syndrome) | n2=en:four-repeat tau plaques in the striatum | rel=r_associated | relid=0 | w=30
  163. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients)
    n1=méningé (syndrome) | n2=en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients) | rel=r_associated | relid=0 | w=30
  164. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:gait ataxia (in some patients)
    n1=méningé (syndrome) | n2=en:gait ataxia (in some patients) | rel=r_associated | relid=0 | w=30
  165. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:gait difficulties, late-onset
    n1=méningé (syndrome) | n2=en:gait difficulties, late-onset | rel=r_associated | relid=0 | w=30
  166. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord
    n1=méningé (syndrome) | n2=en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord | rel=r_associated | relid=0 | w=30
  167. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:glomeruloid vascular proliferation in brain and spinal cord
    n1=méningé (syndrome) | n2=en:glomeruloid vascular proliferation in brain and spinal cord | rel=r_associated | relid=0 | w=30
  168. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:gray matter heterotopia (in some patients)
    n1=méningé (syndrome) | n2=en:gray matter heterotopia (in some patients) | rel=r_associated | relid=0 | w=30
  169. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:gross motor delay
    n1=méningé (syndrome) | n2=en:gross motor delay | rel=r_associated | relid=0 | w=30
  170. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:gyral disorganization
    n1=méningé (syndrome) | n2=en:gyral disorganization | rel=r_associated | relid=0 | w=30
  171. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:head titubations
    n1=méningé (syndrome) | n2=en:head titubations | rel=r_associated | relid=0 | w=30
  172. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:head tremor, mild
    n1=méningé (syndrome) | n2=en:head tremor, mild | rel=r_associated | relid=0 | w=30
  173. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:headache (with pheochromocytoma)
    n1=méningé (syndrome) | n2=en:headache (with pheochromocytoma) | rel=r_associated | relid=0 | w=30
  174. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:headache is usually not a symptom
    n1=méningé (syndrome) | n2=en:headache is usually not a symptom | rel=r_associated | relid=0 | w=30
  175. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:heightened sensitivity to external stimuli
    n1=méningé (syndrome) | n2=en:heightened sensitivity to external stimuli | rel=r_associated | relid=0 | w=30
  176. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hepatic encephalopathy
    n1=méningé (syndrome) | n2=en:hepatic encephalopathy | rel=r_associated | relid=0 | w=30
  177. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:high voltage spikes over the temporal and central regions seen on eeg
    n1=méningé (syndrome) | n2=en:high voltage spikes over the temporal and central regions seen on eeg | rel=r_associated | relid=0 | w=30
  178. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia
    n1=méningé (syndrome) | n2=en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia | rel=r_associated | relid=0 | w=30
  179. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:horner syndrome
    n1=méningé (syndrome) | n2=en:horner syndrome | rel=r_associated | relid=0 | w=30
  180. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hunger and thirst disturbances (in some patients)
    n1=méningé (syndrome) | n2=en:hunger and thirst disturbances (in some patients) | rel=r_associated | relid=0 | w=30
  181. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hydrocephaly, mild
    n1=méningé (syndrome) | n2=en:hydrocephaly, mild | rel=r_associated | relid=0 | w=30
  182. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hyperreflexia (70%)
    n1=méningé (syndrome) | n2=en:hyperreflexia (70%) | rel=r_associated | relid=0 | w=30
  183. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hyperthermia
    n1=méningé (syndrome) | n2=en:hyperthermia | rel=r_associated | relid=0 | w=30
  184. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypnagogic hallucinations
    n1=méningé (syndrome) | n2=en:hypnagogic hallucinations | rel=r_associated | relid=0 | w=30
  185. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypo- and demyelination of the brain
    n1=méningé (syndrome) | n2=en:hypo- and demyelination of the brain | rel=r_associated | relid=0 | w=30
  186. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypocalcemic tetany
    n1=méningé (syndrome) | n2=en:hypocalcemic tetany | rel=r_associated | relid=0 | w=30
  187. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypogenesis of the corpus callosum
    n1=méningé (syndrome) | n2=en:hypogenesis of the corpus callosum | rel=r_associated | relid=0 | w=30
  188. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypoplasia of corpus callosum
    n1=méningé (syndrome) | n2=en:hypoplasia of corpus callosum | rel=r_associated | relid=0 | w=30
  189. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypoplasia of septum pellucidum
    n1=méningé (syndrome) | n2=en:hypoplasia of septum pellucidum | rel=r_associated | relid=0 | w=30
  190. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypoplasia of the corpus callosum (2 patients)
    n1=méningé (syndrome) | n2=en:hypoplasia of the corpus callosum (2 patients) | rel=r_associated | relid=0 | w=30
  191. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypoplasia of the ventral pons
    n1=méningé (syndrome) | n2=en:hypoplasia of the ventral pons | rel=r_associated | relid=0 | w=30
  192. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypoplastic anterior pituitary (in some patients)
    n1=méningé (syndrome) | n2=en:hypoplastic anterior pituitary (in some patients) | rel=r_associated | relid=0 | w=30
  193. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypoplastic corpus callosum (in some)
    n1=méningé (syndrome) | n2=en:hypoplastic corpus callosum (in some) | rel=r_associated | relid=0 | w=30
  194. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypoplastic/atrophic corpus callosum (55%)
    n1=méningé (syndrome) | n2=en:hypoplastic/atrophic corpus callosum (55%) | rel=r_associated | relid=0 | w=30
  195. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypotonia (congenital form)
    n1=méningé (syndrome) | n2=en:hypotonia (congenital form) | rel=r_associated | relid=0 | w=30
  196. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypotonia (hcs and 2p21del)
    n1=méningé (syndrome) | n2=en:hypotonia (hcs and 2p21del) | rel=r_associated | relid=0 | w=30
  197. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypotonia (in some patients)
    n1=méningé (syndrome) | n2=en:hypotonia (in some patients) | rel=r_associated | relid=0 | w=30
  198. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:hypsarrhythmia
    n1=méningé (syndrome) | n2=en:hypsarrhythmia | rel=r_associated | relid=0 | w=30
  199. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ictal eeg showed partial seizures with frontal lobe origin
    n1=méningé (syndrome) | n2=en:ictal eeg showed partial seizures with frontal lobe origin | rel=r_associated | relid=0 | w=30
  200. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:illegible handwriting
    n1=méningé (syndrome) | n2=en:illegible handwriting | rel=r_associated | relid=0 | w=30
  201. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures
    n1=méningé (syndrome) | n2=en:impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures | rel=r_associated | relid=0 | w=30
  202. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:inability to run
    n1=méningé (syndrome) | n2=en:inability to run | rel=r_associated | relid=0 | w=30
  203. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:increased csf lactate
    n1=méningé (syndrome) | n2=en:increased csf lactate | rel=r_associated | relid=0 | w=30
  204. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:increased csf protein
    n1=méningé (syndrome) | n2=en:increased csf protein | rel=r_associated | relid=0 | w=30
  205. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:increased csf protein with normal cell count
    n1=méningé (syndrome) | n2=en:increased csf protein with normal cell count | rel=r_associated | relid=0 | w=30
  206. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:intellectual disability, progressive
    n1=méningé (syndrome) | n2=en:intellectual disability, progressive | rel=r_associated | relid=0 | w=30
  207. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:interhemispheric cysts
    n1=méningé (syndrome) | n2=en:interhemispheric cysts | rel=r_associated | relid=0 | w=30
  208. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:interictal eeg is usually normal
    n1=méningé (syndrome) | n2=en:interictal eeg is usually normal | rel=r_associated | relid=0 | w=30
  209. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis
    n1=méningé (syndrome) | n2=en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis | rel=r_associated | relid=0 | w=30
  210. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:intracellular lewy bodies
    n1=méningé (syndrome) | n2=en:intracellular lewy bodies | rel=r_associated | relid=0 | w=30
  211. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies)
    n1=méningé (syndrome) | n2=en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies) | rel=r_associated | relid=0 | w=30
  212. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:intracerebral calcifications (in some patients)
    n1=méningé (syndrome) | n2=en:intracerebral calcifications (in some patients) | rel=r_associated | relid=0 | w=30
  213. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:involuntary movements may be precipitated by exertion or anxiety
    n1=méningé (syndrome) | n2=en:involuntary movements may be precipitated by exertion or anxiety | rel=r_associated | relid=0 | w=30
  214. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:iron deposition in pallidal nuclei
    n1=méningé (syndrome) | n2=en:iron deposition in pallidal nuclei | rel=r_associated | relid=0 | w=30
  215. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:iron deposition in the globus pallidus and substantia nigra seen on mri
    n1=méningé (syndrome) | n2=en:iron deposition in the globus pallidus and substantia nigra seen on mri | rel=r_associated | relid=0 | w=30
  216. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:irregular spike and slow waves
    n1=méningé (syndrome) | n2=en:irregular spike and slow waves | rel=r_associated | relid=0 | w=30
  217. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lack of bunina bodies
    n1=méningé (syndrome) | n2=en:lack of bunina bodies | rel=r_associated | relid=0 | w=30
  218. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lack of developmental development
    n1=méningé (syndrome) | n2=en:lack of developmental development | rel=r_associated | relid=0 | w=30
  219. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lack of expressive speech
    n1=méningé (syndrome) | n2=en:lack of expressive speech | rel=r_associated | relid=0 | w=30
  220. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lack of head control
    n1=méningé (syndrome) | n2=en:lack of head control | rel=r_associated | relid=0 | w=30
  221. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lack of verbal communication
    n1=méningé (syndrome) | n2=en:lack of verbal communication | rel=r_associated | relid=0 | w=30
  222. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:language acquisition difficulties (in some patients)
    n1=méningé (syndrome) | n2=en:language acquisition difficulties (in some patients) | rel=r_associated | relid=0 | w=30
  223. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:large cerebellum, progressive
    n1=méningé (syndrome) | n2=en:large cerebellum, progressive | rel=r_associated | relid=0 | w=30
  224. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:large sella turcica
    n1=méningé (syndrome) | n2=en:large sella turcica | rel=r_associated | relid=0 | w=30
  225. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:learning difficulties (in 1 patient)
    n1=méningé (syndrome) | n2=en:learning difficulties (in 1 patient) | rel=r_associated | relid=0 | w=30
  226. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:leg pain
    n1=méningé (syndrome) | n2=en:leg pain | rel=r_associated | relid=0 | w=30
  227. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:leigh disease
    n1=méningé (syndrome) | n2=en:leigh disease | rel=r_associated | relid=0 | w=30
  228. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:leptomeningeal melanocytosis (in some patients)
    n1=méningé (syndrome) | n2=en:leptomeningeal melanocytosis (in some patients) | rel=r_associated | relid=0 | w=30
  229. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:leptomeningeal neoplasm
    n1=méningé (syndrome) | n2=en:leptomeningeal neoplasm | rel=r_associated | relid=0 | w=30
  230. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:leptomeningeal thickening
    n1=méningé (syndrome) | n2=en:leptomeningeal thickening | rel=r_associated | relid=0 | w=30
  231. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lesions are symmetrical
    n1=méningé (syndrome) | n2=en:lesions are symmetrical | rel=r_associated | relid=0 | w=30
  232. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lethargy associated with hypoglycemia
    n1=méningé (syndrome) | n2=en:lethargy associated with hypoglycemia | rel=r_associated | relid=0 | w=30
  233. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:leukodystrophy, hypomyelinating
    n1=méningé (syndrome) | n2=en:leukodystrophy, hypomyelinating | rel=r_associated | relid=0 | w=30
  234. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lightheadedness
    n1=méningé (syndrome) | n2=en:lightheadedness | rel=r_associated | relid=0 | w=30
  235. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:limb spasticity
    n1=méningé (syndrome) | n2=en:limb spasticity | rel=r_associated | relid=0 | w=30
  236. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lissencephaly (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:lissencephaly (reported in 1 patient) | rel=r_associated | relid=0 | w=30
  237. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:little spontaneous limb movement
    n1=méningé (syndrome) | n2=en:little spontaneous limb movement | rel=r_associated | relid=0 | w=30
  238. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:loss of cerebellar purkinje cells
    n1=méningé (syndrome) | n2=en:loss of cerebellar purkinje cells | rel=r_associated | relid=0 | w=30
  239. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:loss of gait (in some)
    n1=méningé (syndrome) | n2=en:loss of gait (in some) | rel=r_associated | relid=0 | w=30
  240. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:loss of motor skills
    n1=méningé (syndrome) | n2=en:loss of motor skills | rel=r_associated | relid=0 | w=30
  241. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:loss of myelinated fibers with regenerative clusters on biopsy
    n1=méningé (syndrome) | n2=en:loss of myelinated fibers with regenerative clusters on biopsy | rel=r_associated | relid=0 | w=30
  242. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:loss of white matter
    n1=méningé (syndrome) | n2=en:loss of white matter | rel=r_associated | relid=0 | w=30
  243. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:low-normal iq
    n1=méningé (syndrome) | n2=en:low-normal iq | rel=r_associated | relid=0 | w=30
  244. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lower extremity weakness with febrile episodes (rare)
    n1=méningé (syndrome) | n2=en:lower extremity weakness with febrile episodes (rare) | rel=r_associated | relid=0 | w=30
  245. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lower limbs weakness and atrophy, distal
    n1=méningé (syndrome) | n2=en:lower limbs weakness and atrophy, distal | rel=r_associated | relid=0 | w=30
  246. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lower motor neuron involvement, mild, seen on emg (in some patients)
    n1=méningé (syndrome) | n2=en:lower motor neuron involvement, mild, seen on emg (in some patients) | rel=r_associated | relid=0 | w=30
  247. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lower motor neuron signs, later
    n1=méningé (syndrome) | n2=en:lower motor neuron signs, later | rel=r_associated | relid=0 | w=30
  248. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis
    n1=méningé (syndrome) | n2=en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis | rel=r_associated | relid=0 | w=30
  249. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:lymphocytic infiltration of the brain
    n1=méningé (syndrome) | n2=en:lymphocytic infiltration of the brain | rel=r_associated | relid=0 | w=30
  250. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:meningeal sarcomatosis
    n1=méningé (syndrome) | n2=en:meningeal sarcomatosis | rel=r_associated | relid=0 | w=30
  251. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:meningioma by site
    n1=méningé (syndrome) | n2=en:meningioma by site | rel=r_associated | relid=0 | w=30
  252. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:meningiomatosis
    n1=méningé (syndrome) | n2=en:meningiomatosis | rel=r_associated | relid=0 | w=30
  253. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:meningoencephalocele (wws)
    n1=méningé (syndrome) | n2=en:meningoencephalocele (wws) | rel=r_associated | relid=0 | w=30
  254. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental deterioration beginning 2 to 5 years after onset of seizures
    n1=méningé (syndrome) | n2=en:mental deterioration beginning 2 to 5 years after onset of seizures | rel=r_associated | relid=0 | w=30
  255. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental impairment, mild to moderate
    n1=méningé (syndrome) | n2=en:mental impairment, mild to moderate | rel=r_associated | relid=0 | w=30
  256. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation
    n1=méningé (syndrome) | n2=en:mental retardation | rel=r_associated | relid=0 | w=30
  257. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation (develops later)
    n1=méningé (syndrome) | n2=en:mental retardation (develops later) | rel=r_associated | relid=0 | w=30
  258. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation (in type iia)
    n1=méningé (syndrome) | n2=en:mental retardation (in type iia) | rel=r_associated | relid=0 | w=30
  259. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation (rare less than 1% of cases)
    n1=méningé (syndrome) | n2=en:mental retardation (rare less than 1% of cases) | rel=r_associated | relid=0 | w=30
  260. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation (type i)
    n1=méningé (syndrome) | n2=en:mental retardation (type i) | rel=r_associated | relid=0 | w=30
  261. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation has been reported
    n1=méningé (syndrome) | n2=en:mental retardation has been reported | rel=r_associated | relid=0 | w=30
  262. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation in 5-13%
    n1=méningé (syndrome) | n2=en:mental retardation in 5-13% | rel=r_associated | relid=0 | w=30
  263. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation, mild (1 patient)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (1 patient) | rel=r_associated | relid=0 | w=30
  264. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation, severe in some patients
    n1=méningé (syndrome) | n2=en:mental retardation, severe in some patients | rel=r_associated | relid=0 | w=30
  265. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mental retardation, severe, profound
    n1=méningé (syndrome) | n2=en:mental retardation, severe, profound | rel=r_associated | relid=0 | w=30
  266. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mesial temporal sclerosis (in 1 patient)
    n1=méningé (syndrome) | n2=en:mesial temporal sclerosis (in 1 patient) | rel=r_associated | relid=0 | w=30
  267. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:metastatic malignant neoplasm in the leptomeninges
    n1=méningé (syndrome) | n2=en:metastatic malignant neoplasm in the leptomeninges | rel=r_associated | relid=0 | w=30
  268. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:migraine (uncommon)
    n1=méningé (syndrome) | n2=en:migraine (uncommon) | rel=r_associated | relid=0 | w=30
  269. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mild sensorimotor neuropathy
    n1=méningé (syndrome) | n2=en:mild sensorimotor neuropathy | rel=r_associated | relid=0 | w=30
  270. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mild to moderate learning difficulties
    n1=méningé (syndrome) | n2=en:mild to moderate learning difficulties | rel=r_associated | relid=0 | w=30
  271. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mild-moderate mental retardation (80% affected males)
    n1=méningé (syndrome) | n2=en:mild-moderate mental retardation (80% affected males) | rel=r_associated | relid=0 | w=30
  272. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mirror hand movements (bimanual synkinesis, in some patients)
    n1=méningé (syndrome) | n2=en:mirror hand movements (bimanual synkinesis, in some patients) | rel=r_associated | relid=0 | w=30
  273. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mood lability
    n1=méningé (syndrome) | n2=en:mood lability | rel=r_associated | relid=0 | w=30
  274. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:most patients achieve walking with aid
    n1=méningé (syndrome) | n2=en:most patients achieve walking with aid | rel=r_associated | relid=0 | w=30
  275. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:most patients are wheelchair-bound
    n1=méningé (syndrome) | n2=en:most patients are wheelchair-bound | rel=r_associated | relid=0 | w=30
  276. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:motor development delay (83%)
    n1=méningé (syndrome) | n2=en:motor development delay (83%) | rel=r_associated | relid=0 | w=30
  277. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:motor incoordination
    n1=méningé (syndrome) | n2=en:motor incoordination | rel=r_associated | relid=0 | w=30
  278. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:motor retardation, mild
    n1=méningé (syndrome) | n2=en:motor retardation, mild | rel=r_associated | relid=0 | w=30
  279. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:motor seizures, nocturnal, usually occur in clusters (up to 8 per night) during dozing or on awakening
    n1=méningé (syndrome) | n2=en:motor seizures, nocturnal, usually occur in clusters (up to 8 per night) during dozing or on awakening | rel=r_associated | relid=0 | w=30
  280. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:mri shows high signal intensity of the white matter later
    n1=méningé (syndrome) | n2=en:mri shows high signal intensity of the white matter later | rel=r_associated | relid=0 | w=30
  281. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:multifocal epileptiform discharges on diffuse slow background
    n1=méningé (syndrome) | n2=en:multifocal epileptiform discharges on diffuse slow background | rel=r_associated | relid=0 | w=30
  282. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:myclonus (rare)
    n1=méningé (syndrome) | n2=en:myclonus (rare) | rel=r_associated | relid=0 | w=30
  283. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:myelin-like lamellar structures in schwann cells
    n1=méningé (syndrome) | n2=en:myelin-like lamellar structures in schwann cells | rel=r_associated | relid=0 | w=30
  284. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:myelination defect
    n1=méningé (syndrome) | n2=en:myelination defect | rel=r_associated | relid=0 | w=30
  285. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:myoclonic seizures, progressive
    n1=méningé (syndrome) | n2=en:myoclonic seizures, progressive | rel=r_associated | relid=0 | w=30
  286. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:myotonia
    n1=méningé (syndrome) | n2=en:myotonia | rel=r_associated | relid=0 | w=30
  287. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neural tube defect (in some patients)
    n1=méningé (syndrome) | n2=en:neural tube defect (in some patients) | rel=r_associated | relid=0 | w=30
  288. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neurodegeneration in the basal ganglia
    n1=méningé (syndrome) | n2=en:neurodegeneration in the basal ganglia | rel=r_associated | relid=0 | w=30
  289. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neurodegeneration in the cerebellum
    n1=méningé (syndrome) | n2=en:neurodegeneration in the cerebellum | rel=r_associated | relid=0 | w=30
  290. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neurofibrillary tangles may be present
    n1=méningé (syndrome) | n2=en:neurofibrillary tangles may be present | rel=r_associated | relid=0 | w=30
  291. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neuroimaging shows cortical atrophy
    n1=méningé (syndrome) | n2=en:neuroimaging shows cortical atrophy | rel=r_associated | relid=0 | w=30
  292. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neurologic decompensation
    n1=méningé (syndrome) | n2=en:neurologic decompensation | rel=r_associated | relid=0 | w=30
  293. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neurologic regression following seizure onset
    n1=méningé (syndrome) | n2=en:neurologic regression following seizure onset | rel=r_associated | relid=0 | w=30
  294. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neurologic sequelae not always present
    n1=méningé (syndrome) | n2=en:neurologic sequelae not always present | rel=r_associated | relid=0 | w=30
  295. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neuronal loss in the brainstem
    n1=méningé (syndrome) | n2=en:neuronal loss in the brainstem | rel=r_associated | relid=0 | w=30
  296. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neuronal migration defect
    n1=méningé (syndrome) | n2=en:neuronal migration defect | rel=r_associated | relid=0 | w=30
  297. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:neuropathology shows diffuse demyelination of the cerebral white matter
    n1=méningé (syndrome) | n2=en:neuropathology shows diffuse demyelination of the cerebral white matter | rel=r_associated | relid=0 | w=30
  298. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:no cerebellar signs
    n1=méningé (syndrome) | n2=en:no cerebellar signs | rel=r_associated | relid=0 | w=30
  299. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:no other neurologic disorder
    n1=méningé (syndrome) | n2=en:no other neurologic disorder | rel=r_associated | relid=0 | w=30
  300. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:no response to l-dopa treatment
    n1=méningé (syndrome) | n2=en:no response to l-dopa treatment | rel=r_associated | relid=0 | w=30
  301. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:no seizures
    n1=méningé (syndrome) | n2=en:no seizures | rel=r_associated | relid=0 | w=30
  302. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:no structural brain abnormalities seen on mri
    n1=méningé (syndrome) | n2=en:no structural brain abnormalities seen on mri | rel=r_associated | relid=0 | w=30
  303. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:nocturnal sleep disruption
    n1=méningé (syndrome) | n2=en:nocturnal sleep disruption | rel=r_associated | relid=0 | w=30
  304. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:nodding of head
    n1=méningé (syndrome) | n2=en:nodding of head | rel=r_associated | relid=0 | w=30
  305. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:non-febrile seizures later
    n1=méningé (syndrome) | n2=en:non-febrile seizures later | rel=r_associated | relid=0 | w=30
  306. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:nonspecific leukoencephalopathy (52%)
    n1=méningé (syndrome) | n2=en:nonspecific leukoencephalopathy (52%) | rel=r_associated | relid=0 | w=30
  307. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:nonspecific spongiform degeneration
    n1=méningé (syndrome) | n2=en:nonspecific spongiform degeneration | rel=r_associated | relid=0 | w=30
  308. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:normal intellectual function
    n1=méningé (syndrome) | n2=en:normal intellectual function | rel=r_associated | relid=0 | w=30
  309. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:normal intelligence (majority)
    n1=méningé (syndrome) | n2=en:normal intelligence (majority) | rel=r_associated | relid=0 | w=30
  310. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:normal neurologic development in most cases
    n1=méningé (syndrome) | n2=en:normal neurologic development in most cases | rel=r_associated | relid=0 | w=30
  311. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:occipital encephalocele (in some patients)
    n1=méningé (syndrome) | n2=en:occipital encephalocele (in some patients) | rel=r_associated | relid=0 | w=30
  312. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:occipital lobe infarct (rare)
    n1=méningé (syndrome) | n2=en:occipital lobe infarct (rare) | rel=r_associated | relid=0 | w=30
  313. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:oligodendrocytes with foamy cytoplasm
    n1=méningé (syndrome) | n2=en:oligodendrocytes with foamy cytoplasm | rel=r_associated | relid=0 | w=30
  314. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:optic nerve hypoplasia
    n1=méningé (syndrome) | n2=en:optic nerve hypoplasia | rel=r_associated | relid=0 | w=30
  315. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ossification of the faux cerebri (less common)
    n1=méningé (syndrome) | n2=en:ossification of the faux cerebri (less common) | rel=r_associated | relid=0 | w=30
  316. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:other auras may occur
    n1=méningé (syndrome) | n2=en:other auras may occur | rel=r_associated | relid=0 | w=30
  317. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:paraplegia secondary to spinal cord compression due to severe kyphosis
    n1=méningé (syndrome) | n2=en:paraplegia secondary to spinal cord compression due to severe kyphosis | rel=r_associated | relid=0 | w=30
  318. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:parkinsonism (in some patients)
    n1=méningé (syndrome) | n2=en:parkinsonism (in some patients) | rel=r_associated | relid=0 | w=30
  319. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:parkinsonism (later onset)
    n1=méningé (syndrome) | n2=en:parkinsonism (later onset) | rel=r_associated | relid=0 | w=30
  320. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:parkinsonism, early-onset
    n1=méningé (syndrome) | n2=en:parkinsonism, early-onset | rel=r_associated | relid=0 | w=30
  321. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:partial pachygyria
    n1=méningé (syndrome) | n2=en:partial pachygyria | rel=r_associated | relid=0 | w=30
  322. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:partial response to pyridoxine
    n1=méningé (syndrome) | n2=en:partial response to pyridoxine | rel=r_associated | relid=0 | w=30
  323. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:pathological aspects
    n1=méningé (syndrome) | n2=en:pathological aspects | rel=r_associated | relid=0 | w=30
  324. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:patients may develop a seizure disorder later in life
    n1=méningé (syndrome) | n2=en:patients may develop a seizure disorder later in life | rel=r_associated | relid=0 | w=30
  325. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:paucity of anterior horn motor neurons
    n1=méningé (syndrome) | n2=en:paucity of anterior horn motor neurons | rel=r_associated | relid=0 | w=30
  326. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:periventricular calcifications
    n1=méningé (syndrome) | n2=en:periventricular calcifications | rel=r_associated | relid=0 | w=30
  327. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus
    n1=méningé (syndrome) | n2=en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus | rel=r_associated | relid=0 | w=30
  328. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:pineal gland
    n1=méningé (syndrome) | n2=en:pineal gland | rel=r_associated | relid=0 | w=30
  329. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:poor balance (finding)
    n1=méningé (syndrome) | n2=en:poor balance (finding) | rel=r_associated | relid=0 | w=30
  330. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:poor coordination
    n1=méningé (syndrome) | n2=en:poor coordination | rel=r_associated | relid=0 | w=30
  331. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:poor fine and gross motor coordination
    n1=méningé (syndrome) | n2=en:poor fine and gross motor coordination | rel=r_associated | relid=0 | w=30
  332. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:poor visual-spatial construction
    n1=méningé (syndrome) | n2=en:poor visual-spatial construction | rel=r_associated | relid=0 | w=30
  333. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:postural hand tremor
    n1=méningé (syndrome) | n2=en:postural hand tremor | rel=r_associated | relid=0 | w=30
  334. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments)
    n1=méningé (syndrome) | n2=en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments) | rel=r_associated | relid=0 | w=30
  335. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:progressive cognitive decline following normal development in childhood (in some patients)
    n1=méningé (syndrome) | n2=en:progressive cognitive decline following normal development in childhood (in some patients) | rel=r_associated | relid=0 | w=30
  336. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:progressive gait ataxia
    n1=méningé (syndrome) | n2=en:progressive gait ataxia | rel=r_associated | relid=0 | w=30
  337. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:prominent sulci
    n1=méningé (syndrome) | n2=en:prominent sulci | rel=r_associated | relid=0 | w=30
  338. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:proximal amyotrophy
    n1=méningé (syndrome) | n2=en:proximal amyotrophy | rel=r_associated | relid=0 | w=30
  339. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:proximal muscle weakness
    n1=méningé (syndrome) | n2=en:proximal muscle weakness | rel=r_associated | relid=0 | w=30
  340. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:psammomatous meningioma
    n1=méningé (syndrome) | n2=en:psammomatous meningioma | rel=r_associated | relid=0 | w=30
  341. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:psychiatric disorder
    n1=méningé (syndrome) | n2=en:psychiatric disorder | rel=r_associated | relid=0 | w=30
  342. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:psychomotor deterioration
    n1=méningé (syndrome) | n2=en:psychomotor deterioration | rel=r_associated | relid=0 | w=30
  343. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:psychomotor impairments
    n1=méningé (syndrome) | n2=en:psychomotor impairments | rel=r_associated | relid=0 | w=30
  344. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:psychomotor regression (in some)
    n1=méningé (syndrome) | n2=en:psychomotor regression (in some) | rel=r_associated | relid=0 | w=30
  345. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:psychomotor regression (onset within first year of life)
    n1=méningé (syndrome) | n2=en:psychomotor regression (onset within first year of life) | rel=r_associated | relid=0 | w=30
  346. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:psychomotor retardation
    n1=méningé (syndrome) | n2=en:psychomotor retardation | rel=r_associated | relid=0 | w=30
  347. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:pyramidal signs (1 patient)
    n1=méningé (syndrome) | n2=en:pyramidal signs (1 patient) | rel=r_associated | relid=0 | w=30
  348. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:pyramidal syndrome of the lower limbs
    n1=méningé (syndrome) | n2=en:pyramidal syndrome of the lower limbs | rel=r_associated | relid=0 | w=30
  349. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:quadriplegic dyskinesia
    n1=méningé (syndrome) | n2=en:quadriplegic dyskinesia | rel=r_associated | relid=0 | w=30
  350. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:retrocollis
    n1=méningé (syndrome) | n2=en:retrocollis | rel=r_associated | relid=0 | w=30
  351. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:rhabdoid meningioma
    n1=méningé (syndrome) | n2=en:rhabdoid meningioma | rel=r_associated | relid=0 | w=30
  352. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:rhombencephalosynapsis
    n1=méningé (syndrome) | n2=en:rhombencephalosynapsis | rel=r_associated | relid=0 | w=30
  353. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:rigidity during seizures
    n1=méningé (syndrome) | n2=en:rigidity during seizures | rel=r_associated | relid=0 | w=30
  354. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:roving eye movements (infancy)
    n1=méningé (syndrome) | n2=en:roving eye movements (infancy) | rel=r_associated | relid=0 | w=30
  355. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles
    n1=méningé (syndrome) | n2=en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles | rel=r_associated | relid=0 | w=30
  356. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:secretory meningioma
    n1=méningé (syndrome) | n2=en:secretory meningioma | rel=r_associated | relid=0 | w=30
  357. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:see spg5a (270800)
    n1=méningé (syndrome) | n2=en:see spg5a (270800) | rel=r_associated | relid=0 | w=30
  358. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:seizure (in a subset of patients in infancy)
    n1=méningé (syndrome) | n2=en:seizure (in a subset of patients in infancy) | rel=r_associated | relid=0 | w=30
  359. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:seizures (> 90%)
    n1=méningé (syndrome) | n2=en:seizures (> 90%) | rel=r_associated | relid=0 | w=30
  360. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:seizures (adult)
    n1=méningé (syndrome) | n2=en:seizures (adult) | rel=r_associated | relid=0 | w=30
  361. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:seizures (onset <2 years)
    n1=méningé (syndrome) | n2=en:seizures (onset <2 years) | rel=r_associated | relid=0 | w=30
  362. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:seizures provoked by tactile stimulation or extreme emotion
    n1=méningé (syndrome) | n2=en:seizures provoked by tactile stimulation or extreme emotion | rel=r_associated | relid=0 | w=30
  363. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:seizures, hypoglycemic (in some patients)
    n1=méningé (syndrome) | n2=en:seizures, hypoglycemic (in some patients) | rel=r_associated | relid=0 | w=30
  364. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:seizures, neonatal (2p21del)
    n1=méningé (syndrome) | n2=en:seizures, neonatal (2p21del) | rel=r_associated | relid=0 | w=30
  365. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:seizures, partial with secondary generalization, focal at onset, usually motor
    n1=méningé (syndrome) | n2=en:seizures, partial with secondary generalization, focal at onset, usually motor | rel=r_associated | relid=0 | w=30
  366. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:sensitivity to neuroleptic medication
    n1=méningé (syndrome) | n2=en:sensitivity to neuroleptic medication | rel=r_associated | relid=0 | w=30
  367. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:sensory ataxia (less common)
    n1=méningé (syndrome) | n2=en:sensory ataxia (less common) | rel=r_associated | relid=0 | w=30
  368. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:severe brain damage
    n1=méningé (syndrome) | n2=en:severe brain damage | rel=r_associated | relid=0 | w=30
  369. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:sleep-wake cycle disturbance
    n1=méningé (syndrome) | n2=en:sleep-wake cycle disturbance | rel=r_associated | relid=0 | w=30
  370. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:slow reactions
    n1=méningé (syndrome) | n2=en:slow reactions | rel=r_associated | relid=0 | w=30
  371. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:small thalami
    n1=méningé (syndrome) | n2=en:small thalami | rel=r_associated | relid=0 | w=30
  372. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:smooth, thin cortical mantle (wws)
    n1=méningé (syndrome) | n2=en:smooth, thin cortical mantle (wws) | rel=r_associated | relid=0 | w=30
  373. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:somatosensory evoked potentials show prolonged latency
    n1=méningé (syndrome) | n2=en:somatosensory evoked potentials show prolonged latency | rel=r_associated | relid=0 | w=30
  374. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:somnolence
    n1=méningé (syndrome) | n2=en:somnolence | rel=r_associated | relid=0 | w=30
  375. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:spastic paraplegia
    n1=méningé (syndrome) | n2=en:spastic paraplegia | rel=r_associated | relid=0 | w=30
  376. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:spastic paraplegia (in some patients)
    n1=méningé (syndrome) | n2=en:spastic paraplegia (in some patients) | rel=r_associated | relid=0 | w=30
  377. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:spasticity of lower and upper limbs
    n1=méningé (syndrome) | n2=en:spasticity of lower and upper limbs | rel=r_associated | relid=0 | w=30
  378. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:spasticity, mainly in the lower limbs
    n1=méningé (syndrome) | n2=en:spasticity, mainly in the lower limbs | rel=r_associated | relid=0 | w=30
  379. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:speech deterioration
    n1=méningé (syndrome) | n2=en:speech deterioration | rel=r_associated | relid=0 | w=30
  380. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:spinal arteriovenous malformation
    n1=méningé (syndrome) | n2=en:spinal arteriovenous malformation | rel=r_associated | relid=0 | w=30
  381. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:spinocerebellar ataxia (in some patients)
    n1=méningé (syndrome) | n2=en:spinocerebellar ataxia (in some patients) | rel=r_associated | relid=0 | w=30
  382. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:spongiform changes are mild or may not be present
    n1=méningé (syndrome) | n2=en:spongiform changes are mild or may not be present | rel=r_associated | relid=0 | w=30
  383. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:spongy degeneration
    n1=méningé (syndrome) | n2=en:spongy degeneration | rel=r_associated | relid=0 | w=30
  384. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:stiffness
    n1=méningé (syndrome) | n2=en:stiffness | rel=r_associated | relid=0 | w=30
  385. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:strokes due to coagulopathy
    n1=méningé (syndrome) | n2=en:strokes due to coagulopathy | rel=r_associated | relid=0 | w=30
  386. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:sturge-weber syndrome
    n1=méningé (syndrome) | n2=en:sturge-weber syndrome | rel=r_associated | relid=0 | w=30
  387. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:subarachnoid hemorrhage (rare)
    n1=méningé (syndrome) | n2=en:subarachnoid hemorrhage (rare) | rel=r_associated | relid=0 | w=30
  388. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:subcortical nodular lesions in perivascular white matter
    n1=méningé (syndrome) | n2=en:subcortical nodular lesions in perivascular white matter | rel=r_associated | relid=0 | w=30
  389. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:subcortical white matter abnormalities seen on mri
    n1=méningé (syndrome) | n2=en:subcortical white matter abnormalities seen on mri | rel=r_associated | relid=0 | w=30
  390. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:subependymal heterotopias
    n1=méningé (syndrome) | n2=en:subependymal heterotopias | rel=r_associated | relid=0 | w=30
  391. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:sudden onset of neuropsychiatric symptoms
    n1=méningé (syndrome) | n2=en:sudden onset of neuropsychiatric symptoms | rel=r_associated | relid=0 | w=30
  392. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:syringomyelia
    n1=méningé (syndrome) | n2=en:syringomyelia | rel=r_associated | relid=0 | w=30
  393. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:t2-weighted hyperintensities in the basal ganglia
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintensities in the basal ganglia | rel=r_associated | relid=0 | w=30
  394. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter | rel=r_associated | relid=0 | w=30
  395. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:tau-immunoreactive inclusions in neurons and astrocytes
    n1=méningé (syndrome) | n2=en:tau-immunoreactive inclusions in neurons and astrocytes | rel=r_associated | relid=0 | w=30
  396. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:temporal epileptiform discharges seen on eeg
    n1=méningé (syndrome) | n2=en:temporal epileptiform discharges seen on eeg | rel=r_associated | relid=0 | w=30
  397. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:tendency to walk on toes
    n1=méningé (syndrome) | n2=en:tendency to walk on toes | rel=r_associated | relid=0 | w=30
  398. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:thalamic lesions
    n1=méningé (syndrome) | n2=en:thalamic lesions | rel=r_associated | relid=0 | w=30
  399. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:thin bony cortex
    n1=méningé (syndrome) | n2=en:thin bony cortex | rel=r_associated | relid=0 | w=30
  400. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:third ventricle subependymal focal gliosis
    n1=méningé (syndrome) | n2=en:third ventricle subependymal focal gliosis | rel=r_associated | relid=0 | w=30
  401. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:thrombosis of cerebral veins
    n1=méningé (syndrome) | n2=en:thrombosis of cerebral veins | rel=r_associated | relid=0 | w=30
  402. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:toe-walking gait
    n1=méningé (syndrome) | n2=en:toe-walking gait | rel=r_associated | relid=0 | w=30
  403. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:tonic seizures, refractory
    n1=méningé (syndrome) | n2=en:tonic seizures, refractory | rel=r_associated | relid=0 | w=30
  404. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:tremor (less common)
    n1=méningé (syndrome) | n2=en:tremor (less common) | rel=r_associated | relid=0 | w=30
  405. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:tremor is exacerbated by stress and exercise
    n1=méningé (syndrome) | n2=en:tremor is exacerbated by stress and exercise | rel=r_associated | relid=0 | w=30
  406. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:type iii eeg response is parietooccipital spikes followed by biphasic slow waves and spreading to the frontal region
    n1=méningé (syndrome) | n2=en:type iii eeg response is parietooccipital spikes followed by biphasic slow waves and spreading to the frontal region | rel=r_associated | relid=0 | w=30
  407. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions
    n1=méningé (syndrome) | n2=en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions | rel=r_associated | relid=0 | w=30
  408. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ultrastructure
    n1=méningé (syndrome) | n2=en:ultrastructure | rel=r_associated | relid=0 | w=30
  409. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:unable to walk
    n1=méningé (syndrome) | n2=en:unable to walk | rel=r_associated | relid=0 | w=30
  410. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:undersulcation of the frontal lobes
    n1=méningé (syndrome) | n2=en:undersulcation of the frontal lobes | rel=r_associated | relid=0 | w=30
  411. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:unilateral cerebellar hypoplasia
    n1=méningé (syndrome) | n2=en:unilateral cerebellar hypoplasia | rel=r_associated | relid=0 | w=30
  412. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:unsteady standing
    n1=méningé (syndrome) | n2=en:unsteady standing | rel=r_associated | relid=0 | w=30
  413. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:upper limb involvement
    n1=méningé (syndrome) | n2=en:upper limb involvement | rel=r_associated | relid=0 | w=30
  414. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:upper limb involvement (in some patients)
    n1=méningé (syndrome) | n2=en:upper limb involvement (in some patients) | rel=r_associated | relid=0 | w=30
  415. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:upper limb spasticity (in some patients)
    n1=méningé (syndrome) | n2=en:upper limb spasticity (in some patients) | rel=r_associated | relid=0 | w=30
  416. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:upper limb weakness
    n1=méningé (syndrome) | n2=en:upper limb weakness | rel=r_associated | relid=0 | w=30
  417. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:upper motor neuron signs, early
    n1=méningé (syndrome) | n2=en:upper motor neuron signs, early | rel=r_associated | relid=0 | w=30
  418. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:usually occurs at night
    n1=méningé (syndrome) | n2=en:usually occurs at night | rel=r_associated | relid=0 | w=30
  419. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ventricular asymmetry
    n1=méningé (syndrome) | n2=en:ventricular asymmetry | rel=r_associated | relid=0 | w=30
  420. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ventricular dilatation (in some patients)
    n1=méningé (syndrome) | n2=en:ventricular dilatation (in some patients) | rel=r_associated | relid=0 | w=30
  421. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:ventricular enlargement, mild
    n1=méningé (syndrome) | n2=en:ventricular enlargement, mild | rel=r_associated | relid=0 | w=30
  422. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:vertigo
    n1=méningé (syndrome) | n2=en:vertigo | rel=r_associated | relid=0 | w=30
  423. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:white matter abnormalities (uncommon)
    n1=méningé (syndrome) | n2=en:white matter abnormalities (uncommon) | rel=r_associated | relid=0 | w=30
  424. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:white matter abnormalities seen on mri
    n1=méningé (syndrome) | n2=en:white matter abnormalities seen on mri | rel=r_associated | relid=0 | w=30
  425. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:white matter degeneration
    n1=méningé (syndrome) | n2=en:white matter degeneration | rel=r_associated | relid=0 | w=30
  426. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:white matter lesions in the basal ganglia
    n1=méningé (syndrome) | n2=en:white matter lesions in the basal ganglia | rel=r_associated | relid=0 | w=30
  427. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:white matter vacuolization
    n1=méningé (syndrome) | n2=en:white matter vacuolization | rel=r_associated | relid=0 | w=30
  428. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:wide subarachnoid spaces
    n1=méningé (syndrome) | n2=en:wide subarachnoid spaces | rel=r_associated | relid=0 | w=30
  429. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> en:widespread neuronal loss
    n1=méningé (syndrome) | n2=en:widespread neuronal loss | rel=r_associated | relid=0 | w=30
  430. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> méningiomatose, sai
    n1=méningé (syndrome) | n2=méningiomatose, sai | rel=r_associated | relid=0 | w=30
  431. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> neurologie
    n1=méningé (syndrome) | n2=neurologie | rel=r_associated | relid=0 | w=30
  432. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> pie-mère
    n1=méningé (syndrome) | n2=pie-mère | rel=r_associated | relid=0 | w=30
  433. méningé (syndrome) -- r_associated #0: 30 / 0.361 -> Spécialités médicales
    n1=méningé (syndrome) | n2=Spécialités médicales | rel=r_associated | relid=0 | w=30
  434. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> arachnoïde
    n1=méningé (syndrome) | n2=arachnoïde | rel=r_associated | relid=0 | w=29
  435. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:'eye of the tiger' sign on mri
    n1=méningé (syndrome) | n2=en:'eye of the tiger' sign on mri | rel=r_associated | relid=0 | w=29
  436. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:'spheroid' inclusions in axons
    n1=méningé (syndrome) | n2=en:'spheroid' inclusions in axons | rel=r_associated | relid=0 | w=29
  437. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle
    n1=méningé (syndrome) | n2=en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle | rel=r_associated | relid=0 | w=29
  438. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:abnormal cortical lamination
    n1=méningé (syndrome) | n2=en:abnormal cortical lamination | rel=r_associated | relid=0 | w=29
  439. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:abnormal cortical layering
    n1=méningé (syndrome) | n2=en:abnormal cortical layering | rel=r_associated | relid=0 | w=29
  440. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:abnormal eeg (abnormal slowing of background activity)
    n1=méningé (syndrome) | n2=en:abnormal eeg (abnormal slowing of background activity) | rel=r_associated | relid=0 | w=29
  441. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:abnormal lower motor neuron morphology
    n1=méningé (syndrome) | n2=en:abnormal lower motor neuron morphology | rel=r_associated | relid=0 | w=29
  442. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:abnormal myelination
    n1=méningé (syndrome) | n2=en:abnormal myelination | rel=r_associated | relid=0 | w=29
  443. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:abnormal spike waves
    n1=méningé (syndrome) | n2=en:abnormal spike waves | rel=r_associated | relid=0 | w=29
  444. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:abnormal visual evoked potential
    n1=méningé (syndrome) | n2=en:abnormal visual evoked potential | rel=r_associated | relid=0 | w=29
  445. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:abnormality of the posterior cranial fossa
    n1=méningé (syndrome) | n2=en:abnormality of the posterior cranial fossa | rel=r_associated | relid=0 | w=29
  446. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:absence of myelin in the posterior column of the spinal cord (1 patient)
    n1=méningé (syndrome) | n2=en:absence of myelin in the posterior column of the spinal cord (1 patient) | rel=r_associated | relid=0 | w=29
  447. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:absent development
    n1=méningé (syndrome) | n2=en:absent development | rel=r_associated | relid=0 | w=29
  448. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:absent olfactory bulbs
    n1=méningé (syndrome) | n2=en:absent olfactory bulbs | rel=r_associated | relid=0 | w=29
  449. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:absent olfactory tract or bulbs
    n1=méningé (syndrome) | n2=en:absent olfactory tract or bulbs | rel=r_associated | relid=0 | w=29
  450. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons
    n1=méningé (syndrome) | n2=en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons | rel=r_associated | relid=0 | w=29
  451. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:affected children are unable to sit without support
    n1=méningé (syndrome) | n2=en:affected children are unable to sit without support | rel=r_associated | relid=0 | w=29
  452. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:agenesis of the corpus callosum (1 patient)
    n1=méningé (syndrome) | n2=en:agenesis of the corpus callosum (1 patient) | rel=r_associated | relid=0 | w=29
  453. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:agenesis of the corpus callosum (rare)
    n1=méningé (syndrome) | n2=en:agenesis of the corpus callosum (rare) | rel=r_associated | relid=0 | w=29
  454. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:agenesis or severe hypoplasia of cerebellar vermis
    n1=méningé (syndrome) | n2=en:agenesis or severe hypoplasia of cerebellar vermis | rel=r_associated | relid=0 | w=29
  455. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:alobar holoprosencephaly (rare)
    n1=méningé (syndrome) | n2=en:alobar holoprosencephaly (rare) | rel=r_associated | relid=0 | w=29
  456. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:alpha-synuclein-immunoreactive lewy neurites
    n1=méningé (syndrome) | n2=en:alpha-synuclein-immunoreactive lewy neurites | rel=r_associated | relid=0 | w=29
  457. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord
    n1=méningé (syndrome) | n2=en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord | rel=r_associated | relid=0 | w=29
  458. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:angiitis, cerebral
    n1=méningé (syndrome) | n2=en:angiitis, cerebral | rel=r_associated | relid=0 | w=29
  459. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:ankle clonus (in some patients)
    n1=méningé (syndrome) | n2=en:ankle clonus (in some patients) | rel=r_associated | relid=0 | w=29
  460. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:anomalies of the temporal area
    n1=méningé (syndrome) | n2=en:anomalies of the temporal area | rel=r_associated | relid=0 | w=29
  461. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:aplasia of the vermis
    n1=méningé (syndrome) | n2=en:aplasia of the vermis | rel=r_associated | relid=0 | w=29
  462. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:arachnoidal cysts
    n1=méningé (syndrome) | n2=en:arachnoidal cysts | rel=r_associated | relid=0 | w=29
  463. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:articulatory defect
    n1=méningé (syndrome) | n2=en:articulatory defect | rel=r_associated | relid=0 | w=29
  464. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:asperger syndrome (rare)
    n1=méningé (syndrome) | n2=en:asperger syndrome (rare) | rel=r_associated | relid=0 | w=29
  465. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:associated with paresthesias and dysesthesias
    n1=méningé (syndrome) | n2=en:associated with paresthesias and dysesthesias | rel=r_associated | relid=0 | w=29
  466. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:asymmetry of symptoms
    n1=méningé (syndrome) | n2=en:asymmetry of symptoms | rel=r_associated | relid=0 | w=29
  467. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:ataxia (cvs+)
    n1=méningé (syndrome) | n2=en:ataxia (cvs+) | rel=r_associated | relid=0 | w=29
  468. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:ataxia (type i and type ii, infantile and juvenile)
    n1=méningé (syndrome) | n2=en:ataxia (type i and type ii, infantile and juvenile) | rel=r_associated | relid=0 | w=29
  469. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:ataxia with febrile episodes (rare)
    n1=méningé (syndrome) | n2=en:ataxia with febrile episodes (rare) | rel=r_associated | relid=0 | w=29
  470. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:atrophic pons (in some)
    n1=méningé (syndrome) | n2=en:atrophic pons (in some) | rel=r_associated | relid=0 | w=29
  471. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:atrophy and weakness of limb musculature
    n1=méningé (syndrome) | n2=en:atrophy and weakness of limb musculature | rel=r_associated | relid=0 | w=29
  472. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:atrophy of the posterior columns and spinocerebellar tracts
    n1=méningé (syndrome) | n2=en:atrophy of the posterior columns and spinocerebellar tracts | rel=r_associated | relid=0 | w=29
  473. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:aura (in some instances)
    n1=méningé (syndrome) | n2=en:aura (in some instances) | rel=r_associated | relid=0 | w=29
  474. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension)
    n1=méningé (syndrome) | n2=en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension) | rel=r_associated | relid=0 | w=29
  475. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:autonomic manifestations
    n1=méningé (syndrome) | n2=en:autonomic manifestations | rel=r_associated | relid=0 | w=29
  476. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:axonal 'spheroid' inclusions in the cns
    n1=méningé (syndrome) | n2=en:axonal 'spheroid' inclusions in the cns | rel=r_associated | relid=0 | w=29
  477. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:axonal spheroids in the dorsal column
    n1=méningé (syndrome) | n2=en:axonal spheroids in the dorsal column | rel=r_associated | relid=0 | w=29
  478. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:axonal swelling or thickening in the cns
    n1=méningé (syndrome) | n2=en:axonal swelling or thickening in the cns | rel=r_associated | relid=0 | w=29
  479. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:basal ganglia lesions seen on mri
    n1=méningé (syndrome) | n2=en:basal ganglia lesions seen on mri | rel=r_associated | relid=0 | w=29
  480. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:behavioral variant of frontotemporal dementia
    n1=méningé (syndrome) | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=29
  481. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:bilateral calcification of basal ganglia and cerebellum
    n1=méningé (syndrome) | n2=en:bilateral calcification of basal ganglia and cerebellum | rel=r_associated | relid=0 | w=29
  482. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:bilateral schizencephaly
    n1=méningé (syndrome) | n2=en:bilateral schizencephaly | rel=r_associated | relid=0 | w=29
  483. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:brisk reflexes (1 patient)
    n1=méningé (syndrome) | n2=en:brisk reflexes (1 patient) | rel=r_associated | relid=0 | w=29
  484. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:brisk tendon reflex
    n1=méningé (syndrome) | n2=en:brisk tendon reflex | rel=r_associated | relid=0 | w=29
  485. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:broad-based gait
    n1=méningé (syndrome) | n2=en:broad-based gait | rel=r_associated | relid=0 | w=29
  486. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cavitating leukoencephalopathy
    n1=méningé (syndrome) | n2=en:cavitating leukoencephalopathy | rel=r_associated | relid=0 | w=29
  487. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:central facial nerve paralysis (rare)
    n1=méningé (syndrome) | n2=en:central facial nerve paralysis (rare) | rel=r_associated | relid=0 | w=29
  488. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:central nervous system space
    n1=méningé (syndrome) | n2=en:central nervous system space | rel=r_associated | relid=0 | w=29
  489. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebellar ataxia (may be permanent in 50% of patients)
    n1=méningé (syndrome) | n2=en:cerebellar ataxia (may be permanent in 50% of patients) | rel=r_associated | relid=0 | w=29
  490. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebellar atrophy (in 1 family)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy (in 1 family) | rel=r_associated | relid=0 | w=29
  491. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebellar atrophy (in adulthood)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy (in adulthood) | rel=r_associated | relid=0 | w=29
  492. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebellar degeneration
    n1=méningé (syndrome) | n2=en:cerebellar degeneration | rel=r_associated | relid=0 | w=29
  493. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebellar enlargement
    n1=méningé (syndrome) | n2=en:cerebellar enlargement | rel=r_associated | relid=0 | w=29
  494. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebral atrophy
    n1=méningé (syndrome) | n2=en:cerebral atrophy | rel=r_associated | relid=0 | w=29
  495. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebral atrophy (in severe cases)
    n1=méningé (syndrome) | n2=en:cerebral atrophy (in severe cases) | rel=r_associated | relid=0 | w=29
  496. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebral atrophy, mild, diffuse
    n1=méningé (syndrome) | n2=en:cerebral atrophy, mild, diffuse | rel=r_associated | relid=0 | w=29
  497. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebral convexity meningioma
    n1=méningé (syndrome) | n2=en:cerebral convexity meningioma | rel=r_associated | relid=0 | w=29
  498. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebral malformations
    n1=méningé (syndrome) | n2=en:cerebral malformations | rel=r_associated | relid=0 | w=29
  499. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebral oligogyria
    n1=méningé (syndrome) | n2=en:cerebral oligogyria | rel=r_associated | relid=0 | w=29
  500. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebral white matter atrophy, progressive
    n1=méningé (syndrome) | n2=en:cerebral white matter atrophy, progressive | rel=r_associated | relid=0 | w=29
  501. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cerebrovascular accident (in some patients)
    n1=méningé (syndrome) | n2=en:cerebrovascular accident (in some patients) | rel=r_associated | relid=0 | w=29
  502. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:characteristic arm position with wrist and elbow flexion
    n1=méningé (syndrome) | n2=en:characteristic arm position with wrist and elbow flexion | rel=r_associated | relid=0 | w=29
  503. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:childhood polyphagia
    n1=méningé (syndrome) | n2=en:childhood polyphagia | rel=r_associated | relid=0 | w=29
  504. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:closed-lip schizencephaly
    n1=méningé (syndrome) | n2=en:closed-lip schizencephaly | rel=r_associated | relid=0 | w=29
  505. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:coarsened pattern of sulci and gyri
    n1=méningé (syndrome) | n2=en:coarsened pattern of sulci and gyri | rel=r_associated | relid=0 | w=29
  506. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cognitive decline (in some patients)
    n1=méningé (syndrome) | n2=en:cognitive decline (in some patients) | rel=r_associated | relid=0 | w=29
  507. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cognitive impairment
    n1=méningé (syndrome) | n2=en:cognitive impairment | rel=r_associated | relid=0 | w=29
  508. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cognitive impairment (3 patients)
    n1=méningé (syndrome) | n2=en:cognitive impairment (3 patients) | rel=r_associated | relid=0 | w=29
  509. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cognitive impairment, mild (in 2 of 3 patients)
    n1=méningé (syndrome) | n2=en:cognitive impairment, mild (in 2 of 3 patients) | rel=r_associated | relid=0 | w=29
  510. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:congenital absence of the vermis
    n1=méningé (syndrome) | n2=en:congenital absence of the vermis | rel=r_associated | relid=0 | w=29
  511. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:convulsions, febrile (in some patients)
    n1=méningé (syndrome) | n2=en:convulsions, febrile (in some patients) | rel=r_associated | relid=0 | w=29
  512. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cortical dysplasia (1 patient)
    n1=méningé (syndrome) | n2=en:cortical dysplasia (1 patient) | rel=r_associated | relid=0 | w=29
  513. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cortical dysplasia (2 patients)
    n1=méningé (syndrome) | n2=en:cortical dysplasia (2 patients) | rel=r_associated | relid=0 | w=29
  514. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cortical malformations
    n1=méningé (syndrome) | n2=en:cortical malformations | rel=r_associated | relid=0 | w=29
  515. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cortical simplification
    n1=méningé (syndrome) | n2=en:cortical simplification | rel=r_associated | relid=0 | w=29
  516. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:corticospinal tract atrophy
    n1=méningé (syndrome) | n2=en:corticospinal tract atrophy | rel=r_associated | relid=0 | w=29
  517. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:crowding of the posterior fossa
    n1=méningé (syndrome) | n2=en:crowding of the posterior fossa | rel=r_associated | relid=0 | w=29
  518. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:cystic degeneration of the white matter
    n1=méningé (syndrome) | n2=en:cystic degeneration of the white matter | rel=r_associated | relid=0 | w=29
  519. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dandy-walker malformation (in some patients)
    n1=méningé (syndrome) | n2=en:dandy-walker malformation (in some patients) | rel=r_associated | relid=0 | w=29
  520. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:decreased brain volume (female)
    n1=méningé (syndrome) | n2=en:decreased brain volume (female) | rel=r_associated | relid=0 | w=29
  521. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:decreased brain weight
    n1=méningé (syndrome) | n2=en:decreased brain weight | rel=r_associated | relid=0 | w=29
  522. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:decreased mitochondrial respiratory chain complex activity
    n1=méningé (syndrome) | n2=en:decreased mitochondrial respiratory chain complex activity | rel=r_associated | relid=0 | w=29
  523. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:decreased rapid automatized naming (ran) speed
    n1=méningé (syndrome) | n2=en:decreased rapid automatized naming (ran) speed | rel=r_associated | relid=0 | w=29
  524. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:decreasing responsiveness
    n1=méningé (syndrome) | n2=en:decreasing responsiveness | rel=r_associated | relid=0 | w=29
  525. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:deep hypointensities (mri, t2) suggestive of past microbleeds
    n1=méningé (syndrome) | n2=en:deep hypointensities (mri, t2) suggestive of past microbleeds | rel=r_associated | relid=0 | w=29
  526. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:deficit in reading comprehension
    n1=méningé (syndrome) | n2=en:deficit in reading comprehension | rel=r_associated | relid=0 | w=29
  527. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:degeneration of purkinje cells in the cerebellum
    n1=méningé (syndrome) | n2=en:degeneration of purkinje cells in the cerebellum | rel=r_associated | relid=0 | w=29
  528. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed ambulation
    n1=méningé (syndrome) | n2=en:delayed ambulation | rel=r_associated | relid=0 | w=29
  529. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed development (in some patients)
    n1=méningé (syndrome) | n2=en:delayed development (in some patients) | rel=r_associated | relid=0 | w=29
  530. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed development in early childhood (in some patients)
    n1=méningé (syndrome) | n2=en:delayed development in early childhood (in some patients) | rel=r_associated | relid=0 | w=29
  531. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed development, ranging from mild to severe
    n1=méningé (syndrome) | n2=en:delayed development, ranging from mild to severe | rel=r_associated | relid=0 | w=29
  532. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed development, severe
    n1=méningé (syndrome) | n2=en:delayed development, severe | rel=r_associated | relid=0 | w=29
  533. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed myelination seen on mri
    n1=méningé (syndrome) | n2=en:delayed myelination seen on mri | rel=r_associated | relid=0 | w=29
  534. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed psychomotor development (in some patients)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development (in some patients) | rel=r_associated | relid=0 | w=29
  535. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed psychomotor development, profound
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, profound | rel=r_associated | relid=0 | w=29
  536. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed psychomotor development, profound (patient a)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, profound (patient a) | rel=r_associated | relid=0 | w=29
  537. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:delayed psychomotor development, severe to profound
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, severe to profound | rel=r_associated | relid=0 | w=29
  538. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dementia
    n1=méningé (syndrome) | n2=en:dementia | rel=r_associated | relid=0 | w=29
  539. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dementia (5%)
    n1=méningé (syndrome) | n2=en:dementia (5%) | rel=r_associated | relid=0 | w=29
  540. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dementia (in some patients)
    n1=méningé (syndrome) | n2=en:dementia (in some patients) | rel=r_associated | relid=0 | w=29
  541. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dementia (subtype 3a)
    n1=méningé (syndrome) | n2=en:dementia (subtype 3a) | rel=r_associated | relid=0 | w=29
  542. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:demyelination of the posterior and lateral columns of the spinal cord
    n1=méningé (syndrome) | n2=en:demyelination of the posterior and lateral columns of the spinal cord | rel=r_associated | relid=0 | w=29
  543. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:denervation seen on emg
    n1=méningé (syndrome) | n2=en:denervation seen on emg | rel=r_associated | relid=0 | w=29
  544. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dense calcifications in the cerebellar dentate nucleus
    n1=méningé (syndrome) | n2=en:dense calcifications in the cerebellar dentate nucleus | rel=r_associated | relid=0 | w=29
  545. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:developmental delay (in most patients)
    n1=méningé (syndrome) | n2=en:developmental delay (in most patients) | rel=r_associated | relid=0 | w=29
  546. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:difficulties in fine movement of the hands
    n1=méningé (syndrome) | n2=en:difficulties in fine movement of the hands | rel=r_associated | relid=0 | w=29
  547. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:difficulty speaking during seizures
    n1=méningé (syndrome) | n2=en:difficulty speaking during seizures | rel=r_associated | relid=0 | w=29
  548. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:diffuse cerebral gliosis
    n1=méningé (syndrome) | n2=en:diffuse cerebral gliosis | rel=r_associated | relid=0 | w=29
  549. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare)
    n1=méningé (syndrome) | n2=en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare) | rel=r_associated | relid=0 | w=29
  550. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:diffuse paroxysmal discharges
    n1=méningé (syndrome) | n2=en:diffuse paroxysmal discharges | rel=r_associated | relid=0 | w=29
  551. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dilatation of the lateral and third ventricles
    n1=méningé (syndrome) | n2=en:dilatation of the lateral and third ventricles | rel=r_associated | relid=0 | w=29
  552. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:disordered myelination
    n1=méningé (syndrome) | n2=en:disordered myelination | rel=r_associated | relid=0 | w=29
  553. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:disorganized brain cytoarchitecture
    n1=méningé (syndrome) | n2=en:disorganized brain cytoarchitecture | rel=r_associated | relid=0 | w=29
  554. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:disturbed sleep-wake cycle
    n1=méningé (syndrome) | n2=en:disturbed sleep-wake cycle | rel=r_associated | relid=0 | w=29
  555. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dream enactment
    n1=méningé (syndrome) | n2=en:dream enactment | rel=r_associated | relid=0 | w=29
  556. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dystonia (in 2 patients)
    n1=méningé (syndrome) | n2=en:dystonia (in 2 patients) | rel=r_associated | relid=0 | w=29
  557. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:dystonic vocal tremor
    n1=méningé (syndrome) | n2=en:dystonic vocal tremor | rel=r_associated | relid=0 | w=29
  558. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:ectopic posterior pituitary
    n1=méningé (syndrome) | n2=en:ectopic posterior pituitary | rel=r_associated | relid=0 | w=29
  559. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:eeg shows nonspecific slow-wave paroxysms
    n1=méningé (syndrome) | n2=en:eeg shows nonspecific slow-wave paroxysms | rel=r_associated | relid=0 | w=29
  560. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:eeg shows rolandic sharp waves and spikes
    n1=méningé (syndrome) | n2=en:eeg shows rolandic sharp waves and spikes | rel=r_associated | relid=0 | w=29
  561. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:eeg shows slowed dysrhythmia and multifocal discharges
    n1=méningé (syndrome) | n2=en:eeg shows slowed dysrhythmia and multifocal discharges | rel=r_associated | relid=0 | w=29
  562. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:eeg with focal discharge
    n1=méningé (syndrome) | n2=en:eeg with focal discharge | rel=r_associated | relid=0 | w=29
  563. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:electrophysiologic studies indicate cortical origin
    n1=méningé (syndrome) | n2=en:electrophysiologic studies indicate cortical origin | rel=r_associated | relid=0 | w=29
  564. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:embryologic
    n1=méningé (syndrome) | n2=en:embryologic | rel=r_associated | relid=0 | w=29
  565. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:encephaloceles, frontal
    n1=méningé (syndrome) | n2=en:encephaloceles, frontal | rel=r_associated | relid=0 | w=29
  566. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:encephalomyopathy
    n1=méningé (syndrome) | n2=en:encephalomyopathy | rel=r_associated | relid=0 | w=29
  567. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:enlarged cerebellar cistern
    n1=méningé (syndrome) | n2=en:enlarged cerebellar cistern | rel=r_associated | relid=0 | w=29
  568. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:enlarged cisterna magna
    n1=méningé (syndrome) | n2=en:enlarged cisterna magna | rel=r_associated | relid=0 | w=29
  569. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:epilepsy (in some patients)
    n1=méningé (syndrome) | n2=en:epilepsy (in some patients) | rel=r_associated | relid=0 | w=29
  570. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:epilepsy, multifocal, intractable
    n1=méningé (syndrome) | n2=en:epilepsy, multifocal, intractable | rel=r_associated | relid=0 | w=29
  571. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:epilepsy, myoclonic astatic
    n1=méningé (syndrome) | n2=en:epilepsy, myoclonic astatic | rel=r_associated | relid=0 | w=29
  572. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:epileptic encephalopathy with psychomotor retardation (rare)
    n1=méningé (syndrome) | n2=en:epileptic encephalopathy with psychomotor retardation (rare) | rel=r_associated | relid=0 | w=29
  573. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:episodes typically occur several times a week
    n1=méningé (syndrome) | n2=en:episodes typically occur several times a week | rel=r_associated | relid=0 | w=29
  574. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:exaggerated acoustic startle response
    n1=méningé (syndrome) | n2=en:exaggerated acoustic startle response | rel=r_associated | relid=0 | w=29
  575. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:expressive language delay
    n1=méningé (syndrome) | n2=en:expressive language delay | rel=r_associated | relid=0 | w=29
  576. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:expressive language disorder
    n1=méningé (syndrome) | n2=en:expressive language disorder | rel=r_associated | relid=0 | w=29
  577. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:extrapyramidal signs (less common)
    n1=méningé (syndrome) | n2=en:extrapyramidal signs (less common) | rel=r_associated | relid=0 | w=29
  578. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:extrapyramidal signs may develop
    n1=méningé (syndrome) | n2=en:extrapyramidal signs may develop | rel=r_associated | relid=0 | w=29
  579. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:facial muscle weakness
    n1=méningé (syndrome) | n2=en:facial muscle weakness | rel=r_associated | relid=0 | w=29
  580. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:facial myokymia, mild
    n1=méningé (syndrome) | n2=en:facial myokymia, mild | rel=r_associated | relid=0 | w=29
  581. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:fatal subacute encephalopathy (1 family)
    n1=méningé (syndrome) | n2=en:fatal subacute encephalopathy (1 family) | rel=r_associated | relid=0 | w=29
  582. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:fatigue
    n1=méningé (syndrome) | n2=en:fatigue | rel=r_associated | relid=0 | w=29
  583. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:febrile seizures (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:febrile seizures (reported in 1 patient) | rel=r_associated | relid=0 | w=29
  584. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:flat pons
    n1=méningé (syndrome) | n2=en:flat pons | rel=r_associated | relid=0 | w=29
  585. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:floppiness
    n1=méningé (syndrome) | n2=en:floppiness | rel=r_associated | relid=0 | w=29
  586. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:foot-drop
    n1=méningé (syndrome) | n2=en:foot-drop | rel=r_associated | relid=0 | w=29
  587. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:frontal lobe syndrome
    n1=méningé (syndrome) | n2=en:frontal lobe syndrome | rel=r_associated | relid=0 | w=29
  588. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:frontal release signs
    n1=méningé (syndrome) | n2=en:frontal release signs | rel=r_associated | relid=0 | w=29
  589. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:frontolimbic dementia
    n1=méningé (syndrome) | n2=en:frontolimbic dementia | rel=r_associated | relid=0 | w=29
  590. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:frontotemporal pachygyria (1 patient)
    n1=méningé (syndrome) | n2=en:frontotemporal pachygyria (1 patient) | rel=r_associated | relid=0 | w=29
  591. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:frontotemporal polymicrogyria
    n1=méningé (syndrome) | n2=en:frontotemporal polymicrogyria | rel=r_associated | relid=0 | w=29
  592. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:gait abnormalities (in some patients)
    n1=méningé (syndrome) | n2=en:gait abnormalities (in some patients) | rel=r_associated | relid=0 | w=29
  593. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:gait abnormalities may occur
    n1=méningé (syndrome) | n2=en:gait abnormalities may occur | rel=r_associated | relid=0 | w=29
  594. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:gait and limb ataxia
    n1=méningé (syndrome) | n2=en:gait and limb ataxia | rel=r_associated | relid=0 | w=29
  595. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:gait imbalance
    n1=méningé (syndrome) | n2=en:gait imbalance | rel=r_associated | relid=0 | w=29
  596. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:gait instability, worse in the dark
    n1=méningé (syndrome) | n2=en:gait instability, worse in the dark | rel=r_associated | relid=0 | w=29
  597. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:gait, rigid
    n1=méningé (syndrome) | n2=en:gait, rigid | rel=r_associated | relid=0 | w=29
  598. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:generalized and focal spike and wave complexes seen on eeg
    n1=méningé (syndrome) | n2=en:generalized and focal spike and wave complexes seen on eeg | rel=r_associated | relid=0 | w=29
  599. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:generalized hypotonia
    n1=méningé (syndrome) | n2=en:generalized hypotonia | rel=r_associated | relid=0 | w=29
  600. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:generalized myelin loss
    n1=méningé (syndrome) | n2=en:generalized myelin loss | rel=r_associated | relid=0 | w=29
  601. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:generalized spike-wave activity seen on eeg
    n1=méningé (syndrome) | n2=en:generalized spike-wave activity seen on eeg | rel=r_associated | relid=0 | w=29
  602. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:generalized tonic-clonic seizures (gtcs) (in most patients)
    n1=méningé (syndrome) | n2=en:generalized tonic-clonic seizures (gtcs) (in most patients) | rel=r_associated | relid=0 | w=29
  603. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:generalized tonic-clonic seizures (gtcs) on awakening
    n1=méningé (syndrome) | n2=en:generalized tonic-clonic seizures (gtcs) on awakening | rel=r_associated | relid=0 | w=29
  604. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:gliosis of the white matter
    n1=méningé (syndrome) | n2=en:gliosis of the white matter | rel=r_associated | relid=0 | w=29
  605. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:grade iii meningioma
    n1=méningé (syndrome) | n2=en:grade iii meningioma | rel=r_associated | relid=0 | w=29
  606. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:grimaces
    n1=méningé (syndrome) | n2=en:grimaces | rel=r_associated | relid=0 | w=29
  607. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:gross motor delay (in one family)
    n1=méningé (syndrome) | n2=en:gross motor delay (in one family) | rel=r_associated | relid=0 | w=29
  608. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:gurgling or drooling during seizures
    n1=méningé (syndrome) | n2=en:gurgling or drooling during seizures | rel=r_associated | relid=0 | w=29
  609. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:head bobbing
    n1=méningé (syndrome) | n2=en:head bobbing | rel=r_associated | relid=0 | w=29
  610. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:head movements abnormal
    n1=méningé (syndrome) | n2=en:head movements abnormal | rel=r_associated | relid=0 | w=29
  611. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hemiparesis
    n1=méningé (syndrome) | n2=en:hemiparesis | rel=r_associated | relid=0 | w=29
  612. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hemiplegic migraine
    n1=méningé (syndrome) | n2=en:hemiplegic migraine | rel=r_associated | relid=0 | w=29
  613. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hemispheric atrophy
    n1=méningé (syndrome) | n2=en:hemispheric atrophy | rel=r_associated | relid=0 | w=29
  614. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hemorrhage
    n1=méningé (syndrome) | n2=en:hemorrhage | rel=r_associated | relid=0 | w=29
  615. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:holoprosencephaly
    n1=méningé (syndrome) | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=29
  616. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hydrocephalus (11%)
    n1=méningé (syndrome) | n2=en:hydrocephalus (11%) | rel=r_associated | relid=0 | w=29
  617. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hydrocephalus (12%)
    n1=méningé (syndrome) | n2=en:hydrocephalus (12%) | rel=r_associated | relid=0 | w=29
  618. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hydrocephalus (in some patients)
    n1=méningé (syndrome) | n2=en:hydrocephalus (in some patients) | rel=r_associated | relid=0 | w=29
  619. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hyperactive brainstem reflexes (head retraction, palmomental, snout)
    n1=méningé (syndrome) | n2=en:hyperactive brainstem reflexes (head retraction, palmomental, snout) | rel=r_associated | relid=0 | w=29
  620. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hyperkinetic involuntary movements
    n1=méningé (syndrome) | n2=en:hyperkinetic involuntary movements | rel=r_associated | relid=0 | w=29
  621. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hyperreflexia
    n1=méningé (syndrome) | n2=en:hyperreflexia | rel=r_associated | relid=0 | w=29
  622. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hyperreflexia (type i)
    n1=méningé (syndrome) | n2=en:hyperreflexia (type i) | rel=r_associated | relid=0 | w=29
  623. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypertonia (childhood)
    n1=méningé (syndrome) | n2=en:hypertonia (childhood) | rel=r_associated | relid=0 | w=29
  624. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypertonia and rigidity during seizures
    n1=méningé (syndrome) | n2=en:hypertonia and rigidity during seizures | rel=r_associated | relid=0 | w=29
  625. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypertonia, peripheral dystonia
    n1=méningé (syndrome) | n2=en:hypertonia, peripheral dystonia | rel=r_associated | relid=0 | w=29
  626. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypertonic seizures
    n1=méningé (syndrome) | n2=en:hypertonic seizures | rel=r_associated | relid=0 | w=29
  627. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypoglycemic encephalopathy
    n1=méningé (syndrome) | n2=en:hypoglycemic encephalopathy | rel=r_associated | relid=0 | w=29
  628. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypoplasia of olfactory tract
    n1=méningé (syndrome) | n2=en:hypoplasia of olfactory tract | rel=r_associated | relid=0 | w=29
  629. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypoplasia of the optic tract
    n1=méningé (syndrome) | n2=en:hypoplasia of the optic tract | rel=r_associated | relid=0 | w=29
  630. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction
    n1=méningé (syndrome) | n2=en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction | rel=r_associated | relid=0 | w=29
  631. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypoplastic cerebellar vermis (rare)
    n1=méningé (syndrome) | n2=en:hypoplastic cerebellar vermis (rare) | rel=r_associated | relid=0 | w=29
  632. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypoplastic corpus callosum (rare)
    n1=méningé (syndrome) | n2=en:hypoplastic corpus callosum (rare) | rel=r_associated | relid=0 | w=29
  633. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypoplastic internal capsule (in some)
    n1=méningé (syndrome) | n2=en:hypoplastic internal capsule (in some) | rel=r_associated | relid=0 | w=29
  634. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypoplastic pituitary gland (in some patients)
    n1=méningé (syndrome) | n2=en:hypoplastic pituitary gland (in some patients) | rel=r_associated | relid=0 | w=29
  635. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypotonia in later stages
    n1=méningé (syndrome) | n2=en:hypotonia in later stages | rel=r_associated | relid=0 | w=29
  636. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypotonia, mild, transient
    n1=méningé (syndrome) | n2=en:hypotonia, mild, transient | rel=r_associated | relid=0 | w=29
  637. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:hypotonic seizures
    n1=méningé (syndrome) | n2=en:hypotonic seizures | rel=r_associated | relid=0 | w=29
  638. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:immature myelination
    n1=méningé (syndrome) | n2=en:immature myelination | rel=r_associated | relid=0 | w=29
  639. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:impaired motor control, mild
    n1=méningé (syndrome) | n2=en:impaired motor control, mild | rel=r_associated | relid=0 | w=29
  640. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:incomprehensible speech
    n1=méningé (syndrome) | n2=en:incomprehensible speech | rel=r_associated | relid=0 | w=29
  641. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:incoordination of trunk and limbs
    n1=méningé (syndrome) | n2=en:incoordination of trunk and limbs | rel=r_associated | relid=0 | w=29
  642. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:increased iron deposition in the basal ganglia (40%)
    n1=méningé (syndrome) | n2=en:increased iron deposition in the basal ganglia (40%) | rel=r_associated | relid=0 | w=29
  643. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:increased neurologic sequelae of infections (rare)
    n1=méningé (syndrome) | n2=en:increased neurologic sequelae of infections (rare) | rel=r_associated | relid=0 | w=29
  644. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:interictal eeg may show nonspecific changes in 15 to 20%
    n1=méningé (syndrome) | n2=en:interictal eeg may show nonspecific changes in 15 to 20% | rel=r_associated | relid=0 | w=29
  645. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:intermittent wheelchair dependence (stage 3)
    n1=méningé (syndrome) | n2=en:intermittent wheelchair dependence (stage 3) | rel=r_associated | relid=0 | w=29
  646. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis
    n1=méningé (syndrome) | n2=en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis | rel=r_associated | relid=0 | w=29
  647. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:intracranial hemorrhage
    n1=méningé (syndrome) | n2=en:intracranial hemorrhage | rel=r_associated | relid=0 | w=29
  648. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:intraorbital meningioma
    n1=méningé (syndrome) | n2=en:intraorbital meningioma | rel=r_associated | relid=0 | w=29
  649. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:involuntary repetitive movements
    n1=méningé (syndrome) | n2=en:involuntary repetitive movements | rel=r_associated | relid=0 | w=29
  650. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:irresistible desire to move the legs
    n1=méningé (syndrome) | n2=en:irresistible desire to move the legs | rel=r_associated | relid=0 | w=29
  651. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:ischemic stroke (in some patients)
    n1=méningé (syndrome) | n2=en:ischemic stroke (in some patients) | rel=r_associated | relid=0 | w=29
  652. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lack of development
    n1=méningé (syndrome) | n2=en:lack of development | rel=r_associated | relid=0 | w=29
  653. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lack of independent ambulation (1 patient)
    n1=méningé (syndrome) | n2=en:lack of independent ambulation (1 patient) | rel=r_associated | relid=0 | w=29
  654. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lack of independent sitting or walking
    n1=méningé (syndrome) | n2=en:lack of independent sitting or walking | rel=r_associated | relid=0 | w=29
  655. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lack of spontaneous play
    n1=méningé (syndrome) | n2=en:lack of spontaneous play | rel=r_associated | relid=0 | w=29
  656. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lack of visual attention
    n1=méningé (syndrome) | n2=en:lack of visual attention | rel=r_associated | relid=0 | w=29
  657. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:laminar necrosis
    n1=méningé (syndrome) | n2=en:laminar necrosis | rel=r_associated | relid=0 | w=29
  658. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:large cavum vergae
    n1=méningé (syndrome) | n2=en:large cavum vergae | rel=r_associated | relid=0 | w=29
  659. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lateral corticospinal tracts show atrophy, pallor, and degeneration
    n1=méningé (syndrome) | n2=en:lateral corticospinal tracts show atrophy, pallor, and degeneration | rel=r_associated | relid=0 | w=29
  660. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:learning disabilities (in some patients)
    n1=méningé (syndrome) | n2=en:learning disabilities (in some patients) | rel=r_associated | relid=0 | w=29
  661. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord
    n1=méningé (syndrome) | n2=en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord | rel=r_associated | relid=0 | w=29
  662. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:leukoaraiosis
    n1=méningé (syndrome) | n2=en:leukoaraiosis | rel=r_associated | relid=0 | w=29
  663. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:leukodystrophy (in 1 of 2 patients)
    n1=méningé (syndrome) | n2=en:leukodystrophy (in 1 of 2 patients) | rel=r_associated | relid=0 | w=29
  664. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lewy bodies (not always present)
    n1=méningé (syndrome) | n2=en:lewy bodies (not always present) | rel=r_associated | relid=0 | w=29
  665. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lewy bodies in the substantia nigra
    n1=méningé (syndrome) | n2=en:lewy bodies in the substantia nigra | rel=r_associated | relid=0 | w=29
  666. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lipomyelocystoceles
    n1=méningé (syndrome) | n2=en:lipomyelocystoceles | rel=r_associated | relid=0 | w=29
  667. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles
    n1=méningé (syndrome) | n2=en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles | rel=r_associated | relid=0 | w=29
  668. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:long-tract signs
    n1=méningé (syndrome) | n2=en:long-tract signs | rel=r_associated | relid=0 | w=29
  669. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:loss of cerebellar granular cells
    n1=méningé (syndrome) | n2=en:loss of cerebellar granular cells | rel=r_associated | relid=0 | w=29
  670. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:loss of consciousness (1 patient)
    n1=méningé (syndrome) | n2=en:loss of consciousness (1 patient) | rel=r_associated | relid=0 | w=29
  671. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:loss of dopaminergic neurons
    n1=méningé (syndrome) | n2=en:loss of dopaminergic neurons | rel=r_associated | relid=0 | w=29
  672. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:loss of dopaminergic neurons in the substantia nigra
    n1=méningé (syndrome) | n2=en:loss of dopaminergic neurons in the substantia nigra | rel=r_associated | relid=0 | w=29
  673. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:loss of executive functions
    n1=méningé (syndrome) | n2=en:loss of executive functions | rel=r_associated | relid=0 | w=29
  674. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:loss of motor milestones
    n1=méningé (syndrome) | n2=en:loss of motor milestones | rel=r_associated | relid=0 | w=29
  675. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:loss of purkinje cells in the cerebellar vermis
    n1=méningé (syndrome) | n2=en:loss of purkinje cells in the cerebellar vermis | rel=r_associated | relid=0 | w=29
  676. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:loss of purkinje cells in the cerebellum
    n1=méningé (syndrome) | n2=en:loss of purkinje cells in the cerebellum | rel=r_associated | relid=0 | w=29
  677. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:low densities in the basal ganglia similar to leigh syndrome (256000)
    n1=méningé (syndrome) | n2=en:low densities in the basal ganglia similar to leigh syndrome (256000) | rel=r_associated | relid=0 | w=29
  678. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:low-lying cerebellar tonsils
    n1=méningé (syndrome) | n2=en:low-lying cerebellar tonsils | rel=r_associated | relid=0 | w=29
  679. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lower limb hyperreflexia
    n1=méningé (syndrome) | n2=en:lower limb hyperreflexia | rel=r_associated | relid=0 | w=29
  680. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:lumbosacral meningocele
    n1=méningé (syndrome) | n2=en:lumbosacral meningocele | rel=r_associated | relid=0 | w=29
  681. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:magnetic resonance spectroscopy shows increased lactate in white matter
    n1=méningé (syndrome) | n2=en:magnetic resonance spectroscopy shows increased lactate in white matter | rel=r_associated | relid=0 | w=29
  682. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mask-like facies
    n1=méningé (syndrome) | n2=en:mask-like facies | rel=r_associated | relid=0 | w=29
  683. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:meningeal disorder
    n1=méningé (syndrome) | n2=en:meningeal disorder | rel=r_associated | relid=0 | w=29
  684. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:meningeal neoplasm
    n1=méningé (syndrome) | n2=en:meningeal neoplasm | rel=r_associated | relid=0 | w=29
  685. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:meningoceles, multiple, lateral
    n1=méningé (syndrome) | n2=en:meningoceles, multiple, lateral | rel=r_associated | relid=0 | w=29
  686. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:meningothelial meningioma
    n1=méningé (syndrome) | n2=en:meningothelial meningioma | rel=r_associated | relid=0 | w=29
  687. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental deterioration
    n1=méningé (syndrome) | n2=en:mental deterioration | rel=r_associated | relid=0 | w=29
  688. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation (15%)
    n1=méningé (syndrome) | n2=en:mental retardation (15%) | rel=r_associated | relid=0 | w=29
  689. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation (seen in hhs variant)
    n1=méningé (syndrome) | n2=en:mental retardation (seen in hhs variant) | rel=r_associated | relid=0 | w=29
  690. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation (untreated hypothyroidism)
    n1=méningé (syndrome) | n2=en:mental retardation (untreated hypothyroidism) | rel=r_associated | relid=0 | w=29
  691. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation, borderline to severe
    n1=méningé (syndrome) | n2=en:mental retardation, borderline to severe | rel=r_associated | relid=0 | w=29
  692. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation, mild (carrier females)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (carrier females) | rel=r_associated | relid=0 | w=29
  693. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation, mild (rare)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (rare) | rel=r_associated | relid=0 | w=29
  694. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation, mild to moderate
    n1=méningé (syndrome) | n2=en:mental retardation, mild to moderate | rel=r_associated | relid=0 | w=29
  695. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation, mild to profound
    n1=méningé (syndrome) | n2=en:mental retardation, mild to profound | rel=r_associated | relid=0 | w=29
  696. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation, moderate to severe
    n1=méningé (syndrome) | n2=en:mental retardation, moderate to severe | rel=r_associated | relid=0 | w=29
  697. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation, moderate to severe (iq 40 to 60)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate to severe (iq 40 to 60) | rel=r_associated | relid=0 | w=29
  698. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mental retardation, residual mild-to-severe (in some patients)
    n1=méningé (syndrome) | n2=en:mental retardation, residual mild-to-severe (in some patients) | rel=r_associated | relid=0 | w=29
  699. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mesial temporal brain malformations
    n1=méningé (syndrome) | n2=en:mesial temporal brain malformations | rel=r_associated | relid=0 | w=29
  700. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:microbiological
    n1=méningé (syndrome) | n2=en:microbiological | rel=r_associated | relid=0 | w=29
  701. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:microvascular spaces, dilated
    n1=méningé (syndrome) | n2=en:microvascular spaces, dilated | rel=r_associated | relid=0 | w=29
  702. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:midline brain calcifications
    n1=méningé (syndrome) | n2=en:midline brain calcifications | rel=r_associated | relid=0 | w=29
  703. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:migraine
    n1=méningé (syndrome) | n2=en:migraine | rel=r_associated | relid=0 | w=29
  704. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:migraine headache (less common)
    n1=méningé (syndrome) | n2=en:migraine headache (less common) | rel=r_associated | relid=0 | w=29
  705. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mild global developmental delay
    n1=méningé (syndrome) | n2=en:mild global developmental delay | rel=r_associated | relid=0 | w=29
  706. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mild motor development delay
    n1=méningé (syndrome) | n2=en:mild motor development delay | rel=r_associated | relid=0 | w=29
  707. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mild paraparesis
    n1=méningé (syndrome) | n2=en:mild paraparesis | rel=r_associated | relid=0 | w=29
  708. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mild pyramidal signs (variable expression)
    n1=méningé (syndrome) | n2=en:mild pyramidal signs (variable expression) | rel=r_associated | relid=0 | w=29
  709. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mildly delayed developmental milestones
    n1=méningé (syndrome) | n2=en:mildly delayed developmental milestones | rel=r_associated | relid=0 | w=29
  710. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:moderate cortical atrophy (in some patients)
    n1=méningé (syndrome) | n2=en:moderate cortical atrophy (in some patients) | rel=r_associated | relid=0 | w=29
  711. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:molar tooth sign on brain mri
    n1=méningé (syndrome) | n2=en:molar tooth sign on brain mri | rel=r_associated | relid=0 | w=29
  712. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mosy patients become wheelchair-bound after 10 years
    n1=méningé (syndrome) | n2=en:mosy patients become wheelchair-bound after 10 years | rel=r_associated | relid=0 | w=29
  713. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:motor automatisms
    n1=méningé (syndrome) | n2=en:motor automatisms | rel=r_associated | relid=0 | w=29
  714. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:motor delay (in one patient)
    n1=méningé (syndrome) | n2=en:motor delay (in one patient) | rel=r_associated | relid=0 | w=29
  715. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:motor development delayed (in some patients)
    n1=méningé (syndrome) | n2=en:motor development delayed (in some patients) | rel=r_associated | relid=0 | w=29
  716. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:motor developmental delay, severe
    n1=méningé (syndrome) | n2=en:motor developmental delay, severe | rel=r_associated | relid=0 | w=29
  717. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:motor dysfunction
    n1=méningé (syndrome) | n2=en:motor dysfunction | rel=r_associated | relid=0 | w=29
  718. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mouth movements
    n1=méningé (syndrome) | n2=en:mouth movements | rel=r_associated | relid=0 | w=29
  719. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:movements are exacerbated by anxiety
    n1=méningé (syndrome) | n2=en:movements are exacerbated by anxiety | rel=r_associated | relid=0 | w=29
  720. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mri imaging shows cavitation of the basal ganglia
    n1=méningé (syndrome) | n2=en:mri imaging shows cavitation of the basal ganglia | rel=r_associated | relid=0 | w=29
  721. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mri shows absence of the facial nerve
    n1=méningé (syndrome) | n2=en:mri shows absence of the facial nerve | rel=r_associated | relid=0 | w=29
  722. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mri shows congenital abnormalities of the posterior fossa
    n1=méningé (syndrome) | n2=en:mri shows congenital abnormalities of the posterior fossa | rel=r_associated | relid=0 | w=29
  723. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mri shows generalized atrophy
    n1=méningé (syndrome) | n2=en:mri shows generalized atrophy | rel=r_associated | relid=0 | w=29
  724. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mri shows leukoencephalopathy
    n1=méningé (syndrome) | n2=en:mri shows leukoencephalopathy | rel=r_associated | relid=0 | w=29
  725. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mri shows symmetric, diffuse lesions with csf-like signal intensity
    n1=méningé (syndrome) | n2=en:mri shows symmetric, diffuse lesions with csf-like signal intensity | rel=r_associated | relid=0 | w=29
  726. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:mrs shows decreased creatine in white matter
    n1=méningé (syndrome) | n2=en:mrs shows decreased creatine in white matter | rel=r_associated | relid=0 | w=29
  727. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:multifocal discharges associated with contralateral jerky movements
    n1=méningé (syndrome) | n2=en:multifocal discharges associated with contralateral jerky movements | rel=r_associated | relid=0 | w=29
  728. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:multifocal spikes
    n1=méningé (syndrome) | n2=en:multifocal spikes | rel=r_associated | relid=0 | w=29
  729. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:multiple independent spike foci
    n1=méningé (syndrome) | n2=en:multiple independent spike foci | rel=r_associated | relid=0 | w=29
  730. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:myelomeningocele
    n1=méningé (syndrome) | n2=en:myelomeningocele | rel=r_associated | relid=0 | w=29
  731. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:myoclonic epilepsy (1 patient)
    n1=méningé (syndrome) | n2=en:myoclonic epilepsy (1 patient) | rel=r_associated | relid=0 | w=29
  732. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:myoclonic seizures (subtype 3a)
    n1=méningé (syndrome) | n2=en:myoclonic seizures (subtype 3a) | rel=r_associated | relid=0 | w=29
  733. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:myokymia (in some patients)
    n1=méningé (syndrome) | n2=en:myokymia (in some patients) | rel=r_associated | relid=0 | w=29
  734. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:myotonia (in 1 patient)
    n1=méningé (syndrome) | n2=en:myotonia (in 1 patient) | rel=r_associated | relid=0 | w=29
  735. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neurobehavioral changes associated with hyperammonemia
    n1=méningé (syndrome) | n2=en:neurobehavioral changes associated with hyperammonemia | rel=r_associated | relid=0 | w=29
  736. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neurodevelopmental regression
    n1=méningé (syndrome) | n2=en:neurodevelopmental regression | rel=r_associated | relid=0 | w=29
  737. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neurologic degeneration
    n1=méningé (syndrome) | n2=en:neurologic degeneration | rel=r_associated | relid=0 | w=29
  738. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neurologic involvement (in some patients)
    n1=méningé (syndrome) | n2=en:neurologic involvement (in some patients) | rel=r_associated | relid=0 | w=29
  739. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neurologic regression around age 3 months
    n1=méningé (syndrome) | n2=en:neurologic regression around age 3 months | rel=r_associated | relid=0 | w=29
  740. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neuron loss
    n1=méningé (syndrome) | n2=en:neuron loss | rel=r_associated | relid=0 | w=29
  741. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neuronal loss and gliosis in the cerebral cortex
    n1=méningé (syndrome) | n2=en:neuronal loss and gliosis in the cerebral cortex | rel=r_associated | relid=0 | w=29
  742. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients)
    n1=méningé (syndrome) | n2=en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients) | rel=r_associated | relid=0 | w=29
  743. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives
    n1=méningé (syndrome) | n2=en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives | rel=r_associated | relid=0 | w=29
  744. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neuronal migration disorder
    n1=méningé (syndrome) | n2=en:neuronal migration disorder | rel=r_associated | relid=0 | w=29
  745. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially)
    n1=méningé (syndrome) | n2=en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially) | rel=r_associated | relid=0 | w=29
  746. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:neuropsychologic cognitive abnormalities
    n1=méningé (syndrome) | n2=en:neuropsychologic cognitive abnormalities | rel=r_associated | relid=0 | w=29
  747. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:no sensory symptoms
    n1=méningé (syndrome) | n2=en:no sensory symptoms | rel=r_associated | relid=0 | w=29
  748. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:no speech development (in most patients)
    n1=méningé (syndrome) | n2=en:no speech development (in most patients) | rel=r_associated | relid=0 | w=29
  749. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:no speech problem
    n1=méningé (syndrome) | n2=en:no speech problem | rel=r_associated | relid=0 | w=29
  750. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:nocturnal occurrence, usually during light sleep
    n1=méningé (syndrome) | n2=en:nocturnal occurrence, usually during light sleep | rel=r_associated | relid=0 | w=29
  751. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:nodular heterotopia (rare)
    n1=méningé (syndrome) | n2=en:nodular heterotopia (rare) | rel=r_associated | relid=0 | w=29
  752. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:non-purposeful arm movements, choreoathetoid-like
    n1=méningé (syndrome) | n2=en:non-purposeful arm movements, choreoathetoid-like | rel=r_associated | relid=0 | w=29
  753. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:normal cognition (reported in some patients)
    n1=méningé (syndrome) | n2=en:normal cognition (reported in some patients) | rel=r_associated | relid=0 | w=29
  754. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:normal intelligence (in some patients)
    n1=méningé (syndrome) | n2=en:normal intelligence (in some patients) | rel=r_associated | relid=0 | w=29
  755. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:normal sleep-onset time (normal time of falling asleep)
    n1=méningé (syndrome) | n2=en:normal sleep-onset time (normal time of falling asleep) | rel=r_associated | relid=0 | w=29
  756. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:normal to mild mental retardation
    n1=méningé (syndrome) | n2=en:normal to mild mental retardation | rel=r_associated | relid=0 | w=29
  757. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:normal, timely language development
    n1=méningé (syndrome) | n2=en:normal, timely language development | rel=r_associated | relid=0 | w=29
  758. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:occipital meningocele (less common)
    n1=méningé (syndrome) | n2=en:occipital meningocele (less common) | rel=r_associated | relid=0 | w=29
  759. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:occipital myelomeningocele (less common)
    n1=méningé (syndrome) | n2=en:occipital myelomeningocele (less common) | rel=r_associated | relid=0 | w=29
  760. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:olfactory lobe agenesis
    n1=méningé (syndrome) | n2=en:olfactory lobe agenesis | rel=r_associated | relid=0 | w=29
  761. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:open operculum
    n1=méningé (syndrome) | n2=en:open operculum | rel=r_associated | relid=0 | w=29
  762. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:opisthotonos (type ii)
    n1=méningé (syndrome) | n2=en:opisthotonos (type ii) | rel=r_associated | relid=0 | w=29
  763. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:optic tract agenesis
    n1=méningé (syndrome) | n2=en:optic tract agenesis | rel=r_associated | relid=0 | w=29
  764. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:paraplegia
    n1=méningé (syndrome) | n2=en:paraplegia | rel=r_associated | relid=0 | w=29
  765. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:parenchymal neuromelanosis
    n1=méningé (syndrome) | n2=en:parenchymal neuromelanosis | rel=r_associated | relid=0 | w=29
  766. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:partial or total agenesis of the corpus callosum (33%)
    n1=méningé (syndrome) | n2=en:partial or total agenesis of the corpus callosum (33%) | rel=r_associated | relid=0 | w=29
  767. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:patients may have no structural abnormalities in the central nervous system
    n1=méningé (syndrome) | n2=en:patients may have no structural abnormalities in the central nervous system | rel=r_associated | relid=0 | w=29
  768. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:pediatric terminology
    n1=méningé (syndrome) | n2=en:pediatric terminology | rel=r_associated | relid=0 | w=29
  769. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:peripheral motor neuropathy
    n1=méningé (syndrome) | n2=en:peripheral motor neuropathy | rel=r_associated | relid=0 | w=29
  770. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:periventricular white matter lesions
    n1=méningé (syndrome) | n2=en:periventricular white matter lesions | rel=r_associated | relid=0 | w=29
  771. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:photoparoxysmal and photomyoclonic responses
    n1=méningé (syndrome) | n2=en:photoparoxysmal and photomyoclonic responses | rel=r_associated | relid=0 | w=29
  772. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:pituitary agenesis (rare)
    n1=méningé (syndrome) | n2=en:pituitary agenesis (rare) | rel=r_associated | relid=0 | w=29
  773. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:polymicrogyria (64%)
    n1=méningé (syndrome) | n2=en:polymicrogyria (64%) | rel=r_associated | relid=0 | w=29
  774. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:polymicrogyria, asymmetric or symmetric
    n1=méningé (syndrome) | n2=en:polymicrogyria, asymmetric or symmetric | rel=r_associated | relid=0 | w=29
  775. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:polymicrogyria, bilateral frontoparietal
    n1=méningé (syndrome) | n2=en:polymicrogyria, bilateral frontoparietal | rel=r_associated | relid=0 | w=29
  776. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:polymicrogyria, predominantly frontal and perisylvian
    n1=méningé (syndrome) | n2=en:polymicrogyria, predominantly frontal and perisylvian | rel=r_associated | relid=0 | w=29
  777. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:pontocerebellar arachnoid cyst (reported in 2 patients)
    n1=méningé (syndrome) | n2=en:pontocerebellar arachnoid cyst (reported in 2 patients) | rel=r_associated | relid=0 | w=29
  778. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:poor concentration
    n1=méningé (syndrome) | n2=en:poor concentration | rel=r_associated | relid=0 | w=29
  779. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:poor dendritic maturation
    n1=méningé (syndrome) | n2=en:poor dendritic maturation | rel=r_associated | relid=0 | w=29
  780. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:poor gross motor coordination
    n1=méningé (syndrome) | n2=en:poor gross motor coordination | rel=r_associated | relid=0 | w=29
  781. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:poor language
    n1=méningé (syndrome) | n2=en:poor language | rel=r_associated | relid=0 | w=29
  782. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:poor motor coordination
    n1=méningé (syndrome) | n2=en:poor motor coordination | rel=r_associated | relid=0 | w=29
  783. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:poor myelination
    n1=méningé (syndrome) | n2=en:poor myelination | rel=r_associated | relid=0 | w=29
  784. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:poor vestibuloocular reflex
    n1=méningé (syndrome) | n2=en:poor vestibuloocular reflex | rel=r_associated | relid=0 | w=29
  785. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:posterior column sensory loss
    n1=méningé (syndrome) | n2=en:posterior column sensory loss | rel=r_associated | relid=0 | w=29
  786. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:posterior fossa cyst continuous with the fourth ventricle
    n1=méningé (syndrome) | n2=en:posterior fossa cyst continuous with the fourth ventricle | rel=r_associated | relid=0 | w=29
  787. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:postural instability
    n1=méningé (syndrome) | n2=en:postural instability | rel=r_associated | relid=0 | w=29
  788. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:primitive reflex
    n1=méningé (syndrome) | n2=en:primitive reflex | rel=r_associated | relid=0 | w=29
  789. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:primitive reflexes (in some patients)
    n1=méningé (syndrome) | n2=en:primitive reflexes (in some patients) | rel=r_associated | relid=0 | w=29
  790. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:primitive sylvian fissures
    n1=méningé (syndrome) | n2=en:primitive sylvian fissures | rel=r_associated | relid=0 | w=29
  791. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:progressive cerebral atrophy seen on mri
    n1=méningé (syndrome) | n2=en:progressive cerebral atrophy seen on mri | rel=r_associated | relid=0 | w=29
  792. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:progressive spastic paraplegia
    n1=méningé (syndrome) | n2=en:progressive spastic paraplegia | rel=r_associated | relid=0 | w=29
  793. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:prominent perivascular spaces with surrounding gliosis in periatrial white matter
    n1=méningé (syndrome) | n2=en:prominent perivascular spaces with surrounding gliosis in periatrial white matter | rel=r_associated | relid=0 | w=29
  794. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:pseudotumor
    n1=méningé (syndrome) | n2=en:pseudotumor | rel=r_associated | relid=0 | w=29
  795. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:psychomotor agitation
    n1=méningé (syndrome) | n2=en:psychomotor agitation | rel=r_associated | relid=0 | w=29
  796. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:psychomotor regression
    n1=méningé (syndrome) | n2=en:psychomotor regression | rel=r_associated | relid=0 | w=29
  797. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:psychomotor regression, episodic, often associated with common childhood infections
    n1=méningé (syndrome) | n2=en:psychomotor regression, episodic, often associated with common childhood infections | rel=r_associated | relid=0 | w=29
  798. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:purposeless movements (if left untreated)
    n1=méningé (syndrome) | n2=en:purposeless movements (if left untreated) | rel=r_associated | relid=0 | w=29
  799. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:pyramidal features (rare)
    n1=méningé (syndrome) | n2=en:pyramidal features (rare) | rel=r_associated | relid=0 | w=29
  800. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:pyramidal signs (21% of patients)
    n1=méningé (syndrome) | n2=en:pyramidal signs (21% of patients) | rel=r_associated | relid=0 | w=29
  801. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:quadrupedal gait (palm of hands, legs straight) with diagonal walking
    n1=méningé (syndrome) | n2=en:quadrupedal gait (palm of hands, legs straight) with diagonal walking | rel=r_associated | relid=0 | w=29
  802. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:reduced sleep latency
    n1=méningé (syndrome) | n2=en:reduced sleep latency | rel=r_associated | relid=0 | w=29
  803. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:reflex, deep tendon, absent
    n1=méningé (syndrome) | n2=en:reflex, deep tendon, absent | rel=r_associated | relid=0 | w=29
  804. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:regression of development
    n1=méningé (syndrome) | n2=en:regression of development | rel=r_associated | relid=0 | w=29
  805. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:regression of motor development
    n1=méningé (syndrome) | n2=en:regression of motor development | rel=r_associated | relid=0 | w=29
  806. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:relative preservation of purkinje cells, but they are deformed and disaligned
    n1=méningé (syndrome) | n2=en:relative preservation of purkinje cells, but they are deformed and disaligned | rel=r_associated | relid=0 | w=29
  807. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:relative preservation of the cerebellum
    n1=méningé (syndrome) | n2=en:relative preservation of the cerebellum | rel=r_associated | relid=0 | w=29
  808. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:restlessness at birth
    n1=méningé (syndrome) | n2=en:restlessness at birth | rel=r_associated | relid=0 | w=29
  809. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:results in nocturnal insomnia and chronic sleep deprivation
    n1=méningé (syndrome) | n2=en:results in nocturnal insomnia and chronic sleep deprivation | rel=r_associated | relid=0 | w=29
  810. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:retrocerebellar cyst
    n1=méningé (syndrome) | n2=en:retrocerebellar cyst | rel=r_associated | relid=0 | w=29
  811. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:roentgenographic
    n1=méningé (syndrome) | n2=en:roentgenographic | rel=r_associated | relid=0 | w=29
  812. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:rudimentary white matter
    n1=méningé (syndrome) | n2=en:rudimentary white matter | rel=r_associated | relid=0 | w=29
  813. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:scant iron deposition in the brain (1 family)
    n1=méningé (syndrome) | n2=en:scant iron deposition in the brain (1 family) | rel=r_associated | relid=0 | w=29
  814. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:secondary generalization may occur
    n1=méningé (syndrome) | n2=en:secondary generalization may occur | rel=r_associated | relid=0 | w=29
  815. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:secondary generalization occurs in about 33% of patients
    n1=méningé (syndrome) | n2=en:secondary generalization occurs in about 33% of patients | rel=r_associated | relid=0 | w=29
  816. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:seizure
    n1=méningé (syndrome) | n2=en:seizure | rel=r_associated | relid=0 | w=29
  817. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:seizures (eclampsia)
    n1=méningé (syndrome) | n2=en:seizures (eclampsia) | rel=r_associated | relid=0 | w=29
  818. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:seizures (in some)
    n1=méningé (syndrome) | n2=en:seizures (in some) | rel=r_associated | relid=0 | w=29
  819. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:seizures (rare, in males)
    n1=méningé (syndrome) | n2=en:seizures (rare, in males) | rel=r_associated | relid=0 | w=29
  820. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:seizures affect the vocal cords, lips, mouth, and face
    n1=méningé (syndrome) | n2=en:seizures affect the vocal cords, lips, mouth, and face | rel=r_associated | relid=0 | w=29
  821. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:seizures are poorly controlled
    n1=méningé (syndrome) | n2=en:seizures are poorly controlled | rel=r_associated | relid=0 | w=29
  822. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:seizures occur multiple times per day
    n1=méningé (syndrome) | n2=en:seizures occur multiple times per day | rel=r_associated | relid=0 | w=29
  823. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:seizures, infantile-onset
    n1=méningé (syndrome) | n2=en:seizures, infantile-onset | rel=r_associated | relid=0 | w=29
  824. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:severe expressive language delay
    n1=méningé (syndrome) | n2=en:severe expressive language delay | rel=r_associated | relid=0 | w=29
  825. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:simple partial seizures with secondary generalization
    n1=méningé (syndrome) | n2=en:simple partial seizures with secondary generalization | rel=r_associated | relid=0 | w=29
  826. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:simplified gyral pattern (in one patient)
    n1=méningé (syndrome) | n2=en:simplified gyral pattern (in one patient) | rel=r_associated | relid=0 | w=29
  827. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:skin photosensitivity
    n1=méningé (syndrome) | n2=en:skin photosensitivity | rel=r_associated | relid=0 | w=29
  828. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:sleep disorder (rare)
    n1=méningé (syndrome) | n2=en:sleep disorder (rare) | rel=r_associated | relid=0 | w=29
  829. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:sleep impairment, progressive
    n1=méningé (syndrome) | n2=en:sleep impairment, progressive | rel=r_associated | relid=0 | w=29
  830. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:sleep pattern disturbance
    n1=méningé (syndrome) | n2=en:sleep pattern disturbance | rel=r_associated | relid=0 | w=29
  831. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:sleep talking
    n1=méningé (syndrome) | n2=en:sleep talking | rel=r_associated | relid=0 | w=29
  832. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration
    n1=méningé (syndrome) | n2=en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration | rel=r_associated | relid=0 | w=29
  833. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:small but structurally normal cerebral cortex
    n1=méningé (syndrome) | n2=en:small but structurally normal cerebral cortex | rel=r_associated | relid=0 | w=29
  834. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:small shrunken brain
    n1=méningé (syndrome) | n2=en:small shrunken brain | rel=r_associated | relid=0 | w=29
  835. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:small size of the left hippocampus gyri
    n1=méningé (syndrome) | n2=en:small size of the left hippocampus gyri | rel=r_associated | relid=0 | w=29
  836. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:sparing of optic tracts
    n1=méningé (syndrome) | n2=en:sparing of optic tracts | rel=r_associated | relid=0 | w=29
  837. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:spastic quadriplegia
    n1=méningé (syndrome) | n2=en:spastic quadriplegia | rel=r_associated | relid=0 | w=29
  838. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:spastic quadriplegia, severe
    n1=méningé (syndrome) | n2=en:spastic quadriplegia, severe | rel=r_associated | relid=0 | w=29
  839. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:spasticity (later onset)
    n1=méningé (syndrome) | n2=en:spasticity (later onset) | rel=r_associated | relid=0 | w=29
  840. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:spasticity, primarily lower limbs, but upper limbs may be involved
    n1=méningé (syndrome) | n2=en:spasticity, primarily lower limbs, but upper limbs may be involved | rel=r_associated | relid=0 | w=29
  841. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:spasticity, severe
    n1=méningé (syndrome) | n2=en:spasticity, severe | rel=r_associated | relid=0 | w=29
  842. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:spasticity/paresis (rare)
    n1=méningé (syndrome) | n2=en:spasticity/paresis (rare) | rel=r_associated | relid=0 | w=29
  843. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:specific visual spatial processing defect
    n1=méningé (syndrome) | n2=en:specific visual spatial processing defect | rel=r_associated | relid=0 | w=29
  844. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:speech and language disorder
    n1=méningé (syndrome) | n2=en:speech and language disorder | rel=r_associated | relid=0 | w=29
  845. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:speech delay (10%)
    n1=méningé (syndrome) | n2=en:speech delay (10%) | rel=r_associated | relid=0 | w=29
  846. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:speech delay (59%)
    n1=méningé (syndrome) | n2=en:speech delay (59%) | rel=r_associated | relid=0 | w=29
  847. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:speech disorders (rare)
    n1=méningé (syndrome) | n2=en:speech disorders (rare) | rel=r_associated | relid=0 | w=29
  848. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:speech severely limited or absent
    n1=méningé (syndrome) | n2=en:speech severely limited or absent | rel=r_associated | relid=0 | w=29
  849. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:speech, limited or nonverbal
    n1=méningé (syndrome) | n2=en:speech, limited or nonverbal | rel=r_associated | relid=0 | w=29
  850. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:spinal cord disorder
    n1=méningé (syndrome) | n2=en:spinal cord disorder | rel=r_associated | relid=0 | w=29
  851. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:spinal cord meningioma
    n1=méningé (syndrome) | n2=en:spinal cord meningioma | rel=r_associated | relid=0 | w=29
  852. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:stimulation sensitive segmental myoclonus (stage 2)
    n1=méningé (syndrome) | n2=en:stimulation sensitive segmental myoclonus (stage 2) | rel=r_associated | relid=0 | w=29
  853. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:stroke-like episodes
    n1=méningé (syndrome) | n2=en:stroke-like episodes | rel=r_associated | relid=0 | w=29
  854. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:subcortical band or laminar heterotopia (in female carriers)
    n1=méningé (syndrome) | n2=en:subcortical band or laminar heterotopia (in female carriers) | rel=r_associated | relid=0 | w=29
  855. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:subcortical nodular grey matter heterotopia
    n1=méningé (syndrome) | n2=en:subcortical nodular grey matter heterotopia | rel=r_associated | relid=0 | w=29
  856. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:subnormal cognition
    n1=méningé (syndrome) | n2=en:subnormal cognition | rel=r_associated | relid=0 | w=29
  857. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:suppression-burst pattern see on eeg
    n1=méningé (syndrome) | n2=en:suppression-burst pattern see on eeg | rel=r_associated | relid=0 | w=29
  858. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:supranuclear gaze palsy
    n1=méningé (syndrome) | n2=en:supranuclear gaze palsy | rel=r_associated | relid=0 | w=29
  859. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:sweating problem
    n1=méningé (syndrome) | n2=en:sweating problem | rel=r_associated | relid=0 | w=29
  860. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:swelling of the cerebral white matter
    n1=méningé (syndrome) | n2=en:swelling of the cerebral white matter | rel=r_associated | relid=0 | w=29
  861. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri | rel=r_associated | relid=0 | w=29
  862. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:t2-weighted hyperintensities in the corticospinal tracts and posterior arms of the internal capsule in older patients seen on mri
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintensities in the corticospinal tracts and posterior arms of the internal capsule in older patients seen on mri | rel=r_associated | relid=0 | w=29
  863. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:t2-weighted hyperintensities in the putamen and caudate nuclei
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintensities in the putamen and caudate nuclei | rel=r_associated | relid=0 | w=29
  864. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:tbp- and 1c2-immunoreactive neuronal inclusions
    n1=méningé (syndrome) | n2=en:tbp- and 1c2-immunoreactive neuronal inclusions | rel=r_associated | relid=0 | w=29
  865. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:tectal enlargement
    n1=méningé (syndrome) | n2=en:tectal enlargement | rel=r_associated | relid=0 | w=29
  866. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:temporal lobe seizures (in 1 patient)
    n1=méningé (syndrome) | n2=en:temporal lobe seizures (in 1 patient) | rel=r_associated | relid=0 | w=29
  867. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:tetany, hypocalcemic (in some patients)
    n1=méningé (syndrome) | n2=en:tetany, hypocalcemic (in some patients) | rel=r_associated | relid=0 | w=29
  868. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:thick, maloriented superior cerebellar peduncles
    n1=méningé (syndrome) | n2=en:thick, maloriented superior cerebellar peduncles | rel=r_associated | relid=0 | w=29
  869. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:thickened optic nerve sheath
    n1=méningé (syndrome) | n2=en:thickened optic nerve sheath | rel=r_associated | relid=0 | w=29
  870. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:thin corpus callosum (1/4 patients)
    n1=méningé (syndrome) | n2=en:thin corpus callosum (1/4 patients) | rel=r_associated | relid=0 | w=29
  871. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:thin cortical mantle (wws)
    n1=méningé (syndrome) | n2=en:thin cortical mantle (wws) | rel=r_associated | relid=0 | w=29
  872. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:thin optic chiasm
    n1=méningé (syndrome) | n2=en:thin optic chiasm | rel=r_associated | relid=0 | w=29
  873. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:thinning of the cerebellopontine tracts
    n1=méningé (syndrome) | n2=en:thinning of the cerebellopontine tracts | rel=r_associated | relid=0 | w=29
  874. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:tonic convulsion
    n1=méningé (syndrome) | n2=en:tonic convulsion | rel=r_associated | relid=0 | w=29
  875. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:touch, vibration, and limb position may or may not be affected
    n1=méningé (syndrome) | n2=en:touch, vibration, and limb position may or may not be affected | rel=r_associated | relid=0 | w=29
  876. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:transitional facial palsy (15%)
    n1=méningé (syndrome) | n2=en:transitional facial palsy (15%) | rel=r_associated | relid=0 | w=29
  877. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:tremor (1 patient)
    n1=méningé (syndrome) | n2=en:tremor (1 patient) | rel=r_associated | relid=0 | w=29
  878. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:tremor of the upper limb
    n1=méningé (syndrome) | n2=en:tremor of the upper limb | rel=r_associated | relid=0 | w=29
  879. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:tremor, variable
    n1=méningé (syndrome) | n2=en:tremor, variable | rel=r_associated | relid=0 | w=29
  880. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:tremors, action
    n1=méningé (syndrome) | n2=en:tremors, action | rel=r_associated | relid=0 | w=29
  881. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:truncal ataxia, mild
    n1=méningé (syndrome) | n2=en:truncal ataxia, mild | rel=r_associated | relid=0 | w=29
  882. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:ubiquitin-positive intranuclear neuronal inclusions
    n1=méningé (syndrome) | n2=en:ubiquitin-positive intranuclear neuronal inclusions | rel=r_associated | relid=0 | w=29
  883. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:unintelligible speech, vocalizations, grunting
    n1=méningé (syndrome) | n2=en:unintelligible speech, vocalizations, grunting | rel=r_associated | relid=0 | w=29
  884. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:unstable, ataxic gait
    n1=méningé (syndrome) | n2=en:unstable, ataxic gait | rel=r_associated | relid=0 | w=29
  885. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:upper limb involvement may occur
    n1=méningé (syndrome) | n2=en:upper limb involvement may occur | rel=r_associated | relid=0 | w=29
  886. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:upper limbs may be affected
    n1=méningé (syndrome) | n2=en:upper limbs may be affected | rel=r_associated | relid=0 | w=29
  887. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:upper motor neuron dysfunction
    n1=méningé (syndrome) | n2=en:upper motor neuron dysfunction | rel=r_associated | relid=0 | w=29
  888. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:upper motor neuron signs (in some patients)
    n1=méningé (syndrome) | n2=en:upper motor neuron signs (in some patients) | rel=r_associated | relid=0 | w=29
  889. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:vacuolization (patient a)
    n1=méningé (syndrome) | n2=en:vacuolization (patient a) | rel=r_associated | relid=0 | w=29
  890. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:variable delay (iq range 52-104)
    n1=méningé (syndrome) | n2=en:variable delay (iq range 52-104) | rel=r_associated | relid=0 | w=29
  891. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation
    n1=méningé (syndrome) | n2=en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation | rel=r_associated | relid=0 | w=29
  892. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:varying degree of mental retardation
    n1=méningé (syndrome) | n2=en:varying degree of mental retardation | rel=r_associated | relid=0 | w=29
  893. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:vcp-positive inclusions
    n1=méningé (syndrome) | n2=en:vcp-positive inclusions | rel=r_associated | relid=0 | w=29
  894. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:ventriculomeglia
    n1=méningé (syndrome) | n2=en:ventriculomeglia | rel=r_associated | relid=0 | w=29
  895. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:vestibular dysfunction, mild
    n1=méningé (syndrome) | n2=en:vestibular dysfunction, mild | rel=r_associated | relid=0 | w=29
  896. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:visuospatial agnosia (in a subset of patients)
    n1=méningé (syndrome) | n2=en:visuospatial agnosia (in a subset of patients) | rel=r_associated | relid=0 | w=29
  897. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:white matter abnormalities on mri
    n1=méningé (syndrome) | n2=en:white matter abnormalities on mri | rel=r_associated | relid=0 | w=29
  898. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts
    n1=méningé (syndrome) | n2=en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts | rel=r_associated | relid=0 | w=29
  899. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:white matter immaturity
    n1=méningé (syndrome) | n2=en:white matter immaturity | rel=r_associated | relid=0 | w=29
  900. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:white matter lesions may occur in the thalami, basal ganglia, and periventricular white matter (see leigh syndrome, 256000)
    n1=méningé (syndrome) | n2=en:white matter lesions may occur in the thalami, basal ganglia, and periventricular white matter (see leigh syndrome, 256000) | rel=r_associated | relid=0 | w=29
  901. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:white matter rarefaction and cystic degeneration
    n1=méningé (syndrome) | n2=en:white matter rarefaction and cystic degeneration | rel=r_associated | relid=0 | w=29
  902. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:white matter streaks
    n1=méningé (syndrome) | n2=en:white matter streaks | rel=r_associated | relid=0 | w=29
  903. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> en:widened lateral ventricles
    n1=méningé (syndrome) | n2=en:widened lateral ventricles | rel=r_associated | relid=0 | w=29
  904. méningé (syndrome) -- r_associated #0: 29 / 0.349 -> méningiomes multiples
    n1=méningé (syndrome) | n2=méningiomes multiples | rel=r_associated | relid=0 | w=29
  905. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:3-6 hz polyspike eeg
    n1=méningé (syndrome) | n2=en:3-6 hz polyspike eeg | rel=r_associated | relid=0 | w=28
  906. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:abnormal cell orientation
    n1=méningé (syndrome) | n2=en:abnormal cell orientation | rel=r_associated | relid=0 | w=28
  907. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:abnormal eeg (poor alpha rhythms)
    n1=méningé (syndrome) | n2=en:abnormal eeg (poor alpha rhythms) | rel=r_associated | relid=0 | w=28
  908. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:abnormal eeg with epileptiform changes
    n1=méningé (syndrome) | n2=en:abnormal eeg with epileptiform changes | rel=r_associated | relid=0 | w=28
  909. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:abnormal rapid eye movement sleep
    n1=méningé (syndrome) | n2=en:abnormal rapid eye movement sleep | rel=r_associated | relid=0 | w=28
  910. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:abnormality of the corpus callosum
    n1=méningé (syndrome) | n2=en:abnormality of the corpus callosum | rel=r_associated | relid=0 | w=28
  911. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:absence of neuropathologic findings in the brainstem and anterior horn cells
    n1=méningé (syndrome) | n2=en:absence of neuropathologic findings in the brainstem and anterior horn cells | rel=r_associated | relid=0 | w=28
  912. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:absence of the inferior olives
    n1=méningé (syndrome) | n2=en:absence of the inferior olives | rel=r_associated | relid=0 | w=28
  913. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:absence of the olfactory bulbs and tracts
    n1=méningé (syndrome) | n2=en:absence of the olfactory bulbs and tracts | rel=r_associated | relid=0 | w=28
  914. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:absent or poor expressive speech
    n1=méningé (syndrome) | n2=en:absent or poor expressive speech | rel=r_associated | relid=0 | w=28
  915. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:action myoclonus (triggered by voluntary movements)
    n1=méningé (syndrome) | n2=en:action myoclonus (triggered by voluntary movements) | rel=r_associated | relid=0 | w=28
  916. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:acute episodes of neuropathic symptoms (hcp)
    n1=méningé (syndrome) | n2=en:acute episodes of neuropathic symptoms (hcp) | rel=r_associated | relid=0 | w=28
  917. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:adult grade i meningioma
    n1=méningé (syndrome) | n2=en:adult grade i meningioma | rel=r_associated | relid=0 | w=28
  918. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:adult meningioma
    n1=méningé (syndrome) | n2=en:adult meningioma | rel=r_associated | relid=0 | w=28
  919. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:agitation
    n1=méningé (syndrome) | n2=en:agitation | rel=r_associated | relid=0 | w=28
  920. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:anaplastic (malignant) meningioma
    n1=méningé (syndrome) | n2=en:anaplastic (malignant) meningioma | rel=r_associated | relid=0 | w=28
  921. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:anosmia (in contiguous gene syndrome patients)
    n1=méningé (syndrome) | n2=en:anosmia (in contiguous gene syndrome patients) | rel=r_associated | relid=0 | w=28
  922. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:aplasia of olfactory bulbs, bilateral
    n1=méningé (syndrome) | n2=en:aplasia of olfactory bulbs, bilateral | rel=r_associated | relid=0 | w=28
  923. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:aplasia/hypoplasia of the cerebellar vermis
    n1=méningé (syndrome) | n2=en:aplasia/hypoplasia of the cerebellar vermis | rel=r_associated | relid=0 | w=28
  924. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:aplasia/hypoplasia of the cerebellum
    n1=méningé (syndrome) | n2=en:aplasia/hypoplasia of the cerebellum | rel=r_associated | relid=0 | w=28
  925. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ataxia (early-onset form)
    n1=méningé (syndrome) | n2=en:ataxia (early-onset form) | rel=r_associated | relid=0 | w=28
  926. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ataxia, cerebellar (in some patients)
    n1=méningé (syndrome) | n2=en:ataxia, cerebellar (in some patients) | rel=r_associated | relid=0 | w=28
  927. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ataxia, episodic, occurring after febrile illness or stress
    n1=méningé (syndrome) | n2=en:ataxia, episodic, occurring after febrile illness or stress | rel=r_associated | relid=0 | w=28
  928. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:atrophy of the pituitary (1 patient)
    n1=méningé (syndrome) | n2=en:atrophy of the pituitary (1 patient) | rel=r_associated | relid=0 | w=28
  929. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:atrophy of the pons (in some patients)
    n1=méningé (syndrome) | n2=en:atrophy of the pons (in some patients) | rel=r_associated | relid=0 | w=28
  930. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:attacks characterized by lethargy, incoordination, loss of motor skills
    n1=méningé (syndrome) | n2=en:attacks characterized by lethargy, incoordination, loss of motor skills | rel=r_associated | relid=0 | w=28
  931. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:attention deficit disorder
    n1=méningé (syndrome) | n2=en:attention deficit disorder | rel=r_associated | relid=0 | w=28
  932. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:automatism
    n1=méningé (syndrome) | n2=en:automatism | rel=r_associated | relid=0 | w=28
  933. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:axial dystonia
    n1=méningé (syndrome) | n2=en:axial dystonia | rel=r_associated | relid=0 | w=28
  934. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:axonal dystrophy (in some patients)
    n1=méningé (syndrome) | n2=en:axonal dystrophy (in some patients) | rel=r_associated | relid=0 | w=28
  935. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:band heterotopia (1 patient)
    n1=méningé (syndrome) | n2=en:band heterotopia (1 patient) | rel=r_associated | relid=0 | w=28
  936. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:basal ganglia calcifications (rare)
    n1=méningé (syndrome) | n2=en:basal ganglia calcifications (rare) | rel=r_associated | relid=0 | w=28
  937. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:basal ganglia dysfunction
    n1=méningé (syndrome) | n2=en:basal ganglia dysfunction | rel=r_associated | relid=0 | w=28
  938. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas
    n1=méningé (syndrome) | n2=en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas | rel=r_associated | relid=0 | w=28
  939. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:brain abscess
    n1=méningé (syndrome) | n2=en:brain abscess | rel=r_associated | relid=0 | w=28
  940. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:brain mri shows diffusion abnormalities
    n1=méningé (syndrome) | n2=en:brain mri shows diffusion abnormalities | rel=r_associated | relid=0 | w=28
  941. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:brain mri shows signal abnormalities in the basal ganglia
    n1=méningé (syndrome) | n2=en:brain mri shows signal abnormalities in the basal ganglia | rel=r_associated | relid=0 | w=28
  942. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:brain mrs shows decreased creatine content
    n1=méningé (syndrome) | n2=en:brain mrs shows decreased creatine content | rel=r_associated | relid=0 | w=28
  943. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:brainstem concavity
    n1=méningé (syndrome) | n2=en:brainstem concavity | rel=r_associated | relid=0 | w=28
  944. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:brainstem white matter lesions
    n1=méningé (syndrome) | n2=en:brainstem white matter lesions | rel=r_associated | relid=0 | w=28
  945. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:brisk knee reflexes (early-on)
    n1=méningé (syndrome) | n2=en:brisk knee reflexes (early-on) | rel=r_associated | relid=0 | w=28
  946. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:bulbar dysfunction
    n1=méningé (syndrome) | n2=en:bulbar dysfunction | rel=r_associated | relid=0 | w=28
  947. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:bulbar dysfunction (in some patients)
    n1=méningé (syndrome) | n2=en:bulbar dysfunction (in some patients) | rel=r_associated | relid=0 | w=28
  948. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:bulging of the caudate nuclei
    n1=méningé (syndrome) | n2=en:bulging of the caudate nuclei | rel=r_associated | relid=0 | w=28
  949. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:calcification of the amygdala and the amygdala-hippocampal transition area
    n1=méningé (syndrome) | n2=en:calcification of the amygdala and the amygdala-hippocampal transition area | rel=r_associated | relid=0 | w=28
  950. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:candidal meningitis (in some patients)
    n1=méningé (syndrome) | n2=en:candidal meningitis (in some patients) | rel=r_associated | relid=0 | w=28
  951. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cell loss and gliosis in the basal ganglia
    n1=méningé (syndrome) | n2=en:cell loss and gliosis in the basal ganglia | rel=r_associated | relid=0 | w=28
  952. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:central canal malformation
    n1=méningé (syndrome) | n2=en:central canal malformation | rel=r_associated | relid=0 | w=28
  953. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebellar atrophy, mild (1 patient)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, mild (1 patient) | rel=r_associated | relid=0 | w=28
  954. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebellar atrophy, particularly of the hemispheres
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, particularly of the hemispheres | rel=r_associated | relid=0 | w=28
  955. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebellar cyst
    n1=méningé (syndrome) | n2=en:cerebellar cyst | rel=r_associated | relid=0 | w=28
  956. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebellar hypoplasia (seen in hhs variant)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (seen in hhs variant) | rel=r_associated | relid=0 | w=28
  957. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebellar signs during episodes
    n1=méningé (syndrome) | n2=en:cerebellar signs during episodes | rel=r_associated | relid=0 | w=28
  958. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebellar tonsillar herniation
    n1=méningé (syndrome) | n2=en:cerebellar tonsillar herniation | rel=r_associated | relid=0 | w=28
  959. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebellar white matter lesions on mri
    n1=méningé (syndrome) | n2=en:cerebellar white matter lesions on mri | rel=r_associated | relid=0 | w=28
  960. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebral and cerebellar atrophy
    n1=méningé (syndrome) | n2=en:cerebral and cerebellar atrophy | rel=r_associated | relid=0 | w=28
  961. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebral atrophy, generalized mild
    n1=méningé (syndrome) | n2=en:cerebral atrophy, generalized mild | rel=r_associated | relid=0 | w=28
  962. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebral cavernous malformation
    n1=méningé (syndrome) | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=28
  963. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebral palsy
    n1=méningé (syndrome) | n2=en:cerebral palsy | rel=r_associated | relid=0 | w=28
  964. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cerebral white matter lesions (1 patient)
    n1=méningé (syndrome) | n2=en:cerebral white matter lesions (1 patient) | rel=r_associated | relid=0 | w=28
  965. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:chiari i malformation of the cerebellum (in some patients)
    n1=méningé (syndrome) | n2=en:chiari i malformation of the cerebellum (in some patients) | rel=r_associated | relid=0 | w=28
  966. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:chiari malformation (uncommon)
    n1=méningé (syndrome) | n2=en:chiari malformation (uncommon) | rel=r_associated | relid=0 | w=28
  967. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:chiari type i
    n1=méningé (syndrome) | n2=en:chiari type i | rel=r_associated | relid=0 | w=28
  968. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:chiari type i malformation (in some patients)
    n1=méningé (syndrome) | n2=en:chiari type i malformation (in some patients) | rel=r_associated | relid=0 | w=28
  969. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:childhood meningioma
    n1=méningé (syndrome) | n2=en:childhood meningioma | rel=r_associated | relid=0 | w=28
  970. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:choreoathetosis
    n1=méningé (syndrome) | n2=en:choreoathetosis | rel=r_associated | relid=0 | w=28
  971. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:choroid plexus meningioma
    n1=méningé (syndrome) | n2=en:choroid plexus meningioma | rel=r_associated | relid=0 | w=28
  972. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:chronic headaches
    n1=méningé (syndrome) | n2=en:chronic headaches | rel=r_associated | relid=0 | w=28
  973. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:clumsiness
    n1=méningé (syndrome) | n2=en:clumsiness | rel=r_associated | relid=0 | w=28
  974. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cognition is spared
    n1=méningé (syndrome) | n2=en:cognition is spared | rel=r_associated | relid=0 | w=28
  975. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cognitive decline in adulthood
    n1=méningé (syndrome) | n2=en:cognitive decline in adulthood | rel=r_associated | relid=0 | w=28
  976. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cognitive decline in older patients
    n1=méningé (syndrome) | n2=en:cognitive decline in older patients | rel=r_associated | relid=0 | w=28
  977. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cognitive delay, mild (1 patient)
    n1=méningé (syndrome) | n2=en:cognitive delay, mild (1 patient) | rel=r_associated | relid=0 | w=28
  978. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cognitive delay, mild to severe
    n1=méningé (syndrome) | n2=en:cognitive delay, mild to severe | rel=r_associated | relid=0 | w=28
  979. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cognitive impairment, mild to severe
    n1=méningé (syndrome) | n2=en:cognitive impairment, mild to severe | rel=r_associated | relid=0 | w=28
  980. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cognitive regression, mild
    n1=méningé (syndrome) | n2=en:cognitive regression, mild | rel=r_associated | relid=0 | w=28
  981. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:coma (less common)
    n1=méningé (syndrome) | n2=en:coma (less common) | rel=r_associated | relid=0 | w=28
  982. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:complex partial seizures (in some patients)
    n1=méningé (syndrome) | n2=en:complex partial seizures (in some patients) | rel=r_associated | relid=0 | w=28
  983. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:congenital hyperextension of limb
    n1=méningé (syndrome) | n2=en:congenital hyperextension of limb | rel=r_associated | relid=0 | w=28
  984. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:corprolalia
    n1=méningé (syndrome) | n2=en:corprolalia | rel=r_associated | relid=0 | w=28
  985. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cortical cytotoxic edema
    n1=méningé (syndrome) | n2=en:cortical cytotoxic edema | rel=r_associated | relid=0 | w=28
  986. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cortical myoclonic tremors characterized by 8 to 10-hz discharges
    n1=méningé (syndrome) | n2=en:cortical myoclonic tremors characterized by 8 to 10-hz discharges | rel=r_associated | relid=0 | w=28
  987. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cortical origin of the tremor
    n1=méningé (syndrome) | n2=en:cortical origin of the tremor | rel=r_associated | relid=0 | w=28
  988. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:corticobasal degeneration (in some patients)
    n1=méningé (syndrome) | n2=en:corticobasal degeneration (in some patients) | rel=r_associated | relid=0 | w=28
  989. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:corticospinal tracts with decreased myelin staining
    n1=méningé (syndrome) | n2=en:corticospinal tracts with decreased myelin staining | rel=r_associated | relid=0 | w=28
  990. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cranial nerve palsies can arise with head and neck paragangliomas
    n1=méningé (syndrome) | n2=en:cranial nerve palsies can arise with head and neck paragangliomas | rel=r_associated | relid=0 | w=28
  991. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cystic degeneration of cerebral white matter with preserved cortex
    n1=méningé (syndrome) | n2=en:cystic degeneration of cerebral white matter with preserved cortex | rel=r_associated | relid=0 | w=28
  992. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:cystic lysis of the deep white matter
    n1=méningé (syndrome) | n2=en:cystic lysis of the deep white matter | rel=r_associated | relid=0 | w=28
  993. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dandy-walker malformation (variable)
    n1=méningé (syndrome) | n2=en:dandy-walker malformation (variable) | rel=r_associated | relid=0 | w=28
  994. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dandy-walker malformation (wws)
    n1=méningé (syndrome) | n2=en:dandy-walker malformation (wws) | rel=r_associated | relid=0 | w=28
  995. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:decreased iron content in the substantia nigra
    n1=méningé (syndrome) | n2=en:decreased iron content in the substantia nigra | rel=r_associated | relid=0 | w=28
  996. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:decreased nonverbal iq
    n1=méningé (syndrome) | n2=en:decreased nonverbal iq | rel=r_associated | relid=0 | w=28
  997. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:decreased somatosensory-evoked potentials
    n1=méningé (syndrome) | n2=en:decreased somatosensory-evoked potentials | rel=r_associated | relid=0 | w=28
  998. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:decreased vibratory sense
    n1=méningé (syndrome) | n2=en:decreased vibratory sense | rel=r_associated | relid=0 | w=28
  999. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:deficit in expressive language
    n1=méningé (syndrome) | n2=en:deficit in expressive language | rel=r_associated | relid=0 | w=28
  1000. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:deficits in language expression
    n1=méningé (syndrome) | n2=en:deficits in language expression | rel=r_associated | relid=0 | w=28
  1001. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:degeneration of the dentatorubral and pallidoluysian systems
    n1=méningé (syndrome) | n2=en:degeneration of the dentatorubral and pallidoluysian systems | rel=r_associated | relid=0 | w=28
  1002. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:degeneration of the lateral corticospinal tracts
    n1=méningé (syndrome) | n2=en:degeneration of the lateral corticospinal tracts | rel=r_associated | relid=0 | w=28
  1003. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:delayed cognitive development/learning disabilities (93%)
    n1=méningé (syndrome) | n2=en:delayed cognitive development/learning disabilities (93%) | rel=r_associated | relid=0 | w=28
  1004. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:delayed development (in some)
    n1=méningé (syndrome) | n2=en:delayed development (in some) | rel=r_associated | relid=0 | w=28
  1005. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:delayed developmental milestones
    n1=méningé (syndrome) | n2=en:delayed developmental milestones | rel=r_associated | relid=0 | w=28
  1006. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:delayed motor development due to muscle weakness
    n1=méningé (syndrome) | n2=en:delayed motor development due to muscle weakness | rel=r_associated | relid=0 | w=28
  1007. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:delayed onset of phrase speech (> 36 months)
    n1=méningé (syndrome) | n2=en:delayed onset of phrase speech (> 36 months) | rel=r_associated | relid=0 | w=28
  1008. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:delayed psychomotor development (in most patients)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development (in most patients) | rel=r_associated | relid=0 | w=28
  1009. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:delayed psychomotor development (in some)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development (in some) | rel=r_associated | relid=0 | w=28
  1010. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:delayed speech and language development
    n1=méningé (syndrome) | n2=en:delayed speech and language development | rel=r_associated | relid=0 | w=28
  1011. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:deletion of chromosome 3p associated meningioma
    n1=méningé (syndrome) | n2=en:deletion of chromosome 3p associated meningioma | rel=r_associated | relid=0 | w=28
  1012. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:delirium (later-onset)
    n1=méningé (syndrome) | n2=en:delirium (later-onset) | rel=r_associated | relid=0 | w=28
  1013. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:demyelination with white matter disease in internal capsule, external capsule, genu of corpus callosum, subcortical white matter, and posterior fossa
    n1=méningé (syndrome) | n2=en:demyelination with white matter disease in internal capsule, external capsule, genu of corpus callosum, subcortical white matter, and posterior fossa | rel=r_associated | relid=0 | w=28
  1014. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:demyelination, symmetric
    n1=méningé (syndrome) | n2=en:demyelination, symmetric | rel=r_associated | relid=0 | w=28
  1015. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:developmental delay (20%)
    n1=méningé (syndrome) | n2=en:developmental delay (20%) | rel=r_associated | relid=0 | w=28
  1016. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:developmental delay, primarily motor, resolves in childhood
    n1=méningé (syndrome) | n2=en:developmental delay, primarily motor, resolves in childhood | rel=r_associated | relid=0 | w=28
  1017. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:developmental delay, profound
    n1=méningé (syndrome) | n2=en:developmental delay, profound | rel=r_associated | relid=0 | w=28
  1018. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:developmental delay, progressive
    n1=méningé (syndrome) | n2=en:developmental delay, progressive | rel=r_associated | relid=0 | w=28
  1019. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:developmental regression (in some patients)
    n1=méningé (syndrome) | n2=en:developmental regression (in some patients) | rel=r_associated | relid=0 | w=28
  1020. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:difficulty reading
    n1=méningé (syndrome) | n2=en:difficulty reading | rel=r_associated | relid=0 | w=28
  1021. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:difficulty running
    n1=méningé (syndrome) | n2=en:difficulty running | rel=r_associated | relid=0 | w=28
  1022. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:difficulty standing alone
    n1=méningé (syndrome) | n2=en:difficulty standing alone | rel=r_associated | relid=0 | w=28
  1023. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:diffuse axonal swelling
    n1=méningé (syndrome) | n2=en:diffuse axonal swelling | rel=r_associated | relid=0 | w=28
  1024. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:diffuse brain and spinal cord atrophy on brain ct/mri
    n1=méningé (syndrome) | n2=en:diffuse brain and spinal cord atrophy on brain ct/mri | rel=r_associated | relid=0 | w=28
  1025. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:diffuse cerebral atrophy seen on mri
    n1=méningé (syndrome) | n2=en:diffuse cerebral atrophy seen on mri | rel=r_associated | relid=0 | w=28
  1026. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:diffuse fibrillar astrocytosis (in type iib)
    n1=méningé (syndrome) | n2=en:diffuse fibrillar astrocytosis (in type iib) | rel=r_associated | relid=0 | w=28
  1027. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:diffuse white matter hyperintensities on t2-weighed imaging
    n1=méningé (syndrome) | n2=en:diffuse white matter hyperintensities on t2-weighed imaging | rel=r_associated | relid=0 | w=28
  1028. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dilated venous sinuses
    n1=méningé (syndrome) | n2=en:dilated venous sinuses | rel=r_associated | relid=0 | w=28
  1029. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:disorientation
    n1=méningé (syndrome) | n2=en:disorientation | rel=r_associated | relid=0 | w=28
  1030. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:disproportionately small cerebral cortex
    n1=méningé (syndrome) | n2=en:disproportionately small cerebral cortex | rel=r_associated | relid=0 | w=28
  1031. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:double cortex syndrome
    n1=méningé (syndrome) | n2=en:double cortex syndrome | rel=r_associated | relid=0 | w=28
  1032. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dysarthria (less common)
    n1=méningé (syndrome) | n2=en:dysarthria (less common) | rel=r_associated | relid=0 | w=28
  1033. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dysarthria (most common presenting symptom)
    n1=méningé (syndrome) | n2=en:dysarthria (most common presenting symptom) | rel=r_associated | relid=0 | w=28
  1034. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dysarthria (onset in third decade)
    n1=méningé (syndrome) | n2=en:dysarthria (onset in third decade) | rel=r_associated | relid=0 | w=28
  1035. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dysphonia
    n1=méningé (syndrome) | n2=en:dysphonia | rel=r_associated | relid=0 | w=28
  1036. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dysplasia of the cerebellar hemispheres
    n1=méningé (syndrome) | n2=en:dysplasia of the cerebellar hemispheres | rel=r_associated | relid=0 | w=28
  1037. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dysplastic basal ganglia
    n1=méningé (syndrome) | n2=en:dysplastic basal ganglia | rel=r_associated | relid=0 | w=28
  1038. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dystonia with diurnal variation
    n1=méningé (syndrome) | n2=en:dystonia with diurnal variation | rel=r_associated | relid=0 | w=28
  1039. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dystonia, focal (at onset)
    n1=méningé (syndrome) | n2=en:dystonia, focal (at onset) | rel=r_associated | relid=0 | w=28
  1040. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm)
    n1=méningé (syndrome) | n2=en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm) | rel=r_associated | relid=0 | w=28
  1041. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dystonia, generalized, dopa-unresponsive
    n1=méningé (syndrome) | n2=en:dystonia, generalized, dopa-unresponsive | rel=r_associated | relid=0 | w=28
  1042. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:dystrophic neurites
    n1=méningé (syndrome) | n2=en:dystrophic neurites | rel=r_associated | relid=0 | w=28
  1043. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3)
    n1=méningé (syndrome) | n2=en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3) | rel=r_associated | relid=0 | w=28
  1044. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges
    n1=méningé (syndrome) | n2=en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges | rel=r_associated | relid=0 | w=28
  1045. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:eeg may show migrating focal or multifocal origin (in severe cases)
    n1=méningé (syndrome) | n2=en:eeg may show migrating focal or multifocal origin (in severe cases) | rel=r_associated | relid=0 | w=28
  1046. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:eeg shows epileptiform discharges
    n1=méningé (syndrome) | n2=en:eeg shows epileptiform discharges | rel=r_associated | relid=0 | w=28
  1047. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:emg shows involuntary continuous motor activity at rest
    n1=méningé (syndrome) | n2=en:emg shows involuntary continuous motor activity at rest | rel=r_associated | relid=0 | w=28
  1048. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:emg shows neurogenic changes and denervation
    n1=méningé (syndrome) | n2=en:emg shows neurogenic changes and denervation | rel=r_associated | relid=0 | w=28
  1049. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:encephalocele
    n1=méningé (syndrome) | n2=en:encephalocele | rel=r_associated | relid=0 | w=28
  1050. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:encephalocele (rare)
    n1=méningé (syndrome) | n2=en:encephalocele (rare) | rel=r_associated | relid=0 | w=28
  1051. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:encephalomyelopathy
    n1=méningé (syndrome) | n2=en:encephalomyelopathy | rel=r_associated | relid=0 | w=28
  1052. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:encephalopathic episodes, often associated with infection
    n1=méningé (syndrome) | n2=en:encephalopathic episodes, often associated with infection | rel=r_associated | relid=0 | w=28
  1053. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:encephalopathy, acute, sudden-onset during febrile illness
    n1=méningé (syndrome) | n2=en:encephalopathy, acute, sudden-onset during febrile illness | rel=r_associated | relid=0 | w=28
  1054. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:endothelial intracytoplasmic globular inclusions
    n1=méningé (syndrome) | n2=en:endothelial intracytoplasmic globular inclusions | rel=r_associated | relid=0 | w=28
  1055. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:enhancement of the c-reflex
    n1=méningé (syndrome) | n2=en:enhancement of the c-reflex | rel=r_associated | relid=0 | w=28
  1056. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:enlarged or prominent ventricles (in some patients)
    n1=méningé (syndrome) | n2=en:enlarged or prominent ventricles (in some patients) | rel=r_associated | relid=0 | w=28
  1057. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:enlarged ventricles (1 patient)
    n1=méningé (syndrome) | n2=en:enlarged ventricles (1 patient) | rel=r_associated | relid=0 | w=28
  1058. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:episodic generalized skeletal muscle contractions
    n1=méningé (syndrome) | n2=en:episodic generalized skeletal muscle contractions | rel=r_associated | relid=0 | w=28
  1059. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:episodic sudden headache
    n1=méningé (syndrome) | n2=en:episodic sudden headache | rel=r_associated | relid=0 | w=28
  1060. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:exaggerated moro reflex
    n1=méningé (syndrome) | n2=en:exaggerated moro reflex | rel=r_associated | relid=0 | w=28
  1061. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:expressive aphasia
    n1=méningé (syndrome) | n2=en:expressive aphasia | rel=r_associated | relid=0 | w=28
  1062. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:extensor plantar responses (in some patients)
    n1=méningé (syndrome) | n2=en:extensor plantar responses (in some patients) | rel=r_associated | relid=0 | w=28
  1063. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:extrapyramidal disorder
    n1=méningé (syndrome) | n2=en:extrapyramidal disorder | rel=r_associated | relid=0 | w=28
  1064. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:extrapyramidal symptoms may occur
    n1=méningé (syndrome) | n2=en:extrapyramidal symptoms may occur | rel=r_associated | relid=0 | w=28
  1065. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:facial myokymias
    n1=méningé (syndrome) | n2=en:facial myokymias | rel=r_associated | relid=0 | w=28
  1066. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:facial palsy secondary to cranial hyperostosis
    n1=méningé (syndrome) | n2=en:facial palsy secondary to cranial hyperostosis | rel=r_associated | relid=0 | w=28
  1067. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:facial paralysis
    n1=méningé (syndrome) | n2=en:facial paralysis | rel=r_associated | relid=0 | w=28
  1068. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:fine motor impairment
    n1=méningé (syndrome) | n2=en:fine motor impairment | rel=r_associated | relid=0 | w=28
  1069. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:fine tremors
    n1=méningé (syndrome) | n2=en:fine tremors | rel=r_associated | relid=0 | w=28
  1070. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:flattening of the pons
    n1=méningé (syndrome) | n2=en:flattening of the pons | rel=r_associated | relid=0 | w=28
  1071. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:fluctuating neurologic signs
    n1=méningé (syndrome) | n2=en:fluctuating neurologic signs | rel=r_associated | relid=0 | w=28
  1072. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:fluid filled posterior fossa
    n1=méningé (syndrome) | n2=en:fluid filled posterior fossa | rel=r_associated | relid=0 | w=28
  1073. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:focal dystonia (adult onset)
    n1=méningé (syndrome) | n2=en:focal dystonia (adult onset) | rel=r_associated | relid=0 | w=28
  1074. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:forebrain defects
    n1=méningé (syndrome) | n2=en:forebrain defects | rel=r_associated | relid=0 | w=28
  1075. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:frequency 3.5 hz in midline
    n1=méningé (syndrome) | n2=en:frequency 3.5 hz in midline | rel=r_associated | relid=0 | w=28
  1076. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:frontotemporal dementia (in 30% of patients)
    n1=méningé (syndrome) | n2=en:frontotemporal dementia (in 30% of patients) | rel=r_associated | relid=0 | w=28
  1077. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:frontotemporal leukoencephalopathy
    n1=méningé (syndrome) | n2=en:frontotemporal leukoencephalopathy | rel=r_associated | relid=0 | w=28
  1078. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:frontotemporal lobar atrophy
    n1=méningé (syndrome) | n2=en:frontotemporal lobar atrophy | rel=r_associated | relid=0 | w=28
  1079. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:gait abnormalities (less common)
    n1=méningé (syndrome) | n2=en:gait abnormalities (less common) | rel=r_associated | relid=0 | w=28
  1080. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:gaze deviation
    n1=méningé (syndrome) | n2=en:gaze deviation | rel=r_associated | relid=0 | w=28
  1081. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:generalized clonic or tonic-clonic seizures
    n1=méningé (syndrome) | n2=en:generalized clonic or tonic-clonic seizures | rel=r_associated | relid=0 | w=28
  1082. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:global developmental delay
    n1=méningé (syndrome) | n2=en:global developmental delay | rel=r_associated | relid=0 | w=28
  1083. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:grade i meningioma
    n1=méningé (syndrome) | n2=en:grade i meningioma | rel=r_associated | relid=0 | w=28
  1084. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:gray matter structure of central nervous system
    n1=méningé (syndrome) | n2=en:gray matter structure of central nervous system | rel=r_associated | relid=0 | w=28
  1085. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:gross motor skill delay (infancy)
    n1=méningé (syndrome) | n2=en:gross motor skill delay (infancy) | rel=r_associated | relid=0 | w=28
  1086. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hallucination
    n1=méningé (syndrome) | n2=en:hallucination | rel=r_associated | relid=0 | w=28
  1087. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:head 'tilt' in infancy
    n1=méningé (syndrome) | n2=en:head 'tilt' in infancy | rel=r_associated | relid=0 | w=28
  1088. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:head titubation
    n1=méningé (syndrome) | n2=en:head titubation | rel=r_associated | relid=0 | w=28
  1089. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hemiplegia (rare)
    n1=méningé (syndrome) | n2=en:hemiplegia (rare) | rel=r_associated | relid=0 | w=28
  1090. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum
    n1=méningé (syndrome) | n2=en:herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum | rel=r_associated | relid=0 | w=28
  1091. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:high intensity area in white matter on head mri
    n1=méningé (syndrome) | n2=en:high intensity area in white matter on head mri | rel=r_associated | relid=0 | w=28
  1092. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:high signal intensities at gray/white matter junction
    n1=méningé (syndrome) | n2=en:high signal intensities at gray/white matter junction | rel=r_associated | relid=0 | w=28
  1093. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hippocampal hypoplasia
    n1=méningé (syndrome) | n2=en:hippocampal hypoplasia | rel=r_associated | relid=0 | w=28
  1094. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:holoprosencephaly (100%)
    n1=méningé (syndrome) | n2=en:holoprosencephaly (100%) | rel=r_associated | relid=0 | w=28
  1095. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hydrocephalus (in 2 patients)
    n1=méningé (syndrome) | n2=en:hydrocephalus (in 2 patients) | rel=r_associated | relid=0 | w=28
  1096. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hyperreflexia (2 patients)
    n1=méningé (syndrome) | n2=en:hyperreflexia (2 patients) | rel=r_associated | relid=0 | w=28
  1097. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hyperreflexia (early)
    n1=méningé (syndrome) | n2=en:hyperreflexia (early) | rel=r_associated | relid=0 | w=28
  1098. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults)
    n1=méningé (syndrome) | n2=en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults) | rel=r_associated | relid=0 | w=28
  1099. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hyperreflexia, lower limbs more than upper limbs
    n1=méningé (syndrome) | n2=en:hyperreflexia, lower limbs more than upper limbs | rel=r_associated | relid=0 | w=28
  1100. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypertonia (older children and adolescents)
    n1=méningé (syndrome) | n2=en:hypertonia (older children and adolescents) | rel=r_associated | relid=0 | w=28
  1101. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypodensity of lenticular nuclei
    n1=méningé (syndrome) | n2=en:hypodensity of lenticular nuclei | rel=r_associated | relid=0 | w=28
  1102. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypoglycemic coma
    n1=méningé (syndrome) | n2=en:hypoglycemic coma | rel=r_associated | relid=0 | w=28
  1103. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypomyelination of the brain white matter, diffuse
    n1=méningé (syndrome) | n2=en:hypomyelination of the brain white matter, diffuse | rel=r_associated | relid=0 | w=28
  1104. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypoplasia of the hypothalamus
    n1=méningé (syndrome) | n2=en:hypoplasia of the hypothalamus | rel=r_associated | relid=0 | w=28
  1105. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypothalamus
    n1=méningé (syndrome) | n2=en:hypothalamus | rel=r_associated | relid=0 | w=28
  1106. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypotonia
    n1=méningé (syndrome) | n2=en:hypotonia | rel=r_associated | relid=0 | w=28
  1107. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypotonia (in 1/4 patients)
    n1=méningé (syndrome) | n2=en:hypotonia (in 1/4 patients) | rel=r_associated | relid=0 | w=28
  1108. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypotonia, mild
    n1=méningé (syndrome) | n2=en:hypotonia, mild | rel=r_associated | relid=0 | w=28
  1109. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypotonic
    n1=méningé (syndrome) | n2=en:hypotonic | rel=r_associated | relid=0 | w=28
  1110. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:hypsarrhythmia (in some patients)
    n1=méningé (syndrome) | n2=en:hypsarrhythmia (in some patients) | rel=r_associated | relid=0 | w=28
  1111. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:immature brain with no gyral development
    n1=méningé (syndrome) | n2=en:immature brain with no gyral development | rel=r_associated | relid=0 | w=28
  1112. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:immobile
    n1=méningé (syndrome) | n2=en:immobile | rel=r_associated | relid=0 | w=28
  1113. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:impaired expressive speech
    n1=méningé (syndrome) | n2=en:impaired expressive speech | rel=r_associated | relid=0 | w=28
  1114. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:impairment of gross and fine motor coordination
    n1=méningé (syndrome) | n2=en:impairment of gross and fine motor coordination | rel=r_associated | relid=0 | w=28
  1115. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:inability to sit or stand independently
    n1=méningé (syndrome) | n2=en:inability to sit or stand independently | rel=r_associated | relid=0 | w=28
  1116. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:inability to walk unsupported
    n1=méningé (syndrome) | n2=en:inability to walk unsupported | rel=r_associated | relid=0 | w=28
  1117. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:increased cerebral lactate
    n1=méningé (syndrome) | n2=en:increased cerebral lactate | rel=r_associated | relid=0 | w=28
  1118. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:increased subdural space around frontal lobes
    n1=méningé (syndrome) | n2=en:increased subdural space around frontal lobes | rel=r_associated | relid=0 | w=28
  1119. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:infantile spasm
    n1=méningé (syndrome) | n2=en:infantile spasm | rel=r_associated | relid=0 | w=28
  1120. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:inferior vermis hypoplasia
    n1=méningé (syndrome) | n2=en:inferior vermis hypoplasia | rel=r_associated | relid=0 | w=28
  1121. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:intellectual disability, mild to moderate (in homozygotes)
    n1=méningé (syndrome) | n2=en:intellectual disability, mild to moderate (in homozygotes) | rel=r_associated | relid=0 | w=28
  1122. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:intellectual impairment, mild (in some patients)
    n1=méningé (syndrome) | n2=en:intellectual impairment, mild (in some patients) | rel=r_associated | relid=0 | w=28
  1123. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:intracranial calcifications (1 patient)
    n1=méningé (syndrome) | n2=en:intracranial calcifications (1 patient) | rel=r_associated | relid=0 | w=28
  1124. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:intracranial meningioma
    n1=méningé (syndrome) | n2=en:intracranial meningioma | rel=r_associated | relid=0 | w=28
  1125. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:involuntary writhing movements
    n1=méningé (syndrome) | n2=en:involuntary writhing movements | rel=r_associated | relid=0 | w=28
  1126. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:irregular cortical ribbon
    n1=méningé (syndrome) | n2=en:irregular cortical ribbon | rel=r_associated | relid=0 | w=28
  1127. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:irregular folding of the cortex
    n1=méningé (syndrome) | n2=en:irregular folding of the cortex | rel=r_associated | relid=0 | w=28
  1128. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ischemic cerebrovascular accident
    n1=méningé (syndrome) | n2=en:ischemic cerebrovascular accident | rel=r_associated | relid=0 | w=28
  1129. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ischemic infarction (rare)
    n1=méningé (syndrome) | n2=en:ischemic infarction (rare) | rel=r_associated | relid=0 | w=28
  1130. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ischemic necrotic lesions
    n1=méningé (syndrome) | n2=en:ischemic necrotic lesions | rel=r_associated | relid=0 | w=28
  1131. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like
    n1=méningé (syndrome) | n2=en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like | rel=r_associated | relid=0 | w=28
  1132. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:kernicterus
    n1=méningé (syndrome) | n2=en:kernicterus | rel=r_associated | relid=0 | w=28
  1133. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:lack of inflammatory infiltrate
    n1=méningé (syndrome) | n2=en:lack of inflammatory infiltrate | rel=r_associated | relid=0 | w=28
  1134. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:lack of neurologic development
    n1=méningé (syndrome) | n2=en:lack of neurologic development | rel=r_associated | relid=0 | w=28
  1135. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:lack of speech or only a few words
    n1=méningé (syndrome) | n2=en:lack of speech or only a few words | rel=r_associated | relid=0 | w=28
  1136. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:language development limited to a few words
    n1=méningé (syndrome) | n2=en:language development limited to a few words | rel=r_associated | relid=0 | w=28
  1137. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:learning and developmental delay (in some patients)
    n1=méningé (syndrome) | n2=en:learning and developmental delay (in some patients) | rel=r_associated | relid=0 | w=28
  1138. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:learning difficulties
    n1=méningé (syndrome) | n2=en:learning difficulties | rel=r_associated | relid=0 | w=28
  1139. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:learning difficulties (seen in recessive form)
    n1=méningé (syndrome) | n2=en:learning difficulties (seen in recessive form) | rel=r_associated | relid=0 | w=28
  1140. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:learning disabilities
    n1=méningé (syndrome) | n2=en:learning disabilities | rel=r_associated | relid=0 | w=28
  1141. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:learning disabilities (30%)
    n1=méningé (syndrome) | n2=en:learning disabilities (30%) | rel=r_associated | relid=0 | w=28
  1142. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:leg cramp
    n1=méningé (syndrome) | n2=en:leg cramp | rel=r_associated | relid=0 | w=28
  1143. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation
    n1=méningé (syndrome) | n2=en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation | rel=r_associated | relid=0 | w=28
  1144. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:lesions in the anterior pituitary (less common)
    n1=méningé (syndrome) | n2=en:lesions in the anterior pituitary (less common) | rel=r_associated | relid=0 | w=28
  1145. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:leukoencephalopathy, severe
    n1=méningé (syndrome) | n2=en:leukoencephalopathy, severe | rel=r_associated | relid=0 | w=28
  1146. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:limb dysmetria
    n1=méningé (syndrome) | n2=en:limb dysmetria | rel=r_associated | relid=0 | w=28
  1147. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:limb posturing (if left untreated)
    n1=méningé (syndrome) | n2=en:limb posturing (if left untreated) | rel=r_associated | relid=0 | w=28
  1148. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:limbic malformations
    n1=méningé (syndrome) | n2=en:limbic malformations | rel=r_associated | relid=0 | w=28
  1149. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:limited memory, attention, language
    n1=méningé (syndrome) | n2=en:limited memory, attention, language | rel=r_associated | relid=0 | w=28
  1150. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions)
    n1=méningé (syndrome) | n2=en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions) | rel=r_associated | relid=0 | w=28
  1151. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:little polarity in remaining neurons
    n1=méningé (syndrome) | n2=en:little polarity in remaining neurons | rel=r_associated | relid=0 | w=28
  1152. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:loss of coordination
    n1=méningé (syndrome) | n2=en:loss of coordination | rel=r_associated | relid=0 | w=28
  1153. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:loss of independent ambulation (in some patients)
    n1=méningé (syndrome) | n2=en:loss of independent ambulation (in some patients) | rel=r_associated | relid=0 | w=28
  1154. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:loss of myelin in the pyramidal tracts
    n1=méningé (syndrome) | n2=en:loss of myelin in the pyramidal tracts | rel=r_associated | relid=0 | w=28
  1155. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:loss of purposeful hand movements
    n1=méningé (syndrome) | n2=en:loss of purposeful hand movements | rel=r_associated | relid=0 | w=28
  1156. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:lower motor neuron involvement after long disease duration
    n1=méningé (syndrome) | n2=en:lower motor neuron involvement after long disease duration | rel=r_associated | relid=0 | w=28
  1157. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:lower motor neuron symptoms
    n1=méningé (syndrome) | n2=en:lower motor neuron symptoms | rel=r_associated | relid=0 | w=28
  1158. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:lower motor signs
    n1=méningé (syndrome) | n2=en:lower motor signs | rel=r_associated | relid=0 | w=28
  1159. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter
    n1=méningé (syndrome) | n2=en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter | rel=r_associated | relid=0 | w=28
  1160. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:memory loss
    n1=méningé (syndrome) | n2=en:memory loss | rel=r_associated | relid=0 | w=28
  1161. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:meningitis
    n1=méningé (syndrome) | n2=en:meningitis | rel=r_associated | relid=0 | w=28
  1162. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:meningoencephalitis
    n1=méningé (syndrome) | n2=en:meningoencephalitis | rel=r_associated | relid=0 | w=28
  1163. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mental retardation (50% patients)
    n1=méningé (syndrome) | n2=en:mental retardation (50% patients) | rel=r_associated | relid=0 | w=28
  1164. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mental retardation (6%)
    n1=méningé (syndrome) | n2=en:mental retardation (6%) | rel=r_associated | relid=0 | w=28
  1165. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mental retardation, borderline-mild in carrier females
    n1=méningé (syndrome) | n2=en:mental retardation, borderline-mild in carrier females | rel=r_associated | relid=0 | w=28
  1166. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mental retardation, mild (in some patients)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (in some patients) | rel=r_associated | relid=0 | w=28
  1167. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mental retardation, progressive (50% of patients)
    n1=méningé (syndrome) | n2=en:mental retardation, progressive (50% of patients) | rel=r_associated | relid=0 | w=28
  1168. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:microcephaly
    n1=méningé (syndrome) | n2=en:microcephaly | rel=r_associated | relid=0 | w=28
  1169. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:microcystic meningioma
    n1=méningé (syndrome) | n2=en:microcystic meningioma | rel=r_associated | relid=0 | w=28
  1170. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:migraines (less common)
    n1=méningé (syndrome) | n2=en:migraines (less common) | rel=r_associated | relid=0 | w=28
  1171. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:migrating focal discharges from one cortical region to another seen on eeg
    n1=méningé (syndrome) | n2=en:migrating focal discharges from one cortical region to another seen on eeg | rel=r_associated | relid=0 | w=28
  1172. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mild cognitive impairment (less common)
    n1=méningé (syndrome) | n2=en:mild cognitive impairment (less common) | rel=r_associated | relid=0 | w=28
  1173. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mild mental retardation
    n1=méningé (syndrome) | n2=en:mild mental retardation | rel=r_associated | relid=0 | w=28
  1174. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mild mental retardation (39%) feeding problems/weak suck (43%)
    n1=méningé (syndrome) | n2=en:mild mental retardation (39%) feeding problems/weak suck (43%) | rel=r_associated | relid=0 | w=28
  1175. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mild upper limb involvement
    n1=méningé (syndrome) | n2=en:mild upper limb involvement | rel=r_associated | relid=0 | w=28
  1176. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy
    n1=méningé (syndrome) | n2=en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy | rel=r_associated | relid=0 | w=28
  1177. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:minimal gliosis
    n1=méningé (syndrome) | n2=en:minimal gliosis | rel=r_associated | relid=0 | w=28
  1178. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:minimal or lack of speech
    n1=méningé (syndrome) | n2=en:minimal or lack of speech | rel=r_associated | relid=0 | w=28
  1179. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:misorientation of pyramidal fibers
    n1=méningé (syndrome) | n2=en:misorientation of pyramidal fibers | rel=r_associated | relid=0 | w=28
  1180. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mitochondrial encephalopathy
    n1=méningé (syndrome) | n2=en:mitochondrial encephalopathy | rel=r_associated | relid=0 | w=28
  1181. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:molar tooth sign on mri
    n1=méningé (syndrome) | n2=en:molar tooth sign on mri | rel=r_associated | relid=0 | w=28
  1182. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:most patients do not achieve independent sitting or walking
    n1=méningé (syndrome) | n2=en:most patients do not achieve independent sitting or walking | rel=r_associated | relid=0 | w=28
  1183. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:motor and intellectual disability, severe
    n1=méningé (syndrome) | n2=en:motor and intellectual disability, severe | rel=r_associated | relid=0 | w=28
  1184. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mri may show lesions in basal ganglia, thalamus, and white matter
    n1=méningé (syndrome) | n2=en:mri may show lesions in basal ganglia, thalamus, and white matter | rel=r_associated | relid=0 | w=28
  1185. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:mri shows cerebellar atrophy
    n1=méningé (syndrome) | n2=en:mri shows cerebellar atrophy | rel=r_associated | relid=0 | w=28
  1186. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:multifocal areas of laminar dysmorphic neurons (in type iia)
    n1=méningé (syndrome) | n2=en:multifocal areas of laminar dysmorphic neurons (in type iia) | rel=r_associated | relid=0 | w=28
  1187. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:multifocal white matter lesions
    n1=méningé (syndrome) | n2=en:multifocal white matter lesions | rel=r_associated | relid=0 | w=28
  1188. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:multiple lesions in the white matter
    n1=méningé (syndrome) | n2=en:multiple lesions in the white matter | rel=r_associated | relid=0 | w=28
  1189. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:musician's cramp
    n1=méningé (syndrome) | n2=en:musician's cramp | rel=r_associated | relid=0 | w=28
  1190. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:myelin loss in the corticospinal tracts
    n1=méningé (syndrome) | n2=en:myelin loss in the corticospinal tracts | rel=r_associated | relid=0 | w=28
  1191. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:myoclonic jerks (less common)
    n1=méningé (syndrome) | n2=en:myoclonic jerks (less common) | rel=r_associated | relid=0 | w=28
  1192. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:myoclonus (in a subset of patients)
    n1=méningé (syndrome) | n2=en:myoclonus (in a subset of patients) | rel=r_associated | relid=0 | w=28
  1193. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:myoclonus, cortical, multifocal
    n1=méningé (syndrome) | n2=en:myoclonus, cortical, multifocal | rel=r_associated | relid=0 | w=28
  1194. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:myoclonus, paroxysmal
    n1=méningé (syndrome) | n2=en:myoclonus, paroxysmal | rel=r_associated | relid=0 | w=28
  1195. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:necrotic white matter lesions throughout the brain and brainstem
    n1=méningé (syndrome) | n2=en:necrotic white matter lesions throughout the brain and brainstem | rel=r_associated | relid=0 | w=28
  1196. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:neocortical dysplasia (27%)
    n1=méningé (syndrome) | n2=en:neocortical dysplasia (27%) | rel=r_associated | relid=0 | w=28
  1197. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:nervousness
    n1=méningé (syndrome) | n2=en:nervousness | rel=r_associated | relid=0 | w=28
  1198. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:neurologic deterioration in longterm survivors
    n1=méningé (syndrome) | n2=en:neurologic deterioration in longterm survivors | rel=r_associated | relid=0 | w=28
  1199. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:neuromuscular disturbances, progressive
    n1=méningé (syndrome) | n2=en:neuromuscular disturbances, progressive | rel=r_associated | relid=0 | w=28
  1200. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:neuronal heterotopia
    n1=méningé (syndrome) | n2=en:neuronal heterotopia | rel=r_associated | relid=0 | w=28
  1201. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:neuronal loss and gliosis in the substantia nigra pars compacta
    n1=méningé (syndrome) | n2=en:neuronal loss and gliosis in the substantia nigra pars compacta | rel=r_associated | relid=0 | w=28
  1202. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:neuropathology shows neuronal degeneration
    n1=méningé (syndrome) | n2=en:neuropathology shows neuronal degeneration | rel=r_associated | relid=0 | w=28
  1203. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:neuropil
    n1=méningé (syndrome) | n2=en:neuropil | rel=r_associated | relid=0 | w=28
  1204. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:no autistic features
    n1=méningé (syndrome) | n2=en:no autistic features | rel=r_associated | relid=0 | w=28
  1205. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:no language development
    n1=méningé (syndrome) | n2=en:no language development | rel=r_associated | relid=0 | w=28
  1206. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:no mental retardation
    n1=méningé (syndrome) | n2=en:no mental retardation | rel=r_associated | relid=0 | w=28
  1207. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:no neurofibromas
    n1=méningé (syndrome) | n2=en:no neurofibromas | rel=r_associated | relid=0 | w=28
  1208. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:no tremor
    n1=méningé (syndrome) | n2=en:no tremor | rel=r_associated | relid=0 | w=28
  1209. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:no visual fixation
    n1=méningé (syndrome) | n2=en:no visual fixation | rel=r_associated | relid=0 | w=28
  1210. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:nodular heterotopia of the grey matter
    n1=méningé (syndrome) | n2=en:nodular heterotopia of the grey matter | rel=r_associated | relid=0 | w=28
  1211. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:normal development
    n1=méningé (syndrome) | n2=en:normal development | rel=r_associated | relid=0 | w=28
  1212. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:normal early development
    n1=méningé (syndrome) | n2=en:normal early development | rel=r_associated | relid=0 | w=28
  1213. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:normal intellectual development
    n1=méningé (syndrome) | n2=en:normal intellectual development | rel=r_associated | relid=0 | w=28
  1214. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:normal intelligence in most cases
    n1=méningé (syndrome) | n2=en:normal intelligence in most cases | rel=r_associated | relid=0 | w=28
  1215. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:normal muscle strength
    n1=méningé (syndrome) | n2=en:normal muscle strength | rel=r_associated | relid=0 | w=28
  1216. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:normal psychomotor development until age 2 to 3 years
    n1=méningé (syndrome) | n2=en:normal psychomotor development until age 2 to 3 years | rel=r_associated | relid=0 | w=28
  1217. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:normal to mildly delayed development
    n1=méningé (syndrome) | n2=en:normal to mildly delayed development | rel=r_associated | relid=0 | w=28
  1218. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:nystagmus
    n1=méningé (syndrome) | n2=en:nystagmus | rel=r_associated | relid=0 | w=28
  1219. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:nystagmus, jerky, horizontal, congenital
    n1=méningé (syndrome) | n2=en:nystagmus, jerky, horizontal, congenital | rel=r_associated | relid=0 | w=28
  1220. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:occipital dermal sinus tract
    n1=méningé (syndrome) | n2=en:occipital dermal sinus tract | rel=r_associated | relid=0 | w=28
  1221. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:occipital lobe atrophy
    n1=méningé (syndrome) | n2=en:occipital lobe atrophy | rel=r_associated | relid=0 | w=28
  1222. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:occlusive hydrocephalus, congenital
    n1=méningé (syndrome) | n2=en:occlusive hydrocephalus, congenital | rel=r_associated | relid=0 | w=28
  1223. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ocular motility spared
    n1=méningé (syndrome) | n2=en:ocular motility spared | rel=r_associated | relid=0 | w=28
  1224. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:oculomotor apraxia
    n1=méningé (syndrome) | n2=en:oculomotor apraxia | rel=r_associated | relid=0 | w=28
  1225. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:onset may be triggered by emotional stress, fever, exercise, exposure to heat
    n1=méningé (syndrome) | n2=en:onset may be triggered by emotional stress, fever, exercise, exposure to heat | rel=r_associated | relid=0 | w=28
  1226. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:open spina bifida (myelomeningocele, 182940)
    n1=méningé (syndrome) | n2=en:open spina bifida (myelomeningocele, 182940) | rel=r_associated | relid=0 | w=28
  1227. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:optic nerve sheath meningioma
    n1=méningé (syndrome) | n2=en:optic nerve sheath meningioma | rel=r_associated | relid=0 | w=28
  1228. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:pachygyria (posterior-to-anterior gradient)
    n1=méningé (syndrome) | n2=en:pachygyria (posterior-to-anterior gradient) | rel=r_associated | relid=0 | w=28
  1229. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:pachygyria with preferential frontoparietal involvement (meb)
    n1=méningé (syndrome) | n2=en:pachygyria with preferential frontoparietal involvement (meb) | rel=r_associated | relid=0 | w=28
  1230. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:pachygyria, bilateral frontotemporal
    n1=méningé (syndrome) | n2=en:pachygyria, bilateral frontotemporal | rel=r_associated | relid=0 | w=28
  1231. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:pachygyrias
    n1=méningé (syndrome) | n2=en:pachygyrias | rel=r_associated | relid=0 | w=28
  1232. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:pallidal degeneration
    n1=méningé (syndrome) | n2=en:pallidal degeneration | rel=r_associated | relid=0 | w=28
  1233. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:paresis of extensor muscles of the big toe is presenting symptom
    n1=méningé (syndrome) | n2=en:paresis of extensor muscles of the big toe is presenting symptom | rel=r_associated | relid=0 | w=28
  1234. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:parietal lobe epilepsy
    n1=méningé (syndrome) | n2=en:parietal lobe epilepsy | rel=r_associated | relid=0 | w=28
  1235. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:parkinsonism (later)
    n1=méningé (syndrome) | n2=en:parkinsonism (later) | rel=r_associated | relid=0 | w=28
  1236. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:partial absence of the corpus callosum (in one patient)
    n1=méningé (syndrome) | n2=en:partial absence of the corpus callosum (in one patient) | rel=r_associated | relid=0 | w=28
  1237. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:pathologic calcification, calcified structure
    n1=méningé (syndrome) | n2=en:pathologic calcification, calcified structure | rel=r_associated | relid=0 | w=28
  1238. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:periodic paralysis, usually hypokalemic
    n1=méningé (syndrome) | n2=en:periodic paralysis, usually hypokalemic | rel=r_associated | relid=0 | w=28
  1239. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:perivascular spaces
    n1=méningé (syndrome) | n2=en:perivascular spaces | rel=r_associated | relid=0 | w=28
  1240. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:periventricular white matter hyperintensities, bilateral
    n1=méningé (syndrome) | n2=en:periventricular white matter hyperintensities, bilateral | rel=r_associated | relid=0 | w=28
  1241. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:photophobia
    n1=méningé (syndrome) | n2=en:photophobia | rel=r_associated | relid=0 | w=28
  1242. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:polymicrogyria, temporo-occipital
    n1=méningé (syndrome) | n2=en:polymicrogyria, temporo-occipital | rel=r_associated | relid=0 | w=28
  1243. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:polyneuropathy
    n1=méningé (syndrome) | n2=en:polyneuropathy | rel=r_associated | relid=0 | w=28
  1244. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:poor motor development
    n1=méningé (syndrome) | n2=en:poor motor development | rel=r_associated | relid=0 | w=28
  1245. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:poor or absent speech development
    n1=méningé (syndrome) | n2=en:poor or absent speech development | rel=r_associated | relid=0 | w=28
  1246. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:poor speech
    n1=méningé (syndrome) | n2=en:poor speech | rel=r_associated | relid=0 | w=28
  1247. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:poor spontaneous movements
    n1=méningé (syndrome) | n2=en:poor spontaneous movements | rel=r_associated | relid=0 | w=28
  1248. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:postnatal development of hypertonic extremities
    n1=méningé (syndrome) | n2=en:postnatal development of hypertonic extremities | rel=r_associated | relid=0 | w=28
  1249. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:pre-senile dementia
    n1=méningé (syndrome) | n2=en:pre-senile dementia | rel=r_associated | relid=0 | w=28
  1250. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:progressive cerebellar degeneration
    n1=méningé (syndrome) | n2=en:progressive cerebellar degeneration | rel=r_associated | relid=0 | w=28
  1251. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:progressive extrapyramidal movement disorder
    n1=méningé (syndrome) | n2=en:progressive extrapyramidal movement disorder | rel=r_associated | relid=0 | w=28
  1252. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:progressive intellectual decline
    n1=méningé (syndrome) | n2=en:progressive intellectual decline | rel=r_associated | relid=0 | w=28
  1253. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:progressive myoclonus epilepsy
    n1=méningé (syndrome) | n2=en:progressive myoclonus epilepsy | rel=r_associated | relid=0 | w=28
  1254. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:progressive, symmetric degeneration of the caudate and putamen
    n1=méningé (syndrome) | n2=en:progressive, symmetric degeneration of the caudate and putamen | rel=r_associated | relid=0 | w=28
  1255. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:prominent cortical sulci
    n1=méningé (syndrome) | n2=en:prominent cortical sulci | rel=r_associated | relid=0 | w=28
  1256. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:pseudobulbar palsy
    n1=méningé (syndrome) | n2=en:pseudobulbar palsy | rel=r_associated | relid=0 | w=28
  1257. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:psychomotor delay (evident at 3 months)
    n1=méningé (syndrome) | n2=en:psychomotor delay (evident at 3 months) | rel=r_associated | relid=0 | w=28
  1258. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:psychomotor delay, mild to moderate
    n1=méningé (syndrome) | n2=en:psychomotor delay, mild to moderate | rel=r_associated | relid=0 | w=28
  1259. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:psychomotor deterioration (classical form)
    n1=méningé (syndrome) | n2=en:psychomotor deterioration (classical form) | rel=r_associated | relid=0 | w=28
  1260. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:psychomotor regression may occur
    n1=méningé (syndrome) | n2=en:psychomotor regression may occur | rel=r_associated | relid=0 | w=28
  1261. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:psychomotor regression, severe
    n1=méningé (syndrome) | n2=en:psychomotor regression, severe | rel=r_associated | relid=0 | w=28
  1262. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:psychomotor retardation (in some patients)
    n1=méningé (syndrome) | n2=en:psychomotor retardation (in some patients) | rel=r_associated | relid=0 | w=28
  1263. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:psychomotor retardation, severe to profound
    n1=méningé (syndrome) | n2=en:psychomotor retardation, severe to profound | rel=r_associated | relid=0 | w=28
  1264. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:quadrupedal gait
    n1=méningé (syndrome) | n2=en:quadrupedal gait | rel=r_associated | relid=0 | w=28
  1265. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:quadrupedal gait (in some)
    n1=méningé (syndrome) | n2=en:quadrupedal gait (in some) | rel=r_associated | relid=0 | w=28
  1266. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:reduced consciousness, hypoglycemia-related
    n1=méningé (syndrome) | n2=en:reduced consciousness, hypoglycemia-related | rel=r_associated | relid=0 | w=28
  1267. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:reflex epilepsy, photosensitive
    n1=méningé (syndrome) | n2=en:reflex epilepsy, photosensitive | rel=r_associated | relid=0 | w=28
  1268. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:restrictive behavior, interests, and activities
    n1=méningé (syndrome) | n2=en:restrictive behavior, interests, and activities | rel=r_associated | relid=0 | w=28
  1269. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:retrocerebellar cyst (in some patients)
    n1=méningé (syndrome) | n2=en:retrocerebellar cyst (in some patients) | rel=r_associated | relid=0 | w=28
  1270. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:retrocerebellar cyst (rare)
    n1=méningé (syndrome) | n2=en:retrocerebellar cyst (rare) | rel=r_associated | relid=0 | w=28
  1271. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:retroflexion of the neck
    n1=méningé (syndrome) | n2=en:retroflexion of the neck | rel=r_associated | relid=0 | w=28
  1272. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:reye syndrome
    n1=méningé (syndrome) | n2=en:reye syndrome | rel=r_associated | relid=0 | w=28
  1273. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:rigidity, axial and limb
    n1=méningé (syndrome) | n2=en:rigidity, axial and limb | rel=r_associated | relid=0 | w=28
  1274. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:schizencephaly
    n1=méningé (syndrome) | n2=en:schizencephaly | rel=r_associated | relid=0 | w=28
  1275. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:schizophrenia
    n1=méningé (syndrome) | n2=en:schizophrenia | rel=r_associated | relid=0 | w=28
  1276. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:secondary spinal cord compression may occur
    n1=méningé (syndrome) | n2=en:secondary spinal cord compression may occur | rel=r_associated | relid=0 | w=28
  1277. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:seizure including seizure-like activity in utero starting around 18 weeks gestation
    n1=méningé (syndrome) | n2=en:seizure including seizure-like activity in utero starting around 18 weeks gestation | rel=r_associated | relid=0 | w=28
  1278. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:seizures (50%)
    n1=méningé (syndrome) | n2=en:seizures (50%) | rel=r_associated | relid=0 | w=28
  1279. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:seizures (in 2 of 9 patients)
    n1=méningé (syndrome) | n2=en:seizures (in 2 of 9 patients) | rel=r_associated | relid=0 | w=28
  1280. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:seizures may occur during hypotensive episodes
    n1=méningé (syndrome) | n2=en:seizures may occur during hypotensive episodes | rel=r_associated | relid=0 | w=28
  1281. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:seizures, focal, partial, motor
    n1=méningé (syndrome) | n2=en:seizures, focal, partial, motor | rel=r_associated | relid=0 | w=28
  1282. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:seizures, generalized, afebrile
    n1=méningé (syndrome) | n2=en:seizures, generalized, afebrile | rel=r_associated | relid=0 | w=28
  1283. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:seizures, mild
    n1=méningé (syndrome) | n2=en:seizures, mild | rel=r_associated | relid=0 | w=28
  1284. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:seizures, refractory to treatment
    n1=méningé (syndrome) | n2=en:seizures, refractory to treatment | rel=r_associated | relid=0 | w=28
  1285. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:seizures, tonic-clonic or absence (in some patients)
    n1=méningé (syndrome) | n2=en:seizures, tonic-clonic or absence (in some patients) | rel=r_associated | relid=0 | w=28
  1286. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:self mutilation
    n1=méningé (syndrome) | n2=en:self mutilation | rel=r_associated | relid=0 | w=28
  1287. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:severe developmental delay in survivors
    n1=méningé (syndrome) | n2=en:severe developmental delay in survivors | rel=r_associated | relid=0 | w=28
  1288. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:severe mental retardation (congenital form)
    n1=méningé (syndrome) | n2=en:severe mental retardation (congenital form) | rel=r_associated | relid=0 | w=28
  1289. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:severe mental retardation (iq 10-40)
    n1=méningé (syndrome) | n2=en:severe mental retardation (iq 10-40) | rel=r_associated | relid=0 | w=28
  1290. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:shivering sensation
    n1=méningé (syndrome) | n2=en:shivering sensation | rel=r_associated | relid=0 | w=28
  1291. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:short pons
    n1=méningé (syndrome) | n2=en:short pons | rel=r_associated | relid=0 | w=28
  1292. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:simplified gyral pattern (1 patient)
    n1=méningé (syndrome) | n2=en:simplified gyral pattern (1 patient) | rel=r_associated | relid=0 | w=28
  1293. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:simplified gyration pattern
    n1=méningé (syndrome) | n2=en:simplified gyration pattern | rel=r_associated | relid=0 | w=28
  1294. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:slow spike-wave discharges
    n1=méningé (syndrome) | n2=en:slow spike-wave discharges | rel=r_associated | relid=0 | w=28
  1295. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:slow, broad-based gait
    n1=méningé (syndrome) | n2=en:slow, broad-based gait | rel=r_associated | relid=0 | w=28
  1296. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:slurred speech, episodic
    n1=méningé (syndrome) | n2=en:slurred speech, episodic | rel=r_associated | relid=0 | w=28
  1297. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spastic diplegia, symmetric
    n1=méningé (syndrome) | n2=en:spastic diplegia, symmetric | rel=r_associated | relid=0 | w=28
  1298. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spastic paraparesis (rare)
    n1=méningé (syndrome) | n2=en:spastic paraparesis (rare) | rel=r_associated | relid=0 | w=28
  1299. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spastic-ataxic gait
    n1=méningé (syndrome) | n2=en:spastic-ataxic gait | rel=r_associated | relid=0 | w=28
  1300. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spasticity (1 of 4 patients)
    n1=méningé (syndrome) | n2=en:spasticity (1 of 4 patients) | rel=r_associated | relid=0 | w=28
  1301. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spasticity (in some patients)
    n1=méningé (syndrome) | n2=en:spasticity (in some patients) | rel=r_associated | relid=0 | w=28
  1302. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spasticity (rare)
    n1=méningé (syndrome) | n2=en:spasticity (rare) | rel=r_associated | relid=0 | w=28
  1303. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spasticity in infancy (1 patient)
    n1=méningé (syndrome) | n2=en:spasticity in infancy (1 patient) | rel=r_associated | relid=0 | w=28
  1304. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spasticity, hyperreflexia
    n1=méningé (syndrome) | n2=en:spasticity, hyperreflexia | rel=r_associated | relid=0 | w=28
  1305. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spasticity, lower limbs greater than upper limbs
    n1=méningé (syndrome) | n2=en:spasticity, lower limbs greater than upper limbs | rel=r_associated | relid=0 | w=28
  1306. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:speech articulation problems
    n1=méningé (syndrome) | n2=en:speech articulation problems | rel=r_associated | relid=0 | w=28
  1307. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:speech delay (1 patient)
    n1=méningé (syndrome) | n2=en:speech delay (1 patient) | rel=r_associated | relid=0 | w=28
  1308. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spinal cord compression by tumor infiltration
    n1=méningé (syndrome) | n2=en:spinal cord compression by tumor infiltration | rel=r_associated | relid=0 | w=28
  1309. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spinocerebellar ataxia (upper and lower limb involvement)
    n1=méningé (syndrome) | n2=en:spinocerebellar ataxia (upper and lower limb involvement) | rel=r_associated | relid=0 | w=28
  1310. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:spongiform encephalomyelopathy
    n1=méningé (syndrome) | n2=en:spongiform encephalomyelopathy | rel=r_associated | relid=0 | w=28
  1311. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:stereotypic movements
    n1=méningé (syndrome) | n2=en:stereotypic movements | rel=r_associated | relid=0 | w=28
  1312. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:stiff limbs
    n1=méningé (syndrome) | n2=en:stiff limbs | rel=r_associated | relid=0 | w=28
  1313. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:stretched cerebellar peduncles
    n1=méningé (syndrome) | n2=en:stretched cerebellar peduncles | rel=r_associated | relid=0 | w=28
  1314. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:striatal atrophy
    n1=méningé (syndrome) | n2=en:striatal atrophy | rel=r_associated | relid=0 | w=28
  1315. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:structural abnormalities of cerebellum
    n1=méningé (syndrome) | n2=en:structural abnormalities of cerebellum | rel=r_associated | relid=0 | w=28
  1316. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:subarachnoid hemorrhage
    n1=méningé (syndrome) | n2=en:subarachnoid hemorrhage | rel=r_associated | relid=0 | w=28
  1317. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:subcortical leukodystrophy
    n1=méningé (syndrome) | n2=en:subcortical leukodystrophy | rel=r_associated | relid=0 | w=28
  1318. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:subependymal nodules
    n1=méningé (syndrome) | n2=en:subependymal nodules | rel=r_associated | relid=0 | w=28
  1319. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:suppression-burst pattern
    n1=méningé (syndrome) | n2=en:suppression-burst pattern | rel=r_associated | relid=0 | w=28
  1320. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:supratentorial structures unformed or regressed
    n1=méningé (syndrome) | n2=en:supratentorial structures unformed or regressed | rel=r_associated | relid=0 | w=28
  1321. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients
    n1=méningé (syndrome) | n2=en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients | rel=r_associated | relid=0 | w=28
  1322. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:syndrome screaming
    n1=méningé (syndrome) | n2=en:syndrome screaming | rel=r_associated | relid=0 | w=28
  1323. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem | rel=r_associated | relid=0 | w=28
  1324. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:tdp43-positive inclusions
    n1=méningé (syndrome) | n2=en:tdp43-positive inclusions | rel=r_associated | relid=0 | w=28
  1325. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:tetany, hypocalcemic, episodic
    n1=méningé (syndrome) | n2=en:tetany, hypocalcemic, episodic | rel=r_associated | relid=0 | w=28
  1326. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:tethered spinal cord syndrome
    n1=méningé (syndrome) | n2=en:tethered spinal cord syndrome | rel=r_associated | relid=0 | w=28
  1327. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:thalamic neuronal loss, especially in the medial dorsal nucleus
    n1=méningé (syndrome) | n2=en:thalamic neuronal loss, especially in the medial dorsal nucleus | rel=r_associated | relid=0 | w=28
  1328. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:thick corpus callosum
    n1=méningé (syndrome) | n2=en:thick corpus callosum | rel=r_associated | relid=0 | w=28
  1329. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:thickened frontal cortex
    n1=méningé (syndrome) | n2=en:thickened frontal cortex | rel=r_associated | relid=0 | w=28
  1330. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:thin corpus callosum (1 family)
    n1=méningé (syndrome) | n2=en:thin corpus callosum (1 family) | rel=r_associated | relid=0 | w=28
  1331. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:thin corpus callosum enlarged ventricles
    n1=méningé (syndrome) | n2=en:thin corpus callosum enlarged ventricles | rel=r_associated | relid=0 | w=28
  1332. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:toe-walking in early childhood
    n1=méningé (syndrome) | n2=en:toe-walking in early childhood | rel=r_associated | relid=0 | w=28
  1333. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:torticollis
    n1=méningé (syndrome) | n2=en:torticollis | rel=r_associated | relid=0 | w=28
  1334. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:tow-walking
    n1=méningé (syndrome) | n2=en:tow-walking | rel=r_associated | relid=0 | w=28
  1335. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:tremor (30%)
    n1=méningé (syndrome) | n2=en:tremor (30%) | rel=r_associated | relid=0 | w=28
  1336. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:tremor, action (arms, tongue, head, legs and trunk)
    n1=méningé (syndrome) | n2=en:tremor, action (arms, tongue, head, legs and trunk) | rel=r_associated | relid=0 | w=28
  1337. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family)
    n1=méningé (syndrome) | n2=en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family) | rel=r_associated | relid=0 | w=28
  1338. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:truncal arching
    n1=méningé (syndrome) | n2=en:truncal arching | rel=r_associated | relid=0 | w=28
  1339. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:truncal instability
    n1=méningé (syndrome) | n2=en:truncal instability | rel=r_associated | relid=0 | w=28
  1340. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:upper and lower motor neuron degeneration
    n1=méningé (syndrome) | n2=en:upper and lower motor neuron degeneration | rel=r_associated | relid=0 | w=28
  1341. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:upper limb spasticity, mild
    n1=méningé (syndrome) | n2=en:upper limb spasticity, mild | rel=r_associated | relid=0 | w=28
  1342. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:upper motor neuron degeneration
    n1=méningé (syndrome) | n2=en:upper motor neuron degeneration | rel=r_associated | relid=0 | w=28
  1343. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:upper motor signs
    n1=méningé (syndrome) | n2=en:upper motor signs | rel=r_associated | relid=0 | w=28
  1344. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:upper motor signs (in some patients)
    n1=méningé (syndrome) | n2=en:upper motor signs (in some patients) | rel=r_associated | relid=0 | w=28
  1345. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ventriculomegaly (in some patients)
    n1=méningé (syndrome) | n2=en:ventriculomegaly (in some patients) | rel=r_associated | relid=0 | w=28
  1346. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ventriculomegaly (variable)
    n1=méningé (syndrome) | n2=en:ventriculomegaly (variable) | rel=r_associated | relid=0 | w=28
  1347. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:ventriculomegaly, mild (rare)
    n1=méningé (syndrome) | n2=en:ventriculomegaly, mild (rare) | rel=r_associated | relid=0 | w=28
  1348. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:verbal delay (in some patients)
    n1=méningé (syndrome) | n2=en:verbal delay (in some patients) | rel=r_associated | relid=0 | w=28
  1349. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:vertical orientation of hippocampus
    n1=méningé (syndrome) | n2=en:vertical orientation of hippocampus | rel=r_associated | relid=0 | w=28
  1350. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:vertigo, mild
    n1=méningé (syndrome) | n2=en:vertigo, mild | rel=r_associated | relid=0 | w=28
  1351. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:visual acuity is normal
    n1=méningé (syndrome) | n2=en:visual acuity is normal | rel=r_associated | relid=0 | w=28
  1352. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:visual changes
    n1=méningé (syndrome) | n2=en:visual changes | rel=r_associated | relid=0 | w=28
  1353. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:visual impairment
    n1=méningé (syndrome) | n2=en:visual impairment | rel=r_associated | relid=0 | w=28
  1354. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:waddling gait
    n1=méningé (syndrome) | n2=en:waddling gait | rel=r_associated | relid=0 | w=28
  1355. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:walking delay
    n1=méningé (syndrome) | n2=en:walking delay | rel=r_associated | relid=0 | w=28
  1356. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:white matter lesions in the brainstem may occur
    n1=méningé (syndrome) | n2=en:white matter lesions in the brainstem may occur | rel=r_associated | relid=0 | w=28
  1357. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:wide sylvian fissures with incomplete opercularization
    n1=méningé (syndrome) | n2=en:wide sylvian fissures with incomplete opercularization | rel=r_associated | relid=0 | w=28
  1358. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:widened subarachnoid spaces
    n1=méningé (syndrome) | n2=en:widened subarachnoid spaces | rel=r_associated | relid=0 | w=28
  1359. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> en:widening of the operculum
    n1=méningé (syndrome) | n2=en:widening of the operculum | rel=r_associated | relid=0 | w=28
  1360. méningé (syndrome) -- r_associated #0: 28 / 0.337 -> pachyméninge
    n1=méningé (syndrome) | n2=pachyméninge | rel=r_associated | relid=0 | w=28
  1361. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:'ballooned' neurons with autofluorescent fine granular material
    n1=méningé (syndrome) | n2=en:'ballooned' neurons with autofluorescent fine granular material | rel=r_associated | relid=0 | w=27
  1362. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:abducens nerve palsy (cn vi)
    n1=méningé (syndrome) | n2=en:abducens nerve palsy (cn vi) | rel=r_associated | relid=0 | w=27
  1363. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:abnormal primitive reflexes
    n1=méningé (syndrome) | n2=en:abnormal primitive reflexes | rel=r_associated | relid=0 | w=27
  1364. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:abnormal signals in the thalami seen on mri
    n1=méningé (syndrome) | n2=en:abnormal signals in the thalami seen on mri | rel=r_associated | relid=0 | w=27
  1365. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:absence of the basal ganglia
    n1=méningé (syndrome) | n2=en:absence of the basal ganglia | rel=r_associated | relid=0 | w=27
  1366. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:absent or limited speech development
    n1=méningé (syndrome) | n2=en:absent or limited speech development | rel=r_associated | relid=0 | w=27
  1367. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:absent primitive reflexes
    n1=méningé (syndrome) | n2=en:absent primitive reflexes | rel=r_associated | relid=0 | w=27
  1368. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:acute episodes of neuropathic symptoms
    n1=méningé (syndrome) | n2=en:acute episodes of neuropathic symptoms | rel=r_associated | relid=0 | w=27
  1369. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:agenesis of the corpus callosum (in 1 of 2 patients)
    n1=méningé (syndrome) | n2=en:agenesis of the corpus callosum (in 1 of 2 patients) | rel=r_associated | relid=0 | w=27
  1370. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:agenesis of the corpus callosum (in 2 patients)
    n1=méningé (syndrome) | n2=en:agenesis of the corpus callosum (in 2 patients) | rel=r_associated | relid=0 | w=27
  1371. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:agenesis of the corpus callosum (variable)
    n1=méningé (syndrome) | n2=en:agenesis of the corpus callosum (variable) | rel=r_associated | relid=0 | w=27
  1372. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:agenesis of the occipital lobes (1 patient)
    n1=méningé (syndrome) | n2=en:agenesis of the occipital lobes (1 patient) | rel=r_associated | relid=0 | w=27
  1373. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:agyria (posterior-to-anterior gradient)
    n1=méningé (syndrome) | n2=en:agyria (posterior-to-anterior gradient) | rel=r_associated | relid=0 | w=27
  1374. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:angulation of the frontal horns
    n1=méningé (syndrome) | n2=en:angulation of the frontal horns | rel=r_associated | relid=0 | w=27
  1375. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:anisocoria
    n1=méningé (syndrome) | n2=en:anisocoria | rel=r_associated | relid=0 | w=27
  1376. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ankle clonus
    n1=méningé (syndrome) | n2=en:ankle clonus | rel=r_associated | relid=0 | w=27
  1377. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:anterior horn atrophy
    n1=méningé (syndrome) | n2=en:anterior horn atrophy | rel=r_associated | relid=0 | w=27
  1378. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:anterior horn cell impairment
    n1=méningé (syndrome) | n2=en:anterior horn cell impairment | rel=r_associated | relid=0 | w=27
  1379. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:anterior temporal lobe subcortical cysts
    n1=méningé (syndrome) | n2=en:anterior temporal lobe subcortical cysts | rel=r_associated | relid=0 | w=27
  1380. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:aplasia of corpus callosum
    n1=méningé (syndrome) | n2=en:aplasia of corpus callosum | rel=r_associated | relid=0 | w=27
  1381. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb)
    n1=méningé (syndrome) | n2=en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb) | rel=r_associated | relid=0 | w=27
  1382. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:arachnoid hemangiomata
    n1=méningé (syndrome) | n2=en:arachnoid hemangiomata | rel=r_associated | relid=0 | w=27
  1383. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:arhinencephaly
    n1=méningé (syndrome) | n2=en:arhinencephaly | rel=r_associated | relid=0 | w=27
  1384. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:arrested hydrocephalus (rare)
    n1=méningé (syndrome) | n2=en:arrested hydrocephalus (rare) | rel=r_associated | relid=0 | w=27
  1385. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:astrocytes show reactive changes
    n1=méningé (syndrome) | n2=en:astrocytes show reactive changes | rel=r_associated | relid=0 | w=27
  1386. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:astrocytosis
    n1=méningé (syndrome) | n2=en:astrocytosis | rel=r_associated | relid=0 | w=27
  1387. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ataxia
    n1=méningé (syndrome) | n2=en:ataxia | rel=r_associated | relid=0 | w=27
  1388. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ataxia may develop in middle age (less common)
    n1=méningé (syndrome) | n2=en:ataxia may develop in middle age (less common) | rel=r_associated | relid=0 | w=27
  1389. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ataxia worsens in the dark
    n1=méningé (syndrome) | n2=en:ataxia worsens in the dark | rel=r_associated | relid=0 | w=27
  1390. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ataxias, appendicular
    n1=méningé (syndrome) | n2=en:ataxias, appendicular | rel=r_associated | relid=0 | w=27
  1391. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ataxic gait (juvenile form)
    n1=méningé (syndrome) | n2=en:ataxic gait (juvenile form) | rel=r_associated | relid=0 | w=27
  1392. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ataxic movements
    n1=méningé (syndrome) | n2=en:ataxic movements | rel=r_associated | relid=0 | w=27
  1393. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:atrophy of hippocampal dentate gyrus
    n1=méningé (syndrome) | n2=en:atrophy of hippocampal dentate gyrus | rel=r_associated | relid=0 | w=27
  1394. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:autofluorescent pigment in microglia and macrophages
    n1=méningé (syndrome) | n2=en:autofluorescent pigment in microglia and macrophages | rel=r_associated | relid=0 | w=27
  1395. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:autonomic involvement may occur
    n1=méningé (syndrome) | n2=en:autonomic involvement may occur | rel=r_associated | relid=0 | w=27
  1396. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:axonal dystrophy
    n1=méningé (syndrome) | n2=en:axonal dystrophy | rel=r_associated | relid=0 | w=27
  1397. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib)
    n1=méningé (syndrome) | n2=en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib) | rel=r_associated | relid=0 | w=27
  1398. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain atrophy (1 family)
    n1=méningé (syndrome) | n2=en:brain atrophy (1 family) | rel=r_associated | relid=0 | w=27
  1399. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain calcification (if left untreated)
    n1=méningé (syndrome) | n2=en:brain calcification (if left untreated) | rel=r_associated | relid=0 | w=27
  1400. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain edema following head injury (less common)
    n1=méningé (syndrome) | n2=en:brain edema following head injury (less common) | rel=r_associated | relid=0 | w=27
  1401. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain imaging shows functional defects in the cortical and subcortical motor-related areas of the frontal lobe
    n1=méningé (syndrome) | n2=en:brain imaging shows functional defects in the cortical and subcortical motor-related areas of the frontal lobe | rel=r_associated | relid=0 | w=27
  1402. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain injury
    n1=méningé (syndrome) | n2=en:brain injury | rel=r_associated | relid=0 | w=27
  1403. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family)
    n1=méningé (syndrome) | n2=en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family) | rel=r_associated | relid=0 | w=27
  1404. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain mri shows cerebellar hypoplasia
    n1=méningé (syndrome) | n2=en:brain mri shows cerebellar hypoplasia | rel=r_associated | relid=0 | w=27
  1405. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain mri shows flattening of the ventral pons
    n1=méningé (syndrome) | n2=en:brain mri shows flattening of the ventral pons | rel=r_associated | relid=0 | w=27
  1406. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain mri shows hyperintensities in the basal ganglia
    n1=méningé (syndrome) | n2=en:brain mri shows hyperintensities in the basal ganglia | rel=r_associated | relid=0 | w=27
  1407. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain mri shows lesions consistent with epileptic episodes
    n1=méningé (syndrome) | n2=en:brain mri shows lesions consistent with epileptic episodes | rel=r_associated | relid=0 | w=27
  1408. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain mri shows lesions in the basal ganglia
    n1=méningé (syndrome) | n2=en:brain mri shows lesions in the basal ganglia | rel=r_associated | relid=0 | w=27
  1409. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain small vessel disease with hemorrhage
    n1=méningé (syndrome) | n2=en:brain small vessel disease with hemorrhage | rel=r_associated | relid=0 | w=27
  1410. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brain stem atrophy, progressive
    n1=méningé (syndrome) | n2=en:brain stem atrophy, progressive | rel=r_associated | relid=0 | w=27
  1411. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brainstem hypoplasia (1 patient)
    n1=méningé (syndrome) | n2=en:brainstem hypoplasia (1 patient) | rel=r_associated | relid=0 | w=27
  1412. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brainstem may show neuronal loss
    n1=méningé (syndrome) | n2=en:brainstem may show neuronal loss | rel=r_associated | relid=0 | w=27
  1413. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:brisk lower limb reflexes (in some patients)
    n1=méningé (syndrome) | n2=en:brisk lower limb reflexes (in some patients) | rel=r_associated | relid=0 | w=27
  1414. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:broad gait
    n1=méningé (syndrome) | n2=en:broad gait | rel=r_associated | relid=0 | w=27
  1415. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:broad-based gait (1 patient)
    n1=méningé (syndrome) | n2=en:broad-based gait (1 patient) | rel=r_associated | relid=0 | w=27
  1416. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:bulbar dysfunction (e.g. dysarthria and dysphagia)
    n1=méningé (syndrome) | n2=en:bulbar dysfunction (e.g. dysarthria and dysphagia) | rel=r_associated | relid=0 | w=27
  1417. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:bulbar involvement
    n1=méningé (syndrome) | n2=en:bulbar involvement | rel=r_associated | relid=0 | w=27
  1418. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:burst suppression pattern seen on eeg
    n1=méningé (syndrome) | n2=en:burst suppression pattern seen on eeg | rel=r_associated | relid=0 | w=27
  1419. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord
    n1=méningé (syndrome) | n2=en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord | rel=r_associated | relid=0 | w=27
  1420. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cavum vergae
    n1=méningé (syndrome) | n2=en:cavum vergae | rel=r_associated | relid=0 | w=27
  1421. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ccerebellar ataxia
    n1=méningé (syndrome) | n2=en:ccerebellar ataxia | rel=r_associated | relid=0 | w=27
  1422. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar ataxia during episodes
    n1=méningé (syndrome) | n2=en:cerebellar ataxia during episodes | rel=r_associated | relid=0 | w=27
  1423. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar ataxia, slowly progressive
    n1=méningé (syndrome) | n2=en:cerebellar ataxia, slowly progressive | rel=r_associated | relid=0 | w=27
  1424. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar atrophy (especially in the superior cerebellar vermis)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy (especially in the superior cerebellar vermis) | rel=r_associated | relid=0 | w=27
  1425. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar atrophy (juvenile form)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy (juvenile form) | rel=r_associated | relid=0 | w=27
  1426. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar atrophy in older patients
    n1=méningé (syndrome) | n2=en:cerebellar atrophy in older patients | rel=r_associated | relid=0 | w=27
  1427. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri
    n1=méningé (syndrome) | n2=en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri | rel=r_associated | relid=0 | w=27
  1428. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar atrophy, diffuse, severe
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, diffuse, severe | rel=r_associated | relid=0 | w=27
  1429. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar cell paucity, more marked in vermis than hemispheres
    n1=méningé (syndrome) | n2=en:cerebellar cell paucity, more marked in vermis than hemispheres | rel=r_associated | relid=0 | w=27
  1430. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar gangliocytoma manifesting as seizure and tremor
    n1=méningé (syndrome) | n2=en:cerebellar gangliocytoma manifesting as seizure and tremor | rel=r_associated | relid=0 | w=27
  1431. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar hemorrhage (rare)
    n1=méningé (syndrome) | n2=en:cerebellar hemorrhage (rare) | rel=r_associated | relid=0 | w=27
  1432. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar signs
    n1=méningé (syndrome) | n2=en:cerebellar signs | rel=r_associated | relid=0 | w=27
  1433. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebellar vermis aplasia or hypoplasia
    n1=méningé (syndrome) | n2=en:cerebellar vermis aplasia or hypoplasia | rel=r_associated | relid=0 | w=27
  1434. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebral atrophy, progressive
    n1=méningé (syndrome) | n2=en:cerebral atrophy, progressive | rel=r_associated | relid=0 | w=27
  1435. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebral cortex with spongiform changes
    n1=méningé (syndrome) | n2=en:cerebral cortex with spongiform changes | rel=r_associated | relid=0 | w=27
  1436. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cerebral infarction
    n1=méningé (syndrome) | n2=en:cerebral infarction | rel=r_associated | relid=0 | w=27
  1437. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:chiari i malformation on mri
    n1=méningé (syndrome) | n2=en:chiari i malformation on mri | rel=r_associated | relid=0 | w=27
  1438. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:chorea of all limbs
    n1=méningé (syndrome) | n2=en:chorea of all limbs | rel=r_associated | relid=0 | w=27
  1439. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:choreoathetosis (in a subset of patients)
    n1=méningé (syndrome) | n2=en:choreoathetosis (in a subset of patients) | rel=r_associated | relid=0 | w=27
  1440. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:choreoathetosis of the face, trunk, extremities
    n1=méningé (syndrome) | n2=en:choreoathetosis of the face, trunk, extremities | rel=r_associated | relid=0 | w=27
  1441. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma
    n1=méningé (syndrome) | n2=en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma | rel=r_associated | relid=0 | w=27
  1442. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:clumsiness (mild)
    n1=méningé (syndrome) | n2=en:clumsiness (mild) | rel=r_associated | relid=0 | w=27
  1443. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cns component
    n1=méningé (syndrome) | n2=en:cns component | rel=r_associated | relid=0 | w=27
  1444. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cobblestone lissencephaly
    n1=méningé (syndrome) | n2=en:cobblestone lissencephaly | rel=r_associated | relid=0 | w=27
  1445. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cognitive decline (1 family)
    n1=méningé (syndrome) | n2=en:cognitive decline (1 family) | rel=r_associated | relid=0 | w=27
  1446. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cognitive decline, rapid
    n1=méningé (syndrome) | n2=en:cognitive decline, rapid | rel=r_associated | relid=0 | w=27
  1447. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cognitive defects in executive function and attention
    n1=méningé (syndrome) | n2=en:cognitive defects in executive function and attention | rel=r_associated | relid=0 | w=27
  1448. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cognitive dysfunction (in some patients)
    n1=méningé (syndrome) | n2=en:cognitive dysfunction (in some patients) | rel=r_associated | relid=0 | w=27
  1449. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cognitive impairment (1 family)
    n1=méningé (syndrome) | n2=en:cognitive impairment (1 family) | rel=r_associated | relid=0 | w=27
  1450. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:coma
    n1=méningé (syndrome) | n2=en:coma | rel=r_associated | relid=0 | w=27
  1451. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:complete or partial absence of the corpus callosum (wws)
    n1=méningé (syndrome) | n2=en:complete or partial absence of the corpus callosum (wws) | rel=r_associated | relid=0 | w=27
  1452. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:confusion, paroxysmal
    n1=méningé (syndrome) | n2=en:confusion, paroxysmal | rel=r_associated | relid=0 | w=27
  1453. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:congenital cerebellar hypoplasia
    n1=méningé (syndrome) | n2=en:congenital cerebellar hypoplasia | rel=r_associated | relid=0 | w=27
  1454. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:congenital hypotonia, mild
    n1=méningé (syndrome) | n2=en:congenital hypotonia, mild | rel=r_associated | relid=0 | w=27
  1455. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:corpus callosum, thin (rare)
    n1=méningé (syndrome) | n2=en:corpus callosum, thin (rare) | rel=r_associated | relid=0 | w=27
  1456. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cranial nerve anomalies
    n1=méningé (syndrome) | n2=en:cranial nerve anomalies | rel=r_associated | relid=0 | w=27
  1457. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cranial nerve dysfunction
    n1=méningé (syndrome) | n2=en:cranial nerve dysfunction | rel=r_associated | relid=0 | w=27
  1458. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:crawling and standing not achieved
    n1=méningé (syndrome) | n2=en:crawling and standing not achieved | rel=r_associated | relid=0 | w=27
  1459. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ct scan shows dense calcifications in the basal ganglia
    n1=méningé (syndrome) | n2=en:ct scan shows dense calcifications in the basal ganglia | rel=r_associated | relid=0 | w=27
  1460. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cyst of septum pellucidum
    n1=méningé (syndrome) | n2=en:cyst of septum pellucidum | rel=r_associated | relid=0 | w=27
  1461. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:cytopathic effect
    n1=méningé (syndrome) | n2=en:cytopathic effect | rel=r_associated | relid=0 | w=27
  1462. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dandy-walker malformation (1 patient)
    n1=méningé (syndrome) | n2=en:dandy-walker malformation (1 patient) | rel=r_associated | relid=0 | w=27
  1463. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:decerebrate or decorticate posturing late
    n1=méningé (syndrome) | n2=en:decerebrate or decorticate posturing late | rel=r_associated | relid=0 | w=27
  1464. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:decerebrate posturings
    n1=méningé (syndrome) | n2=en:decerebrate posturings | rel=r_associated | relid=0 | w=27
  1465. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:decreased delineation of the basal ganglia (in some patients)
    n1=méningé (syndrome) | n2=en:decreased delineation of the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=27
  1466. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:decreased fine motor coordination
    n1=méningé (syndrome) | n2=en:decreased fine motor coordination | rel=r_associated | relid=0 | w=27
  1467. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:decreased sleep latency
    n1=méningé (syndrome) | n2=en:decreased sleep latency | rel=r_associated | relid=0 | w=27
  1468. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:deep white matter hypodensities
    n1=méningé (syndrome) | n2=en:deep white matter hypodensities | rel=r_associated | relid=0 | w=27
  1469. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:deja vu feeling
    n1=méningé (syndrome) | n2=en:deja vu feeling | rel=r_associated | relid=0 | w=27
  1470. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:delayed development, after 8-15 months
    n1=méningé (syndrome) | n2=en:delayed development, after 8-15 months | rel=r_associated | relid=0 | w=27
  1471. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:delayed development, variable (in some patients)
    n1=méningé (syndrome) | n2=en:delayed development, variable (in some patients) | rel=r_associated | relid=0 | w=27
  1472. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:delayed intellectual development
    n1=méningé (syndrome) | n2=en:delayed intellectual development | rel=r_associated | relid=0 | w=27
  1473. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:delayed motor development (1 patient)
    n1=méningé (syndrome) | n2=en:delayed motor development (1 patient) | rel=r_associated | relid=0 | w=27
  1474. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:delayed motor development, severe
    n1=méningé (syndrome) | n2=en:delayed motor development, severe | rel=r_associated | relid=0 | w=27
  1475. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:delayed myelination (1/4 patients)
    n1=méningé (syndrome) | n2=en:delayed myelination (1/4 patients) | rel=r_associated | relid=0 | w=27
  1476. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:delayed opercularization
    n1=méningé (syndrome) | n2=en:delayed opercularization | rel=r_associated | relid=0 | w=27
  1477. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:delayed or absent independent walking
    n1=méningé (syndrome) | n2=en:delayed or absent independent walking | rel=r_associated | relid=0 | w=27
  1478. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:delayed psychomotor development, severe (in 2 of 6 patients)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, severe (in 2 of 6 patients) | rel=r_associated | relid=0 | w=27
  1479. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental delay
    n1=méningé (syndrome) | n2=en:developmental delay | rel=r_associated | relid=0 | w=27
  1480. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental delay (1 family)
    n1=méningé (syndrome) | n2=en:developmental delay (1 family) | rel=r_associated | relid=0 | w=27
  1481. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental delay if undiagnosed or untreated
    n1=méningé (syndrome) | n2=en:developmental delay if undiagnosed or untreated | rel=r_associated | relid=0 | w=27
  1482. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental delay or regression
    n1=méningé (syndrome) | n2=en:developmental delay or regression | rel=r_associated | relid=0 | w=27
  1483. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental delay, mild to moderate
    n1=méningé (syndrome) | n2=en:developmental delay, mild to moderate | rel=r_associated | relid=0 | w=27
  1484. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental delay, severe
    n1=méningé (syndrome) | n2=en:developmental delay, severe | rel=r_associated | relid=0 | w=27
  1485. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental delay, severe (2p21del)
    n1=méningé (syndrome) | n2=en:developmental delay, severe (2p21del) | rel=r_associated | relid=0 | w=27
  1486. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental regression
    n1=méningé (syndrome) | n2=en:developmental regression | rel=r_associated | relid=0 | w=27
  1487. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental regression after the first year
    n1=méningé (syndrome) | n2=en:developmental regression after the first year | rel=r_associated | relid=0 | w=27
  1488. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental regression before age 6 months
    n1=méningé (syndrome) | n2=en:developmental regression before age 6 months | rel=r_associated | relid=0 | w=27
  1489. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental regression in about 50% of patients
    n1=méningé (syndrome) | n2=en:developmental regression in about 50% of patients | rel=r_associated | relid=0 | w=27
  1490. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:developmental regression, severe
    n1=méningé (syndrome) | n2=en:developmental regression, severe | rel=r_associated | relid=0 | w=27
  1491. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:difficulties with equilibrium
    n1=méningé (syndrome) | n2=en:difficulties with equilibrium | rel=r_associated | relid=0 | w=27
  1492. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem
    n1=méningé (syndrome) | n2=en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem | rel=r_associated | relid=0 | w=27
  1493. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:diffuse cerebral atrophy on ct and mri
    n1=méningé (syndrome) | n2=en:diffuse cerebral atrophy on ct and mri | rel=r_associated | relid=0 | w=27
  1494. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:diffuse hyperintense signal abnormalities in the white matter (in children)
    n1=méningé (syndrome) | n2=en:diffuse hyperintense signal abnormalities in the white matter (in children) | rel=r_associated | relid=0 | w=27
  1495. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:diffuse signal abnormality of central white matter
    n1=méningé (syndrome) | n2=en:diffuse signal abnormality of central white matter | rel=r_associated | relid=0 | w=27
  1496. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dilated fourth ventricle
    n1=méningé (syndrome) | n2=en:dilated fourth ventricle | rel=r_associated | relid=0 | w=27
  1497. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:distal amyotrophy
    n1=méningé (syndrome) | n2=en:distal amyotrophy | rel=r_associated | relid=0 | w=27
  1498. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:disturbance of attention
    n1=méningé (syndrome) | n2=en:disturbance of attention | rel=r_associated | relid=0 | w=27
  1499. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dizziness may occur
    n1=méningé (syndrome) | n2=en:dizziness may occur | rel=r_associated | relid=0 | w=27
  1500. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dural and choroid plexus calcifications
    n1=méningé (syndrome) | n2=en:dural and choroid plexus calcifications | rel=r_associated | relid=0 | w=27
  1501. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dysarthria (1 family)
    n1=méningé (syndrome) | n2=en:dysarthria (1 family) | rel=r_associated | relid=0 | w=27
  1502. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dysarthria, mild (1 family)
    n1=méningé (syndrome) | n2=en:dysarthria, mild (1 family) | rel=r_associated | relid=0 | w=27
  1503. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dysarthria, slowly progressive
    n1=méningé (syndrome) | n2=en:dysarthria, slowly progressive | rel=r_associated | relid=0 | w=27
  1504. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dysautonomia
    n1=méningé (syndrome) | n2=en:dysautonomia | rel=r_associated | relid=0 | w=27
  1505. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dysmetria (1 family)
    n1=méningé (syndrome) | n2=en:dysmetria (1 family) | rel=r_associated | relid=0 | w=27
  1506. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dysmetria (type i)
    n1=méningé (syndrome) | n2=en:dysmetria (type i) | rel=r_associated | relid=0 | w=27
  1507. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dysmorphic basal ganglia (in some)
    n1=méningé (syndrome) | n2=en:dysmorphic basal ganglia (in some) | rel=r_associated | relid=0 | w=27
  1508. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dysplastic cerebellum
    n1=méningé (syndrome) | n2=en:dysplastic cerebellum | rel=r_associated | relid=0 | w=27
  1509. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dysplastic superior cerebellar vermis
    n1=méningé (syndrome) | n2=en:dysplastic superior cerebellar vermis | rel=r_associated | relid=0 | w=27
  1510. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:dystonia 18 (disorder)
    n1=méningé (syndrome) | n2=en:dystonia 18 (disorder) | rel=r_associated | relid=0 | w=27
  1511. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:echolalia
    n1=méningé (syndrome) | n2=en:echolalia | rel=r_associated | relid=0 | w=27
  1512. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:eeg shows generalized polyspike and wave discharges (4-6 hz)
    n1=méningé (syndrome) | n2=en:eeg shows generalized polyspike and wave discharges (4-6 hz) | rel=r_associated | relid=0 | w=27
  1513. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:eeg shows generalized, bilateral, synchronous, symmetrical discharge
    n1=méningé (syndrome) | n2=en:eeg shows generalized, bilateral, synchronous, symmetrical discharge | rel=r_associated | relid=0 | w=27
  1514. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:emg shows neurogenic changes
    n1=méningé (syndrome) | n2=en:emg shows neurogenic changes | rel=r_associated | relid=0 | w=27
  1515. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:emg with spontaneous discharge of normal motor unit potentials
    n1=méningé (syndrome) | n2=en:emg with spontaneous discharge of normal motor unit potentials | rel=r_associated | relid=0 | w=27
  1516. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:encephalocele (single case)
    n1=méningé (syndrome) | n2=en:encephalocele (single case) | rel=r_associated | relid=0 | w=27
  1517. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:encephalocele of orbit
    n1=méningé (syndrome) | n2=en:encephalocele of orbit | rel=r_associated | relid=0 | w=27
  1518. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:enlarged lateral and third ventricles
    n1=méningé (syndrome) | n2=en:enlarged lateral and third ventricles | rel=r_associated | relid=0 | w=27
  1519. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions
    n1=méningé (syndrome) | n2=en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions | rel=r_associated | relid=0 | w=27
  1520. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:epilepsy, frontal lobe
    n1=méningé (syndrome) | n2=en:epilepsy, frontal lobe | rel=r_associated | relid=0 | w=27
  1521. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:epilepsy, refractory (onset in adolescence or young adulthood)
    n1=méningé (syndrome) | n2=en:epilepsy, refractory (onset in adolescence or young adulthood) | rel=r_associated | relid=0 | w=27
  1522. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:episodes begin with muscle tightening
    n1=méningé (syndrome) | n2=en:episodes begin with muscle tightening | rel=r_associated | relid=0 | w=27
  1523. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:episodic confusion
    n1=méningé (syndrome) | n2=en:episodic confusion | rel=r_associated | relid=0 | w=27
  1524. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:essential tremor
    n1=méningé (syndrome) | n2=en:essential tremor | rel=r_associated | relid=0 | w=27
  1525. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:excessive daytime somnolence
    n1=méningé (syndrome) | n2=en:excessive daytime somnolence | rel=r_associated | relid=0 | w=27
  1526. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:extensor posturing
    n1=méningé (syndrome) | n2=en:extensor posturing | rel=r_associated | relid=0 | w=27
  1527. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:external capsule and claustrum may be involved
    n1=méningé (syndrome) | n2=en:external capsule and claustrum may be involved | rel=r_associated | relid=0 | w=27
  1528. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:extrapyramidal signs (in some patients) thinning of the corpus callosum
    n1=méningé (syndrome) | n2=en:extrapyramidal signs (in some patients) thinning of the corpus callosum | rel=r_associated | relid=0 | w=27
  1529. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:extremity ataxia
    n1=méningé (syndrome) | n2=en:extremity ataxia | rel=r_associated | relid=0 | w=27
  1530. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:fenestrated basilar artery
    n1=méningé (syndrome) | n2=en:fenestrated basilar artery | rel=r_associated | relid=0 | w=27
  1531. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:fibrillary plaques in the cerebellar cortex
    n1=méningé (syndrome) | n2=en:fibrillary plaques in the cerebellar cortex | rel=r_associated | relid=0 | w=27
  1532. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:focal discharges
    n1=méningé (syndrome) | n2=en:focal discharges | rel=r_associated | relid=0 | w=27
  1533. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:focal lissencephaly
    n1=méningé (syndrome) | n2=en:focal lissencephaly | rel=r_associated | relid=0 | w=27
  1534. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:focal neurologic signs
    n1=méningé (syndrome) | n2=en:focal neurologic signs | rel=r_associated | relid=0 | w=27
  1535. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:focal thickening of the cortex on mri (in type iib)
    n1=méningé (syndrome) | n2=en:focal thickening of the cortex on mri (in type iib) | rel=r_associated | relid=0 | w=27
  1536. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:focal white matter lesions (in type iib)
    n1=méningé (syndrome) | n2=en:focal white matter lesions (in type iib) | rel=r_associated | relid=0 | w=27
  1537. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:frequency 6 hz in lateral gaze
    n1=méningé (syndrome) | n2=en:frequency 6 hz in lateral gaze | rel=r_associated | relid=0 | w=27
  1538. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:frequent falls
    n1=méningé (syndrome) | n2=en:frequent falls | rel=r_associated | relid=0 | w=27
  1539. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:frequent headache
    n1=méningé (syndrome) | n2=en:frequent headache | rel=r_associated | relid=0 | w=27
  1540. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:frontal lobe origin
    n1=méningé (syndrome) | n2=en:frontal lobe origin | rel=r_associated | relid=0 | w=27
  1541. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:frontotemporal atrophy
    n1=méningé (syndrome) | n2=en:frontotemporal atrophy | rel=r_associated | relid=0 | w=27
  1542. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:gait disturbance
    n1=méningé (syndrome) | n2=en:gait disturbance | rel=r_associated | relid=0 | w=27
  1543. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:gait unsteady
    n1=méningé (syndrome) | n2=en:gait unsteady | rel=r_associated | relid=0 | w=27
  1544. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:generalized amyotrophy
    n1=méningé (syndrome) | n2=en:generalized amyotrophy | rel=r_associated | relid=0 | w=27
  1545. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:generalized cortical atrophy (in one patient)
    n1=méningé (syndrome) | n2=en:generalized cortical atrophy (in one patient) | rel=r_associated | relid=0 | w=27
  1546. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:generalized seizures
    n1=méningé (syndrome) | n2=en:generalized seizures | rel=r_associated | relid=0 | w=27
  1547. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:generalized slowing
    n1=méningé (syndrome) | n2=en:generalized slowing | rel=r_associated | relid=0 | w=27
  1548. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:generalized spike wave discharges
    n1=méningé (syndrome) | n2=en:generalized spike wave discharges | rel=r_associated | relid=0 | w=27
  1549. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:giant cortical somatosensory evoked potentials (seps)
    n1=méningé (syndrome) | n2=en:giant cortical somatosensory evoked potentials (seps) | rel=r_associated | relid=0 | w=27
  1550. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:gilles de la tourette syndrome (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:gilles de la tourette syndrome (reported in 1 patient) | rel=r_associated | relid=0 | w=27
  1551. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:global cerebral atrophy, mild (in some patients)
    n1=méningé (syndrome) | n2=en:global cerebral atrophy, mild (in some patients) | rel=r_associated | relid=0 | w=27
  1552. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:global developmental delay, variable severity
    n1=méningé (syndrome) | n2=en:global developmental delay, variable severity | rel=r_associated | relid=0 | w=27
  1553. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:grade ii meningioma
    n1=méningé (syndrome) | n2=en:grade ii meningioma | rel=r_associated | relid=0 | w=27
  1554. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:head tremor (14% of patients)
    n1=méningé (syndrome) | n2=en:head tremor (14% of patients) | rel=r_associated | relid=0 | w=27
  1555. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:head tremor (in some patients)
    n1=méningé (syndrome) | n2=en:head tremor (in some patients) | rel=r_associated | relid=0 | w=27
  1556. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hemimegalencephaly
    n1=méningé (syndrome) | n2=en:hemimegalencephaly | rel=r_associated | relid=0 | w=27
  1557. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hemiparesis, paroxysmal
    n1=méningé (syndrome) | n2=en:hemiparesis, paroxysmal | rel=r_associated | relid=0 | w=27
  1558. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hemorrhagic cerebrovascular accident
    n1=méningé (syndrome) | n2=en:hemorrhagic cerebrovascular accident | rel=r_associated | relid=0 | w=27
  1559. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:high-steppage gait
    n1=méningé (syndrome) | n2=en:high-steppage gait | rel=r_associated | relid=0 | w=27
  1560. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:holoprosencephaly (1 patient)
    n1=méningé (syndrome) | n2=en:holoprosencephaly (1 patient) | rel=r_associated | relid=0 | w=27
  1561. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hydrocephalus (uncommon)
    n1=méningé (syndrome) | n2=en:hydrocephalus (uncommon) | rel=r_associated | relid=0 | w=27
  1562. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hyperactivity
    n1=méningé (syndrome) | n2=en:hyperactivity | rel=r_associated | relid=0 | w=27
  1563. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hyperekplexia (rare)
    n1=méningé (syndrome) | n2=en:hyperekplexia (rare) | rel=r_associated | relid=0 | w=27
  1564. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hyperintense lesions in the basal ganglia on mri
    n1=méningé (syndrome) | n2=en:hyperintense lesions in the basal ganglia on mri | rel=r_associated | relid=0 | w=27
  1565. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypersomnolent
    n1=méningé (syndrome) | n2=en:hypersomnolent | rel=r_associated | relid=0 | w=27
  1566. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypertonia (in some patients)
    n1=méningé (syndrome) | n2=en:hypertonia (in some patients) | rel=r_associated | relid=0 | w=27
  1567. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypertonia (type ii)
    n1=méningé (syndrome) | n2=en:hypertonia (type ii) | rel=r_associated | relid=0 | w=27
  1568. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypnapompic hallucinations
    n1=méningé (syndrome) | n2=en:hypnapompic hallucinations | rel=r_associated | relid=0 | w=27
  1569. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypodensity of caudate
    n1=méningé (syndrome) | n2=en:hypodensity of caudate | rel=r_associated | relid=0 | w=27
  1570. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypoplasia of the medulla oblongata
    n1=méningé (syndrome) | n2=en:hypoplasia of the medulla oblongata | rel=r_associated | relid=0 | w=27
  1571. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypoplasia of the mesencephalic tectum
    n1=méningé (syndrome) | n2=en:hypoplasia of the mesencephalic tectum | rel=r_associated | relid=0 | w=27
  1572. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypoplasia of the pyramidal tract
    n1=méningé (syndrome) | n2=en:hypoplasia of the pyramidal tract | rel=r_associated | relid=0 | w=27
  1573. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hyporeflexia
    n1=méningé (syndrome) | n2=en:hyporeflexia | rel=r_associated | relid=0 | w=27
  1574. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypotonia (early-onset form)
    n1=méningé (syndrome) | n2=en:hypotonia (early-onset form) | rel=r_associated | relid=0 | w=27
  1575. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypotonia (type i and type ii, infantile)
    n1=méningé (syndrome) | n2=en:hypotonia (type i and type ii, infantile) | rel=r_associated | relid=0 | w=27
  1576. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypotonia progressing to hypertonia
    n1=méningé (syndrome) | n2=en:hypotonia progressing to hypertonia | rel=r_associated | relid=0 | w=27
  1577. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:hypotonia, proximal, severe
    n1=méningé (syndrome) | n2=en:hypotonia, proximal, severe | rel=r_associated | relid=0 | w=27
  1578. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ictal eeg shows focal onset in central, parietal, or temporal regions
    n1=méningé (syndrome) | n2=en:ictal eeg shows focal onset in central, parietal, or temporal regions | rel=r_associated | relid=0 | w=27
  1579. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:idiopathic generalized epilepsy in childhood (homozygous patient)
    n1=méningé (syndrome) | n2=en:idiopathic generalized epilepsy in childhood (homozygous patient) | rel=r_associated | relid=0 | w=27
  1580. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:impaired ambulation due to muscle weakness
    n1=méningé (syndrome) | n2=en:impaired ambulation due to muscle weakness | rel=r_associated | relid=0 | w=27
  1581. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:impaired expression of language
    n1=méningé (syndrome) | n2=en:impaired expression of language | rel=r_associated | relid=0 | w=27
  1582. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:inability to hold neck up ('limber neck') onset at 6 months
    n1=méningé (syndrome) | n2=en:inability to hold neck up ('limber neck') onset at 6 months | rel=r_associated | relid=0 | w=27
  1583. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:infantile encephalopathy
    n1=méningé (syndrome) | n2=en:infantile encephalopathy | rel=r_associated | relid=0 | w=27
  1584. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:infantile encephalopathy, progressive
    n1=méningé (syndrome) | n2=en:infantile encephalopathy, progressive | rel=r_associated | relid=0 | w=27
  1585. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:inflexible adherence to routines or rituals
    n1=méningé (syndrome) | n2=en:inflexible adherence to routines or rituals | rel=r_associated | relid=0 | w=27
  1586. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:intellectual disability
    n1=méningé (syndrome) | n2=en:intellectual disability | rel=r_associated | relid=0 | w=27
  1587. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:intention tremor (in some patients)
    n1=méningé (syndrome) | n2=en:intention tremor (in some patients) | rel=r_associated | relid=0 | w=27
  1588. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:interictal ataxia may occur later in disease course
    n1=méningé (syndrome) | n2=en:interictal ataxia may occur later in disease course | rel=r_associated | relid=0 | w=27
  1589. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:interictal eeg may be normal or abnormal
    n1=méningé (syndrome) | n2=en:interictal eeg may be normal or abnormal | rel=r_associated | relid=0 | w=27
  1590. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:interventricular cysts
    n1=méningé (syndrome) | n2=en:interventricular cysts | rel=r_associated | relid=0 | w=27
  1591. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:intracranial calcification affecting the basal ganglia (in some patients)
    n1=méningé (syndrome) | n2=en:intracranial calcification affecting the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=27
  1592. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:intraventricular meningioma
    n1=méningé (syndrome) | n2=en:intraventricular meningioma | rel=r_associated | relid=0 | w=27
  1593. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:iq 85-115 (female)
    n1=méningé (syndrome) | n2=en:iq 85-115 (female) | rel=r_associated | relid=0 | w=27
  1594. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:iron deposits in the globus pallidus, caudate, and substantia nigra
    n1=méningé (syndrome) | n2=en:iron deposits in the globus pallidus, caudate, and substantia nigra | rel=r_associated | relid=0 | w=27
  1595. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:ischemic infarct of brain
    n1=méningé (syndrome) | n2=en:ischemic infarct of brain | rel=r_associated | relid=0 | w=27
  1596. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:jerk-locked premyoclonus spikes
    n1=méningé (syndrome) | n2=en:jerk-locked premyoclonus spikes | rel=r_associated | relid=0 | w=27
  1597. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:kearns-sayre syndrome (530000), in a subset of patients
    n1=méningé (syndrome) | n2=en:kearns-sayre syndrome (530000), in a subset of patients | rel=r_associated | relid=0 | w=27
  1598. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:lack of psychomotor development (1 patient)
    n1=méningé (syndrome) | n2=en:lack of psychomotor development (1 patient) | rel=r_associated | relid=0 | w=27
  1599. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:lack of speech or poor speech
    n1=méningé (syndrome) | n2=en:lack of speech or poor speech | rel=r_associated | relid=0 | w=27
  1600. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:lack of upper motor neuron signs
    n1=méningé (syndrome) | n2=en:lack of upper motor neuron signs | rel=r_associated | relid=0 | w=27
  1601. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:lethargy
    n1=méningé (syndrome) | n2=en:lethargy | rel=r_associated | relid=0 | w=27
  1602. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:limb dystonia
    n1=méningé (syndrome) | n2=en:limb dystonia | rel=r_associated | relid=0 | w=27
  1603. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions)
    n1=méningé (syndrome) | n2=en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions) | rel=r_associated | relid=0 | w=27
  1604. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of ability to walk
    n1=méningé (syndrome) | n2=en:loss of ability to walk | rel=r_associated | relid=0 | w=27
  1605. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of any acquired abilities in early childhood
    n1=méningé (syndrome) | n2=en:loss of any acquired abilities in early childhood | rel=r_associated | relid=0 | w=27
  1606. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of developmental milestones
    n1=méningé (syndrome) | n2=en:loss of developmental milestones | rel=r_associated | relid=0 | w=27
  1607. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of language ability
    n1=méningé (syndrome) | n2=en:loss of language ability | rel=r_associated | relid=0 | w=27
  1608. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of motor functions
    n1=méningé (syndrome) | n2=en:loss of motor functions | rel=r_associated | relid=0 | w=27
  1609. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of myelin and oligodendroglia
    n1=méningé (syndrome) | n2=en:loss of myelin and oligodendroglia | rel=r_associated | relid=0 | w=27
  1610. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of myelin in the descending lateral spinal cord tracts
    n1=méningé (syndrome) | n2=en:loss of myelin in the descending lateral spinal cord tracts | rel=r_associated | relid=0 | w=27
  1611. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord
    n1=méningé (syndrome) | n2=en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord | rel=r_associated | relid=0 | w=27
  1612. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of pigmented neurons in the substantia nigra
    n1=méningé (syndrome) | n2=en:loss of pigmented neurons in the substantia nigra | rel=r_associated | relid=0 | w=27
  1613. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of postural tone
    n1=méningé (syndrome) | n2=en:loss of postural tone | rel=r_associated | relid=0 | w=27
  1614. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:loss of spontaneous movements
    n1=méningé (syndrome) | n2=en:loss of spontaneous movements | rel=r_associated | relid=0 | w=27
  1615. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:low apparent diffusion coefficient (adc) values
    n1=méningé (syndrome) | n2=en:low apparent diffusion coefficient (adc) values | rel=r_associated | relid=0 | w=27
  1616. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:lower limb hypotrophy
    n1=méningé (syndrome) | n2=en:lower limb hypotrophy | rel=r_associated | relid=0 | w=27
  1617. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:lower limb weakness, proximal
    n1=méningé (syndrome) | n2=en:lower limb weakness, proximal | rel=r_associated | relid=0 | w=27
  1618. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:major developmental milestones are not attained
    n1=méningé (syndrome) | n2=en:major developmental milestones are not attained | rel=r_associated | relid=0 | w=27
  1619. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:malformations of cortical development
    n1=méningé (syndrome) | n2=en:malformations of cortical development | rel=r_associated | relid=0 | w=27
  1620. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:megacisterna magna (in some patients)
    n1=méningé (syndrome) | n2=en:megacisterna magna (in some patients) | rel=r_associated | relid=0 | w=27
  1621. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:meningeal carcinomatosis
    n1=méningé (syndrome) | n2=en:meningeal carcinomatosis | rel=r_associated | relid=0 | w=27
  1622. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mental impairment may develop with repeated acute episodes
    n1=méningé (syndrome) | n2=en:mental impairment may develop with repeated acute episodes | rel=r_associated | relid=0 | w=27
  1623. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mental retardation (30%)
    n1=méningé (syndrome) | n2=en:mental retardation (30%) | rel=r_associated | relid=0 | w=27
  1624. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mental retardation (70%)
    n1=méningé (syndrome) | n2=en:mental retardation (70%) | rel=r_associated | relid=0 | w=27
  1625. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mental retardation (in some)
    n1=méningé (syndrome) | n2=en:mental retardation (in some) | rel=r_associated | relid=0 | w=27
  1626. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mental retardation (moderate to severe in males)
    n1=méningé (syndrome) | n2=en:mental retardation (moderate to severe in males) | rel=r_associated | relid=0 | w=27
  1627. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mental retardation (range mild to severe)
    n1=méningé (syndrome) | n2=en:mental retardation (range mild to severe) | rel=r_associated | relid=0 | w=27
  1628. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mental retardation, mild, some patients (iq 70-80)
    n1=méningé (syndrome) | n2=en:mental retardation, mild, some patients (iq 70-80) | rel=r_associated | relid=0 | w=27
  1629. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mental retardation, moderate (in sister)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate (in sister) | rel=r_associated | relid=0 | w=27
  1630. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mental retardation, moderate to severe (in some patients)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate to severe (in some patients) | rel=r_associated | relid=0 | w=27
  1631. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:microbleeds
    n1=méningé (syndrome) | n2=en:microbleeds | rel=r_associated | relid=0 | w=27
  1632. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:microcystic degeneration
    n1=méningé (syndrome) | n2=en:microcystic degeneration | rel=r_associated | relid=0 | w=27
  1633. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:micrographia
    n1=méningé (syndrome) | n2=en:micrographia | rel=r_associated | relid=0 | w=27
  1634. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:microlissencephalies
    n1=méningé (syndrome) | n2=en:microlissencephalies | rel=r_associated | relid=0 | w=27
  1635. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:migraine headaches (ipsilateral to facial hemangioma)
    n1=méningé (syndrome) | n2=en:migraine headaches (ipsilateral to facial hemangioma) | rel=r_associated | relid=0 | w=27
  1636. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:migrating partial seizures
    n1=méningé (syndrome) | n2=en:migrating partial seizures | rel=r_associated | relid=0 | w=27
  1637. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mild cortical atrophy (in 1 patient)
    n1=méningé (syndrome) | n2=en:mild cortical atrophy (in 1 patient) | rel=r_associated | relid=0 | w=27
  1638. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mild cortical atrophy on ct or mri
    n1=méningé (syndrome) | n2=en:mild cortical atrophy on ct or mri | rel=r_associated | relid=0 | w=27
  1639. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mild memory loss
    n1=méningé (syndrome) | n2=en:mild memory loss | rel=r_associated | relid=0 | w=27
  1640. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mild structural abnormalities seen mri (in some patients)
    n1=méningé (syndrome) | n2=en:mild structural abnormalities seen mri (in some patients) | rel=r_associated | relid=0 | w=27
  1641. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mild-moderate ventricular dilatation
    n1=méningé (syndrome) | n2=en:mild-moderate ventricular dilatation | rel=r_associated | relid=0 | w=27
  1642. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mild-severe mental retardation (20%)
    n1=méningé (syndrome) | n2=en:mild-severe mental retardation (20%) | rel=r_associated | relid=0 | w=27
  1643. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mirror movements, involuntary, affecting the hand and fingers
    n1=méningé (syndrome) | n2=en:mirror movements, involuntary, affecting the hand and fingers | rel=r_associated | relid=0 | w=27
  1644. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mobility poor
    n1=méningé (syndrome) | n2=en:mobility poor | rel=r_associated | relid=0 | w=27
  1645. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:motor and vocal tics
    n1=méningé (syndrome) | n2=en:motor and vocal tics | rel=r_associated | relid=0 | w=27
  1646. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:motor developmental delay
    n1=méningé (syndrome) | n2=en:motor developmental delay | rel=r_associated | relid=0 | w=27
  1647. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:moyamoya disease
    n1=méningé (syndrome) | n2=en:moyamoya disease | rel=r_associated | relid=0 | w=27
  1648. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mri is best imaging modality to detect lesions
    n1=méningé (syndrome) | n2=en:mri is best imaging modality to detect lesions | rel=r_associated | relid=0 | w=27
  1649. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mri shows brain asymmetry
    n1=méningé (syndrome) | n2=en:mri shows brain asymmetry | rel=r_associated | relid=0 | w=27
  1650. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mri shows decreased signal intensity in the pallidal nuclei with central hyperintensity ('eye of the tiger' sign)
    n1=méningé (syndrome) | n2=en:mri shows decreased signal intensity in the pallidal nuclei with central hyperintensity ('eye of the tiger' sign) | rel=r_associated | relid=0 | w=27
  1651. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mri shows delayed myelination (1 of 6 patients)
    n1=méningé (syndrome) | n2=en:mri shows delayed myelination (1 of 6 patients) | rel=r_associated | relid=0 | w=27
  1652. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:mri shows frontal and temporal cortical atrophy
    n1=méningé (syndrome) | n2=en:mri shows frontal and temporal cortical atrophy | rel=r_associated | relid=0 | w=27
  1653. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:multifocal epileptic activity
    n1=méningé (syndrome) | n2=en:multifocal epileptic activity | rel=r_associated | relid=0 | w=27
  1654. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:multifocal spike waves
    n1=méningé (syndrome) | n2=en:multifocal spike waves | rel=r_associated | relid=0 | w=27
  1655. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:muscle cramp
    n1=méningé (syndrome) | n2=en:muscle cramp | rel=r_associated | relid=0 | w=27
  1656. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:myoclonus (in 1 family)
    n1=méningé (syndrome) | n2=en:myoclonus (in 1 family) | rel=r_associated | relid=0 | w=27
  1657. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:myoclonus (subtype 3a)
    n1=méningé (syndrome) | n2=en:myoclonus (subtype 3a) | rel=r_associated | relid=0 | w=27
  1658. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:myoclonus (type i and type ii, infantile and juvenile)
    n1=méningé (syndrome) | n2=en:myoclonus (type i and type ii, infantile and juvenile) | rel=r_associated | relid=0 | w=27
  1659. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:nerve degeneration
    n1=méningé (syndrome) | n2=en:nerve degeneration | rel=r_associated | relid=0 | w=27
  1660. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:neurofibrillary degeneration (morphologic abnormality)
    n1=méningé (syndrome) | n2=en:neurofibrillary degeneration (morphologic abnormality) | rel=r_associated | relid=0 | w=27
  1661. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:neurofibrillary mapt (tau)-positive tangles
    n1=méningé (syndrome) | n2=en:neurofibrillary mapt (tau)-positive tangles | rel=r_associated | relid=0 | w=27
  1662. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:neuron apoptotic process
    n1=méningé (syndrome) | n2=en:neuron apoptotic process | rel=r_associated | relid=0 | w=27
  1663. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:neuronal inclusion bodies stain for neuroserpin
    n1=méningé (syndrome) | n2=en:neuronal inclusion bodies stain for neuroserpin | rel=r_associated | relid=0 | w=27
  1664. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:neuronal loss (patient a)
    n1=méningé (syndrome) | n2=en:neuronal loss (patient a) | rel=r_associated | relid=0 | w=27
  1665. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:neuronal loss, particularly of cerebellar purkinje cells
    n1=méningé (syndrome) | n2=en:neuronal loss, particularly of cerebellar purkinje cells | rel=r_associated | relid=0 | w=27
  1666. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum
    n1=méningé (syndrome) | n2=en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum | rel=r_associated | relid=0 | w=27
  1667. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:no lewy bodies
    n1=méningé (syndrome) | n2=en:no lewy bodies | rel=r_associated | relid=0 | w=27
  1668. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:no other neurologic deficits
    n1=méningé (syndrome) | n2=en:no other neurologic deficits | rel=r_associated | relid=0 | w=27
  1669. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:no pick bodies or lewy bodies
    n1=méningé (syndrome) | n2=en:no pick bodies or lewy bodies | rel=r_associated | relid=0 | w=27
  1670. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:no spontaneous movements
    n1=méningé (syndrome) | n2=en:no spontaneous movements | rel=r_associated | relid=0 | w=27
  1671. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:no voluntary movement
    n1=méningé (syndrome) | n2=en:no voluntary movement | rel=r_associated | relid=0 | w=27
  1672. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:nocturnal occurrence
    n1=méningé (syndrome) | n2=en:nocturnal occurrence | rel=r_associated | relid=0 | w=27
  1673. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:nodular heterotopia (in some patients)
    n1=méningé (syndrome) | n2=en:nodular heterotopia (in some patients) | rel=r_associated | relid=0 | w=27
  1674. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:normal brain mri or ct scan
    n1=méningé (syndrome) | n2=en:normal brain mri or ct scan | rel=r_associated | relid=0 | w=27
  1675. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:normal intelligence in carrier females
    n1=méningé (syndrome) | n2=en:normal intelligence in carrier females | rel=r_associated | relid=0 | w=27
  1676. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:normal intelligence in iib
    n1=méningé (syndrome) | n2=en:normal intelligence in iib | rel=r_associated | relid=0 | w=27
  1677. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:normal intelligence in majority
    n1=méningé (syndrome) | n2=en:normal intelligence in majority | rel=r_associated | relid=0 | w=27
  1678. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:normal interictal neurologic examination
    n1=méningé (syndrome) | n2=en:normal interictal neurologic examination | rel=r_associated | relid=0 | w=27
  1679. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:normal motor conduction studies (initially)
    n1=méningé (syndrome) | n2=en:normal motor conduction studies (initially) | rel=r_associated | relid=0 | w=27
  1680. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:normal neurological development is possible
    n1=méningé (syndrome) | n2=en:normal neurological development is possible | rel=r_associated | relid=0 | w=27
  1681. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:nystagmus decreases on convergence
    n1=méningé (syndrome) | n2=en:nystagmus decreases on convergence | rel=r_associated | relid=0 | w=27
  1682. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:occipital encephalocele (wws)
    n1=méningé (syndrome) | n2=en:occipital encephalocele (wws) | rel=r_associated | relid=0 | w=27
  1683. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:occipital encephaloceles
    n1=méningé (syndrome) | n2=en:occipital encephaloceles | rel=r_associated | relid=0 | w=27
  1684. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:olfactory groove meningioma
    n1=méningé (syndrome) | n2=en:olfactory groove meningioma | rel=r_associated | relid=0 | w=27
  1685. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:over time, white matter vanishes and is replaced by csf
    n1=méningé (syndrome) | n2=en:over time, white matter vanishes and is replaced by csf | rel=r_associated | relid=0 | w=27
  1686. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:pachygyria, most prominent in the frontal lobes
    n1=méningé (syndrome) | n2=en:pachygyria, most prominent in the frontal lobes | rel=r_associated | relid=0 | w=27
  1687. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:paraparesis
    n1=méningé (syndrome) | n2=en:paraparesis | rel=r_associated | relid=0 | w=27
  1688. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:parkinsonism (in some)
    n1=méningé (syndrome) | n2=en:parkinsonism (in some) | rel=r_associated | relid=0 | w=27
  1689. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:paroxysmal dystonia
    n1=méningé (syndrome) | n2=en:paroxysmal dystonia | rel=r_associated | relid=0 | w=27
  1690. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:paroxysmal lethargy
    n1=méningé (syndrome) | n2=en:paroxysmal lethargy | rel=r_associated | relid=0 | w=27
  1691. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:paroxysmal nonkinesigenic dyskinesia
    n1=méningé (syndrome) | n2=en:paroxysmal nonkinesigenic dyskinesia | rel=r_associated | relid=0 | w=27
  1692. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:partial agenesis of corpus callosum
    n1=méningé (syndrome) | n2=en:partial agenesis of corpus callosum | rel=r_associated | relid=0 | w=27
  1693. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:partial or complete agenesis of corpus callosum
    n1=méningé (syndrome) | n2=en:partial or complete agenesis of corpus callosum | rel=r_associated | relid=0 | w=27
  1694. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:partial seizures, simple and complex
    n1=méningé (syndrome) | n2=en:partial seizures, simple and complex | rel=r_associated | relid=0 | w=27
  1695. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:patellar and ankle clonus
    n1=méningé (syndrome) | n2=en:patellar and ankle clonus | rel=r_associated | relid=0 | w=27
  1696. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds
    n1=méningé (syndrome) | n2=en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds | rel=r_associated | relid=0 | w=27
  1697. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:periventricular white matter abnormalities (in some patients)
    n1=méningé (syndrome) | n2=en:periventricular white matter abnormalities (in some patients) | rel=r_associated | relid=0 | w=27
  1698. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:periventricular white matter gliosis (in some patients)
    n1=méningé (syndrome) | n2=en:periventricular white matter gliosis (in some patients) | rel=r_associated | relid=0 | w=27
  1699. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:persistent falcine venous sinus
    n1=méningé (syndrome) | n2=en:persistent falcine venous sinus | rel=r_associated | relid=0 | w=27
  1700. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:pigmentary loss in the substantia nigra
    n1=méningé (syndrome) | n2=en:pigmentary loss in the substantia nigra | rel=r_associated | relid=0 | w=27
  1701. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:polymicrogyria (meb)
    n1=méningé (syndrome) | n2=en:polymicrogyria (meb) | rel=r_associated | relid=0 | w=27
  1702. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:pontine dysraphia
    n1=méningé (syndrome) | n2=en:pontine dysraphia | rel=r_associated | relid=0 | w=27
  1703. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:pontoneocerebellar hypoplasia
    n1=méningé (syndrome) | n2=en:pontoneocerebellar hypoplasia | rel=r_associated | relid=0 | w=27
  1704. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:poor delineation of cerebral cortical regions
    n1=méningé (syndrome) | n2=en:poor delineation of cerebral cortical regions | rel=r_associated | relid=0 | w=27
  1705. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:poor feeding (congenital form form)
    n1=méningé (syndrome) | n2=en:poor feeding (congenital form form) | rel=r_associated | relid=0 | w=27
  1706. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:poor head and trunk control in infancy
    n1=méningé (syndrome) | n2=en:poor head and trunk control in infancy | rel=r_associated | relid=0 | w=27
  1707. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:poor neonatal suck and swallow reflexes
    n1=méningé (syndrome) | n2=en:poor neonatal suck and swallow reflexes | rel=r_associated | relid=0 | w=27
  1708. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:poor school performance
    n1=méningé (syndrome) | n2=en:poor school performance | rel=r_associated | relid=0 | w=27
  1709. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:porencephaly (in some patients)
    n1=méningé (syndrome) | n2=en:porencephaly (in some patients) | rel=r_associated | relid=0 | w=27
  1710. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:posterior fossa cysts (wws)
    n1=méningé (syndrome) | n2=en:posterior fossa cysts (wws) | rel=r_associated | relid=0 | w=27
  1711. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:postural tremor (later onset, spreads to all limbs and neck)
    n1=méningé (syndrome) | n2=en:postural tremor (later onset, spreads to all limbs and neck) | rel=r_associated | relid=0 | w=27
  1712. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:praxis
    n1=méningé (syndrome) | n2=en:praxis | rel=r_associated | relid=0 | w=27
  1713. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:premature stroke
    n1=méningé (syndrome) | n2=en:premature stroke | rel=r_associated | relid=0 | w=27
  1714. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:prion protein-positive senile plaques
    n1=méningé (syndrome) | n2=en:prion protein-positive senile plaques | rel=r_associated | relid=0 | w=27
  1715. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients)
    n1=méningé (syndrome) | n2=en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients) | rel=r_associated | relid=0 | w=27
  1716. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:profound intellectual disabilities
    n1=méningé (syndrome) | n2=en:profound intellectual disabilities | rel=r_associated | relid=0 | w=27
  1717. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:progressive bulbar palsy
    n1=méningé (syndrome) | n2=en:progressive bulbar palsy | rel=r_associated | relid=0 | w=27
  1718. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:progressive impairment of gait
    n1=méningé (syndrome) | n2=en:progressive impairment of gait | rel=r_associated | relid=0 | w=27
  1719. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:progressive neurologic deterioration
    n1=méningé (syndrome) | n2=en:progressive neurologic deterioration | rel=r_associated | relid=0 | w=27
  1720. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:progressive spastic quadriplegia
    n1=méningé (syndrome) | n2=en:progressive spastic quadriplegia | rel=r_associated | relid=0 | w=27
  1721. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:prolonged seizure
    n1=méningé (syndrome) | n2=en:prolonged seizure | rel=r_associated | relid=0 | w=27
  1722. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:prolonged somatosensory evoked potentials (seps)
    n1=méningé (syndrome) | n2=en:prolonged somatosensory evoked potentials (seps) | rel=r_associated | relid=0 | w=27
  1723. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:psychomotor delay after second year
    n1=méningé (syndrome) | n2=en:psychomotor delay after second year | rel=r_associated | relid=0 | w=27
  1724. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:psychomotor delay, severe
    n1=méningé (syndrome) | n2=en:psychomotor delay, severe | rel=r_associated | relid=0 | w=27
  1725. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:psychomotor retardation, mild
    n1=méningé (syndrome) | n2=en:psychomotor retardation, mild | rel=r_associated | relid=0 | w=27
  1726. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:psychomotor retardation, profound, in those who survive
    n1=méningé (syndrome) | n2=en:psychomotor retardation, profound, in those who survive | rel=r_associated | relid=0 | w=27
  1727. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:pyramidal hypertonia
    n1=méningé (syndrome) | n2=en:pyramidal hypertonia | rel=r_associated | relid=0 | w=27
  1728. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:pyramidal tract signs (in some patients)
    n1=méningé (syndrome) | n2=en:pyramidal tract signs (in some patients) | rel=r_associated | relid=0 | w=27
  1729. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:quadriplegia, flaccid
    n1=méningé (syndrome) | n2=en:quadriplegia, flaccid | rel=r_associated | relid=0 | w=27
  1730. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:reactive gliosis
    n1=méningé (syndrome) | n2=en:reactive gliosis | rel=r_associated | relid=0 | w=27
  1731. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:reduced posterior white matter volume (in some patients)
    n1=méningé (syndrome) | n2=en:reduced posterior white matter volume (in some patients) | rel=r_associated | relid=0 | w=27
  1732. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:resting tremor (in some patients)
    n1=méningé (syndrome) | n2=en:resting tremor (in some patients) | rel=r_associated | relid=0 | w=27
  1733. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:scanning speech
    n1=méningé (syndrome) | n2=en:scanning speech | rel=r_associated | relid=0 | w=27
  1734. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:scattered cns demyelination
    n1=méningé (syndrome) | n2=en:scattered cns demyelination | rel=r_associated | relid=0 | w=27
  1735. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:scissoring
    n1=méningé (syndrome) | n2=en:scissoring | rel=r_associated | relid=0 | w=27
  1736. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:scissors gait
    n1=méningé (syndrome) | n2=en:scissors gait | rel=r_associated | relid=0 | w=27
  1737. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:secondary generalization
    n1=méningé (syndrome) | n2=en:secondary generalization | rel=r_associated | relid=0 | w=27
  1738. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:secondary generalized tonic-clonic seizures may occur
    n1=méningé (syndrome) | n2=en:secondary generalized tonic-clonic seizures may occur | rel=r_associated | relid=0 | w=27
  1739. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:secondary hypertonia
    n1=méningé (syndrome) | n2=en:secondary hypertonia | rel=r_associated | relid=0 | w=27
  1740. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:segmental sensory loss, especially of pain and temperature
    n1=méningé (syndrome) | n2=en:segmental sensory loss, especially of pain and temperature | rel=r_associated | relid=0 | w=27
  1741. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:seizures (meb)
    n1=méningé (syndrome) | n2=en:seizures (meb) | rel=r_associated | relid=0 | w=27
  1742. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:seizures (uncommon)
    n1=méningé (syndrome) | n2=en:seizures (uncommon) | rel=r_associated | relid=0 | w=27
  1743. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:seizures often associated with infections
    n1=méningé (syndrome) | n2=en:seizures often associated with infections | rel=r_associated | relid=0 | w=27
  1744. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:seizures, multiple types
    n1=méningé (syndrome) | n2=en:seizures, multiple types | rel=r_associated | relid=0 | w=27
  1745. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:seizures, onset age 5 to 10 years
    n1=méningé (syndrome) | n2=en:seizures, onset age 5 to 10 years | rel=r_associated | relid=0 | w=27
  1746. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:seizures, severe, drug-resistant, intractable
    n1=méningé (syndrome) | n2=en:seizures, severe, drug-resistant, intractable | rel=r_associated | relid=0 | w=27
  1747. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:seizures, sudden-onset, drug-resistant
    n1=méningé (syndrome) | n2=en:seizures, sudden-onset, drug-resistant | rel=r_associated | relid=0 | w=27
  1748. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:seizures, tonic, clonic, focal
    n1=méningé (syndrome) | n2=en:seizures, tonic, clonic, focal | rel=r_associated | relid=0 | w=27
  1749. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:septum pellucidum deficient or cavum
    n1=méningé (syndrome) | n2=en:septum pellucidum deficient or cavum | rel=r_associated | relid=0 | w=27
  1750. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:severe cognitive impairment
    n1=méningé (syndrome) | n2=en:severe cognitive impairment | rel=r_associated | relid=0 | w=27
  1751. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:severe psychomotor retardation from birth
    n1=méningé (syndrome) | n2=en:severe psychomotor retardation from birth | rel=r_associated | relid=0 | w=27
  1752. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:sinus pericranii (rare)
    n1=méningé (syndrome) | n2=en:sinus pericranii (rare) | rel=r_associated | relid=0 | w=27
  1753. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:sleep abnormalities
    n1=méningé (syndrome) | n2=en:sleep abnormalities | rel=r_associated | relid=0 | w=27
  1754. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:sleep apnea (in 1/4 patients)
    n1=méningé (syndrome) | n2=en:sleep apnea (in 1/4 patients) | rel=r_associated | relid=0 | w=27
  1755. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:sleep disturbances common
    n1=méningé (syndrome) | n2=en:sleep disturbances common | rel=r_associated | relid=0 | w=27
  1756. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:sleep paralysis at beginning or end of sleep period (in 60% of patients)
    n1=méningé (syndrome) | n2=en:sleep paralysis at beginning or end of sleep period (in 60% of patients) | rel=r_associated | relid=0 | w=27
  1757. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:small pituitary gland (in some patients)
    n1=méningé (syndrome) | n2=en:small pituitary gland (in some patients) | rel=r_associated | relid=0 | w=27
  1758. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:some patients have neurologic involvement
    n1=méningé (syndrome) | n2=en:some patients have neurologic involvement | rel=r_associated | relid=0 | w=27
  1759. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:spastic ataxia
    n1=méningé (syndrome) | n2=en:spastic ataxia | rel=r_associated | relid=0 | w=27
  1760. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:spastic dystonia
    n1=méningé (syndrome) | n2=en:spastic dystonia | rel=r_associated | relid=0 | w=27
  1761. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:spastic paraparesis (1 patient)
    n1=méningé (syndrome) | n2=en:spastic paraparesis (1 patient) | rel=r_associated | relid=0 | w=27
  1762. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:spasticity may be present
    n1=méningé (syndrome) | n2=en:spasticity may be present | rel=r_associated | relid=0 | w=27
  1763. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:speech articulation defects
    n1=méningé (syndrome) | n2=en:speech articulation defects | rel=r_associated | relid=0 | w=27
  1764. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:speech difficulties due to hypoglossia
    n1=méningé (syndrome) | n2=en:speech difficulties due to hypoglossia | rel=r_associated | relid=0 | w=27
  1765. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:speech disorder (in 1 of 6 patients)
    n1=méningé (syndrome) | n2=en:speech disorder (in 1 of 6 patients) | rel=r_associated | relid=0 | w=27
  1766. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:speech limited
    n1=méningé (syndrome) | n2=en:speech limited | rel=r_associated | relid=0 | w=27
  1767. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:spina bifida
    n1=méningé (syndrome) | n2=en:spina bifida | rel=r_associated | relid=0 | w=27
  1768. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:staring
    n1=méningé (syndrome) | n2=en:staring | rel=r_associated | relid=0 | w=27
  1769. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:staring spells
    n1=méningé (syndrome) | n2=en:staring spells | rel=r_associated | relid=0 | w=27
  1770. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:status epilepticus (in 1 of 6 patients)
    n1=méningé (syndrome) | n2=en:status epilepticus (in 1 of 6 patients) | rel=r_associated | relid=0 | w=27
  1771. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:stiff gait
    n1=méningé (syndrome) | n2=en:stiff gait | rel=r_associated | relid=0 | w=27
  1772. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:stiffness while walking
    n1=méningé (syndrome) | n2=en:stiffness while walking | rel=r_associated | relid=0 | w=27
  1773. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:stoke-like lesions
    n1=méningé (syndrome) | n2=en:stoke-like lesions | rel=r_associated | relid=0 | w=27
  1774. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:stroke-like episodes (in some patients)
    n1=méningé (syndrome) | n2=en:stroke-like episodes (in some patients) | rel=r_associated | relid=0 | w=27
  1775. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:structural brain abnormalities
    n1=méningé (syndrome) | n2=en:structural brain abnormalities | rel=r_associated | relid=0 | w=27
  1776. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:structure of central sensory visual system
    n1=méningé (syndrome) | n2=en:structure of central sensory visual system | rel=r_associated | relid=0 | w=27
  1777. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:structure of decussation of superior cerebellar peduncles
    n1=méningé (syndrome) | n2=en:structure of decussation of superior cerebellar peduncles | rel=r_associated | relid=0 | w=27
  1778. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:subacute neurologic deterioration
    n1=méningé (syndrome) | n2=en:subacute neurologic deterioration | rel=r_associated | relid=0 | w=27
  1779. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:subcortical lesions
    n1=méningé (syndrome) | n2=en:subcortical lesions | rel=r_associated | relid=0 | w=27
  1780. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:sudden awakening
    n1=méningé (syndrome) | n2=en:sudden awakening | rel=r_associated | relid=0 | w=27
  1781. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:symmetric spinal nerve root neurofibromas
    n1=méningé (syndrome) | n2=en:symmetric spinal nerve root neurofibromas | rel=r_associated | relid=0 | w=27
  1782. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:syringomyelia (in some patients)
    n1=méningé (syndrome) | n2=en:syringomyelia (in some patients) | rel=r_associated | relid=0 | w=27
  1783. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra
    n1=méningé (syndrome) | n2=en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra | rel=r_associated | relid=0 | w=27
  1784. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:t2-weighted mri shows hyperintensities in the thalamus, basal ganglia, and brainstem during acute illness (may later resolve)
    n1=méningé (syndrome) | n2=en:t2-weighted mri shows hyperintensities in the thalamus, basal ganglia, and brainstem during acute illness (may later resolve) | rel=r_associated | relid=0 | w=27
  1785. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:t2-weighted signal abnormalities in the deep white matter
    n1=méningé (syndrome) | n2=en:t2-weighted signal abnormalities in the deep white matter | rel=r_associated | relid=0 | w=27
  1786. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:tethered cord (rare)
    n1=méningé (syndrome) | n2=en:tethered cord (rare) | rel=r_associated | relid=0 | w=27
  1787. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:tonic-clonic seizures (less common)
    n1=méningé (syndrome) | n2=en:tonic-clonic seizures (less common) | rel=r_associated | relid=0 | w=27
  1788. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:tremor (3 patients)
    n1=méningé (syndrome) | n2=en:tremor (3 patients) | rel=r_associated | relid=0 | w=27
  1789. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:tremor (57% of patients)
    n1=méningé (syndrome) | n2=en:tremor (57% of patients) | rel=r_associated | relid=0 | w=27
  1790. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:tremor (in some patients)
    n1=méningé (syndrome) | n2=en:tremor (in some patients) | rel=r_associated | relid=0 | w=27
  1791. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:tremor with febrile episodes (rare)
    n1=méningé (syndrome) | n2=en:tremor with febrile episodes (rare) | rel=r_associated | relid=0 | w=27
  1792. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:tremor, action, progressive
    n1=méningé (syndrome) | n2=en:tremor, action, progressive | rel=r_associated | relid=0 | w=27
  1793. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:tremor, static
    n1=méningé (syndrome) | n2=en:tremor, static | rel=r_associated | relid=0 | w=27
  1794. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:type i arnold chiari malformation
    n1=méningé (syndrome) | n2=en:type i arnold chiari malformation | rel=r_associated | relid=0 | w=27
  1795. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:unsteadiness, episodic
    n1=méningé (syndrome) | n2=en:unsteadiness, episodic | rel=r_associated | relid=0 | w=27
  1796. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:upper limb ataxia
    n1=méningé (syndrome) | n2=en:upper limb ataxia | rel=r_associated | relid=0 | w=27
  1797. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:upper limbs may show mild involvement
    n1=méningé (syndrome) | n2=en:upper limbs may show mild involvement | rel=r_associated | relid=0 | w=27
  1798. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:variable mental retardation (40%)
    n1=méningé (syndrome) | n2=en:variable mental retardation (40%) | rel=r_associated | relid=0 | w=27
  1799. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:vermian hypoplasia
    n1=méningé (syndrome) | n2=en:vermian hypoplasia | rel=r_associated | relid=0 | w=27
  1800. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:visceroautonomic dysfunction
    n1=méningé (syndrome) | n2=en:visceroautonomic dysfunction | rel=r_associated | relid=0 | w=27
  1801. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:weakness
    n1=méningé (syndrome) | n2=en:weakness | rel=r_associated | relid=0 | w=27
  1802. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:white matter abnormalities (in some)
    n1=méningé (syndrome) | n2=en:white matter abnormalities (in some) | rel=r_associated | relid=0 | w=27
  1803. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:white matter changes may occur (in adulthood)
    n1=méningé (syndrome) | n2=en:white matter changes may occur (in adulthood) | rel=r_associated | relid=0 | w=27
  1804. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:white matter lacks axons and myelin
    n1=méningé (syndrome) | n2=en:white matter lacks axons and myelin | rel=r_associated | relid=0 | w=27
  1805. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> en:writing fatigability
    n1=méningé (syndrome) | n2=en:writing fatigability | rel=r_associated | relid=0 | w=27
  1806. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> médecine
    (science)
    n1=méningé (syndrome) | n2=médecine
    (science)
    | rel=r_associated | relid=0 | w=27
  1807. méningé (syndrome) -- r_associated #0: 27 / 0.325 -> méningiome multiple
    n1=méningé (syndrome) | n2=méningiome multiple | rel=r_associated | relid=0 | w=27
  1808. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:'dragonfly' pattern on imaging
    n1=méningé (syndrome) | n2=en:'dragonfly' pattern on imaging | rel=r_associated | relid=0 | w=26
  1809. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan
    n1=méningé (syndrome) | n2=en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan | rel=r_associated | relid=0 | w=26
  1810. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:abnormal gyral pattern
    n1=méningé (syndrome) | n2=en:abnormal gyral pattern | rel=r_associated | relid=0 | w=26
  1811. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:abnormal sleep pattern
    n1=méningé (syndrome) | n2=en:abnormal sleep pattern | rel=r_associated | relid=0 | w=26
  1812. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:abnormality of ocular smooth pursuit
    n1=méningé (syndrome) | n2=en:abnormality of ocular smooth pursuit | rel=r_associated | relid=0 | w=26
  1813. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:absence of lower motor neuron involvement
    n1=méningé (syndrome) | n2=en:absence of lower motor neuron involvement | rel=r_associated | relid=0 | w=26
  1814. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:absence of the cerebellar vermis
    n1=méningé (syndrome) | n2=en:absence of the cerebellar vermis | rel=r_associated | relid=0 | w=26
  1815. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:absence or atrophy of the putamen
    n1=méningé (syndrome) | n2=en:absence or atrophy of the putamen | rel=r_associated | relid=0 | w=26
  1816. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:absent optic nerves, chiasm, and tracts
    n1=méningé (syndrome) | n2=en:absent optic nerves, chiasm, and tracts | rel=r_associated | relid=0 | w=26
  1817. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:acute cerebrovascular accidents
    n1=méningé (syndrome) | n2=en:acute cerebrovascular accidents | rel=r_associated | relid=0 | w=26
  1818. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:affected arteries show loss of smooth muscle cells
    n1=méningé (syndrome) | n2=en:affected arteries show loss of smooth muscle cells | rel=r_associated | relid=0 | w=26
  1819. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:agenesis of pineal gland
    n1=méningé (syndrome) | n2=en:agenesis of pineal gland | rel=r_associated | relid=0 | w=26
  1820. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:alpha-synuclein-containing inclusions
    n1=méningé (syndrome) | n2=en:alpha-synuclein-containing inclusions | rel=r_associated | relid=0 | w=26
  1821. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:alzheimer disease, early onset
    n1=méningé (syndrome) | n2=en:alzheimer disease, early onset | rel=r_associated | relid=0 | w=26
  1822. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:amyotrophy, distal, severe
    n1=méningé (syndrome) | n2=en:amyotrophy, distal, severe | rel=r_associated | relid=0 | w=26
  1823. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:anterior basal encephalocele
    n1=méningé (syndrome) | n2=en:anterior basal encephalocele | rel=r_associated | relid=0 | w=26
  1824. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:anterior pituitary hypoplasia
    n1=méningé (syndrome) | n2=en:anterior pituitary hypoplasia | rel=r_associated | relid=0 | w=26
  1825. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:appendicular hypertonia
    n1=méningé (syndrome) | n2=en:appendicular hypertonia | rel=r_associated | relid=0 | w=26
  1826. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:apraxia, verbal
    n1=méningé (syndrome) | n2=en:apraxia, verbal | rel=r_associated | relid=0 | w=26
  1827. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:associated with syringomyelia (186700)
    n1=méningé (syndrome) | n2=en:associated with syringomyelia (186700) | rel=r_associated | relid=0 | w=26
  1828. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:ataxia (deletion patients)
    n1=méningé (syndrome) | n2=en:ataxia (deletion patients) | rel=r_associated | relid=0 | w=26
  1829. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:ataxia (if untreated)
    n1=méningé (syndrome) | n2=en:ataxia (if untreated) | rel=r_associated | relid=0 | w=26
  1830. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:ataxia (uncommon)
    n1=méningé (syndrome) | n2=en:ataxia (uncommon) | rel=r_associated | relid=0 | w=26
  1831. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:ataxia in those who survive
    n1=méningé (syndrome) | n2=en:ataxia in those who survive | rel=r_associated | relid=0 | w=26
  1832. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:athetoid and dystonic hand movements (in some patients)
    n1=méningé (syndrome) | n2=en:athetoid and dystonic hand movements (in some patients) | rel=r_associated | relid=0 | w=26
  1833. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:athetosis (in some patients)
    n1=méningé (syndrome) | n2=en:athetosis (in some patients) | rel=r_associated | relid=0 | w=26
  1834. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:atrophy and weakness of the tongue, jaw, and throat muscles
    n1=méningé (syndrome) | n2=en:atrophy and weakness of the tongue, jaw, and throat muscles | rel=r_associated | relid=0 | w=26
  1835. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:atrophy of the motor cortex in older patients seen on mri
    n1=méningé (syndrome) | n2=en:atrophy of the motor cortex in older patients seen on mri | rel=r_associated | relid=0 | w=26
  1836. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:atypical absence seizure
    n1=méningé (syndrome) | n2=en:atypical absence seizure | rel=r_associated | relid=0 | w=26
  1837. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:atypical meningioma
    n1=méningé (syndrome) | n2=en:atypical meningioma | rel=r_associated | relid=0 | w=26
  1838. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:autism or autistic features
    n1=méningé (syndrome) | n2=en:autism or autistic features | rel=r_associated | relid=0 | w=26
  1839. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:autonomic features may occur
    n1=méningé (syndrome) | n2=en:autonomic features may occur | rel=r_associated | relid=0 | w=26
  1840. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:autonomic signs
    n1=méningé (syndrome) | n2=en:autonomic signs | rel=r_associated | relid=0 | w=26
  1841. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:axial rigidity
    n1=méningé (syndrome) | n2=en:axial rigidity | rel=r_associated | relid=0 | w=26
  1842. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:basal ganglia cysts
    n1=méningé (syndrome) | n2=en:basal ganglia cysts | rel=r_associated | relid=0 | w=26
  1843. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:benign meningioma
    n1=méningé (syndrome) | n2=en:benign meningioma | rel=r_associated | relid=0 | w=26
  1844. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:bilateral convulsive seizures
    n1=méningé (syndrome) | n2=en:bilateral convulsive seizures | rel=r_associated | relid=0 | w=26
  1845. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:bilateral striatal necrosis
    n1=méningé (syndrome) | n2=en:bilateral striatal necrosis | rel=r_associated | relid=0 | w=26
  1846. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:biopsy shows white matter hypomyelination, demyelination, gliosis
    n1=méningé (syndrome) | n2=en:biopsy shows white matter hypomyelination, demyelination, gliosis | rel=r_associated | relid=0 | w=26
  1847. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:blake's pouch (rare)
    n1=méningé (syndrome) | n2=en:blake's pouch (rare) | rel=r_associated | relid=0 | w=26
  1848. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:blurring of the gray-white junction (in type iib)
    n1=méningé (syndrome) | n2=en:blurring of the gray-white junction (in type iib) | rel=r_associated | relid=0 | w=26
  1849. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:brain atrophy, particularly of the frontal and temporal lobes
    n1=méningé (syndrome) | n2=en:brain atrophy, particularly of the frontal and temporal lobes | rel=r_associated | relid=0 | w=26
  1850. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:brain imaging shows cortical atrophy
    n1=méningé (syndrome) | n2=en:brain imaging shows cortical atrophy | rel=r_associated | relid=0 | w=26
  1851. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:brain iron accumulation (in some patients)
    n1=méningé (syndrome) | n2=en:brain iron accumulation (in some patients) | rel=r_associated | relid=0 | w=26
  1852. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:brain mri shows hypoplastic pituitary
    n1=méningé (syndrome) | n2=en:brain mri shows hypoplastic pituitary | rel=r_associated | relid=0 | w=26
  1853. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:brain mri shows t2-weighted hyperintensities (17%)
    n1=méningé (syndrome) | n2=en:brain mri shows t2-weighted hyperintensities (17%) | rel=r_associated | relid=0 | w=26
  1854. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd)
    n1=méningé (syndrome) | n2=en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd) | rel=r_associated | relid=0 | w=26
  1855. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:brain stem
    n1=méningé (syndrome) | n2=en:brain stem | rel=r_associated | relid=0 | w=26
  1856. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:brainstem atrophy
    n1=méningé (syndrome) | n2=en:brainstem atrophy | rel=r_associated | relid=0 | w=26
  1857. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:brainstem hypoplasia (in some patients)
    n1=méningé (syndrome) | n2=en:brainstem hypoplasia (in some patients) | rel=r_associated | relid=0 | w=26
  1858. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:c3hex, decreased ability to smell
    n1=méningé (syndrome) | n2=en:c3hex, decreased ability to smell | rel=r_associated | relid=0 | w=26
  1859. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:calicification of the falx cerebri
    n1=méningé (syndrome) | n2=en:calicification of the falx cerebri | rel=r_associated | relid=0 | w=26
  1860. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:central hypotonia
    n1=méningé (syndrome) | n2=en:central hypotonia | rel=r_associated | relid=0 | w=26
  1861. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:central nervous system involvement (in some patients)
    n1=méningé (syndrome) | n2=en:central nervous system involvement (in some patients) | rel=r_associated | relid=0 | w=26
  1862. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar ataxia, gait and stance
    n1=méningé (syndrome) | n2=en:cerebellar ataxia, gait and stance | rel=r_associated | relid=0 | w=26
  1863. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar ataxia, severe
    n1=méningé (syndrome) | n2=en:cerebellar ataxia, severe | rel=r_associated | relid=0 | w=26
  1864. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar atrophy (especially of the vermis)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy (especially of the vermis) | rel=r_associated | relid=0 | w=26
  1865. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar calcifications
    n1=méningé (syndrome) | n2=en:cerebellar calcifications | rel=r_associated | relid=0 | w=26
  1866. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar dysfunction, progressive
    n1=méningé (syndrome) | n2=en:cerebellar dysfunction, progressive | rel=r_associated | relid=0 | w=26
  1867. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar hypoplasia (1 patient)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (1 patient) | rel=r_associated | relid=0 | w=26
  1868. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar hypoplasia (reported in 1 family)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (reported in 1 family) | rel=r_associated | relid=0 | w=26
  1869. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar hypoplasia due to enlarged foramen magnum
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia due to enlarged foramen magnum | rel=r_associated | relid=0 | w=26
  1870. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar signs (less common)
    n1=méningé (syndrome) | n2=en:cerebellar signs (less common) | rel=r_associated | relid=0 | w=26
  1871. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar signs may develop
    n1=méningé (syndrome) | n2=en:cerebellar signs may develop | rel=r_associated | relid=0 | w=26
  1872. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar stroke
    n1=méningé (syndrome) | n2=en:cerebellar stroke | rel=r_associated | relid=0 | w=26
  1873. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar tonsil herniation
    n1=méningé (syndrome) | n2=en:cerebellar tonsil herniation | rel=r_associated | relid=0 | w=26
  1874. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar vermis hypoplasia
    n1=méningé (syndrome) | n2=en:cerebellar vermis hypoplasia | rel=r_associated | relid=0 | w=26
  1875. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebellar vermis hypoplasia (in some patients)
    n1=méningé (syndrome) | n2=en:cerebellar vermis hypoplasia (in some patients) | rel=r_associated | relid=0 | w=26
  1876. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebral atrophy, diffuse, severe
    n1=méningé (syndrome) | n2=en:cerebral atrophy, diffuse, severe | rel=r_associated | relid=0 | w=26
  1877. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebral atrophy, frontotemporal, progressive
    n1=méningé (syndrome) | n2=en:cerebral atrophy, frontotemporal, progressive | rel=r_associated | relid=0 | w=26
  1878. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebral hypomyelination
    n1=méningé (syndrome) | n2=en:cerebral hypomyelination | rel=r_associated | relid=0 | w=26
  1879. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebral thrombosis
    n1=méningé (syndrome) | n2=en:cerebral thrombosis | rel=r_associated | relid=0 | w=26
  1880. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency)
    n1=méningé (syndrome) | n2=en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency) | rel=r_associated | relid=0 | w=26
  1881. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cerebral vasculitis or vasculopathy (rare)
    n1=méningé (syndrome) | n2=en:cerebral vasculitis or vasculopathy (rare) | rel=r_associated | relid=0 | w=26
  1882. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:characteristic findings on mri
    n1=méningé (syndrome) | n2=en:characteristic findings on mri | rel=r_associated | relid=0 | w=26
  1883. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:chorea of hands
    n1=méningé (syndrome) | n2=en:chorea of hands | rel=r_associated | relid=0 | w=26
  1884. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:choreoathetoid movements
    n1=méningé (syndrome) | n2=en:choreoathetoid movements | rel=r_associated | relid=0 | w=26
  1885. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:choristoma
    n1=méningé (syndrome) | n2=en:choristoma | rel=r_associated | relid=0 | w=26
  1886. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:clumsiness in childhood
    n1=méningé (syndrome) | n2=en:clumsiness in childhood | rel=r_associated | relid=0 | w=26
  1887. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cognitive deterioration
    n1=méningé (syndrome) | n2=en:cognitive deterioration | rel=r_associated | relid=0 | w=26
  1888. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cognitive dysfunction
    n1=méningé (syndrome) | n2=en:cognitive dysfunction | rel=r_associated | relid=0 | w=26
  1889. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cognitive impairment (rare)
    n1=méningé (syndrome) | n2=en:cognitive impairment (rare) | rel=r_associated | relid=0 | w=26
  1890. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cogwheel rigidities
    n1=méningé (syndrome) | n2=en:cogwheel rigidities | rel=r_associated | relid=0 | w=26
  1891. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:colpocephaly
    n1=méningé (syndrome) | n2=en:colpocephaly | rel=r_associated | relid=0 | w=26
  1892. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:coma (in up to 33% of patients)
    n1=méningé (syndrome) | n2=en:coma (in up to 33% of patients) | rel=r_associated | relid=0 | w=26
  1893. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:complex partial seizures, often with secondary generalization, are the most common type
    n1=méningé (syndrome) | n2=en:complex partial seizures, often with secondary generalization, are the most common type | rel=r_associated | relid=0 | w=26
  1894. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:concentration impairment
    n1=méningé (syndrome) | n2=en:concentration impairment | rel=r_associated | relid=0 | w=26
  1895. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:corpus callosum lipoma
    n1=méningé (syndrome) | n2=en:corpus callosum lipoma | rel=r_associated | relid=0 | w=26
  1896. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cortical and subcortical hyperintensities
    n1=méningé (syndrome) | n2=en:cortical and subcortical hyperintensities | rel=r_associated | relid=0 | w=26
  1897. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cortical atrophy (43%)
    n1=méningé (syndrome) | n2=en:cortical atrophy (43%) | rel=r_associated | relid=0 | w=26
  1898. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cortical degeneration
    n1=méningé (syndrome) | n2=en:cortical degeneration | rel=r_associated | relid=0 | w=26
  1899. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cortical venous thromboses
    n1=méningé (syndrome) | n2=en:cortical venous thromboses | rel=r_associated | relid=0 | w=26
  1900. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:cyst of septum pellucidum (in some patients)
    n1=méningé (syndrome) | n2=en:cyst of septum pellucidum (in some patients) | rel=r_associated | relid=0 | w=26
  1901. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:decrease in abstract thinking
    n1=méningé (syndrome) | n2=en:decrease in abstract thinking | rel=r_associated | relid=0 | w=26
  1902. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:decreased active movements
    n1=méningé (syndrome) | n2=en:decreased active movements | rel=r_associated | relid=0 | w=26
  1903. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:decreased motor nerve conduction velocity
    n1=méningé (syndrome) | n2=en:decreased motor nerve conduction velocity | rel=r_associated | relid=0 | w=26
  1904. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:decreased spontaneous movements at birth
    n1=méningé (syndrome) | n2=en:decreased spontaneous movements at birth | rel=r_associated | relid=0 | w=26
  1905. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:defects in visual cue processing
    n1=méningé (syndrome) | n2=en:defects in visual cue processing | rel=r_associated | relid=0 | w=26
  1906. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:deficits in abstraction
    n1=méningé (syndrome) | n2=en:deficits in abstraction | rel=r_associated | relid=0 | w=26
  1907. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:degeneration of anterior horn cells
    n1=méningé (syndrome) | n2=en:degeneration of anterior horn cells | rel=r_associated | relid=0 | w=26
  1908. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:delayed cerebral myelination
    n1=méningé (syndrome) | n2=en:delayed cerebral myelination | rel=r_associated | relid=0 | w=26
  1909. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:delayed cognitive development, mild (reported in 1 family)
    n1=méningé (syndrome) | n2=en:delayed cognitive development, mild (reported in 1 family) | rel=r_associated | relid=0 | w=26
  1910. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:delayed development (about 25%)
    n1=méningé (syndrome) | n2=en:delayed development (about 25%) | rel=r_associated | relid=0 | w=26
  1911. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:delayed myelination (in some patients)
    n1=méningé (syndrome) | n2=en:delayed myelination (in some patients) | rel=r_associated | relid=0 | w=26
  1912. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:delayed psychomotor development (stops at development levels of 1-2 years)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development (stops at development levels of 1-2 years) | rel=r_associated | relid=0 | w=26
  1913. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:delayed psychomotor development, mild
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, mild | rel=r_associated | relid=0 | w=26
  1914. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:delayed psychomotor development, moderate to severe
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, moderate to severe | rel=r_associated | relid=0 | w=26
  1915. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:delayed walking (less common)
    n1=méningé (syndrome) | n2=en:delayed walking (less common) | rel=r_associated | relid=0 | w=26
  1916. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dementia (later-onset)
    n1=méningé (syndrome) | n2=en:dementia (later-onset) | rel=r_associated | relid=0 | w=26
  1917. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dementia in a subset of patients
    n1=méningé (syndrome) | n2=en:dementia in a subset of patients | rel=r_associated | relid=0 | w=26
  1918. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dementia, progressive (more common in males)
    n1=méningé (syndrome) | n2=en:dementia, progressive (more common in males) | rel=r_associated | relid=0 | w=26
  1919. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:developmental arrest, 2nd year of life
    n1=méningé (syndrome) | n2=en:developmental arrest, 2nd year of life | rel=r_associated | relid=0 | w=26
  1920. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:developmental delay (microdeletion patients only)
    n1=méningé (syndrome) | n2=en:developmental delay (microdeletion patients only) | rel=r_associated | relid=0 | w=26
  1921. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:developmental delay (seen in recessive form)
    n1=méningé (syndrome) | n2=en:developmental delay (seen in recessive form) | rel=r_associated | relid=0 | w=26
  1922. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:developmental delay, significant
    n1=méningé (syndrome) | n2=en:developmental delay, significant | rel=r_associated | relid=0 | w=26
  1923. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:developmental regression after onset of seizures
    n1=méningé (syndrome) | n2=en:developmental regression after onset of seizures | rel=r_associated | relid=0 | w=26
  1924. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:developmental stagnation
    n1=méningé (syndrome) | n2=en:developmental stagnation | rel=r_associated | relid=0 | w=26
  1925. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:developmental stagnation at onset of seizures
    n1=méningé (syndrome) | n2=en:developmental stagnation at onset of seizures | rel=r_associated | relid=0 | w=26
  1926. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:difficulty in phonologic coding
    n1=méningé (syndrome) | n2=en:difficulty in phonologic coding | rel=r_associated | relid=0 | w=26
  1927. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:difficulty walking, running
    n1=méningé (syndrome) | n2=en:difficulty walking, running | rel=r_associated | relid=0 | w=26
  1928. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes)
    n1=méningé (syndrome) | n2=en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes) | rel=r_associated | relid=0 | w=26
  1929. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:diffuse hyporeflexia (later)
    n1=méningé (syndrome) | n2=en:diffuse hyporeflexia (later) | rel=r_associated | relid=0 | w=26
  1930. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:diffuse hypotonia
    n1=méningé (syndrome) | n2=en:diffuse hypotonia | rel=r_associated | relid=0 | w=26
  1931. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:diffuse leptomeningeal enhancement seen on mri
    n1=méningé (syndrome) | n2=en:diffuse leptomeningeal enhancement seen on mri | rel=r_associated | relid=0 | w=26
  1932. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:diffuse white matter dysmyelination
    n1=méningé (syndrome) | n2=en:diffuse white matter dysmyelination | rel=r_associated | relid=0 | w=26
  1933. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dilatation of the 3rd ventricle (in one family)
    n1=méningé (syndrome) | n2=en:dilatation of the 3rd ventricle (in one family) | rel=r_associated | relid=0 | w=26
  1934. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dilatation of the lateral ventricles (in one family)
    n1=méningé (syndrome) | n2=en:dilatation of the lateral ventricles (in one family) | rel=r_associated | relid=0 | w=26
  1935. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dilated lateral ventricles (1 patient)
    n1=méningé (syndrome) | n2=en:dilated lateral ventricles (1 patient) | rel=r_associated | relid=0 | w=26
  1936. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:disordered sleep pattern (in some patients)
    n1=méningé (syndrome) | n2=en:disordered sleep pattern (in some patients) | rel=r_associated | relid=0 | w=26
  1937. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysarthria (74%)
    n1=méningé (syndrome) | n2=en:dysarthria (74%) | rel=r_associated | relid=0 | w=26
  1938. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysarthria (in some patients)
    n1=méningé (syndrome) | n2=en:dysarthria (in some patients) | rel=r_associated | relid=0 | w=26
  1939. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysarthrias, spastic
    n1=méningé (syndrome) | n2=en:dysarthrias, spastic | rel=r_associated | relid=0 | w=26
  1940. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dyscalculia
    n1=méningé (syndrome) | n2=en:dyscalculia | rel=r_associated | relid=0 | w=26
  1941. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysdiadochokinesis
    n1=méningé (syndrome) | n2=en:dysdiadochokinesis | rel=r_associated | relid=0 | w=26
  1942. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysfunction of the autonomic nervous system
    n1=méningé (syndrome) | n2=en:dysfunction of the autonomic nervous system | rel=r_associated | relid=0 | w=26
  1943. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysgenesis or agenesis of the corpus callosum (in some)
    n1=méningé (syndrome) | n2=en:dysgenesis or agenesis of the corpus callosum (in some) | rel=r_associated | relid=0 | w=26
  1944. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysgraphias
    n1=méningé (syndrome) | n2=en:dysgraphias | rel=r_associated | relid=0 | w=26
  1945. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysmorphic basal ganglia (in some patients)
    n1=méningé (syndrome) | n2=en:dysmorphic basal ganglia (in some patients) | rel=r_associated | relid=0 | w=26
  1946. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysmyelination of the brain and spinal cord
    n1=méningé (syndrome) | n2=en:dysmyelination of the brain and spinal cord | rel=r_associated | relid=0 | w=26
  1947. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dysplastic pons
    n1=méningé (syndrome) | n2=en:dysplastic pons | rel=r_associated | relid=0 | w=26
  1948. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dystonia (may spontaneously remit in childhood or adolescence)
    n1=méningé (syndrome) | n2=en:dystonia (may spontaneously remit in childhood or adolescence) | rel=r_associated | relid=0 | w=26
  1949. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dystonia, episodic, primary affects hands and feet
    n1=méningé (syndrome) | n2=en:dystonia, episodic, primary affects hands and feet | rel=r_associated | relid=0 | w=26
  1950. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dystonia, progressive
    n1=méningé (syndrome) | n2=en:dystonia, progressive | rel=r_associated | relid=0 | w=26
  1951. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:dystonic tongue protrusion
    n1=méningé (syndrome) | n2=en:dystonic tongue protrusion | rel=r_associated | relid=0 | w=26
  1952. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:eeg shows 3-hz spike-wave discharges
    n1=méningé (syndrome) | n2=en:eeg shows 3-hz spike-wave discharges | rel=r_associated | relid=0 | w=26
  1953. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:eeg shows spike and wave or polyspike and wave discharges
    n1=méningé (syndrome) | n2=en:eeg shows spike and wave or polyspike and wave discharges | rel=r_associated | relid=0 | w=26
  1954. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:eeg shows with a multifocal pattern with spikes and sharp waves
    n1=méningé (syndrome) | n2=en:eeg shows with a multifocal pattern with spikes and sharp waves | rel=r_associated | relid=0 | w=26
  1955. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:elongated superior cerebellar peduncles
    n1=méningé (syndrome) | n2=en:elongated superior cerebellar peduncles | rel=r_associated | relid=0 | w=26
  1956. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:emg shows bursts of activity originating in the masseter muscle and spreading to the orbicularis oris and oculi muscles
    n1=méningé (syndrome) | n2=en:emg shows bursts of activity originating in the masseter muscle and spreading to the orbicularis oris and oculi muscles | rel=r_associated | relid=0 | w=26
  1957. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:encephalitis
    n1=méningé (syndrome) | n2=en:encephalitis | rel=r_associated | relid=0 | w=26
  1958. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:encephalopathy
    n1=méningé (syndrome) | n2=en:encephalopathy | rel=r_associated | relid=0 | w=26
  1959. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:encephalopathy, acute-onset
    n1=méningé (syndrome) | n2=en:encephalopathy, acute-onset | rel=r_associated | relid=0 | w=26
  1960. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:epilepsia partialis continua
    n1=méningé (syndrome) | n2=en:epilepsia partialis continua | rel=r_associated | relid=0 | w=26
  1961. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:episodes last up to 2 minutes
    n1=méningé (syndrome) | n2=en:episodes last up to 2 minutes | rel=r_associated | relid=0 | w=26
  1962. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:equivocal plantar response
    n1=méningé (syndrome) | n2=en:equivocal plantar response | rel=r_associated | relid=0 | w=26
  1963. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:expressive speech deficit
    n1=méningé (syndrome) | n2=en:expressive speech deficit | rel=r_associated | relid=0 | w=26
  1964. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:extensor plantar responses (reported in 1 family)
    n1=méningé (syndrome) | n2=en:extensor plantar responses (reported in 1 family) | rel=r_associated | relid=0 | w=26
  1965. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:extrapyramidal features
    n1=méningé (syndrome) | n2=en:extrapyramidal features | rel=r_associated | relid=0 | w=26
  1966. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:extrapyramidal muscular rigidity
    n1=méningé (syndrome) | n2=en:extrapyramidal muscular rigidity | rel=r_associated | relid=0 | w=26
  1967. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:extrapyramidal signs (in 1 patient)
    n1=méningé (syndrome) | n2=en:extrapyramidal signs (in 1 patient) | rel=r_associated | relid=0 | w=26
  1968. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:facial, pharyngeal, and masticatory muscle diplegia
    n1=méningé (syndrome) | n2=en:facial, pharyngeal, and masticatory muscle diplegia | rel=r_associated | relid=0 | w=26
  1969. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:fall
    n1=méningé (syndrome) | n2=en:fall | rel=r_associated | relid=0 | w=26
  1970. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:febrile seizures (1 patient)
    n1=méningé (syndrome) | n2=en:febrile seizures (1 patient) | rel=r_associated | relid=0 | w=26
  1971. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:febrile seizures (usually remit by age 6 years)
    n1=méningé (syndrome) | n2=en:febrile seizures (usually remit by age 6 years) | rel=r_associated | relid=0 | w=26
  1972. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:fifth ventricle
    n1=méningé (syndrome) | n2=en:fifth ventricle | rel=r_associated | relid=0 | w=26
  1973. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:fine motor delay
    n1=méningé (syndrome) | n2=en:fine motor delay | rel=r_associated | relid=0 | w=26
  1974. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:focal cortical dysplasia
    n1=méningé (syndrome) | n2=en:focal cortical dysplasia | rel=r_associated | relid=0 | w=26
  1975. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:focal dystonia (e.g., writer's cramp)
    n1=méningé (syndrome) | n2=en:focal dystonia (e.g., writer's cramp) | rel=r_associated | relid=0 | w=26
  1976. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:focal nodular heterotopia
    n1=méningé (syndrome) | n2=en:focal nodular heterotopia | rel=r_associated | relid=0 | w=26
  1977. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:focal parietal pachygyria
    n1=méningé (syndrome) | n2=en:focal parietal pachygyria | rel=r_associated | relid=0 | w=26
  1978. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:focal, segmental or multifocal dystonia
    n1=méningé (syndrome) | n2=en:focal, segmental or multifocal dystonia | rel=r_associated | relid=0 | w=26
  1979. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:frequent falls with preservation of consciousness
    n1=méningé (syndrome) | n2=en:frequent falls with preservation of consciousness | rel=r_associated | relid=0 | w=26
  1980. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:frontoparietal polymicrogyria
    n1=méningé (syndrome) | n2=en:frontoparietal polymicrogyria | rel=r_associated | relid=0 | w=26
  1981. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:frontotemporal dementia (1 patient)
    n1=méningé (syndrome) | n2=en:frontotemporal dementia (1 patient) | rel=r_associated | relid=0 | w=26
  1982. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:frontotemporal/subcortical dementia
    n1=méningé (syndrome) | n2=en:frontotemporal/subcortical dementia | rel=r_associated | relid=0 | w=26
  1983. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:gait ataxias, cerebellar
    n1=méningé (syndrome) | n2=en:gait ataxias, cerebellar | rel=r_associated | relid=0 | w=26
  1984. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:gait, drop foot
    n1=méningé (syndrome) | n2=en:gait, drop foot | rel=r_associated | relid=0 | w=26
  1985. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:generalized dystonia
    n1=méningé (syndrome) | n2=en:generalized dystonia | rel=r_associated | relid=0 | w=26
  1986. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:generalized tonic-clonic seizures in 50%
    n1=méningé (syndrome) | n2=en:generalized tonic-clonic seizures in 50% | rel=r_associated | relid=0 | w=26
  1987. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:glial activation
    n1=méningé (syndrome) | n2=en:glial activation | rel=r_associated | relid=0 | w=26
  1988. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:global and focal neurologic abnormalities (less than 30%)
    n1=méningé (syndrome) | n2=en:global and focal neurologic abnormalities (less than 30%) | rel=r_associated | relid=0 | w=26
  1989. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:granular material in neurons
    n1=méningé (syndrome) | n2=en:granular material in neurons | rel=r_associated | relid=0 | w=26
  1990. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:head tremor
    n1=méningé (syndrome) | n2=en:head tremor | rel=r_associated | relid=0 | w=26
  1991. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:headaches, severe, unilateral
    n1=méningé (syndrome) | n2=en:headaches, severe, unilateral | rel=r_associated | relid=0 | w=26
  1992. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hemiclonic seizures
    n1=méningé (syndrome) | n2=en:hemiclonic seizures | rel=r_associated | relid=0 | w=26
  1993. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hippocampal atrophy (1 patient)
    n1=méningé (syndrome) | n2=en:hippocampal atrophy (1 patient) | rel=r_associated | relid=0 | w=26
  1994. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:holoprosencephaly (less common)
    n1=méningé (syndrome) | n2=en:holoprosencephaly (less common) | rel=r_associated | relid=0 | w=26
  1995. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hyperirritability
    n1=méningé (syndrome) | n2=en:hyperirritability | rel=r_associated | relid=0 | w=26
  1996. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hyperreflexia (33%)
    n1=méningé (syndrome) | n2=en:hyperreflexia (33%) | rel=r_associated | relid=0 | w=26
  1997. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hyperreflexia in some
    n1=méningé (syndrome) | n2=en:hyperreflexia in some | rel=r_associated | relid=0 | w=26
  1998. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypertonia in neonatal period
    n1=méningé (syndrome) | n2=en:hypertonia in neonatal period | rel=r_associated | relid=0 | w=26
  1999. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypertonia late
    n1=méningé (syndrome) | n2=en:hypertonia late | rel=r_associated | relid=0 | w=26
  2000. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypodysplasia of the corpus callosum
    n1=méningé (syndrome) | n2=en:hypodysplasia of the corpus callosum | rel=r_associated | relid=0 | w=26
  2001. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypokinesia
    n1=méningé (syndrome) | n2=en:hypokinesia | rel=r_associated | relid=0 | w=26
  2002. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypokinetic movements
    n1=méningé (syndrome) | n2=en:hypokinetic movements | rel=r_associated | relid=0 | w=26
  2003. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a)
    n1=méningé (syndrome) | n2=en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a) | rel=r_associated | relid=0 | w=26
  2004. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypoplasia of anterior or entire pituitary gland (frequent)
    n1=méningé (syndrome) | n2=en:hypoplasia of anterior or entire pituitary gland (frequent) | rel=r_associated | relid=0 | w=26
  2005. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypoplasia of the pons
    n1=méningé (syndrome) | n2=en:hypoplasia of the pons | rel=r_associated | relid=0 | w=26
  2006. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypoplastic olfactory lobes
    n1=méningé (syndrome) | n2=en:hypoplastic olfactory lobes | rel=r_associated | relid=0 | w=26
  2007. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hyporeflexia (occurs later)
    n1=méningé (syndrome) | n2=en:hyporeflexia (occurs later) | rel=r_associated | relid=0 | w=26
  2008. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hyporeflexia of lower limbs
    n1=méningé (syndrome) | n2=en:hyporeflexia of lower limbs | rel=r_associated | relid=0 | w=26
  2009. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypothalamic hamartoma
    n1=méningé (syndrome) | n2=en:hypothalamic hamartoma | rel=r_associated | relid=0 | w=26
  2010. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypotonia (1 patient)
    n1=méningé (syndrome) | n2=en:hypotonia (1 patient) | rel=r_associated | relid=0 | w=26
  2011. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypotonia (newborn)
    n1=méningé (syndrome) | n2=en:hypotonia (newborn) | rel=r_associated | relid=0 | w=26
  2012. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypotonia (rare)
    n1=méningé (syndrome) | n2=en:hypotonia (rare) | rel=r_associated | relid=0 | w=26
  2013. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypotonia changing to hypertonia
    n1=méningé (syndrome) | n2=en:hypotonia changing to hypertonia | rel=r_associated | relid=0 | w=26
  2014. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg
    n1=méningé (syndrome) | n2=en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg | rel=r_associated | relid=0 | w=26
  2015. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:immunology aspects
    n1=méningé (syndrome) | n2=en:immunology aspects | rel=r_associated | relid=0 | w=26
  2016. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:impaired cognition (in some patients)
    n1=méningé (syndrome) | n2=en:impaired cognition (in some patients) | rel=r_associated | relid=0 | w=26
  2017. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:impaired gait due to peripheral neuropathy
    n1=méningé (syndrome) | n2=en:impaired gait due to peripheral neuropathy | rel=r_associated | relid=0 | w=26
  2018. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:impaired voluntary movement
    n1=méningé (syndrome) | n2=en:impaired voluntary movement | rel=r_associated | relid=0 | w=26
  2019. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:inability to communicate
    n1=méningé (syndrome) | n2=en:inability to communicate | rel=r_associated | relid=0 | w=26
  2020. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:inability to hold head
    n1=méningé (syndrome) | n2=en:inability to hold head | rel=r_associated | relid=0 | w=26
  2021. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:inability to sit or control head
    n1=méningé (syndrome) | n2=en:inability to sit or control head | rel=r_associated | relid=0 | w=26
  2022. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:inability to walk independently
    n1=méningé (syndrome) | n2=en:inability to walk independently | rel=r_associated | relid=0 | w=26
  2023. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:increased activity period
    n1=méningé (syndrome) | n2=en:increased activity period | rel=r_associated | relid=0 | w=26
  2024. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:increased iron deposition in the basal ganglia
    n1=méningé (syndrome) | n2=en:increased iron deposition in the basal ganglia | rel=r_associated | relid=0 | w=26
  2025. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:individuals can stand or walk with support by 4 to 6 years of age
    n1=méningé (syndrome) | n2=en:individuals can stand or walk with support by 4 to 6 years of age | rel=r_associated | relid=0 | w=26
  2026. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:infantile seizures (approximately 80% of patients)
    n1=méningé (syndrome) | n2=en:infantile seizures (approximately 80% of patients) | rel=r_associated | relid=0 | w=26
  2027. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients)
    n1=méningé (syndrome) | n2=en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients) | rel=r_associated | relid=0 | w=26
  2028. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:intellectual disabilities (in 1 family)
    n1=méningé (syndrome) | n2=en:intellectual disabilities (in 1 family) | rel=r_associated | relid=0 | w=26
  2029. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:intellectual disability, mild (1 patient)
    n1=méningé (syndrome) | n2=en:intellectual disability, mild (1 patient) | rel=r_associated | relid=0 | w=26
  2030. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:intellectual disability, mild (in some patients)
    n1=méningé (syndrome) | n2=en:intellectual disability, mild (in some patients) | rel=r_associated | relid=0 | w=26
  2031. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:intellectual disability, mild to moderate
    n1=méningé (syndrome) | n2=en:intellectual disability, mild to moderate | rel=r_associated | relid=0 | w=26
  2032. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:intellectual impairment, mild
    n1=méningé (syndrome) | n2=en:intellectual impairment, mild | rel=r_associated | relid=0 | w=26
  2033. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:interictal eeg shows 3-4 hz general spike-wave complexes
    n1=méningé (syndrome) | n2=en:interictal eeg shows 3-4 hz general spike-wave complexes | rel=r_associated | relid=0 | w=26
  2034. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:intracranial lipoma (cerebello-pontine)
    n1=méningé (syndrome) | n2=en:intracranial lipoma (cerebello-pontine) | rel=r_associated | relid=0 | w=26
  2035. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:intractable epilepsy
    n1=méningé (syndrome) | n2=en:intractable epilepsy | rel=r_associated | relid=0 | w=26
  2036. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:involuntary dystonic or choreiform movements
    n1=méningé (syndrome) | n2=en:involuntary dystonic or choreiform movements | rel=r_associated | relid=0 | w=26
  2037. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:ipsilateral cranial nerve hypoplasia
    n1=méningé (syndrome) | n2=en:ipsilateral cranial nerve hypoplasia | rel=r_associated | relid=0 | w=26
  2038. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:jerky movements in infancy
    n1=méningé (syndrome) | n2=en:jerky movements in infancy | rel=r_associated | relid=0 | w=26
  2039. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:lack of developmental milestones
    n1=méningé (syndrome) | n2=en:lack of developmental milestones | rel=r_associated | relid=0 | w=26
  2040. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:lack of spontaneous movement
    n1=méningé (syndrome) | n2=en:lack of spontaneous movement | rel=r_associated | relid=0 | w=26
  2041. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:lack of volitional movement
    n1=méningé (syndrome) | n2=en:lack of volitional movement | rel=r_associated | relid=0 | w=26
  2042. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging
    n1=méningé (syndrome) | n2=en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging | rel=r_associated | relid=0 | w=26
  2043. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:learning disabilities (in females)
    n1=méningé (syndrome) | n2=en:learning disabilities (in females) | rel=r_associated | relid=0 | w=26
  2044. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation
    n1=méningé (syndrome) | n2=en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation | rel=r_associated | relid=0 | w=26
  2045. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:leukoencephalopathy
    n1=méningé (syndrome) | n2=en:leukoencephalopathy | rel=r_associated | relid=0 | w=26
  2046. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:lissencephaly, posterior to anterior gradient
    n1=méningé (syndrome) | n2=en:lissencephaly, posterior to anterior gradient | rel=r_associated | relid=0 | w=26
  2047. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:locomotor delay (early-onset form)
    n1=méningé (syndrome) | n2=en:locomotor delay (early-onset form) | rel=r_associated | relid=0 | w=26
  2048. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:loss of anterior horn cells and gliosis in the spinal cord
    n1=méningé (syndrome) | n2=en:loss of anterior horn cells and gliosis in the spinal cord | rel=r_associated | relid=0 | w=26
  2049. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:loss of lower alpha-motor neurons in the anterior horn of the spinal cord and lower brainstem
    n1=méningé (syndrome) | n2=en:loss of lower alpha-motor neurons in the anterior horn of the spinal cord and lower brainstem | rel=r_associated | relid=0 | w=26
  2050. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:low iq
    n1=méningé (syndrome) | n2=en:low iq | rel=r_associated | relid=0 | w=26
  2051. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:lower limb muscle weakness (occurs later)
    n1=méningé (syndrome) | n2=en:lower limb muscle weakness (occurs later) | rel=r_associated | relid=0 | w=26
  2052. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:lower motor neuron degeneration
    n1=méningé (syndrome) | n2=en:lower motor neuron degeneration | rel=r_associated | relid=0 | w=26
  2053. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:macrocephaly (due to dandy-walker malformation)
    n1=méningé (syndrome) | n2=en:macrocephaly (due to dandy-walker malformation) | rel=r_associated | relid=0 | w=26
  2054. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mega cisterna magna
    n1=méningé (syndrome) | n2=en:mega cisterna magna | rel=r_associated | relid=0 | w=26
  2055. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental lethargy
    n1=méningé (syndrome) | n2=en:mental lethargy | rel=r_associated | relid=0 | w=26
  2056. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation (20%)
    n1=méningé (syndrome) | n2=en:mental retardation (20%) | rel=r_associated | relid=0 | w=26
  2057. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation (cvs+)
    n1=méningé (syndrome) | n2=en:mental retardation (cvs+) | rel=r_associated | relid=0 | w=26
  2058. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation (if untreated in infancy)
    n1=méningé (syndrome) | n2=en:mental retardation (if untreated in infancy) | rel=r_associated | relid=0 | w=26
  2059. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation (in some patients)
    n1=méningé (syndrome) | n2=en:mental retardation (in some patients) | rel=r_associated | relid=0 | w=26
  2060. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation (less common)
    n1=méningé (syndrome) | n2=en:mental retardation (less common) | rel=r_associated | relid=0 | w=26
  2061. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation (one-third)
    n1=méningé (syndrome) | n2=en:mental retardation (one-third) | rel=r_associated | relid=0 | w=26
  2062. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation (secondary to intracranial bleed)
    n1=méningé (syndrome) | n2=en:mental retardation (secondary to intracranial bleed) | rel=r_associated | relid=0 | w=26
  2063. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation (uncommon)
    n1=méningé (syndrome) | n2=en:mental retardation (uncommon) | rel=r_associated | relid=0 | w=26
  2064. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation can occur in patients with repeated episodes of dehydration
    n1=méningé (syndrome) | n2=en:mental retardation can occur in patients with repeated episodes of dehydration | rel=r_associated | relid=0 | w=26
  2065. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation, mild (18%)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (18%) | rel=r_associated | relid=0 | w=26
  2066. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation, mild to moderate (iq 30-76)
    n1=méningé (syndrome) | n2=en:mental retardation, mild to moderate (iq 30-76) | rel=r_associated | relid=0 | w=26
  2067. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation, mild-moderate (28%, usually in males)
    n1=méningé (syndrome) | n2=en:mental retardation, mild-moderate (28%, usually in males) | rel=r_associated | relid=0 | w=26
  2068. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation, moderate (in 1 patient)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate (in 1 patient) | rel=r_associated | relid=0 | w=26
  2069. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation, moderate to profound
    n1=méningé (syndrome) | n2=en:mental retardation, moderate to profound | rel=r_associated | relid=0 | w=26
  2070. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mental retardation, moderate-severe (2p21del)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate-severe (2p21del) | rel=r_associated | relid=0 | w=26
  2071. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:microvacuolation
    n1=méningé (syndrome) | n2=en:microvacuolation | rel=r_associated | relid=0 | w=26
  2072. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:midbrain atrophy
    n1=méningé (syndrome) | n2=en:midbrain atrophy | rel=r_associated | relid=0 | w=26
  2073. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:migraine headaches (onset in adolescence)
    n1=méningé (syndrome) | n2=en:migraine headaches (onset in adolescence) | rel=r_associated | relid=0 | w=26
  2074. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mild cerebellar hypoplasia
    n1=méningé (syndrome) | n2=en:mild cerebellar hypoplasia | rel=r_associated | relid=0 | w=26
  2075. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mild cognitive deterioration in adults
    n1=méningé (syndrome) | n2=en:mild cognitive deterioration in adults | rel=r_associated | relid=0 | w=26
  2076. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mild distal sensory deficits
    n1=méningé (syndrome) | n2=en:mild distal sensory deficits | rel=r_associated | relid=0 | w=26
  2077. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mild mental decline
    n1=méningé (syndrome) | n2=en:mild mental decline | rel=r_associated | relid=0 | w=26
  2078. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mild spasticity
    n1=méningé (syndrome) | n2=en:mild spasticity | rel=r_associated | relid=0 | w=26
  2079. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mildly decreased intelligence has been reported
    n1=méningé (syndrome) | n2=en:mildly decreased intelligence has been reported | rel=r_associated | relid=0 | w=26
  2080. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mildly delayed motor development
    n1=méningé (syndrome) | n2=en:mildly delayed motor development | rel=r_associated | relid=0 | w=26
  2081. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:minor motor impairment (stage 2)
    n1=méningé (syndrome) | n2=en:minor motor impairment (stage 2) | rel=r_associated | relid=0 | w=26
  2082. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:motor abnormalities
    n1=méningé (syndrome) | n2=en:motor abnormalities | rel=r_associated | relid=0 | w=26
  2083. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:motor disturbances
    n1=méningé (syndrome) | n2=en:motor disturbances | rel=r_associated | relid=0 | w=26
  2084. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:motor dyspraxia
    n1=méningé (syndrome) | n2=en:motor dyspraxia | rel=r_associated | relid=0 | w=26
  2085. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:motor neuron disease
    n1=méningé (syndrome) | n2=en:motor neuron disease | rel=r_associated | relid=0 | w=26
  2086. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:motor regression
    n1=méningé (syndrome) | n2=en:motor regression | rel=r_associated | relid=0 | w=26
  2087. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:motor tic
    n1=méningé (syndrome) | n2=en:motor tic | rel=r_associated | relid=0 | w=26
  2088. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:movement of visual image - finding
    n1=méningé (syndrome) | n2=en:movement of visual image - finding | rel=r_associated | relid=0 | w=26
  2089. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mr spectroscopy shows decreased n-acetyl aspartate
    n1=méningé (syndrome) | n2=en:mr spectroscopy shows decreased n-acetyl aspartate | rel=r_associated | relid=0 | w=26
  2090. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mri shows globus pallidus signal abnormalities
    n1=méningé (syndrome) | n2=en:mri shows globus pallidus signal abnormalities | rel=r_associated | relid=0 | w=26
  2091. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mri shows hypointensity of the thalami early-on
    n1=méningé (syndrome) | n2=en:mri shows hypointensity of the thalami early-on | rel=r_associated | relid=0 | w=26
  2092. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mrs shows decreased choline in affected white matter
    n1=méningé (syndrome) | n2=en:mrs shows decreased choline in affected white matter | rel=r_associated | relid=0 | w=26
  2093. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:multifocal discharges seen on eeg (in some patients)
    n1=méningé (syndrome) | n2=en:multifocal discharges seen on eeg (in some patients) | rel=r_associated | relid=0 | w=26
  2094. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:multifocal seizure
    n1=méningé (syndrome) | n2=en:multifocal seizure | rel=r_associated | relid=0 | w=26
  2095. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:multifocal spikes and progressive slowing of background activity seen on eeg
    n1=méningé (syndrome) | n2=en:multifocal spikes and progressive slowing of background activity seen on eeg | rel=r_associated | relid=0 | w=26
  2096. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:multiple sclerosis-like illness (516003.0001)
    n1=méningé (syndrome) | n2=en:multiple sclerosis-like illness (516003.0001) | rel=r_associated | relid=0 | w=26
  2097. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:mutism
    n1=méningé (syndrome) | n2=en:mutism | rel=r_associated | relid=0 | w=26
  2098. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:myelomeningocele (rare)
    n1=méningé (syndrome) | n2=en:myelomeningocele (rare) | rel=r_associated | relid=0 | w=26
  2099. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:myoclonic jerk
    n1=méningé (syndrome) | n2=en:myoclonic jerk | rel=r_associated | relid=0 | w=26
  2100. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:myoclonic jerks (rare)
    n1=méningé (syndrome) | n2=en:myoclonic jerks (rare) | rel=r_associated | relid=0 | w=26
  2101. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:myoclonic spasms, superimposed episodic, severe, painful (characterized by activation of antagonistic muscle pairs, may involve facial muscles)
    n1=méningé (syndrome) | n2=en:myoclonic spasms, superimposed episodic, severe, painful (characterized by activation of antagonistic muscle pairs, may involve facial muscles) | rel=r_associated | relid=0 | w=26
  2102. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:myotonic seizures
    n1=méningé (syndrome) | n2=en:myotonic seizures | rel=r_associated | relid=0 | w=26
  2103. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:necrotic process
    n1=méningé (syndrome) | n2=en:necrotic process | rel=r_associated | relid=0 | w=26
  2104. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neonatal irritability
    n1=méningé (syndrome) | n2=en:neonatal irritability | rel=r_associated | relid=0 | w=26
  2105. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern
    n1=méningé (syndrome) | n2=en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern | rel=r_associated | relid=0 | w=26
  2106. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neural tube defects (4%)
    n1=méningé (syndrome) | n2=en:neural tube defects (4%) | rel=r_associated | relid=0 | w=26
  2107. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neurogenic bladder
    n1=méningé (syndrome) | n2=en:neurogenic bladder | rel=r_associated | relid=0 | w=26
  2108. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neurologic abnormalities in about 7%
    n1=méningé (syndrome) | n2=en:neurologic abnormalities in about 7% | rel=r_associated | relid=0 | w=26
  2109. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neurologic symptoms, if present, usually result from associated syringomyelia
    n1=méningé (syndrome) | n2=en:neurologic symptoms, if present, usually result from associated syringomyelia | rel=r_associated | relid=0 | w=26
  2110. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neuronal loss and gliosis in caudate and putamen
    n1=méningé (syndrome) | n2=en:neuronal loss and gliosis in caudate and putamen | rel=r_associated | relid=0 | w=26
  2111. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neuronal loss, diffuse
    n1=méningé (syndrome) | n2=en:neuronal loss, diffuse | rel=r_associated | relid=0 | w=26
  2112. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells
    n1=méningé (syndrome) | n2=en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells | rel=r_associated | relid=0 | w=26
  2113. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neurophysiologic abnormalities (eeg, sep, vep)
    n1=méningé (syndrome) | n2=en:neurophysiologic abnormalities (eeg, sep, vep) | rel=r_associated | relid=0 | w=26
  2114. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neuropsychologic impairment
    n1=méningé (syndrome) | n2=en:neuropsychologic impairment | rel=r_associated | relid=0 | w=26
  2115. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:neurosarcoidosis (5-16% of patients)
    n1=méningé (syndrome) | n2=en:neurosarcoidosis (5-16% of patients) | rel=r_associated | relid=0 | w=26
  2116. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:no amyloid plaques
    n1=méningé (syndrome) | n2=en:no amyloid plaques | rel=r_associated | relid=0 | w=26
  2117. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:no motor skills acquired (in some)
    n1=méningé (syndrome) | n2=en:no motor skills acquired (in some) | rel=r_associated | relid=0 | w=26
  2118. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:no speech acquisition
    n1=méningé (syndrome) | n2=en:no speech acquisition | rel=r_associated | relid=0 | w=26
  2119. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:no structural brain anomalies
    n1=méningé (syndrome) | n2=en:no structural brain anomalies | rel=r_associated | relid=0 | w=26
  2120. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:normal development in some patients
    n1=méningé (syndrome) | n2=en:normal development in some patients | rel=r_associated | relid=0 | w=26
  2121. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:normal development until 6-18 months
    n1=méningé (syndrome) | n2=en:normal development until 6-18 months | rel=r_associated | relid=0 | w=26
  2122. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:normal initial psychomotor development
    n1=méningé (syndrome) | n2=en:normal initial psychomotor development | rel=r_associated | relid=0 | w=26
  2123. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit
    n1=méningé (syndrome) | n2=en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit | rel=r_associated | relid=0 | w=26
  2124. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:nystagmus, mild
    n1=méningé (syndrome) | n2=en:nystagmus, mild | rel=r_associated | relid=0 | w=26
  2125. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:olivopontocerebellar hypoplasia, fetal-onset
    n1=méningé (syndrome) | n2=en:olivopontocerebellar hypoplasia, fetal-onset | rel=r_associated | relid=0 | w=26
  2126. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:only walking achieved
    n1=méningé (syndrome) | n2=en:only walking achieved | rel=r_associated | relid=0 | w=26
  2127. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:opsoclonus
    n1=méningé (syndrome) | n2=en:opsoclonus | rel=r_associated | relid=0 | w=26
  2128. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pachymeningitis cervicalis (cervical cord compression due to thickened dura)
    n1=méningé (syndrome) | n2=en:pachymeningitis cervicalis (cervical cord compression due to thickened dura) | rel=r_associated | relid=0 | w=26
  2129. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pain affects upper body
    n1=méningé (syndrome) | n2=en:pain affects upper body | rel=r_associated | relid=0 | w=26
  2130. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:papillary meningioma
    n1=méningé (syndrome) | n2=en:papillary meningioma | rel=r_associated | relid=0 | w=26
  2131. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:paralysis
    n1=méningé (syndrome) | n2=en:paralysis | rel=r_associated | relid=0 | w=26
  2132. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:paralysis, episodic, after strenuous exercise
    n1=méningé (syndrome) | n2=en:paralysis, episodic, after strenuous exercise | rel=r_associated | relid=0 | w=26
  2133. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:parasagittal meningioma
    n1=méningé (syndrome) | n2=en:parasagittal meningioma | rel=r_associated | relid=0 | w=26
  2134. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:paresis (hcp)
    n1=méningé (syndrome) | n2=en:paresis (hcp) | rel=r_associated | relid=0 | w=26
  2135. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms)
    n1=méningé (syndrome) | n2=en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms) | rel=r_associated | relid=0 | w=26
  2136. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:paroxysmal choreoathetosis
    n1=méningé (syndrome) | n2=en:paroxysmal choreoathetosis | rel=r_associated | relid=0 | w=26
  2137. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:partial agenesis of the corpus callosum (rare)
    n1=méningé (syndrome) | n2=en:partial agenesis of the corpus callosum (rare) | rel=r_associated | relid=0 | w=26
  2138. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:partial seizure
    n1=méningé (syndrome) | n2=en:partial seizure | rel=r_associated | relid=0 | w=26
  2139. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:patchy demyelination of subcortical white matter
    n1=méningé (syndrome) | n2=en:patchy demyelination of subcortical white matter | rel=r_associated | relid=0 | w=26
  2140. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:patients show normal psychomotor development
    n1=méningé (syndrome) | n2=en:patients show normal psychomotor development | rel=r_associated | relid=0 | w=26
  2141. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:periodic stiffness
    n1=méningé (syndrome) | n2=en:periodic stiffness | rel=r_associated | relid=0 | w=26
  2142. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:periventricular gray matter heterotopia
    n1=méningé (syndrome) | n2=en:periventricular gray matter heterotopia | rel=r_associated | relid=0 | w=26
  2143. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:periventricular hemorrhagic infarction
    n1=méningé (syndrome) | n2=en:periventricular hemorrhagic infarction | rel=r_associated | relid=0 | w=26
  2144. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:photoparoxysmal response (in some)
    n1=méningé (syndrome) | n2=en:photoparoxysmal response (in some) | rel=r_associated | relid=0 | w=26
  2145. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:physiopathological
    n1=méningé (syndrome) | n2=en:physiopathological | rel=r_associated | relid=0 | w=26
  2146. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pituitary gland hypoplasia
    n1=méningé (syndrome) | n2=en:pituitary gland hypoplasia | rel=r_associated | relid=0 | w=26
  2147. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pituitary hypoplasia (in some patients)
    n1=méningé (syndrome) | n2=en:pituitary hypoplasia (in some patients) | rel=r_associated | relid=0 | w=26
  2148. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pontine hypoplasia (1 family)
    n1=méningé (syndrome) | n2=en:pontine hypoplasia (1 family) | rel=r_associated | relid=0 | w=26
  2149. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:poor cognition
    n1=méningé (syndrome) | n2=en:poor cognition | rel=r_associated | relid=0 | w=26
  2150. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:poor head control
    n1=méningé (syndrome) | n2=en:poor head control | rel=r_associated | relid=0 | w=26
  2151. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:poor or absent independent walking
    n1=méningé (syndrome) | n2=en:poor or absent independent walking | rel=r_associated | relid=0 | w=26
  2152. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:posterior fossa arachnoid cyst
    n1=méningé (syndrome) | n2=en:posterior fossa arachnoid cyst | rel=r_associated | relid=0 | w=26
  2153. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:posterior pachygyria
    n1=méningé (syndrome) | n2=en:posterior pachygyria | rel=r_associated | relid=0 | w=26
  2154. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:postural instability (63%)
    n1=méningé (syndrome) | n2=en:postural instability (63%) | rel=r_associated | relid=0 | w=26
  2155. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:posturing
    n1=méningé (syndrome) | n2=en:posturing | rel=r_associated | relid=0 | w=26
  2156. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:presenile and senile dementia
    n1=méningé (syndrome) | n2=en:presenile and senile dementia | rel=r_associated | relid=0 | w=26
  2157. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:progressive psychomotor deterioration
    n1=méningé (syndrome) | n2=en:progressive psychomotor deterioration | rel=r_associated | relid=0 | w=26
  2158. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:progressive spastic diplegia to quadriplegia
    n1=méningé (syndrome) | n2=en:progressive spastic diplegia to quadriplegia | rel=r_associated | relid=0 | w=26
  2159. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:prominent perivascular spaces
    n1=méningé (syndrome) | n2=en:prominent perivascular spaces | rel=r_associated | relid=0 | w=26
  2160. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pseudobulbar signs
    n1=méningé (syndrome) | n2=en:pseudobulbar signs | rel=r_associated | relid=0 | w=26
  2161. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pseudobulbar symptoms (uncontrolled laughter, weeping)
    n1=méningé (syndrome) | n2=en:pseudobulbar symptoms (uncontrolled laughter, weeping) | rel=r_associated | relid=0 | w=26
  2162. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:psychomotor regression, progressive
    n1=méningé (syndrome) | n2=en:psychomotor regression, progressive | rel=r_associated | relid=0 | w=26
  2163. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:psychomotor retardation, profound
    n1=méningé (syndrome) | n2=en:psychomotor retardation, profound | rel=r_associated | relid=0 | w=26
  2164. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pyramidal signs (less common)
    n1=méningé (syndrome) | n2=en:pyramidal signs (less common) | rel=r_associated | relid=0 | w=26
  2165. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pyramidal signs, mild
    n1=méningé (syndrome) | n2=en:pyramidal signs, mild | rel=r_associated | relid=0 | w=26
  2166. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:pyramidal system
    n1=méningé (syndrome) | n2=en:pyramidal system | rel=r_associated | relid=0 | w=26
  2167. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:rapid initial onset of symptoms (hours to weeks)
    n1=méningé (syndrome) | n2=en:rapid initial onset of symptoms (hours to weeks) | rel=r_associated | relid=0 | w=26
  2168. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:rare secondary generalization
    n1=méningé (syndrome) | n2=en:rare secondary generalization | rel=r_associated | relid=0 | w=26
  2169. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:reduced consciousness
    n1=méningé (syndrome) | n2=en:reduced consciousness | rel=r_associated | relid=0 | w=26
  2170. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:reduced tendon reflexes
    n1=méningé (syndrome) | n2=en:reduced tendon reflexes | rel=r_associated | relid=0 | w=26
  2171. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:reduction of white matter, generalized
    n1=méningé (syndrome) | n2=en:reduction of white matter, generalized | rel=r_associated | relid=0 | w=26
  2172. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:rem sleep behavior disorder
    n1=méningé (syndrome) | n2=en:rem sleep behavior disorder | rel=r_associated | relid=0 | w=26
  2173. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:resting tremors
    n1=méningé (syndrome) | n2=en:resting tremors | rel=r_associated | relid=0 | w=26
  2174. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:sagittal sinus thrombosis
    n1=méningé (syndrome) | n2=en:sagittal sinus thrombosis | rel=r_associated | relid=0 | w=26
  2175. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:school problem (finding)
    n1=méningé (syndrome) | n2=en:school problem (finding) | rel=r_associated | relid=0 | w=26
  2176. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:secondary involvement of proximal and trunk muscles
    n1=méningé (syndrome) | n2=en:secondary involvement of proximal and trunk muscles | rel=r_associated | relid=0 | w=26
  2177. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:secondary seizures (in some patients)
    n1=méningé (syndrome) | n2=en:secondary seizures (in some patients) | rel=r_associated | relid=0 | w=26
  2178. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizure, febrile (2/3 children)
    n1=méningé (syndrome) | n2=en:seizure, febrile (2/3 children) | rel=r_associated | relid=0 | w=26
  2179. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizures (40%)
    n1=méningé (syndrome) | n2=en:seizures (40%) | rel=r_associated | relid=0 | w=26
  2180. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizures (cvs+)
    n1=méningé (syndrome) | n2=en:seizures (cvs+) | rel=r_associated | relid=0 | w=26
  2181. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizures (in 1 of 3 patients)
    n1=méningé (syndrome) | n2=en:seizures (in 1 of 3 patients) | rel=r_associated | relid=0 | w=26
  2182. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizures (juvenile form)
    n1=méningé (syndrome) | n2=en:seizures (juvenile form) | rel=r_associated | relid=0 | w=26
  2183. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizures (mean onset 4-5 months)
    n1=méningé (syndrome) | n2=en:seizures (mean onset 4-5 months) | rel=r_associated | relid=0 | w=26
  2184. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizures (reported in 2 patients)
    n1=méningé (syndrome) | n2=en:seizures (reported in 2 patients) | rel=r_associated | relid=0 | w=26
  2185. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizures (type i and type ii, juvenile)
    n1=méningé (syndrome) | n2=en:seizures (type i and type ii, juvenile) | rel=r_associated | relid=0 | w=26
  2186. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizures occur in clusters over 1 or several days
    n1=méningé (syndrome) | n2=en:seizures occur in clusters over 1 or several days | rel=r_associated | relid=0 | w=26
  2187. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:seizures recur in 33% of patients
    n1=méningé (syndrome) | n2=en:seizures recur in 33% of patients | rel=r_associated | relid=0 | w=26
  2188. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle
    n1=méningé (syndrome) | n2=en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle | rel=r_associated | relid=0 | w=26
  2189. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:severe cognitive deficits (develop later)
    n1=méningé (syndrome) | n2=en:severe cognitive deficits (develop later) | rel=r_associated | relid=0 | w=26
  2190. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:severe delay in myelination
    n1=méningé (syndrome) | n2=en:severe delay in myelination | rel=r_associated | relid=0 | w=26
  2191. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:severe muscular hypotonia
    n1=méningé (syndrome) | n2=en:severe muscular hypotonia | rel=r_associated | relid=0 | w=26
  2192. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:severe psychomotor retardation
    n1=méningé (syndrome) | n2=en:severe psychomotor retardation | rel=r_associated | relid=0 | w=26
  2193. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:shorter daily total sleep times compared to age-matched controls
    n1=méningé (syndrome) | n2=en:shorter daily total sleep times compared to age-matched controls | rel=r_associated | relid=0 | w=26
  2194. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:simple partial seizures
    n1=méningé (syndrome) | n2=en:simple partial seizures | rel=r_associated | relid=0 | w=26
  2195. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:simplified cortical gyration pattern
    n1=méningé (syndrome) | n2=en:simplified cortical gyration pattern | rel=r_associated | relid=0 | w=26
  2196. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:sleep disturbances
    n1=méningé (syndrome) | n2=en:sleep disturbances | rel=r_associated | relid=0 | w=26
  2197. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:sleep disturbances (in some patients)
    n1=méningé (syndrome) | n2=en:sleep disturbances (in some patients) | rel=r_associated | relid=0 | w=26
  2198. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:slowly progressive neurologic deterioration
    n1=méningé (syndrome) | n2=en:slowly progressive neurologic deterioration | rel=r_associated | relid=0 | w=26
  2199. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:slurred speech
    n1=méningé (syndrome) | n2=en:slurred speech | rel=r_associated | relid=0 | w=26
  2200. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:small brain
    n1=méningé (syndrome) | n2=en:small brain | rel=r_associated | relid=0 | w=26
  2201. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:small sella
    n1=méningé (syndrome) | n2=en:small sella | rel=r_associated | relid=0 | w=26
  2202. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:small, thin cerebellum
    n1=méningé (syndrome) | n2=en:small, thin cerebellum | rel=r_associated | relid=0 | w=26
  2203. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:smooth brain surface
    n1=méningé (syndrome) | n2=en:smooth brain surface | rel=r_associated | relid=0 | w=26
  2204. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:social communication disorder
    n1=méningé (syndrome) | n2=en:social communication disorder | rel=r_associated | relid=0 | w=26
  2205. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spastic paraplegia, later onset (in one patient)
    n1=méningé (syndrome) | n2=en:spastic paraplegia, later onset (in one patient) | rel=r_associated | relid=0 | w=26
  2206. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spastic quadriplegia (in one patient)
    n1=méningé (syndrome) | n2=en:spastic quadriplegia (in one patient) | rel=r_associated | relid=0 | w=26
  2207. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spastic tetraparesis
    n1=méningé (syndrome) | n2=en:spastic tetraparesis | rel=r_associated | relid=0 | w=26
  2208. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spasticity (1 family)
    n1=méningé (syndrome) | n2=en:spasticity (1 family) | rel=r_associated | relid=0 | w=26
  2209. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spasticity (later)
    n1=méningé (syndrome) | n2=en:spasticity (later) | rel=r_associated | relid=0 | w=26
  2210. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spasticity, mild (in some patients)
    n1=méningé (syndrome) | n2=en:spasticity, mild (in some patients) | rel=r_associated | relid=0 | w=26
  2211. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spasticity, severe, affecting lower limbs
    n1=méningé (syndrome) | n2=en:spasticity, severe, affecting lower limbs | rel=r_associated | relid=0 | w=26
  2212. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:specialized branches of medicine
    n1=méningé (syndrome) | n2=en:specialized branches of medicine | rel=r_associated | relid=0 | w=26
  2213. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:speech development delayed (in some patients)
    n1=méningé (syndrome) | n2=en:speech development delayed (in some patients) | rel=r_associated | relid=0 | w=26
  2214. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:speech never acquired
    n1=méningé (syndrome) | n2=en:speech never acquired | rel=r_associated | relid=0 | w=26
  2215. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spinal cord compression
    n1=méningé (syndrome) | n2=en:spinal cord compression | rel=r_associated | relid=0 | w=26
  2216. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spinal cord glial hyperplasia
    n1=méningé (syndrome) | n2=en:spinal cord glial hyperplasia | rel=r_associated | relid=0 | w=26
  2217. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spinal neurofibromas (64%)
    n1=méningé (syndrome) | n2=en:spinal neurofibromas (64%) | rel=r_associated | relid=0 | w=26
  2218. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:spinocerebellar degeneration
    n1=méningé (syndrome) | n2=en:spinocerebellar degeneration | rel=r_associated | relid=0 | w=26
  2219. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:stance ataxia
    n1=méningé (syndrome) | n2=en:stance ataxia | rel=r_associated | relid=0 | w=26
  2220. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:start with tonic posturing
    n1=méningé (syndrome) | n2=en:start with tonic posturing | rel=r_associated | relid=0 | w=26
  2221. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:startle myoclonus
    n1=méningé (syndrome) | n2=en:startle myoclonus | rel=r_associated | relid=0 | w=26
  2222. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:stenosis of the aqueduct of sylvius (rare)
    n1=méningé (syndrome) | n2=en:stenosis of the aqueduct of sylvius (rare) | rel=r_associated | relid=0 | w=26
  2223. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:structural abnormalities in the basal ganglia (especially caudate)
    n1=méningé (syndrome) | n2=en:structural abnormalities in the basal ganglia (especially caudate) | rel=r_associated | relid=0 | w=26
  2224. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:subcortical lesions with edema
    n1=méningé (syndrome) | n2=en:subcortical lesions with edema | rel=r_associated | relid=0 | w=26
  2225. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:subcortical white matter abnormalities (rare)
    n1=méningé (syndrome) | n2=en:subcortical white matter abnormalities (rare) | rel=r_associated | relid=0 | w=26
  2226. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:subnormal intelligence (62%)
    n1=méningé (syndrome) | n2=en:subnormal intelligence (62%) | rel=r_associated | relid=0 | w=26
  2227. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:superficial laminar spongiosis
    n1=méningé (syndrome) | n2=en:superficial laminar spongiosis | rel=r_associated | relid=0 | w=26
  2228. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:symptoms are exacerbated during pregnancy
    n1=méningé (syndrome) | n2=en:symptoms are exacerbated during pregnancy | rel=r_associated | relid=0 | w=26
  2229. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:synkinesia (rare)
    n1=méningé (syndrome) | n2=en:synkinesia (rare) | rel=r_associated | relid=0 | w=26
  2230. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:tau-positive inclusions may be found
    n1=méningé (syndrome) | n2=en:tau-positive inclusions may be found | rel=r_associated | relid=0 | w=26
  2231. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:temporal lobe heterotopias
    n1=méningé (syndrome) | n2=en:temporal lobe heterotopias | rel=r_associated | relid=0 | w=26
  2232. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:thickening of the skull (less common)
    n1=méningé (syndrome) | n2=en:thickening of the skull (less common) | rel=r_associated | relid=0 | w=26
  2233. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:tremor
    n1=méningé (syndrome) | n2=en:tremor | rel=r_associated | relid=0 | w=26
  2234. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:trigeminal neuralgia
    n1=méningé (syndrome) | n2=en:trigeminal neuralgia | rel=r_associated | relid=0 | w=26
  2235. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:trismus (rare)
    n1=méningé (syndrome) | n2=en:trismus (rare) | rel=r_associated | relid=0 | w=26
  2236. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves
    n1=méningé (syndrome) | n2=en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves | rel=r_associated | relid=0 | w=26
  2237. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:upper and lower motor neuron disease
    n1=méningé (syndrome) | n2=en:upper and lower motor neuron disease | rel=r_associated | relid=0 | w=26
  2238. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:upper limb dysmetria
    n1=méningé (syndrome) | n2=en:upper limb dysmetria | rel=r_associated | relid=0 | w=26
  2239. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:upper limb hyperreflexia (in some patients)
    n1=méningé (syndrome) | n2=en:upper limb hyperreflexia (in some patients) | rel=r_associated | relid=0 | w=26
  2240. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:upper limb involvement (onset in the first decade)
    n1=méningé (syndrome) | n2=en:upper limb involvement (onset in the first decade) | rel=r_associated | relid=0 | w=26
  2241. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:upper limbs affected
    n1=méningé (syndrome) | n2=en:upper limbs affected | rel=r_associated | relid=0 | w=26
  2242. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:use of ultrasonography
    n1=méningé (syndrome) | n2=en:use of ultrasonography | rel=r_associated | relid=0 | w=26
  2243. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:very poor expressive speech
    n1=méningé (syndrome) | n2=en:very poor expressive speech | rel=r_associated | relid=0 | w=26
  2244. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:vestibular anomalies (less common)
    n1=méningé (syndrome) | n2=en:vestibular anomalies (less common) | rel=r_associated | relid=0 | w=26
  2245. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade)
    n1=méningé (syndrome) | n2=en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade) | rel=r_associated | relid=0 | w=26
  2246. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:vibrissae
    n1=méningé (syndrome) | n2=en:vibrissae | rel=r_associated | relid=0 | w=26
  2247. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:visual auras
    n1=méningé (syndrome) | n2=en:visual auras | rel=r_associated | relid=0 | w=26
  2248. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:visual hallucination
    n1=méningé (syndrome) | n2=en:visual hallucination | rel=r_associated | relid=0 | w=26
  2249. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:walking impairment due to myoclonus late in disease
    n1=méningé (syndrome) | n2=en:walking impairment due to myoclonus late in disease | rel=r_associated | relid=0 | w=26
  2250. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:weakness of hip and ankle flexion
    n1=méningé (syndrome) | n2=en:weakness of hip and ankle flexion | rel=r_associated | relid=0 | w=26
  2251. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:white matter changes
    n1=méningé (syndrome) | n2=en:white matter changes | rel=r_associated | relid=0 | w=26
  2252. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:white matter changes on brain imaging (less common)
    n1=méningé (syndrome) | n2=en:white matter changes on brain imaging (less common) | rel=r_associated | relid=0 | w=26
  2253. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:white matter dysmyelination/demyelination (71%)
    n1=méningé (syndrome) | n2=en:white matter dysmyelination/demyelination (71%) | rel=r_associated | relid=0 | w=26
  2254. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:white matter lesions (1 patient)
    n1=méningé (syndrome) | n2=en:white matter lesions (1 patient) | rel=r_associated | relid=0 | w=26
  2255. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> en:white matter lesions seen on brain imaging
    n1=méningé (syndrome) | n2=en:white matter lesions seen on brain imaging | rel=r_associated | relid=0 | w=26
  2256. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> méningiomatose
    n1=méningé (syndrome) | n2=méningiomatose | rel=r_associated | relid=0 | w=26
  2257. méningé (syndrome) -- r_associated #0: 26 / 0.313 -> tumeur
    n1=méningé (syndrome) | n2=tumeur | rel=r_associated | relid=0 | w=26
  2258. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> cerveau
    (anatomie)
    n1=méningé (syndrome) | n2=cerveau
    (anatomie)
    | rel=r_associated | relid=0 | w=25
  2259. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:'double contour' convolutional calcification on ct scan
    n1=méningé (syndrome) | n2=en:'double contour' convolutional calcification on ct scan | rel=r_associated | relid=0 | w=25
  2260. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:'dragonfly-like' pattern
    n1=méningé (syndrome) | n2=en:'dragonfly-like' pattern | rel=r_associated | relid=0 | w=25
  2261. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:abnormal gyri
    n1=méningé (syndrome) | n2=en:abnormal gyri | rel=r_associated | relid=0 | w=25
  2262. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:abnormal hippocampus
    n1=méningé (syndrome) | n2=en:abnormal hippocampus | rel=r_associated | relid=0 | w=25
  2263. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:abnormal interictal eeg (in some patients)
    n1=méningé (syndrome) | n2=en:abnormal interictal eeg (in some patients) | rel=r_associated | relid=0 | w=25
  2264. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:absent cortical responses of somatosensory evoked potentials
    n1=méningé (syndrome) | n2=en:absent cortical responses of somatosensory evoked potentials | rel=r_associated | relid=0 | w=25
  2265. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:absent olfactory tracts and bulbs
    n1=méningé (syndrome) | n2=en:absent olfactory tracts and bulbs | rel=r_associated | relid=0 | w=25
  2266. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:absent or immature dentate nuclei
    n1=méningé (syndrome) | n2=en:absent or immature dentate nuclei | rel=r_associated | relid=0 | w=25
  2267. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:absent posterior pituitary bright spot
    n1=méningé (syndrome) | n2=en:absent posterior pituitary bright spot | rel=r_associated | relid=0 | w=25
  2268. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:absent speech
    n1=méningé (syndrome) | n2=en:absent speech | rel=r_associated | relid=0 | w=25
  2269. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:actin- and actin depolymerizing factor/cofilin-immunoreactive eosinophilic spherical structures in the striatum
    n1=méningé (syndrome) | n2=en:actin- and actin depolymerizing factor/cofilin-immunoreactive eosinophilic spherical structures in the striatum | rel=r_associated | relid=0 | w=25
  2270. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:action and postural tremor
    n1=méningé (syndrome) | n2=en:action and postural tremor | rel=r_associated | relid=0 | w=25
  2271. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:acute necrotizing encephalopathy
    n1=méningé (syndrome) | n2=en:acute necrotizing encephalopathy | rel=r_associated | relid=0 | w=25
  2272. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:agenesis or hypogenesis of the cerebellar vermis
    n1=méningé (syndrome) | n2=en:agenesis or hypogenesis of the cerebellar vermis | rel=r_associated | relid=0 | w=25
  2273. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:aggregation of snca-immunopositive inclusions
    n1=méningé (syndrome) | n2=en:aggregation of snca-immunopositive inclusions | rel=r_associated | relid=0 | w=25
  2274. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:aggression
    n1=méningé (syndrome) | n2=en:aggression | rel=r_associated | relid=0 | w=25
  2275. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:amyloid-like plaques, immunoreactive to prp, predominantly in the cerebellum
    n1=méningé (syndrome) | n2=en:amyloid-like plaques, immunoreactive to prp, predominantly in the cerebellum | rel=r_associated | relid=0 | w=25
  2276. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:amyotrophic lateral sclerosis
    n1=méningé (syndrome) | n2=en:amyotrophic lateral sclerosis | rel=r_associated | relid=0 | w=25
  2277. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:anencephaly
    n1=méningé (syndrome) | n2=en:anencephaly | rel=r_associated | relid=0 | w=25
  2278. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:anencephaly (1 patient)
    n1=méningé (syndrome) | n2=en:anencephaly (1 patient) | rel=r_associated | relid=0 | w=25
  2279. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:anterior pituitary adenoma
    n1=méningé (syndrome) | n2=en:anterior pituitary adenoma | rel=r_associated | relid=0 | w=25
  2280. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:anterior sacral meningocele
    n1=méningé (syndrome) | n2=en:anterior sacral meningocele | rel=r_associated | relid=0 | w=25
  2281. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:aphasia
    n1=méningé (syndrome) | n2=en:aphasia | rel=r_associated | relid=0 | w=25
  2282. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:arachnoid cysts (in one family)
    n1=méningé (syndrome) | n2=en:arachnoid cysts (in one family) | rel=r_associated | relid=0 | w=25
  2283. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:areflexia (30%)
    n1=méningé (syndrome) | n2=en:areflexia (30%) | rel=r_associated | relid=0 | w=25
  2284. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:areflexia of upper limbs
    n1=méningé (syndrome) | n2=en:areflexia of upper limbs | rel=r_associated | relid=0 | w=25
  2285. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:argyrophilic hyperphosphorylated tau-positive inclusions (pick bodies)
    n1=méningé (syndrome) | n2=en:argyrophilic hyperphosphorylated tau-positive inclusions (pick bodies) | rel=r_associated | relid=0 | w=25
  2286. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:arm flexion
    n1=méningé (syndrome) | n2=en:arm flexion | rel=r_associated | relid=0 | w=25
  2287. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:arm pain
    n1=méningé (syndrome) | n2=en:arm pain | rel=r_associated | relid=0 | w=25
  2288. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:arrest of psychomotor development after seizure onset
    n1=méningé (syndrome) | n2=en:arrest of psychomotor development after seizure onset | rel=r_associated | relid=0 | w=25
  2289. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:articulation difficulties
    n1=méningé (syndrome) | n2=en:articulation difficulties | rel=r_associated | relid=0 | w=25
  2290. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:articulation, unintelligible
    n1=méningé (syndrome) | n2=en:articulation, unintelligible | rel=r_associated | relid=0 | w=25
  2291. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:astrogliosis (in some patients)
    n1=méningé (syndrome) | n2=en:astrogliosis (in some patients) | rel=r_associated | relid=0 | w=25
  2292. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:atretic occipital cephalocele
    n1=méningé (syndrome) | n2=en:atretic occipital cephalocele | rel=r_associated | relid=0 | w=25
  2293. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:atrophy may be more severe in the left hemisphere
    n1=méningé (syndrome) | n2=en:atrophy may be more severe in the left hemisphere | rel=r_associated | relid=0 | w=25
  2294. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:atrophy of the granular cell layer of the cerebellum
    n1=méningé (syndrome) | n2=en:atrophy of the granular cell layer of the cerebellum | rel=r_associated | relid=0 | w=25
  2295. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:autonomic abnormalities
    n1=méningé (syndrome) | n2=en:autonomic abnormalities | rel=r_associated | relid=0 | w=25
  2296. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:autonomic disturbances
    n1=méningé (syndrome) | n2=en:autonomic disturbances | rel=r_associated | relid=0 | w=25
  2297. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:autonomic dysfunction may occur
    n1=méningé (syndrome) | n2=en:autonomic dysfunction may occur | rel=r_associated | relid=0 | w=25
  2298. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:autonomic involvement affecting limbs during episodes
    n1=méningé (syndrome) | n2=en:autonomic involvement affecting limbs during episodes | rel=r_associated | relid=0 | w=25
  2299. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:axial imbalance (34%)
    n1=méningé (syndrome) | n2=en:axial imbalance (34%) | rel=r_associated | relid=0 | w=25
  2300. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:axonal swellings or spheroids
    n1=méningé (syndrome) | n2=en:axonal swellings or spheroids | rel=r_associated | relid=0 | w=25
  2301. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:babinski sign
    n1=méningé (syndrome) | n2=en:babinski sign | rel=r_associated | relid=0 | w=25
  2302. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:basal ganglion degeneration
    n1=méningé (syndrome) | n2=en:basal ganglion degeneration | rel=r_associated | relid=0 | w=25
  2303. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:benign neoplasm of the meninges
    n1=méningé (syndrome) | n2=en:benign neoplasm of the meninges | rel=r_associated | relid=0 | w=25
  2304. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:bilateral striatal lucencies on imaging
    n1=méningé (syndrome) | n2=en:bilateral striatal lucencies on imaging | rel=r_associated | relid=0 | w=25
  2305. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:bilateral thalamic lesions on mri
    n1=méningé (syndrome) | n2=en:bilateral thalamic lesions on mri | rel=r_associated | relid=0 | w=25
  2306. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:brain imaging shows generalized atrophy
    n1=méningé (syndrome) | n2=en:brain imaging shows generalized atrophy | rel=r_associated | relid=0 | w=25
  2307. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:brain mrs shows reduced choline and inositol peaks in the parieto-occipital white matter
    n1=méningé (syndrome) | n2=en:brain mrs shows reduced choline and inositol peaks in the parieto-occipital white matter | rel=r_associated | relid=0 | w=25
  2308. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:brain tissue shows abnormal spherical aggregates of iron and ferritin in the basal ganglia, forebrain, and cerebellum
    n1=méningé (syndrome) | n2=en:brain tissue shows abnormal spherical aggregates of iron and ferritin in the basal ganglia, forebrain, and cerebellum | rel=r_associated | relid=0 | w=25
  2309. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:brain white matter hyperintensities on mri
    n1=méningé (syndrome) | n2=en:brain white matter hyperintensities on mri | rel=r_associated | relid=0 | w=25
  2310. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:bulbar paresis
    n1=méningé (syndrome) | n2=en:bulbar paresis | rel=r_associated | relid=0 | w=25
  2311. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cavum septum pellucidum atrophy
    n1=méningé (syndrome) | n2=en:cavum septum pellucidum atrophy | rel=r_associated | relid=0 | w=25
  2312. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cerebellar atrophy, severe
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, severe | rel=r_associated | relid=0 | w=25
  2313. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cerebellar dysarthria
    n1=méningé (syndrome) | n2=en:cerebellar dysarthria | rel=r_associated | relid=0 | w=25
  2314. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cerebellar hypoplasia, mild (in some patients)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia, mild (in some patients) | rel=r_associated | relid=0 | w=25
  2315. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cerebral atrophy (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:cerebral atrophy (reported in 1 patient) | rel=r_associated | relid=0 | w=25
  2316. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cerebral atrophy diffuse
    n1=méningé (syndrome) | n2=en:cerebral atrophy diffuse | rel=r_associated | relid=0 | w=25
  2317. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cerebral cortical neurodegeneration
    n1=méningé (syndrome) | n2=en:cerebral cortical neurodegeneration | rel=r_associated | relid=0 | w=25
  2318. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cerebral degeneration
    n1=méningé (syndrome) | n2=en:cerebral degeneration | rel=r_associated | relid=0 | w=25
  2319. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cerebrospinal fluid
    n1=méningé (syndrome) | n2=en:cerebrospinal fluid | rel=r_associated | relid=0 | w=25
  2320. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:chiari malformation type ii
    n1=méningé (syndrome) | n2=en:chiari malformation type ii | rel=r_associated | relid=0 | w=25
  2321. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:chorea-ballism
    n1=méningé (syndrome) | n2=en:chorea-ballism | rel=r_associated | relid=0 | w=25
  2322. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:chronic pain
    n1=méningé (syndrome) | n2=en:chronic pain | rel=r_associated | relid=0 | w=25
  2323. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cns infarctions
    n1=méningé (syndrome) | n2=en:cns infarctions | rel=r_associated | relid=0 | w=25
  2324. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cobblestone lissencephaly (posterior brain regions more affected than anterior regions)
    n1=méningé (syndrome) | n2=en:cobblestone lissencephaly (posterior brain regions more affected than anterior regions) | rel=r_associated | relid=0 | w=25
  2325. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cognitive dysfunction (rare)
    n1=méningé (syndrome) | n2=en:cognitive dysfunction (rare) | rel=r_associated | relid=0 | w=25
  2326. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cognitive impairment (1 patient)
    n1=méningé (syndrome) | n2=en:cognitive impairment (1 patient) | rel=r_associated | relid=0 | w=25
  2327. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:communicating hydrocephalus
    n1=méningé (syndrome) | n2=en:communicating hydrocephalus | rel=r_associated | relid=0 | w=25
  2328. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:complex partial seizures
    n1=méningé (syndrome) | n2=en:complex partial seizures | rel=r_associated | relid=0 | w=25
  2329. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:compromised expressive language development, severe
    n1=méningé (syndrome) | n2=en:compromised expressive language development, severe | rel=r_associated | relid=0 | w=25
  2330. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:congenital porencephaly
    n1=méningé (syndrome) | n2=en:congenital porencephaly | rel=r_associated | relid=0 | w=25
  2331. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:continuous spike-wave discharges during sleep
    n1=méningé (syndrome) | n2=en:continuous spike-wave discharges during sleep | rel=r_associated | relid=0 | w=25
  2332. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:contralateral hemiparesis, congenital
    n1=méningé (syndrome) | n2=en:contralateral hemiparesis, congenital | rel=r_associated | relid=0 | w=25
  2333. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:convulsive seizures
    n1=méningé (syndrome) | n2=en:convulsive seizures | rel=r_associated | relid=0 | w=25
  2334. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:corpus callosum agenesis
    n1=méningé (syndrome) | n2=en:corpus callosum agenesis | rel=r_associated | relid=0 | w=25
  2335. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cortical and subcortical neuronal loss in the frontal and temporal regions
    n1=méningé (syndrome) | n2=en:cortical and subcortical neuronal loss in the frontal and temporal regions | rel=r_associated | relid=0 | w=25
  2336. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cortical dysplasia, focal (in some patients)
    n1=méningé (syndrome) | n2=en:cortical dysplasia, focal (in some patients) | rel=r_associated | relid=0 | w=25
  2337. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:cortical hypergyria (in some patients)
    n1=méningé (syndrome) | n2=en:cortical hypergyria (in some patients) | rel=r_associated | relid=0 | w=25
  2338. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:corticospinal tract hypoplasia
    n1=méningé (syndrome) | n2=en:corticospinal tract hypoplasia | rel=r_associated | relid=0 | w=25
  2339. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:decreased amount of myelin-specific proteins
    n1=méningé (syndrome) | n2=en:decreased amount of myelin-specific proteins | rel=r_associated | relid=0 | w=25
  2340. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:decreased iq
    n1=méningé (syndrome) | n2=en:decreased iq | rel=r_associated | relid=0 | w=25
  2341. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:decreased speech
    n1=méningé (syndrome) | n2=en:decreased speech | rel=r_associated | relid=0 | w=25
  2342. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:decreased upper extremity reflexes
    n1=méningé (syndrome) | n2=en:decreased upper extremity reflexes | rel=r_associated | relid=0 | w=25
  2343. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:deep posterior interpeduncular fossa
    n1=méningé (syndrome) | n2=en:deep posterior interpeduncular fossa | rel=r_associated | relid=0 | w=25
  2344. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:defect in axonal guidance
    n1=méningé (syndrome) | n2=en:defect in axonal guidance | rel=r_associated | relid=0 | w=25
  2345. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:deficient myelination
    n1=méningé (syndrome) | n2=en:deficient myelination | rel=r_associated | relid=0 | w=25
  2346. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:delayed myelination (1 patient)
    n1=méningé (syndrome) | n2=en:delayed myelination (1 patient) | rel=r_associated | relid=0 | w=25
  2347. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:delayed myelination on brain mri (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:delayed myelination on brain mri (reported in 1 patient) | rel=r_associated | relid=0 | w=25
  2348. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:delayed walking, mild (in some patients)
    n1=méningé (syndrome) | n2=en:delayed walking, mild (in some patients) | rel=r_associated | relid=0 | w=25
  2349. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dementia, progressive, with onset of disease
    n1=méningé (syndrome) | n2=en:dementia, progressive, with onset of disease | rel=r_associated | relid=0 | w=25
  2350. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:demyelinization
    n1=méningé (syndrome) | n2=en:demyelinization | rel=r_associated | relid=0 | w=25
  2351. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dermoid cyst
    n1=méningé (syndrome) | n2=en:dermoid cyst | rel=r_associated | relid=0 | w=25
  2352. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:developmental delay, variable
    n1=méningé (syndrome) | n2=en:developmental delay, variable | rel=r_associated | relid=0 | w=25
  2353. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:developmental regression after age 2 years
    n1=méningé (syndrome) | n2=en:developmental regression after age 2 years | rel=r_associated | relid=0 | w=25
  2354. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:diffuse lewy bodies throughout the brain (cortical and subcortical regions)
    n1=méningé (syndrome) | n2=en:diffuse lewy bodies throughout the brain (cortical and subcortical regions) | rel=r_associated | relid=0 | w=25
  2355. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:diffuse periventricular leukoencephalopathy
    n1=méningé (syndrome) | n2=en:diffuse periventricular leukoencephalopathy | rel=r_associated | relid=0 | w=25
  2356. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:diffuse slowing
    n1=méningé (syndrome) | n2=en:diffuse slowing | rel=r_associated | relid=0 | w=25
  2357. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:diffuse slowing of background
    n1=méningé (syndrome) | n2=en:diffuse slowing of background | rel=r_associated | relid=0 | w=25
  2358. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:diffuse, severe neuronal loss
    n1=méningé (syndrome) | n2=en:diffuse, severe neuronal loss | rel=r_associated | relid=0 | w=25
  2359. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dilation of lateral ventricles
    n1=méningé (syndrome) | n2=en:dilation of lateral ventricles | rel=r_associated | relid=0 | w=25
  2360. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:disorganised speech
    n1=méningé (syndrome) | n2=en:disorganised speech | rel=r_associated | relid=0 | w=25
  2361. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:distal sensory impairment
    n1=méningé (syndrome) | n2=en:distal sensory impairment | rel=r_associated | relid=0 | w=25
  2362. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dizziness
    n1=méningé (syndrome) | n2=en:dizziness | rel=r_associated | relid=0 | w=25
  2363. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dural ectasia
    n1=méningé (syndrome) | n2=en:dural ectasia | rel=r_associated | relid=0 | w=25
  2364. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dysarthria (mild)
    n1=méningé (syndrome) | n2=en:dysarthria (mild) | rel=r_associated | relid=0 | w=25
  2365. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dysautonomia may occur
    n1=méningé (syndrome) | n2=en:dysautonomia may occur | rel=r_associated | relid=0 | w=25
  2366. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dysmetria (in some patients)
    n1=méningé (syndrome) | n2=en:dysmetria (in some patients) | rel=r_associated | relid=0 | w=25
  2367. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dysmetric saccades
    n1=méningé (syndrome) | n2=en:dysmetric saccades | rel=r_associated | relid=0 | w=25
  2368. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dysmorphic basal ganglia (1 patient)
    n1=méningé (syndrome) | n2=en:dysmorphic basal ganglia (1 patient) | rel=r_associated | relid=0 | w=25
  2369. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dysmyelinating leukodystrophy
    n1=méningé (syndrome) | n2=en:dysmyelinating leukodystrophy | rel=r_associated | relid=0 | w=25
  2370. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dysplastic cerebellar vermis
    n1=méningé (syndrome) | n2=en:dysplastic cerebellar vermis | rel=r_associated | relid=0 | w=25
  2371. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dystonia (1 family)
    n1=méningé (syndrome) | n2=en:dystonia (1 family) | rel=r_associated | relid=0 | w=25
  2372. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dystonia (1 patient)
    n1=méningé (syndrome) | n2=en:dystonia (1 patient) | rel=r_associated | relid=0 | w=25
  2373. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dystonia (in severe cases)
    n1=méningé (syndrome) | n2=en:dystonia (in severe cases) | rel=r_associated | relid=0 | w=25
  2374. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dystonia (less common)
    n1=méningé (syndrome) | n2=en:dystonia (less common) | rel=r_associated | relid=0 | w=25
  2375. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dystonia disorders
    n1=méningé (syndrome) | n2=en:dystonia disorders | rel=r_associated | relid=0 | w=25
  2376. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dystonia, limb, exercise-induced
    n1=méningé (syndrome) | n2=en:dystonia, limb, exercise-induced | rel=r_associated | relid=0 | w=25
  2377. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dystonia, trunk and limbs (upper and lower)
    n1=méningé (syndrome) | n2=en:dystonia, trunk and limbs (upper and lower) | rel=r_associated | relid=0 | w=25
  2378. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dystonic posturing (rare)
    n1=méningé (syndrome) | n2=en:dystonic posturing (rare) | rel=r_associated | relid=0 | w=25
  2379. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:dystonic posturing of the hands
    n1=méningé (syndrome) | n2=en:dystonic posturing of the hands | rel=r_associated | relid=0 | w=25
  2380. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:early severe fetal akinesia sequence
    n1=méningé (syndrome) | n2=en:early severe fetal akinesia sequence | rel=r_associated | relid=0 | w=25
  2381. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:ectopic dorsal pontine transverse bundle of fibers forms the 'cap'
    n1=méningé (syndrome) | n2=en:ectopic dorsal pontine transverse bundle of fibers forms the 'cap' | rel=r_associated | relid=0 | w=25
  2382. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eeg during episodes shows desynchronization
    n1=méningé (syndrome) | n2=en:eeg during episodes shows desynchronization | rel=r_associated | relid=0 | w=25
  2383. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eeg later shows generalized spike or polyspike waves and focal spikes
    n1=méningé (syndrome) | n2=en:eeg later shows generalized spike or polyspike waves and focal spikes | rel=r_associated | relid=0 | w=25
  2384. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eeg shows 3-4-hz spike and multispike slow wave complexes
    n1=méningé (syndrome) | n2=en:eeg shows 3-4-hz spike and multispike slow wave complexes | rel=r_associated | relid=0 | w=25
  2385. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eeg shows 3-4-hz spike waves
    n1=méningé (syndrome) | n2=en:eeg shows 3-4-hz spike waves | rel=r_associated | relid=0 | w=25
  2386. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eeg shows centrotemporal spike-wave discharges
    n1=méningé (syndrome) | n2=en:eeg shows centrotemporal spike-wave discharges | rel=r_associated | relid=0 | w=25
  2387. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eeg shows hypsarrhythmia (in 1 of 6 patients)
    n1=méningé (syndrome) | n2=en:eeg shows hypsarrhythmia (in 1 of 6 patients) | rel=r_associated | relid=0 | w=25
  2388. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eeg shows multifocal discharges
    n1=méningé (syndrome) | n2=en:eeg shows multifocal discharges | rel=r_associated | relid=0 | w=25
  2389. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eeg shows unilateral centrotemporal spikes
    n1=méningé (syndrome) | n2=en:eeg shows unilateral centrotemporal spikes | rel=r_associated | relid=0 | w=25
  2390. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eeg with burst suppression
    n1=méningé (syndrome) | n2=en:eeg with burst suppression | rel=r_associated | relid=0 | w=25
  2391. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:electroencephalogram abnormal
    n1=méningé (syndrome) | n2=en:electroencephalogram abnormal | rel=r_associated | relid=0 | w=25
  2392. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:encephalocele (1 patient)
    n1=méningé (syndrome) | n2=en:encephalocele (1 patient) | rel=r_associated | relid=0 | w=25
  2393. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:encephalopathy (in some patients)
    n1=méningé (syndrome) | n2=en:encephalopathy (in some patients) | rel=r_associated | relid=0 | w=25
  2394. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:enlarged cerebellum
    n1=méningé (syndrome) | n2=en:enlarged cerebellum | rel=r_associated | relid=0 | w=25
  2395. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:enlarged corpus callosum
    n1=méningé (syndrome) | n2=en:enlarged corpus callosum | rel=r_associated | relid=0 | w=25
  2396. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:enlarged lateral ventricles (occipital>frontal)
    n1=méningé (syndrome) | n2=en:enlarged lateral ventricles (occipital>frontal) | rel=r_associated | relid=0 | w=25
  2397. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:episodic hemiplegia
    n1=méningé (syndrome) | n2=en:episodic hemiplegia | rel=r_associated | relid=0 | w=25
  2398. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:episodic subtype, headaches occur in clusters
    n1=méningé (syndrome) | n2=en:episodic subtype, headaches occur in clusters | rel=r_associated | relid=0 | w=25
  2399. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:extensor plantar responses (1 family)
    n1=méningé (syndrome) | n2=en:extensor plantar responses (1 family) | rel=r_associated | relid=0 | w=25
  2400. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:extra superior temporal gyrus (female)
    n1=méningé (syndrome) | n2=en:extra superior temporal gyrus (female) | rel=r_associated | relid=0 | w=25
  2401. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:extrapyramidal dyskinesia
    n1=méningé (syndrome) | n2=en:extrapyramidal dyskinesia | rel=r_associated | relid=0 | w=25
  2402. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:extrapyramidal symptoms (later-onset)
    n1=méningé (syndrome) | n2=en:extrapyramidal symptoms (later-onset) | rel=r_associated | relid=0 | w=25
  2403. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:eye
    n1=méningé (syndrome) | n2=en:eye | rel=r_associated | relid=0 | w=25
  2404. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:facial-faucial-finger mini-myoclonus (fff)
    n1=méningé (syndrome) | n2=en:facial-faucial-finger mini-myoclonus (fff) | rel=r_associated | relid=0 | w=25
  2405. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:faciomandibular myoclonus, nocturnal
    n1=méningé (syndrome) | n2=en:faciomandibular myoclonus, nocturnal | rel=r_associated | relid=0 | w=25
  2406. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:fasciculations, tongue
    n1=méningé (syndrome) | n2=en:fasciculations, tongue | rel=r_associated | relid=0 | w=25
  2407. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:febrile seizure
    n1=méningé (syndrome) | n2=en:febrile seizure | rel=r_associated | relid=0 | w=25
  2408. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:febrile seizures (in some)
    n1=méningé (syndrome) | n2=en:febrile seizures (in some) | rel=r_associated | relid=0 | w=25
  2409. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:focal cerebellar dysplasia
    n1=méningé (syndrome) | n2=en:focal cerebellar dysplasia | rel=r_associated | relid=0 | w=25
  2410. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:focal hyperplasia of the choroid plexus
    n1=méningé (syndrome) | n2=en:focal hyperplasia of the choroid plexus | rel=r_associated | relid=0 | w=25
  2411. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:focal tremor
    n1=méningé (syndrome) | n2=en:focal tremor | rel=r_associated | relid=0 | w=25
  2412. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:frontotemporal dementia
    n1=méningé (syndrome) | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=25
  2413. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:fusion of the basal ganglia
    n1=méningé (syndrome) | n2=en:fusion of the basal ganglia | rel=r_associated | relid=0 | w=25
  2414. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:fusion of the cerebellar hemispheres
    n1=méningé (syndrome) | n2=en:fusion of the cerebellar hemispheres | rel=r_associated | relid=0 | w=25
  2415. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:gait disability
    n1=méningé (syndrome) | n2=en:gait disability | rel=r_associated | relid=0 | w=25
  2416. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:gait impairment (55%)
    n1=méningé (syndrome) | n2=en:gait impairment (55%) | rel=r_associated | relid=0 | w=25
  2417. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:generalized cerebral hypoplasia/atrophy (45%)
    n1=méningé (syndrome) | n2=en:generalized cerebral hypoplasia/atrophy (45%) | rel=r_associated | relid=0 | w=25
  2418. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:generalized cortical atrophy, most prominent in the frontal and parietal lobes
    n1=méningé (syndrome) | n2=en:generalized cortical atrophy, most prominent in the frontal and parietal lobes | rel=r_associated | relid=0 | w=25
  2419. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:generalized stiffening
    n1=méningé (syndrome) | n2=en:generalized stiffening | rel=r_associated | relid=0 | w=25
  2420. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:giant granules in schwann cells
    n1=méningé (syndrome) | n2=en:giant granules in schwann cells | rel=r_associated | relid=0 | w=25
  2421. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:gyral simplification
    n1=méningé (syndrome) | n2=en:gyral simplification | rel=r_associated | relid=0 | w=25
  2422. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hamartomatous lesions of the brain
    n1=méningé (syndrome) | n2=en:hamartomatous lesions of the brain | rel=r_associated | relid=0 | w=25
  2423. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hand muscle weakness
    n1=méningé (syndrome) | n2=en:hand muscle weakness | rel=r_associated | relid=0 | w=25
  2424. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:has tingling sensation
    n1=méningé (syndrome) | n2=en:has tingling sensation | rel=r_associated | relid=0 | w=25
  2425. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:headache
    n1=méningé (syndrome) | n2=en:headache | rel=r_associated | relid=0 | w=25
  2426. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:headache is unilateral
    n1=méningé (syndrome) | n2=en:headache is unilateral | rel=r_associated | relid=0 | w=25
  2427. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:headache recurrent
    n1=méningé (syndrome) | n2=en:headache recurrent | rel=r_associated | relid=0 | w=25
  2428. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hemosiderin deposition
    n1=méningé (syndrome) | n2=en:hemosiderin deposition | rel=r_associated | relid=0 | w=25
  2429. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:high voltage, fast rhythms seen on eeg
    n1=méningé (syndrome) | n2=en:high voltage, fast rhythms seen on eeg | rel=r_associated | relid=0 | w=25
  2430. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hydrocephalus (rare)
    n1=méningé (syndrome) | n2=en:hydrocephalus (rare) | rel=r_associated | relid=0 | w=25
  2431. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hydrocephalus, occasional
    n1=méningé (syndrome) | n2=en:hydrocephalus, occasional | rel=r_associated | relid=0 | w=25
  2432. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hyperactive deep tendon reflexes
    n1=méningé (syndrome) | n2=en:hyperactive deep tendon reflexes | rel=r_associated | relid=0 | w=25
  2433. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hyperintensities in the basal ganglia (rare)
    n1=méningé (syndrome) | n2=en:hyperintensities in the basal ganglia (rare) | rel=r_associated | relid=0 | w=25
  2434. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hyperintensities in the basal ganglia and/or thalamus
    n1=méningé (syndrome) | n2=en:hyperintensities in the basal ganglia and/or thalamus | rel=r_associated | relid=0 | w=25
  2435. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hyperreflexia (less common)
    n1=méningé (syndrome) | n2=en:hyperreflexia (less common) | rel=r_associated | relid=0 | w=25
  2436. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hyperreflexia (some patients)
    n1=méningé (syndrome) | n2=en:hyperreflexia (some patients) | rel=r_associated | relid=0 | w=25
  2437. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hyperreflexia may occur
    n1=méningé (syndrome) | n2=en:hyperreflexia may occur | rel=r_associated | relid=0 | w=25
  2438. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hypertonia (after age 2 years)
    n1=méningé (syndrome) | n2=en:hypertonia (after age 2 years) | rel=r_associated | relid=0 | w=25
  2439. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hypertonia of the extremities
    n1=méningé (syndrome) | n2=en:hypertonia of the extremities | rel=r_associated | relid=0 | w=25
  2440. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hypokinesia in infancy
    n1=méningé (syndrome) | n2=en:hypokinesia in infancy | rel=r_associated | relid=0 | w=25
  2441. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hypoplasia and displacement of the corticospinal fibers within the brainstem
    n1=méningé (syndrome) | n2=en:hypoplasia and displacement of the corticospinal fibers within the brainstem | rel=r_associated | relid=0 | w=25
  2442. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hypoplastic anterior pituitary gland
    n1=méningé (syndrome) | n2=en:hypoplastic anterior pituitary gland | rel=r_associated | relid=0 | w=25
  2443. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hyposmia/anosmia (in some patients)
    n1=méningé (syndrome) | n2=en:hyposmia/anosmia (in some patients) | rel=r_associated | relid=0 | w=25
  2444. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hypotonia, severe (rare)
    n1=méningé (syndrome) | n2=en:hypotonia, severe (rare) | rel=r_associated | relid=0 | w=25
  2445. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:hypotrophic brainstem
    n1=méningé (syndrome) | n2=en:hypotrophic brainstem | rel=r_associated | relid=0 | w=25
  2446. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:ictal eeg with bisynchronous spike waves
    n1=méningé (syndrome) | n2=en:ictal eeg with bisynchronous spike waves | rel=r_associated | relid=0 | w=25
  2447. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:idiopathic torsion dystonia
    n1=méningé (syndrome) | n2=en:idiopathic torsion dystonia | rel=r_associated | relid=0 | w=25
  2448. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:imaging shows signal abnormalities in basal ganglia
    n1=méningé (syndrome) | n2=en:imaging shows signal abnormalities in basal ganglia | rel=r_associated | relid=0 | w=25
  2449. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:impaired horizontal smooth pursuit
    n1=méningé (syndrome) | n2=en:impaired horizontal smooth pursuit | rel=r_associated | relid=0 | w=25
  2450. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:impaired proprioception
    n1=méningé (syndrome) | n2=en:impaired proprioception | rel=r_associated | relid=0 | w=25
  2451. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:inability to generate syntactic grammar rules (i.e., tense, gender, number)
    n1=méningé (syndrome) | n2=en:inability to generate syntactic grammar rules (i.e., tense, gender, number) | rel=r_associated | relid=0 | w=25
  2452. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:increased falls
    n1=méningé (syndrome) | n2=en:increased falls | rel=r_associated | relid=0 | w=25
  2453. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:increased signal intensity on t(2)-weighted scans in the periventricular and centrum ovale area
    n1=méningé (syndrome) | n2=en:increased signal intensity on t(2)-weighted scans in the periventricular and centrum ovale area | rel=r_associated | relid=0 | w=25
  2454. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:increased tone in the upper limbs (occur later)
    n1=méningé (syndrome) | n2=en:increased tone in the upper limbs (occur later) | rel=r_associated | relid=0 | w=25
  2455. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:infrequent generalized seizures
    n1=méningé (syndrome) | n2=en:infrequent generalized seizures | rel=r_associated | relid=0 | w=25
  2456. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:intellectual disability (in most patients)
    n1=méningé (syndrome) | n2=en:intellectual disability (in most patients) | rel=r_associated | relid=0 | w=25
  2457. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:intermittent migraine headaches
    n1=méningé (syndrome) | n2=en:intermittent migraine headaches | rel=r_associated | relid=0 | w=25
  2458. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:intermittent, transient episodes of worsening of ataxia
    n1=méningé (syndrome) | n2=en:intermittent, transient episodes of worsening of ataxia | rel=r_associated | relid=0 | w=25
  2459. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:intracellular accumulation of material resulting in fingerprint profiles on ultrastructural analysis
    n1=méningé (syndrome) | n2=en:intracellular accumulation of material resulting in fingerprint profiles on ultrastructural analysis | rel=r_associated | relid=0 | w=25
  2460. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:intracranial bleeding (1 patient)
    n1=méningé (syndrome) | n2=en:intracranial bleeding (1 patient) | rel=r_associated | relid=0 | w=25
  2461. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:intraneuronal inclusions
    n1=méningé (syndrome) | n2=en:intraneuronal inclusions | rel=r_associated | relid=0 | w=25
  2462. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:involuntary movements of extremities, neck, trunk, and/or face
    n1=méningé (syndrome) | n2=en:involuntary movements of extremities, neck, trunk, and/or face | rel=r_associated | relid=0 | w=25
  2463. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:iron accumulation in the globus pallidus and substantia nigra seen on mri
    n1=méningé (syndrome) | n2=en:iron accumulation in the globus pallidus and substantia nigra seen on mri | rel=r_associated | relid=0 | w=25
  2464. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:iron-containing deposits in various brain regions
    n1=méningé (syndrome) | n2=en:iron-containing deposits in various brain regions | rel=r_associated | relid=0 | w=25
  2465. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:irritation
    n1=méningé (syndrome) | n2=en:irritation | rel=r_associated | relid=0 | w=25
  2466. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:lack of ependymal cells
    n1=méningé (syndrome) | n2=en:lack of ependymal cells | rel=r_associated | relid=0 | w=25
  2467. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:lack of independent ambulation
    n1=méningé (syndrome) | n2=en:lack of independent ambulation | rel=r_associated | relid=0 | w=25
  2468. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:lack of speech acquisition
    n1=méningé (syndrome) | n2=en:lack of speech acquisition | rel=r_associated | relid=0 | w=25
  2469. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:language delay (55%)
    n1=méningé (syndrome) | n2=en:language delay (55%) | rel=r_associated | relid=0 | w=25
  2470. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:large subcortical cysts in frontal and temporal lobes
    n1=méningé (syndrome) | n2=en:large subcortical cysts in frontal and temporal lobes | rel=r_associated | relid=0 | w=25
  2471. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:learning difficulties in affected females
    n1=méningé (syndrome) | n2=en:learning difficulties in affected females | rel=r_associated | relid=0 | w=25
  2472. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:learning difficulties, mild (1 family)
    n1=méningé (syndrome) | n2=en:learning difficulties, mild (1 family) | rel=r_associated | relid=0 | w=25
  2473. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:learning problems
    n1=méningé (syndrome) | n2=en:learning problems | rel=r_associated | relid=0 | w=25
  2474. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:lesions in the caudate and putamen seen on mri
    n1=méningé (syndrome) | n2=en:lesions in the caudate and putamen seen on mri | rel=r_associated | relid=0 | w=25
  2475. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:leukoencephalopathy in the frontal and parietal lobes (later)
    n1=méningé (syndrome) | n2=en:leukoencephalopathy in the frontal and parietal lobes (later) | rel=r_associated | relid=0 | w=25
  2476. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:lissencephaly
    n1=méningé (syndrome) | n2=en:lissencephaly | rel=r_associated | relid=0 | w=25
  2477. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:loss of ability to walk later
    n1=méningé (syndrome) | n2=en:loss of ability to walk later | rel=r_associated | relid=0 | w=25
  2478. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:loss of ankle reflexes
    n1=méningé (syndrome) | n2=en:loss of ankle reflexes | rel=r_associated | relid=0 | w=25
  2479. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:loss of balance may occur
    n1=méningé (syndrome) | n2=en:loss of balance may occur | rel=r_associated | relid=0 | w=25
  2480. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:loss of motor neurons in the spinal cord
    n1=méningé (syndrome) | n2=en:loss of motor neurons in the spinal cord | rel=r_associated | relid=0 | w=25
  2481. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:loss of neurons affecting all cortical layers
    n1=méningé (syndrome) | n2=en:loss of neurons affecting all cortical layers | rel=r_associated | relid=0 | w=25
  2482. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:loss of reflexes due to myopathy
    n1=méningé (syndrome) | n2=en:loss of reflexes due to myopathy | rel=r_associated | relid=0 | w=25
  2483. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:loss of very early milestones
    n1=méningé (syndrome) | n2=en:loss of very early milestones | rel=r_associated | relid=0 | w=25
  2484. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:lower limb spasticity
    n1=méningé (syndrome) | n2=en:lower limb spasticity | rel=r_associated | relid=0 | w=25
  2485. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:malformation, cerebral arteriovenous
    n1=méningé (syndrome) | n2=en:malformation, cerebral arteriovenous | rel=r_associated | relid=0 | w=25
  2486. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:markedly delayed nerve conduction velocities
    n1=méningé (syndrome) | n2=en:markedly delayed nerve conduction velocities | rel=r_associated | relid=0 | w=25
  2487. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mean sleep latency is less than 5 to 8 minutes
    n1=méningé (syndrome) | n2=en:mean sleep latency is less than 5 to 8 minutes | rel=r_associated | relid=0 | w=25
  2488. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:memory impairment, progressive
    n1=méningé (syndrome) | n2=en:memory impairment, progressive | rel=r_associated | relid=0 | w=25
  2489. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:meningismus
    n1=méningé (syndrome) | n2=en:meningismus | rel=r_associated | relid=0 | w=25
  2490. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental delay or retardation (uncommon)
    n1=méningé (syndrome) | n2=en:mental delay or retardation (uncommon) | rel=r_associated | relid=0 | w=25
  2491. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation (18% of patients)
    n1=méningé (syndrome) | n2=en:mental retardation (18% of patients) | rel=r_associated | relid=0 | w=25
  2492. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation (2 patients)
    n1=méningé (syndrome) | n2=en:mental retardation (2 patients) | rel=r_associated | relid=0 | w=25
  2493. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation (in 2 patients) learning disability (in 1 patient)
    n1=méningé (syndrome) | n2=en:mental retardation (in 2 patients) learning disability (in 1 patient) | rel=r_associated | relid=0 | w=25
  2494. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation (iq 45-75)
    n1=méningé (syndrome) | n2=en:mental retardation (iq 45-75) | rel=r_associated | relid=0 | w=25
  2495. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation (iq 50-60 combined griffiths and stanford-binet scale)
    n1=méningé (syndrome) | n2=en:mental retardation (iq 50-60 combined griffiths and stanford-binet scale) | rel=r_associated | relid=0 | w=25
  2496. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation (rare)
    n1=méningé (syndrome) | n2=en:mental retardation (rare) | rel=r_associated | relid=0 | w=25
  2497. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:mental retardation (reported in 1 patient) | rel=r_associated | relid=0 | w=25
  2498. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation (sometimes)
    n1=méningé (syndrome) | n2=en:mental retardation (sometimes) | rel=r_associated | relid=0 | w=25
  2499. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation from rapid mental regression
    n1=méningé (syndrome) | n2=en:mental retardation from rapid mental regression | rel=r_associated | relid=0 | w=25
  2500. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation, borderline (1 patient)
    n1=méningé (syndrome) | n2=en:mental retardation, borderline (1 patient) | rel=r_associated | relid=0 | w=25
  2501. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation, mild (1 family)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (1 family) | rel=r_associated | relid=0 | w=25
  2502. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation, mild (10%)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (10%) | rel=r_associated | relid=0 | w=25
  2503. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation, mild (11%)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (11%) | rel=r_associated | relid=0 | w=25
  2504. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation, mild (20% have more severe mental retardation)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (20% have more severe mental retardation) | rel=r_associated | relid=0 | w=25
  2505. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation, mild to moderate (in 12%)
    n1=méningé (syndrome) | n2=en:mental retardation, mild to moderate (in 12%) | rel=r_associated | relid=0 | w=25
  2506. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation, mild to moderate (in some patients)
    n1=méningé (syndrome) | n2=en:mental retardation, mild to moderate (in some patients) | rel=r_associated | relid=0 | w=25
  2507. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation, moderate (in some patients)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate (in some patients) | rel=r_associated | relid=0 | w=25
  2508. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mental retardation, variable degree (in some patients)
    n1=méningé (syndrome) | n2=en:mental retardation, variable degree (in some patients) | rel=r_associated | relid=0 | w=25
  2509. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:metaplastic meningioma
    n1=méningé (syndrome) | n2=en:metaplastic meningioma | rel=r_associated | relid=0 | w=25
  2510. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:migraine, with or without aura
    n1=méningé (syndrome) | n2=en:migraine, with or without aura | rel=r_associated | relid=0 | w=25
  2511. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mild mental retardation (in 1/4 patients)
    n1=méningé (syndrome) | n2=en:mild mental retardation (in 1/4 patients) | rel=r_associated | relid=0 | w=25
  2512. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mildly enlarged ventricles
    n1=méningé (syndrome) | n2=en:mildly enlarged ventricles | rel=r_associated | relid=0 | w=25
  2513. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mildly thin corpus callosum
    n1=méningé (syndrome) | n2=en:mildly thin corpus callosum | rel=r_associated | relid=0 | w=25
  2514. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:minimal to absent speech
    n1=méningé (syndrome) | n2=en:minimal to absent speech | rel=r_associated | relid=0 | w=25
  2515. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:molar tooth sign on brain mri (subset of patients)
    n1=méningé (syndrome) | n2=en:molar tooth sign on brain mri (subset of patients) | rel=r_associated | relid=0 | w=25
  2516. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:molar tooth sign seen on mri
    n1=méningé (syndrome) | n2=en:molar tooth sign seen on mri | rel=r_associated | relid=0 | w=25
  2517. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:motor deterioration
    n1=méningé (syndrome) | n2=en:motor deterioration | rel=r_associated | relid=0 | w=25
  2518. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:motor neuron disease, lower
    n1=méningé (syndrome) | n2=en:motor neuron disease, lower | rel=r_associated | relid=0 | w=25
  2519. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mri - diffuse or focal cerebral and cerebellar white matter disease
    n1=méningé (syndrome) | n2=en:mri - diffuse or focal cerebral and cerebellar white matter disease | rel=r_associated | relid=0 | w=25
  2520. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mri may be normal, especially in type iib
    n1=méningé (syndrome) | n2=en:mri may be normal, especially in type iib | rel=r_associated | relid=0 | w=25
  2521. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mri shows atretic occipital cephalocele with bony skull defect
    n1=méningé (syndrome) | n2=en:mri shows atretic occipital cephalocele with bony skull defect | rel=r_associated | relid=0 | w=25
  2522. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mri shows brainstem hypoplasia
    n1=méningé (syndrome) | n2=en:mri shows brainstem hypoplasia | rel=r_associated | relid=0 | w=25
  2523. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mri shows increased t2-weighted signals in the globus pallidi
    n1=méningé (syndrome) | n2=en:mri shows increased t2-weighted signals in the globus pallidi | rel=r_associated | relid=0 | w=25
  2524. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:mri shows subcortical leukoencephalopathy with cavitation
    n1=méningé (syndrome) | n2=en:mri shows subcortical leukoencephalopathy with cavitation | rel=r_associated | relid=0 | w=25
  2525. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:multifocal epileptiform spikes seen on eeg
    n1=méningé (syndrome) | n2=en:multifocal epileptiform spikes seen on eeg | rel=r_associated | relid=0 | w=25
  2526. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:multifocal spike and wave activity
    n1=méningé (syndrome) | n2=en:multifocal spike and wave activity | rel=r_associated | relid=0 | w=25
  2527. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:multiple aneurysms
    n1=méningé (syndrome) | n2=en:multiple aneurysms | rel=r_associated | relid=0 | w=25
  2528. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:muscle biopsy shows neurogenic changes
    n1=méningé (syndrome) | n2=en:muscle biopsy shows neurogenic changes | rel=r_associated | relid=0 | w=25
  2529. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:muscle weakness
    n1=méningé (syndrome) | n2=en:muscle weakness | rel=r_associated | relid=0 | w=25
  2530. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:muscle weakness lower limb
    n1=méningé (syndrome) | n2=en:muscle weakness lower limb | rel=r_associated | relid=0 | w=25
  2531. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:muscle weakness, distal (lower limbs more affected than upper limbs), due to motor neuronopathy
    n1=méningé (syndrome) | n2=en:muscle weakness, distal (lower limbs more affected than upper limbs), due to motor neuronopathy | rel=r_associated | relid=0 | w=25
  2532. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy
    n1=méningé (syndrome) | n2=en:muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy | rel=r_associated | relid=0 | w=25
  2533. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:muscular rigidity
    n1=méningé (syndrome) | n2=en:muscular rigidity | rel=r_associated | relid=0 | w=25
  2534. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:myoclonic seizure, refractory
    n1=méningé (syndrome) | n2=en:myoclonic seizure, refractory | rel=r_associated | relid=0 | w=25
  2535. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:neonatal epileptic encephalopathy (nee)
    n1=méningé (syndrome) | n2=en:neonatal epileptic encephalopathy (nee) | rel=r_associated | relid=0 | w=25
  2536. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:neurodegeneration (patient a)
    n1=méningé (syndrome) | n2=en:neurodegeneration (patient a) | rel=r_associated | relid=0 | w=25
  2537. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:neurodegeneration in the substantia nigra
    n1=méningé (syndrome) | n2=en:neurodegeneration in the substantia nigra | rel=r_associated | relid=0 | w=25
  2538. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:neurologic dysfunction, progressive
    n1=méningé (syndrome) | n2=en:neurologic dysfunction, progressive | rel=r_associated | relid=0 | w=25
  2539. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:neurologic regression
    n1=méningé (syndrome) | n2=en:neurologic regression | rel=r_associated | relid=0 | w=25
  2540. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:neurologic sequelae of stroke
    n1=méningé (syndrome) | n2=en:neurologic sequelae of stroke | rel=r_associated | relid=0 | w=25
  2541. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:neuronal loss in the cerebral cortex
    n1=méningé (syndrome) | n2=en:neuronal loss in the cerebral cortex | rel=r_associated | relid=0 | w=25
  2542. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:neuropathologic examination shows extensive spongiosis and gliosis
    n1=méningé (syndrome) | n2=en:neuropathologic examination shows extensive spongiosis and gliosis | rel=r_associated | relid=0 | w=25
  2543. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:neuropathology shows fmr1 mrna-positive inclusions in neurons and astrocytes
    n1=méningé (syndrome) | n2=en:neuropathology shows fmr1 mrna-positive inclusions in neurons and astrocytes | rel=r_associated | relid=0 | w=25
  2544. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:nigrostriatal degeneration
    n1=méningé (syndrome) | n2=en:nigrostriatal degeneration | rel=r_associated | relid=0 | w=25
  2545. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:no dementia
    n1=méningé (syndrome) | n2=en:no dementia | rel=r_associated | relid=0 | w=25
  2546. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:no developmental progress
    n1=méningé (syndrome) | n2=en:no developmental progress | rel=r_associated | relid=0 | w=25
  2547. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:no gaze contact
    n1=méningé (syndrome) | n2=en:no gaze contact | rel=r_associated | relid=0 | w=25
  2548. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:normal early development, up to 8 to 15 months of age
    n1=méningé (syndrome) | n2=en:normal early development, up to 8 to 15 months of age | rel=r_associated | relid=0 | w=25
  2549. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:normal early developmental milestones
    n1=méningé (syndrome) | n2=en:normal early developmental milestones | rel=r_associated | relid=0 | w=25
  2550. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:normal intelligence to mild or moderate mental retardation
    n1=méningé (syndrome) | n2=en:normal intelligence to mild or moderate mental retardation | rel=r_associated | relid=0 | w=25
  2551. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:normal iq in infancy, then iq drops with age
    n1=méningé (syndrome) | n2=en:normal iq in infancy, then iq drops with age | rel=r_associated | relid=0 | w=25
  2552. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:normal motor development
    n1=méningé (syndrome) | n2=en:normal motor development | rel=r_associated | relid=0 | w=25
  2553. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:normal psychomotor development in most
    n1=méningé (syndrome) | n2=en:normal psychomotor development in most | rel=r_associated | relid=0 | w=25
  2554. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:numbness
    n1=méningé (syndrome) | n2=en:numbness | rel=r_associated | relid=0 | w=25
  2555. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:occurs most often during the night or early morning
    n1=méningé (syndrome) | n2=en:occurs most often during the night or early morning | rel=r_associated | relid=0 | w=25
  2556. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:olfactory or auditory hallucinations
    n1=méningé (syndrome) | n2=en:olfactory or auditory hallucinations | rel=r_associated | relid=0 | w=25
  2557. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:olivopontocerebellar atrophy
    n1=méningé (syndrome) | n2=en:olivopontocerebellar atrophy | rel=r_associated | relid=0 | w=25
  2558. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:orthostatic hypotension
    n1=méningé (syndrome) | n2=en:orthostatic hypotension | rel=r_associated | relid=0 | w=25
  2559. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:pachygyria, frontoparietal
    n1=méningé (syndrome) | n2=en:pachygyria, frontoparietal | rel=r_associated | relid=0 | w=25
  2560. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:pachygyria, usually posterior
    n1=méningé (syndrome) | n2=en:pachygyria, usually posterior | rel=r_associated | relid=0 | w=25
  2561. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:paraspinal masses
    n1=méningé (syndrome) | n2=en:paraspinal masses | rel=r_associated | relid=0 | w=25
  2562. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:parkinsonism (less common)
    n1=méningé (syndrome) | n2=en:parkinsonism (less common) | rel=r_associated | relid=0 | w=25
  2563. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:paroxysmal oculogyric crises
    n1=méningé (syndrome) | n2=en:paroxysmal oculogyric crises | rel=r_associated | relid=0 | w=25
  2564. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:partial agenesis of corpus callosum (rare, in males)
    n1=méningé (syndrome) | n2=en:partial agenesis of corpus callosum (rare, in males) | rel=r_associated | relid=0 | w=25
  2565. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:pathology includes spongiform changes, diffuse nerve cell degeneration and glial proliferation
    n1=méningé (syndrome) | n2=en:pathology includes spongiform changes, diffuse nerve cell degeneration and glial proliferation | rel=r_associated | relid=0 | w=25
  2566. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:periodic paralysis (finding)
    n1=méningé (syndrome) | n2=en:periodic paralysis (finding) | rel=r_associated | relid=0 | w=25
  2567. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:perisylvian polymicrogyria
    n1=méningé (syndrome) | n2=en:perisylvian polymicrogyria | rel=r_associated | relid=0 | w=25
  2568. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:periventricular cysts
    n1=méningé (syndrome) | n2=en:periventricular cysts | rel=r_associated | relid=0 | w=25
  2569. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:periventricular leukomalacia (reported in 2 patients)
    n1=méningé (syndrome) | n2=en:periventricular leukomalacia (reported in 2 patients) | rel=r_associated | relid=0 | w=25
  2570. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:periventricular white matter changes (meb)
    n1=méningé (syndrome) | n2=en:periventricular white matter changes (meb) | rel=r_associated | relid=0 | w=25
  2571. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:perseveration
    n1=méningé (syndrome) | n2=en:perseveration | rel=r_associated | relid=0 | w=25
  2572. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:petit mal epilepsy
    n1=méningé (syndrome) | n2=en:petit mal epilepsy | rel=r_associated | relid=0 | w=25
  2573. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:pineal hypertrophy
    n1=méningé (syndrome) | n2=en:pineal hypertrophy | rel=r_associated | relid=0 | w=25
  2574. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:plaque, amyloid
    n1=méningé (syndrome) | n2=en:plaque, amyloid | rel=r_associated | relid=0 | w=25
  2575. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:polymicrogyria
    n1=méningé (syndrome) | n2=en:polymicrogyria | rel=r_associated | relid=0 | w=25
  2576. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:polymicrogyria, diffuse, asymmetric
    n1=méningé (syndrome) | n2=en:polymicrogyria, diffuse, asymmetric | rel=r_associated | relid=0 | w=25
  2577. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:polymicrogyria, frontal
    n1=méningé (syndrome) | n2=en:polymicrogyria, frontal | rel=r_associated | relid=0 | w=25
  2578. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:polymicrogyria, occipital
    n1=méningé (syndrome) | n2=en:polymicrogyria, occipital | rel=r_associated | relid=0 | w=25
  2579. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:poor or absent speech acquisition
    n1=méningé (syndrome) | n2=en:poor or absent speech acquisition | rel=r_associated | relid=0 | w=25
  2580. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:poor responsiveness
    n1=méningé (syndrome) | n2=en:poor responsiveness | rel=r_associated | relid=0 | w=25
  2581. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:posterior fossa compression syndrome
    n1=méningé (syndrome) | n2=en:posterior fossa compression syndrome | rel=r_associated | relid=0 | w=25
  2582. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:posterior fossa cyst (in 1 of 2 patients)
    n1=méningé (syndrome) | n2=en:posterior fossa cyst (in 1 of 2 patients) | rel=r_associated | relid=0 | w=25
  2583. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:postural dystonia (onset is restricted to 1 extremity, usually lower, with foot dystonia)
    n1=méningé (syndrome) | n2=en:postural dystonia (onset is restricted to 1 extremity, usually lower, with foot dystonia) | rel=r_associated | relid=0 | w=25
  2584. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:preservation of u fibers
    n1=méningé (syndrome) | n2=en:preservation of u fibers | rel=r_associated | relid=0 | w=25
  2585. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:progression to paralysis and atrophy of distal lower limb muscles
    n1=méningé (syndrome) | n2=en:progression to paralysis and atrophy of distal lower limb muscles | rel=r_associated | relid=0 | w=25
  2586. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:progressive spasticity
    n1=méningé (syndrome) | n2=en:progressive spasticity | rel=r_associated | relid=0 | w=25
  2587. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:prominent ventricles (in some patients)
    n1=méningé (syndrome) | n2=en:prominent ventricles (in some patients) | rel=r_associated | relid=0 | w=25
  2588. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:proximal limb muscle stiffness
    n1=méningé (syndrome) | n2=en:proximal limb muscle stiffness | rel=r_associated | relid=0 | w=25
  2589. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:proximal muscle weakness in lower limbs
    n1=méningé (syndrome) | n2=en:proximal muscle weakness in lower limbs | rel=r_associated | relid=0 | w=25
  2590. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:proximal weakness occurs first
    n1=méningé (syndrome) | n2=en:proximal weakness occurs first | rel=r_associated | relid=0 | w=25
  2591. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:pseudobulbar palsy (e.g. involuntary weeping or laughter)
    n1=méningé (syndrome) | n2=en:pseudobulbar palsy (e.g. involuntary weeping or laughter) | rel=r_associated | relid=0 | w=25
  2592. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:psychomotor regression beginning in infancy
    n1=méningé (syndrome) | n2=en:psychomotor regression beginning in infancy | rel=r_associated | relid=0 | w=25
  2593. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:psychomotor regression in infants
    n1=méningé (syndrome) | n2=en:psychomotor regression in infants | rel=r_associated | relid=0 | w=25
  2594. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:psychosis
    n1=méningé (syndrome) | n2=en:psychosis | rel=r_associated | relid=0 | w=25
  2595. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:psychosis (rare)
    n1=méningé (syndrome) | n2=en:psychosis (rare) | rel=r_associated | relid=0 | w=25
  2596. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:pyramidal signs (in some patients)
    n1=méningé (syndrome) | n2=en:pyramidal signs (in some patients) | rel=r_associated | relid=0 | w=25
  2597. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:pyramidal signs, mild (uncommon)
    n1=méningé (syndrome) | n2=en:pyramidal signs, mild (uncommon) | rel=r_associated | relid=0 | w=25
  2598. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:pyramidal tract dysfunction (juvenile-onset, less common)
    n1=méningé (syndrome) | n2=en:pyramidal tract dysfunction (juvenile-onset, less common) | rel=r_associated | relid=0 | w=25
  2599. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:quadrupedal locomotion (in some patients)
    n1=méningé (syndrome) | n2=en:quadrupedal locomotion (in some patients) | rel=r_associated | relid=0 | w=25
  2600. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:recurrent muscle twitches (symptom)
    n1=méningé (syndrome) | n2=en:recurrent muscle twitches (symptom) | rel=r_associated | relid=0 | w=25
  2601. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:reduced brain size
    n1=méningé (syndrome) | n2=en:reduced brain size | rel=r_associated | relid=0 | w=25
  2602. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:reduced size of the pituitary gland
    n1=méningé (syndrome) | n2=en:reduced size of the pituitary gland | rel=r_associated | relid=0 | w=25
  2603. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:relative sparing of language
    n1=méningé (syndrome) | n2=en:relative sparing of language | rel=r_associated | relid=0 | w=25
  2604. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:rigidity (later)
    n1=méningé (syndrome) | n2=en:rigidity (later) | rel=r_associated | relid=0 | w=25
  2605. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:rotary head movements ('rolling,' 'tremor')
    n1=méningé (syndrome) | n2=en:rotary head movements ('rolling,' 'tremor') | rel=r_associated | relid=0 | w=25
  2606. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:segmental callosal hypoplasia, mild
    n1=méningé (syndrome) | n2=en:segmental callosal hypoplasia, mild | rel=r_associated | relid=0 | w=25
  2607. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizure disorder (homozygote)
    n1=méningé (syndrome) | n2=en:seizure disorder (homozygote) | rel=r_associated | relid=0 | w=25
  2608. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizure, focal or multifocal onset
    n1=méningé (syndrome) | n2=en:seizure, focal or multifocal onset | rel=r_associated | relid=0 | w=25
  2609. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures (in 1 of 2 sibs)
    n1=méningé (syndrome) | n2=en:seizures (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=25
  2610. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures (in 2 of 6 patients)
    n1=méningé (syndrome) | n2=en:seizures (in 2 of 6 patients) | rel=r_associated | relid=0 | w=25
  2611. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures (in one patient)
    n1=méningé (syndrome) | n2=en:seizures (in one patient) | rel=r_associated | relid=0 | w=25
  2612. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures (rare)
    n1=méningé (syndrome) | n2=en:seizures (rare) | rel=r_associated | relid=0 | w=25
  2613. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures occur in clusters
    n1=méningé (syndrome) | n2=en:seizures occur in clusters | rel=r_associated | relid=0 | w=25
  2614. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures usually last 1 to 5 minutes (less commonly up to 10 minutes)
    n1=méningé (syndrome) | n2=en:seizures usually last 1 to 5 minutes (less commonly up to 10 minutes) | rel=r_associated | relid=0 | w=25
  2615. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures, diurnal partial, rare (in some patients)
    n1=méningé (syndrome) | n2=en:seizures, diurnal partial, rare (in some patients) | rel=r_associated | relid=0 | w=25
  2616. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures, febrile (1 family)
    n1=méningé (syndrome) | n2=en:seizures, febrile (1 family) | rel=r_associated | relid=0 | w=25
  2617. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures, generalized tonic/clonic, myoclonic, atonic, or atypical absence, aggravated by fatigue and fasting with frequency ranges from daily to monthly (in some patients)
    n1=méningé (syndrome) | n2=en:seizures, generalized tonic/clonic, myoclonic, atonic, or atypical absence, aggravated by fatigue and fasting with frequency ranges from daily to monthly (in some patients) | rel=r_associated | relid=0 | w=25
  2618. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures, partial, often hemifacial
    n1=méningé (syndrome) | n2=en:seizures, partial, often hemifacial | rel=r_associated | relid=0 | w=25
  2619. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures, particularly absence (in some patients)
    n1=méningé (syndrome) | n2=en:seizures, particularly absence (in some patients) | rel=r_associated | relid=0 | w=25
  2620. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures, severe, intractable
    n1=méningé (syndrome) | n2=en:seizures, severe, intractable | rel=r_associated | relid=0 | w=25
  2621. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:seizures, tonic-clonic (1 patient)
    n1=méningé (syndrome) | n2=en:seizures, tonic-clonic (1 patient) | rel=r_associated | relid=0 | w=25
  2622. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:severe behavioral problems at age 3-4
    n1=méningé (syndrome) | n2=en:severe behavioral problems at age 3-4 | rel=r_associated | relid=0 | w=25
  2623. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:severe speech delay
    n1=méningé (syndrome) | n2=en:severe speech delay | rel=r_associated | relid=0 | w=25
  2624. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:simplified gyration in the frontal cortex (less common)
    n1=méningé (syndrome) | n2=en:simplified gyration in the frontal cortex (less common) | rel=r_associated | relid=0 | w=25
  2625. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:sleep disorder with severe insomnia (in adulthood)
    n1=méningé (syndrome) | n2=en:sleep disorder with severe insomnia (in adulthood) | rel=r_associated | relid=0 | w=25
  2626. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:small cerebellum (especially vermis)
    n1=méningé (syndrome) | n2=en:small cerebellum (especially vermis) | rel=r_associated | relid=0 | w=25
  2627. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spastic cerebral palsy
    n1=méningé (syndrome) | n2=en:spastic cerebral palsy | rel=r_associated | relid=0 | w=25
  2628. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spastic diplegia (in some patients)
    n1=méningé (syndrome) | n2=en:spastic diplegia (in some patients) | rel=r_associated | relid=0 | w=25
  2629. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spasticity (patient a)
    n1=méningé (syndrome) | n2=en:spasticity (patient a) | rel=r_associated | relid=0 | w=25
  2630. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spasticity of facial muscles
    n1=méningé (syndrome) | n2=en:spasticity of facial muscles | rel=r_associated | relid=0 | w=25
  2631. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spasticity, more apparent in the lower limbs
    n1=méningé (syndrome) | n2=en:spasticity, more apparent in the lower limbs | rel=r_associated | relid=0 | w=25
  2632. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:speech abnormalities (palilalia)
    n1=méningé (syndrome) | n2=en:speech abnormalities (palilalia) | rel=r_associated | relid=0 | w=25
  2633. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:speech absent or delayed
    n1=méningé (syndrome) | n2=en:speech absent or delayed | rel=r_associated | relid=0 | w=25
  2634. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:speech and language regression
    n1=méningé (syndrome) | n2=en:speech and language regression | rel=r_associated | relid=0 | w=25
  2635. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:speech delay
    n1=méningé (syndrome) | n2=en:speech delay | rel=r_associated | relid=0 | w=25
  2636. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:speech disorder
    n1=méningé (syndrome) | n2=en:speech disorder | rel=r_associated | relid=0 | w=25
  2637. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spheroids contain neurofilaments
    n1=méningé (syndrome) | n2=en:spheroids contain neurofilaments | rel=r_associated | relid=0 | w=25
  2638. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spinal cord paresis
    n1=méningé (syndrome) | n2=en:spinal cord paresis | rel=r_associated | relid=0 | w=25
  2639. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spinal cord syrinx (in 2 patients)
    n1=méningé (syndrome) | n2=en:spinal cord syrinx (in 2 patients) | rel=r_associated | relid=0 | w=25
  2640. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spinal neuropathy
    n1=méningé (syndrome) | n2=en:spinal neuropathy | rel=r_associated | relid=0 | w=25
  2641. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spinal tract degeneration
    n1=méningé (syndrome) | n2=en:spinal tract degeneration | rel=r_associated | relid=0 | w=25
  2642. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:spongy gliosis
    n1=méningé (syndrome) | n2=en:spongy gliosis | rel=r_associated | relid=0 | w=25
  2643. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:status epilepticus rarely occurs
    n1=méningé (syndrome) | n2=en:status epilepticus rarely occurs | rel=r_associated | relid=0 | w=25
  2644. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:stroke (in some patients)
    n1=méningé (syndrome) | n2=en:stroke (in some patients) | rel=r_associated | relid=0 | w=25
  2645. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:subarachnoid cyst
    n1=méningé (syndrome) | n2=en:subarachnoid cyst | rel=r_associated | relid=0 | w=25
  2646. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:subcortical cysts may occur elsewhere
    n1=méningé (syndrome) | n2=en:subcortical cysts may occur elsewhere | rel=r_associated | relid=0 | w=25
  2647. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:subcortical cysts temporal lobe
    n1=méningé (syndrome) | n2=en:subcortical cysts temporal lobe | rel=r_associated | relid=0 | w=25
  2648. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:subcortical dementia, progressive (6% of patients)
    n1=méningé (syndrome) | n2=en:subcortical dementia, progressive (6% of patients) | rel=r_associated | relid=0 | w=25
  2649. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:subcortical lacunar lesions seen early in disease
    n1=méningé (syndrome) | n2=en:subcortical lacunar lesions seen early in disease | rel=r_associated | relid=0 | w=25
  2650. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:subependymal heterotopic nodules
    n1=méningé (syndrome) | n2=en:subependymal heterotopic nodules | rel=r_associated | relid=0 | w=25
  2651. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:substantia nigra gliosis
    n1=méningé (syndrome) | n2=en:substantia nigra gliosis | rel=r_associated | relid=0 | w=25
  2652. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:sudden arousal from slow-wave sleep with screaming, autonomic, and behavioral manifestations of intense fear (sleep terrors)
    n1=méningé (syndrome) | n2=en:sudden arousal from slow-wave sleep with screaming, autonomic, and behavioral manifestations of intense fear (sleep terrors) | rel=r_associated | relid=0 | w=25
  2653. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:swelling of the deep white matter seen on mri
    n1=méningé (syndrome) | n2=en:swelling of the deep white matter seen on mri | rel=r_associated | relid=0 | w=25
  2654. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:symptoms of hypothalamic disturbances (in some patients)
    n1=méningé (syndrome) | n2=en:symptoms of hypothalamic disturbances (in some patients) | rel=r_associated | relid=0 | w=25
  2655. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:temporal lobe epilepsy (1 patient)
    n1=méningé (syndrome) | n2=en:temporal lobe epilepsy (1 patient) | rel=r_associated | relid=0 | w=25
  2656. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:thin corpus callosum (1 patient)
    n1=méningé (syndrome) | n2=en:thin corpus callosum (1 patient) | rel=r_associated | relid=0 | w=25
  2657. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:thin pituitary stalk
    n1=méningé (syndrome) | n2=en:thin pituitary stalk | rel=r_associated | relid=0 | w=25
  2658. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:tip-toe gait
    n1=méningé (syndrome) | n2=en:tip-toe gait | rel=r_associated | relid=0 | w=25
  2659. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:tonic spasms
    n1=méningé (syndrome) | n2=en:tonic spasms | rel=r_associated | relid=0 | w=25
  2660. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:transient ataxia
    n1=méningé (syndrome) | n2=en:transient ataxia | rel=r_associated | relid=0 | w=25
  2661. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:tremor due to hyperthyroidism
    n1=méningé (syndrome) | n2=en:tremor due to hyperthyroidism | rel=r_associated | relid=0 | w=25
  2662. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:tremor, small-amplitude, high-frequency, restricted to the hands
    n1=méningé (syndrome) | n2=en:tremor, small-amplitude, high-frequency, restricted to the hands | rel=r_associated | relid=0 | w=25
  2663. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:truncal ataxia, severe
    n1=méningé (syndrome) | n2=en:truncal ataxia, severe | rel=r_associated | relid=0 | w=25
  2664. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:tussive syncopes
    n1=méningé (syndrome) | n2=en:tussive syncopes | rel=r_associated | relid=0 | w=25
  2665. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:twitching of the fingers and toes
    n1=méningé (syndrome) | n2=en:twitching of the fingers and toes | rel=r_associated | relid=0 | w=25
  2666. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:type i eeg response is occipital spikes
    n1=méningé (syndrome) | n2=en:type i eeg response is occipital spikes | rel=r_associated | relid=0 | w=25
  2667. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:ubiquitin-positive inclusions
    n1=méningé (syndrome) | n2=en:ubiquitin-positive inclusions | rel=r_associated | relid=0 | w=25
  2668. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:unable to grasp objects
    n1=méningé (syndrome) | n2=en:unable to grasp objects | rel=r_associated | relid=0 | w=25
  2669. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:underdeveloped corpus callosum (3 patients)
    n1=méningé (syndrome) | n2=en:underdeveloped corpus callosum (3 patients) | rel=r_associated | relid=0 | w=25
  2670. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:unusual aura symptoms include alien limb phenomenon, diplopia, apraxia, dysarthria, impaired hearing, vertigo
    n1=méningé (syndrome) | n2=en:unusual aura symptoms include alien limb phenomenon, diplopia, apraxia, dysarthria, impaired hearing, vertigo | rel=r_associated | relid=0 | w=25
  2671. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:upper limb hyperreflexia (some)
    n1=méningé (syndrome) | n2=en:upper limb hyperreflexia (some) | rel=r_associated | relid=0 | w=25
  2672. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:vacuolizing myelinopathy
    n1=méningé (syndrome) | n2=en:vacuolizing myelinopathy | rel=r_associated | relid=0 | w=25
  2673. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:ventriculomegaly (38%)
    n1=méningé (syndrome) | n2=en:ventriculomegaly (38%) | rel=r_associated | relid=0 | w=25
  2674. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:vertigo, episodic (onset in second or third decade)
    n1=méningé (syndrome) | n2=en:vertigo, episodic (onset in second or third decade) | rel=r_associated | relid=0 | w=25
  2675. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:visual symptoms (in 60% of patients)
    n1=méningé (syndrome) | n2=en:visual symptoms (in 60% of patients) | rel=r_associated | relid=0 | w=25
  2676. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:west syndrome
    n1=méningé (syndrome) | n2=en:west syndrome | rel=r_associated | relid=0 | w=25
  2677. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:white mater abnormalities in the posterior periventricular region
    n1=méningé (syndrome) | n2=en:white mater abnormalities in the posterior periventricular region | rel=r_associated | relid=0 | w=25
  2678. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:white matter abnormalities (rare)
    n1=méningé (syndrome) | n2=en:white matter abnormalities (rare) | rel=r_associated | relid=0 | w=25
  2679. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:white matter abnormalities in the periventricular regions (1 patient)
    n1=méningé (syndrome) | n2=en:white matter abnormalities in the periventricular regions (1 patient) | rel=r_associated | relid=0 | w=25
  2680. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:white matter lesions in the supratentorial white matter, brainstem, cerebellum, and spinal cord
    n1=méningé (syndrome) | n2=en:white matter lesions in the supratentorial white matter, brainstem, cerebellum, and spinal cord | rel=r_associated | relid=0 | w=25
  2681. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> en:wide sylvian fissures
    n1=méningé (syndrome) | n2=en:wide sylvian fissures | rel=r_associated | relid=0 | w=25
  2682. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> méningiomatose diffuse
    n1=méningé (syndrome) | n2=méningiomatose diffuse | rel=r_associated | relid=0 | w=25
  2683. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> méningiome angiomateux
    n1=méningé (syndrome) | n2=méningiome angiomateux | rel=r_associated | relid=0 | w=25
  2684. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> neurochirurgie
    n1=méningé (syndrome) | n2=neurochirurgie | rel=r_associated | relid=0 | w=25
  2685. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> pathologie
    n1=méningé (syndrome) | n2=pathologie | rel=r_associated | relid=0 | w=25
  2686. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> système nerveux central
    n1=méningé (syndrome) | n2=système nerveux central | rel=r_associated | relid=0 | w=25
  2687. méningé (syndrome) -- r_associated #0: 25 / 0.301 -> zoologie
    n1=méningé (syndrome) | n2=zoologie | rel=r_associated | relid=0 | w=25
  2688. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:a subset of patients develop frontotemporal dementia
    n1=méningé (syndrome) | n2=en:a subset of patients develop frontotemporal dementia | rel=r_associated | relid=0 | w=24
  2689. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:abnormal behavior
    n1=méningé (syndrome) | n2=en:abnormal behavior | rel=r_associated | relid=0 | w=24
  2690. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:abnormal coordination
    n1=méningé (syndrome) | n2=en:abnormal coordination | rel=r_associated | relid=0 | w=24
  2691. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:abnormal cortical eeg discharges triggered by intermittent light
    n1=méningé (syndrome) | n2=en:abnormal cortical eeg discharges triggered by intermittent light | rel=r_associated | relid=0 | w=24
  2692. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:abnormal lipid peak on brain mrs
    n1=méningé (syndrome) | n2=en:abnormal lipid peak on brain mrs | rel=r_associated | relid=0 | w=24
  2693. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:abnormal sleep-wake cycles
    n1=méningé (syndrome) | n2=en:abnormal sleep-wake cycles | rel=r_associated | relid=0 | w=24
  2694. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:abnormal visual evoked potential (vep)
    n1=méningé (syndrome) | n2=en:abnormal visual evoked potential (vep) | rel=r_associated | relid=0 | w=24
  2695. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:abnormality of the cerebellum
    n1=méningé (syndrome) | n2=en:abnormality of the cerebellum | rel=r_associated | relid=0 | w=24
  2696. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:abnormally marked pontobulbar sulcus
    n1=méningé (syndrome) | n2=en:abnormally marked pontobulbar sulcus | rel=r_associated | relid=0 | w=24
  2697. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:absence of anterior pituitary
    n1=méningé (syndrome) | n2=en:absence of anterior pituitary | rel=r_associated | relid=0 | w=24
  2698. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:absence of primitive reflexes
    n1=méningé (syndrome) | n2=en:absence of primitive reflexes | rel=r_associated | relid=0 | w=24
  2699. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:absence of spontaneous movements
    n1=méningé (syndrome) | n2=en:absence of spontaneous movements | rel=r_associated | relid=0 | w=24
  2700. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:absent superior division of oculomotor nerve and corresponding alpha motor neurons
    n1=méningé (syndrome) | n2=en:absent superior division of oculomotor nerve and corresponding alpha motor neurons | rel=r_associated | relid=0 | w=24
  2701. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:accumulation of autofluorescent material in neurons
    n1=méningé (syndrome) | n2=en:accumulation of autofluorescent material in neurons | rel=r_associated | relid=0 | w=24
  2702. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:accumulation of pas-positive diastase-resistant neuronal inclusion bodies in the cerebral cortex (collins bodies)
    n1=méningé (syndrome) | n2=en:accumulation of pas-positive diastase-resistant neuronal inclusion bodies in the cerebral cortex (collins bodies) | rel=r_associated | relid=0 | w=24
  2703. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:action myoclonus
    n1=méningé (syndrome) | n2=en:action myoclonus | rel=r_associated | relid=0 | w=24
  2704. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:afebrile seizure
    n1=méningé (syndrome) | n2=en:afebrile seizure | rel=r_associated | relid=0 | w=24
  2705. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:alpha-synuclein-immunreactive lewy bodies
    n1=méningé (syndrome) | n2=en:alpha-synuclein-immunreactive lewy bodies | rel=r_associated | relid=0 | w=24
  2706. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:anarthria speech disorder
    n1=méningé (syndrome) | n2=en:anarthria speech disorder | rel=r_associated | relid=0 | w=24
  2707. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:ankle reflex absent
    n1=méningé (syndrome) | n2=en:ankle reflex absent | rel=r_associated | relid=0 | w=24
  2708. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:anomia
    n1=méningé (syndrome) | n2=en:anomia | rel=r_associated | relid=0 | w=24
  2709. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:anosmia (in some patients)
    n1=méningé (syndrome) | n2=en:anosmia (in some patients) | rel=r_associated | relid=0 | w=24
  2710. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:approximately 30% of patients show normal early development
    n1=méningé (syndrome) | n2=en:approximately 30% of patients show normal early development | rel=r_associated | relid=0 | w=24
  2711. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:apraxia (in some patients)
    n1=méningé (syndrome) | n2=en:apraxia (in some patients) | rel=r_associated | relid=0 | w=24
  2712. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:arachnoid cyst (in some patients)
    n1=méningé (syndrome) | n2=en:arachnoid cyst (in some patients) | rel=r_associated | relid=0 | w=24
  2713. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:areflexia of lower limbs
    n1=méningé (syndrome) | n2=en:areflexia of lower limbs | rel=r_associated | relid=0 | w=24
  2714. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:astrocyte
    n1=méningé (syndrome) | n2=en:astrocyte | rel=r_associated | relid=0 | w=24
  2715. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:ataxia with jerky arm movements
    n1=méningé (syndrome) | n2=en:ataxia with jerky arm movements | rel=r_associated | relid=0 | w=24
  2716. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:ataxia, gait and appendicular
    n1=méningé (syndrome) | n2=en:ataxia, gait and appendicular | rel=r_associated | relid=0 | w=24
  2717. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:ataxias, sensory
    n1=méningé (syndrome) | n2=en:ataxias, sensory | rel=r_associated | relid=0 | w=24
  2718. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:athetosis
    n1=méningé (syndrome) | n2=en:athetosis | rel=r_associated | relid=0 | w=24
  2719. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:atrophy of the spinal cord
    n1=méningé (syndrome) | n2=en:atrophy of the spinal cord | rel=r_associated | relid=0 | w=24
  2720. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:autism
    n1=méningé (syndrome) | n2=en:autism | rel=r_associated | relid=0 | w=24
  2721. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:autism (rare)
    n1=méningé (syndrome) | n2=en:autism (rare) | rel=r_associated | relid=0 | w=24
  2722. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:autofluorescent lipopigment in neurons
    n1=méningé (syndrome) | n2=en:autofluorescent lipopigment in neurons | rel=r_associated | relid=0 | w=24
  2723. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:autonomic instability (22%)
    n1=méningé (syndrome) | n2=en:autonomic instability (22%) | rel=r_associated | relid=0 | w=24
  2724. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:autonomic involvement
    n1=méningé (syndrome) | n2=en:autonomic involvement | rel=r_associated | relid=0 | w=24
  2725. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:average intellect
    n1=méningé (syndrome) | n2=en:average intellect | rel=r_associated | relid=0 | w=24
  2726. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:basal ganglia atrophy
    n1=méningé (syndrome) | n2=en:basal ganglia atrophy | rel=r_associated | relid=0 | w=24
  2727. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:basal ganglia atrophy, progressive
    n1=méningé (syndrome) | n2=en:basal ganglia atrophy, progressive | rel=r_associated | relid=0 | w=24
  2728. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:basal ganglia gliosis
    n1=méningé (syndrome) | n2=en:basal ganglia gliosis | rel=r_associated | relid=0 | w=24
  2729. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:basal ganglia lesions may be present before onset of clinical symptoms
    n1=méningé (syndrome) | n2=en:basal ganglia lesions may be present before onset of clinical symptoms | rel=r_associated | relid=0 | w=24
  2730. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:begins in limbs, later generalized (childhood onset)
    n1=méningé (syndrome) | n2=en:begins in limbs, later generalized (childhood onset) | rel=r_associated | relid=0 | w=24
  2731. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:biopsy shows foamy lipid-laden macrophages
    n1=méningé (syndrome) | n2=en:biopsy shows foamy lipid-laden macrophages | rel=r_associated | relid=0 | w=24
  2732. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:brain imaging shows diffuse white matter abnormalities
    n1=méningé (syndrome) | n2=en:brain imaging shows diffuse white matter abnormalities | rel=r_associated | relid=0 | w=24
  2733. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:brain imaging shows white-matter hypodensities and demyelination
    n1=méningé (syndrome) | n2=en:brain imaging shows white-matter hypodensities and demyelination | rel=r_associated | relid=0 | w=24
  2734. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:brain mri shows cerebellar atrophy (1 patient)
    n1=méningé (syndrome) | n2=en:brain mri shows cerebellar atrophy (1 patient) | rel=r_associated | relid=0 | w=24
  2735. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:buccolingofacial dyspraxia
    n1=méningé (syndrome) | n2=en:buccolingofacial dyspraxia | rel=r_associated | relid=0 | w=24
  2736. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:bulbar spasticity
    n1=méningé (syndrome) | n2=en:bulbar spasticity | rel=r_associated | relid=0 | w=24
  2737. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:bulbar weakness
    n1=méningé (syndrome) | n2=en:bulbar weakness | rel=r_associated | relid=0 | w=24
  2738. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:burst suppression pattern on neonatal eeg
    n1=méningé (syndrome) | n2=en:burst suppression pattern on neonatal eeg | rel=r_associated | relid=0 | w=24
  2739. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:by 10-15 years after onset, postural dystonia spreads to all limbs
    n1=méningé (syndrome) | n2=en:by 10-15 years after onset, postural dystonia spreads to all limbs | rel=r_associated | relid=0 | w=24
  2740. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cavitating white matter degeneration
    n1=méningé (syndrome) | n2=en:cavitating white matter degeneration | rel=r_associated | relid=0 | w=24
  2741. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:central facial palsy (in some patients)
    n1=méningé (syndrome) | n2=en:central facial palsy (in some patients) | rel=r_associated | relid=0 | w=24
  2742. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:central nervous system involvement in approximately 50% of patients
    n1=méningé (syndrome) | n2=en:central nervous system involvement in approximately 50% of patients | rel=r_associated | relid=0 | w=24
  2743. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar and brainstem atrophy, mild (1 patient)
    n1=méningé (syndrome) | n2=en:cerebellar and brainstem atrophy, mild (1 patient) | rel=r_associated | relid=0 | w=24
  2744. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar ataxia (seen in hhs variant)
    n1=méningé (syndrome) | n2=en:cerebellar ataxia (seen in hhs variant) | rel=r_associated | relid=0 | w=24
  2745. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar atrophy
    n1=méningé (syndrome) | n2=en:cerebellar atrophy | rel=r_associated | relid=0 | w=24
  2746. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar atrophy, mild (in 1 of 3 families)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, mild (in 1 of 3 families) | rel=r_associated | relid=0 | w=24
  2747. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy) | rel=r_associated | relid=0 | w=24
  2748. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar cortical degeneration
    n1=méningé (syndrome) | n2=en:cerebellar cortical degeneration | rel=r_associated | relid=0 | w=24
  2749. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar cyst (rare)
    n1=méningé (syndrome) | n2=en:cerebellar cyst (rare) | rel=r_associated | relid=0 | w=24
  2750. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar hypoplasia (in some)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (in some) | rel=r_associated | relid=0 | w=24
  2751. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar hypoplasia (variable)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (variable) | rel=r_associated | relid=0 | w=24
  2752. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar hypoplasia, mild asymmetric (rare)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia, mild asymmetric (rare) | rel=r_associated | relid=0 | w=24
  2753. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar hypoplasia, particularly of the hemispheres
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia, particularly of the hemispheres | rel=r_associated | relid=0 | w=24
  2754. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar hypoplasia, severe (wws)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia, severe (wws) | rel=r_associated | relid=0 | w=24
  2755. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar signs (more common in variant cjd)
    n1=méningé (syndrome) | n2=en:cerebellar signs (more common in variant cjd) | rel=r_associated | relid=0 | w=24
  2756. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellar vermis hypoplasia (in 1 patient)
    n1=méningé (syndrome) | n2=en:cerebellar vermis hypoplasia (in 1 patient) | rel=r_associated | relid=0 | w=24
  2757. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebellopontine angle meningioma
    n1=méningé (syndrome) | n2=en:cerebellopontine angle meningioma | rel=r_associated | relid=0 | w=24
  2758. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebral arterial hemorrhage
    n1=méningé (syndrome) | n2=en:cerebral arterial hemorrhage | rel=r_associated | relid=0 | w=24
  2759. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebral cyst
    n1=méningé (syndrome) | n2=en:cerebral cyst | rel=r_associated | relid=0 | w=24
  2760. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cerebrovascular ischemia
    n1=méningé (syndrome) | n2=en:cerebrovascular ischemia | rel=r_associated | relid=0 | w=24
  2761. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cervical cord compression
    n1=méningé (syndrome) | n2=en:cervical cord compression | rel=r_associated | relid=0 | w=24
  2762. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:chorea, prominent (in some patients)
    n1=méningé (syndrome) | n2=en:chorea, prominent (in some patients) | rel=r_associated | relid=0 | w=24
  2763. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:choreoathetosis (described in 1 patient)
    n1=méningé (syndrome) | n2=en:choreoathetosis (described in 1 patient) | rel=r_associated | relid=0 | w=24
  2764. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:choreoathetosis (in 79%), more frequent at disease onset
    n1=méningé (syndrome) | n2=en:choreoathetosis (in 79%), more frequent at disease onset | rel=r_associated | relid=0 | w=24
  2765. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:choreodystonia of the upper limbs
    n1=méningé (syndrome) | n2=en:choreodystonia of the upper limbs | rel=r_associated | relid=0 | w=24
  2766. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:choroid plexus calcification
    n1=méningé (syndrome) | n2=en:choroid plexus calcification | rel=r_associated | relid=0 | w=24
  2767. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:choroid plexus papilloma (in some patients)
    n1=méningé (syndrome) | n2=en:choroid plexus papilloma (in some patients) | rel=r_associated | relid=0 | w=24
  2768. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:clonic convulsion
    n1=méningé (syndrome) | n2=en:clonic convulsion | rel=r_associated | relid=0 | w=24
  2769. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:clonus may occur
    n1=méningé (syndrome) | n2=en:clonus may occur | rel=r_associated | relid=0 | w=24
  2770. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cns venous malformations
    n1=méningé (syndrome) | n2=en:cns venous malformations | rel=r_associated | relid=0 | w=24
  2771. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cognitive defects (rare)
    n1=méningé (syndrome) | n2=en:cognitive defects (rare) | rel=r_associated | relid=0 | w=24
  2772. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cognitive regression
    n1=méningé (syndrome) | n2=en:cognitive regression | rel=r_associated | relid=0 | w=24
  2773. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cogwheel rigidity (in some patients)
    n1=méningé (syndrome) | n2=en:cogwheel rigidity (in some patients) | rel=r_associated | relid=0 | w=24
  2774. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:complete or partial absence of the corpus callosum
    n1=méningé (syndrome) | n2=en:complete or partial absence of the corpus callosum | rel=r_associated | relid=0 | w=24
  2775. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:constructional apraxia (in a subset of patients)
    n1=méningé (syndrome) | n2=en:constructional apraxia (in a subset of patients) | rel=r_associated | relid=0 | w=24
  2776. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cortical and brainstem neuronal loss
    n1=méningé (syndrome) | n2=en:cortical and brainstem neuronal loss | rel=r_associated | relid=0 | w=24
  2777. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cortical atrophy (in 2 siblings)
    n1=méningé (syndrome) | n2=en:cortical atrophy (in 2 siblings) | rel=r_associated | relid=0 | w=24
  2778. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cortical atrophy (in some patients)
    n1=méningé (syndrome) | n2=en:cortical atrophy (in some patients) | rel=r_associated | relid=0 | w=24
  2779. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cortical dysgenesis
    n1=méningé (syndrome) | n2=en:cortical dysgenesis | rel=r_associated | relid=0 | w=24
  2780. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:cortical thinning
    n1=méningé (syndrome) | n2=en:cortical thinning | rel=r_associated | relid=0 | w=24
  2781. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dandy walker variant
    n1=méningé (syndrome) | n2=en:dandy walker variant | rel=r_associated | relid=0 | w=24
  2782. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:decreased cerebral volume, especially of the frontal lobes
    n1=méningé (syndrome) | n2=en:decreased cerebral volume, especially of the frontal lobes | rel=r_associated | relid=0 | w=24
  2783. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:decreased mental processing speed
    n1=méningé (syndrome) | n2=en:decreased mental processing speed | rel=r_associated | relid=0 | w=24
  2784. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:decreased n-acetylaspartate
    n1=méningé (syndrome) | n2=en:decreased n-acetylaspartate | rel=r_associated | relid=0 | w=24
  2785. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:decreased supratentorial volume
    n1=méningé (syndrome) | n2=en:decreased supratentorial volume | rel=r_associated | relid=0 | w=24
  2786. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:decreased tendon reflex
    n1=méningé (syndrome) | n2=en:decreased tendon reflex | rel=r_associated | relid=0 | w=24
  2787. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:deep white matter changes
    n1=méningé (syndrome) | n2=en:deep white matter changes | rel=r_associated | relid=0 | w=24
  2788. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:deep white matter lesions, particularly affecting the frontal and parietal lobes
    n1=méningé (syndrome) | n2=en:deep white matter lesions, particularly affecting the frontal and parietal lobes | rel=r_associated | relid=0 | w=24
  2789. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:defect in morphosyntactic rules
    n1=méningé (syndrome) | n2=en:defect in morphosyntactic rules | rel=r_associated | relid=0 | w=24
  2790. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:delayed cognitive development (in some patients)
    n1=méningé (syndrome) | n2=en:delayed cognitive development (in some patients) | rel=r_associated | relid=0 | w=24
  2791. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:delayed development may occur
    n1=méningé (syndrome) | n2=en:delayed development may occur | rel=r_associated | relid=0 | w=24
  2792. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:delayed motor development, mild, transient
    n1=méningé (syndrome) | n2=en:delayed motor development, mild, transient | rel=r_associated | relid=0 | w=24
  2793. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:delayed myelination (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:delayed myelination (reported in 1 patient) | rel=r_associated | relid=0 | w=24
  2794. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:delayed myelination, mild
    n1=méningé (syndrome) | n2=en:delayed myelination, mild | rel=r_associated | relid=0 | w=24
  2795. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:delayed psychomotor development (in severe cases)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development (in severe cases) | rel=r_associated | relid=0 | w=24
  2796. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:delayed psychomotor development, mild (in some patients)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, mild (in some patients) | rel=r_associated | relid=0 | w=24
  2797. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:delayed walking (rare)
    n1=méningé (syndrome) | n2=en:delayed walking (rare) | rel=r_associated | relid=0 | w=24
  2798. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:delayed walking and running in early childhood
    n1=méningé (syndrome) | n2=en:delayed walking and running in early childhood | rel=r_associated | relid=0 | w=24
  2799. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dementia (1 family)
    n1=méningé (syndrome) | n2=en:dementia (1 family) | rel=r_associated | relid=0 | w=24
  2800. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dementia, rapidly progressive
    n1=méningé (syndrome) | n2=en:dementia, rapidly progressive | rel=r_associated | relid=0 | w=24
  2801. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:developmental delay (female)
    n1=méningé (syndrome) | n2=en:developmental delay (female) | rel=r_associated | relid=0 | w=24
  2802. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:developmental delay (homozygote)
    n1=méningé (syndrome) | n2=en:developmental delay (homozygote) | rel=r_associated | relid=0 | w=24
  2803. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:developmental delay (in some patients who survive infancy)
    n1=méningé (syndrome) | n2=en:developmental delay (in some patients who survive infancy) | rel=r_associated | relid=0 | w=24
  2804. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:developmental delay (in some patients)
    n1=méningé (syndrome) | n2=en:developmental delay (in some patients) | rel=r_associated | relid=0 | w=24
  2805. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:developmental delay (in some)
    n1=méningé (syndrome) | n2=en:developmental delay (in some) | rel=r_associated | relid=0 | w=24
  2806. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:developmental delay, variable severity
    n1=méningé (syndrome) | n2=en:developmental delay, variable severity | rel=r_associated | relid=0 | w=24
  2807. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:developmental regression, after age 2 years (some)
    n1=méningé (syndrome) | n2=en:developmental regression, after age 2 years (some) | rel=r_associated | relid=0 | w=24
  2808. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:developmental retardation, severe
    n1=méningé (syndrome) | n2=en:developmental retardation, severe | rel=r_associated | relid=0 | w=24
  2809. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:diffuse brain swelling occurs during coma
    n1=méningé (syndrome) | n2=en:diffuse brain swelling occurs during coma | rel=r_associated | relid=0 | w=24
  2810. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dilation of cerebral ventricles
    n1=méningé (syndrome) | n2=en:dilation of cerebral ventricles | rel=r_associated | relid=0 | w=24
  2811. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:diplegia
    n1=méningé (syndrome) | n2=en:diplegia | rel=r_associated | relid=0 | w=24
  2812. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:disorganization of the anterior cerebellar vermis
    n1=méningé (syndrome) | n2=en:disorganization of the anterior cerebellar vermis | rel=r_associated | relid=0 | w=24
  2813. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:disorganized cortical architecture
    n1=méningé (syndrome) | n2=en:disorganized cortical architecture | rel=r_associated | relid=0 | w=24
  2814. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:distal sensory loss to all modalities, lower limbs more affected than upper limbs
    n1=méningé (syndrome) | n2=en:distal sensory loss to all modalities, lower limbs more affected than upper limbs | rel=r_associated | relid=0 | w=24
  2815. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dopamine-responsive parkinsonism
    n1=méningé (syndrome) | n2=en:dopamine-responsive parkinsonism | rel=r_associated | relid=0 | w=24
  2816. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dyskinesia, limb, exertion-induced
    n1=méningé (syndrome) | n2=en:dyskinesia, limb, exertion-induced | rel=r_associated | relid=0 | w=24
  2817. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dyslexia
    n1=méningé (syndrome) | n2=en:dyslexia | rel=r_associated | relid=0 | w=24
  2818. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dysmetrias, cerebellar
    n1=méningé (syndrome) | n2=en:dysmetrias, cerebellar | rel=r_associated | relid=0 | w=24
  2819. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dysmorphic corpus callosum
    n1=méningé (syndrome) | n2=en:dysmorphic corpus callosum | rel=r_associated | relid=0 | w=24
  2820. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dystonia may become generalized
    n1=méningé (syndrome) | n2=en:dystonia may become generalized | rel=r_associated | relid=0 | w=24
  2821. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dystonic hand posturing (44% of patients)
    n1=méningé (syndrome) | n2=en:dystonic hand posturing (44% of patients) | rel=r_associated | relid=0 | w=24
  2822. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:dystonic tremor
    n1=méningé (syndrome) | n2=en:dystonic tremor | rel=r_associated | relid=0 | w=24
  2823. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:eeg - alpha slowing, 4-6 hz spike waves, myoclonus on photic stimulation (stage 2)
    n1=méningé (syndrome) | n2=en:eeg - alpha slowing, 4-6 hz spike waves, myoclonus on photic stimulation (stage 2) | rel=r_associated | relid=0 | w=24
  2824. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:eeg abnormalities in 20-50%
    n1=méningé (syndrome) | n2=en:eeg abnormalities in 20-50% | rel=r_associated | relid=0 | w=24
  2825. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:eeg and symptomatology suggest mesial temporal origin
    n1=méningé (syndrome) | n2=en:eeg and symptomatology suggest mesial temporal origin | rel=r_associated | relid=0 | w=24
  2826. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:eeg is usually normal
    n1=méningé (syndrome) | n2=en:eeg is usually normal | rel=r_associated | relid=0 | w=24
  2827. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:eeg shows frontal lobe origin
    n1=méningé (syndrome) | n2=en:eeg shows frontal lobe origin | rel=r_associated | relid=0 | w=24
  2828. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:eeg shows hypsarrhythmia
    n1=méningé (syndrome) | n2=en:eeg shows hypsarrhythmia | rel=r_associated | relid=0 | w=24
  2829. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:eeg shows photosensitivity
    n1=méningé (syndrome) | n2=en:eeg shows photosensitivity | rel=r_associated | relid=0 | w=24
  2830. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:electroencephalogram (eeg) abnormalities
    n1=méningé (syndrome) | n2=en:electroencephalogram (eeg) abnormalities | rel=r_associated | relid=0 | w=24
  2831. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:emg shows neurogenic findings
    n1=méningé (syndrome) | n2=en:emg shows neurogenic findings | rel=r_associated | relid=0 | w=24
  2832. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:empty sella syndrome
    n1=méningé (syndrome) | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=24
  2833. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:encephalopathic attacks, episodic, associated with infection
    n1=méningé (syndrome) | n2=en:encephalopathic attacks, episodic, associated with infection | rel=r_associated | relid=0 | w=24
  2834. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:encephalopathy, episodic
    n1=méningé (syndrome) | n2=en:encephalopathy, episodic | rel=r_associated | relid=0 | w=24
  2835. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:enlarged cisterna magna (in some patients)
    n1=méningé (syndrome) | n2=en:enlarged cisterna magna (in some patients) | rel=r_associated | relid=0 | w=24
  2836. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:enlarged ventricles (in some)
    n1=méningé (syndrome) | n2=en:enlarged ventricles (in some) | rel=r_associated | relid=0 | w=24
  2837. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:epileptic encephalopathy (in 2 of 3 patients)
    n1=méningé (syndrome) | n2=en:epileptic encephalopathy (in 2 of 3 patients) | rel=r_associated | relid=0 | w=24
  2838. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:episodes of weakness can last 1 day to several weeks and can occur 1-3 times per month
    n1=méningé (syndrome) | n2=en:episodes of weakness can last 1 day to several weeks and can occur 1-3 times per month | rel=r_associated | relid=0 | w=24
  2839. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:essential tremor (1 family)
    n1=méningé (syndrome) | n2=en:essential tremor (1 family) | rel=r_associated | relid=0 | w=24
  2840. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:extensor plantar responses (1 patient)
    n1=méningé (syndrome) | n2=en:extensor plantar responses (1 patient) | rel=r_associated | relid=0 | w=24
  2841. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:extensor plantar responses (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:extensor plantar responses (reported in 1 patient) | rel=r_associated | relid=0 | w=24
  2842. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:extrapyramidal signs, mild
    n1=méningé (syndrome) | n2=en:extrapyramidal signs, mild | rel=r_associated | relid=0 | w=24
  2843. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:facial muscle weakness of muscles innervated by cn vii
    n1=méningé (syndrome) | n2=en:facial muscle weakness of muscles innervated by cn vii | rel=r_associated | relid=0 | w=24
  2844. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:failure to achieve sitting or walking (severe form)
    n1=méningé (syndrome) | n2=en:failure to achieve sitting or walking (severe form) | rel=r_associated | relid=0 | w=24
  2845. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:fearful expression
    n1=méningé (syndrome) | n2=en:fearful expression | rel=r_associated | relid=0 | w=24
  2846. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:febrile seizures in infancy
    n1=méningé (syndrome) | n2=en:febrile seizures in infancy | rel=r_associated | relid=0 | w=24
  2847. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:fetal akinesia deformation sequence
    n1=méningé (syndrome) | n2=en:fetal akinesia deformation sequence | rel=r_associated | relid=0 | w=24
  2848. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:fibrous astrocyte
    n1=méningé (syndrome) | n2=en:fibrous astrocyte | rel=r_associated | relid=0 | w=24
  2849. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:fibrous meningioma
    n1=méningé (syndrome) | n2=en:fibrous meningioma | rel=r_associated | relid=0 | w=24
  2850. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:finger twitching
    n1=méningé (syndrome) | n2=en:finger twitching | rel=r_associated | relid=0 | w=24
  2851. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:focal clonic seizure
    n1=méningé (syndrome) | n2=en:focal clonic seizure | rel=r_associated | relid=0 | w=24
  2852. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:focal interhemispheric fusion
    n1=méningé (syndrome) | n2=en:focal interhemispheric fusion | rel=r_associated | relid=0 | w=24
  2853. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:focal microgyria
    n1=méningé (syndrome) | n2=en:focal microgyria | rel=r_associated | relid=0 | w=24
  2854. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:focal neurologic deficit
    n1=méningé (syndrome) | n2=en:focal neurologic deficit | rel=r_associated | relid=0 | w=24
  2855. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:frequency of 1 to 20 episodes per day
    n1=méningé (syndrome) | n2=en:frequency of 1 to 20 episodes per day | rel=r_associated | relid=0 | w=24
  2856. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:frontal lobe hypoplasia
    n1=méningé (syndrome) | n2=en:frontal lobe hypoplasia | rel=r_associated | relid=0 | w=24
  2857. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:frontotemporal dementia, variable severity
    n1=méningé (syndrome) | n2=en:frontotemporal dementia, variable severity | rel=r_associated | relid=0 | w=24
  2858. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:fusion of the left and right thalami
    n1=méningé (syndrome) | n2=en:fusion of the left and right thalami | rel=r_associated | relid=0 | w=24
  2859. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:gait abnormalities due to muscle weakness
    n1=méningé (syndrome) | n2=en:gait abnormalities due to muscle weakness | rel=r_associated | relid=0 | w=24
  2860. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:gait difficulties due to contractures of the lower limbs
    n1=méningé (syndrome) | n2=en:gait difficulties due to contractures of the lower limbs | rel=r_associated | relid=0 | w=24
  2861. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:glial inclusions
    n1=méningé (syndrome) | n2=en:glial inclusions | rel=r_associated | relid=0 | w=24
  2862. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:globular thalamus (1 patient)
    n1=méningé (syndrome) | n2=en:globular thalamus (1 patient) | rel=r_associated | relid=0 | w=24
  2863. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:granular osmiophilic cytoplasmic deposits in schwann cells
    n1=méningé (syndrome) | n2=en:granular osmiophilic cytoplasmic deposits in schwann cells | rel=r_associated | relid=0 | w=24
  2864. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:granulovacuolar degeneration
    n1=méningé (syndrome) | n2=en:granulovacuolar degeneration | rel=r_associated | relid=0 | w=24
  2865. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:gray matter
    n1=méningé (syndrome) | n2=en:gray matter | rel=r_associated | relid=0 | w=24
  2866. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:gross motor delay, mild
    n1=méningé (syndrome) | n2=en:gross motor delay, mild | rel=r_associated | relid=0 | w=24
  2867. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hand muscle atrophy
    n1=méningé (syndrome) | n2=en:hand muscle atrophy | rel=r_associated | relid=0 | w=24
  2868. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hemisensory attacks
    n1=méningé (syndrome) | n2=en:hemisensory attacks | rel=r_associated | relid=0 | w=24
  2869. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hereditary meningioma
    n1=méningé (syndrome) | n2=en:hereditary meningioma | rel=r_associated | relid=0 | w=24
  2870. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:herniation of the cerebellar tonsils through the foramen magnum 5 mm or greater
    n1=méningé (syndrome) | n2=en:herniation of the cerebellar tonsils through the foramen magnum 5 mm or greater | rel=r_associated | relid=0 | w=24
  2871. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:heterotopic neurons in the white matter (36%)
    n1=méningé (syndrome) | n2=en:heterotopic neurons in the white matter (36%) | rel=r_associated | relid=0 | w=24
  2872. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hiccough
    n1=méningé (syndrome) | n2=en:hiccough | rel=r_associated | relid=0 | w=24
  2873. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:high-stepping gait
    n1=méningé (syndrome) | n2=en:high-stepping gait | rel=r_associated | relid=0 | w=24
  2874. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hydrocephalus (in 1 patient)
    n1=méningé (syndrome) | n2=en:hydrocephalus (in 1 patient) | rel=r_associated | relid=0 | w=24
  2875. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hydrocephalus (less common)
    n1=méningé (syndrome) | n2=en:hydrocephalus (less common) | rel=r_associated | relid=0 | w=24
  2876. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hydrocephalus (variable)
    n1=méningé (syndrome) | n2=en:hydrocephalus (variable) | rel=r_associated | relid=0 | w=24
  2877. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hyperactive startle reflex
    n1=méningé (syndrome) | n2=en:hyperactive startle reflex | rel=r_associated | relid=0 | w=24
  2878. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hyperreflexia (later)
    n1=méningé (syndrome) | n2=en:hyperreflexia (later) | rel=r_associated | relid=0 | w=24
  2879. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hyperreflexia in the lower limbs (in some patients)
    n1=méningé (syndrome) | n2=en:hyperreflexia in the lower limbs (in some patients) | rel=r_associated | relid=0 | w=24
  2880. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hyperreflexia, especially of the lower limbs
    n1=méningé (syndrome) | n2=en:hyperreflexia, especially of the lower limbs | rel=r_associated | relid=0 | w=24
  2881. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypocalcemic seizures
    n1=méningé (syndrome) | n2=en:hypocalcemic seizures | rel=r_associated | relid=0 | w=24
  2882. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypoplastic cerebrum
    n1=méningé (syndrome) | n2=en:hypoplastic cerebrum | rel=r_associated | relid=0 | w=24
  2883. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypoplastic or absent optic chiasm
    n1=méningé (syndrome) | n2=en:hypoplastic or absent optic chiasm | rel=r_associated | relid=0 | w=24
  2884. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hyposmia/anosmia
    n1=méningé (syndrome) | n2=en:hyposmia/anosmia | rel=r_associated | relid=0 | w=24
  2885. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypotonia (93%)
    n1=méningé (syndrome) | n2=en:hypotonia (93%) | rel=r_associated | relid=0 | w=24
  2886. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypotonia (early infancy)
    n1=méningé (syndrome) | n2=en:hypotonia (early infancy) | rel=r_associated | relid=0 | w=24
  2887. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypotonia, global, severe
    n1=méningé (syndrome) | n2=en:hypotonia, global, severe | rel=r_associated | relid=0 | w=24
  2888. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypotonia, neonatal (> 90%)
    n1=méningé (syndrome) | n2=en:hypotonia, neonatal (> 90%) | rel=r_associated | relid=0 | w=24
  2889. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypoxic convulsions
    n1=méningé (syndrome) | n2=en:hypoxic convulsions | rel=r_associated | relid=0 | w=24
  2890. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypperreflexia
    n1=méningé (syndrome) | n2=en:hypperreflexia | rel=r_associated | relid=0 | w=24
  2891. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:hypsarrhythmia (1 patient)
    n1=méningé (syndrome) | n2=en:hypsarrhythmia (1 patient) | rel=r_associated | relid=0 | w=24
  2892. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:impaired language development
    n1=méningé (syndrome) | n2=en:impaired language development | rel=r_associated | relid=0 | w=24
  2893. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:impaired psychomotor development
    n1=méningé (syndrome) | n2=en:impaired psychomotor development | rel=r_associated | relid=0 | w=24
  2894. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:incomplete myelination
    n1=méningé (syndrome) | n2=en:incomplete myelination | rel=r_associated | relid=0 | w=24
  2895. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:increased muscle tone in the lower limbs
    n1=méningé (syndrome) | n2=en:increased muscle tone in the lower limbs | rel=r_associated | relid=0 | w=24
  2896. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:increased risk of seizures in childhood or adulthood (11-16%)
    n1=méningé (syndrome) | n2=en:increased risk of seizures in childhood or adulthood (11-16%) | rel=r_associated | relid=0 | w=24
  2897. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:individuals require less sleep in a 24-hour period compared to age-matched controls
    n1=méningé (syndrome) | n2=en:individuals require less sleep in a 24-hour period compared to age-matched controls | rel=r_associated | relid=0 | w=24
  2898. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:insomnia
    n1=méningé (syndrome) | n2=en:insomnia | rel=r_associated | relid=0 | w=24
  2899. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:intellectual disability, mild to severe
    n1=méningé (syndrome) | n2=en:intellectual disability, mild to severe | rel=r_associated | relid=0 | w=24
  2900. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:interictal dystonia may occur later in disease course
    n1=méningé (syndrome) | n2=en:interictal dystonia may occur later in disease course | rel=r_associated | relid=0 | w=24
  2901. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:interictal periods of normal health
    n1=méningé (syndrome) | n2=en:interictal periods of normal health | rel=r_associated | relid=0 | w=24
  2902. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:intraspinal neoplasm
    n1=méningé (syndrome) | n2=en:intraspinal neoplasm | rel=r_associated | relid=0 | w=24
  2903. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:ipsilateral brain hypoplasia
    n1=méningé (syndrome) | n2=en:ipsilateral brain hypoplasia | rel=r_associated | relid=0 | w=24
  2904. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:iron deposition in the basal ganglia (in some patients)
    n1=méningé (syndrome) | n2=en:iron deposition in the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=24
  2905. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:isolated focal dystonia may occur
    n1=méningé (syndrome) | n2=en:isolated focal dystonia may occur | rel=r_associated | relid=0 | w=24
  2906. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:joubert syndrome
    n1=méningé (syndrome) | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=24
  2907. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:lack of peer relationships
    n1=méningé (syndrome) | n2=en:lack of peer relationships | rel=r_associated | relid=0 | w=24
  2908. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:lack of psychomotor development (severe connatal form)
    n1=méningé (syndrome) | n2=en:lack of psychomotor development (severe connatal form) | rel=r_associated | relid=0 | w=24
  2909. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:lack of skein-like inclusions
    n1=méningé (syndrome) | n2=en:lack of skein-like inclusions | rel=r_associated | relid=0 | w=24
  2910. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:lacunar infarcts develop after age 40 years
    n1=méningé (syndrome) | n2=en:lacunar infarcts develop after age 40 years | rel=r_associated | relid=0 | w=24
  2911. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:late diaphragmatic involvement
    n1=méningé (syndrome) | n2=en:late diaphragmatic involvement | rel=r_associated | relid=0 | w=24
  2912. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:lesions in the basal ganglia
    n1=méningé (syndrome) | n2=en:lesions in the basal ganglia | rel=r_associated | relid=0 | w=24
  2913. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:leukodystrophy and white matter changes, which improve with age
    n1=méningé (syndrome) | n2=en:leukodystrophy and white matter changes, which improve with age | rel=r_associated | relid=0 | w=24
  2914. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:leukomalacia (rare)
    n1=méningé (syndrome) | n2=en:leukomalacia (rare) | rel=r_associated | relid=0 | w=24
  2915. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:lewy bodies
    n1=méningé (syndrome) | n2=en:lewy bodies | rel=r_associated | relid=0 | w=24
  2916. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:limb ataxia, progressive
    n1=méningé (syndrome) | n2=en:limb ataxia, progressive | rel=r_associated | relid=0 | w=24
  2917. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:limb dystonia (18%)
    n1=méningé (syndrome) | n2=en:limb dystonia (18%) | rel=r_associated | relid=0 | w=24
  2918. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:limb fasciculations
    n1=méningé (syndrome) | n2=en:limb fasciculations | rel=r_associated | relid=0 | w=24
  2919. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:limb muscle stiffness is often asymmetric
    n1=méningé (syndrome) | n2=en:limb muscle stiffness is often asymmetric | rel=r_associated | relid=0 | w=24
  2920. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:long, thickened cerebellar peduncles
    n1=méningé (syndrome) | n2=en:long, thickened cerebellar peduncles | rel=r_associated | relid=0 | w=24
  2921. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:loss of consciousness
    n1=méningé (syndrome) | n2=en:loss of consciousness | rel=r_associated | relid=0 | w=24
  2922. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:loss of deep tendon reflexes (later)
    n1=méningé (syndrome) | n2=en:loss of deep tendon reflexes (later) | rel=r_associated | relid=0 | w=24
  2923. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:loss of speech
    n1=méningé (syndrome) | n2=en:loss of speech | rel=r_associated | relid=0 | w=24
  2924. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:loss of speech development
    n1=méningé (syndrome) | n2=en:loss of speech development | rel=r_associated | relid=0 | w=24
  2925. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:low density white matter on ct scan
    n1=méningé (syndrome) | n2=en:low density white matter on ct scan | rel=r_associated | relid=0 | w=24
  2926. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:lower limb dystonia
    n1=méningé (syndrome) | n2=en:lower limb dystonia | rel=r_associated | relid=0 | w=24
  2927. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:lower motor neuron dysfunction
    n1=méningé (syndrome) | n2=en:lower motor neuron dysfunction | rel=r_associated | relid=0 | w=24
  2928. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:magnetic resonance spectroscopy (mrs) shows increased lactate in the central nervous system
    n1=méningé (syndrome) | n2=en:magnetic resonance spectroscopy (mrs) shows increased lactate in the central nervous system | rel=r_associated | relid=0 | w=24
  2929. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:major developmental delay
    n1=méningé (syndrome) | n2=en:major developmental delay | rel=r_associated | relid=0 | w=24
  2930. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:meningeal solitary fibrous tumor/hemangiopericytoma
    n1=méningé (syndrome) | n2=en:meningeal solitary fibrous tumor/hemangiopericytoma | rel=r_associated | relid=0 | w=24
  2931. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental deterioration in a subset of patients
    n1=méningé (syndrome) | n2=en:mental deterioration in a subset of patients | rel=r_associated | relid=0 | w=24
  2932. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation (1 family)
    n1=méningé (syndrome) | n2=en:mental retardation (1 family) | rel=r_associated | relid=0 | w=24
  2933. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation (31%)
    n1=méningé (syndrome) | n2=en:mental retardation (31%) | rel=r_associated | relid=0 | w=24
  2934. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation (7%)
    n1=méningé (syndrome) | n2=en:mental retardation (7%) | rel=r_associated | relid=0 | w=24
  2935. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation (early-onset form)
    n1=méningé (syndrome) | n2=en:mental retardation (early-onset form) | rel=r_associated | relid=0 | w=24
  2936. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation (in a subset of patients)
    n1=méningé (syndrome) | n2=en:mental retardation (in a subset of patients) | rel=r_associated | relid=0 | w=24
  2937. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation (iq 20-78)
    n1=méningé (syndrome) | n2=en:mental retardation (iq 20-78) | rel=r_associated | relid=0 | w=24
  2938. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation (one patient)
    n1=méningé (syndrome) | n2=en:mental retardation (one patient) | rel=r_associated | relid=0 | w=24
  2939. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, mild (2 families)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (2 families) | rel=r_associated | relid=0 | w=24
  2940. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, mild (iq range from 50 to 70)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (iq range from 50 to 70) | rel=r_associated | relid=0 | w=24
  2941. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, mild to severe
    n1=méningé (syndrome) | n2=en:mental retardation, mild to severe | rel=r_associated | relid=0 | w=24
  2942. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, mild-moderate (some)
    n1=méningé (syndrome) | n2=en:mental retardation, mild-moderate (some) | rel=r_associated | relid=0 | w=24
  2943. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, mild, in most carrier females
    n1=méningé (syndrome) | n2=en:mental retardation, mild, in most carrier females | rel=r_associated | relid=0 | w=24
  2944. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, moderate to severe (10-15% of patients)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate to severe (10-15% of patients) | rel=r_associated | relid=0 | w=24
  2945. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, profound (wws)
    n1=méningé (syndrome) | n2=en:mental retardation, profound (wws) | rel=r_associated | relid=0 | w=24
  2946. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, severe (meb)
    n1=méningé (syndrome) | n2=en:mental retardation, severe (meb) | rel=r_associated | relid=0 | w=24
  2947. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, severe to profound
    n1=méningé (syndrome) | n2=en:mental retardation, severe to profound | rel=r_associated | relid=0 | w=24
  2948. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mental retardation, variable severity
    n1=méningé (syndrome) | n2=en:mental retardation, variable severity | rel=r_associated | relid=0 | w=24
  2949. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:metabolic aspects
    n1=méningé (syndrome) | n2=en:metabolic aspects | rel=r_associated | relid=0 | w=24
  2950. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:midline forebrain defects
    n1=méningé (syndrome) | n2=en:midline forebrain defects | rel=r_associated | relid=0 | w=24
  2951. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:migraine (40% of patients)
    n1=méningé (syndrome) | n2=en:migraine (40% of patients) | rel=r_associated | relid=0 | w=24
  2952. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:migrating discharges from one cortical region to another seen on eeg (in some patients)
    n1=méningé (syndrome) | n2=en:migrating discharges from one cortical region to another seen on eeg (in some patients) | rel=r_associated | relid=0 | w=24
  2953. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mild cognitive decline (1 patient)
    n1=méningé (syndrome) | n2=en:mild cognitive decline (1 patient) | rel=r_associated | relid=0 | w=24
  2954. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mild loss of neurons in the cerebellum
    n1=méningé (syndrome) | n2=en:mild loss of neurons in the cerebellum | rel=r_associated | relid=0 | w=24
  2955. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mild mental deterioration
    n1=méningé (syndrome) | n2=en:mild mental deterioration | rel=r_associated | relid=0 | w=24
  2956. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mirror movements disorder
    n1=méningé (syndrome) | n2=en:mirror movements disorder | rel=r_associated | relid=0 | w=24
  2957. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mixed cerebellar/pseudobulbar dysarthria
    n1=méningé (syndrome) | n2=en:mixed cerebellar/pseudobulbar dysarthria | rel=r_associated | relid=0 | w=24
  2958. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:moderate mental retardation (i.q. 35-49)
    n1=méningé (syndrome) | n2=en:moderate mental retardation (i.q. 35-49) | rel=r_associated | relid=0 | w=24
  2959. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:moderately thickened cortex
    n1=méningé (syndrome) | n2=en:moderately thickened cortex | rel=r_associated | relid=0 | w=24
  2960. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:monopareses
    n1=méningé (syndrome) | n2=en:monopareses | rel=r_associated | relid=0 | w=24
  2961. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:morning myoclonic jerks
    n1=méningé (syndrome) | n2=en:morning myoclonic jerks | rel=r_associated | relid=0 | w=24
  2962. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:motor stereotypy
    n1=méningé (syndrome) | n2=en:motor stereotypy | rel=r_associated | relid=0 | w=24
  2963. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mri may show atrophy of the cerebrum
    n1=méningé (syndrome) | n2=en:mri may show atrophy of the cerebrum | rel=r_associated | relid=0 | w=24
  2964. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mri shows dysmyelination
    n1=méningé (syndrome) | n2=en:mri shows dysmyelination | rel=r_associated | relid=0 | w=24
  2965. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mri shows no normal myelination
    n1=méningé (syndrome) | n2=en:mri shows no normal myelination | rel=r_associated | relid=0 | w=24
  2966. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:mri shows short, thick corpus callosum
    n1=méningé (syndrome) | n2=en:mri shows short, thick corpus callosum | rel=r_associated | relid=0 | w=24
  2967. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:muscle stiffness and rigidity, chronic, fluctuating
    n1=méningé (syndrome) | n2=en:muscle stiffness and rigidity, chronic, fluctuating | rel=r_associated | relid=0 | w=24
  2968. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:muscle weakness, symmetric, proximal due to motor neuronopathy
    n1=méningé (syndrome) | n2=en:muscle weakness, symmetric, proximal due to motor neuronopathy | rel=r_associated | relid=0 | w=24
  2969. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:myoclonus (less common)
    n1=méningé (syndrome) | n2=en:myoclonus (less common) | rel=r_associated | relid=0 | w=24
  2970. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:myoclonus, axial (predominantly in upper limbs, occurs at rest and increases with activity or changes in posture)
    n1=méningé (syndrome) | n2=en:myoclonus, axial (predominantly in upper limbs, occurs at rest and increases with activity or changes in posture) | rel=r_associated | relid=0 | w=24
  2971. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neck drop
    n1=méningé (syndrome) | n2=en:neck drop | rel=r_associated | relid=0 | w=24
  2972. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neocortical atrophy
    n1=méningé (syndrome) | n2=en:neocortical atrophy | rel=r_associated | relid=0 | w=24
  2973. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neonatal hypotonia
    n1=méningé (syndrome) | n2=en:neonatal hypotonia | rel=r_associated | relid=0 | w=24
  2974. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neonatal irresponsiveness
    n1=méningé (syndrome) | n2=en:neonatal irresponsiveness | rel=r_associated | relid=0 | w=24
  2975. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neuroaxonal abnormalities
    n1=méningé (syndrome) | n2=en:neuroaxonal abnormalities | rel=r_associated | relid=0 | w=24
  2976. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neurocognitive impairment, mild (homozygous patient)
    n1=méningé (syndrome) | n2=en:neurocognitive impairment, mild (homozygous patient) | rel=r_associated | relid=0 | w=24
  2977. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neurogenic muscle atrophy, especially in the lower limbs
    n1=méningé (syndrome) | n2=en:neurogenic muscle atrophy, especially in the lower limbs | rel=r_associated | relid=0 | w=24
  2978. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neuronal and vascular calcifications
    n1=méningé (syndrome) | n2=en:neuronal and vascular calcifications | rel=r_associated | relid=0 | w=24
  2979. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neuronal loss and gliosis in the dentate nucleus
    n1=méningé (syndrome) | n2=en:neuronal loss and gliosis in the dentate nucleus | rel=r_associated | relid=0 | w=24
  2980. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neuronal loss in central nervous system
    n1=méningé (syndrome) | n2=en:neuronal loss in central nervous system | rel=r_associated | relid=0 | w=24
  2981. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neuronal loss in the purkinje cell layer of the cerebellar vermis
    n1=méningé (syndrome) | n2=en:neuronal loss in the purkinje cell layer of the cerebellar vermis | rel=r_associated | relid=0 | w=24
  2982. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neuronal loss in the substantia nigra
    n1=méningé (syndrome) | n2=en:neuronal loss in the substantia nigra | rel=r_associated | relid=0 | w=24
  2983. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:neuropathologic examination shows severe demyelination
    n1=méningé (syndrome) | n2=en:neuropathologic examination shows severe demyelination | rel=r_associated | relid=0 | w=24
  2984. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:no neurofibrillary tangles
    n1=méningé (syndrome) | n2=en:no neurofibrillary tangles | rel=r_associated | relid=0 | w=24
  2985. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:no seizures (hcs)
    n1=méningé (syndrome) | n2=en:no seizures (hcs) | rel=r_associated | relid=0 | w=24
  2986. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:no tau pathology
    n1=méningé (syndrome) | n2=en:no tau pathology | rel=r_associated | relid=0 | w=24
  2987. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:normal cognition and intellectual function
    n1=méningé (syndrome) | n2=en:normal cognition and intellectual function | rel=r_associated | relid=0 | w=24
  2988. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:normal early psychomotor development
    n1=méningé (syndrome) | n2=en:normal early psychomotor development | rel=r_associated | relid=0 | w=24
  2989. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:normal fine motor activity
    n1=méningé (syndrome) | n2=en:normal fine motor activity | rel=r_associated | relid=0 | w=24
  2990. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:normal psychomotor development
    n1=méningé (syndrome) | n2=en:normal psychomotor development | rel=r_associated | relid=0 | w=24
  2991. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:occasional degeneration of the globus pallidus
    n1=méningé (syndrome) | n2=en:occasional degeneration of the globus pallidus | rel=r_associated | relid=0 | w=24
  2992. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:opisthotonus
    n1=méningé (syndrome) | n2=en:opisthotonus | rel=r_associated | relid=0 | w=24
  2993. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:organic writer's cramp
    n1=méningé (syndrome) | n2=en:organic writer's cramp | rel=r_associated | relid=0 | w=24
  2994. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:orofacial dyspraxia, linguistic and nonlinguistic
    n1=méningé (syndrome) | n2=en:orofacial dyspraxia, linguistic and nonlinguistic | rel=r_associated | relid=0 | w=24
  2995. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:other cranial nerves may be involved
    n1=méningé (syndrome) | n2=en:other cranial nerves may be involved | rel=r_associated | relid=0 | w=24
  2996. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:other seizure types (in some patients)
    n1=méningé (syndrome) | n2=en:other seizure types (in some patients) | rel=r_associated | relid=0 | w=24
  2997. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:pachygyria (rare)
    n1=méningé (syndrome) | n2=en:pachygyria (rare) | rel=r_associated | relid=0 | w=24
  2998. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:pain, episodic
    n1=méningé (syndrome) | n2=en:pain, episodic | rel=r_associated | relid=0 | w=24
  2999. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:parkinsonism may occur
    n1=méningé (syndrome) | n2=en:parkinsonism may occur | rel=r_associated | relid=0 | w=24
  3000. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:partial agenesis of the corpus callosum (in 1 of 2 sibs)
    n1=méningé (syndrome) | n2=en:partial agenesis of the corpus callosum (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=24
  3001. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:partial or complete absence of the cerebellar vermis consistent with dandy walker malformation
    n1=méningé (syndrome) | n2=en:partial or complete absence of the cerebellar vermis consistent with dandy walker malformation | rel=r_associated | relid=0 | w=24
  3002. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:patients may only achieve sitting or walking
    n1=méningé (syndrome) | n2=en:patients may only achieve sitting or walking | rel=r_associated | relid=0 | w=24
  3003. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:periventricular and subcortical white matter abnormalities
    n1=méningé (syndrome) | n2=en:periventricular and subcortical white matter abnormalities | rel=r_associated | relid=0 | w=24
  3004. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:periventricular nodular heterotopia
    n1=méningé (syndrome) | n2=en:periventricular nodular heterotopia | rel=r_associated | relid=0 | w=24
  3005. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:periventricular nodular heterotopia seen on mri
    n1=méningé (syndrome) | n2=en:periventricular nodular heterotopia seen on mri | rel=r_associated | relid=0 | w=24
  3006. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:periventricular white matter abnormalities
    n1=méningé (syndrome) | n2=en:periventricular white matter abnormalities | rel=r_associated | relid=0 | w=24
  3007. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:persistent cavum septum pellucidum
    n1=méningé (syndrome) | n2=en:persistent cavum septum pellucidum | rel=r_associated | relid=0 | w=24
  3008. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:personality change
    n1=méningé (syndrome) | n2=en:personality change | rel=r_associated | relid=0 | w=24
  3009. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:pituitary gland adenoma
    n1=méningé (syndrome) | n2=en:pituitary gland adenoma | rel=r_associated | relid=0 | w=24
  3010. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:pontine atrophy
    n1=méningé (syndrome) | n2=en:pontine atrophy | rel=r_associated | relid=0 | w=24
  3011. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:poor coordination (83%)
    n1=méningé (syndrome) | n2=en:poor coordination (83%) | rel=r_associated | relid=0 | w=24
  3012. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:poor or absent speech
    n1=méningé (syndrome) | n2=en:poor or absent speech | rel=r_associated | relid=0 | w=24
  3013. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:poor visual-motor integration (range 41-80)
    n1=méningé (syndrome) | n2=en:poor visual-motor integration (range 41-80) | rel=r_associated | relid=0 | w=24
  3014. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:posterior fossa crowding, progressive
    n1=méningé (syndrome) | n2=en:posterior fossa crowding, progressive | rel=r_associated | relid=0 | w=24
  3015. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:posterior fossa cyst
    n1=méningé (syndrome) | n2=en:posterior fossa cyst | rel=r_associated | relid=0 | w=24
  3016. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:posterior fossa malformations
    n1=méningé (syndrome) | n2=en:posterior fossa malformations | rel=r_associated | relid=0 | w=24
  3017. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:posterior slow-wave activity on eeg
    n1=méningé (syndrome) | n2=en:posterior slow-wave activity on eeg | rel=r_associated | relid=0 | w=24
  3018. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:progressive forgetfulness
    n1=méningé (syndrome) | n2=en:progressive forgetfulness | rel=r_associated | relid=0 | w=24
  3019. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:progressive language deterioration
    n1=méningé (syndrome) | n2=en:progressive language deterioration | rel=r_associated | relid=0 | w=24
  3020. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:progressive loss of movement control
    n1=méningé (syndrome) | n2=en:progressive loss of movement control | rel=r_associated | relid=0 | w=24
  3021. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:prominent csf spaces (in some patients)
    n1=méningé (syndrome) | n2=en:prominent csf spaces (in some patients) | rel=r_associated | relid=0 | w=24
  3022. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:prominent trigone and occipital horns
    n1=méningé (syndrome) | n2=en:prominent trigone and occipital horns | rel=r_associated | relid=0 | w=24
  3023. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:proximal weakness occurs later
    n1=méningé (syndrome) | n2=en:proximal weakness occurs later | rel=r_associated | relid=0 | w=24
  3024. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:prp immunoreactivity limited to cerebellum and putamen
    n1=méningé (syndrome) | n2=en:prp immunoreactivity limited to cerebellum and putamen | rel=r_associated | relid=0 | w=24
  3025. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:psychotic episodes
    n1=méningé (syndrome) | n2=en:psychotic episodes | rel=r_associated | relid=0 | w=24
  3026. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:pyramidal signs (in some)
    n1=méningé (syndrome) | n2=en:pyramidal signs (in some) | rel=r_associated | relid=0 | w=24
  3027. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:pyramidal syndrome
    n1=méningé (syndrome) | n2=en:pyramidal syndrome | rel=r_associated | relid=0 | w=24
  3028. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:rapid, instantaneous neurologic decline may occur after fright
    n1=méningé (syndrome) | n2=en:rapid, instantaneous neurologic decline may occur after fright | rel=r_associated | relid=0 | w=24
  3029. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:rapidly progressive brainstem degeneration
    n1=méningé (syndrome) | n2=en:rapidly progressive brainstem degeneration | rel=r_associated | relid=0 | w=24
  3030. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:reduced numbers of neurons
    n1=méningé (syndrome) | n2=en:reduced numbers of neurons | rel=r_associated | relid=0 | w=24
  3031. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:reduced white matter volume
    n1=méningé (syndrome) | n2=en:reduced white matter volume | rel=r_associated | relid=0 | w=24
  3032. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:reduction or loss of acquired skills (e.g., purposeful hand use, speech)
    n1=méningé (syndrome) | n2=en:reduction or loss of acquired skills (e.g., purposeful hand use, speech) | rel=r_associated | relid=0 | w=24
  3033. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures (1 family)
    n1=méningé (syndrome) | n2=en:seizures (1 family) | rel=r_associated | relid=0 | w=24
  3034. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures (3 patients)
    n1=méningé (syndrome) | n2=en:seizures (3 patients) | rel=r_associated | relid=0 | w=24
  3035. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures (in 35%)
    n1=méningé (syndrome) | n2=en:seizures (in 35%) | rel=r_associated | relid=0 | w=24
  3036. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures (reported in 1 family)
    n1=méningé (syndrome) | n2=en:seizures (reported in 1 family) | rel=r_associated | relid=0 | w=24
  3037. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures (tetany)
    n1=méningé (syndrome) | n2=en:seizures (tetany) | rel=r_associated | relid=0 | w=24
  3038. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures (variable)
    n1=méningé (syndrome) | n2=en:seizures (variable) | rel=r_associated | relid=0 | w=24
  3039. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures in 15-30%
    n1=méningé (syndrome) | n2=en:seizures in 15-30% | rel=r_associated | relid=0 | w=24
  3040. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause
    n1=méningé (syndrome) | n2=en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause | rel=r_associated | relid=0 | w=24
  3041. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures usually last less than 15 minutes
    n1=méningé (syndrome) | n2=en:seizures usually last less than 15 minutes | rel=r_associated | relid=0 | w=24
  3042. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures usually occur less than 3 times
    n1=méningé (syndrome) | n2=en:seizures usually occur less than 3 times | rel=r_associated | relid=0 | w=24
  3043. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures, continuous, refractory
    n1=méningé (syndrome) | n2=en:seizures, continuous, refractory | rel=r_associated | relid=0 | w=24
  3044. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:seizures, partial complex (rare)
    n1=méningé (syndrome) | n2=en:seizures, partial complex (rare) | rel=r_associated | relid=0 | w=24
  3045. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:sensorineural hearing loss
    n1=méningé (syndrome) | n2=en:sensorineural hearing loss | rel=r_associated | relid=0 | w=24
  3046. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:severe demyelination of the white matter
    n1=méningé (syndrome) | n2=en:severe demyelination of the white matter | rel=r_associated | relid=0 | w=24
  3047. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:severe global developmental delay
    n1=méningé (syndrome) | n2=en:severe global developmental delay | rel=r_associated | relid=0 | w=24
  3048. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:severe psychomotor retardation (iq 35-65)
    n1=méningé (syndrome) | n2=en:severe psychomotor retardation (iq 35-65) | rel=r_associated | relid=0 | w=24
  3049. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:severe speech impairment
    n1=méningé (syndrome) | n2=en:severe speech impairment | rel=r_associated | relid=0 | w=24
  3050. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:severely delayed psychomotor development
    n1=méningé (syndrome) | n2=en:severely delayed psychomotor development | rel=r_associated | relid=0 | w=24
  3051. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:severity of symptoms peak in the second decade and do not progress
    n1=méningé (syndrome) | n2=en:severity of symptoms peak in the second decade and do not progress | rel=r_associated | relid=0 | w=24
  3052. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:shrunken inferior olivary nuclei
    n1=méningé (syndrome) | n2=en:shrunken inferior olivary nuclei | rel=r_associated | relid=0 | w=24
  3053. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:signal abnormalities in the posterior limbs of the internal capsules, middle cerebral peduncles, pyramidal tracts in the pons, and middle cerebellar peduncles seen on mri
    n1=méningé (syndrome) | n2=en:signal abnormalities in the posterior limbs of the internal capsules, middle cerebral peduncles, pyramidal tracts in the pons, and middle cerebellar peduncles seen on mri | rel=r_associated | relid=0 | w=24
  3054. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:signal changes in the caudate and putamen
    n1=méningé (syndrome) | n2=en:signal changes in the caudate and putamen | rel=r_associated | relid=0 | w=24
  3055. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:simplified cortical gyral pattern
    n1=méningé (syndrome) | n2=en:simplified cortical gyral pattern | rel=r_associated | relid=0 | w=24
  3056. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:sleep benefit (31%)
    n1=méningé (syndrome) | n2=en:sleep benefit (31%) | rel=r_associated | relid=0 | w=24
  3057. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:sleep-onset rem
    n1=méningé (syndrome) | n2=en:sleep-onset rem | rel=r_associated | relid=0 | w=24
  3058. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:slow gross motor activity
    n1=méningé (syndrome) | n2=en:slow gross motor activity | rel=r_associated | relid=0 | w=24
  3059. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:small brain with no other malformation see on mri
    n1=méningé (syndrome) | n2=en:small brain with no other malformation see on mri | rel=r_associated | relid=0 | w=24
  3060. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:small cerebral cortex
    n1=méningé (syndrome) | n2=en:small cerebral cortex | rel=r_associated | relid=0 | w=24
  3061. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:small hippocampi (1 patient)
    n1=méningé (syndrome) | n2=en:small hippocampi (1 patient) | rel=r_associated | relid=0 | w=24
  3062. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:small, smooth cerebellum
    n1=méningé (syndrome) | n2=en:small, smooth cerebellum | rel=r_associated | relid=0 | w=24
  3063. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:some may not achieve ambulation
    n1=méningé (syndrome) | n2=en:some may not achieve ambulation | rel=r_associated | relid=0 | w=24
  3064. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:sparing of the inferior olives
    n1=méningé (syndrome) | n2=en:sparing of the inferior olives | rel=r_associated | relid=0 | w=24
  3065. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:spasticity (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:spasticity (reported in 1 patient) | rel=r_associated | relid=0 | w=24
  3066. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:spasticity of pharyngeal muscles
    n1=méningé (syndrome) | n2=en:spasticity of pharyngeal muscles | rel=r_associated | relid=0 | w=24
  3067. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:spasticity, usually of the lower limbs
    n1=méningé (syndrome) | n2=en:spasticity, usually of the lower limbs | rel=r_associated | relid=0 | w=24
  3068. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:speech deficits
    n1=méningé (syndrome) | n2=en:speech deficits | rel=r_associated | relid=0 | w=24
  3069. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:speech limited to single word or no words
    n1=méningé (syndrome) | n2=en:speech limited to single word or no words | rel=r_associated | relid=0 | w=24
  3070. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:spina bifida occulta
    n1=méningé (syndrome) | n2=en:spina bifida occulta | rel=r_associated | relid=0 | w=24
  3071. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:spinal stenosis
    n1=méningé (syndrome) | n2=en:spinal stenosis | rel=r_associated | relid=0 | w=24
  3072. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:spongiform degeneration
    n1=méningé (syndrome) | n2=en:spongiform degeneration | rel=r_associated | relid=0 | w=24
  3073. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:status epilepticus (in some)
    n1=méningé (syndrome) | n2=en:status epilepticus (in some) | rel=r_associated | relid=0 | w=24
  3074. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:stenosis of the jugular foramen
    n1=méningé (syndrome) | n2=en:stenosis of the jugular foramen | rel=r_associated | relid=0 | w=24
  3075. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:stiffness of the lower limbs
    n1=méningé (syndrome) | n2=en:stiffness of the lower limbs | rel=r_associated | relid=0 | w=24
  3076. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:striatal lesions
    n1=méningé (syndrome) | n2=en:striatal lesions | rel=r_associated | relid=0 | w=24
  3077. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:structural brain anomalies
    n1=méningé (syndrome) | n2=en:structural brain anomalies | rel=r_associated | relid=0 | w=24
  3078. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:subclinical absence seizures
    n1=méningé (syndrome) | n2=en:subclinical absence seizures | rel=r_associated | relid=0 | w=24
  3079. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:subcortical atrophy (in some patients)
    n1=méningé (syndrome) | n2=en:subcortical atrophy (in some patients) | rel=r_associated | relid=0 | w=24
  3080. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:subcortical focal lacunae
    n1=méningé (syndrome) | n2=en:subcortical focal lacunae | rel=r_associated | relid=0 | w=24
  3081. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:subcortical temporal white matter disease, moderate
    n1=méningé (syndrome) | n2=en:subcortical temporal white matter disease, moderate | rel=r_associated | relid=0 | w=24
  3082. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:subcortical white matter lesions in the temporal lobes seen on brain mri
    n1=méningé (syndrome) | n2=en:subcortical white matter lesions in the temporal lobes seen on brain mri | rel=r_associated | relid=0 | w=24
  3083. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:syncope
    n1=méningé (syndrome) | n2=en:syncope | rel=r_associated | relid=0 | w=24
  3084. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:synkinesis
    n1=méningé (syndrome) | n2=en:synkinesis | rel=r_associated | relid=0 | w=24
  3085. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:t2-weighted hyperintensities in subcortical brain regions seen on mri
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintensities in subcortical brain regions seen on mri | rel=r_associated | relid=0 | w=24
  3086. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:tau inclusions are 'flame-shaped' or 'tuft-like'
    n1=méningé (syndrome) | n2=en:tau inclusions are 'flame-shaped' or 'tuft-like' | rel=r_associated | relid=0 | w=24
  3087. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:tau-containing inclusions
    n1=méningé (syndrome) | n2=en:tau-containing inclusions | rel=r_associated | relid=0 | w=24
  3088. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:tdp43-positive neuronal and glial cytoplasmic inclusions
    n1=méningé (syndrome) | n2=en:tdp43-positive neuronal and glial cytoplasmic inclusions | rel=r_associated | relid=0 | w=24
  3089. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:thick, short corpus callosum
    n1=méningé (syndrome) | n2=en:thick, short corpus callosum | rel=r_associated | relid=0 | w=24
  3090. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:thin corpus callosum (in some patients)
    n1=méningé (syndrome) | n2=en:thin corpus callosum (in some patients) | rel=r_associated | relid=0 | w=24
  3091. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:tonic clonic seizures, infrequent (in one patient)
    n1=méningé (syndrome) | n2=en:tonic clonic seizures, infrequent (in one patient) | rel=r_associated | relid=0 | w=24
  3092. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:total body paralysis, paroxysmal
    n1=méningé (syndrome) | n2=en:total body paralysis, paroxysmal | rel=r_associated | relid=0 | w=24
  3093. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:transient mild dystonia may precede abrupt onset of disorder by several years
    n1=méningé (syndrome) | n2=en:transient mild dystonia may precede abrupt onset of disorder by several years | rel=r_associated | relid=0 | w=24
  3094. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:transient, reversible neurologic deficits
    n1=méningé (syndrome) | n2=en:transient, reversible neurologic deficits | rel=r_associated | relid=0 | w=24
  3095. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:tremor of hands
    n1=méningé (syndrome) | n2=en:tremor of hands | rel=r_associated | relid=0 | w=24
  3096. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:type iv eeg response is generalized spike-wave discharges
    n1=méningé (syndrome) | n2=en:type iv eeg response is generalized spike-wave discharges | rel=r_associated | relid=0 | w=24
  3097. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:unable to stand
    n1=méningé (syndrome) | n2=en:unable to stand | rel=r_associated | relid=0 | w=24
  3098. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:unresponsiveness
    n1=méningé (syndrome) | n2=en:unresponsiveness | rel=r_associated | relid=0 | w=24
  3099. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:upper limb weakness may occur later
    n1=méningé (syndrome) | n2=en:upper limb weakness may occur later | rel=r_associated | relid=0 | w=24
  3100. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:upper limbs may show hyperreflexia
    n1=méningé (syndrome) | n2=en:upper limbs may show hyperreflexia | rel=r_associated | relid=0 | w=24
  3101. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:ventricular anomalies
    n1=méningé (syndrome) | n2=en:ventricular anomalies | rel=r_associated | relid=0 | w=24
  3102. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:ventricular dilatation (rare)
    n1=méningé (syndrome) | n2=en:ventricular dilatation (rare) | rel=r_associated | relid=0 | w=24
  3103. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:visual blackouts (stage 1)
    n1=méningé (syndrome) | n2=en:visual blackouts (stage 1) | rel=r_associated | relid=0 | w=24
  3104. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:walking during slow-wave sleep (sleepwalking)
    n1=méningé (syndrome) | n2=en:walking during slow-wave sleep (sleepwalking) | rel=r_associated | relid=0 | w=24
  3105. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:walking independently at 2.5 years to 4 years of age
    n1=méningé (syndrome) | n2=en:walking independently at 2.5 years to 4 years of age | rel=r_associated | relid=0 | w=24
  3106. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:weak or absent tendon reflexes of knees and ankles (in some patients)
    n1=méningé (syndrome) | n2=en:weak or absent tendon reflexes of knees and ankles (in some patients) | rel=r_associated | relid=0 | w=24
  3107. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:white matter abnormalities (1 patient)
    n1=méningé (syndrome) | n2=en:white matter abnormalities (1 patient) | rel=r_associated | relid=0 | w=24
  3108. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:white matter signal abnormalities in the deep white matter and periventricular regions
    n1=méningé (syndrome) | n2=en:white matter signal abnormalities in the deep white matter and periventricular regions | rel=r_associated | relid=0 | w=24
  3109. méningé (syndrome) -- r_associated #0: 24 / 0.289 -> en:word finding difficulty (disorder)
    n1=méningé (syndrome) | n2=en:word finding difficulty (disorder) | rel=r_associated | relid=0 | w=24
  3110. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:abnormal purkinje cells
    n1=méningé (syndrome) | n2=en:abnormal purkinje cells | rel=r_associated | relid=0 | w=23
  3111. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:abnormal visual sensitivity of the brain in reaction to intermittent photic stimulation
    n1=méningé (syndrome) | n2=en:abnormal visual sensitivity of the brain in reaction to intermittent photic stimulation | rel=r_associated | relid=0 | w=23
  3112. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:absence of cerebral aneurysms
    n1=méningé (syndrome) | n2=en:absence of cerebral aneurysms | rel=r_associated | relid=0 | w=23
  3113. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:absence of language development
    n1=méningé (syndrome) | n2=en:absence of language development | rel=r_associated | relid=0 | w=23
  3114. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:absence seizures (stage 2 and 3)
    n1=méningé (syndrome) | n2=en:absence seizures (stage 2 and 3) | rel=r_associated | relid=0 | w=23
  3115. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:absence seizures may occur
    n1=méningé (syndrome) | n2=en:absence seizures may occur | rel=r_associated | relid=0 | w=23
  3116. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:adipose tissue in subarachnoid space
    n1=méningé (syndrome) | n2=en:adipose tissue in subarachnoid space | rel=r_associated | relid=0 | w=23
  3117. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:agenesis of the anterior commissure
    n1=méningé (syndrome) | n2=en:agenesis of the anterior commissure | rel=r_associated | relid=0 | w=23
  3118. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:agenesis of the corpus callosum (patient a)
    n1=méningé (syndrome) | n2=en:agenesis of the corpus callosum (patient a) | rel=r_associated | relid=0 | w=23
  3119. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:agenesis or hypoplasia of the corpus callosum
    n1=méningé (syndrome) | n2=en:agenesis or hypoplasia of the corpus callosum | rel=r_associated | relid=0 | w=23
  3120. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:agyria (1 patient)
    n1=méningé (syndrome) | n2=en:agyria (1 patient) | rel=r_associated | relid=0 | w=23
  3121. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:alobar hpe shows absence of interhemispheric cleavage and single ventricle
    n1=méningé (syndrome) | n2=en:alobar hpe shows absence of interhemispheric cleavage and single ventricle | rel=r_associated | relid=0 | w=23
  3122. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:alpha-synuclein immunoreactive neuronal and glial inclusions
    n1=méningé (syndrome) | n2=en:alpha-synuclein immunoreactive neuronal and glial inclusions | rel=r_associated | relid=0 | w=23
  3123. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:ankle clonus (in some)
    n1=méningé (syndrome) | n2=en:ankle clonus (in some) | rel=r_associated | relid=0 | w=23
  3124. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:ankle or knee clonus
    n1=méningé (syndrome) | n2=en:ankle or knee clonus | rel=r_associated | relid=0 | w=23
  3125. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:anomalies of the folding of the right sylvian area
    n1=méningé (syndrome) | n2=en:anomalies of the folding of the right sylvian area | rel=r_associated | relid=0 | w=23
  3126. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:anterior pachygyria and posterior agyria
    n1=méningé (syndrome) | n2=en:anterior pachygyria and posterior agyria | rel=r_associated | relid=0 | w=23
  3127. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:anxiety
    n1=méningé (syndrome) | n2=en:anxiety | rel=r_associated | relid=0 | w=23
  3128. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:apathy
    n1=méningé (syndrome) | n2=en:apathy | rel=r_associated | relid=0 | w=23
  3129. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:aplasia of the inferior half of the cerebellar vermis
    n1=méningé (syndrome) | n2=en:aplasia of the inferior half of the cerebellar vermis | rel=r_associated | relid=0 | w=23
  3130. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:apraxias
    n1=méningé (syndrome) | n2=en:apraxias | rel=r_associated | relid=0 | w=23
  3131. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:arachnoid cyst
    n1=méningé (syndrome) | n2=en:arachnoid cyst | rel=r_associated | relid=0 | w=23
  3132. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:arachnoid mater
    n1=méningé (syndrome) | n2=en:arachnoid mater | rel=r_associated | relid=0 | w=23
  3133. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:arnold-chiari i malformation
    n1=méningé (syndrome) | n2=en:arnold-chiari i malformation | rel=r_associated | relid=0 | w=23
  3134. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:astrocytic gliosis
    n1=méningé (syndrome) | n2=en:astrocytic gliosis | rel=r_associated | relid=0 | w=23
  3135. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:ataxia (less common)
    n1=méningé (syndrome) | n2=en:ataxia (less common) | rel=r_associated | relid=0 | w=23
  3136. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:ataxia, cerebellar, limb and gait
    n1=méningé (syndrome) | n2=en:ataxia, cerebellar, limb and gait | rel=r_associated | relid=0 | w=23
  3137. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:ataxia, episodic (episodes last from hours to days)
    n1=méningé (syndrome) | n2=en:ataxia, episodic (episodes last from hours to days) | rel=r_associated | relid=0 | w=23
  3138. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:atelencephaly
    n1=méningé (syndrome) | n2=en:atelencephaly | rel=r_associated | relid=0 | w=23
  3139. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:athetosis, mild (in one patient)
    n1=méningé (syndrome) | n2=en:athetosis, mild (in one patient) | rel=r_associated | relid=0 | w=23
  3140. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:atrophy of cerebellum, brainstem, cervical spinal cord
    n1=méningé (syndrome) | n2=en:atrophy of cerebellum, brainstem, cervical spinal cord | rel=r_associated | relid=0 | w=23
  3141. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:atrophy of the cerebellar vermis seen on mri
    n1=méningé (syndrome) | n2=en:atrophy of the cerebellar vermis seen on mri | rel=r_associated | relid=0 | w=23
  3142. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:atrophy of the frontal and parietal cortex
    n1=méningé (syndrome) | n2=en:atrophy of the frontal and parietal cortex | rel=r_associated | relid=0 | w=23
  3143. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:atrophy of the spinal cord and cerebellar tracts
    n1=méningé (syndrome) | n2=en:atrophy of the spinal cord and cerebellar tracts | rel=r_associated | relid=0 | w=23
  3144. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:attacks of disabling daytime drowsiness and low alertness
    n1=méningé (syndrome) | n2=en:attacks of disabling daytime drowsiness and low alertness | rel=r_associated | relid=0 | w=23
  3145. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:autonomic nervous system disorders
    n1=méningé (syndrome) | n2=en:autonomic nervous system disorders | rel=r_associated | relid=0 | w=23
  3146. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:autonomic symptoms
    n1=méningé (syndrome) | n2=en:autonomic symptoms | rel=r_associated | relid=0 | w=23
  3147. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:axial hypotonia (rare)
    n1=méningé (syndrome) | n2=en:axial hypotonia (rare) | rel=r_associated | relid=0 | w=23
  3148. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:axonal loss
    n1=méningé (syndrome) | n2=en:axonal loss | rel=r_associated | relid=0 | w=23
  3149. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:background slowing
    n1=méningé (syndrome) | n2=en:background slowing | rel=r_associated | relid=0 | w=23
  3150. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:beta-amyloid-positive senile plaques
    n1=méningé (syndrome) | n2=en:beta-amyloid-positive senile plaques | rel=r_associated | relid=0 | w=23
  3151. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:between 2 and 7% of children will develop afebrile seizure disorders later in life
    n1=méningé (syndrome) | n2=en:between 2 and 7% of children will develop afebrile seizure disorders later in life | rel=r_associated | relid=0 | w=23
  3152. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:bilateral signals in the basal ganglia
    n1=méningé (syndrome) | n2=en:bilateral signals in the basal ganglia | rel=r_associated | relid=0 | w=23
  3153. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:biopsy in both types shows neuronal cytomegaly (large, bizarre, maloriented neurons) in the laminar cortex
    n1=méningé (syndrome) | n2=en:biopsy in both types shows neuronal cytomegaly (large, bizarre, maloriented neurons) in the laminar cortex | rel=r_associated | relid=0 | w=23
  3154. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:board and poorly defined gyri
    n1=méningé (syndrome) | n2=en:board and poorly defined gyri | rel=r_associated | relid=0 | w=23
  3155. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:bradykinesia (in severe cases)
    n1=méningé (syndrome) | n2=en:bradykinesia (in severe cases) | rel=r_associated | relid=0 | w=23
  3156. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:brain and spinal cord structure
    n1=méningé (syndrome) | n2=en:brain and spinal cord structure | rel=r_associated | relid=0 | w=23
  3157. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:brain atrophy (1 patient)
    n1=méningé (syndrome) | n2=en:brain atrophy (1 patient) | rel=r_associated | relid=0 | w=23
  3158. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:brain atrophy seen on mri
    n1=méningé (syndrome) | n2=en:brain atrophy seen on mri | rel=r_associated | relid=0 | w=23
  3159. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:brain imaging shows hypomyelination
    n1=méningé (syndrome) | n2=en:brain imaging shows hypomyelination | rel=r_associated | relid=0 | w=23
  3160. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:brain imaging shows lesions in the thalami, brainstem, and cerebellum
    n1=méningé (syndrome) | n2=en:brain imaging shows lesions in the thalami, brainstem, and cerebellum | rel=r_associated | relid=0 | w=23
  3161. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:brain mri shows cortical atrophy
    n1=méningé (syndrome) | n2=en:brain mri shows cortical atrophy | rel=r_associated | relid=0 | w=23
  3162. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:brain mri shows hypoplasia of the corpus callosum
    n1=méningé (syndrome) | n2=en:brain mri shows hypoplasia of the corpus callosum | rel=r_associated | relid=0 | w=23
  3163. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:brainstem damage
    n1=méningé (syndrome) | n2=en:brainstem damage | rel=r_associated | relid=0 | w=23
  3164. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:brainstem dysplasia
    n1=méningé (syndrome) | n2=en:brainstem dysplasia | rel=r_associated | relid=0 | w=23
  3165. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:breathing difficulty due to vocal cord paralysis
    n1=méningé (syndrome) | n2=en:breathing difficulty due to vocal cord paralysis | rel=r_associated | relid=0 | w=23
  3166. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:broca's aphasia
    n1=méningé (syndrome) | n2=en:broca's aphasia | rel=r_associated | relid=0 | w=23
  3167. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:bulbar signs
    n1=méningé (syndrome) | n2=en:bulbar signs | rel=r_associated | relid=0 | w=23
  3168. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cauda equina syndrome
    n1=méningé (syndrome) | n2=en:cauda equina syndrome | rel=r_associated | relid=0 | w=23
  3169. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cellular secretion
    n1=méningé (syndrome) | n2=en:cellular secretion | rel=r_associated | relid=0 | w=23
  3170. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:central nervous system neoplasm
    n1=méningé (syndrome) | n2=en:central nervous system neoplasm | rel=r_associated | relid=0 | w=23
  3171. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:central neural pathway/tract
    n1=méningé (syndrome) | n2=en:central neural pathway/tract | rel=r_associated | relid=0 | w=23
  3172. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar ataxia
    n1=méningé (syndrome) | n2=en:cerebellar ataxia | rel=r_associated | relid=0 | w=23
  3173. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar ataxia (1 patient)
    n1=méningé (syndrome) | n2=en:cerebellar ataxia (1 patient) | rel=r_associated | relid=0 | w=23
  3174. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar atrophy in most cases
    n1=méningé (syndrome) | n2=en:cerebellar atrophy in most cases | rel=r_associated | relid=0 | w=23
  3175. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar atrophy seen on mri
    n1=méningé (syndrome) | n2=en:cerebellar atrophy seen on mri | rel=r_associated | relid=0 | w=23
  3176. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar heterotopias
    n1=méningé (syndrome) | n2=en:cerebellar heterotopias | rel=r_associated | relid=0 | w=23
  3177. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar hypoplasia (in 1 of 2 patients)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (in 1 of 2 patients) | rel=r_associated | relid=0 | w=23
  3178. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar hypoplasia (in 1 of 2 sibs)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=23
  3179. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar hypoplasia or agenesis
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia or agenesis | rel=r_associated | relid=0 | w=23
  3180. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar hypoplasia predominantly affecting the vermis
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia predominantly affecting the vermis | rel=r_associated | relid=0 | w=23
  3181. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar hypoplasia/atrophy (27%)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia/atrophy (27%) | rel=r_associated | relid=0 | w=23
  3182. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebellar lesion nos
    n1=méningé (syndrome) | n2=en:cerebellar lesion nos | rel=r_associated | relid=0 | w=23
  3183. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebral atrophy (in 1 family)
    n1=méningé (syndrome) | n2=en:cerebral atrophy (in 1 family) | rel=r_associated | relid=0 | w=23
  3184. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebral atrophy (in some patients)
    n1=méningé (syndrome) | n2=en:cerebral atrophy (in some patients) | rel=r_associated | relid=0 | w=23
  3185. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebral atrophy (rare)
    n1=méningé (syndrome) | n2=en:cerebral atrophy (rare) | rel=r_associated | relid=0 | w=23
  3186. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebral atrophy, mild
    n1=méningé (syndrome) | n2=en:cerebral atrophy, mild | rel=r_associated | relid=0 | w=23
  3187. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebral cortex myoclonus
    n1=méningé (syndrome) | n2=en:cerebral cortex myoclonus | rel=r_associated | relid=0 | w=23
  3188. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebral cortical atrophy, especially frontal lobes
    n1=méningé (syndrome) | n2=en:cerebral cortical atrophy, especially frontal lobes | rel=r_associated | relid=0 | w=23
  3189. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebral dysmyelination
    n1=méningé (syndrome) | n2=en:cerebral dysmyelination | rel=r_associated | relid=0 | w=23
  3190. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cerebrovascular ischemic attacks, transient (proceed secondary neurologic findings)
    n1=méningé (syndrome) | n2=en:cerebrovascular ischemic attacks, transient (proceed secondary neurologic findings) | rel=r_associated | relid=0 | w=23
  3191. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cervical myelopathy
    n1=méningé (syndrome) | n2=en:cervical myelopathy | rel=r_associated | relid=0 | w=23
  3192. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:characteristic electroencephalogram (eeg) discharges
    n1=méningé (syndrome) | n2=en:characteristic electroencephalogram (eeg) discharges | rel=r_associated | relid=0 | w=23
  3193. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:characteristic periodic eeg complexes (only in sporadic and familial cjd, not in variant cjd)
    n1=méningé (syndrome) | n2=en:characteristic periodic eeg complexes (only in sporadic and familial cjd, not in variant cjd) | rel=r_associated | relid=0 | w=23
  3194. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:choreic movements, episodic
    n1=méningé (syndrome) | n2=en:choreic movements, episodic | rel=r_associated | relid=0 | w=23
  3195. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:clear cell meningioma
    n1=méningé (syndrome) | n2=en:clear cell meningioma | rel=r_associated | relid=0 | w=23
  3196. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cognition is preserved
    n1=méningé (syndrome) | n2=en:cognition is preserved | rel=r_associated | relid=0 | w=23
  3197. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cognitive decline (rare)
    n1=méningé (syndrome) | n2=en:cognitive decline (rare) | rel=r_associated | relid=0 | w=23
  3198. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cognitive delay
    n1=méningé (syndrome) | n2=en:cognitive delay | rel=r_associated | relid=0 | w=23
  3199. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cognitive impairment (cvs+)
    n1=méningé (syndrome) | n2=en:cognitive impairment (cvs+) | rel=r_associated | relid=0 | w=23
  3200. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cognitive impairment (in some patients)
    n1=méningé (syndrome) | n2=en:cognitive impairment (in some patients) | rel=r_associated | relid=0 | w=23
  3201. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cognitive impairment, mild (44%)
    n1=méningé (syndrome) | n2=en:cognitive impairment, mild (44%) | rel=r_associated | relid=0 | w=23
  3202. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cognitive impairment, mild to moderate
    n1=méningé (syndrome) | n2=en:cognitive impairment, mild to moderate | rel=r_associated | relid=0 | w=23
  3203. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:coma may occur after force feeding of high protein diet
    n1=méningé (syndrome) | n2=en:coma may occur after force feeding of high protein diet | rel=r_associated | relid=0 | w=23
  3204. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:communication defects
    n1=méningé (syndrome) | n2=en:communication defects | rel=r_associated | relid=0 | w=23
  3205. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:corpus callosum, agenesis of (in some patients)
    n1=méningé (syndrome) | n2=en:corpus callosum, agenesis of (in some patients) | rel=r_associated | relid=0 | w=23
  3206. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cortical and subcortical regions involved
    n1=méningé (syndrome) | n2=en:cortical and subcortical regions involved | rel=r_associated | relid=0 | w=23
  3207. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cortical atrophy (frontal area)
    n1=méningé (syndrome) | n2=en:cortical atrophy (frontal area) | rel=r_associated | relid=0 | w=23
  3208. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cortical atrophy, progressive
    n1=méningé (syndrome) | n2=en:cortical atrophy, progressive | rel=r_associated | relid=0 | w=23
  3209. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:cortical reflex myoclonus
    n1=méningé (syndrome) | n2=en:cortical reflex myoclonus | rel=r_associated | relid=0 | w=23
  3210. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:corticospinal signs (87% of patients in 1 report)
    n1=méningé (syndrome) | n2=en:corticospinal signs (87% of patients in 1 report) | rel=r_associated | relid=0 | w=23
  3211. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:corticospinal tract disease in lower limbs (in adulthood)
    n1=méningé (syndrome) | n2=en:corticospinal tract disease in lower limbs (in adulthood) | rel=r_associated | relid=0 | w=23
  3212. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:decreased amount of myelin-specific lipids
    n1=méningé (syndrome) | n2=en:decreased amount of myelin-specific lipids | rel=r_associated | relid=0 | w=23
  3213. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:decreased csf volume in posterior fossa
    n1=méningé (syndrome) | n2=en:decreased csf volume in posterior fossa | rel=r_associated | relid=0 | w=23
  3214. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:decreased or absent gyri (in some patients)
    n1=méningé (syndrome) | n2=en:decreased or absent gyri (in some patients) | rel=r_associated | relid=0 | w=23
  3215. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:decreased volume of the cerebral white matter
    n1=méningé (syndrome) | n2=en:decreased volume of the cerebral white matter | rel=r_associated | relid=0 | w=23
  3216. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:decreased volume of the posterior cranial fossa with normal hindbrain volume
    n1=méningé (syndrome) | n2=en:decreased volume of the posterior cranial fossa with normal hindbrain volume | rel=r_associated | relid=0 | w=23
  3217. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:decreased white matter volume
    n1=méningé (syndrome) | n2=en:decreased white matter volume | rel=r_associated | relid=0 | w=23
  3218. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:defects in auditory cue processing
    n1=méningé (syndrome) | n2=en:defects in auditory cue processing | rel=r_associated | relid=0 | w=23
  3219. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:defects in fine motor skills
    n1=méningé (syndrome) | n2=en:defects in fine motor skills | rel=r_associated | relid=0 | w=23
  3220. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:deficit in nonword repetition (nwr)
    n1=méningé (syndrome) | n2=en:deficit in nonword repetition (nwr) | rel=r_associated | relid=0 | w=23
  3221. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:deficit in spelling
    n1=méningé (syndrome) | n2=en:deficit in spelling | rel=r_associated | relid=0 | w=23
  3222. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:delayed adaptive hand use
    n1=méningé (syndrome) | n2=en:delayed adaptive hand use | rel=r_associated | relid=0 | w=23
  3223. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:delayed cerebellar development (in some patients)
    n1=méningé (syndrome) | n2=en:delayed cerebellar development (in some patients) | rel=r_associated | relid=0 | w=23
  3224. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:delayed development (1 family)
    n1=méningé (syndrome) | n2=en:delayed development (1 family) | rel=r_associated | relid=0 | w=23
  3225. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:delayed development, variable severity, from birth in some patients
    n1=méningé (syndrome) | n2=en:delayed development, variable severity, from birth in some patients | rel=r_associated | relid=0 | w=23
  3226. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:delayed independent walking
    n1=méningé (syndrome) | n2=en:delayed independent walking | rel=r_associated | relid=0 | w=23
  3227. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:delayed psychomotor development (in 1 family)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development (in 1 family) | rel=r_associated | relid=0 | w=23
  3228. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:delayed psychomotor development, severe (> 90%)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, severe (> 90%) | rel=r_associated | relid=0 | w=23
  3229. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:deletion of chromosome 22 associated meningioma
    n1=méningé (syndrome) | n2=en:deletion of chromosome 22 associated meningioma | rel=r_associated | relid=0 | w=23
  3230. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:deletion of the short arm of chromosome 1 (1p) associated meningioma
    n1=méningé (syndrome) | n2=en:deletion of the short arm of chromosome 1 (1p) associated meningioma | rel=r_associated | relid=0 | w=23
  3231. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:dementia (<20%)
    n1=méningé (syndrome) | n2=en:dementia (<20%) | rel=r_associated | relid=0 | w=23
  3232. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:dementia may occur
    n1=méningé (syndrome) | n2=en:dementia may occur | rel=r_associated | relid=0 | w=23
  3233. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:demyelination
    n1=méningé (syndrome) | n2=en:demyelination | rel=r_associated | relid=0 | w=23
  3234. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:developmental delay (apparent after the first year of life)
    n1=méningé (syndrome) | n2=en:developmental delay (apparent after the first year of life) | rel=r_associated | relid=0 | w=23
  3235. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:developmental delay, moderate (in some patients)
    n1=méningé (syndrome) | n2=en:developmental delay, moderate (in some patients) | rel=r_associated | relid=0 | w=23
  3236. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:developmental regression in affected children
    n1=méningé (syndrome) | n2=en:developmental regression in affected children | rel=r_associated | relid=0 | w=23
  3237. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:developmental retardation (in some patients)
    n1=méningé (syndrome) | n2=en:developmental retardation (in some patients) | rel=r_associated | relid=0 | w=23
  3238. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:developmental retardation, profound
    n1=méningé (syndrome) | n2=en:developmental retardation, profound | rel=r_associated | relid=0 | w=23
  3239. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:diffuse leukoencephalopathy
    n1=méningé (syndrome) | n2=en:diffuse leukoencephalopathy | rel=r_associated | relid=0 | w=23
  3240. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:diffuse spongiform leukoencephalopathy
    n1=méningé (syndrome) | n2=en:diffuse spongiform leukoencephalopathy | rel=r_associated | relid=0 | w=23
  3241. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:diffuse white matter abnormalities on brain mri
    n1=méningé (syndrome) | n2=en:diffuse white matter abnormalities on brain mri | rel=r_associated | relid=0 | w=23
  3242. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:diffuse white matter loss
    n1=méningé (syndrome) | n2=en:diffuse white matter loss | rel=r_associated | relid=0 | w=23
  3243. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:distal tapering of the carotid, cerebellar, and meningeal arteries
    n1=méningé (syndrome) | n2=en:distal tapering of the carotid, cerebellar, and meningeal arteries | rel=r_associated | relid=0 | w=23
  3244. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:distal weakness occurs later
    n1=méningé (syndrome) | n2=en:distal weakness occurs later | rel=r_associated | relid=0 | w=23
  3245. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:disturbed equilibrium
    n1=méningé (syndrome) | n2=en:disturbed equilibrium | rel=r_associated | relid=0 | w=23
  3246. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:disturbed myelination affecting the periventricular and subcortical white matter
    n1=méningé (syndrome) | n2=en:disturbed myelination affecting the periventricular and subcortical white matter | rel=r_associated | relid=0 | w=23
  3247. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:dizziness, episodic
    n1=méningé (syndrome) | n2=en:dizziness, episodic | rel=r_associated | relid=0 | w=23
  3248. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:drop attack
    n1=méningé (syndrome) | n2=en:drop attack | rel=r_associated | relid=0 | w=23
  3249. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:drug-resistent seizures (rare)
    n1=méningé (syndrome) | n2=en:drug-resistent seizures (rare) | rel=r_associated | relid=0 | w=23
  3250. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:dysgenesis of the corpus callosum (1 patient)
    n1=méningé (syndrome) | n2=en:dysgenesis of the corpus callosum (1 patient) | rel=r_associated | relid=0 | w=23
  3251. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:dyskinesia, episodic
    n1=méningé (syndrome) | n2=en:dyskinesia, episodic | rel=r_associated | relid=0 | w=23
  3252. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:dysphasia
    n1=méningé (syndrome) | n2=en:dysphasia | rel=r_associated | relid=0 | w=23
  3253. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:dystonia
    n1=méningé (syndrome) | n2=en:dystonia | rel=r_associated | relid=0 | w=23
  3254. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:dystonia (57%)
    n1=méningé (syndrome) | n2=en:dystonia (57%) | rel=r_associated | relid=0 | w=23
  3255. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:dystonic posture
    n1=méningé (syndrome) | n2=en:dystonic posture | rel=r_associated | relid=0 | w=23
  3256. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:ectopic posterior pituitary (in some patients)
    n1=méningé (syndrome) | n2=en:ectopic posterior pituitary (in some patients) | rel=r_associated | relid=0 | w=23
  3257. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:eeg shows abundant slow waves and fast spike activity
    n1=méningé (syndrome) | n2=en:eeg shows abundant slow waves and fast spike activity | rel=r_associated | relid=0 | w=23
  3258. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:eeg shows active generalized spike and wave and polyspike pattern
    n1=méningé (syndrome) | n2=en:eeg shows active generalized spike and wave and polyspike pattern | rel=r_associated | relid=0 | w=23
  3259. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:eeg shows multifocal epileptic activity
    n1=méningé (syndrome) | n2=en:eeg shows multifocal epileptic activity | rel=r_associated | relid=0 | w=23
  3260. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:eeg shows spike and multispike waves, 3-4 hz
    n1=méningé (syndrome) | n2=en:eeg shows spike and multispike waves, 3-4 hz | rel=r_associated | relid=0 | w=23
  3261. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:eeg with photoparoxysmal response
    n1=méningé (syndrome) | n2=en:eeg with photoparoxysmal response | rel=r_associated | relid=0 | w=23
  3262. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:elevated pterin levels (tetrahydrobiopterin, neopterin) in cerebrospinal fluid
    n1=méningé (syndrome) | n2=en:elevated pterin levels (tetrahydrobiopterin, neopterin) in cerebrospinal fluid | rel=r_associated | relid=0 | w=23
  3263. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:elevation and splaying of the superior cerebellar peduncles
    n1=méningé (syndrome) | n2=en:elevation and splaying of the superior cerebellar peduncles | rel=r_associated | relid=0 | w=23
  3264. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:emg shows evidence of denervation
    n1=méningé (syndrome) | n2=en:emg shows evidence of denervation | rel=r_associated | relid=0 | w=23
  3265. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:encephalopathy (in 1 patient)
    n1=méningé (syndrome) | n2=en:encephalopathy (in 1 patient) | rel=r_associated | relid=0 | w=23
  3266. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:encephalopathy, acute, episodic
    n1=méningé (syndrome) | n2=en:encephalopathy, acute, episodic | rel=r_associated | relid=0 | w=23
  3267. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:encephalopathy, episodic, associated with febrile illnesses
    n1=méningé (syndrome) | n2=en:encephalopathy, episodic, associated with febrile illnesses | rel=r_associated | relid=0 | w=23
  3268. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:enlarged ventricles (in some patients)
    n1=méningé (syndrome) | n2=en:enlarged ventricles (in some patients) | rel=r_associated | relid=0 | w=23
  3269. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:epilepsy (in 2 of 3 patients)
    n1=méningé (syndrome) | n2=en:epilepsy (in 2 of 3 patients) | rel=r_associated | relid=0 | w=23
  3270. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:epilepsy, rolandic
    n1=méningé (syndrome) | n2=en:epilepsy, rolandic | rel=r_associated | relid=0 | w=23
  3271. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:epilepsy, temporal lobe
    n1=méningé (syndrome) | n2=en:epilepsy, temporal lobe | rel=r_associated | relid=0 | w=23
  3272. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:epileptic drop attack
    n1=méningé (syndrome) | n2=en:epileptic drop attack | rel=r_associated | relid=0 | w=23
  3273. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:epileptic encephalopathy
    n1=méningé (syndrome) | n2=en:epileptic encephalopathy | rel=r_associated | relid=0 | w=23
  3274. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:episodes may last less than 30 minutes or greater than several hours
    n1=méningé (syndrome) | n2=en:episodes may last less than 30 minutes or greater than several hours | rel=r_associated | relid=0 | w=23
  3275. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:episodic acute neurologic deterioration/encephalopathy, recurrent
    n1=méningé (syndrome) | n2=en:episodic acute neurologic deterioration/encephalopathy, recurrent | rel=r_associated | relid=0 | w=23
  3276. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:episodic ataxia
    n1=méningé (syndrome) | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=23
  3277. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:expressive speech absent
    n1=méningé (syndrome) | n2=en:expressive speech absent | rel=r_associated | relid=0 | w=23
  3278. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:extensive melanosis of leptomeninges, amygdala, and cerebellar hemispheres
    n1=méningé (syndrome) | n2=en:extensive melanosis of leptomeninges, amygdala, and cerebellar hemispheres | rel=r_associated | relid=0 | w=23
  3279. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:extrapyramidal sign
    n1=méningé (syndrome) | n2=en:extrapyramidal sign | rel=r_associated | relid=0 | w=23
  3280. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:fasciculation-like movements
    n1=méningé (syndrome) | n2=en:fasciculation-like movements | rel=r_associated | relid=0 | w=23
  3281. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:fasciculations (after long disease duration)
    n1=méningé (syndrome) | n2=en:fasciculations (after long disease duration) | rel=r_associated | relid=0 | w=23
  3282. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:fine motor task disruption
    n1=méningé (syndrome) | n2=en:fine motor task disruption | rel=r_associated | relid=0 | w=23
  3283. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:flexor plantar response
    n1=méningé (syndrome) | n2=en:flexor plantar response | rel=r_associated | relid=0 | w=23
  3284. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:fluctuations in consciousness
    n1=méningé (syndrome) | n2=en:fluctuations in consciousness | rel=r_associated | relid=0 | w=23
  3285. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:focal paroxysmal discharges
    n1=méningé (syndrome) | n2=en:focal paroxysmal discharges | rel=r_associated | relid=0 | w=23
  3286. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:frontal lobe atrophy
    n1=méningé (syndrome) | n2=en:frontal lobe atrophy | rel=r_associated | relid=0 | w=23
  3287. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:frontotemporal atrophy, mild, seen on mri
    n1=méningé (syndrome) | n2=en:frontotemporal atrophy, mild, seen on mri | rel=r_associated | relid=0 | w=23
  3288. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:frontotemporal lobar atrophy with 'knife-edge' distinction
    n1=méningé (syndrome) | n2=en:frontotemporal lobar atrophy with 'knife-edge' distinction | rel=r_associated | relid=0 | w=23
  3289. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:gait apraxia
    n1=méningé (syndrome) | n2=en:gait apraxia | rel=r_associated | relid=0 | w=23
  3290. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:gait disturbance (ataxia)
    n1=méningé (syndrome) | n2=en:gait disturbance (ataxia) | rel=r_associated | relid=0 | w=23
  3291. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:generalized spike-wave discharges see on eeg
    n1=méningé (syndrome) | n2=en:generalized spike-wave discharges see on eeg | rel=r_associated | relid=0 | w=23
  3292. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:generalized tonic-clonic seizures on awakening
    n1=méningé (syndrome) | n2=en:generalized tonic-clonic seizures on awakening | rel=r_associated | relid=0 | w=23
  3293. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:gliosis (patient a)
    n1=méningé (syndrome) | n2=en:gliosis (patient a) | rel=r_associated | relid=0 | w=23
  3294. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:global brain atrophy
    n1=méningé (syndrome) | n2=en:global brain atrophy | rel=r_associated | relid=0 | w=23
  3295. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:global developmental delay if untreated
    n1=méningé (syndrome) | n2=en:global developmental delay if untreated | rel=r_associated | relid=0 | w=23
  3296. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:global hypotonia
    n1=méningé (syndrome) | n2=en:global hypotonia | rel=r_associated | relid=0 | w=23
  3297. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:global reduction in cerebral blood flow on pet scan
    n1=méningé (syndrome) | n2=en:global reduction in cerebral blood flow on pet scan | rel=r_associated | relid=0 | w=23
  3298. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:grand mal seizure
    n1=méningé (syndrome) | n2=en:grand mal seizure | rel=r_associated | relid=0 | w=23
  3299. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:gray matter appears relatively unaffected
    n1=méningé (syndrome) | n2=en:gray matter appears relatively unaffected | rel=r_associated | relid=0 | w=23
  3300. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hallucinations (rare)
    n1=méningé (syndrome) | n2=en:hallucinations (rare) | rel=r_associated | relid=0 | w=23
  3301. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hand tremor (in some patients)
    n1=méningé (syndrome) | n2=en:hand tremor (in some patients) | rel=r_associated | relid=0 | w=23
  3302. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:high pain threshold
    n1=méningé (syndrome) | n2=en:high pain threshold | rel=r_associated | relid=0 | w=23
  3303. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:high signal intensities in periventricular white matter
    n1=méningé (syndrome) | n2=en:high signal intensities in periventricular white matter | rel=r_associated | relid=0 | w=23
  3304. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:holoprosencephaly (variable)
    n1=méningé (syndrome) | n2=en:holoprosencephaly (variable) | rel=r_associated | relid=0 | w=23
  3305. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hydrocephalus, normal pressure
    n1=méningé (syndrome) | n2=en:hydrocephalus, normal pressure | rel=r_associated | relid=0 | w=23
  3306. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hyperexplexia
    n1=méningé (syndrome) | n2=en:hyperexplexia | rel=r_associated | relid=0 | w=23
  3307. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypermotor automatisms
    n1=méningé (syndrome) | n2=en:hypermotor automatisms | rel=r_associated | relid=0 | w=23
  3308. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hyperreflexia proximally
    n1=méningé (syndrome) | n2=en:hyperreflexia proximally | rel=r_associated | relid=0 | w=23
  3309. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hyperreflexia, lower limbs, mild
    n1=méningé (syndrome) | n2=en:hyperreflexia, lower limbs, mild | rel=r_associated | relid=0 | w=23
  3310. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypersensitive to stimuli
    n1=méningé (syndrome) | n2=en:hypersensitive to stimuli | rel=r_associated | relid=0 | w=23
  3311. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypertonia
    n1=méningé (syndrome) | n2=en:hypertonia | rel=r_associated | relid=0 | w=23
  3312. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypertonia in early stage
    n1=méningé (syndrome) | n2=en:hypertonia in early stage | rel=r_associated | relid=0 | w=23
  3313. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypertonia, mild, transient
    n1=méningé (syndrome) | n2=en:hypertonia, mild, transient | rel=r_associated | relid=0 | w=23
  3314. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypoglycemia-related seizures
    n1=méningé (syndrome) | n2=en:hypoglycemia-related seizures | rel=r_associated | relid=0 | w=23
  3315. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypoglycemic seizures
    n1=méningé (syndrome) | n2=en:hypoglycemic seizures | rel=r_associated | relid=0 | w=23
  3316. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypometabolism of the frontal lobe and thalamic regions
    n1=méningé (syndrome) | n2=en:hypometabolism of the frontal lobe and thalamic regions | rel=r_associated | relid=0 | w=23
  3317. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypoplastic or absent middle cerebellar peduncles
    n1=méningé (syndrome) | n2=en:hypoplastic or absent middle cerebellar peduncles | rel=r_associated | relid=0 | w=23
  3318. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypotonia at birth
    n1=méningé (syndrome) | n2=en:hypotonia at birth | rel=r_associated | relid=0 | w=23
  3319. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypotonicity (in some patients)
    n1=méningé (syndrome) | n2=en:hypotonicity (in some patients) | rel=r_associated | relid=0 | w=23
  3320. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:hypsarrhythmia seen on eeg
    n1=méningé (syndrome) | n2=en:hypsarrhythmia seen on eeg | rel=r_associated | relid=0 | w=23
  3321. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:imbalance
    n1=méningé (syndrome) | n2=en:imbalance | rel=r_associated | relid=0 | w=23
  3322. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:impaired balance
    n1=méningé (syndrome) | n2=en:impaired balance | rel=r_associated | relid=0 | w=23
  3323. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:impaired balance (2 patients)
    n1=méningé (syndrome) | n2=en:impaired balance (2 patients) | rel=r_associated | relid=0 | w=23
  3324. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:impaired executive function (in some patients)
    n1=méningé (syndrome) | n2=en:impaired executive function (in some patients) | rel=r_associated | relid=0 | w=23
  3325. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:impaired fine motor skills
    n1=méningé (syndrome) | n2=en:impaired fine motor skills | rel=r_associated | relid=0 | w=23
  3326. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:impaired tandem gait
    n1=méningé (syndrome) | n2=en:impaired tandem gait | rel=r_associated | relid=0 | w=23
  3327. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:impaired vertical visual pursuit
    n1=méningé (syndrome) | n2=en:impaired vertical visual pursuit | rel=r_associated | relid=0 | w=23
  3328. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:impaired vibration sensation in the lower limbs
    n1=méningé (syndrome) | n2=en:impaired vibration sensation in the lower limbs | rel=r_associated | relid=0 | w=23
  3329. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:impaired visuospatial skills
    n1=méningé (syndrome) | n2=en:impaired visuospatial skills | rel=r_associated | relid=0 | w=23
  3330. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:inability to reach
    n1=méningé (syndrome) | n2=en:inability to reach | rel=r_associated | relid=0 | w=23
  3331. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:inability to run (in some patients)
    n1=méningé (syndrome) | n2=en:inability to run (in some patients) | rel=r_associated | relid=0 | w=23
  3332. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:inability to sit or walk independently
    n1=méningé (syndrome) | n2=en:inability to sit or walk independently | rel=r_associated | relid=0 | w=23
  3333. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:inability to stand on toes
    n1=méningé (syndrome) | n2=en:inability to stand on toes | rel=r_associated | relid=0 | w=23
  3334. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:increased deep tendon reflexes (if left untreated)
    n1=méningé (syndrome) | n2=en:increased deep tendon reflexes (if left untreated) | rel=r_associated | relid=0 | w=23
  3335. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:increased intracranial pressure preoperatively (in some patients)
    n1=méningé (syndrome) | n2=en:increased intracranial pressure preoperatively (in some patients) | rel=r_associated | relid=0 | w=23
  3336. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:increased startle response
    n1=méningé (syndrome) | n2=en:increased startle response | rel=r_associated | relid=0 | w=23
  3337. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:infantile nystagmus
    n1=méningé (syndrome) | n2=en:infantile nystagmus | rel=r_associated | relid=0 | w=23
  3338. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:infarction
    n1=méningé (syndrome) | n2=en:infarction | rel=r_associated | relid=0 | w=23
  3339. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:inferior olivary nuclei show fetal pattern
    n1=méningé (syndrome) | n2=en:inferior olivary nuclei show fetal pattern | rel=r_associated | relid=0 | w=23
  3340. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intellectual disability, mild (uncommon)
    n1=méningé (syndrome) | n2=en:intellectual disability, mild (uncommon) | rel=r_associated | relid=0 | w=23
  3341. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intellectual disability, moderate (in some patients)
    n1=méningé (syndrome) | n2=en:intellectual disability, moderate (in some patients) | rel=r_associated | relid=0 | w=23
  3342. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intellectual disability, moderate to severe
    n1=méningé (syndrome) | n2=en:intellectual disability, moderate to severe | rel=r_associated | relid=0 | w=23
  3343. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intellectual function may be high in milder cases
    n1=méningé (syndrome) | n2=en:intellectual function may be high in milder cases | rel=r_associated | relid=0 | w=23
  3344. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intention tremor (1 patient)
    n1=méningé (syndrome) | n2=en:intention tremor (1 patient) | rel=r_associated | relid=0 | w=23
  3345. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intention tremor in those who survive
    n1=méningé (syndrome) | n2=en:intention tremor in those who survive | rel=r_associated | relid=0 | w=23
  3346. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:interhemispheric lipoma
    n1=méningé (syndrome) | n2=en:interhemispheric lipoma | rel=r_associated | relid=0 | w=23
  3347. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:interosseus muscle atrophy
    n1=méningé (syndrome) | n2=en:interosseus muscle atrophy | rel=r_associated | relid=0 | w=23
  3348. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intracranial calcification by x-ray or ct
    n1=méningé (syndrome) | n2=en:intracranial calcification by x-ray or ct | rel=r_associated | relid=0 | w=23
  3349. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intracranial calcifications (in some patients)
    n1=méningé (syndrome) | n2=en:intracranial calcifications (in some patients) | rel=r_associated | relid=0 | w=23
  3350. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intracranial cysts
    n1=méningé (syndrome) | n2=en:intracranial cysts | rel=r_associated | relid=0 | w=23
  3351. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:intraparenchymal brain hemorrhage, multifocal
    n1=méningé (syndrome) | n2=en:intraparenchymal brain hemorrhage, multifocal | rel=r_associated | relid=0 | w=23
  3352. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:involuntary movements, asymmetric
    n1=méningé (syndrome) | n2=en:involuntary movements, asymmetric | rel=r_associated | relid=0 | w=23
  3353. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:iron accumulation in the basal ganglia seen on mri
    n1=méningé (syndrome) | n2=en:iron accumulation in the basal ganglia seen on mri | rel=r_associated | relid=0 | w=23
  3354. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:isolated absence of pain sensation
    n1=méningé (syndrome) | n2=en:isolated absence of pain sensation | rel=r_associated | relid=0 | w=23
  3355. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:lack of head or postural control (in severe cases)
    n1=méningé (syndrome) | n2=en:lack of head or postural control (in severe cases) | rel=r_associated | relid=0 | w=23
  3356. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:lack of motor milestones
    n1=méningé (syndrome) | n2=en:lack of motor milestones | rel=r_associated | relid=0 | w=23
  3357. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:lack of speech development (some patients)
    n1=méningé (syndrome) | n2=en:lack of speech development (some patients) | rel=r_associated | relid=0 | w=23
  3358. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:language delay
    n1=méningé (syndrome) | n2=en:language delay | rel=r_associated | relid=0 | w=23
  3359. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:language delay/disorder
    n1=méningé (syndrome) | n2=en:language delay/disorder | rel=r_associated | relid=0 | w=23
  3360. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:large basal ganglia
    n1=méningé (syndrome) | n2=en:large basal ganglia | rel=r_associated | relid=0 | w=23
  3361. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:late ambulation
    n1=méningé (syndrome) | n2=en:late ambulation | rel=r_associated | relid=0 | w=23
  3362. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:learning difficulties (in some patients)
    n1=méningé (syndrome) | n2=en:learning difficulties (in some patients) | rel=r_associated | relid=0 | w=23
  3363. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:learning disabilities (in some)
    n1=méningé (syndrome) | n2=en:learning disabilities (in some) | rel=r_associated | relid=0 | w=23
  3364. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:learning disabilities (major)
    n1=méningé (syndrome) | n2=en:learning disabilities (major) | rel=r_associated | relid=0 | w=23
  3365. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:learning disability (90% patients)
    n1=méningé (syndrome) | n2=en:learning disability (90% patients) | rel=r_associated | relid=0 | w=23
  3366. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:lesions show signal increase on t2- and signal decrease on t1-weighted images
    n1=méningé (syndrome) | n2=en:lesions show signal increase on t2- and signal decrease on t1-weighted images | rel=r_associated | relid=0 | w=23
  3367. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:lewy bodies throughout the brain
    n1=méningé (syndrome) | n2=en:lewy bodies throughout the brain | rel=r_associated | relid=0 | w=23
  3368. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:limb hypertonia (in some patients)
    n1=méningé (syndrome) | n2=en:limb hypertonia (in some patients) | rel=r_associated | relid=0 | w=23
  3369. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:limb muscle weakness (distal greater than proximal)
    n1=méningé (syndrome) | n2=en:limb muscle weakness (distal greater than proximal) | rel=r_associated | relid=0 | w=23
  3370. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:limited expressive language
    n1=méningé (syndrome) | n2=en:limited expressive language | rel=r_associated | relid=0 | w=23
  3371. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:lobar holoprosencephalies
    n1=méningé (syndrome) | n2=en:lobar holoprosencephalies | rel=r_associated | relid=0 | w=23
  3372. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:loss of ability to walk in first decade
    n1=méningé (syndrome) | n2=en:loss of ability to walk in first decade | rel=r_associated | relid=0 | w=23
  3373. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:loss of independent ambulation
    n1=méningé (syndrome) | n2=en:loss of independent ambulation | rel=r_associated | relid=0 | w=23
  3374. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:loss of myelin
    n1=méningé (syndrome) | n2=en:loss of myelin | rel=r_associated | relid=0 | w=23
  3375. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:loss of purkinje cells
    n1=méningé (syndrome) | n2=en:loss of purkinje cells | rel=r_associated | relid=0 | w=23
  3376. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:loss of speech (1 patient)
    n1=méningé (syndrome) | n2=en:loss of speech (1 patient) | rel=r_associated | relid=0 | w=23
  3377. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:low-normal intelligence
    n1=méningé (syndrome) | n2=en:low-normal intelligence | rel=r_associated | relid=0 | w=23
  3378. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:macroencephaly
    n1=méningé (syndrome) | n2=en:macroencephaly | rel=r_associated | relid=0 | w=23
  3379. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:malignant neoplasm of the meninges
    n1=méningé (syndrome) | n2=en:malignant neoplasm of the meninges | rel=r_associated | relid=0 | w=23
  3380. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:medulloblastoma with leptomeningeal spread
    n1=méningé (syndrome) | n2=en:medulloblastoma with leptomeningeal spread | rel=r_associated | relid=0 | w=23
  3381. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:memory impairment
    n1=méningé (syndrome) | n2=en:memory impairment | rel=r_associated | relid=0 | w=23
  3382. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental handicap
    n1=méningé (syndrome) | n2=en:mental handicap | rel=r_associated | relid=0 | w=23
  3383. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental impairment
    n1=méningé (syndrome) | n2=en:mental impairment | rel=r_associated | relid=0 | w=23
  3384. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation (about 40%)
    n1=méningé (syndrome) | n2=en:mental retardation (about 40%) | rel=r_associated | relid=0 | w=23
  3385. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation (average iq 51)
    n1=méningé (syndrome) | n2=en:mental retardation (average iq 51) | rel=r_associated | relid=0 | w=23
  3386. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation (if left untreated)
    n1=méningé (syndrome) | n2=en:mental retardation (if left untreated) | rel=r_associated | relid=0 | w=23
  3387. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation (in most patients)
    n1=méningé (syndrome) | n2=en:mental retardation (in most patients) | rel=r_associated | relid=0 | w=23
  3388. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation (reported in 1 family)
    n1=méningé (syndrome) | n2=en:mental retardation (reported in 1 family) | rel=r_associated | relid=0 | w=23
  3389. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation (some)
    n1=méningé (syndrome) | n2=en:mental retardation (some) | rel=r_associated | relid=0 | w=23
  3390. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation by age 30 years
    n1=méningé (syndrome) | n2=en:mental retardation by age 30 years | rel=r_associated | relid=0 | w=23
  3391. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation due to repeated episodes of hypoglycemia
    n1=méningé (syndrome) | n2=en:mental retardation due to repeated episodes of hypoglycemia | rel=r_associated | relid=0 | w=23
  3392. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation in 75%
    n1=méningé (syndrome) | n2=en:mental retardation in 75% | rel=r_associated | relid=0 | w=23
  3393. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation, in subgroup of patients
    n1=méningé (syndrome) | n2=en:mental retardation, in subgroup of patients | rel=r_associated | relid=0 | w=23
  3394. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation, moderate to severe (iq 35-50)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate to severe (iq 35-50) | rel=r_associated | relid=0 | w=23
  3395. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation, severe (if untreated)
    n1=méningé (syndrome) | n2=en:mental retardation, severe (if untreated) | rel=r_associated | relid=0 | w=23
  3396. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mental retardation, variable (in some patients)
    n1=méningé (syndrome) | n2=en:mental retardation, variable (in some patients) | rel=r_associated | relid=0 | w=23
  3397. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:migraine headaches (cvs+)
    n1=méningé (syndrome) | n2=en:migraine headaches (cvs+) | rel=r_associated | relid=0 | w=23
  3398. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:migrating clonic jerks (in some patients)
    n1=méningé (syndrome) | n2=en:migrating clonic jerks (in some patients) | rel=r_associated | relid=0 | w=23
  3399. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mild brain anomalies on mri (e.g., dilated ventricles) (in some patients)
    n1=méningé (syndrome) | n2=en:mild brain anomalies on mri (e.g., dilated ventricles) (in some patients) | rel=r_associated | relid=0 | w=23
  3400. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mild cognitive disorder
    n1=méningé (syndrome) | n2=en:mild cognitive disorder | rel=r_associated | relid=0 | w=23
  3401. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mild to severe mental retardation (24%)
    n1=méningé (syndrome) | n2=en:mild to severe mental retardation (24%) | rel=r_associated | relid=0 | w=23
  3402. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mildly delayed motor development due to vestibular dysfunction
    n1=méningé (syndrome) | n2=en:mildly delayed motor development due to vestibular dysfunction | rel=r_associated | relid=0 | w=23
  3403. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mitochondrial dna depletion in brain tissue
    n1=méningé (syndrome) | n2=en:mitochondrial dna depletion in brain tissue | rel=r_associated | relid=0 | w=23
  3404. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:moderate to severe hypotonia
    n1=méningé (syndrome) | n2=en:moderate to severe hypotonia | rel=r_associated | relid=0 | w=23
  3405. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:monotonous speech
    n1=méningé (syndrome) | n2=en:monotonous speech | rel=r_associated | relid=0 | w=23
  3406. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:motor deterioration in second decade
    n1=méningé (syndrome) | n2=en:motor deterioration in second decade | rel=r_associated | relid=0 | w=23
  3407. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:motor neuron disease (less common)
    n1=méningé (syndrome) | n2=en:motor neuron disease (less common) | rel=r_associated | relid=0 | w=23
  3408. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mri shows cerebral atrophy
    n1=méningé (syndrome) | n2=en:mri shows cerebral atrophy | rel=r_associated | relid=0 | w=23
  3409. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mri shows diffuse white matter hyperintensities on t2-weighted imaging
    n1=méningé (syndrome) | n2=en:mri shows diffuse white matter hyperintensities on t2-weighted imaging | rel=r_associated | relid=0 | w=23
  3410. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:mri shows t2-weighted signals in the basal ganglia
    n1=méningé (syndrome) | n2=en:mri shows t2-weighted signals in the basal ganglia | rel=r_associated | relid=0 | w=23
  3411. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:muscle weakness of limb
    n1=méningé (syndrome) | n2=en:muscle weakness of limb | rel=r_associated | relid=0 | w=23
  3412. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:muscle weakness, distal, upper and lower
    n1=méningé (syndrome) | n2=en:muscle weakness, distal, upper and lower | rel=r_associated | relid=0 | w=23
  3413. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:muscular hypotonia of the trunk
    n1=méningé (syndrome) | n2=en:muscular hypotonia of the trunk | rel=r_associated | relid=0 | w=23
  3414. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:myelination defects (type ii)
    n1=méningé (syndrome) | n2=en:myelination defects (type ii) | rel=r_associated | relid=0 | w=23
  3415. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:myoclonic seizures may occur
    n1=méningé (syndrome) | n2=en:myoclonic seizures may occur | rel=r_associated | relid=0 | w=23
  3416. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:neonatal/early-infantile onset encephalopathy
    n1=méningé (syndrome) | n2=en:neonatal/early-infantile onset encephalopathy | rel=r_associated | relid=0 | w=23
  3417. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:neuronal loss in the hippocampus
    n1=méningé (syndrome) | n2=en:neuronal loss in the hippocampus | rel=r_associated | relid=0 | w=23
  3418. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:neuronal loss in the inferior olives
    n1=méningé (syndrome) | n2=en:neuronal loss in the inferior olives | rel=r_associated | relid=0 | w=23
  3419. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:neuropathologic examination shows calcification of the small brain vessels
    n1=méningé (syndrome) | n2=en:neuropathologic examination shows calcification of the small brain vessels | rel=r_associated | relid=0 | w=23
  3420. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:neurophysiologic abnormalities (eeg, vep, sep)
    n1=méningé (syndrome) | n2=en:neurophysiologic abnormalities (eeg, vep, sep) | rel=r_associated | relid=0 | w=23
  3421. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:neurophysiologic studies show evidence of denervation and renervation
    n1=méningé (syndrome) | n2=en:neurophysiologic studies show evidence of denervation and renervation | rel=r_associated | relid=0 | w=23
  3422. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:never learn to walk (some patients)
    n1=méningé (syndrome) | n2=en:never learn to walk (some patients) | rel=r_associated | relid=0 | w=23
  3423. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:no cerebellar vermis aplasia/hypoplasia
    n1=méningé (syndrome) | n2=en:no cerebellar vermis aplasia/hypoplasia | rel=r_associated | relid=0 | w=23
  3424. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:no head control
    n1=méningé (syndrome) | n2=en:no head control | rel=r_associated | relid=0 | w=23
  3425. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:no language
    n1=méningé (syndrome) | n2=en:no language | rel=r_associated | relid=0 | w=23
  3426. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:nocturnal seizures
    n1=méningé (syndrome) | n2=en:nocturnal seizures | rel=r_associated | relid=0 | w=23
  3427. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:nonprogressive cerebellar ataxia
    n1=méningé (syndrome) | n2=en:nonprogressive cerebellar ataxia | rel=r_associated | relid=0 | w=23
  3428. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:nonverbal (in some patients)
    n1=méningé (syndrome) | n2=en:nonverbal (in some patients) | rel=r_associated | relid=0 | w=23
  3429. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:normal cognition (1 patient)
    n1=méningé (syndrome) | n2=en:normal cognition (1 patient) | rel=r_associated | relid=0 | w=23
  3430. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:normal neuromuscular studies
    n1=méningé (syndrome) | n2=en:normal neuromuscular studies | rel=r_associated | relid=0 | w=23
  3431. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:obstruction of the foramen of monro (variable)
    n1=méningé (syndrome) | n2=en:obstruction of the foramen of monro (variable) | rel=r_associated | relid=0 | w=23
  3432. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:occipital meningocele
    n1=méningé (syndrome) | n2=en:occipital meningocele | rel=r_associated | relid=0 | w=23
  3433. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:only some achieve rolling or sitting
    n1=méningé (syndrome) | n2=en:only some achieve rolling or sitting | rel=r_associated | relid=0 | w=23
  3434. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:open sylvian fissures
    n1=méningé (syndrome) | n2=en:open sylvian fissures | rel=r_associated | relid=0 | w=23
  3435. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:opisthotonic posturing
    n1=méningé (syndrome) | n2=en:opisthotonic posturing | rel=r_associated | relid=0 | w=23
  3436. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:orofacial dystonia
    n1=méningé (syndrome) | n2=en:orofacial dystonia | rel=r_associated | relid=0 | w=23
  3437. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:pachygyria (1 patient)
    n1=méningé (syndrome) | n2=en:pachygyria (1 patient) | rel=r_associated | relid=0 | w=23
  3438. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:pain
    n1=méningé (syndrome) | n2=en:pain | rel=r_associated | relid=0 | w=23
  3439. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:paradoxical cerebral emboli
    n1=méningé (syndrome) | n2=en:paradoxical cerebral emboli | rel=r_associated | relid=0 | w=23
  3440. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:parasitology
    n1=méningé (syndrome) | n2=en:parasitology | rel=r_associated | relid=0 | w=23
  3441. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:paresthesia
    n1=méningé (syndrome) | n2=en:paresthesia | rel=r_associated | relid=0 | w=23
  3442. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:parkinsonism has been described in 1 family
    n1=méningé (syndrome) | n2=en:parkinsonism has been described in 1 family | rel=r_associated | relid=0 | w=23
  3443. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:parkinsonism, l-dopa responsive
    n1=méningé (syndrome) | n2=en:parkinsonism, l-dopa responsive | rel=r_associated | relid=0 | w=23
  3444. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:partial empty sella turcica
    n1=méningé (syndrome) | n2=en:partial empty sella turcica | rel=r_associated | relid=0 | w=23
  3445. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:partial migrating seizures seen on eeg (in some patients)
    n1=méningé (syndrome) | n2=en:partial migrating seizures seen on eeg (in some patients) | rel=r_associated | relid=0 | w=23
  3446. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:patients achieve ambulation
    n1=méningé (syndrome) | n2=en:patients achieve ambulation | rel=r_associated | relid=0 | w=23
  3447. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:peak frequency of vomiting every 10 to 15 minutes
    n1=méningé (syndrome) | n2=en:peak frequency of vomiting every 10 to 15 minutes | rel=r_associated | relid=0 | w=23
  3448. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:peculiar gait (if left untreated)
    n1=méningé (syndrome) | n2=en:peculiar gait (if left untreated) | rel=r_associated | relid=0 | w=23
  3449. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:peripheral hypertonia
    n1=méningé (syndrome) | n2=en:peripheral hypertonia | rel=r_associated | relid=0 | w=23
  3450. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:peripheral sensory neuropathy
    n1=méningé (syndrome) | n2=en:peripheral sensory neuropathy | rel=r_associated | relid=0 | w=23
  3451. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:periventricular leukomalacia
    n1=méningé (syndrome) | n2=en:periventricular leukomalacia | rel=r_associated | relid=0 | w=23
  3452. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:periventricular white matter changes
    n1=méningé (syndrome) | n2=en:periventricular white matter changes | rel=r_associated | relid=0 | w=23
  3453. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:phonophobia
    n1=méningé (syndrome) | n2=en:phonophobia | rel=r_associated | relid=0 | w=23
  3454. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:platybasia
    n1=méningé (syndrome) | n2=en:platybasia | rel=r_associated | relid=0 | w=23
  3455. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:polymicrogyria (rare)
    n1=méningé (syndrome) | n2=en:polymicrogyria (rare) | rel=r_associated | relid=0 | w=23
  3456. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:polymicrogyria, anterior to posterior gradient
    n1=méningé (syndrome) | n2=en:polymicrogyria, anterior to posterior gradient | rel=r_associated | relid=0 | w=23
  3457. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:polymicrogyria, most severe in the frontoparietal regions
    n1=méningé (syndrome) | n2=en:polymicrogyria, most severe in the frontoparietal regions | rel=r_associated | relid=0 | w=23
  3458. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:poor eye contact
    n1=méningé (syndrome) | n2=en:poor eye contact | rel=r_associated | relid=0 | w=23
  3459. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:poor language and speech development
    n1=méningé (syndrome) | n2=en:poor language and speech development | rel=r_associated | relid=0 | w=23
  3460. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:poor speech or no speech
    n1=méningé (syndrome) | n2=en:poor speech or no speech | rel=r_associated | relid=0 | w=23
  3461. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:porencephalic changes
    n1=méningé (syndrome) | n2=en:porencephalic changes | rel=r_associated | relid=0 | w=23
  3462. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:porencephalic cyst
    n1=méningé (syndrome) | n2=en:porencephalic cyst | rel=r_associated | relid=0 | w=23
  3463. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:primarily affects distal lower limbs
    n1=méningé (syndrome) | n2=en:primarily affects distal lower limbs | rel=r_associated | relid=0 | w=23
  3464. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:primary melanocytic lesion of meninges
    n1=méningé (syndrome) | n2=en:primary melanocytic lesion of meninges | rel=r_associated | relid=0 | w=23
  3465. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:primitive reflexes (palmomental, snout, glabellar)
    n1=méningé (syndrome) | n2=en:primitive reflexes (palmomental, snout, glabellar) | rel=r_associated | relid=0 | w=23
  3466. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:progression to tetraplegia and decerebrate state
    n1=méningé (syndrome) | n2=en:progression to tetraplegia and decerebrate state | rel=r_associated | relid=0 | w=23
  3467. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:progressive cns degeneration
    n1=méningé (syndrome) | n2=en:progressive cns degeneration | rel=r_associated | relid=0 | w=23
  3468. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:progressive ventriculomegaly
    n1=méningé (syndrome) | n2=en:progressive ventriculomegaly | rel=r_associated | relid=0 | w=23
  3469. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:psychomotor delay (in one family)
    n1=méningé (syndrome) | n2=en:psychomotor delay (in one family) | rel=r_associated | relid=0 | w=23
  3470. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:psychomotor regression (in milder cases)
    n1=méningé (syndrome) | n2=en:psychomotor regression (in milder cases) | rel=r_associated | relid=0 | w=23
  3471. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:psychomotor regression (in some patients)
    n1=méningé (syndrome) | n2=en:psychomotor regression (in some patients) | rel=r_associated | relid=0 | w=23
  3472. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:psychomotor retardation (in 1 patient)
    n1=méningé (syndrome) | n2=en:psychomotor retardation (in 1 patient) | rel=r_associated | relid=0 | w=23
  3473. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:psychomotor retardation in those that survive
    n1=méningé (syndrome) | n2=en:psychomotor retardation in those that survive | rel=r_associated | relid=0 | w=23
  3474. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:psychomotor retardation, mild to moderate
    n1=méningé (syndrome) | n2=en:psychomotor retardation, mild to moderate | rel=r_associated | relid=0 | w=23
  3475. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:psychomotor retardation, moderate
    n1=méningé (syndrome) | n2=en:psychomotor retardation, moderate | rel=r_associated | relid=0 | w=23
  3476. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:psychomotor retardation, variable
    n1=méningé (syndrome) | n2=en:psychomotor retardation, variable | rel=r_associated | relid=0 | w=23
  3477. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:pulsating quality
    n1=méningé (syndrome) | n2=en:pulsating quality | rel=r_associated | relid=0 | w=23
  3478. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:putamen atrophy
    n1=méningé (syndrome) | n2=en:putamen atrophy | rel=r_associated | relid=0 | w=23
  3479. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:pyramidal sign
    n1=méningé (syndrome) | n2=en:pyramidal sign | rel=r_associated | relid=0 | w=23
  3480. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:pyramidal symptoms
    n1=méningé (syndrome) | n2=en:pyramidal symptoms | rel=r_associated | relid=0 | w=23
  3481. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:pyramidal tetraparesis
    n1=méningé (syndrome) | n2=en:pyramidal tetraparesis | rel=r_associated | relid=0 | w=23
  3482. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:quadriplegia
    n1=méningé (syndrome) | n2=en:quadriplegia | rel=r_associated | relid=0 | w=23
  3483. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:quadriplegia, episodic
    n1=méningé (syndrome) | n2=en:quadriplegia, episodic | rel=r_associated | relid=0 | w=23
  3484. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:rapid complete resolution of symptoms
    n1=méningé (syndrome) | n2=en:rapid complete resolution of symptoms | rel=r_associated | relid=0 | w=23
  3485. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:rapid onset
    n1=méningé (syndrome) | n2=en:rapid onset | rel=r_associated | relid=0 | w=23
  3486. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:recurrent bacterial meningitis
    n1=méningé (syndrome) | n2=en:recurrent bacterial meningitis | rel=r_associated | relid=0 | w=23
  3487. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:recurrent encephalopathy
    n1=méningé (syndrome) | n2=en:recurrent encephalopathy | rel=r_associated | relid=0 | w=23
  3488. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:recurrent meningitis
    n1=méningé (syndrome) | n2=en:recurrent meningitis | rel=r_associated | relid=0 | w=23
  3489. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:recurrent subcortical infarcts (strokes)
    n1=méningé (syndrome) | n2=en:recurrent subcortical infarcts (strokes) | rel=r_associated | relid=0 | w=23
  3490. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:reduced concentration span
    n1=méningé (syndrome) | n2=en:reduced concentration span | rel=r_associated | relid=0 | w=23
  3491. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:reduced white matter
    n1=méningé (syndrome) | n2=en:reduced white matter | rel=r_associated | relid=0 | w=23
  3492. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:relative preservation of the cerebellar folia
    n1=méningé (syndrome) | n2=en:relative preservation of the cerebellar folia | rel=r_associated | relid=0 | w=23
  3493. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:rigidity (juvenile form)
    n1=méningé (syndrome) | n2=en:rigidity (juvenile form) | rel=r_associated | relid=0 | w=23
  3494. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:rigidity of limbs
    n1=méningé (syndrome) | n2=en:rigidity of limbs | rel=r_associated | relid=0 | w=23
  3495. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:secondary motor complications develop in 50% of those on levodopa therapy
    n1=méningé (syndrome) | n2=en:secondary motor complications develop in 50% of those on levodopa therapy | rel=r_associated | relid=0 | w=23
  3496. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:see juvenile myoclonic epilepsy (606904)
    n1=méningé (syndrome) | n2=en:see juvenile myoclonic epilepsy (606904) | rel=r_associated | relid=0 | w=23
  3497. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:seizure disorder
    n1=méningé (syndrome) | n2=en:seizure disorder | rel=r_associated | relid=0 | w=23
  3498. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:seizures, generalized, may occur
    n1=méningé (syndrome) | n2=en:seizures, generalized, may occur | rel=r_associated | relid=0 | w=23
  3499. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:seizures, intractable
    n1=méningé (syndrome) | n2=en:seizures, intractable | rel=r_associated | relid=0 | w=23
  3500. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:seizures, intractable (in 1 family)
    n1=méningé (syndrome) | n2=en:seizures, intractable (in 1 family) | rel=r_associated | relid=0 | w=23
  3501. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:seizures, recurrent, refractory
    n1=méningé (syndrome) | n2=en:seizures, recurrent, refractory | rel=r_associated | relid=0 | w=23
  3502. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:self-injurious behavior, median onset age 2 years
    n1=méningé (syndrome) | n2=en:self-injurious behavior, median onset age 2 years | rel=r_associated | relid=0 | w=23
  3503. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:shuffling gaits
    n1=méningé (syndrome) | n2=en:shuffling gaits | rel=r_associated | relid=0 | w=23
  3504. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:sleep apnea
    n1=méningé (syndrome) | n2=en:sleep apnea | rel=r_associated | relid=0 | w=23
  3505. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:slow gait
    n1=méningé (syndrome) | n2=en:slow gait | rel=r_associated | relid=0 | w=23
  3506. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:slowed background activity
    n1=méningé (syndrome) | n2=en:slowed background activity | rel=r_associated | relid=0 | w=23
  3507. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:slowing mental development by 1.5 to 3 years of age
    n1=méningé (syndrome) | n2=en:slowing mental development by 1.5 to 3 years of age | rel=r_associated | relid=0 | w=23
  3508. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:small brain size (some patients)
    n1=méningé (syndrome) | n2=en:small brain size (some patients) | rel=r_associated | relid=0 | w=23
  3509. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:small caudate
    n1=méningé (syndrome) | n2=en:small caudate | rel=r_associated | relid=0 | w=23
  3510. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:small cavum septum
    n1=méningé (syndrome) | n2=en:small cavum septum | rel=r_associated | relid=0 | w=23
  3511. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:small rotary component may be present
    n1=méningé (syndrome) | n2=en:small rotary component may be present | rel=r_associated | relid=0 | w=23
  3512. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:social and occupational deterioration
    n1=méningé (syndrome) | n2=en:social and occupational deterioration | rel=r_associated | relid=0 | w=23
  3513. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:some patients do not achieve ability to walk
    n1=méningé (syndrome) | n2=en:some patients do not achieve ability to walk | rel=r_associated | relid=0 | w=23
  3514. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:some patients may develop afebrile seizures later in life
    n1=méningé (syndrome) | n2=en:some patients may develop afebrile seizures later in life | rel=r_associated | relid=0 | w=23
  3515. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:some patients only achieve sitting
    n1=méningé (syndrome) | n2=en:some patients only achieve sitting | rel=r_associated | relid=0 | w=23
  3516. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:sparing of central white matter structures
    n1=méningé (syndrome) | n2=en:sparing of central white matter structures | rel=r_associated | relid=0 | w=23
  3517. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spastic diplegia (1 patient)
    n1=méningé (syndrome) | n2=en:spastic diplegia (1 patient) | rel=r_associated | relid=0 | w=23
  3518. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spastic diplegia, progressive
    n1=méningé (syndrome) | n2=en:spastic diplegia, progressive | rel=r_associated | relid=0 | w=23
  3519. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spastic gait
    n1=méningé (syndrome) | n2=en:spastic gait | rel=r_associated | relid=0 | w=23
  3520. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spastic paralysis
    n1=méningé (syndrome) | n2=en:spastic paralysis | rel=r_associated | relid=0 | w=23
  3521. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spastic paraplegia, severe
    n1=méningé (syndrome) | n2=en:spastic paraplegia, severe | rel=r_associated | relid=0 | w=23
  3522. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spastic tetraparesis (in severe cases)
    n1=méningé (syndrome) | n2=en:spastic tetraparesis (in severe cases) | rel=r_associated | relid=0 | w=23
  3523. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spastic tetraplegia (onset in the second decade)
    n1=méningé (syndrome) | n2=en:spastic tetraplegia (onset in the second decade) | rel=r_associated | relid=0 | w=23
  3524. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spastic-ataxic tetraparesis
    n1=méningé (syndrome) | n2=en:spastic-ataxic tetraparesis | rel=r_associated | relid=0 | w=23
  3525. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:speech delay (in all patients)
    n1=méningé (syndrome) | n2=en:speech delay (in all patients) | rel=r_associated | relid=0 | w=23
  3526. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:speech delay (in some patients)
    n1=méningé (syndrome) | n2=en:speech delay (in some patients) | rel=r_associated | relid=0 | w=23
  3527. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:speech difficulties (48%)
    n1=méningé (syndrome) | n2=en:speech difficulties (48%) | rel=r_associated | relid=0 | w=23
  3528. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:speech hesitancy
    n1=méningé (syndrome) | n2=en:speech hesitancy | rel=r_associated | relid=0 | w=23
  3529. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spina bifida (less common)
    n1=méningé (syndrome) | n2=en:spina bifida (less common) | rel=r_associated | relid=0 | w=23
  3530. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spinal cord atrophy (rare)
    n1=méningé (syndrome) | n2=en:spinal cord atrophy (rare) | rel=r_associated | relid=0 | w=23
  3531. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spinal muscular atrophy
    n1=méningé (syndrome) | n2=en:spinal muscular atrophy | rel=r_associated | relid=0 | w=23
  3532. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:spongiosis, mild
    n1=méningé (syndrome) | n2=en:spongiosis, mild | rel=r_associated | relid=0 | w=23
  3533. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:status epilepticus may occur
    n1=méningé (syndrome) | n2=en:status epilepticus may occur | rel=r_associated | relid=0 | w=23
  3534. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:stroke (rare)
    n1=méningé (syndrome) | n2=en:stroke (rare) | rel=r_associated | relid=0 | w=23
  3535. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:stroke (uncommon)
    n1=méningé (syndrome) | n2=en:stroke (uncommon) | rel=r_associated | relid=0 | w=23
  3536. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:structural changes in the temporal lobe
    n1=méningé (syndrome) | n2=en:structural changes in the temporal lobe | rel=r_associated | relid=0 | w=23
  3537. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:subcortical origin of the myoclonus based on neurophysiologic studies
    n1=méningé (syndrome) | n2=en:subcortical origin of the myoclonus based on neurophysiologic studies | rel=r_associated | relid=0 | w=23
  3538. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:symmetric ventriculomegaly
    n1=méningé (syndrome) | n2=en:symmetric ventriculomegaly | rel=r_associated | relid=0 | w=23
  3539. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:symmetrical progressive demyelination
    n1=méningé (syndrome) | n2=en:symmetrical progressive demyelination | rel=r_associated | relid=0 | w=23
  3540. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:t2-weighted hyperintensities in the supratentorial white matter seen on brain mri
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintensities in the supratentorial white matter seen on brain mri | rel=r_associated | relid=0 | w=23
  3541. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:tfg- and tdp43-positive intraneuronal inclusions in some sensory and motor spinal cord neurons
    n1=méningé (syndrome) | n2=en:tfg- and tdp43-positive intraneuronal inclusions in some sensory and motor spinal cord neurons | rel=r_associated | relid=0 | w=23
  3542. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:thick cortex
    n1=méningé (syndrome) | n2=en:thick cortex | rel=r_associated | relid=0 | w=23
  3543. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:thin brainstem
    n1=méningé (syndrome) | n2=en:thin brainstem | rel=r_associated | relid=0 | w=23
  3544. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:tongue movements, protrusions
    n1=méningé (syndrome) | n2=en:tongue movements, protrusions | rel=r_associated | relid=0 | w=23
  3545. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:transitional meningioma
    n1=méningé (syndrome) | n2=en:transitional meningioma | rel=r_associated | relid=0 | w=23
  3546. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:tremor (rare)
    n1=méningé (syndrome) | n2=en:tremor (rare) | rel=r_associated | relid=0 | w=23
  3547. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:tremor, postural (arms, tongue, head, legs and trunk)
    n1=méningé (syndrome) | n2=en:tremor, postural (arms, tongue, head, legs and trunk) | rel=r_associated | relid=0 | w=23
  3548. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:tremors, limb
    n1=méningé (syndrome) | n2=en:tremors, limb | rel=r_associated | relid=0 | w=23
  3549. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:trigeminal anesthesia
    n1=méningé (syndrome) | n2=en:trigeminal anesthesia | rel=r_associated | relid=0 | w=23
  3550. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:truncal titubation
    n1=méningé (syndrome) | n2=en:truncal titubation | rel=r_associated | relid=0 | w=23
  3551. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:unable to sit unsupported
    n1=méningé (syndrome) | n2=en:unable to sit unsupported | rel=r_associated | relid=0 | w=23
  3552. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:uncoordinated movements
    n1=méningé (syndrome) | n2=en:uncoordinated movements | rel=r_associated | relid=0 | w=23
  3553. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:unsteady gait due to muscle weakness
    n1=méningé (syndrome) | n2=en:unsteady gait due to muscle weakness | rel=r_associated | relid=0 | w=23
  3554. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:upper and lower neuron manifestations
    n1=méningé (syndrome) | n2=en:upper and lower neuron manifestations | rel=r_associated | relid=0 | w=23
  3555. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:upper body involvement
    n1=méningé (syndrome) | n2=en:upper body involvement | rel=r_associated | relid=0 | w=23
  3556. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:upper extremity action tremor
    n1=méningé (syndrome) | n2=en:upper extremity action tremor | rel=r_associated | relid=0 | w=23
  3557. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:upper limb dystonia
    n1=méningé (syndrome) | n2=en:upper limb dystonia | rel=r_associated | relid=0 | w=23
  3558. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:upper limb spasticity (some)
    n1=méningé (syndrome) | n2=en:upper limb spasticity (some) | rel=r_associated | relid=0 | w=23
  3559. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:upper limbs more often affected than lower limbs
    n1=méningé (syndrome) | n2=en:upper limbs more often affected than lower limbs | rel=r_associated | relid=0 | w=23
  3560. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:vacuolated neurons
    n1=méningé (syndrome) | n2=en:vacuolated neurons | rel=r_associated | relid=0 | w=23
  3561. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:variable mental retardation
    n1=méningé (syndrome) | n2=en:variable mental retardation | rel=r_associated | relid=0 | w=23
  3562. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:variable neurologic deterioration (likely result of hemophagocytic syndrome)
    n1=méningé (syndrome) | n2=en:variable neurologic deterioration (likely result of hemophagocytic syndrome) | rel=r_associated | relid=0 | w=23
  3563. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:variable outcome after acute illness
    n1=méningé (syndrome) | n2=en:variable outcome after acute illness | rel=r_associated | relid=0 | w=23
  3564. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:ventricles slightly enlarged
    n1=méningé (syndrome) | n2=en:ventricles slightly enlarged | rel=r_associated | relid=0 | w=23
  3565. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:viruses
    n1=méningé (syndrome) | n2=en:viruses | rel=r_associated | relid=0 | w=23
  3566. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:white matter alterations (in one family)
    n1=méningé (syndrome) | n2=en:white matter alterations (in one family) | rel=r_associated | relid=0 | w=23
  3567. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:white matter hyperintensities
    n1=méningé (syndrome) | n2=en:white matter hyperintensities | rel=r_associated | relid=0 | w=23
  3568. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:white matter hyperintensities in t2 imaging
    n1=méningé (syndrome) | n2=en:white matter hyperintensities in t2 imaging | rel=r_associated | relid=0 | w=23
  3569. méningé (syndrome) -- r_associated #0: 23 / 0.277 -> en:widespread brain calcifications
    n1=méningé (syndrome) | n2=en:widespread brain calcifications | rel=r_associated | relid=0 | w=23
  3570. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:abnormal 'hobby horse' ataxic gait
    n1=méningé (syndrome) | n2=en:abnormal 'hobby horse' ataxic gait | rel=r_associated | relid=0 | w=22
  3571. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:abnormal brain myelination
    n1=méningé (syndrome) | n2=en:abnormal brain myelination | rel=r_associated | relid=0 | w=22
  3572. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:abnormal cortical gyration
    n1=méningé (syndrome) | n2=en:abnormal cortical gyration | rel=r_associated | relid=0 | w=22
  3573. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:abnormal gait (67%)
    n1=méningé (syndrome) | n2=en:abnormal gait (67%) | rel=r_associated | relid=0 | w=22
  3574. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:abnormal gait due to muscle weakness
    n1=méningé (syndrome) | n2=en:abnormal gait due to muscle weakness | rel=r_associated | relid=0 | w=22
  3575. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:abnormal movement
    n1=méningé (syndrome) | n2=en:abnormal movement | rel=r_associated | relid=0 | w=22
  3576. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:abnormal sulci
    n1=méningé (syndrome) | n2=en:abnormal sulci | rel=r_associated | relid=0 | w=22
  3577. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:abnormal white matter signals, in the basal ganglia or cerebellum seen on brain mri
    n1=méningé (syndrome) | n2=en:abnormal white matter signals, in the basal ganglia or cerebellum seen on brain mri | rel=r_associated | relid=0 | w=22
  3578. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:absence of neurologic manifestations
    n1=méningé (syndrome) | n2=en:absence of neurologic manifestations | rel=r_associated | relid=0 | w=22
  3579. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:absent myelination of the brain (severe connatal form)
    n1=méningé (syndrome) | n2=en:absent myelination of the brain (severe connatal form) | rel=r_associated | relid=0 | w=22
  3580. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:absent or delayed speech development
    n1=méningé (syndrome) | n2=en:absent or delayed speech development | rel=r_associated | relid=0 | w=22
  3581. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:absent rem sleep
    n1=méningé (syndrome) | n2=en:absent rem sleep | rel=r_associated | relid=0 | w=22
  3582. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:action dystonia
    n1=méningé (syndrome) | n2=en:action dystonia | rel=r_associated | relid=0 | w=22
  3583. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:acute neurologic decompensation (in later-onset cases)
    n1=méningé (syndrome) | n2=en:acute neurologic decompensation (in later-onset cases) | rel=r_associated | relid=0 | w=22
  3584. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:acute neurologic deficits due to cerebrovascular disease
    n1=méningé (syndrome) | n2=en:acute neurologic deficits due to cerebrovascular disease | rel=r_associated | relid=0 | w=22
  3585. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:acute poliomyelitis
    n1=méningé (syndrome) | n2=en:acute poliomyelitis | rel=r_associated | relid=0 | w=22
  3586. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:agenesis of the corpus callosum (less common)
    n1=méningé (syndrome) | n2=en:agenesis of the corpus callosum (less common) | rel=r_associated | relid=0 | w=22
  3587. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:agenesis of the rostrum of corpus callosum
    n1=méningé (syndrome) | n2=en:agenesis of the rostrum of corpus callosum | rel=r_associated | relid=0 | w=22
  3588. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:akinesia
    n1=méningé (syndrome) | n2=en:akinesia | rel=r_associated | relid=0 | w=22
  3589. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:akinetic mutism (in some patients)
    n1=méningé (syndrome) | n2=en:akinetic mutism (in some patients) | rel=r_associated | relid=0 | w=22
  3590. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:alpha-b-crystallin expression in oligodendrocytes
    n1=méningé (syndrome) | n2=en:alpha-b-crystallin expression in oligodendrocytes | rel=r_associated | relid=0 | w=22
  3591. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:altered breathing patterns
    n1=méningé (syndrome) | n2=en:altered breathing patterns | rel=r_associated | relid=0 | w=22
  3592. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:ambulation difficulty
    n1=méningé (syndrome) | n2=en:ambulation difficulty | rel=r_associated | relid=0 | w=22
  3593. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:anosmia
    n1=méningé (syndrome) | n2=en:anosmia | rel=r_associated | relid=0 | w=22
  3594. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:anterior commissure not evident
    n1=méningé (syndrome) | n2=en:anterior commissure not evident | rel=r_associated | relid=0 | w=22
  3595. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:apoptotic neurons
    n1=méningé (syndrome) | n2=en:apoptotic neurons | rel=r_associated | relid=0 | w=22
  3596. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:aspects of radionuclide imaging
    n1=méningé (syndrome) | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=22
  3597. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:association between poor metabolizers (pm) and parkinson disease
    n1=méningé (syndrome) | n2=en:association between poor metabolizers (pm) and parkinson disease | rel=r_associated | relid=0 | w=22
  3598. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:asymmetric brain development
    n1=méningé (syndrome) | n2=en:asymmetric brain development | rel=r_associated | relid=0 | w=22
  3599. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:ataxia (in some patients)
    n1=méningé (syndrome) | n2=en:ataxia (in some patients) | rel=r_associated | relid=0 | w=22
  3600. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:ataxia, cerebellar (upper and lower limbs affected)
    n1=méningé (syndrome) | n2=en:ataxia, cerebellar (upper and lower limbs affected) | rel=r_associated | relid=0 | w=22
  3601. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:atlantoaxial instability
    n1=méningé (syndrome) | n2=en:atlantoaxial instability | rel=r_associated | relid=0 | w=22
  3602. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:atrophy of corpus callosum
    n1=méningé (syndrome) | n2=en:atrophy of corpus callosum | rel=r_associated | relid=0 | w=22
  3603. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:atrophy of the dentate nucleus
    n1=méningé (syndrome) | n2=en:atrophy of the dentate nucleus | rel=r_associated | relid=0 | w=22
  3604. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:atrophy, thin hemisphere
    n1=méningé (syndrome) | n2=en:atrophy, thin hemisphere | rel=r_associated | relid=0 | w=22
  3605. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:atrophy/degeneration involving the spinal cord
    n1=méningé (syndrome) | n2=en:atrophy/degeneration involving the spinal cord | rel=r_associated | relid=0 | w=22
  3606. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:attention deficit hyperactivity disorder
    n1=méningé (syndrome) | n2=en:attention deficit hyperactivity disorder | rel=r_associated | relid=0 | w=22
  3607. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:auditory, olfactory, and visual auras
    n1=méningé (syndrome) | n2=en:auditory, olfactory, and visual auras | rel=r_associated | relid=0 | w=22
  3608. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:aura
    n1=méningé (syndrome) | n2=en:aura | rel=r_associated | relid=0 | w=22
  3609. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:axial muscle stiffness, symmetric
    n1=méningé (syndrome) | n2=en:axial muscle stiffness, symmetric | rel=r_associated | relid=0 | w=22
  3610. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:axonal swelling of spinal nerve roots and cranial nerves
    n1=méningé (syndrome) | n2=en:axonal swelling of spinal nerve roots and cranial nerves | rel=r_associated | relid=0 | w=22
  3611. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:axonal swelling or thickening
    n1=méningé (syndrome) | n2=en:axonal swelling or thickening | rel=r_associated | relid=0 | w=22
  3612. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:ballooned neurons
    n1=méningé (syndrome) | n2=en:ballooned neurons | rel=r_associated | relid=0 | w=22
  3613. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:basal ganglia lucencies
    n1=méningé (syndrome) | n2=en:basal ganglia lucencies | rel=r_associated | relid=0 | w=22
  3614. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:bilateral perisylvian cortical malformations on mri
    n1=méningé (syndrome) | n2=en:bilateral perisylvian cortical malformations on mri | rel=r_associated | relid=0 | w=22
  3615. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:bradykinesia
    n1=méningé (syndrome) | n2=en:bradykinesia | rel=r_associated | relid=0 | w=22
  3616. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:brain imaging shows calcification of the dentate nucleus
    n1=méningé (syndrome) | n2=en:brain imaging shows calcification of the dentate nucleus | rel=r_associated | relid=0 | w=22
  3617. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:brain iron accumulation in the basal ganglia (in some patients)
    n1=méningé (syndrome) | n2=en:brain iron accumulation in the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=22
  3618. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:brain mri shows molar tooth sign
    n1=méningé (syndrome) | n2=en:brain mri shows molar tooth sign | rel=r_associated | relid=0 | w=22
  3619. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:brain mri shows proportionate pontocerebellar hypoplasia
    n1=méningé (syndrome) | n2=en:brain mri shows proportionate pontocerebellar hypoplasia | rel=r_associated | relid=0 | w=22
  3620. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:brain vascular anomalies (rare)
    n1=méningé (syndrome) | n2=en:brain vascular anomalies (rare) | rel=r_associated | relid=0 | w=22
  3621. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:bulbar dysfunction (juvenile-onset, less common)
    n1=méningé (syndrome) | n2=en:bulbar dysfunction (juvenile-onset, less common) | rel=r_associated | relid=0 | w=22
  3622. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:calcifications of cerebral ventricles
    n1=méningé (syndrome) | n2=en:calcifications of cerebral ventricles | rel=r_associated | relid=0 | w=22
  3623. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cataplexy, paroxysmal weakness or paralysis
    n1=méningé (syndrome) | n2=en:cataplexy, paroxysmal weakness or paralysis | rel=r_associated | relid=0 | w=22
  3624. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:caudate nuclei atrophy
    n1=méningé (syndrome) | n2=en:caudate nuclei atrophy | rel=r_associated | relid=0 | w=22
  3625. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:central nervous system
    n1=méningé (syndrome) | n2=en:central nervous system | rel=r_associated | relid=0 | w=22
  3626. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:central nervous system malformations (40%)
    n1=méningé (syndrome) | n2=en:central nervous system malformations (40%) | rel=r_associated | relid=0 | w=22
  3627. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:central nervous system part
    n1=méningé (syndrome) | n2=en:central nervous system part | rel=r_associated | relid=0 | w=22
  3628. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar ataxia (rare)
    n1=méningé (syndrome) | n2=en:cerebellar ataxia (rare) | rel=r_associated | relid=0 | w=22
  3629. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar atrophy (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy (reported in 1 patient) | rel=r_associated | relid=0 | w=22
  3630. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar atrophy, progressive
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, progressive | rel=r_associated | relid=0 | w=22
  3631. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar cortex shows normal layers
    n1=méningé (syndrome) | n2=en:cerebellar cortex shows normal layers | rel=r_associated | relid=0 | w=22
  3632. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar dysplasia
    n1=méningé (syndrome) | n2=en:cerebellar dysplasia | rel=r_associated | relid=0 | w=22
  3633. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar hemangioblastoma
    n1=méningé (syndrome) | n2=en:cerebellar hemangioblastoma | rel=r_associated | relid=0 | w=22
  3634. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar herniation (rare)
    n1=méningé (syndrome) | n2=en:cerebellar herniation (rare) | rel=r_associated | relid=0 | w=22
  3635. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar hypoplasia (in most patients)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (in most patients) | rel=r_associated | relid=0 | w=22
  3636. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar hypoplasia (in some patients)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (in some patients) | rel=r_associated | relid=0 | w=22
  3637. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar hypoplasia (seen in recessive form)
    n1=méningé (syndrome) | n2=en:cerebellar hypoplasia (seen in recessive form) | rel=r_associated | relid=0 | w=22
  3638. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellar neuronal loss
    n1=méningé (syndrome) | n2=en:cerebellar neuronal loss | rel=r_associated | relid=0 | w=22
  3639. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebellum
    n1=méningé (syndrome) | n2=en:cerebellum | rel=r_associated | relid=0 | w=22
  3640. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebral atrophy (1 patient)
    n1=méningé (syndrome) | n2=en:cerebral atrophy (1 patient) | rel=r_associated | relid=0 | w=22
  3641. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebral atrophy, progressive, from anterior to posterior
    n1=méningé (syndrome) | n2=en:cerebral atrophy, progressive, from anterior to posterior | rel=r_associated | relid=0 | w=22
  3642. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebral atrophy, severe
    n1=méningé (syndrome) | n2=en:cerebral atrophy, severe | rel=r_associated | relid=0 | w=22
  3643. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebral calcification
    n1=méningé (syndrome) | n2=en:cerebral calcification | rel=r_associated | relid=0 | w=22
  3644. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebral cortical and cerebellar atrophy (patient a)
    n1=méningé (syndrome) | n2=en:cerebral cortical and cerebellar atrophy (patient a) | rel=r_associated | relid=0 | w=22
  3645. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebral demyelination and inflammation
    n1=méningé (syndrome) | n2=en:cerebral demyelination and inflammation | rel=r_associated | relid=0 | w=22
  3646. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebral hemorrhage
    n1=méningé (syndrome) | n2=en:cerebral hemorrhage | rel=r_associated | relid=0 | w=22
  3647. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebral infarction dandy-walker malformation
    n1=méningé (syndrome) | n2=en:cerebral infarction dandy-walker malformation | rel=r_associated | relid=0 | w=22
  3648. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebrospinal fluid glucose decreased
    n1=méningé (syndrome) | n2=en:cerebrospinal fluid glucose decreased | rel=r_associated | relid=0 | w=22
  3649. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebrospinal fluid may show decreased levels of homovanillic acid (hva)
    n1=méningé (syndrome) | n2=en:cerebrospinal fluid may show decreased levels of homovanillic acid (hva) | rel=r_associated | relid=0 | w=22
  3650. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cerebrovascular accident
    n1=méningé (syndrome) | n2=en:cerebrovascular accident | rel=r_associated | relid=0 | w=22
  3651. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:chemical aspects
    n1=méningé (syndrome) | n2=en:chemical aspects | rel=r_associated | relid=0 | w=22
  3652. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:chorea
    n1=méningé (syndrome) | n2=en:chorea | rel=r_associated | relid=0 | w=22
  3653. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:chorea (in some patients)
    n1=méningé (syndrome) | n2=en:chorea (in some patients) | rel=r_associated | relid=0 | w=22
  3654. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:choreoathetosis (in some patients)
    n1=méningé (syndrome) | n2=en:choreoathetosis (in some patients) | rel=r_associated | relid=0 | w=22
  3655. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:choroid plexus cyst
    n1=méningé (syndrome) | n2=en:choroid plexus cyst | rel=r_associated | relid=0 | w=22
  3656. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:coarse tremors
    n1=méningé (syndrome) | n2=en:coarse tremors | rel=r_associated | relid=0 | w=22
  3657. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cobblestone lissencephaly, posterior frontal and parietal regions
    n1=méningé (syndrome) | n2=en:cobblestone lissencephaly, posterior frontal and parietal regions | rel=r_associated | relid=0 | w=22
  3658. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cognitive decline (later in life)
    n1=méningé (syndrome) | n2=en:cognitive decline (later in life) | rel=r_associated | relid=0 | w=22
  3659. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cognitive defects (variable from mild to severe)
    n1=méningé (syndrome) | n2=en:cognitive defects (variable from mild to severe) | rel=r_associated | relid=0 | w=22
  3660. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cognitive impairment, gradual onset
    n1=méningé (syndrome) | n2=en:cognitive impairment, gradual onset | rel=r_associated | relid=0 | w=22
  3661. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:coma (if untreated)
    n1=méningé (syndrome) | n2=en:coma (if untreated) | rel=r_associated | relid=0 | w=22
  3662. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:coma during episodes (in some patients)
    n1=méningé (syndrome) | n2=en:coma during episodes (in some patients) | rel=r_associated | relid=0 | w=22
  3663. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:confusion (later-onset)
    n1=méningé (syndrome) | n2=en:confusion (later-onset) | rel=r_associated | relid=0 | w=22
  3664. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cortical atrophy (rare)
    n1=méningé (syndrome) | n2=en:cortical atrophy (rare) | rel=r_associated | relid=0 | w=22
  3665. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cortical blindness (in 1 moroccan patient)
    n1=méningé (syndrome) | n2=en:cortical blindness (in 1 moroccan patient) | rel=r_associated | relid=0 | w=22
  3666. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cortical dysgenesis, complex
    n1=méningé (syndrome) | n2=en:cortical dysgenesis, complex | rel=r_associated | relid=0 | w=22
  3667. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cortical gyral simplification
    n1=méningé (syndrome) | n2=en:cortical gyral simplification | rel=r_associated | relid=0 | w=22
  3668. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cystic lesions consistent with leigh syndrome (256000)
    n1=méningé (syndrome) | n2=en:cystic lesions consistent with leigh syndrome (256000) | rel=r_associated | relid=0 | w=22
  3669. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:cystic lesions in the basal ganglia, brainstem, and cerebral hemispheres similar to leigh syndrome (256000)
    n1=méningé (syndrome) | n2=en:cystic lesions in the basal ganglia, brainstem, and cerebral hemispheres similar to leigh syndrome (256000) | rel=r_associated | relid=0 | w=22
  3670. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dandy-walker malformation (in 1 of 4 patients)
    n1=méningé (syndrome) | n2=en:dandy-walker malformation (in 1 of 4 patients) | rel=r_associated | relid=0 | w=22
  3671. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dandy-walker malformation (rare)
    n1=méningé (syndrome) | n2=en:dandy-walker malformation (rare) | rel=r_associated | relid=0 | w=22
  3672. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:decorticate posture
    n1=méningé (syndrome) | n2=en:decorticate posture | rel=r_associated | relid=0 | w=22
  3673. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:decreased creatine signal seen on magnetic resonance spectroscopy
    n1=méningé (syndrome) | n2=en:decreased creatine signal seen on magnetic resonance spectroscopy | rel=r_associated | relid=0 | w=22
  3674. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:decreased numbers of astrocytes
    n1=méningé (syndrome) | n2=en:decreased numbers of astrocytes | rel=r_associated | relid=0 | w=22
  3675. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:decreased or absent motor evoked potentials (mep), indicating dysfunction of the corticospinal tracts
    n1=méningé (syndrome) | n2=en:decreased or absent motor evoked potentials (mep), indicating dysfunction of the corticospinal tracts | rel=r_associated | relid=0 | w=22
  3676. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:decreased pain response
    n1=méningé (syndrome) | n2=en:decreased pain response | rel=r_associated | relid=0 | w=22
  3677. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:decreased vibration sense, suggesting posterior column involvement
    n1=méningé (syndrome) | n2=en:decreased vibration sense, suggesting posterior column involvement | rel=r_associated | relid=0 | w=22
  3678. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:defective myelination of the deep white matter
    n1=méningé (syndrome) | n2=en:defective myelination of the deep white matter | rel=r_associated | relid=0 | w=22
  3679. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:defective opercularization
    n1=méningé (syndrome) | n2=en:defective opercularization | rel=r_associated | relid=0 | w=22
  3680. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:delay in gross motor development due to weakness
    n1=méningé (syndrome) | n2=en:delay in gross motor development due to weakness | rel=r_associated | relid=0 | w=22
  3681. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:delay of gross motor function
    n1=méningé (syndrome) | n2=en:delay of gross motor function | rel=r_associated | relid=0 | w=22
  3682. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:delayed motor and speech development, mild (1 family)
    n1=méningé (syndrome) | n2=en:delayed motor and speech development, mild (1 family) | rel=r_associated | relid=0 | w=22
  3683. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:delayed motor development (secondary to skeletal abnormalities)
    n1=méningé (syndrome) | n2=en:delayed motor development (secondary to skeletal abnormalities) | rel=r_associated | relid=0 | w=22
  3684. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:delayed motor milestones due to muscle weakness
    n1=méningé (syndrome) | n2=en:delayed motor milestones due to muscle weakness | rel=r_associated | relid=0 | w=22
  3685. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:delayed psychomotor development after onset of seizures
    n1=méningé (syndrome) | n2=en:delayed psychomotor development after onset of seizures | rel=r_associated | relid=0 | w=22
  3686. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:delayed psychomotor development, profound (1 patient)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, profound (1 patient) | rel=r_associated | relid=0 | w=22
  3687. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:delayed psychomotor development, severe
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, severe | rel=r_associated | relid=0 | w=22
  3688. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:delusion
    n1=méningé (syndrome) | n2=en:delusion | rel=r_associated | relid=0 | w=22
  3689. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dementia, presenile, progressive, beginning around age 30 years
    n1=méningé (syndrome) | n2=en:dementia, presenile, progressive, beginning around age 30 years | rel=r_associated | relid=0 | w=22
  3690. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:deterioration of motor development
    n1=méningé (syndrome) | n2=en:deterioration of motor development | rel=r_associated | relid=0 | w=22
  3691. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:developmental delay (mild-severe)
    n1=méningé (syndrome) | n2=en:developmental delay (mild-severe) | rel=r_associated | relid=0 | w=22
  3692. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:developmental delay (rare)
    n1=méningé (syndrome) | n2=en:developmental delay (rare) | rel=r_associated | relid=0 | w=22
  3693. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:developmental delay, mild (in some patients)
    n1=méningé (syndrome) | n2=en:developmental delay, mild (in some patients) | rel=r_associated | relid=0 | w=22
  3694. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:difficulty in spelling
    n1=méningé (syndrome) | n2=en:difficulty in spelling | rel=r_associated | relid=0 | w=22
  3695. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:difficulty running and climbing stairs
    n1=méningé (syndrome) | n2=en:difficulty running and climbing stairs | rel=r_associated | relid=0 | w=22
  3696. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:difficulty walking and climbing stairs
    n1=méningé (syndrome) | n2=en:difficulty walking and climbing stairs | rel=r_associated | relid=0 | w=22
  3697. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:difficulty walking in childhood
    n1=méningé (syndrome) | n2=en:difficulty walking in childhood | rel=r_associated | relid=0 | w=22
  3698. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:difficulty with writing and drawing
    n1=méningé (syndrome) | n2=en:difficulty with writing and drawing | rel=r_associated | relid=0 | w=22
  3699. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:diffuse swelling of cerebral white matter
    n1=méningé (syndrome) | n2=en:diffuse swelling of cerebral white matter | rel=r_associated | relid=0 | w=22
  3700. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:diffuse white matter changes (meb)
    n1=méningé (syndrome) | n2=en:diffuse white matter changes (meb) | rel=r_associated | relid=0 | w=22
  3701. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:disorganized slow background activity seen on eeg
    n1=méningé (syndrome) | n2=en:disorganized slow background activity seen on eeg | rel=r_associated | relid=0 | w=22
  3702. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:distal muscle weakness
    n1=méningé (syndrome) | n2=en:distal muscle weakness | rel=r_associated | relid=0 | w=22
  3703. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dysarthria (1 patient)
    n1=méningé (syndrome) | n2=en:dysarthria (1 patient) | rel=r_associated | relid=0 | w=22
  3704. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dysgenesis or agenesis of the cerebellar vermis
    n1=méningé (syndrome) | n2=en:dysgenesis or agenesis of the cerebellar vermis | rel=r_associated | relid=0 | w=22
  3705. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dysmetria, mild
    n1=méningé (syndrome) | n2=en:dysmetria, mild | rel=r_associated | relid=0 | w=22
  3706. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dysmyelination of the brain, myelin is not formed properly
    n1=méningé (syndrome) | n2=en:dysmyelination of the brain, myelin is not formed properly | rel=r_associated | relid=0 | w=22
  3707. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dystonia (<20%) (finding)
    n1=méningé (syndrome) | n2=en:dystonia (<20%) (finding) | rel=r_associated | relid=0 | w=22
  3708. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dystonia (14% of patients)
    n1=méningé (syndrome) | n2=en:dystonia (14% of patients) | rel=r_associated | relid=0 | w=22
  3709. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dystonia at onset (16%)
    n1=méningé (syndrome) | n2=en:dystonia at onset (16%) | rel=r_associated | relid=0 | w=22
  3710. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:dystonic movements (in 1 of 6 patients)
    n1=méningé (syndrome) | n2=en:dystonic movements (in 1 of 6 patients) | rel=r_associated | relid=0 | w=22
  3711. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:early-onset myoclonic seizures
    n1=méningé (syndrome) | n2=en:early-onset myoclonic seizures | rel=r_associated | relid=0 | w=22
  3712. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:eeg shows generalized polyspike and wave discharges (4-5 hz)
    n1=méningé (syndrome) | n2=en:eeg shows generalized polyspike and wave discharges (4-5 hz) | rel=r_associated | relid=0 | w=22
  3713. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:emg shows fibrillations and fasiculations
    n1=méningé (syndrome) | n2=en:emg shows fibrillations and fasiculations | rel=r_associated | relid=0 | w=22
  3714. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:emg shows neurogenic abnormalities
    n1=méningé (syndrome) | n2=en:emg shows neurogenic abnormalities | rel=r_associated | relid=0 | w=22
  3715. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:encephalocele (uncommon)
    n1=méningé (syndrome) | n2=en:encephalocele (uncommon) | rel=r_associated | relid=0 | w=22
  3716. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:encephalopathy associated with hypoglycemia
    n1=méningé (syndrome) | n2=en:encephalopathy associated with hypoglycemia | rel=r_associated | relid=0 | w=22
  3717. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:episodic vomiting
    n1=méningé (syndrome) | n2=en:episodic vomiting | rel=r_associated | relid=0 | w=22
  3718. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:exaggerated startle response
    n1=méningé (syndrome) | n2=en:exaggerated startle response | rel=r_associated | relid=0 | w=22
  3719. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:exaggerated startle response to tactile or acoustic stimuli
    n1=méningé (syndrome) | n2=en:exaggerated startle response to tactile or acoustic stimuli | rel=r_associated | relid=0 | w=22
  3720. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:facial muscle sparing
    n1=méningé (syndrome) | n2=en:facial muscle sparing | rel=r_associated | relid=0 | w=22
  3721. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:facial paresis, congenital bilateral
    n1=méningé (syndrome) | n2=en:facial paresis, congenital bilateral | rel=r_associated | relid=0 | w=22
  3722. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:fasciculation
    n1=méningé (syndrome) | n2=en:fasciculation | rel=r_associated | relid=0 | w=22
  3723. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:fibrillation
    n1=méningé (syndrome) | n2=en:fibrillation | rel=r_associated | relid=0 | w=22
  3724. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:fine motor skills delayed
    n1=méningé (syndrome) | n2=en:fine motor skills delayed | rel=r_associated | relid=0 | w=22
  3725. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:fine motor/coordination problems (12%)
    n1=méningé (syndrome) | n2=en:fine motor/coordination problems (12%) | rel=r_associated | relid=0 | w=22
  3726. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:fine rapid hand tremor, 4-12 hz
    n1=méningé (syndrome) | n2=en:fine rapid hand tremor, 4-12 hz | rel=r_associated | relid=0 | w=22
  3727. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:flattening of the caudate
    n1=méningé (syndrome) | n2=en:flattening of the caudate | rel=r_associated | relid=0 | w=22
  3728. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:floppy infant
    n1=méningé (syndrome) | n2=en:floppy infant | rel=r_associated | relid=0 | w=22
  3729. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:focal dystonia, upper limb
    n1=méningé (syndrome) | n2=en:focal dystonia, upper limb | rel=r_associated | relid=0 | w=22
  3730. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:focal dystonia, usually of the hands
    n1=méningé (syndrome) | n2=en:focal dystonia, usually of the hands | rel=r_associated | relid=0 | w=22
  3731. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:frontotemporal hypoplasia
    n1=méningé (syndrome) | n2=en:frontotemporal hypoplasia | rel=r_associated | relid=0 | w=22
  3732. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:fused hemispheres (wws)
    n1=méningé (syndrome) | n2=en:fused hemispheres (wws) | rel=r_associated | relid=0 | w=22
  3733. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:gait impairment
    n1=méningé (syndrome) | n2=en:gait impairment | rel=r_associated | relid=0 | w=22
  3734. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:generalized slowing seen on eeg
    n1=méningé (syndrome) | n2=en:generalized slowing seen on eeg | rel=r_associated | relid=0 | w=22
  3735. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:generalized tonic-clonic seizures (rare)
    n1=méningé (syndrome) | n2=en:generalized tonic-clonic seizures (rare) | rel=r_associated | relid=0 | w=22
  3736. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:germinal cysts over the caudate
    n1=méningé (syndrome) | n2=en:germinal cysts over the caudate | rel=r_associated | relid=0 | w=22
  3737. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:glial cell
    n1=méningé (syndrome) | n2=en:glial cell | rel=r_associated | relid=0 | w=22
  3738. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:gliosis
    n1=méningé (syndrome) | n2=en:gliosis | rel=r_associated | relid=0 | w=22
  3739. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:gliosis (27%)
    n1=méningé (syndrome) | n2=en:gliosis (27%) | rel=r_associated | relid=0 | w=22
  3740. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:globular basal ganglia (1 patient)
    n1=méningé (syndrome) | n2=en:globular basal ganglia (1 patient) | rel=r_associated | relid=0 | w=22
  3741. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:gowers sign
    n1=méningé (syndrome) | n2=en:gowers sign | rel=r_associated | relid=0 | w=22
  3742. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:head-rolling movements
    n1=méningé (syndrome) | n2=en:head-rolling movements | rel=r_associated | relid=0 | w=22
  3743. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hemihypoasthesia
    n1=méningé (syndrome) | n2=en:hemihypoasthesia | rel=r_associated | relid=0 | w=22
  3744. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hyperactive deep tendon reflexes in early stage
    n1=méningé (syndrome) | n2=en:hyperactive deep tendon reflexes in early stage | rel=r_associated | relid=0 | w=22
  3745. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hyperextension of the neck
    n1=méningé (syndrome) | n2=en:hyperextension of the neck | rel=r_associated | relid=0 | w=22
  3746. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hyperintense lesions of the globi pallidi
    n1=méningé (syndrome) | n2=en:hyperintense lesions of the globi pallidi | rel=r_associated | relid=0 | w=22
  3747. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypermetric saccades
    n1=méningé (syndrome) | n2=en:hypermetric saccades | rel=r_associated | relid=0 | w=22
  3748. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypersensitivity to sound
    n1=méningé (syndrome) | n2=en:hypersensitivity to sound | rel=r_associated | relid=0 | w=22
  3749. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypertonia of lower limbs, later
    n1=méningé (syndrome) | n2=en:hypertonia of lower limbs, later | rel=r_associated | relid=0 | w=22
  3750. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypodensity of cerebral white matter seen on mri
    n1=méningé (syndrome) | n2=en:hypodensity of cerebral white matter seen on mri | rel=r_associated | relid=0 | w=22
  3751. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypomimia
    n1=méningé (syndrome) | n2=en:hypomimia | rel=r_associated | relid=0 | w=22
  3752. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypomyelination
    n1=méningé (syndrome) | n2=en:hypomyelination | rel=r_associated | relid=0 | w=22
  3753. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypoplasia of corpus callosum and cerebellar vermis
    n1=méningé (syndrome) | n2=en:hypoplasia of corpus callosum and cerebellar vermis | rel=r_associated | relid=0 | w=22
  3754. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypoplasia of the optic chiasm
    n1=méningé (syndrome) | n2=en:hypoplasia of the optic chiasm | rel=r_associated | relid=0 | w=22
  3755. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypoplasia of the posterior corpus callosum (in some patients)
    n1=méningé (syndrome) | n2=en:hypoplasia of the posterior corpus callosum (in some patients) | rel=r_associated | relid=0 | w=22
  3756. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypoplasia or dysgenesis of the corpus callosum (in some patients)
    n1=méningé (syndrome) | n2=en:hypoplasia or dysgenesis of the corpus callosum (in some patients) | rel=r_associated | relid=0 | w=22
  3757. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypoplastic corpus callosum (in some patients)
    n1=méningé (syndrome) | n2=en:hypoplastic corpus callosum (in some patients) | rel=r_associated | relid=0 | w=22
  3758. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypoplastic pons
    n1=méningé (syndrome) | n2=en:hypoplastic pons | rel=r_associated | relid=0 | w=22
  3759. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hyporeflexia (early)
    n1=méningé (syndrome) | n2=en:hyporeflexia (early) | rel=r_associated | relid=0 | w=22
  3760. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hyporeflexia to hyperreflexia
    n1=méningé (syndrome) | n2=en:hyporeflexia to hyperreflexia | rel=r_associated | relid=0 | w=22
  3761. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypotonia (96%)
    n1=méningé (syndrome) | n2=en:hypotonia (96%) | rel=r_associated | relid=0 | w=22
  3762. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypotonia (less common)
    n1=méningé (syndrome) | n2=en:hypotonia (less common) | rel=r_associated | relid=0 | w=22
  3763. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:hypotonia, poor moro reflex
    n1=méningé (syndrome) | n2=en:hypotonia, poor moro reflex | rel=r_associated | relid=0 | w=22
  3764. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:ictal eeg shows focal, temporal, unilateral, rhythmic slow wave activity of high amplitude
    n1=méningé (syndrome) | n2=en:ictal eeg shows focal, temporal, unilateral, rhythmic slow wave activity of high amplitude | rel=r_associated | relid=0 | w=22
  3765. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:imaging shows noncalcified subependymal periventricular heterotopic nodules of gray matter
    n1=méningé (syndrome) | n2=en:imaging shows noncalcified subependymal periventricular heterotopic nodules of gray matter | rel=r_associated | relid=0 | w=22
  3766. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:impaired processing of language
    n1=méningé (syndrome) | n2=en:impaired processing of language | rel=r_associated | relid=0 | w=22
  3767. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:impaired vibration sensation at ankles
    n1=méningé (syndrome) | n2=en:impaired vibration sensation at ankles | rel=r_associated | relid=0 | w=22
  3768. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:impaired walking ability (in some patients)
    n1=méningé (syndrome) | n2=en:impaired walking ability (in some patients) | rel=r_associated | relid=0 | w=22
  3769. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:impairment of balance
    n1=méningé (syndrome) | n2=en:impairment of balance | rel=r_associated | relid=0 | w=22
  3770. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:inability to hold head up
    n1=méningé (syndrome) | n2=en:inability to hold head up | rel=r_associated | relid=0 | w=22
  3771. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:inability to sit
    n1=méningé (syndrome) | n2=en:inability to sit | rel=r_associated | relid=0 | w=22
  3772. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:inability to stand without assistance
    n1=méningé (syndrome) | n2=en:inability to stand without assistance | rel=r_associated | relid=0 | w=22
  3773. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:increased white matter abnormalities on t2 signalling (in type iib)
    n1=méningé (syndrome) | n2=en:increased white matter abnormalities on t2 signalling (in type iib) | rel=r_associated | relid=0 | w=22
  3774. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:independent walking never achieved
    n1=méningé (syndrome) | n2=en:independent walking never achieved | rel=r_associated | relid=0 | w=22
  3775. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:infantile irritability (if left untreated)
    n1=méningé (syndrome) | n2=en:infantile irritability (if left untreated) | rel=r_associated | relid=0 | w=22
  3776. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:infantile muscular hypotonia
    n1=méningé (syndrome) | n2=en:infantile muscular hypotonia | rel=r_associated | relid=0 | w=22
  3777. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:infantile seizures
    n1=méningé (syndrome) | n2=en:infantile seizures | rel=r_associated | relid=0 | w=22
  3778. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:initial normal development
    n1=méningé (syndrome) | n2=en:initial normal development | rel=r_associated | relid=0 | w=22
  3779. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:intellect high (in some patients)
    n1=méningé (syndrome) | n2=en:intellect high (in some patients) | rel=r_associated | relid=0 | w=22
  3780. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:intellectual disability (in 1 ashkenazi patient)
    n1=méningé (syndrome) | n2=en:intellectual disability (in 1 ashkenazi patient) | rel=r_associated | relid=0 | w=22
  3781. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:intellectual impairment (rare)
    n1=méningé (syndrome) | n2=en:intellectual impairment (rare) | rel=r_associated | relid=0 | w=22
  3782. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:interictal neurologic impairment
    n1=méningé (syndrome) | n2=en:interictal neurologic impairment | rel=r_associated | relid=0 | w=22
  3783. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:intracerebral periventricular calcifications
    n1=méningé (syndrome) | n2=en:intracerebral periventricular calcifications | rel=r_associated | relid=0 | w=22
  3784. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:intracranial hypertension
    n1=méningé (syndrome) | n2=en:intracranial hypertension | rel=r_associated | relid=0 | w=22
  3785. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:intracranial thin-walled sinusoidal vessel (cavernous) malformations
    n1=méningé (syndrome) | n2=en:intracranial thin-walled sinusoidal vessel (cavernous) malformations | rel=r_associated | relid=0 | w=22
  3786. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:involuntary rhythmic myoclonic movements ('tremor'), upper extremities
    n1=méningé (syndrome) | n2=en:involuntary rhythmic myoclonic movements ('tremor'), upper extremities | rel=r_associated | relid=0 | w=22
  3787. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lack of communication
    n1=méningé (syndrome) | n2=en:lack of communication | rel=r_associated | relid=0 | w=22
  3788. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lack of independent walking (in some patients)
    n1=méningé (syndrome) | n2=en:lack of independent walking (in some patients) | rel=r_associated | relid=0 | w=22
  3789. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lack of motor development
    n1=méningé (syndrome) | n2=en:lack of motor development | rel=r_associated | relid=0 | w=22
  3790. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lack of motor development (wws)
    n1=méningé (syndrome) | n2=en:lack of motor development (wws) | rel=r_associated | relid=0 | w=22
  3791. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lack of speech (in severe cases)
    n1=méningé (syndrome) | n2=en:lack of speech (in severe cases) | rel=r_associated | relid=0 | w=22
  3792. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lack of speech development
    n1=méningé (syndrome) | n2=en:lack of speech development | rel=r_associated | relid=0 | w=22
  3793. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:language disorder
    n1=méningé (syndrome) | n2=en:language disorder | rel=r_associated | relid=0 | w=22
  3794. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:learning difficulties (less common)
    n1=méningé (syndrome) | n2=en:learning difficulties (less common) | rel=r_associated | relid=0 | w=22
  3795. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:learning disabilities (1 family)
    n1=méningé (syndrome) | n2=en:learning disabilities (1 family) | rel=r_associated | relid=0 | w=22
  3796. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:leigh syndrome (245000), in a subset of patients
    n1=méningé (syndrome) | n2=en:leigh syndrome (245000), in a subset of patients | rel=r_associated | relid=0 | w=22
  3797. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lesions in the caudate and putamen
    n1=méningé (syndrome) | n2=en:lesions in the caudate and putamen | rel=r_associated | relid=0 | w=22
  3798. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lesions in the internal capsule after age 40 years
    n1=méningé (syndrome) | n2=en:lesions in the internal capsule after age 40 years | rel=r_associated | relid=0 | w=22
  3799. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lethargy, neonatal
    n1=méningé (syndrome) | n2=en:lethargy, neonatal | rel=r_associated | relid=0 | w=22
  3800. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:leukodystrophy
    n1=méningé (syndrome) | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=22
  3801. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:leukodystrophy (in some patients)
    n1=méningé (syndrome) | n2=en:leukodystrophy (in some patients) | rel=r_associated | relid=0 | w=22
  3802. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:leukodystrophy, demyelinating
    n1=méningé (syndrome) | n2=en:leukodystrophy, demyelinating | rel=r_associated | relid=0 | w=22
  3803. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:leukoencephalopathy in the periventricular and deep white matter and brainstem, cerebellum, and spinal cord tracts
    n1=méningé (syndrome) | n2=en:leukoencephalopathy in the periventricular and deep white matter and brainstem, cerebellum, and spinal cord tracts | rel=r_associated | relid=0 | w=22
  3804. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:leukoencephalopathy on ct and mri
    n1=méningé (syndrome) | n2=en:leukoencephalopathy on ct and mri | rel=r_associated | relid=0 | w=22
  3805. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:light-induced sneezing
    n1=méningé (syndrome) | n2=en:light-induced sneezing | rel=r_associated | relid=0 | w=22
  3806. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:limb hypertonia
    n1=méningé (syndrome) | n2=en:limb hypertonia | rel=r_associated | relid=0 | w=22
  3807. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:limb incoordination (in some patients)
    n1=méningé (syndrome) | n2=en:limb incoordination (in some patients) | rel=r_associated | relid=0 | w=22
  3808. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:limited verbal comprehension
    n1=méningé (syndrome) | n2=en:limited verbal comprehension | rel=r_associated | relid=0 | w=22
  3809. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:limited walking ability
    n1=méningé (syndrome) | n2=en:limited walking ability | rel=r_associated | relid=0 | w=22
  3810. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lingual-facial-buccal dyskinesia
    n1=méningé (syndrome) | n2=en:lingual-facial-buccal dyskinesia | rel=r_associated | relid=0 | w=22
  3811. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lipoma, anterior sacral
    n1=méningé (syndrome) | n2=en:lipoma, anterior sacral | rel=r_associated | relid=0 | w=22
  3812. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:little or no speech acquisition
    n1=méningé (syndrome) | n2=en:little or no speech acquisition | rel=r_associated | relid=0 | w=22
  3813. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:long perforating arteries of the brain are affected
    n1=méningé (syndrome) | n2=en:long perforating arteries of the brain are affected | rel=r_associated | relid=0 | w=22
  3814. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:loss of ambulation
    n1=méningé (syndrome) | n2=en:loss of ambulation | rel=r_associated | relid=0 | w=22
  3815. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:loss of cerebral white matter (in 1 of 3 patients)
    n1=méningé (syndrome) | n2=en:loss of cerebral white matter (in 1 of 3 patients) | rel=r_associated | relid=0 | w=22
  3816. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:loss of independent ambulation approximately 30 years after onset
    n1=méningé (syndrome) | n2=en:loss of independent ambulation approximately 30 years after onset | rel=r_associated | relid=0 | w=22
  3817. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:loss of independent ambulation by age 10 years
    n1=méningé (syndrome) | n2=en:loss of independent ambulation by age 10 years | rel=r_associated | relid=0 | w=22
  3818. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:loss of motor neurons in the anterior horn of the spinal cord
    n1=méningé (syndrome) | n2=en:loss of motor neurons in the anterior horn of the spinal cord | rel=r_associated | relid=0 | w=22
  3819. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:loss of myelinated fibers in spinal cord roots
    n1=méningé (syndrome) | n2=en:loss of myelinated fibers in spinal cord roots | rel=r_associated | relid=0 | w=22
  3820. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:loss of primary reflexes
    n1=méningé (syndrome) | n2=en:loss of primary reflexes | rel=r_associated | relid=0 | w=22
  3821. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lower limb atrophy
    n1=méningé (syndrome) | n2=en:lower limb atrophy | rel=r_associated | relid=0 | w=22
  3822. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:lymphoplasmacyte-rich meningioma
    n1=méningé (syndrome) | n2=en:lymphoplasmacyte-rich meningioma | rel=r_associated | relid=0 | w=22
  3823. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:malformation of the insula
    n1=méningé (syndrome) | n2=en:malformation of the insula | rel=r_associated | relid=0 | w=22
  3824. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:medulloblastoma
    n1=méningé (syndrome) | n2=en:medulloblastoma | rel=r_associated | relid=0 | w=22
  3825. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:megacisterna magna (rare)
    n1=méningé (syndrome) | n2=en:megacisterna magna (rare) | rel=r_associated | relid=0 | w=22
  3826. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:meningeal melanocytoma
    n1=méningé (syndrome) | n2=en:meningeal melanocytoma | rel=r_associated | relid=0 | w=22
  3827. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:meningioma (in some patients)
    n1=méningé (syndrome) | n2=en:meningioma (in some patients) | rel=r_associated | relid=0 | w=22
  3828. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental deficiency
    n1=méningé (syndrome) | n2=en:mental deficiency | rel=r_associated | relid=0 | w=22
  3829. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation (2/3 patients)
    n1=méningé (syndrome) | n2=en:mental retardation (2/3 patients) | rel=r_associated | relid=0 | w=22
  3830. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation (average iq 56)
    n1=méningé (syndrome) | n2=en:mental retardation (average iq 56) | rel=r_associated | relid=0 | w=22
  3831. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation (in 2 of 6 patients)
    n1=méningé (syndrome) | n2=en:mental retardation (in 2 of 6 patients) | rel=r_associated | relid=0 | w=22
  3832. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation (in most)
    n1=méningé (syndrome) | n2=en:mental retardation (in most) | rel=r_associated | relid=0 | w=22
  3833. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation (iq 24-85) (variable)
    n1=méningé (syndrome) | n2=en:mental retardation (iq 24-85) (variable) | rel=r_associated | relid=0 | w=22
  3834. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation (males)
    n1=méningé (syndrome) | n2=en:mental retardation (males) | rel=r_associated | relid=0 | w=22
  3835. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation (rarely noted)
    n1=méningé (syndrome) | n2=en:mental retardation (rarely noted) | rel=r_associated | relid=0 | w=22
  3836. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation, mild (in some females)
    n1=méningé (syndrome) | n2=en:mental retardation, mild (in some females) | rel=r_associated | relid=0 | w=22
  3837. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation, mild-borderline, nonprogressive
    n1=méningé (syndrome) | n2=en:mental retardation, mild-borderline, nonprogressive | rel=r_associated | relid=0 | w=22
  3838. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation, moderate (apparent by age 4 years)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate (apparent by age 4 years) | rel=r_associated | relid=0 | w=22
  3839. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mental retardation, occasional
    n1=méningé (syndrome) | n2=en:mental retardation, occasional | rel=r_associated | relid=0 | w=22
  3840. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:microbleeds (most smaller than 5 mm) occur after age 40 years
    n1=méningé (syndrome) | n2=en:microbleeds (most smaller than 5 mm) occur after age 40 years | rel=r_associated | relid=0 | w=22
  3841. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:migraine (in affected males)
    n1=méningé (syndrome) | n2=en:migraine (in affected males) | rel=r_associated | relid=0 | w=22
  3842. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:migraine with aura
    n1=méningé (syndrome) | n2=en:migraine with aura | rel=r_associated | relid=0 | w=22
  3843. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mild cognitive impairment (in 2 patients)
    n1=méningé (syndrome) | n2=en:mild cognitive impairment (in 2 patients) | rel=r_associated | relid=0 | w=22
  3844. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mirror movements, involuntary, usually of the upper limb and hand
    n1=méningé (syndrome) | n2=en:mirror movements, involuntary, usually of the upper limb and hand | rel=r_associated | relid=0 | w=22
  3845. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:misshapen posterior fossa
    n1=méningé (syndrome) | n2=en:misshapen posterior fossa | rel=r_associated | relid=0 | w=22
  3846. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mobius syndrome
    n1=méningé (syndrome) | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=22
  3847. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:moderate learning difficulties
    n1=méningé (syndrome) | n2=en:moderate learning difficulties | rel=r_associated | relid=0 | w=22
  3848. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:monotone speech
    n1=méningé (syndrome) | n2=en:monotone speech | rel=r_associated | relid=0 | w=22
  3849. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:most patients remain stable or improve in years after the abrupt onset of symptoms
    n1=méningé (syndrome) | n2=en:most patients remain stable or improve in years after the abrupt onset of symptoms | rel=r_associated | relid=0 | w=22
  3850. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:movement abnormalities of the extremities
    n1=méningé (syndrome) | n2=en:movement abnormalities of the extremities | rel=r_associated | relid=0 | w=22
  3851. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mri shows decreased signal intensities in the basal ganglia
    n1=méningé (syndrome) | n2=en:mri shows decreased signal intensities in the basal ganglia | rel=r_associated | relid=0 | w=22
  3852. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mri shows defects of the corpus callosum
    n1=méningé (syndrome) | n2=en:mri shows defects of the corpus callosum | rel=r_associated | relid=0 | w=22
  3853. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:mri shows white matter lesions
    n1=méningé (syndrome) | n2=en:mri shows white matter lesions | rel=r_associated | relid=0 | w=22
  3854. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:multifocal cerebral white matter abnormalities
    n1=méningé (syndrome) | n2=en:multifocal cerebral white matter abnormalities | rel=r_associated | relid=0 | w=22
  3855. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:muscle atrophy
    n1=méningé (syndrome) | n2=en:muscle atrophy | rel=r_associated | relid=0 | w=22
  3856. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:muscle weakness, proximal, due to neuronopathy begins in the lower limbs and then progresses to upper limbs
    n1=méningé (syndrome) | n2=en:muscle weakness, proximal, due to neuronopathy begins in the lower limbs and then progresses to upper limbs | rel=r_associated | relid=0 | w=22
  3857. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:myelin microvacuolation
    n1=méningé (syndrome) | n2=en:myelin microvacuolation | rel=r_associated | relid=0 | w=22
  3858. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:myokymia
    n1=méningé (syndrome) | n2=en:myokymia | rel=r_associated | relid=0 | w=22
  3859. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:narcolepsy
    n1=méningé (syndrome) | n2=en:narcolepsy | rel=r_associated | relid=0 | w=22
  3860. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:neck pain
    n1=méningé (syndrome) | n2=en:neck pain | rel=r_associated | relid=0 | w=22
  3861. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:neural tube defects may occur
    n1=méningé (syndrome) | n2=en:neural tube defects may occur | rel=r_associated | relid=0 | w=22
  3862. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:neuroaxonal spheroids
    n1=méningé (syndrome) | n2=en:neuroaxonal spheroids | rel=r_associated | relid=0 | w=22
  3863. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:neurodegeneration leading to profound mental retardation
    n1=méningé (syndrome) | n2=en:neurodegeneration leading to profound mental retardation | rel=r_associated | relid=0 | w=22
  3864. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:neurofibrillary tangles composed of disordered microtubules
    n1=méningé (syndrome) | n2=en:neurofibrillary tangles composed of disordered microtubules | rel=r_associated | relid=0 | w=22
  3865. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:neurofibromas can occur at cervical, thoracic, lumbar, and sacral levels
    n1=méningé (syndrome) | n2=en:neurofibromas can occur at cervical, thoracic, lumbar, and sacral levels | rel=r_associated | relid=0 | w=22
  3866. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:neurologic crises with coma (in some patients)
    n1=méningé (syndrome) | n2=en:neurologic crises with coma (in some patients) | rel=r_associated | relid=0 | w=22
  3867. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:neurologic regression after age 2 years
    n1=méningé (syndrome) | n2=en:neurologic regression after age 2 years | rel=r_associated | relid=0 | w=22
  3868. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:neuronal loss and gliosis in the inferior olives
    n1=méningé (syndrome) | n2=en:neuronal loss and gliosis in the inferior olives | rel=r_associated | relid=0 | w=22
  3869. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:no bulbar involvement
    n1=méningé (syndrome) | n2=en:no bulbar involvement | rel=r_associated | relid=0 | w=22
  3870. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:no central nervous system abnormalities
    n1=méningé (syndrome) | n2=en:no central nervous system abnormalities | rel=r_associated | relid=0 | w=22
  3871. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:no cognitive decline
    n1=méningé (syndrome) | n2=en:no cognitive decline | rel=r_associated | relid=0 | w=22
  3872. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:no myoclonus
    n1=méningé (syndrome) | n2=en:no myoclonus | rel=r_associated | relid=0 | w=22
  3873. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:no sensory deficit
    n1=méningé (syndrome) | n2=en:no sensory deficit | rel=r_associated | relid=0 | w=22
  3874. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:nodular heterotopia (less common)
    n1=méningé (syndrome) | n2=en:nodular heterotopia (less common) | rel=r_associated | relid=0 | w=22
  3875. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:normal cognition (in some patients)
    n1=méningé (syndrome) | n2=en:normal cognition (in some patients) | rel=r_associated | relid=0 | w=22
  3876. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:normal cognition (reported in 1 patient who survived to age 20 years)
    n1=méningé (syndrome) | n2=en:normal cognition (reported in 1 patient who survived to age 20 years) | rel=r_associated | relid=0 | w=22
  3877. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:normal mental development
    n1=méningé (syndrome) | n2=en:normal mental development | rel=r_associated | relid=0 | w=22
  3878. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:nystagmus, horizontal
    n1=méningé (syndrome) | n2=en:nystagmus, horizontal | rel=r_associated | relid=0 | w=22
  3879. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:obsessive compulsive behavior
    n1=méningé (syndrome) | n2=en:obsessive compulsive behavior | rel=r_associated | relid=0 | w=22
  3880. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:ocular palsies
    n1=méningé (syndrome) | n2=en:ocular palsies | rel=r_associated | relid=0 | w=22
  3881. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:optic ataxia (in a subset of patients)
    n1=méningé (syndrome) | n2=en:optic ataxia (in a subset of patients) | rel=r_associated | relid=0 | w=22
  3882. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:oromandibular dystonia
    n1=méningé (syndrome) | n2=en:oromandibular dystonia | rel=r_associated | relid=0 | w=22
  3883. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pachygyria (less common)
    n1=méningé (syndrome) | n2=en:pachygyria (less common) | rel=r_associated | relid=0 | w=22
  3884. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pachygyria, occipital
    n1=méningé (syndrome) | n2=en:pachygyria, occipital | rel=r_associated | relid=0 | w=22
  3885. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:palatal myoclonus
    n1=méningé (syndrome) | n2=en:palatal myoclonus | rel=r_associated | relid=0 | w=22
  3886. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pallor of dorsal columns of the spinal cord
    n1=méningé (syndrome) | n2=en:pallor of dorsal columns of the spinal cord | rel=r_associated | relid=0 | w=22
  3887. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:paraparesis, spastic
    n1=méningé (syndrome) | n2=en:paraparesis, spastic | rel=r_associated | relid=0 | w=22
  3888. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:partial epilepsy
    n1=méningé (syndrome) | n2=en:partial epilepsy | rel=r_associated | relid=0 | w=22
  3889. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:patients 20-30 years old have hyperintense lesions on t2-weighted mri in the frontal and anterior temporal lobes
    n1=méningé (syndrome) | n2=en:patients 20-30 years old have hyperintense lesions on t2-weighted mri in the frontal and anterior temporal lobes | rel=r_associated | relid=0 | w=22
  3890. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pericystic abnormal myelination
    n1=méningé (syndrome) | n2=en:pericystic abnormal myelination | rel=r_associated | relid=0 | w=22
  3891. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:peripheral nervous system disorder
    n1=méningé (syndrome) | n2=en:peripheral nervous system disorder | rel=r_associated | relid=0 | w=22
  3892. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:persistent cavus septum pellucidum
    n1=méningé (syndrome) | n2=en:persistent cavus septum pellucidum | rel=r_associated | relid=0 | w=22
  3893. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:photosensitive tonic-clonic seizures
    n1=méningé (syndrome) | n2=en:photosensitive tonic-clonic seizures | rel=r_associated | relid=0 | w=22
  3894. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pituitary agenesis
    n1=méningé (syndrome) | n2=en:pituitary agenesis | rel=r_associated | relid=0 | w=22
  3895. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pituitary aplasia or dysplasia
    n1=méningé (syndrome) | n2=en:pituitary aplasia or dysplasia | rel=r_associated | relid=0 | w=22
  3896. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:polymicrogyria, usually frontal (in some patients)
    n1=méningé (syndrome) | n2=en:polymicrogyria, usually frontal (in some patients) | rel=r_associated | relid=0 | w=22
  3897. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:polyneuropathies, motor
    n1=méningé (syndrome) | n2=en:polyneuropathies, motor | rel=r_associated | relid=0 | w=22
  3898. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pons damage
    n1=méningé (syndrome) | n2=en:pons damage | rel=r_associated | relid=0 | w=22
  3899. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pontocerebellar atrophy
    n1=méningé (syndrome) | n2=en:pontocerebellar atrophy | rel=r_associated | relid=0 | w=22
  3900. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:poor communication
    n1=méningé (syndrome) | n2=en:poor communication | rel=r_associated | relid=0 | w=22
  3901. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:poor differentiation of gray and white matter on t2-weighted mri
    n1=méningé (syndrome) | n2=en:poor differentiation of gray and white matter on t2-weighted mri | rel=r_associated | relid=0 | w=22
  3902. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:poor fine motor coordination
    n1=méningé (syndrome) | n2=en:poor fine motor coordination | rel=r_associated | relid=0 | w=22
  3903. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:poor fine motor skills
    n1=méningé (syndrome) | n2=en:poor fine motor skills | rel=r_associated | relid=0 | w=22
  3904. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:poor or absent smooth pursuit
    n1=méningé (syndrome) | n2=en:poor or absent smooth pursuit | rel=r_associated | relid=0 | w=22
  3905. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:poor-absent neurologic development
    n1=méningé (syndrome) | n2=en:poor-absent neurologic development | rel=r_associated | relid=0 | w=22
  3906. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:postural tremor, slow, irregular (in some patients)
    n1=méningé (syndrome) | n2=en:postural tremor, slow, irregular (in some patients) | rel=r_associated | relid=0 | w=22
  3907. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:profound global developmental delay
    n1=méningé (syndrome) | n2=en:profound global developmental delay | rel=r_associated | relid=0 | w=22
  3908. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:profound mental retardation and hypotonia in survivors
    n1=méningé (syndrome) | n2=en:profound mental retardation and hypotonia in survivors | rel=r_associated | relid=0 | w=22
  3909. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:progressive ataxia (onset second year of life)
    n1=méningé (syndrome) | n2=en:progressive ataxia (onset second year of life) | rel=r_associated | relid=0 | w=22
  3910. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:progressive choreoathetosis
    n1=méningé (syndrome) | n2=en:progressive choreoathetosis | rel=r_associated | relid=0 | w=22
  3911. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:progressive leukoencephalopathy
    n1=méningé (syndrome) | n2=en:progressive leukoencephalopathy | rel=r_associated | relid=0 | w=22
  3912. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pseudotumor cerebri
    n1=méningé (syndrome) | n2=en:pseudotumor cerebri | rel=r_associated | relid=0 | w=22
  3913. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:psychomotor arrest and regression
    n1=méningé (syndrome) | n2=en:psychomotor arrest and regression | rel=r_associated | relid=0 | w=22
  3914. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:psychomotor delay (rare)
    n1=méningé (syndrome) | n2=en:psychomotor delay (rare) | rel=r_associated | relid=0 | w=22
  3915. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:psychomotor retardation (2/4 patients)
    n1=méningé (syndrome) | n2=en:psychomotor retardation (2/4 patients) | rel=r_associated | relid=0 | w=22
  3916. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pyramidal signs (1 family)
    n1=méningé (syndrome) | n2=en:pyramidal signs (1 family) | rel=r_associated | relid=0 | w=22
  3917. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:pyramidal tract involvement
    n1=méningé (syndrome) | n2=en:pyramidal tract involvement | rel=r_associated | relid=0 | w=22
  3918. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:rapid, jerky movements
    n1=méningé (syndrome) | n2=en:rapid, jerky movements | rel=r_associated | relid=0 | w=22
  3919. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:rare dementia
    n1=méningé (syndrome) | n2=en:rare dementia | rel=r_associated | relid=0 | w=22
  3920. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:recurrent meningioma
    n1=méningé (syndrome) | n2=en:recurrent meningioma | rel=r_associated | relid=0 | w=22
  3921. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:reduced brain gyri
    n1=méningé (syndrome) | n2=en:reduced brain gyri | rel=r_associated | relid=0 | w=22
  3922. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:relief with motor activation
    n1=méningé (syndrome) | n2=en:relief with motor activation | rel=r_associated | relid=0 | w=22
  3923. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:residual ataxia
    n1=méningé (syndrome) | n2=en:residual ataxia | rel=r_associated | relid=0 | w=22
  3924. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:seizures (50% of patients)
    n1=méningé (syndrome) | n2=en:seizures (50% of patients) | rel=r_associated | relid=0 | w=22
  3925. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:seizures (in some patients)
    n1=méningé (syndrome) | n2=en:seizures (in some patients) | rel=r_associated | relid=0 | w=22
  3926. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:seizures often begin focally with head and eye deviation
    n1=méningé (syndrome) | n2=en:seizures often begin focally with head and eye deviation | rel=r_associated | relid=0 | w=22
  3927. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:seizures often begin with head and eye deviation
    n1=méningé (syndrome) | n2=en:seizures often begin with head and eye deviation | rel=r_associated | relid=0 | w=22
  3928. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:seizures, early onset
    n1=méningé (syndrome) | n2=en:seizures, early onset | rel=r_associated | relid=0 | w=22
  3929. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:seizures, nocturnal, usually occur in daily clusters
    n1=méningé (syndrome) | n2=en:seizures, nocturnal, usually occur in daily clusters | rel=r_associated | relid=0 | w=22
  3930. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:seizures, refractory
    n1=méningé (syndrome) | n2=en:seizures, refractory | rel=r_associated | relid=0 | w=22
  3931. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:seizures, refractory, infantile-onset
    n1=méningé (syndrome) | n2=en:seizures, refractory, infantile-onset | rel=r_associated | relid=0 | w=22
  3932. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:seizures, tonic, hyperekplectic
    n1=méningé (syndrome) | n2=en:seizures, tonic, hyperekplectic | rel=r_associated | relid=0 | w=22
  3933. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:severe form may never achieve sitting or walking
    n1=méningé (syndrome) | n2=en:severe form may never achieve sitting or walking | rel=r_associated | relid=0 | w=22
  3934. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:severe involvement of globus pallidus
    n1=méningé (syndrome) | n2=en:severe involvement of globus pallidus | rel=r_associated | relid=0 | w=22
  3935. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:severely impaired or absent speech
    n1=méningé (syndrome) | n2=en:severely impaired or absent speech | rel=r_associated | relid=0 | w=22
  3936. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:simplified gyral pattern (in some patients)
    n1=méningé (syndrome) | n2=en:simplified gyral pattern (in some patients) | rel=r_associated | relid=0 | w=22
  3937. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:slow paraparetic gait
    n1=méningé (syndrome) | n2=en:slow paraparetic gait | rel=r_associated | relid=0 | w=22
  3938. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:slowing mental development by 1.5 to 3 years
    n1=méningé (syndrome) | n2=en:slowing mental development by 1.5 to 3 years | rel=r_associated | relid=0 | w=22
  3939. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:small anterior commissure
    n1=méningé (syndrome) | n2=en:small anterior commissure | rel=r_associated | relid=0 | w=22
  3940. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:small frontal lobes (in one patient)
    n1=méningé (syndrome) | n2=en:small frontal lobes (in one patient) | rel=r_associated | relid=0 | w=22
  3941. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:some patients have no structural brain abnormalities
    n1=méningé (syndrome) | n2=en:some patients have no structural brain abnormalities | rel=r_associated | relid=0 | w=22
  3942. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:some patients never achieve independent ambulation
    n1=méningé (syndrome) | n2=en:some patients never achieve independent ambulation | rel=r_associated | relid=0 | w=22
  3943. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:spasmodic dysphonia
    n1=méningé (syndrome) | n2=en:spasmodic dysphonia | rel=r_associated | relid=0 | w=22
  3944. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:spastic paraplegia, slowly progressive
    n1=méningé (syndrome) | n2=en:spastic paraplegia, slowly progressive | rel=r_associated | relid=0 | w=22
  3945. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:spastic tetraplegia (in some patients)
    n1=méningé (syndrome) | n2=en:spastic tetraplegia (in some patients) | rel=r_associated | relid=0 | w=22
  3946. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:spasticity
    n1=méningé (syndrome) | n2=en:spasticity | rel=r_associated | relid=0 | w=22
  3947. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:spasticity (in some)
    n1=méningé (syndrome) | n2=en:spasticity (in some) | rel=r_associated | relid=0 | w=22
  3948. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:spasticity (type ii)
    n1=méningé (syndrome) | n2=en:spasticity (type ii) | rel=r_associated | relid=0 | w=22
  3949. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:spasticity, distal
    n1=méningé (syndrome) | n2=en:spasticity, distal | rel=r_associated | relid=0 | w=22
  3950. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:speech disability
    n1=méningé (syndrome) | n2=en:speech disability | rel=r_associated | relid=0 | w=22
  3951. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:spinocerebellar tract degeneration
    n1=méningé (syndrome) | n2=en:spinocerebellar tract degeneration | rel=r_associated | relid=0 | w=22
  3952. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:spinocerebellar tract disease in lower limbs (in adulthood)
    n1=méningé (syndrome) | n2=en:spinocerebellar tract disease in lower limbs (in adulthood) | rel=r_associated | relid=0 | w=22
  3953. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:status dystonicus
    n1=méningé (syndrome) | n2=en:status dystonicus | rel=r_associated | relid=0 | w=22
  3954. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:status epilepticus
    n1=méningé (syndrome) | n2=en:status epilepticus | rel=r_associated | relid=0 | w=22
  3955. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:striatal necrosis
    n1=méningé (syndrome) | n2=en:striatal necrosis | rel=r_associated | relid=0 | w=22
  3956. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:stroke-like symptoms
    n1=méningé (syndrome) | n2=en:stroke-like symptoms | rel=r_associated | relid=0 | w=22
  3957. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:structure of central auditory system
    n1=méningé (syndrome) | n2=en:structure of central auditory system | rel=r_associated | relid=0 | w=22
  3958. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:subcortical heterotopia
    n1=méningé (syndrome) | n2=en:subcortical heterotopia | rel=r_associated | relid=0 | w=22
  3959. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:subcortical hypomyelination
    n1=méningé (syndrome) | n2=en:subcortical hypomyelination | rel=r_associated | relid=0 | w=22
  3960. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:subependymal hemorrhage
    n1=méningé (syndrome) | n2=en:subependymal hemorrhage | rel=r_associated | relid=0 | w=22
  3961. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:subependymal pseudocyst
    n1=méningé (syndrome) | n2=en:subependymal pseudocyst | rel=r_associated | relid=0 | w=22
  3962. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:surgical aspects
    n1=méningé (syndrome) | n2=en:surgical aspects | rel=r_associated | relid=0 | w=22
  3963. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:swollen achromatic cells (pick cells)
    n1=méningé (syndrome) | n2=en:swollen achromatic cells (pick cells) | rel=r_associated | relid=0 | w=22
  3964. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:symptoms occur at rest
    n1=méningé (syndrome) | n2=en:symptoms occur at rest | rel=r_associated | relid=0 | w=22
  3965. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:symptoms stabilize within 4 weeks
    n1=méningé (syndrome) | n2=en:symptoms stabilize within 4 weeks | rel=r_associated | relid=0 | w=22
  3966. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:syringomyelia, noncommunicating (80% of cases)
    n1=méningé (syndrome) | n2=en:syringomyelia, noncommunicating (80% of cases) | rel=r_associated | relid=0 | w=22
  3967. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:t2-weighted hyperintensities in deep cerebral white matter, brainstem, and cerebellar white matter with sparing of the periventricular rim
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintensities in deep cerebral white matter, brainstem, and cerebellar white matter with sparing of the periventricular rim | rel=r_associated | relid=0 | w=22
  3968. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:temporal lobe infarct (rare)
    n1=méningé (syndrome) | n2=en:temporal lobe infarct (rare) | rel=r_associated | relid=0 | w=22
  3969. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:tethered spinal cord
    n1=méningé (syndrome) | n2=en:tethered spinal cord | rel=r_associated | relid=0 | w=22
  3970. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:thenar muscle atrophy
    n1=méningé (syndrome) | n2=en:thenar muscle atrophy | rel=r_associated | relid=0 | w=22
  3971. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:thenar muscle weakness
    n1=méningé (syndrome) | n2=en:thenar muscle weakness | rel=r_associated | relid=0 | w=22
  3972. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:thickened cortices
    n1=méningé (syndrome) | n2=en:thickened cortices | rel=r_associated | relid=0 | w=22
  3973. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:tonic head extension
    n1=méningé (syndrome) | n2=en:tonic head extension | rel=r_associated | relid=0 | w=22
  3974. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:tonic posturing
    n1=méningé (syndrome) | n2=en:tonic posturing | rel=r_associated | relid=0 | w=22
  3975. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:tonus dysregulation
    n1=méningé (syndrome) | n2=en:tonus dysregulation | rel=r_associated | relid=0 | w=22
  3976. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:transient ischemic attack
    n1=méningé (syndrome) | n2=en:transient ischemic attack | rel=r_associated | relid=0 | w=22
  3977. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:tremor of palate
    n1=méningé (syndrome) | n2=en:tremor of palate | rel=r_associated | relid=0 | w=22
  3978. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:upper limb spasticity
    n1=méningé (syndrome) | n2=en:upper limb spasticity | rel=r_associated | relid=0 | w=22
  3979. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:vasculopathy of the small arteries penetrating the white matter
    n1=méningé (syndrome) | n2=en:vasculopathy of the small arteries penetrating the white matter | rel=r_associated | relid=0 | w=22
  3980. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:ventricular dilatation (29%)
    n1=méningé (syndrome) | n2=en:ventricular dilatation (29%) | rel=r_associated | relid=0 | w=22
  3981. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:vestibular dysfunction
    n1=méningé (syndrome) | n2=en:vestibular dysfunction | rel=r_associated | relid=0 | w=22
  3982. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:visual hallucinations may occur
    n1=méningé (syndrome) | n2=en:visual hallucinations may occur | rel=r_associated | relid=0 | w=22
  3983. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:visual inattention
    n1=méningé (syndrome) | n2=en:visual inattention | rel=r_associated | relid=0 | w=22
  3984. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:white matter hyperintensities in various brain regions
    n1=méningé (syndrome) | n2=en:white matter hyperintensities in various brain regions | rel=r_associated | relid=0 | w=22
  3985. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:white matter hypodensities seen on mri
    n1=méningé (syndrome) | n2=en:white matter hypodensities seen on mri | rel=r_associated | relid=0 | w=22
  3986. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:white matter lesion
    n1=méningé (syndrome) | n2=en:white matter lesion | rel=r_associated | relid=0 | w=22
  3987. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:widening of cortical sulci
    n1=méningé (syndrome) | n2=en:widening of cortical sulci | rel=r_associated | relid=0 | w=22
  3988. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:widening of the ventricles
    n1=méningé (syndrome) | n2=en:widening of the ventricles | rel=r_associated | relid=0 | w=22
  3989. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> en:widespread tau (mapt)-positive glial and neuronal inclusions
    n1=méningé (syndrome) | n2=en:widespread tau (mapt)-positive glial and neuronal inclusions | rel=r_associated | relid=0 | w=22
  3990. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> maladie
    n1=méningé (syndrome) | n2=maladie | rel=r_associated | relid=0 | w=22
  3991. méningé (syndrome) -- r_associated #0: 22 / 0.265 -> maladie
    (médecine)
    n1=méningé (syndrome) | n2=maladie
    (médecine)
    | rel=r_associated | relid=0 | w=22
  3992. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:a subset of patients have neurologic abnormalities
    n1=méningé (syndrome) | n2=en:a subset of patients have neurologic abnormalities | rel=r_associated | relid=0 | w=21
  3993. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:abnormal eeg activity during sleep
    n1=méningé (syndrome) | n2=en:abnormal eeg activity during sleep | rel=r_associated | relid=0 | w=21
  3994. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:abnormal hypothalamo-pituitary axis
    n1=méningé (syndrome) | n2=en:abnormal hypothalamo-pituitary axis | rel=r_associated | relid=0 | w=21
  3995. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:abnormal posture
    n1=méningé (syndrome) | n2=en:abnormal posture | rel=r_associated | relid=0 | w=21
  3996. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:absence of olfactory bulbs
    n1=méningé (syndrome) | n2=en:absence of olfactory bulbs | rel=r_associated | relid=0 | w=21
  3997. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:absence of vestibular schwannomas at age greater than 18 years
    n1=méningé (syndrome) | n2=en:absence of vestibular schwannomas at age greater than 18 years | rel=r_associated | relid=0 | w=21
  3998. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:absence or hypoplasia of the anterior limb of the internal capsule
    n1=méningé (syndrome) | n2=en:absence or hypoplasia of the anterior limb of the internal capsule | rel=r_associated | relid=0 | w=21
  3999. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:absent corpus callosum (variable)
    n1=méningé (syndrome) | n2=en:absent corpus callosum (variable) | rel=r_associated | relid=0 | w=21
  4000. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:absent or delayed psychomotor development, severe
    n1=méningé (syndrome) | n2=en:absent or delayed psychomotor development, severe | rel=r_associated | relid=0 | w=21
  4001. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:actual effective cognition
    n1=méningé (syndrome) | n2=en:actual effective cognition | rel=r_associated | relid=0 | w=21
  4002. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:affected arteries have electron-dense granular material close to vascular smooth muscle cell membranes
    n1=méningé (syndrome) | n2=en:affected arteries have electron-dense granular material close to vascular smooth muscle cell membranes | rel=r_associated | relid=0 | w=21
  4003. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:agenesis of corpus callosum, partial or complete (rare)
    n1=méningé (syndrome) | n2=en:agenesis of corpus callosum, partial or complete (rare) | rel=r_associated | relid=0 | w=21
  4004. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:agnosia
    n1=méningé (syndrome) | n2=en:agnosia | rel=r_associated | relid=0 | w=21
  4005. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:altered mental status
    n1=méningé (syndrome) | n2=en:altered mental status | rel=r_associated | relid=0 | w=21
  4006. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:amyloid plaques may be present
    n1=méningé (syndrome) | n2=en:amyloid plaques may be present | rel=r_associated | relid=0 | w=21
  4007. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:amyloid-like plaques are not immunoreactive to app (104760)
    n1=méningé (syndrome) | n2=en:amyloid-like plaques are not immunoreactive to app (104760) | rel=r_associated | relid=0 | w=21
  4008. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:aqueductal stenosis
    n1=méningé (syndrome) | n2=en:aqueductal stenosis | rel=r_associated | relid=0 | w=21
  4009. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:arhinencephaly (1 patient)
    n1=méningé (syndrome) | n2=en:arhinencephaly (1 patient) | rel=r_associated | relid=0 | w=21
  4010. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:ataxia (1 patient)
    n1=méningé (syndrome) | n2=en:ataxia (1 patient) | rel=r_associated | relid=0 | w=21
  4011. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:ataxia, (1 family)
    n1=méningé (syndrome) | n2=en:ataxia, (1 family) | rel=r_associated | relid=0 | w=21
  4012. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:ataxic gait
    n1=méningé (syndrome) | n2=en:ataxic gait | rel=r_associated | relid=0 | w=21
  4013. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:athetosis (later)
    n1=méningé (syndrome) | n2=en:athetosis (later) | rel=r_associated | relid=0 | w=21
  4014. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:attenuated gyri
    n1=méningé (syndrome) | n2=en:attenuated gyri | rel=r_associated | relid=0 | w=21
  4015. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:axial hypotonia (1 patient)
    n1=méningé (syndrome) | n2=en:axial hypotonia (1 patient) | rel=r_associated | relid=0 | w=21
  4016. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:axonal 'spheroid' inclusions
    n1=méningé (syndrome) | n2=en:axonal 'spheroid' inclusions | rel=r_associated | relid=0 | w=21
  4017. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:balloon cells (in type iib)
    n1=méningé (syndrome) | n2=en:balloon cells (in type iib) | rel=r_associated | relid=0 | w=21
  4018. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:basal ganglia calcification
    n1=méningé (syndrome) | n2=en:basal ganglia calcification | rel=r_associated | relid=0 | w=21
  4019. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:basal ganglia calcifications (in some patients)
    n1=méningé (syndrome) | n2=en:basal ganglia calcifications (in some patients) | rel=r_associated | relid=0 | w=21
  4020. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:blindness
    n1=méningé (syndrome) | n2=en:blindness | rel=r_associated | relid=0 | w=21
  4021. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:brain
    n1=méningé (syndrome) | n2=en:brain | rel=r_associated | relid=0 | w=21
  4022. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:brain atrophy (in some patients)
    n1=méningé (syndrome) | n2=en:brain atrophy (in some patients) | rel=r_associated | relid=0 | w=21
  4023. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:brain imaging shows decreased white matter density
    n1=méningé (syndrome) | n2=en:brain imaging shows decreased white matter density | rel=r_associated | relid=0 | w=21
  4024. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:brain mri shows abnormal gyral pattern in frontal lobes
    n1=méningé (syndrome) | n2=en:brain mri shows abnormal gyral pattern in frontal lobes | rel=r_associated | relid=0 | w=21
  4025. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:brain mri shows cerebellar atrophy
    n1=méningé (syndrome) | n2=en:brain mri shows cerebellar atrophy | rel=r_associated | relid=0 | w=21
  4026. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:brain tissue shows cavitation of the basal ganglia
    n1=méningé (syndrome) | n2=en:brain tissue shows cavitation of the basal ganglia | rel=r_associated | relid=0 | w=21
  4027. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:brainstem lesions, hyperintense on t2-weighted imaging
    n1=méningé (syndrome) | n2=en:brainstem lesions, hyperintense on t2-weighted imaging | rel=r_associated | relid=0 | w=21
  4028. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:bulbar symptoms may occur (less common)
    n1=méningé (syndrome) | n2=en:bulbar symptoms may occur (less common) | rel=r_associated | relid=0 | w=21
  4029. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:burning pain in the limbs
    n1=méningé (syndrome) | n2=en:burning pain in the limbs | rel=r_associated | relid=0 | w=21
  4030. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:calcification may occur in other brain regions, including cerebellum, thalamus, white matter
    n1=méningé (syndrome) | n2=en:calcification may occur in other brain regions, including cerebellum, thalamus, white matter | rel=r_associated | relid=0 | w=21
  4031. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:calcifications may be seen in the thalamus, hippocampus, subcortical white matter, and cortex
    n1=méningé (syndrome) | n2=en:calcifications may be seen in the thalamus, hippocampus, subcortical white matter, and cortex | rel=r_associated | relid=0 | w=21
  4032. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cataplexy
    n1=méningé (syndrome) | n2=en:cataplexy | rel=r_associated | relid=0 | w=21
  4033. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:catatonic behavior
    n1=méningé (syndrome) | n2=en:catatonic behavior | rel=r_associated | relid=0 | w=21
  4034. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:central nervous system degeneration
    n1=méningé (syndrome) | n2=en:central nervous system degeneration | rel=r_associated | relid=0 | w=21
  4035. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar ataxia, adult-onset (in 1 family)
    n1=méningé (syndrome) | n2=en:cerebellar ataxia, adult-onset (in 1 family) | rel=r_associated | relid=0 | w=21
  4036. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar ataxia, limb and trunk
    n1=méningé (syndrome) | n2=en:cerebellar ataxia, limb and trunk | rel=r_associated | relid=0 | w=21
  4037. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar atrophy (96% of patients)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy (96% of patients) | rel=r_associated | relid=0 | w=21
  4038. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar atrophy (in some patients)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy (in some patients) | rel=r_associated | relid=0 | w=21
  4039. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar atrophy, mild
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, mild | rel=r_associated | relid=0 | w=21
  4040. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar atrophy, progressive (in some patients)
    n1=méningé (syndrome) | n2=en:cerebellar atrophy, progressive (in some patients) | rel=r_associated | relid=0 | w=21
  4041. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar cysts (meb)
    n1=méningé (syndrome) | n2=en:cerebellar cysts (meb) | rel=r_associated | relid=0 | w=21
  4042. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar origin most likely
    n1=méningé (syndrome) | n2=en:cerebellar origin most likely | rel=r_associated | relid=0 | w=21
  4043. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar signs (in some patients)
    n1=méningé (syndrome) | n2=en:cerebellar signs (in some patients) | rel=r_associated | relid=0 | w=21
  4044. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar signs (may be permanent in 50% of patients)
    n1=méningé (syndrome) | n2=en:cerebellar signs (may be permanent in 50% of patients) | rel=r_associated | relid=0 | w=21
  4045. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebellar signs, mild (in 1 of 3 families)
    n1=méningé (syndrome) | n2=en:cerebellar signs, mild (in 1 of 3 families) | rel=r_associated | relid=0 | w=21
  4046. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebral cortical atrophy, diffuse
    n1=méningé (syndrome) | n2=en:cerebral cortical atrophy, diffuse | rel=r_associated | relid=0 | w=21
  4047. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebral edema
    n1=méningé (syndrome) | n2=en:cerebral edema | rel=r_associated | relid=0 | w=21
  4048. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebral hypoplasia
    n1=méningé (syndrome) | n2=en:cerebral hypoplasia | rel=r_associated | relid=0 | w=21
  4049. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebral spongiosis
    n1=méningé (syndrome) | n2=en:cerebral spongiosis | rel=r_associated | relid=0 | w=21
  4050. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cerebral white matter lesion
    n1=méningé (syndrome) | n2=en:cerebral white matter lesion | rel=r_associated | relid=0 | w=21
  4051. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:chorea, mild (in some)
    n1=méningé (syndrome) | n2=en:chorea, mild (in some) | rel=r_associated | relid=0 | w=21
  4052. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:choreic movements (10 to 22% of patients)
    n1=méningé (syndrome) | n2=en:choreic movements (10 to 22% of patients) | rel=r_associated | relid=0 | w=21
  4053. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:chronic lymphocytic meningitis
    n1=méningé (syndrome) | n2=en:chronic lymphocytic meningitis | rel=r_associated | relid=0 | w=21
  4054. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:chronic subtype, headaches occur without remission for 1 year
    n1=méningé (syndrome) | n2=en:chronic subtype, headaches occur without remission for 1 year | rel=r_associated | relid=0 | w=21
  4055. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:clumsiness, unsteadiness
    n1=méningé (syndrome) | n2=en:clumsiness, unsteadiness | rel=r_associated | relid=0 | w=21
  4056. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:clumsy gait
    n1=méningé (syndrome) | n2=en:clumsy gait | rel=r_associated | relid=0 | w=21
  4057. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cognitive decline (1 patient)
    n1=méningé (syndrome) | n2=en:cognitive decline (1 patient) | rel=r_associated | relid=0 | w=21
  4058. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cognitive defects develop later in the disease
    n1=méningé (syndrome) | n2=en:cognitive defects develop later in the disease | rel=r_associated | relid=0 | w=21
  4059. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cognitive deficits (less common)
    n1=méningé (syndrome) | n2=en:cognitive deficits (less common) | rel=r_associated | relid=0 | w=21
  4060. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cognitive deficits may occur
    n1=méningé (syndrome) | n2=en:cognitive deficits may occur | rel=r_associated | relid=0 | w=21
  4061. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cognitive deficits, mild (in some patients)
    n1=méningé (syndrome) | n2=en:cognitive deficits, mild (in some patients) | rel=r_associated | relid=0 | w=21
  4062. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cognitive function, variable
    n1=méningé (syndrome) | n2=en:cognitive function, variable | rel=r_associated | relid=0 | w=21
  4063. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cognitive impairment (in 1 of 3 patients)
    n1=méningé (syndrome) | n2=en:cognitive impairment (in 1 of 3 patients) | rel=r_associated | relid=0 | w=21
  4064. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cognitive impairment, mild (1 patient)
    n1=méningé (syndrome) | n2=en:cognitive impairment, mild (1 patient) | rel=r_associated | relid=0 | w=21
  4065. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:complex partial seizure with impairment of consciousness
    n1=méningé (syndrome) | n2=en:complex partial seizure with impairment of consciousness | rel=r_associated | relid=0 | w=21
  4066. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:confusion
    n1=méningé (syndrome) | n2=en:confusion | rel=r_associated | relid=0 | w=21
  4067. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:consciousness fluctuating
    n1=méningé (syndrome) | n2=en:consciousness fluctuating | rel=r_associated | relid=0 | w=21
  4068. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:continuous spike-waves during slow-wave sleep
    n1=méningé (syndrome) | n2=en:continuous spike-waves during slow-wave sleep | rel=r_associated | relid=0 | w=21
  4069. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:contractures (older children and adolescents)
    n1=méningé (syndrome) | n2=en:contractures (older children and adolescents) | rel=r_associated | relid=0 | w=21
  4070. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:corpus callosum abnormalities (in some patients)
    n1=méningé (syndrome) | n2=en:corpus callosum abnormalities (in some patients) | rel=r_associated | relid=0 | w=21
  4071. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cortical and subcortical atrophy (1 patient)
    n1=méningé (syndrome) | n2=en:cortical and subcortical atrophy (1 patient) | rel=r_associated | relid=0 | w=21
  4072. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cortical atrophy with loss of pyramidal neurons in the motor cortex
    n1=méningé (syndrome) | n2=en:cortical atrophy with loss of pyramidal neurons in the motor cortex | rel=r_associated | relid=0 | w=21
  4073. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cortical dysplasia
    n1=méningé (syndrome) | n2=en:cortical dysplasia | rel=r_associated | relid=0 | w=21
  4074. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cortical neuronal loss
    n1=méningé (syndrome) | n2=en:cortical neuronal loss | rel=r_associated | relid=0 | w=21
  4075. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cortical tubers
    n1=méningé (syndrome) | n2=en:cortical tubers | rel=r_associated | relid=0 | w=21
  4076. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cranial nerve palsy, intermittent, transient
    n1=méningé (syndrome) | n2=en:cranial nerve palsy, intermittent, transient | rel=r_associated | relid=0 | w=21
  4077. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:cystic destruction of brain tissue, including basal ganglia
    n1=méningé (syndrome) | n2=en:cystic destruction of brain tissue, including basal ganglia | rel=r_associated | relid=0 | w=21
  4078. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:deafness
    n1=méningé (syndrome) | n2=en:deafness | rel=r_associated | relid=0 | w=21
  4079. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:decreased cerebellar folia
    n1=méningé (syndrome) | n2=en:decreased cerebellar folia | rel=r_associated | relid=0 | w=21
  4080. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:decreased cognition (later-onset)
    n1=méningé (syndrome) | n2=en:decreased cognition (later-onset) | rel=r_associated | relid=0 | w=21
  4081. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:decreased iq (1 patient)
    n1=méningé (syndrome) | n2=en:decreased iq (1 patient) | rel=r_associated | relid=0 | w=21
  4082. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:decreased iq (some patients)
    n1=méningé (syndrome) | n2=en:decreased iq (some patients) | rel=r_associated | relid=0 | w=21
  4083. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:decreased myelin
    n1=méningé (syndrome) | n2=en:decreased myelin | rel=r_associated | relid=0 | w=21
  4084. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:decreased need for sleep
    n1=méningé (syndrome) | n2=en:decreased need for sleep | rel=r_associated | relid=0 | w=21
  4085. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:decreased reflexes (in some patients)
    n1=méningé (syndrome) | n2=en:decreased reflexes (in some patients) | rel=r_associated | relid=0 | w=21
  4086. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:decreased white matter
    n1=méningé (syndrome) | n2=en:decreased white matter | rel=r_associated | relid=0 | w=21
  4087. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:deep interpeduncular fossa
    n1=méningé (syndrome) | n2=en:deep interpeduncular fossa | rel=r_associated | relid=0 | w=21
  4088. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:deficit in phonologic short-term memory
    n1=méningé (syndrome) | n2=en:deficit in phonologic short-term memory | rel=r_associated | relid=0 | w=21
  4089. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:deformed temporal lobes
    n1=méningé (syndrome) | n2=en:deformed temporal lobes | rel=r_associated | relid=0 | w=21
  4090. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:delayed brainstem development (in some patients)
    n1=méningé (syndrome) | n2=en:delayed brainstem development (in some patients) | rel=r_associated | relid=0 | w=21
  4091. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:delayed development if untreated
    n1=méningé (syndrome) | n2=en:delayed development if untreated | rel=r_associated | relid=0 | w=21
  4092. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:delayed gross motor development (in some patients)
    n1=méningé (syndrome) | n2=en:delayed gross motor development (in some patients) | rel=r_associated | relid=0 | w=21
  4093. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:delayed gyration
    n1=méningé (syndrome) | n2=en:delayed gyration | rel=r_associated | relid=0 | w=21
  4094. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:delayed myelination
    n1=méningé (syndrome) | n2=en:delayed myelination | rel=r_associated | relid=0 | w=21
  4095. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:delayed psychomotor development (1 patient)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development (1 patient) | rel=r_associated | relid=0 | w=21
  4096. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:delayed psychomotor development (mild to severe)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development (mild to severe) | rel=r_associated | relid=0 | w=21
  4097. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:delayed psychomotor development, mild (in 3 of 5 patients)
    n1=méningé (syndrome) | n2=en:delayed psychomotor development, mild (in 3 of 5 patients) | rel=r_associated | relid=0 | w=21
  4098. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:delayed walking (1 family)
    n1=méningé (syndrome) | n2=en:delayed walking (1 family) | rel=r_associated | relid=0 | w=21
  4099. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dementia (onset in fifth decade)
    n1=méningé (syndrome) | n2=en:dementia (onset in fifth decade) | rel=r_associated | relid=0 | w=21
  4100. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:developmental delay (type ii)
    n1=méningé (syndrome) | n2=en:developmental delay (type ii) | rel=r_associated | relid=0 | w=21
  4101. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:developmental delay (uncommon)
    n1=méningé (syndrome) | n2=en:developmental delay (uncommon) | rel=r_associated | relid=0 | w=21
  4102. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:developmental delay evident by 12-24 months of age
    n1=méningé (syndrome) | n2=en:developmental delay evident by 12-24 months of age | rel=r_associated | relid=0 | w=21
  4103. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:developmental delay, mild (in some)
    n1=méningé (syndrome) | n2=en:developmental delay, mild (in some) | rel=r_associated | relid=0 | w=21
  4104. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:difficulties in fine bimanual activities
    n1=méningé (syndrome) | n2=en:difficulties in fine bimanual activities | rel=r_associated | relid=0 | w=21
  4105. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:difficulty sleeping
    n1=méningé (syndrome) | n2=en:difficulty sleeping | rel=r_associated | relid=0 | w=21
  4106. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:diffuse cerebellar atrophy
    n1=méningé (syndrome) | n2=en:diffuse cerebellar atrophy | rel=r_associated | relid=0 | w=21
  4107. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:diffuse hypomyelination
    n1=méningé (syndrome) | n2=en:diffuse hypomyelination | rel=r_associated | relid=0 | w=21
  4108. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:diffuse lewy body pathology
    n1=méningé (syndrome) | n2=en:diffuse lewy body pathology | rel=r_associated | relid=0 | w=21
  4109. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:diffuse white matter abnormalities seen on brain mri
    n1=méningé (syndrome) | n2=en:diffuse white matter abnormalities seen on brain mri | rel=r_associated | relid=0 | w=21
  4110. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dilated perivascular spaces
    n1=méningé (syndrome) | n2=en:dilated perivascular spaces | rel=r_associated | relid=0 | w=21
  4111. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dilated ventricles (finding)
    n1=méningé (syndrome) | n2=en:dilated ventricles (finding) | rel=r_associated | relid=0 | w=21
  4112. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dilation of lateral ventricles (in some patients)
    n1=méningé (syndrome) | n2=en:dilation of lateral ventricles (in some patients) | rel=r_associated | relid=0 | w=21
  4113. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:diminished visual activity
    n1=méningé (syndrome) | n2=en:diminished visual activity | rel=r_associated | relid=0 | w=21
  4114. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:discrepancy between verbal and nonverbal abilities
    n1=méningé (syndrome) | n2=en:discrepancy between verbal and nonverbal abilities | rel=r_associated | relid=0 | w=21
  4115. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:distal muscle weakness and atrophy due to motor neuronopathy
    n1=méningé (syndrome) | n2=en:distal muscle weakness and atrophy due to motor neuronopathy | rel=r_associated | relid=0 | w=21
  4116. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:distal muscle weakness, upper and lower limbs
    n1=méningé (syndrome) | n2=en:distal muscle weakness, upper and lower limbs | rel=r_associated | relid=0 | w=21
  4117. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dysarthria may occur
    n1=méningé (syndrome) | n2=en:dysarthria may occur | rel=r_associated | relid=0 | w=21
  4118. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dysarthria, mild (in some patients)
    n1=méningé (syndrome) | n2=en:dysarthria, mild (in some patients) | rel=r_associated | relid=0 | w=21
  4119. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dysdiadochokinesis (1 family)
    n1=méningé (syndrome) | n2=en:dysdiadochokinesis (1 family) | rel=r_associated | relid=0 | w=21
  4120. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dysfunction of lateral corticospinal tracts
    n1=méningé (syndrome) | n2=en:dysfunction of lateral corticospinal tracts | rel=r_associated | relid=0 | w=21
  4121. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dysgenesis of corpus callosum
    n1=méningé (syndrome) | n2=en:dysgenesis of corpus callosum | rel=r_associated | relid=0 | w=21
  4122. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dyskinetic movements
    n1=méningé (syndrome) | n2=en:dyskinetic movements | rel=r_associated | relid=0 | w=21
  4123. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dysmetria (in 1 of 3 families)
    n1=méningé (syndrome) | n2=en:dysmetria (in 1 of 3 families) | rel=r_associated | relid=0 | w=21
  4124. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dysmorphic basal ganglia
    n1=méningé (syndrome) | n2=en:dysmorphic basal ganglia | rel=r_associated | relid=0 | w=21
  4125. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dysphagia
    n1=méningé (syndrome) | n2=en:dysphagia | rel=r_associated | relid=0 | w=21
  4126. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dysplastic cerebellar gangliocytoma
    n1=méningé (syndrome) | n2=en:dysplastic cerebellar gangliocytoma | rel=r_associated | relid=0 | w=21
  4127. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dystonia (in some patients)
    n1=méningé (syndrome) | n2=en:dystonia (in some patients) | rel=r_associated | relid=0 | w=21
  4128. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:dystonia, severe (in all limbs)
    n1=méningé (syndrome) | n2=en:dystonia, severe (in all limbs) | rel=r_associated | relid=0 | w=21
  4129. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:early and severe foot extensor muscle involvement
    n1=méningé (syndrome) | n2=en:early and severe foot extensor muscle involvement | rel=r_associated | relid=0 | w=21
  4130. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:early involvement of the corticospinal pathways
    n1=méningé (syndrome) | n2=en:early involvement of the corticospinal pathways | rel=r_associated | relid=0 | w=21
  4131. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:eeg - polyspike on photic stimulation (stage 1)
    n1=méningé (syndrome) | n2=en:eeg - polyspike on photic stimulation (stage 1) | rel=r_associated | relid=0 | w=21
  4132. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:eeg shows burst suppression
    n1=méningé (syndrome) | n2=en:eeg shows burst suppression | rel=r_associated | relid=0 | w=21
  4133. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:eeg shows suppression-burst pattern
    n1=méningé (syndrome) | n2=en:eeg shows suppression-burst pattern | rel=r_associated | relid=0 | w=21
  4134. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:eeg with paroxysmal activity
    n1=méningé (syndrome) | n2=en:eeg with paroxysmal activity | rel=r_associated | relid=0 | w=21
  4135. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:elevated white cell count in cerebrospinal fluid
    n1=méningé (syndrome) | n2=en:elevated white cell count in cerebrospinal fluid | rel=r_associated | relid=0 | w=21
  4136. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:emg shows continuous motor unit firing at rest
    n1=méningé (syndrome) | n2=en:emg shows continuous motor unit firing at rest | rel=r_associated | relid=0 | w=21
  4137. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:encephalopathy during episodes
    n1=méningé (syndrome) | n2=en:encephalopathy during episodes | rel=r_associated | relid=0 | w=21
  4138. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:encephalopathy, acute, sudden-onset after febrile illness
    n1=méningé (syndrome) | n2=en:encephalopathy, acute, sudden-onset after febrile illness | rel=r_associated | relid=0 | w=21
  4139. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:encephalopathy, severe, neonatal
    n1=méningé (syndrome) | n2=en:encephalopathy, severe, neonatal | rel=r_associated | relid=0 | w=21
  4140. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:enlarged extraaxial space on brain imaging
    n1=méningé (syndrome) | n2=en:enlarged extraaxial space on brain imaging | rel=r_associated | relid=0 | w=21
  4141. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:enlarged motor unit action potentials
    n1=méningé (syndrome) | n2=en:enlarged motor unit action potentials | rel=r_associated | relid=0 | w=21
  4142. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:entire central nervous system
    n1=méningé (syndrome) | n2=en:entire central nervous system | rel=r_associated | relid=0 | w=21
  4143. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:enzymology
    n1=méningé (syndrome) | n2=en:enzymology | rel=r_associated | relid=0 | w=21
  4144. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:epilepsies, myoclonic
    n1=méningé (syndrome) | n2=en:epilepsies, myoclonic | rel=r_associated | relid=0 | w=21
  4145. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:epileptic encephalopathy (in some patients)
    n1=méningé (syndrome) | n2=en:epileptic encephalopathy (in some patients) | rel=r_associated | relid=0 | w=21
  4146. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:episodes of decreased alertness, hypotonia, and poor respiration requiring mechanical ventilation
    n1=méningé (syndrome) | n2=en:episodes of decreased alertness, hypotonia, and poor respiration requiring mechanical ventilation | rel=r_associated | relid=0 | w=21
  4147. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:evolution to severe encephalopathy
    n1=méningé (syndrome) | n2=en:evolution to severe encephalopathy | rel=r_associated | relid=0 | w=21
  4148. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:extensor plantar responses (later)
    n1=méningé (syndrome) | n2=en:extensor plantar responses (later) | rel=r_associated | relid=0 | w=21
  4149. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:extensor plantar responses (variable)
    n1=méningé (syndrome) | n2=en:extensor plantar responses (variable) | rel=r_associated | relid=0 | w=21
  4150. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:extrapyramidal dyskinesias (1 patient)
    n1=méningé (syndrome) | n2=en:extrapyramidal dyskinesias (1 patient) | rel=r_associated | relid=0 | w=21
  4151. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:facial nerve palsy
    n1=méningé (syndrome) | n2=en:facial nerve palsy | rel=r_associated | relid=0 | w=21
  4152. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:facial nerve weakness
    n1=méningé (syndrome) | n2=en:facial nerve weakness | rel=r_associated | relid=0 | w=21
  4153. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:failure of opercularization of the frontal and temporal lobes on ct
    n1=méningé (syndrome) | n2=en:failure of opercularization of the frontal and temporal lobes on ct | rel=r_associated | relid=0 | w=21
  4154. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:falx cerebri, precocious calcification of
    n1=méningé (syndrome) | n2=en:falx cerebri, precocious calcification of | rel=r_associated | relid=0 | w=21
  4155. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:favorable response to levodopa
    n1=méningé (syndrome) | n2=en:favorable response to levodopa | rel=r_associated | relid=0 | w=21
  4156. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:festinating (parkinsonian) gait
    n1=méningé (syndrome) | n2=en:festinating (parkinsonian) gait | rel=r_associated | relid=0 | w=21
  4157. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:first dorsal interossei muscle weakness
    n1=méningé (syndrome) | n2=en:first dorsal interossei muscle weakness | rel=r_associated | relid=0 | w=21
  4158. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:fluid-filled cavity within the cerebral hemispheres, can be unilateral or bilateral and may or may not communicate with cerebrospinal fluid (csf) spaces
    n1=méningé (syndrome) | n2=en:fluid-filled cavity within the cerebral hemispheres, can be unilateral or bilateral and may or may not communicate with cerebrospinal fluid (csf) spaces | rel=r_associated | relid=0 | w=21
  4159. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:frightening sensation
    n1=méningé (syndrome) | n2=en:frightening sensation | rel=r_associated | relid=0 | w=21
  4160. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:frontal cortical atophy
    n1=méningé (syndrome) | n2=en:frontal cortical atophy | rel=r_associated | relid=0 | w=21
  4161. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:frontotemporoparietal cortical dysplasia
    n1=méningé (syndrome) | n2=en:frontotemporoparietal cortical dysplasia | rel=r_associated | relid=0 | w=21
  4162. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:fusion of the dentate nuclei and the superior cerebellar peduncles
    n1=méningé (syndrome) | n2=en:fusion of the dentate nuclei and the superior cerebellar peduncles | rel=r_associated | relid=0 | w=21
  4163. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:generalized cerebral, cerebellar, and brainstem atrophy, progressive
    n1=méningé (syndrome) | n2=en:generalized cerebral, cerebellar, and brainstem atrophy, progressive | rel=r_associated | relid=0 | w=21
  4164. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:generalized tonic-clonic seizures (often develop in adolescence)
    n1=méningé (syndrome) | n2=en:generalized tonic-clonic seizures (often develop in adolescence) | rel=r_associated | relid=0 | w=21
  4165. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:generalized tonic-clonic seizures (stage 2 and 3)
    n1=méningé (syndrome) | n2=en:generalized tonic-clonic seizures (stage 2 and 3) | rel=r_associated | relid=0 | w=21
  4166. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:gliosis in the brainstem
    n1=méningé (syndrome) | n2=en:gliosis in the brainstem | rel=r_associated | relid=0 | w=21
  4167. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:gliosis in the striatum, medial thalamic nuclei, and inferior olives
    n1=méningé (syndrome) | n2=en:gliosis in the striatum, medial thalamic nuclei, and inferior olives | rel=r_associated | relid=0 | w=21
  4168. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:globally delayed development
    n1=méningé (syndrome) | n2=en:globally delayed development | rel=r_associated | relid=0 | w=21
  4169. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:gtcs during 'leisure' time (evening)
    n1=méningé (syndrome) | n2=en:gtcs during 'leisure' time (evening) | rel=r_associated | relid=0 | w=21
  4170. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:head lag
    n1=méningé (syndrome) | n2=en:head lag | rel=r_associated | relid=0 | w=21
  4171. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:head oscillations
    n1=méningé (syndrome) | n2=en:head oscillations | rel=r_associated | relid=0 | w=21
  4172. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:headache, episodic
    n1=méningé (syndrome) | n2=en:headache, episodic | rel=r_associated | relid=0 | w=21
  4173. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:headache, suboccipital, migraine-like (most common symptom) precipitated by coughing, sneezing, bending forward, lifting, neck extension
    n1=méningé (syndrome) | n2=en:headache, suboccipital, migraine-like (most common symptom) precipitated by coughing, sneezing, bending forward, lifting, neck extension | rel=r_associated | relid=0 | w=21
  4174. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hemiparesis (in some patients)
    n1=méningé (syndrome) | n2=en:hemiparesis (in some patients) | rel=r_associated | relid=0 | w=21
  4175. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hemiplegia
    n1=méningé (syndrome) | n2=en:hemiplegia | rel=r_associated | relid=0 | w=21
  4176. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hemiplegic migraine in some patients
    n1=méningé (syndrome) | n2=en:hemiplegic migraine in some patients | rel=r_associated | relid=0 | w=21
  4177. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hippocampal atrophy (in 2 siblings)
    n1=méningé (syndrome) | n2=en:hippocampal atrophy (in 2 siblings) | rel=r_associated | relid=0 | w=21
  4178. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hydranencephaly
    n1=méningé (syndrome) | n2=en:hydranencephaly | rel=r_associated | relid=0 | w=21
  4179. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hydrocephalus
    n1=méningé (syndrome) | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=21
  4180. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hyperkinesia
    n1=méningé (syndrome) | n2=en:hyperkinesia | rel=r_associated | relid=0 | w=21
  4181. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypermotor behavior
    n1=méningé (syndrome) | n2=en:hypermotor behavior | rel=r_associated | relid=0 | w=21
  4182. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypertonicity
    n1=méningé (syndrome) | n2=en:hypertonicity | rel=r_associated | relid=0 | w=21
  4183. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypodensity of the white matter
    n1=méningé (syndrome) | n2=en:hypodensity of the white matter | rel=r_associated | relid=0 | w=21
  4184. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypomyelinating leukoencephalopathy
    n1=méningé (syndrome) | n2=en:hypomyelinating leukoencephalopathy | rel=r_associated | relid=0 | w=21
  4185. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypomyelination (1 patient)
    n1=méningé (syndrome) | n2=en:hypomyelination (1 patient) | rel=r_associated | relid=0 | w=21
  4186. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypoplasia of dentate nucleus
    n1=méningé (syndrome) | n2=en:hypoplasia of dentate nucleus | rel=r_associated | relid=0 | w=21
  4187. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypoplasia of the brainstem
    n1=méningé (syndrome) | n2=en:hypoplasia of the brainstem | rel=r_associated | relid=0 | w=21
  4188. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypoplastic corpus callosum (1 patient)
    n1=méningé (syndrome) | n2=en:hypoplastic corpus callosum (1 patient) | rel=r_associated | relid=0 | w=21
  4189. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hyporeflexia or areflexia
    n1=méningé (syndrome) | n2=en:hyporeflexia or areflexia | rel=r_associated | relid=0 | w=21
  4190. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypotonia (in males)
    n1=méningé (syndrome) | n2=en:hypotonia (in males) | rel=r_associated | relid=0 | w=21
  4191. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypotonia in infancy and early childhood
    n1=méningé (syndrome) | n2=en:hypotonia in infancy and early childhood | rel=r_associated | relid=0 | w=21
  4192. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypotonia, axial, severe
    n1=méningé (syndrome) | n2=en:hypotonia, axial, severe | rel=r_associated | relid=0 | w=21
  4193. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:hypotonia, profound muscular (in some patients)
    n1=méningé (syndrome) | n2=en:hypotonia, profound muscular (in some patients) | rel=r_associated | relid=0 | w=21
  4194. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:ictal eeg shows diffuse slow delta and theta activity
    n1=méningé (syndrome) | n2=en:ictal eeg shows diffuse slow delta and theta activity | rel=r_associated | relid=0 | w=21
  4195. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:ictal eeg shows focal onset, often posterior region of brain
    n1=méningé (syndrome) | n2=en:ictal eeg shows focal onset, often posterior region of brain | rel=r_associated | relid=0 | w=21
  4196. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:impaired long-term verbal memory
    n1=méningé (syndrome) | n2=en:impaired long-term verbal memory | rel=r_associated | relid=0 | w=21
  4197. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:inability to walk unaided
    n1=méningé (syndrome) | n2=en:inability to walk unaided | rel=r_associated | relid=0 | w=21
  4198. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:inarticulate speech delayed gross motor skills
    n1=méningé (syndrome) | n2=en:inarticulate speech delayed gross motor skills | rel=r_associated | relid=0 | w=21
  4199. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:incoordination of the hands
    n1=méningé (syndrome) | n2=en:incoordination of the hands | rel=r_associated | relid=0 | w=21
  4200. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:increased lactate in the brain
    n1=méningé (syndrome) | n2=en:increased lactate in the brain | rel=r_associated | relid=0 | w=21
  4201. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:increased t2 signal intensities in the middle cerebellar peduncles
    n1=méningé (syndrome) | n2=en:increased t2 signal intensities in the middle cerebellar peduncles | rel=r_associated | relid=0 | w=21
  4202. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:infantile hemiplegias
    n1=méningé (syndrome) | n2=en:infantile hemiplegias | rel=r_associated | relid=0 | w=21
  4203. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:initial hypotonia, followed by spasticity
    n1=méningé (syndrome) | n2=en:initial hypotonia, followed by spasticity | rel=r_associated | relid=0 | w=21
  4204. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:insomnia, refractory
    n1=méningé (syndrome) | n2=en:insomnia, refractory | rel=r_associated | relid=0 | w=21
  4205. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:intellectual delay
    n1=méningé (syndrome) | n2=en:intellectual delay | rel=r_associated | relid=0 | w=21
  4206. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:intellectual disability (in some patients)
    n1=méningé (syndrome) | n2=en:intellectual disability (in some patients) | rel=r_associated | relid=0 | w=21
  4207. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:interictal downbeat nystagmus
    n1=méningé (syndrome) | n2=en:interictal downbeat nystagmus | rel=r_associated | relid=0 | w=21
  4208. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:intermittent episodes associated with lethargy, vomiting
    n1=méningé (syndrome) | n2=en:intermittent episodes associated with lethargy, vomiting | rel=r_associated | relid=0 | w=21
  4209. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:intracerebral cysts (in some patients)
    n1=méningé (syndrome) | n2=en:intracerebral cysts (in some patients) | rel=r_associated | relid=0 | w=21
  4210. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:intracranial calcifications in the anterior mesial temporal lobes
    n1=méningé (syndrome) | n2=en:intracranial calcifications in the anterior mesial temporal lobes | rel=r_associated | relid=0 | w=21
  4211. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:intracranial calcifications, band-like, particularly periventricular and in the basal ganglia and thalamus
    n1=méningé (syndrome) | n2=en:intracranial calcifications, band-like, particularly periventricular and in the basal ganglia and thalamus | rel=r_associated | relid=0 | w=21
  4212. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:involuntary jerking movements
    n1=méningé (syndrome) | n2=en:involuntary jerking movements | rel=r_associated | relid=0 | w=21
  4213. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:involuntary movements
    n1=méningé (syndrome) | n2=en:involuntary movements | rel=r_associated | relid=0 | w=21
  4214. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:involuntary rhythmic myoclonic movements ('tremor') of the distal extremities, usually fingers
    n1=méningé (syndrome) | n2=en:involuntary rhythmic myoclonic movements ('tremor') of the distal extremities, usually fingers | rel=r_associated | relid=0 | w=21
  4215. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:iron deposition in the globus pallidus (variable)
    n1=méningé (syndrome) | n2=en:iron deposition in the globus pallidus (variable) | rel=r_associated | relid=0 | w=21
  4216. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:ischemic stroke in the basal ganglia (rare)
    n1=méningé (syndrome) | n2=en:ischemic stroke in the basal ganglia (rare) | rel=r_associated | relid=0 | w=21
  4217. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:jacksonian seizure
    n1=méningé (syndrome) | n2=en:jacksonian seizure | rel=r_associated | relid=0 | w=21
  4218. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:jerking movements
    n1=méningé (syndrome) | n2=en:jerking movements | rel=r_associated | relid=0 | w=21
  4219. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:jerky head movements
    n1=méningé (syndrome) | n2=en:jerky head movements | rel=r_associated | relid=0 | w=21
  4220. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:jerky limb movements
    n1=méningé (syndrome) | n2=en:jerky limb movements | rel=r_associated | relid=0 | w=21
  4221. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:knee and ankle clonus
    n1=méningé (syndrome) | n2=en:knee and ankle clonus | rel=r_associated | relid=0 | w=21
  4222. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:late-onset spinocerebellar degeneration
    n1=méningé (syndrome) | n2=en:late-onset spinocerebellar degeneration | rel=r_associated | relid=0 | w=21
  4223. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:learning disability (early in life)
    n1=méningé (syndrome) | n2=en:learning disability (early in life) | rel=r_associated | relid=0 | w=21
  4224. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:leg stiffness
    n1=méningé (syndrome) | n2=en:leg stiffness | rel=r_associated | relid=0 | w=21
  4225. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:leigh syndrome (in some patients)
    n1=méningé (syndrome) | n2=en:leigh syndrome (in some patients) | rel=r_associated | relid=0 | w=21
  4226. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:little spontaneous movement
    n1=méningé (syndrome) | n2=en:little spontaneous movement | rel=r_associated | relid=0 | w=21
  4227. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:loss of dorsal root ganglion cells
    n1=méningé (syndrome) | n2=en:loss of dorsal root ganglion cells | rel=r_associated | relid=0 | w=21
  4228. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:loss of fine motor skills
    n1=méningé (syndrome) | n2=en:loss of fine motor skills | rel=r_associated | relid=0 | w=21
  4229. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:loss of hypocretin (orexin)-secreting neurons in the hypothalamus
    n1=méningé (syndrome) | n2=en:loss of hypocretin (orexin)-secreting neurons in the hypothalamus | rel=r_associated | relid=0 | w=21
  4230. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:loss of independent ambulation within a few years
    n1=méningé (syndrome) | n2=en:loss of independent ambulation within a few years | rel=r_associated | relid=0 | w=21
  4231. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:loss of myelin in the cerebral and cerebellar white matter
    n1=méningé (syndrome) | n2=en:loss of myelin in the cerebral and cerebellar white matter | rel=r_associated | relid=0 | w=21
  4232. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:loss of pain and temperature in a cape-like distribution
    n1=méningé (syndrome) | n2=en:loss of pain and temperature in a cape-like distribution | rel=r_associated | relid=0 | w=21
  4233. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:lower limb hyperreflexia (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:lower limb hyperreflexia (reported in 1 patient) | rel=r_associated | relid=0 | w=21
  4234. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:lower limb hypertonia
    n1=méningé (syndrome) | n2=en:lower limb hypertonia | rel=r_associated | relid=0 | w=21
  4235. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:lower limb muscle atrophy
    n1=méningé (syndrome) | n2=en:lower limb muscle atrophy | rel=r_associated | relid=0 | w=21
  4236. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:lower limb spasticity, mild
    n1=méningé (syndrome) | n2=en:lower limb spasticity, mild | rel=r_associated | relid=0 | w=21
  4237. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:lower limbs affected before upper limbs
    n1=méningé (syndrome) | n2=en:lower limbs affected before upper limbs | rel=r_associated | relid=0 | w=21
  4238. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:lower motor neuron disease affecting upper and lower limbs
    n1=méningé (syndrome) | n2=en:lower motor neuron disease affecting upper and lower limbs | rel=r_associated | relid=0 | w=21
  4239. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:lower motor neuron dysfunction involving upper and lower limbs
    n1=méningé (syndrome) | n2=en:lower motor neuron dysfunction involving upper and lower limbs | rel=r_associated | relid=0 | w=21
  4240. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:malformations of cortical development, variable
    n1=méningé (syndrome) | n2=en:malformations of cortical development, variable | rel=r_associated | relid=0 | w=21
  4241. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:malformations of the mid- and hindbrain
    n1=méningé (syndrome) | n2=en:malformations of the mid- and hindbrain | rel=r_associated | relid=0 | w=21
  4242. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:memory defects
    n1=méningé (syndrome) | n2=en:memory defects | rel=r_associated | relid=0 | w=21
  4243. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:meningeal
    n1=méningé (syndrome) | n2=en:meningeal | rel=r_associated | relid=0 | w=21
  4244. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental deterioration in childhood
    n1=méningé (syndrome) | n2=en:mental deterioration in childhood | rel=r_associated | relid=0 | w=21
  4245. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation (25%)
    n1=méningé (syndrome) | n2=en:mental retardation (25%) | rel=r_associated | relid=0 | w=21
  4246. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation (3 patients)
    n1=méningé (syndrome) | n2=en:mental retardation (3 patients) | rel=r_associated | relid=0 | w=21
  4247. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation (38%)
    n1=méningé (syndrome) | n2=en:mental retardation (38%) | rel=r_associated | relid=0 | w=21
  4248. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation (47%)
    n1=méningé (syndrome) | n2=en:mental retardation (47%) | rel=r_associated | relid=0 | w=21
  4249. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation (in some cases)
    n1=méningé (syndrome) | n2=en:mental retardation (in some cases) | rel=r_associated | relid=0 | w=21
  4250. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation (variable expression)
    n1=méningé (syndrome) | n2=en:mental retardation (variable expression) | rel=r_associated | relid=0 | w=21
  4251. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation by the age of 7 years
    n1=méningé (syndrome) | n2=en:mental retardation by the age of 7 years | rel=r_associated | relid=0 | w=21
  4252. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation if untreated
    n1=méningé (syndrome) | n2=en:mental retardation if untreated | rel=r_associated | relid=0 | w=21
  4253. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation in survivors
    n1=méningé (syndrome) | n2=en:mental retardation in survivors | rel=r_associated | relid=0 | w=21
  4254. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation may occur
    n1=méningé (syndrome) | n2=en:mental retardation may occur | rel=r_associated | relid=0 | w=21
  4255. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation, mild to moderate (20% of patients)
    n1=méningé (syndrome) | n2=en:mental retardation, mild to moderate (20% of patients) | rel=r_associated | relid=0 | w=21
  4256. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mental retardation, moderate to severe (type ii, infantile and juvenile)
    n1=méningé (syndrome) | n2=en:mental retardation, moderate to severe (type ii, infantile and juvenile) | rel=r_associated | relid=0 | w=21
  4257. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:metastatic meningioma
    n1=méningé (syndrome) | n2=en:metastatic meningioma | rel=r_associated | relid=0 | w=21
  4258. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:microgyria
    n1=méningé (syndrome) | n2=en:microgyria | rel=r_associated | relid=0 | w=21
  4259. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:migraine (in some patients)
    n1=méningé (syndrome) | n2=en:migraine (in some patients) | rel=r_associated | relid=0 | w=21
  4260. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:migraine with aura, usually visual (in 50% of patients)
    n1=méningé (syndrome) | n2=en:migraine with aura, usually visual (in 50% of patients) | rel=r_associated | relid=0 | w=21
  4261. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:migraine without aura
    n1=méningé (syndrome) | n2=en:migraine without aura | rel=r_associated | relid=0 | w=21
  4262. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mild cognitive impairment (in some patients)
    n1=méningé (syndrome) | n2=en:mild cognitive impairment (in some patients) | rel=r_associated | relid=0 | w=21
  4263. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mild mental retardation (some)
    n1=méningé (syndrome) | n2=en:mild mental retardation (some) | rel=r_associated | relid=0 | w=21
  4264. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mild psychomotor delay
    n1=méningé (syndrome) | n2=en:mild psychomotor delay | rel=r_associated | relid=0 | w=21
  4265. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:moro reflex absent
    n1=méningé (syndrome) | n2=en:moro reflex absent | rel=r_associated | relid=0 | w=21
  4266. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:most never acquire independent ambulation
    n1=méningé (syndrome) | n2=en:most never acquire independent ambulation | rel=r_associated | relid=0 | w=21
  4267. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:motor symptoms may be present
    n1=méningé (syndrome) | n2=en:motor symptoms may be present | rel=r_associated | relid=0 | w=21
  4268. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:movement disorder
    n1=méningé (syndrome) | n2=en:movement disorder | rel=r_associated | relid=0 | w=21
  4269. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:movements ('tremors') characterized by 8 to 10-hz discharges
    n1=méningé (syndrome) | n2=en:movements ('tremors') characterized by 8 to 10-hz discharges | rel=r_associated | relid=0 | w=21
  4270. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mri shows global lack of myelination in the cerebral hemispheres
    n1=méningé (syndrome) | n2=en:mri shows global lack of myelination in the cerebral hemispheres | rel=r_associated | relid=0 | w=21
  4271. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:mri shows symmetric lesions of the basal ganglia (particularly caudate and putamen)
    n1=méningé (syndrome) | n2=en:mri shows symmetric lesions of the basal ganglia (particularly caudate and putamen) | rel=r_associated | relid=0 | w=21
  4272. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:multifocal discharges
    n1=méningé (syndrome) | n2=en:multifocal discharges | rel=r_associated | relid=0 | w=21
  4273. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:multifocal intractable seizures
    n1=méningé (syndrome) | n2=en:multifocal intractable seizures | rel=r_associated | relid=0 | w=21
  4274. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:myelomeningocele (less common)
    n1=méningé (syndrome) | n2=en:myelomeningocele (less common) | rel=r_associated | relid=0 | w=21
  4275. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:myoclonic seizures (1 patient)
    n1=méningé (syndrome) | n2=en:myoclonic seizures (1 patient) | rel=r_associated | relid=0 | w=21
  4276. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:myoclonic seizures, frequent, long-lasting (many hours)
    n1=méningé (syndrome) | n2=en:myoclonic seizures, frequent, long-lasting (many hours) | rel=r_associated | relid=0 | w=21
  4277. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:myoclonic-astatic seizures
    n1=méningé (syndrome) | n2=en:myoclonic-astatic seizures | rel=r_associated | relid=0 | w=21
  4278. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:myokymia, especially facial
    n1=méningé (syndrome) | n2=en:myokymia, especially facial | rel=r_associated | relid=0 | w=21
  4279. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:myopathy
    n1=méningé (syndrome) | n2=en:myopathy | rel=r_associated | relid=0 | w=21
  4280. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:nerve paralysis
    n1=méningé (syndrome) | n2=en:nerve paralysis | rel=r_associated | relid=0 | w=21
  4281. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:neuroaxonal dystrophies
    n1=méningé (syndrome) | n2=en:neuroaxonal dystrophies | rel=r_associated | relid=0 | w=21
  4282. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:neurodevelopmental impairment (early-onset form)
    n1=méningé (syndrome) | n2=en:neurodevelopmental impairment (early-onset form) | rel=r_associated | relid=0 | w=21
  4283. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:neurologic involvement is rare
    n1=méningé (syndrome) | n2=en:neurologic involvement is rare | rel=r_associated | relid=0 | w=21
  4284. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:neurologic regression after prolonged episodes
    n1=méningé (syndrome) | n2=en:neurologic regression after prolonged episodes | rel=r_associated | relid=0 | w=21
  4285. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:neuronal loss in basal ganglia
    n1=méningé (syndrome) | n2=en:neuronal loss in basal ganglia | rel=r_associated | relid=0 | w=21
  4286. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:neuronal loss in the cerebrum and cerebellum
    n1=méningé (syndrome) | n2=en:neuronal loss in the cerebrum and cerebellum | rel=r_associated | relid=0 | w=21
  4287. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:neuronal loss in the dentate nuclei
    n1=méningé (syndrome) | n2=en:neuronal loss in the dentate nuclei | rel=r_associated | relid=0 | w=21
  4288. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:neuronal loss in the locus ceruleus
    n1=méningé (syndrome) | n2=en:neuronal loss in the locus ceruleus | rel=r_associated | relid=0 | w=21
  4289. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:neuropathology shows neuronal loss in basal ganglia, brainstem, and cerebellum
    n1=méningé (syndrome) | n2=en:neuropathology shows neuronal loss in basal ganglia, brainstem, and cerebellum | rel=r_associated | relid=0 | w=21
  4290. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:never able to walk
    n1=méningé (syndrome) | n2=en:never able to walk | rel=r_associated | relid=0 | w=21
  4291. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:no development
    n1=méningé (syndrome) | n2=en:no development | rel=r_associated | relid=0 | w=21
  4292. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:no hippocampal sclerosis
    n1=méningé (syndrome) | n2=en:no hippocampal sclerosis | rel=r_associated | relid=0 | w=21
  4293. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:no hydrocephalus
    n1=méningé (syndrome) | n2=en:no hydrocephalus | rel=r_associated | relid=0 | w=21
  4294. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:no overt seizures
    n1=méningé (syndrome) | n2=en:no overt seizures | rel=r_associated | relid=0 | w=21
  4295. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:nocturnal seizures (in some patients)
    n1=méningé (syndrome) | n2=en:nocturnal seizures (in some patients) | rel=r_associated | relid=0 | w=21
  4296. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:nodular heterotopia
    n1=méningé (syndrome) | n2=en:nodular heterotopia | rel=r_associated | relid=0 | w=21
  4297. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:normal development (in 2 of 6 patients)
    n1=méningé (syndrome) | n2=en:normal development (in 2 of 6 patients) | rel=r_associated | relid=0 | w=21
  4298. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:normal interictal eeg
    n1=méningé (syndrome) | n2=en:normal interictal eeg | rel=r_associated | relid=0 | w=21
  4299. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:nuclear magnetic resonance imaging brain normal
    n1=méningé (syndrome) | n2=en:nuclear magnetic resonance imaging brain normal | rel=r_associated | relid=0 | w=21
  4300. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:occipital headache
    n1=méningé (syndrome) | n2=en:occipital headache | rel=r_associated | relid=0 | w=21
  4301. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:occipital neural tube defects
    n1=méningé (syndrome) | n2=en:occipital neural tube defects | rel=r_associated | relid=0 | w=21
  4302. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:ocular muscle abnormalities
    n1=méningé (syndrome) | n2=en:ocular muscle abnormalities | rel=r_associated | relid=0 | w=21
  4303. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:olivopontocerebellar hypoplasia, severe
    n1=méningé (syndrome) | n2=en:olivopontocerebellar hypoplasia, severe | rel=r_associated | relid=0 | w=21
  4304. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:optic tract and chiasm hypoplasia
    n1=méningé (syndrome) | n2=en:optic tract and chiasm hypoplasia | rel=r_associated | relid=0 | w=21
  4305. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:pachymacrogyria
    n1=méningé (syndrome) | n2=en:pachymacrogyria | rel=r_associated | relid=0 | w=21
  4306. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:pain (sharp, boring, drilling, piercing)
    n1=méningé (syndrome) | n2=en:pain (sharp, boring, drilling, piercing) | rel=r_associated | relid=0 | w=21
  4307. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:paraneoplastic syndrome
    n1=méningé (syndrome) | n2=en:paraneoplastic syndrome | rel=r_associated | relid=0 | w=21
  4308. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:paraventricular cysts
    n1=méningé (syndrome) | n2=en:paraventricular cysts | rel=r_associated | relid=0 | w=21
  4309. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:parkinsonism
    n1=méningé (syndrome) | n2=en:parkinsonism | rel=r_associated | relid=0 | w=21
  4310. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:patchy diffuse hyperintensities on t2-weighted mri
    n1=méningé (syndrome) | n2=en:patchy diffuse hyperintensities on t2-weighted mri | rel=r_associated | relid=0 | w=21
  4311. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:patellar tendon reflexes hyperactive
    n1=méningé (syndrome) | n2=en:patellar tendon reflexes hyperactive | rel=r_associated | relid=0 | w=21
  4312. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:pathologic changes in anterior horn cells and lateral corticospinal tracts
    n1=méningé (syndrome) | n2=en:pathologic changes in anterior horn cells and lateral corticospinal tracts | rel=r_associated | relid=0 | w=21
  4313. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:patients 30-40 years old have hyperintense lesions in periventricular areas, the external capsule, basal ganglia, thalamus, and brainstem
    n1=méningé (syndrome) | n2=en:patients 30-40 years old have hyperintense lesions in periventricular areas, the external capsule, basal ganglia, thalamus, and brainstem | rel=r_associated | relid=0 | w=21
  4314. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:peculiar stance and sitting posture (if left untreated)
    n1=méningé (syndrome) | n2=en:peculiar stance and sitting posture (if left untreated) | rel=r_associated | relid=0 | w=21
  4315. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:pharyngeal gag reflex negative
    n1=méningé (syndrome) | n2=en:pharyngeal gag reflex negative | rel=r_associated | relid=0 | w=21
  4316. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:phonology deficits
    n1=méningé (syndrome) | n2=en:phonology deficits | rel=r_associated | relid=0 | w=21
  4317. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:photosensitivity in one-third of patients
    n1=méningé (syndrome) | n2=en:photosensitivity in one-third of patients | rel=r_associated | relid=0 | w=21
  4318. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:polyglucosan bodies (round intracellular inclusions) found in neuronal and astrocytic processes
    n1=méningé (syndrome) | n2=en:polyglucosan bodies (round intracellular inclusions) found in neuronal and astrocytic processes | rel=r_associated | relid=0 | w=21
  4319. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:polygyria
    n1=méningé (syndrome) | n2=en:polygyria | rel=r_associated | relid=0 | w=21
  4320. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:polymicrogyria (reported in 1 patient)
    n1=méningé (syndrome) | n2=en:polymicrogyria (reported in 1 patient) | rel=r_associated | relid=0 | w=21
  4321. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:pontine hypoplasia, mild
    n1=méningé (syndrome) | n2=en:pontine hypoplasia, mild | rel=r_associated | relid=0 | w=21
  4322. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:poor adaptive skills
    n1=méningé (syndrome) | n2=en:poor adaptive skills | rel=r_associated | relid=0 | w=21
  4323. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:poor hand-eye coordination
    n1=méningé (syndrome) | n2=en:poor hand-eye coordination | rel=r_associated | relid=0 | w=21
  4324. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:poor speech or lack of speech development
    n1=méningé (syndrome) | n2=en:poor speech or lack of speech development | rel=r_associated | relid=0 | w=21
  4325. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:posterior column degeneration
    n1=méningé (syndrome) | n2=en:posterior column degeneration | rel=r_associated | relid=0 | w=21
  4326. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:posterior fossa abnormalities (rare)
    n1=méningé (syndrome) | n2=en:posterior fossa abnormalities (rare) | rel=r_associated | relid=0 | w=21
  4327. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:progressive cerebellar ataxia
    n1=méningé (syndrome) | n2=en:progressive cerebellar ataxia | rel=r_associated | relid=0 | w=21
  4328. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:progressive encephalopathy
    n1=méningé (syndrome) | n2=en:progressive encephalopathy | rel=r_associated | relid=0 | w=21
  4329. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:progressive inability to walk
    n1=méningé (syndrome) | n2=en:progressive inability to walk | rel=r_associated | relid=0 | w=21
  4330. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:progressive pyramidal and cerebellar signs
    n1=méningé (syndrome) | n2=en:progressive pyramidal and cerebellar signs | rel=r_associated | relid=0 | w=21
  4331. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:progressive truncal ataxia
    n1=méningé (syndrome) | n2=en:progressive truncal ataxia | rel=r_associated | relid=0 | w=21
  4332. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:progressive white matter lesions in the brain
    n1=méningé (syndrome) | n2=en:progressive white matter lesions in the brain | rel=r_associated | relid=0 | w=21
  4333. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:proximal weakness of the lower extremities
    n1=méningé (syndrome) | n2=en:proximal weakness of the lower extremities | rel=r_associated | relid=0 | w=21
  4334. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:pseudolaminar spongiform changes
    n1=méningé (syndrome) | n2=en:pseudolaminar spongiform changes | rel=r_associated | relid=0 | w=21
  4335. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:psychiatric symptoms (delusions, hallucinations)
    n1=méningé (syndrome) | n2=en:psychiatric symptoms (delusions, hallucinations) | rel=r_associated | relid=0 | w=21
  4336. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:quadriparesis
    n1=méningé (syndrome) | n2=en:quadriparesis | rel=r_associated | relid=0 | w=21
  4337. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:rapid regression
    n1=méningé (syndrome) | n2=en:rapid regression | rel=r_associated | relid=0 | w=21
  4338. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:recurrent seizures nos
    n1=méningé (syndrome) | n2=en:recurrent seizures nos | rel=r_associated | relid=0 | w=21
  4339. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:reduced cerebral white matter
    n1=méningé (syndrome) | n2=en:reduced cerebral white matter | rel=r_associated | relid=0 | w=21
  4340. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:regression of early motor skills
    n1=méningé (syndrome) | n2=en:regression of early motor skills | rel=r_associated | relid=0 | w=21
  4341. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:response to pyridoxal phosphate
    n1=méningé (syndrome) | n2=en:response to pyridoxal phosphate | rel=r_associated | relid=0 | w=21
  4342. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:resting myoclonus
    n1=méningé (syndrome) | n2=en:resting myoclonus | rel=r_associated | relid=0 | w=21
  4343. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:romberg's sign positive
    n1=méningé (syndrome) | n2=en:romberg's sign positive | rel=r_associated | relid=0 | w=21
  4344. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:salaam seizures
    n1=méningé (syndrome) | n2=en:salaam seizures | rel=r_associated | relid=0 | w=21
  4345. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures (1 patient)
    n1=méningé (syndrome) | n2=en:seizures (1 patient) | rel=r_associated | relid=0 | w=21
  4346. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures (2-10% of patients)
    n1=méningé (syndrome) | n2=en:seizures (2-10% of patients) | rel=r_associated | relid=0 | w=21
  4347. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures (about 50% of patients)
    n1=méningé (syndrome) | n2=en:seizures (about 50% of patients) | rel=r_associated | relid=0 | w=21
  4348. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures (if left untreated)
    n1=méningé (syndrome) | n2=en:seizures (if left untreated) | rel=r_associated | relid=0 | w=21
  4349. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures (less common)
    n1=méningé (syndrome) | n2=en:seizures (less common) | rel=r_associated | relid=0 | w=21
  4350. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures (may be difficult to control)
    n1=méningé (syndrome) | n2=en:seizures (may be difficult to control) | rel=r_associated | relid=0 | w=21
  4351. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures in the newborn, refractory
    n1=méningé (syndrome) | n2=en:seizures in the newborn, refractory | rel=r_associated | relid=0 | w=21
  4352. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures, complex partial, episodic
    n1=méningé (syndrome) | n2=en:seizures, complex partial, episodic | rel=r_associated | relid=0 | w=21
  4353. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures, complex, myoclonic
    n1=méningé (syndrome) | n2=en:seizures, complex, myoclonic | rel=r_associated | relid=0 | w=21
  4354. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures, early-onset (1 family)
    n1=méningé (syndrome) | n2=en:seizures, early-onset (1 family) | rel=r_associated | relid=0 | w=21
  4355. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures, juvenile myoclonic
    n1=méningé (syndrome) | n2=en:seizures, juvenile myoclonic | rel=r_associated | relid=0 | w=21
  4356. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures, partial, unilateral
    n1=méningé (syndrome) | n2=en:seizures, partial, unilateral | rel=r_associated | relid=0 | w=21
  4357. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures, poorly controlled
    n1=méningé (syndrome) | n2=en:seizures, poorly controlled | rel=r_associated | relid=0 | w=21
  4358. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:seizures, tonic-clonic (rare)
    n1=méningé (syndrome) | n2=en:seizures, tonic-clonic (rare) | rel=r_associated | relid=0 | w=21
  4359. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:selective loss of cerebellar purkinje cells
    n1=méningé (syndrome) | n2=en:selective loss of cerebellar purkinje cells | rel=r_associated | relid=0 | w=21
  4360. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:semilobar holoprosencephalies
    n1=méningé (syndrome) | n2=en:semilobar holoprosencephalies | rel=r_associated | relid=0 | w=21
  4361. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:sensory aura may occur
    n1=méningé (syndrome) | n2=en:sensory aura may occur | rel=r_associated | relid=0 | w=21
  4362. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:severe expressive speech delay
    n1=méningé (syndrome) | n2=en:severe expressive speech delay | rel=r_associated | relid=0 | w=21
  4363. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:severe hydrocephalus
    n1=méningé (syndrome) | n2=en:severe hydrocephalus | rel=r_associated | relid=0 | w=21
  4364. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:severe mental retardation (i.q. 20-34)
    n1=méningé (syndrome) | n2=en:severe mental retardation (i.q. 20-34) | rel=r_associated | relid=0 | w=21
  4365. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:severe neonatal hypotonia improving with age
    n1=méningé (syndrome) | n2=en:severe neonatal hypotonia improving with age | rel=r_associated | relid=0 | w=21
  4366. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:severe prenatal onset hydrocephalus
    n1=méningé (syndrome) | n2=en:severe prenatal onset hydrocephalus | rel=r_associated | relid=0 | w=21
  4367. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:simplified gyral pattern (in 1 of 2 sibs)
    n1=méningé (syndrome) | n2=en:simplified gyral pattern (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=21
  4368. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:sleep disorder
    n1=méningé (syndrome) | n2=en:sleep disorder | rel=r_associated | relid=0 | w=21
  4369. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:sleepiness
    n1=méningé (syndrome) | n2=en:sleepiness | rel=r_associated | relid=0 | w=21
  4370. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:slow speech
    n1=méningé (syndrome) | n2=en:slow speech | rel=r_associated | relid=0 | w=21
  4371. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:small cerebellum
    n1=méningé (syndrome) | n2=en:small cerebellum | rel=r_associated | relid=0 | w=21
  4372. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:small midbrain
    n1=méningé (syndrome) | n2=en:small midbrain | rel=r_associated | relid=0 | w=21
  4373. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:some patients have periodic wave complexes on eeg
    n1=méningé (syndrome) | n2=en:some patients have periodic wave complexes on eeg | rel=r_associated | relid=0 | w=21
  4374. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:some patients may show normal early development
    n1=méningé (syndrome) | n2=en:some patients may show normal early development | rel=r_associated | relid=0 | w=21
  4375. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spasmodic torticollis
    n1=méningé (syndrome) | n2=en:spasmodic torticollis | rel=r_associated | relid=0 | w=21
  4376. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spastic diplegia
    n1=méningé (syndrome) | n2=en:spastic diplegia | rel=r_associated | relid=0 | w=21
  4377. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spastic paraplegia, pure
    n1=méningé (syndrome) | n2=en:spastic paraplegia, pure | rel=r_associated | relid=0 | w=21
  4378. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spastic quadriplegia, residual mild-to-severe (in some patients)
    n1=méningé (syndrome) | n2=en:spastic quadriplegia, residual mild-to-severe (in some patients) | rel=r_associated | relid=0 | w=21
  4379. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spasticity (less common)
    n1=méningé (syndrome) | n2=en:spasticity (less common) | rel=r_associated | relid=0 | w=21
  4380. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spasticity may occur
    n1=méningé (syndrome) | n2=en:spasticity may occur | rel=r_associated | relid=0 | w=21
  4381. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spasticity, progressive, develops in childhood
    n1=méningé (syndrome) | n2=en:spasticity, progressive, develops in childhood | rel=r_associated | relid=0 | w=21
  4382. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spect scan may show hypermetabolism of the temporal lobe
    n1=méningé (syndrome) | n2=en:spect scan may show hypermetabolism of the temporal lobe | rel=r_associated | relid=0 | w=21
  4383. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:speech and language delay (rare)
    n1=méningé (syndrome) | n2=en:speech and language delay (rare) | rel=r_associated | relid=0 | w=21
  4384. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:speech and language delay, severe
    n1=méningé (syndrome) | n2=en:speech and language delay, severe | rel=r_associated | relid=0 | w=21
  4385. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:speech impairment
    n1=méningé (syndrome) | n2=en:speech impairment | rel=r_associated | relid=0 | w=21
  4386. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spinal cord atrophy (1 family)
    n1=méningé (syndrome) | n2=en:spinal cord atrophy (1 family) | rel=r_associated | relid=0 | w=21
  4387. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spinal cysts (in some patients)
    n1=méningé (syndrome) | n2=en:spinal cysts (in some patients) | rel=r_associated | relid=0 | w=21
  4388. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:spinocerebellar ataxia
    n1=méningé (syndrome) | n2=en:spinocerebellar ataxia | rel=r_associated | relid=0 | w=21
  4389. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:staring episodes during seizures
    n1=méningé (syndrome) | n2=en:staring episodes during seizures | rel=r_associated | relid=0 | w=21
  4390. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:status epilepticus (in some patients)
    n1=méningé (syndrome) | n2=en:status epilepticus (in some patients) | rel=r_associated | relid=0 | w=21
  4391. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:stimulation sensitive generalized myoclonus (stage 3)
    n1=méningé (syndrome) | n2=en:stimulation sensitive generalized myoclonus (stage 3) | rel=r_associated | relid=0 | w=21
  4392. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:subcortical and periventricular white matter abnormalities seen on mri (in some patients)
    n1=méningé (syndrome) | n2=en:subcortical and periventricular white matter abnormalities seen on mri (in some patients) | rel=r_associated | relid=0 | w=21
  4393. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:subcortical cysts in frontal and temporal lobes
    n1=méningé (syndrome) | n2=en:subcortical cysts in frontal and temporal lobes | rel=r_associated | relid=0 | w=21
  4394. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:subcortical gliosis
    n1=méningé (syndrome) | n2=en:subcortical gliosis | rel=r_associated | relid=0 | w=21
  4395. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:subcortical white matter calcifications
    n1=méningé (syndrome) | n2=en:subcortical white matter calcifications | rel=r_associated | relid=0 | w=21
  4396. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:subependymal calcifications
    n1=méningé (syndrome) | n2=en:subependymal calcifications | rel=r_associated | relid=0 | w=21
  4397. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:t2-weighted hyperintensities in deep brain regions
    n1=méningé (syndrome) | n2=en:t2-weighted hyperintensities in deep brain regions | rel=r_associated | relid=0 | w=21
  4398. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:t2-weighted hypodensities in the basal ganglia
    n1=méningé (syndrome) | n2=en:t2-weighted hypodensities in the basal ganglia | rel=r_associated | relid=0 | w=21
  4399. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:tau immunreactivity
    n1=méningé (syndrome) | n2=en:tau immunreactivity | rel=r_associated | relid=0 | w=21
  4400. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:tdp43-positive neuronal inclusions
    n1=méningé (syndrome) | n2=en:tdp43-positive neuronal inclusions | rel=r_associated | relid=0 | w=21
  4401. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:tetany
    n1=méningé (syndrome) | n2=en:tetany | rel=r_associated | relid=0 | w=21
  4402. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:tethered cord (uncommon)
    n1=méningé (syndrome) | n2=en:tethered cord (uncommon) | rel=r_associated | relid=0 | w=21
  4403. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:tetraplegic spasticity
    n1=méningé (syndrome) | n2=en:tetraplegic spasticity | rel=r_associated | relid=0 | w=21
  4404. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:thalamic hypoplasia
    n1=méningé (syndrome) | n2=en:thalamic hypoplasia | rel=r_associated | relid=0 | w=21
  4405. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:thick and elongated superior cerebellar peduncles
    n1=méningé (syndrome) | n2=en:thick and elongated superior cerebellar peduncles | rel=r_associated | relid=0 | w=21
  4406. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:thin cerebral cortex
    n1=méningé (syndrome) | n2=en:thin cerebral cortex | rel=r_associated | relid=0 | w=21
  4407. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing)
    n1=méningé (syndrome) | n2=en:torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing) | rel=r_associated | relid=0 | w=21
  4408. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:tremor (later-onset)
    n1=méningé (syndrome) | n2=en:tremor (later-onset) | rel=r_associated | relid=0 | w=21
  4409. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:tremor, mild
    n1=méningé (syndrome) | n2=en:tremor, mild | rel=r_associated | relid=0 | w=21
  4410. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:ubqln2- and tdp43-immunopositive inclusions in spinal motor, brainstem, and hippocampal neurons
    n1=méningé (syndrome) | n2=en:ubqln2- and tdp43-immunopositive inclusions in spinal motor, brainstem, and hippocampal neurons | rel=r_associated | relid=0 | w=21
  4411. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:unable to talk
    n1=méningé (syndrome) | n2=en:unable to talk | rel=r_associated | relid=0 | w=21
  4412. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:unidentified bright objects on brain mri
    n1=méningé (syndrome) | n2=en:unidentified bright objects on brain mri | rel=r_associated | relid=0 | w=21
  4413. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:unilateral headache location
    n1=méningé (syndrome) | n2=en:unilateral headache location | rel=r_associated | relid=0 | w=21
  4414. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:unresponsive to stimuli
    n1=méningé (syndrome) | n2=en:unresponsive to stimuli | rel=r_associated | relid=0 | w=21
  4415. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:upbeat central vestibular nystagmus
    n1=méningé (syndrome) | n2=en:upbeat central vestibular nystagmus | rel=r_associated | relid=0 | w=21
  4416. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:upper extremities may be involved
    n1=méningé (syndrome) | n2=en:upper extremities may be involved | rel=r_associated | relid=0 | w=21
  4417. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:upper motor involvement (some patient)
    n1=méningé (syndrome) | n2=en:upper motor involvement (some patient) | rel=r_associated | relid=0 | w=21
  4418. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:upper motor neuron signs
    n1=méningé (syndrome) | n2=en:upper motor neuron signs | rel=r_associated | relid=0 | w=21
  4419. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:variable intracranial abnormalities
    n1=méningé (syndrome) | n2=en:variable intracranial abnormalities | rel=r_associated | relid=0 | w=21
  4420. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:vasovagal syncope
    n1=méningé (syndrome) | n2=en:vasovagal syncope | rel=r_associated | relid=0 | w=21
  4421. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:ventricular enlargement
    n1=méningé (syndrome) | n2=en:ventricular enlargement | rel=r_associated | relid=0 | w=21
  4422. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:virtual absence of pyramidal tracts (wws)
    n1=méningé (syndrome) | n2=en:virtual absence of pyramidal tracts (wws) | rel=r_associated | relid=0 | w=21
  4423. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:vocalization (finding)
    n1=méningé (syndrome) | n2=en:vocalization (finding) | rel=r_associated | relid=0 | w=21
  4424. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:white matter
    n1=méningé (syndrome) | n2=en:white matter | rel=r_associated | relid=0 | w=21
  4425. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:white matter abnormalities seen on mri which resolve over time
    n1=méningé (syndrome) | n2=en:white matter abnormalities seen on mri which resolve over time | rel=r_associated | relid=0 | w=21
  4426. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:white matter hypodensities on brain imaging
    n1=méningé (syndrome) | n2=en:white matter hypodensities on brain imaging | rel=r_associated | relid=0 | w=21
  4427. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:white matter neuronal heterotopia
    n1=méningé (syndrome) | n2=en:white matter neuronal heterotopia | rel=r_associated | relid=0 | w=21
  4428. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:white matter signal abnormalities in various brain regions
    n1=méningé (syndrome) | n2=en:white matter signal abnormalities in various brain regions | rel=r_associated | relid=0 | w=21
  4429. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:widening of the spinal canal
    n1=méningé (syndrome) | n2=en:widening of the spinal canal | rel=r_associated | relid=0 | w=21
  4430. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> en:widespread brain atrophy
    n1=méningé (syndrome) | n2=en:widespread brain atrophy | rel=r_associated | relid=0 | w=21
  4431. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> leptoméninge
    n1=méningé (syndrome) | n2=leptoméninge | rel=r_associated | relid=0 | w=21
  4432. méningé (syndrome) -- r_associated #0: 21 / 0.253 -> membrane
    n1=méningé (syndrome) | n2=membrane | rel=r_associated | relid=0 | w=21
  4433. méningé (syndrome) -- r_associated #0: 20 / 0.241 -> en:epidemic cerebrospinal meningitis
    n1=méningé (syndrome) | n2=en:epidemic cerebrospinal meningitis | rel=r_associated | relid=0 | w=20
  4434. méningé (syndrome) -- r_associated #0: 20 / 0.241 -> Méningiomes
    n1=méningé (syndrome) | n2=Méningiomes | rel=r_associated | relid=0 | w=20
  4435. méningé (syndrome) -- r_associated #0: 20 / 0.241 -> Méningite
    n1=méningé (syndrome) | n2=Méningite | rel=r_associated | relid=0 | w=20
  4436. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> carcinologie
    (oncologie)
    n1=méningé (syndrome) | n2=carcinologie
    (oncologie)
    | rel=r_associated | relid=0 | w=15
  4437. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> dure-mère
    n1=méningé (syndrome) | n2=dure-mère | rel=r_associated | relid=0 | w=15
  4438. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> en:arachnoid membrane
    n1=méningé (syndrome) | n2=en:arachnoid membrane | rel=r_associated | relid=0 | w=15
  4439. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> en:chirurgia
    n1=méningé (syndrome) | n2=en:chirurgia | rel=r_associated | relid=0 | w=15
  4440. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> en:nervous system tumor morphology
    n1=méningé (syndrome) | n2=en:nervous system tumor morphology | rel=r_associated | relid=0 | w=15
  4441. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> en:neurofibromatosis type 1
    n1=méningé (syndrome) | n2=en:neurofibromatosis type 1 | rel=r_associated | relid=0 | w=15
  4442. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> en:neurologia
    n1=méningé (syndrome) | n2=en:neurologia | rel=r_associated | relid=0 | w=15
  4443. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> en:oncology
    n1=méningé (syndrome) | n2=en:oncology | rel=r_associated | relid=0 | w=15
  4444. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> en:surgery
    n1=méningé (syndrome) | n2=en:surgery | rel=r_associated | relid=0 | w=15
  4445. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> en:surgical operation
    n1=méningé (syndrome) | n2=en:surgical operation | rel=r_associated | relid=0 | w=15
  4446. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> en:surgical procedure
    n1=méningé (syndrome) | n2=en:surgical procedure | rel=r_associated | relid=0 | w=15
  4447. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> encéphale
    n1=méningé (syndrome) | n2=encéphale | rel=r_associated | relid=0 | w=15
  4448. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> maladie
    (médecine, vétérinaire)
    n1=méningé (syndrome) | n2=maladie
    (médecine, vétérinaire)
    | rel=r_associated | relid=0 | w=15
  4449. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> méninge dure
    n1=méningé (syndrome) | n2=méninge dure | rel=r_associated | relid=0 | w=15
  4450. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> méninge externe
    n1=méningé (syndrome) | n2=méninge externe | rel=r_associated | relid=0 | w=15
  4451. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> méningiome cutané
    n1=méningé (syndrome) | n2=méningiome cutané | rel=r_associated | relid=0 | w=15
  4452. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> méningiome du nerf optique
    n1=méningé (syndrome) | n2=méningiome du nerf optique | rel=r_associated | relid=0 | w=15
  4453. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> méningisme
    n1=méningé (syndrome) | n2=méningisme | rel=r_associated | relid=0 | w=15
  4454. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> moelle épinière
    n1=méningé (syndrome) | n2=moelle épinière | rel=r_associated | relid=0 | w=15
  4455. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> opération chirurgicale
    n1=méningé (syndrome) | n2=opération chirurgicale | rel=r_associated | relid=0 | w=15
  4456. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> système nerveux
    n1=méningé (syndrome) | n2=système nerveux | rel=r_associated | relid=0 | w=15
  4457. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> tissus vivants
    n1=méningé (syndrome) | n2=tissus vivants | rel=r_associated | relid=0 | w=15
  4458. méningé (syndrome) -- r_associated #0: 15 / 0.181 -> Zoologie
    n1=méningé (syndrome) | n2=Zoologie | rel=r_associated | relid=0 | w=15
  4459. méningé (syndrome) -- r_associated #0: 10 / - -> _SW
    n1=méningé (syndrome) | n2=_SW | rel=r_associated | relid=0 | w=10
  4460. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome
    [peut]
    se trouver
    [endroit]
    cerveau
    n1=méningé (syndrome) | n2=méningiome
    [peut]
    se trouver
    [endroit]
    cerveau | rel=r_associated | relid=0 | w=10
  4461. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome
    [peut]
    se trouver dans
    [objet]
    cerveau
    n1=méningé (syndrome) | n2=méningiome
    [peut]
    se trouver dans
    [objet]
    cerveau | rel=r_associated | relid=0 | w=10
  4462. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> chercheur
    [peut]
    se creuser
    [objet]
    méninges
    n1=méningé (syndrome) | n2=chercheur
    [peut]
    se creuser
    [objet]
    méninges | rel=r_associated | relid=0 | w=10
  4463. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> chercheur
    [peut]
    se creuser
    n1=méningé (syndrome) | n2=chercheur
    [peut]
    se creuser | rel=r_associated | relid=0 | w=10
  4464. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> 953 méningiomes (c70.-)
    n1=méningé (syndrome) | n2=953 méningiomes (c70.-) | rel=r_associated | relid=0 | w=10
  4465. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> anatomie
    (ensemble des organes)
    n1=méningé (syndrome) | n2=anatomie
    (ensemble des organes)
    | rel=r_associated | relid=0 | w=10
  4466. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> anesthésie péridurale
    n1=méningé (syndrome) | n2=anesthésie péridurale | rel=r_associated | relid=0 | w=10
  4467. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> angiomateux
    n1=méningé (syndrome) | n2=angiomateux | rel=r_associated | relid=0 | w=10
  4468. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> angiome
    n1=méningé (syndrome) | n2=angiome | rel=r_associated | relid=0 | w=10
  4469. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> arachnoïde, sai
    n1=méningé (syndrome) | n2=arachnoïde, sai | rel=r_associated | relid=0 | w=10
  4470. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> arachnoïde
    (Nom)
    n1=méningé (syndrome) | n2=arachnoïde
    (Nom)
    | rel=r_associated | relid=0 | w=10
  4471. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> arachnoides
    n1=méningé (syndrome) | n2=arachnoides | rel=r_associated | relid=0 | w=10
  4472. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> arachnoïdienne
    n1=méningé (syndrome) | n2=arachnoïdienne | rel=r_associated | relid=0 | w=10
  4473. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> bénin
    n1=méningé (syndrome) | n2=bénin | rel=r_associated | relid=0 | w=10
  4474. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> bénin
    (médecine, non cancéreux)
    n1=méningé (syndrome) | n2=bénin
    (médecine, non cancéreux)
    | rel=r_associated | relid=0 | w=10
  4475. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> cellules grises
    n1=méningé (syndrome) | n2=cellules grises | rel=r_associated | relid=0 | w=10
  4476. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> cerveau humain
    n1=méningé (syndrome) | n2=cerveau humain | rel=r_associated | relid=0 | w=10
  4477. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> cervelle
    n1=méningé (syndrome) | n2=cervelle | rel=r_associated | relid=0 | w=10
  4478. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> Chirurgie
    n1=méningé (syndrome) | n2=Chirurgie | rel=r_associated | relid=0 | w=10
  4479. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> de forme méningée
    n1=méningé (syndrome) | n2=de forme méningée | rel=r_associated | relid=0 | w=10
  4480. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> Dupre
    n1=méningé (syndrome) | n2=Dupre | rel=r_associated | relid=0 | w=10
  4481. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> dure
    n1=méningé (syndrome) | n2=dure | rel=r_associated | relid=0 | w=10
  4482. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:abdominal tumors (immunodeficiency-associated form)
    n1=méningé (syndrome) | n2=en:abdominal tumors (immunodeficiency-associated form) | rel=r_associated | relid=0 | w=10
  4483. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:aberrant ductule of epididymis
    n1=méningé (syndrome) | n2=en:aberrant ductule of epididymis | rel=r_associated | relid=0 | w=10
  4484. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:accelerated neoplasm growth
    n1=méningé (syndrome) | n2=en:accelerated neoplasm growth | rel=r_associated | relid=0 | w=10
  4485. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:acinar cell
    n1=méningé (syndrome) | n2=en:acinar cell | rel=r_associated | relid=0 | w=10
  4486. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:acinar cell neoplasm
    n1=méningé (syndrome) | n2=en:acinar cell neoplasm | rel=r_associated | relid=0 | w=10
  4487. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:acoustic schwannoma
    n1=méningé (syndrome) | n2=en:acoustic schwannoma | rel=r_associated | relid=0 | w=10
  4488. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:acute leukemia
    n1=méningé (syndrome) | n2=en:acute leukemia | rel=r_associated | relid=0 | w=10
  4489. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:acute lymphoblastic leukemia
    n1=méningé (syndrome) | n2=en:acute lymphoblastic leukemia | rel=r_associated | relid=0 | w=10
  4490. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:acute lymphoblastic leukemia (in 1 patient)
    n1=méningé (syndrome) | n2=en:acute lymphoblastic leukemia (in 1 patient) | rel=r_associated | relid=0 | w=10
  4491. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:acute megakaryoblastic leukemia
    n1=méningé (syndrome) | n2=en:acute megakaryoblastic leukemia | rel=r_associated | relid=0 | w=10
  4492. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:acute monocytic leukemia
    n1=méningé (syndrome) | n2=en:acute monocytic leukemia | rel=r_associated | relid=0 | w=10
  4493. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:acute myeloid leukemia
    n1=méningé (syndrome) | n2=en:acute myeloid leukemia | rel=r_associated | relid=0 | w=10
  4494. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adenocarcinoma
    n1=méningé (syndrome) | n2=en:adenocarcinoma | rel=r_associated | relid=0 | w=10
  4495. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adenocarcinoma (some)
    n1=méningé (syndrome) | n2=en:adenocarcinoma (some) | rel=r_associated | relid=0 | w=10
  4496. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adenoid cystic carcinoma
    n1=méningé (syndrome) | n2=en:adenoid cystic carcinoma | rel=r_associated | relid=0 | w=10
  4497. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adenoma and/or adenocarcinoma
    n1=méningé (syndrome) | n2=en:adenoma and/or adenocarcinoma | rel=r_associated | relid=0 | w=10
  4498. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adipocytic tumors (all subtypes)
    n1=méningé (syndrome) | n2=en:adipocytic tumors (all subtypes) | rel=r_associated | relid=0 | w=10
  4499. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adnexal and/or skin appendage neoplasm
    n1=méningé (syndrome) | n2=en:adnexal and/or skin appendage neoplasm | rel=r_associated | relid=0 | w=10
  4500. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adrenal cortex carcinoma
    n1=méningé (syndrome) | n2=en:adrenal cortex carcinoma | rel=r_associated | relid=0 | w=10
  4501. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adrenal gland pheochromocytoma
    n1=méningé (syndrome) | n2=en:adrenal gland pheochromocytoma | rel=r_associated | relid=0 | w=10
  4502. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adrenal glands are most common site
    n1=méningé (syndrome) | n2=en:adrenal glands are most common site | rel=r_associated | relid=0 | w=10
  4503. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adrenal medulllary cell
    n1=méningé (syndrome) | n2=en:adrenal medulllary cell | rel=r_associated | relid=0 | w=10
  4504. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult anaplastic (malignant) meningioma
    n1=méningé (syndrome) | n2=en:adult anaplastic (malignant) meningioma | rel=r_associated | relid=0 | w=10
  4505. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult atypical meningioma
    n1=méningé (syndrome) | n2=en:adult atypical meningioma | rel=r_associated | relid=0 | w=10
  4506. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult brain meningioma
    n1=méningé (syndrome) | n2=en:adult brain meningioma | rel=r_associated | relid=0 | w=10
  4507. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult central nervous system neoplasm
    n1=méningé (syndrome) | n2=en:adult central nervous system neoplasm | rel=r_associated | relid=0 | w=10
  4508. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult grade ii meningioma
    n1=méningé (syndrome) | n2=en:adult grade ii meningioma | rel=r_associated | relid=0 | w=10
  4509. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult grade iii meningioma
    n1=méningé (syndrome) | n2=en:adult grade iii meningioma | rel=r_associated | relid=0 | w=10
  4510. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult medulloblastoma
    n1=méningé (syndrome) | n2=en:adult medulloblastoma | rel=r_associated | relid=0 | w=10
  4511. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult meningeal melanoma
    n1=méningé (syndrome) | n2=en:adult meningeal melanoma | rel=r_associated | relid=0 | w=10
  4512. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult papillary meningioma
    n1=méningé (syndrome) | n2=en:adult papillary meningioma | rel=r_associated | relid=0 | w=10
  4513. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult primary melanocytic lesion of meninges
    n1=méningé (syndrome) | n2=en:adult primary melanocytic lesion of meninges | rel=r_associated | relid=0 | w=10
  4514. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:adult vascular tumor
    n1=méningé (syndrome) | n2=en:adult vascular tumor | rel=r_associated | relid=0 | w=10
  4515. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:afferent nerve
    n1=méningé (syndrome) | n2=en:afferent nerve | rel=r_associated | relid=0 | w=10
  4516. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:air sac
    n1=méningé (syndrome) | n2=en:air sac | rel=r_associated | relid=0 | w=10
  4517. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:alpha cell
    n1=méningé (syndrome) | n2=en:alpha cell | rel=r_associated | relid=0 | w=10
  4518. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:alveolar cell carcinoma (some)
    n1=méningé (syndrome) | n2=en:alveolar cell carcinoma (some) | rel=r_associated | relid=0 | w=10
  4519. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:amphiarthrosis
    n1=méningé (syndrome) | n2=en:amphiarthrosis | rel=r_associated | relid=0 | w=10
  4520. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ampulla of vater adenocarcinoma
    n1=méningé (syndrome) | n2=en:ampulla of vater adenocarcinoma | rel=r_associated | relid=0 | w=10
  4521. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ampullary cupula
    n1=méningé (syndrome) | n2=en:ampullary cupula | rel=r_associated | relid=0 | w=10
  4522. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ampullary membranous limb
    n1=méningé (syndrome) | n2=en:ampullary membranous limb | rel=r_associated | relid=0 | w=10
  4523. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anaplastic (malignant) intracranial meningioma
    n1=méningé (syndrome) | n2=en:anaplastic (malignant) intracranial meningioma | rel=r_associated | relid=0 | w=10
  4524. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anaplastic (malignant) intraspinal meningioma
    n1=méningé (syndrome) | n2=en:anaplastic (malignant) intraspinal meningioma | rel=r_associated | relid=0 | w=10
  4525. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anaplastic medulloblastoma
    n1=méningé (syndrome) | n2=en:anaplastic medulloblastoma | rel=r_associated | relid=0 | w=10
  4526. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anastomotic vessel
    n1=méningé (syndrome) | n2=en:anastomotic vessel | rel=r_associated | relid=0 | w=10
  4527. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anatomical curvature
    n1=méningé (syndrome) | n2=en:anatomical curvature | rel=r_associated | relid=0 | w=10
  4528. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anatomical feature
    n1=méningé (syndrome) | n2=en:anatomical feature | rel=r_associated | relid=0 | w=10
  4529. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anatomical flexure
    n1=méningé (syndrome) | n2=en:anatomical flexure | rel=r_associated | relid=0 | w=10
  4530. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anatomical internal os
    n1=méningé (syndrome) | n2=en:anatomical internal os | rel=r_associated | relid=0 | w=10
  4531. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anatomical pole
    n1=méningé (syndrome) | n2=en:anatomical pole | rel=r_associated | relid=0 | w=10
  4532. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anatomical space structure
    n1=méningé (syndrome) | n2=en:anatomical space structure | rel=r_associated | relid=0 | w=10
  4533. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anatomical tail
    n1=méningé (syndrome) | n2=en:anatomical tail | rel=r_associated | relid=0 | w=10
  4534. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anatomical zone
    n1=méningé (syndrome) | n2=en:anatomical zone | rel=r_associated | relid=0 | w=10
  4535. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:android pelvis
    n1=méningé (syndrome) | n2=en:android pelvis | rel=r_associated | relid=0 | w=10
  4536. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:angioblastic meningioma
    n1=méningé (syndrome) | n2=en:angioblastic meningioma | rel=r_associated | relid=0 | w=10
  4537. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:angiocentric glioma
    n1=méningé (syndrome) | n2=en:angiocentric glioma | rel=r_associated | relid=0 | w=10
  4538. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:angiofibroma
    n1=méningé (syndrome) | n2=en:angiofibroma | rel=r_associated | relid=0 | w=10
  4539. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:angiokeratoma
    n1=méningé (syndrome) | n2=en:angiokeratoma | rel=r_associated | relid=0 | w=10
  4540. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:angiolipoma
    n1=méningé (syndrome) | n2=en:angiolipoma | rel=r_associated | relid=0 | w=10
  4541. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:angiosarcoma
    n1=méningé (syndrome) | n2=en:angiosarcoma | rel=r_associated | relid=0 | w=10
  4542. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anterior cranial fossa meningioma
    n1=méningé (syndrome) | n2=en:anterior cranial fossa meningioma | rel=r_associated | relid=0 | w=10
  4543. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anterior foramen magnum meningioma
    n1=méningé (syndrome) | n2=en:anterior foramen magnum meningioma | rel=r_associated | relid=0 | w=10
  4544. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anterior parolfactory sulcus (human only)
    n1=méningé (syndrome) | n2=en:anterior parolfactory sulcus (human only) | rel=r_associated | relid=0 | w=10
  4545. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anterior root
    n1=méningé (syndrome) | n2=en:anterior root | rel=r_associated | relid=0 | w=10
  4546. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anterior visual pathway meningioma
    n1=méningé (syndrome) | n2=en:anterior visual pathway meningioma | rel=r_associated | relid=0 | w=10
  4547. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:anthropoid pelvis
    n1=méningé (syndrome) | n2=en:anthropoid pelvis | rel=r_associated | relid=0 | w=10
  4548. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:apex of the lung
    n1=méningé (syndrome) | n2=en:apex of the lung | rel=r_associated | relid=0 | w=10
  4549. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:aplastic anemia
    n1=méningé (syndrome) | n2=en:aplastic anemia | rel=r_associated | relid=0 | w=10
  4550. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:appendix epiploica
    n1=méningé (syndrome) | n2=en:appendix epiploica | rel=r_associated | relid=0 | w=10
  4551. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:approximately 10% of cases are paraneoplastic
    n1=méningé (syndrome) | n2=en:approximately 10% of cases are paraneoplastic | rel=r_associated | relid=0 | w=10
  4552. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:arachnoid villus
    n1=méningé (syndrome) | n2=en:arachnoid villus | rel=r_associated | relid=0 | w=10
  4553. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:arachnoiditis
    n1=méningé (syndrome) | n2=en:arachnoiditis | rel=r_associated | relid=0 | w=10
  4554. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:argentaffin cell
    n1=méningé (syndrome) | n2=en:argentaffin cell | rel=r_associated | relid=0 | w=10
  4555. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:argyrophilic cell
    n1=méningé (syndrome) | n2=en:argyrophilic cell | rel=r_associated | relid=0 | w=10
  4556. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:arterial circle
    n1=méningé (syndrome) | n2=en:arterial circle | rel=r_associated | relid=0 | w=10
  4557. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:artery
    n1=méningé (syndrome) | n2=en:artery | rel=r_associated | relid=0 | w=10
  4558. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:articular branch
    n1=méningé (syndrome) | n2=en:articular branch | rel=r_associated | relid=0 | w=10
  4559. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:articular fossa
    n1=méningé (syndrome) | n2=en:articular fossa | rel=r_associated | relid=0 | w=10
  4560. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:articular head
    n1=méningé (syndrome) | n2=en:articular head | rel=r_associated | relid=0 | w=10
  4561. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:articular recess
    n1=méningé (syndrome) | n2=en:articular recess | rel=r_associated | relid=0 | w=10
  4562. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:articular vascular plexus
    n1=méningé (syndrome) | n2=en:articular vascular plexus | rel=r_associated | relid=0 | w=10
  4563. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:aseptic meningitis
    n1=méningé (syndrome) | n2=en:aseptic meningitis | rel=r_associated | relid=0 | w=10
  4564. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:aspect of cranium
    n1=méningé (syndrome) | n2=en:aspect of cranium | rel=r_associated | relid=0 | w=10
  4565. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:aspects of mortality statistics
    n1=méningé (syndrome) | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=10
  4566. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:aspects of radiation effects
    n1=méningé (syndrome) | n2=en:aspects of radiation effects | rel=r_associated | relid=0 | w=10
  4567. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:associated with other malignancies
    n1=méningé (syndrome) | n2=en:associated with other malignancies | rel=r_associated | relid=0 | w=10
  4568. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:association fibre
    n1=méningé (syndrome) | n2=en:association fibre | rel=r_associated | relid=0 | w=10
  4569. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:astrocytic tumor
    n1=méningé (syndrome) | n2=en:astrocytic tumor | rel=r_associated | relid=0 | w=10
  4570. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:astrocytoma
    n1=méningé (syndrome) | n2=en:astrocytoma | rel=r_associated | relid=0 | w=10
  4571. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:atlantooccipital membrane
    n1=méningé (syndrome) | n2=en:atlantooccipital membrane | rel=r_associated | relid=0 | w=10
  4572. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:auditory system
    n1=méningé (syndrome) | n2=en:auditory system | rel=r_associated | relid=0 | w=10
  4573. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:auricular muscle
    n1=méningé (syndrome) | n2=en:auricular muscle | rel=r_associated | relid=0 | w=10
  4574. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:autonomic branch
    n1=méningé (syndrome) | n2=en:autonomic branch | rel=r_associated | relid=0 | w=10
  4575. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:b-cell lymphomas
    n1=méningé (syndrome) | n2=en:b-cell lymphomas | rel=r_associated | relid=0 | w=10
  4576. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:b-cell non-hodgkin lymphoma
    n1=méningé (syndrome) | n2=en:b-cell non-hodgkin lymphoma | rel=r_associated | relid=0 | w=10
  4577. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bacterial meningitis
    n1=méningé (syndrome) | n2=en:bacterial meningitis | rel=r_associated | relid=0 | w=10
  4578. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:band cell
    n1=méningé (syndrome) | n2=en:band cell | rel=r_associated | relid=0 | w=10
  4579. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bannayan syndrome
    n1=méningé (syndrome) | n2=en:bannayan syndrome | rel=r_associated | relid=0 | w=10
  4580. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:basal cell neoplasm
    n1=méningé (syndrome) | n2=en:basal cell neoplasm | rel=r_associated | relid=0 | w=10
  4581. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:basal cell nevus
    n1=méningé (syndrome) | n2=en:basal cell nevus | rel=r_associated | relid=0 | w=10
  4582. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:basaloid cell
    n1=méningé (syndrome) | n2=en:basaloid cell | rel=r_associated | relid=0 | w=10
  4583. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:base of the lung
    n1=méningé (syndrome) | n2=en:base of the lung | rel=r_associated | relid=0 | w=10
  4584. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:basocellular neoplasms
    n1=méningé (syndrome) | n2=en:basocellular neoplasms | rel=r_associated | relid=0 | w=10
  4585. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:basocellular neoplasms develop after second decade
    n1=méningé (syndrome) | n2=en:basocellular neoplasms develop after second decade | rel=r_associated | relid=0 | w=10
  4586. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign brain neoplasm
    n1=méningé (syndrome) | n2=en:benign brain neoplasm | rel=r_associated | relid=0 | w=10
  4587. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign digestive system neoplasm
    n1=méningé (syndrome) | n2=en:benign digestive system neoplasm | rel=r_associated | relid=0 | w=10
  4588. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign endocrine neoplasm
    n1=méningé (syndrome) | n2=en:benign endocrine neoplasm | rel=r_associated | relid=0 | w=10
  4589. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign epithelial neoplasm
    n1=méningé (syndrome) | n2=en:benign epithelial neoplasm | rel=r_associated | relid=0 | w=10
  4590. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign female reproductive system neoplasm
    n1=méningé (syndrome) | n2=en:benign female reproductive system neoplasm | rel=r_associated | relid=0 | w=10
  4591. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign genitourinary tract neoplasm
    n1=méningé (syndrome) | n2=en:benign genitourinary tract neoplasm | rel=r_associated | relid=0 | w=10
  4592. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign intracranial meningioma
    n1=méningé (syndrome) | n2=en:benign intracranial meningioma | rel=r_associated | relid=0 | w=10
  4593. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign male reproductive system neoplasm
    n1=méningé (syndrome) | n2=en:benign male reproductive system neoplasm | rel=r_associated | relid=0 | w=10
  4594. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign multirecurrent endothelioleukocytal meningitis
    n1=méningé (syndrome) | n2=en:benign multirecurrent endothelioleukocytal meningitis | rel=r_associated | relid=0 | w=10
  4595. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign neoplasm
    n1=méningé (syndrome) | n2=en:benign neoplasm | rel=r_associated | relid=0 | w=10
  4596. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign neoplasm of central nervous system
    n1=méningé (syndrome) | n2=en:benign neoplasm of central nervous system | rel=r_associated | relid=0 | w=10
  4597. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign neoplasm of cerebral meninges
    n1=méningé (syndrome) | n2=en:benign neoplasm of cerebral meninges | rel=r_associated | relid=0 | w=10
  4598. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign neoplasm of meninges
    n1=méningé (syndrome) | n2=en:benign neoplasm of meninges | rel=r_associated | relid=0 | w=10
  4599. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign neoplasm of spinal intradural space
    n1=méningé (syndrome) | n2=en:benign neoplasm of spinal intradural space | rel=r_associated | relid=0 | w=10
  4600. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign neoplasm of spinal meninges
    n1=méningé (syndrome) | n2=en:benign neoplasm of spinal meninges | rel=r_associated | relid=0 | w=10
  4601. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign nervous system neoplasm
    n1=méningé (syndrome) | n2=en:benign nervous system neoplasm | rel=r_associated | relid=0 | w=10
  4602. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign optic nerve tumor
    n1=méningé (syndrome) | n2=en:benign optic nerve tumor | rel=r_associated | relid=0 | w=10
  4603. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign skin neoplasm
    n1=méningé (syndrome) | n2=en:benign skin neoplasm | rel=r_associated | relid=0 | w=10
  4604. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign soft tissue neoplasm
    n1=méningé (syndrome) | n2=en:benign soft tissue neoplasm | rel=r_associated | relid=0 | w=10
  4605. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign spinal cord neoplasm
    n1=méningé (syndrome) | n2=en:benign spinal cord neoplasm | rel=r_associated | relid=0 | w=10
  4606. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign teratoma
    n1=méningé (syndrome) | n2=en:benign teratoma | rel=r_associated | relid=0 | w=10
  4607. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign tumors of the eye, heart, and lungs
    n1=méningé (syndrome) | n2=en:benign tumors of the eye, heart, and lungs | rel=r_associated | relid=0 | w=10
  4608. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:benign vascular neoplasm
    n1=méningé (syndrome) | n2=en:benign vascular neoplasm | rel=r_associated | relid=0 | w=10
  4609. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:beta cell
    n1=méningé (syndrome) | n2=en:beta cell | rel=r_associated | relid=0 | w=10
  4610. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bilateral optic nerve meningioma
    n1=méningé (syndrome) | n2=en:bilateral optic nerve meningioma | rel=r_associated | relid=0 | w=10
  4611. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:biological polymorphism
    n1=méningé (syndrome) | n2=en:biological polymorphism | rel=r_associated | relid=0 | w=10
  4612. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bladder carcinoma
    n1=méningé (syndrome) | n2=en:bladder carcinoma | rel=r_associated | relid=0 | w=10
  4613. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bladder neoplasm
    n1=méningé (syndrome) | n2=en:bladder neoplasm | rel=r_associated | relid=0 | w=10
  4614. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bladder urothelial carcinoma
    n1=méningé (syndrome) | n2=en:bladder urothelial carcinoma | rel=r_associated | relid=0 | w=10
  4615. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:blast cell
    n1=méningé (syndrome) | n2=en:blast cell | rel=r_associated | relid=0 | w=10
  4616. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:blood cell precursor - general anatomical term
    n1=méningé (syndrome) | n2=en:blood cell precursor - general anatomical term | rel=r_associated | relid=0 | w=10
  4617. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:blood vessel
    n1=méningé (syndrome) | n2=en:blood vessel | rel=r_associated | relid=0 | w=10
  4618. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:blood vessel neoplasm
    n1=méningé (syndrome) | n2=en:blood vessel neoplasm | rel=r_associated | relid=0 | w=10
  4619. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:blood-brain barrier
    n1=méningé (syndrome) | n2=en:blood-brain barrier | rel=r_associated | relid=0 | w=10
  4620. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:body constitution
    n1=méningé (syndrome) | n2=en:body constitution | rel=r_associated | relid=0 | w=10
  4621. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:body covering or investment
    n1=méningé (syndrome) | n2=en:body covering or investment | rel=r_associated | relid=0 | w=10
  4622. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bone
    n1=méningé (syndrome) | n2=en:bone | rel=r_associated | relid=0 | w=10
  4623. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bone hemangioma
    n1=méningé (syndrome) | n2=en:bone hemangioma | rel=r_associated | relid=0 | w=10
  4624. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bone marrow blood-forming cell
    n1=méningé (syndrome) | n2=en:bone marrow blood-forming cell | rel=r_associated | relid=0 | w=10
  4625. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bone neoplasm
    n1=méningé (syndrome) | n2=en:bone neoplasm | rel=r_associated | relid=0 | w=10
  4626. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bone-forming neoplasm
    n1=méningé (syndrome) | n2=en:bone-forming neoplasm | rel=r_associated | relid=0 | w=10
  4627. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:brain morphology
    n1=méningé (syndrome) | n2=en:brain morphology | rel=r_associated | relid=0 | w=10
  4628. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:brain neoplasm
    n1=méningé (syndrome) | n2=en:brain neoplasm | rel=r_associated | relid=0 | w=10
  4629. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:brain observable
    n1=méningé (syndrome) | n2=en:brain observable | rel=r_associated | relid=0 | w=10
  4630. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:brain stem intraparenchymal clear cell meningioma
    n1=méningé (syndrome) | n2=en:brain stem intraparenchymal clear cell meningioma | rel=r_associated | relid=0 | w=10
  4631. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:brains
    n1=méningé (syndrome) | n2=en:brains | rel=r_associated | relid=0 | w=10
  4632. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast angiosarcoma
    n1=méningé (syndrome) | n2=en:breast angiosarcoma | rel=r_associated | relid=0 | w=10
  4633. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast angiosarcoma metastatic
    n1=méningé (syndrome) | n2=en:breast angiosarcoma metastatic | rel=r_associated | relid=0 | w=10
  4634. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast cancer (rare)
    n1=méningé (syndrome) | n2=en:breast cancer (rare) | rel=r_associated | relid=0 | w=10
  4635. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast cancer, early-onset (in some patients)
    n1=méningé (syndrome) | n2=en:breast cancer, early-onset (in some patients) | rel=r_associated | relid=0 | w=10
  4636. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast cancer, lobular
    n1=méningé (syndrome) | n2=en:breast cancer, lobular | rel=r_associated | relid=0 | w=10
  4637. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast carcinoma
    n1=méningé (syndrome) | n2=en:breast carcinoma | rel=r_associated | relid=0 | w=10
  4638. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast hemangioma
    n1=méningé (syndrome) | n2=en:breast hemangioma | rel=r_associated | relid=0 | w=10
  4639. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast lobe
    n1=méningé (syndrome) | n2=en:breast lobe | rel=r_associated | relid=0 | w=10
  4640. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast neoplasm
    n1=méningé (syndrome) | n2=en:breast neoplasm | rel=r_associated | relid=0 | w=10
  4641. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast neoplasms benign (incl nipple)
    n1=méningé (syndrome) | n2=en:breast neoplasms benign (incl nipple) | rel=r_associated | relid=0 | w=10
  4642. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:breast neoplasms malignant and unspecified (incl nipple)
    n1=méningé (syndrome) | n2=en:breast neoplasms malignant and unspecified (incl nipple) | rel=r_associated | relid=0 | w=10
  4643. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bronchiole
    n1=méningé (syndrome) | n2=en:bronchiole | rel=r_associated | relid=0 | w=10
  4644. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bronchogenic carcinoma (some)
    n1=méningé (syndrome) | n2=en:bronchogenic carcinoma (some) | rel=r_associated | relid=0 | w=10
  4645. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bronchopericardial membrane
    n1=méningé (syndrome) | n2=en:bronchopericardial membrane | rel=r_associated | relid=0 | w=10
  4646. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bronchopulmonary segment
    n1=méningé (syndrome) | n2=en:bronchopulmonary segment | rel=r_associated | relid=0 | w=10
  4647. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bronchus
    n1=méningé (syndrome) | n2=en:bronchus | rel=r_associated | relid=0 | w=10
  4648. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:bulging tumor sign
    n1=méningé (syndrome) | n2=en:bulging tumor sign | rel=r_associated | relid=0 | w=10
  4649. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:burkitt lymphoma (b-cell lymphoma)
    n1=méningé (syndrome) | n2=en:burkitt lymphoma (b-cell lymphoma) | rel=r_associated | relid=0 | w=10
  4650. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:buttock
    n1=méningé (syndrome) | n2=en:buttock | rel=r_associated | relid=0 | w=10
  4651. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:capsule of nonsynovial joint
    n1=méningé (syndrome) | n2=en:capsule of nonsynovial joint | rel=r_associated | relid=0 | w=10
  4652. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:carcinoid tumor
    n1=méningé (syndrome) | n2=en:carcinoid tumor | rel=r_associated | relid=0 | w=10
  4653. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:carcinoma in situ
    n1=méningé (syndrome) | n2=en:carcinoma in situ | rel=r_associated | relid=0 | w=10
  4654. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cardiac atrium
    n1=méningé (syndrome) | n2=en:cardiac atrium | rel=r_associated | relid=0 | w=10
  4655. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cardiac haemangioma benign
    n1=méningé (syndrome) | n2=en:cardiac haemangioma benign | rel=r_associated | relid=0 | w=10
  4656. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cardiocyte - general anatomical term
    n1=méningé (syndrome) | n2=en:cardiocyte - general anatomical term | rel=r_associated | relid=0 | w=10
  4657. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:carotid body paraganglioma
    n1=méningé (syndrome) | n2=en:carotid body paraganglioma | rel=r_associated | relid=0 | w=10
  4658. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:carotid body tumors (most common location)
    n1=méningé (syndrome) | n2=en:carotid body tumors (most common location) | rel=r_associated | relid=0 | w=10
  4659. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:carotid body tumors (most common)
    n1=méningé (syndrome) | n2=en:carotid body tumors (most common) | rel=r_associated | relid=0 | w=10
  4660. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cartilage
    n1=méningé (syndrome) | n2=en:cartilage | rel=r_associated | relid=0 | w=10
  4661. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cartilage-forming neoplasm
    n1=méningé (syndrome) | n2=en:cartilage-forming neoplasm | rel=r_associated | relid=0 | w=10
  4662. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cavernous sinus meningioma
    n1=méningé (syndrome) | n2=en:cavernous sinus meningioma | rel=r_associated | relid=0 | w=10
  4663. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cdisc sdtm anatomical location terminology
    n1=méningé (syndrome) | n2=en:cdisc sdtm anatomical location terminology | rel=r_associated | relid=0 | w=10
  4664. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cdisc sdtm terminology
    n1=méningé (syndrome) | n2=en:cdisc sdtm terminology | rel=r_associated | relid=0 | w=10
  4665. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cdisc send biospecimens terminology
    n1=méningé (syndrome) | n2=en:cdisc send biospecimens terminology | rel=r_associated | relid=0 | w=10
  4666. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cdisc send terminology
    n1=méningé (syndrome) | n2=en:cdisc send terminology | rel=r_associated | relid=0 | w=10
  4667. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cell
    n1=méningé (syndrome) | n2=en:cell | rel=r_associated | relid=0 | w=10
  4668. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cell part
    n1=méningé (syndrome) | n2=en:cell part | rel=r_associated | relid=0 | w=10
  4669. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cells, lymphoid
    n1=méningé (syndrome) | n2=en:cells, lymphoid | rel=r_associated | relid=0 | w=10
  4670. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cellular aspects of
    n1=méningé (syndrome) | n2=en:cellular aspects of | rel=r_associated | relid=0 | w=10
  4671. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cellular morphology
    n1=méningé (syndrome) | n2=en:cellular morphology | rel=r_associated | relid=0 | w=10
  4672. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system carcinoma
    n1=méningé (syndrome) | n2=en:central nervous system carcinoma | rel=r_associated | relid=0 | w=10
  4673. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system cyst
    n1=méningé (syndrome) | n2=en:central nervous system cyst | rel=r_associated | relid=0 | w=10
  4674. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system dermoid tumour
    n1=méningé (syndrome) | n2=en:central nervous system dermoid tumour | rel=r_associated | relid=0 | w=10
  4675. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system embryonal neoplasm
    n1=méningé (syndrome) | n2=en:central nervous system embryonal neoplasm | rel=r_associated | relid=0 | w=10
  4676. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system embryonal tumor, not otherwise specified with leptomeningeal spread
    n1=méningé (syndrome) | n2=en:central nervous system embryonal tumor, not otherwise specified with leptomeningeal spread | rel=r_associated | relid=0 | w=10
  4677. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system ewing sarcoma/peripheral primitive neuroectodermal tumor
    n1=méningé (syndrome) | n2=en:central nervous system ewing sarcoma/peripheral primitive neuroectodermal tumor | rel=r_associated | relid=0 | w=10
  4678. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system germ cell tumor
    n1=méningé (syndrome) | n2=en:central nervous system germ cell tumor | rel=r_associated | relid=0 | w=10
  4679. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system hemangioblastoma
    n1=méningé (syndrome) | n2=en:central nervous system hemangioblastoma | rel=r_associated | relid=0 | w=10
  4680. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system hematopoietic neoplasm
    n1=méningé (syndrome) | n2=en:central nervous system hematopoietic neoplasm | rel=r_associated | relid=0 | w=10
  4681. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system leukemia
    n1=méningé (syndrome) | n2=en:central nervous system leukemia | rel=r_associated | relid=0 | w=10
  4682. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system lymphoma
    n1=méningé (syndrome) | n2=en:central nervous system lymphoma | rel=r_associated | relid=0 | w=10
  4683. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system melanocytic neoplasm
    n1=méningé (syndrome) | n2=en:central nervous system melanocytic neoplasm | rel=r_associated | relid=0 | w=10
  4684. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system mesenchymal, non-meningothelial neoplasm
    n1=méningé (syndrome) | n2=en:central nervous system mesenchymal, non-meningothelial neoplasm | rel=r_associated | relid=0 | w=10
  4685. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system paraganglioma
    n1=méningé (syndrome) | n2=en:central nervous system paraganglioma | rel=r_associated | relid=0 | w=10
  4686. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:central nervous system pressure
    n1=méningé (syndrome) | n2=en:central nervous system pressure | rel=r_associated | relid=0 | w=10
  4687. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebellar haemangioma
    n1=méningé (syndrome) | n2=en:cerebellar haemangioma | rel=r_associated | relid=0 | w=10
  4688. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebellar medulloblastoma
    n1=méningé (syndrome) | n2=en:cerebellar medulloblastoma | rel=r_associated | relid=0 | w=10
  4689. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebellar neoplasm
    n1=méningé (syndrome) | n2=en:cerebellar neoplasm | rel=r_associated | relid=0 | w=10
  4690. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebellar papillary meningioma
    n1=méningé (syndrome) | n2=en:cerebellar papillary meningioma | rel=r_associated | relid=0 | w=10
  4691. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebellar vermis medulloblastoma
    n1=méningé (syndrome) | n2=en:cerebellar vermis medulloblastoma | rel=r_associated | relid=0 | w=10
  4692. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebellopontine angle neoplasm
    n1=méningé (syndrome) | n2=en:cerebellopontine angle neoplasm | rel=r_associated | relid=0 | w=10
  4693. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebral germinoma
    n1=méningé (syndrome) | n2=en:cerebral germinoma | rel=r_associated | relid=0 | w=10
  4694. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebral hamartomata
    n1=méningé (syndrome) | n2=en:cerebral hamartomata | rel=r_associated | relid=0 | w=10
  4695. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebral hemangioma
    n1=méningé (syndrome) | n2=en:cerebral hemangioma | rel=r_associated | relid=0 | w=10
  4696. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebral meninges
    n1=méningé (syndrome) | n2=en:cerebral meninges | rel=r_associated | relid=0 | w=10
  4697. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebral meningioma
    n1=méningé (syndrome) | n2=en:cerebral meningioma | rel=r_associated | relid=0 | w=10
  4698. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cerebrospinal fluid pressure observable
    n1=méningé (syndrome) | n2=en:cerebrospinal fluid pressure observable | rel=r_associated | relid=0 | w=10
  4699. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cervical cancer (rare)
    n1=méningé (syndrome) | n2=en:cervical cancer (rare) | rel=r_associated | relid=0 | w=10
  4700. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cervical carcinoma
    n1=méningé (syndrome) | n2=en:cervical carcinoma | rel=r_associated | relid=0 | w=10
  4701. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cervical intervertebral foramina
    n1=méningé (syndrome) | n2=en:cervical intervertebral foramina | rel=r_associated | relid=0 | w=10
  4702. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cervical intraspinal meningioma
    n1=méningé (syndrome) | n2=en:cervical intraspinal meningioma | rel=r_associated | relid=0 | w=10
  4703. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chamber of eyeball
    n1=méningé (syndrome) | n2=en:chamber of eyeball | rel=r_associated | relid=0 | w=10
  4704. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chemically induced
    n1=méningé (syndrome) | n2=en:chemically induced | rel=r_associated | relid=0 | w=10
  4705. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chief cell
    n1=méningé (syndrome) | n2=en:chief cell | rel=r_associated | relid=0 | w=10
  4706. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:childhood atypical teratoid/rhabdoid tumor
    n1=méningé (syndrome) | n2=en:childhood atypical teratoid/rhabdoid tumor | rel=r_associated | relid=0 | w=10
  4707. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:childhood brain meningioma
    n1=méningé (syndrome) | n2=en:childhood brain meningioma | rel=r_associated | relid=0 | w=10
  4708. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:childhood central nervous system neoplasm
    n1=méningé (syndrome) | n2=en:childhood central nervous system neoplasm | rel=r_associated | relid=0 | w=10
  4709. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:childhood grade ii meningioma
    n1=méningé (syndrome) | n2=en:childhood grade ii meningioma | rel=r_associated | relid=0 | w=10
  4710. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:childhood grade iii meningioma
    n1=méningé (syndrome) | n2=en:childhood grade iii meningioma | rel=r_associated | relid=0 | w=10
  4711. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:childhood medulloblastoma
    n1=méningé (syndrome) | n2=en:childhood medulloblastoma | rel=r_associated | relid=0 | w=10
  4712. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:childhood meningeal melanoma
    n1=méningé (syndrome) | n2=en:childhood meningeal melanoma | rel=r_associated | relid=0 | w=10
  4713. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:childhood vascular neoplasm
    n1=méningé (syndrome) | n2=en:childhood vascular neoplasm | rel=r_associated | relid=0 | w=10
  4714. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chondrogenic neoplasm
    n1=méningé (syndrome) | n2=en:chondrogenic neoplasm | rel=r_associated | relid=0 | w=10
  4715. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chordae tendineae
    n1=méningé (syndrome) | n2=en:chordae tendineae | rel=r_associated | relid=0 | w=10
  4716. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chordoid meningioma
    n1=méningé (syndrome) | n2=en:chordoid meningioma | rel=r_associated | relid=0 | w=10
  4717. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chordoma
    n1=méningé (syndrome) | n2=en:chordoma | rel=r_associated | relid=0 | w=10
  4718. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:choroid hemangioma
    n1=méningé (syndrome) | n2=en:choroid hemangioma | rel=r_associated | relid=0 | w=10
  4719. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:choroid plexus carcinoma
    n1=méningé (syndrome) | n2=en:choroid plexus carcinoma | rel=r_associated | relid=0 | w=10
  4720. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:choroid plexus neoplasm
    n1=méningé (syndrome) | n2=en:choroid plexus neoplasm | rel=r_associated | relid=0 | w=10
  4721. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:choroid plexus papilloma
    n1=méningé (syndrome) | n2=en:choroid plexus papilloma | rel=r_associated | relid=0 | w=10
  4722. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chromaffin cell neoplasm
    n1=méningé (syndrome) | n2=en:chromaffin cell neoplasm | rel=r_associated | relid=0 | w=10
  4723. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chromophilic cell
    n1=méningé (syndrome) | n2=en:chromophilic cell | rel=r_associated | relid=0 | w=10
  4724. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chromophobe cell
    n1=méningé (syndrome) | n2=en:chromophobe cell | rel=r_associated | relid=0 | w=10
  4725. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chronic lymphocytic leukemia
    n1=méningé (syndrome) | n2=en:chronic lymphocytic leukemia | rel=r_associated | relid=0 | w=10
  4726. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chronic lymphocytic leukemia, b-cell, susceptibility to
    n1=méningé (syndrome) | n2=en:chronic lymphocytic leukemia, b-cell, susceptibility to | rel=r_associated | relid=0 | w=10
  4727. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:chronic myelogenous leukemia, bcr-abl1 positive
    n1=méningé (syndrome) | n2=en:chronic myelogenous leukemia, bcr-abl1 positive | rel=r_associated | relid=0 | w=10
  4728. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ciliary process
    n1=méningé (syndrome) | n2=en:ciliary process | rel=r_associated | relid=0 | w=10
  4729. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cistern
    n1=méningé (syndrome) | n2=en:cistern | rel=r_associated | relid=0 | w=10
  4730. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:classic medulloblastoma
    n1=méningé (syndrome) | n2=en:classic medulloblastoma | rel=r_associated | relid=0 | w=10
  4731. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:clear cell
    n1=méningé (syndrome) | n2=en:clear cell | rel=r_associated | relid=0 | w=10
  4732. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:clear cell acanthoma
    n1=méningé (syndrome) | n2=en:clear cell acanthoma | rel=r_associated | relid=0 | w=10
  4733. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:clear cell neoplasm
    n1=méningé (syndrome) | n2=en:clear cell neoplasm | rel=r_associated | relid=0 | w=10
  4734. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:clear cell renal cell carcinoma
    n1=méningé (syndrome) | n2=en:clear cell renal cell carcinoma | rel=r_associated | relid=0 | w=10
  4735. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:clinical data interchange standards consortium terminology
    n1=méningé (syndrome) | n2=en:clinical data interchange standards consortium terminology | rel=r_associated | relid=0 | w=10
  4736. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:clivus meningioma
    n1=méningé (syndrome) | n2=en:clivus meningioma | rel=r_associated | relid=0 | w=10
  4737. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:collateral vessel
    n1=méningé (syndrome) | n2=en:collateral vessel | rel=r_associated | relid=0 | w=10
  4738. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:colon adenocarcinoma
    n1=méningé (syndrome) | n2=en:colon adenocarcinoma | rel=r_associated | relid=0 | w=10
  4739. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:colon carcinoma
    n1=méningé (syndrome) | n2=en:colon carcinoma | rel=r_associated | relid=0 | w=10
  4740. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:colorectal cancer (in some patients)
    n1=méningé (syndrome) | n2=en:colorectal cancer (in some patients) | rel=r_associated | relid=0 | w=10
  4741. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:colorectal cancer, early onset
    n1=méningé (syndrome) | n2=en:colorectal cancer, early onset | rel=r_associated | relid=0 | w=10
  4742. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:colorectal carcinoma
    n1=méningé (syndrome) | n2=en:colorectal carcinoma | rel=r_associated | relid=0 | w=10
  4743. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:column
    n1=méningé (syndrome) | n2=en:column | rel=r_associated | relid=0 | w=10
  4744. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:commissural fibre
    n1=méningé (syndrome) | n2=en:commissural fibre | rel=r_associated | relid=0 | w=10
  4745. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:compartmental model region
    n1=méningé (syndrome) | n2=en:compartmental model region | rel=r_associated | relid=0 | w=10
  4746. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:complex epithelial neoplasm
    n1=méningé (syndrome) | n2=en:complex epithelial neoplasm | rel=r_associated | relid=0 | w=10
  4747. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:complex mixed and stromal neoplasms
    n1=méningé (syndrome) | n2=en:complex mixed and stromal neoplasms | rel=r_associated | relid=0 | w=10
  4748. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:complex mixed and/or stromal neoplasm
    n1=méningé (syndrome) | n2=en:complex mixed and/or stromal neoplasm | rel=r_associated | relid=0 | w=10
  4749. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:complication aspects
    n1=méningé (syndrome) | n2=en:complication aspects | rel=r_associated | relid=0 | w=10
  4750. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:compound eye
    n1=méningé (syndrome) | n2=en:compound eye | rel=r_associated | relid=0 | w=10
  4751. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:congenital cerebral haemangioma
    n1=méningé (syndrome) | n2=en:congenital cerebral haemangioma | rel=r_associated | relid=0 | w=10
  4752. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:congenital hemangioma
    n1=méningé (syndrome) | n2=en:congenital hemangioma | rel=r_associated | relid=0 | w=10
  4753. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:congenital mesh qualifier
    n1=méningé (syndrome) | n2=en:congenital mesh qualifier | rel=r_associated | relid=0 | w=10
  4754. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:conjunctiva
    n1=méningé (syndrome) | n2=en:conjunctiva | rel=r_associated | relid=0 | w=10
  4755. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cord of brachial plexus
    n1=méningé (syndrome) | n2=en:cord of brachial plexus | rel=r_associated | relid=0 | w=10
  4756. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:corpora paraaortica
    n1=méningé (syndrome) | n2=en:corpora paraaortica | rel=r_associated | relid=0 | w=10
  4757. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cortical column
    n1=méningé (syndrome) | n2=en:cortical column | rel=r_associated | relid=0 | w=10
  4758. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cowden syndrome
    n1=méningé (syndrome) | n2=en:cowden syndrome | rel=r_associated | relid=0 | w=10
  4759. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cranial subarachnoid space
    n1=méningé (syndrome) | n2=en:cranial subarachnoid space | rel=r_associated | relid=0 | w=10
  4760. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:craniopharyngioma
    n1=méningé (syndrome) | n2=en:craniopharyngioma | rel=r_associated | relid=0 | w=10
  4761. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ctrp terminology
    n1=méningé (syndrome) | n2=en:ctrp terminology | rel=r_associated | relid=0 | w=10
  4762. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cusp
    n1=méningé (syndrome) | n2=en:cusp | rel=r_associated | relid=0 | w=10
  4763. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cutaneous branch
    n1=méningé (syndrome) | n2=en:cutaneous branch | rel=r_associated | relid=0 | w=10
  4764. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cutaneous leiomyosarcoma (less common)
    n1=méningé (syndrome) | n2=en:cutaneous leiomyosarcoma (less common) | rel=r_associated | relid=0 | w=10
  4765. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cutaneous melanoma
    n1=méningé (syndrome) | n2=en:cutaneous melanoma | rel=r_associated | relid=0 | w=10
  4766. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cutaneous meningioma
    n1=méningé (syndrome) | n2=en:cutaneous meningioma | rel=r_associated | relid=0 | w=10
  4767. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cutaneous vascular neoplasm
    n1=méningé (syndrome) | n2=en:cutaneous vascular neoplasm | rel=r_associated | relid=0 | w=10
  4768. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cutaneous vein
    n1=méningé (syndrome) | n2=en:cutaneous vein | rel=r_associated | relid=0 | w=10
  4769. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cylindromas may show malignant transformation
    n1=méningé (syndrome) | n2=en:cylindromas may show malignant transformation | rel=r_associated | relid=0 | w=10
  4770. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cyst
    n1=méningé (syndrome) | n2=en:cyst | rel=r_associated | relid=0 | w=10
  4771. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cystadenoma
    n1=méningé (syndrome) | n2=en:cystadenoma | rel=r_associated | relid=0 | w=10
  4772. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:cystic, mucinous and/or serous neoplasm
    n1=méningé (syndrome) | n2=en:cystic, mucinous and/or serous neoplasm | rel=r_associated | relid=0 | w=10
  4773. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:deep artery of arm
    n1=méningé (syndrome) | n2=en:deep artery of arm | rel=r_associated | relid=0 | w=10
  4774. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:deep femoral artery
    n1=méningé (syndrome) | n2=en:deep femoral artery | rel=r_associated | relid=0 | w=10
  4775. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:deep vein
    n1=méningé (syndrome) | n2=en:deep vein | rel=r_associated | relid=0 | w=10
  4776. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:delta cell
    n1=méningé (syndrome) | n2=en:delta cell | rel=r_associated | relid=0 | w=10
  4777. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:denticulate suture
    n1=méningé (syndrome) | n2=en:denticulate suture | rel=r_associated | relid=0 | w=10
  4778. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:desmoid-type fibromatosis
    n1=méningé (syndrome) | n2=en:desmoid-type fibromatosis | rel=r_associated | relid=0 | w=10
  4779. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:desmoplastic small cell tumor
    n1=méningé (syndrome) | n2=en:desmoplastic small cell tumor | rel=r_associated | relid=0 | w=10
  4780. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:desmoplastic/nodular medulloblastoma
    n1=méningé (syndrome) | n2=en:desmoplastic/nodular medulloblastoma | rel=r_associated | relid=0 | w=10
  4781. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:development of tumors in adulthood
    n1=méningé (syndrome) | n2=en:development of tumors in adulthood | rel=r_associated | relid=0 | w=10
  4782. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:diagnosis aspect
    n1=méningé (syndrome) | n2=en:diagnosis aspect | rel=r_associated | relid=0 | w=10
  4783. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:diaphragma sellae meningioma
    n1=méningé (syndrome) | n2=en:diaphragma sellae meningioma | rel=r_associated | relid=0 | w=10
  4784. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:diastema of teeth
    n1=méningé (syndrome) | n2=en:diastema of teeth | rel=r_associated | relid=0 | w=10
  4785. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:digestive system carcinoma
    n1=méningé (syndrome) | n2=en:digestive system carcinoma | rel=r_associated | relid=0 | w=10
  4786. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:digestive system neoplasms
    n1=méningé (syndrome) | n2=en:digestive system neoplasms | rel=r_associated | relid=0 | w=10
  4787. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:digit
    n1=méningé (syndrome) | n2=en:digit | rel=r_associated | relid=0 | w=10
  4788. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:diploid nucleated cell
    n1=méningé (syndrome) | n2=en:diploid nucleated cell | rel=r_associated | relid=0 | w=10
  4789. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:distal interphalangeal joint
    n1=méningé (syndrome) | n2=en:distal interphalangeal joint | rel=r_associated | relid=0 | w=10
  4790. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:dorsal root of the spinal nerve
    n1=méningé (syndrome) | n2=en:dorsal root of the spinal nerve | rel=r_associated | relid=0 | w=10
  4791. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:dorsal vein
    n1=méningé (syndrome) | n2=en:dorsal vein | rel=r_associated | relid=0 | w=10
  4792. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:drug effect
    n1=méningé (syndrome) | n2=en:drug effect | rel=r_associated | relid=0 | w=10
  4793. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:duct
    n1=méningé (syndrome) | n2=en:duct | rel=r_associated | relid=0 | w=10
  4794. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:duct system
    n1=méningé (syndrome) | n2=en:duct system | rel=r_associated | relid=0 | w=10
  4795. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ductal and lobular neoplasms
    n1=méningé (syndrome) | n2=en:ductal and lobular neoplasms | rel=r_associated | relid=0 | w=10
  4796. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ductal breast carcinoma
    n1=méningé (syndrome) | n2=en:ductal breast carcinoma | rel=r_associated | relid=0 | w=10
  4797. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ductal, lobular and/or medullary neoplasm
    n1=méningé (syndrome) | n2=en:ductal, lobular and/or medullary neoplasm | rel=r_associated | relid=0 | w=10
  4798. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:duodenal carcinoid
    n1=méningé (syndrome) | n2=en:duodenal carcinoid | rel=r_associated | relid=0 | w=10
  4799. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:duodenal carcinoma
    n1=méningé (syndrome) | n2=en:duodenal carcinoma | rel=r_associated | relid=0 | w=10
  4800. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:dura mater
    n1=méningé (syndrome) | n2=en:dura mater | rel=r_associated | relid=0 | w=10
  4801. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:dural extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
    n1=méningé (syndrome) | n2=en:dural extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue | rel=r_associated | relid=0 | w=10
  4802. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:dural tail sign
    n1=méningé (syndrome) | n2=en:dural tail sign | rel=r_associated | relid=0 | w=10
  4803. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:dysgerminoma
    n1=méningé (syndrome) | n2=en:dysgerminoma | rel=r_associated | relid=0 | w=10
  4804. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:dysplasia with neoplasia
    n1=méningé (syndrome) | n2=en:dysplasia with neoplasia | rel=r_associated | relid=0 | w=10
  4805. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:early filling vein sign
    n1=méningé (syndrome) | n2=en:early filling vein sign | rel=r_associated | relid=0 | w=10
  4806. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:early-onset hepatocellular carcinoma
    n1=méningé (syndrome) | n2=en:early-onset hepatocellular carcinoma | rel=r_associated | relid=0 | w=10
  4807. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ebv-induced b-cell lymphoma
    n1=méningé (syndrome) | n2=en:ebv-induced b-cell lymphoma | rel=r_associated | relid=0 | w=10
  4808. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ectopic meningioma
    n1=méningé (syndrome) | n2=en:ectopic meningioma | rel=r_associated | relid=0 | w=10
  4809. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:efferent duct
    n1=méningé (syndrome) | n2=en:efferent duct | rel=r_associated | relid=0 | w=10
  4810. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:egg shell
    n1=méningé (syndrome) | n2=en:egg shell | rel=r_associated | relid=0 | w=10
  4811. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:electric organ
    n1=méningé (syndrome) | n2=en:electric organ | rel=r_associated | relid=0 | w=10
  4812. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:embryonal carcinoma
    n1=méningé (syndrome) | n2=en:embryonal carcinoma | rel=r_associated | relid=0 | w=10
  4813. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:embryonal neoplasm
    n1=méningé (syndrome) | n2=en:embryonal neoplasm | rel=r_associated | relid=0 | w=10
  4814. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:endocrine cell
    n1=méningé (syndrome) | n2=en:endocrine cell | rel=r_associated | relid=0 | w=10
  4815. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:endocrine neoplasms malignant and unspecified
    n1=méningé (syndrome) | n2=en:endocrine neoplasms malignant and unspecified | rel=r_associated | relid=0 | w=10
  4816. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:endolymphatic sac tumor
    n1=méningé (syndrome) | n2=en:endolymphatic sac tumor | rel=r_associated | relid=0 | w=10
  4817. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:endometrial adenocarcinoma
    n1=méningé (syndrome) | n2=en:endometrial adenocarcinoma | rel=r_associated | relid=0 | w=10
  4818. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:endometrial carcinoma
    n1=méningé (syndrome) | n2=en:endometrial carcinoma | rel=r_associated | relid=0 | w=10
  4819. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:endometrioid stromal sarcoma
    n1=méningé (syndrome) | n2=en:endometrioid stromal sarcoma | rel=r_associated | relid=0 | w=10
  4820. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:endotheliomatosis
    n1=méningé (syndrome) | n2=en:endotheliomatosis | rel=r_associated | relid=0 | w=10
  4821. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:enteropathy-associated t-cell lymphoma
    n1=méningé (syndrome) | n2=en:enteropathy-associated t-cell lymphoma | rel=r_associated | relid=0 | w=10
  4822. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:entire meninges
    n1=méningé (syndrome) | n2=en:entire meninges | rel=r_associated | relid=0 | w=10
  4823. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:eosinophilic meningitis
    n1=méningé (syndrome) | n2=en:eosinophilic meningitis | rel=r_associated | relid=0 | w=10
  4824. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ependyma and remnants of the central canal of the spinal cord
    n1=méningé (syndrome) | n2=en:ependyma and remnants of the central canal of the spinal cord | rel=r_associated | relid=0 | w=10
  4825. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ependymal tumor
    n1=méningé (syndrome) | n2=en:ependymal tumor | rel=r_associated | relid=0 | w=10
  4826. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ependymoma
    n1=méningé (syndrome) | n2=en:ependymoma | rel=r_associated | relid=0 | w=10
  4827. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:epidemiologic
    n1=méningé (syndrome) | n2=en:epidemiologic | rel=r_associated | relid=0 | w=10
  4828. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:epidural spinal canal meningioma
    n1=méningé (syndrome) | n2=en:epidural spinal canal meningioma | rel=r_associated | relid=0 | w=10
  4829. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:epidural spinal canal neoplasm
    n1=méningé (syndrome) | n2=en:epidural spinal canal neoplasm | rel=r_associated | relid=0 | w=10
  4830. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:epithelial neoplasm
    n1=méningé (syndrome) | n2=en:epithelial neoplasm | rel=r_associated | relid=0 | w=10
  4831. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:esophageal carcinoma
    n1=méningé (syndrome) | n2=en:esophageal carcinoma | rel=r_associated | relid=0 | w=10
  4832. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ethnologic
    n1=méningé (syndrome) | n2=en:ethnologic | rel=r_associated | relid=0 | w=10
  4833. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:etiology aspects
    n1=méningé (syndrome) | n2=en:etiology aspects | rel=r_associated | relid=0 | w=10
  4834. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ewing sarcoma
    n1=méningé (syndrome) | n2=en:ewing sarcoma | rel=r_associated | relid=0 | w=10
  4835. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:excretory duct of lacrimal gland
    n1=méningé (syndrome) | n2=en:excretory duct of lacrimal gland | rel=r_associated | relid=0 | w=10
  4836. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:exocrine cell
    n1=méningé (syndrome) | n2=en:exocrine cell | rel=r_associated | relid=0 | w=10
  4837. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:exposure as collected domain
    n1=méningé (syndrome) | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=10
  4838. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:extra-adrenal paraganglioma
    n1=méningé (syndrome) | n2=en:extra-adrenal paraganglioma | rel=r_associated | relid=0 | w=10
  4839. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:extra-adrenal sympathetic paraganglioma
    n1=méningé (syndrome) | n2=en:extra-adrenal sympathetic paraganglioma | rel=r_associated | relid=0 | w=10
  4840. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:eye and adnexa
    n1=méningé (syndrome) | n2=en:eye and adnexa | rel=r_associated | relid=0 | w=10
  4841. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:eye haemangioma
    n1=méningé (syndrome) | n2=en:eye haemangioma | rel=r_associated | relid=0 | w=10
  4842. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:eye neoplasm
    n1=méningé (syndrome) | n2=en:eye neoplasm | rel=r_associated | relid=0 | w=10
  4843. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:eye, brain and other parts of central nervous system
    n1=méningé (syndrome) | n2=en:eye, brain and other parts of central nervous system | rel=r_associated | relid=0 | w=10
  4844. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:eyelid
    n1=méningé (syndrome) | n2=en:eyelid | rel=r_associated | relid=0 | w=10
  4845. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:falx cerebri meningioma
    n1=méningé (syndrome) | n2=en:falx cerebri meningioma | rel=r_associated | relid=0 | w=10
  4846. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:familial adenomatous polyposis associated medulloblastoma
    n1=méningé (syndrome) | n2=en:familial adenomatous polyposis associated medulloblastoma | rel=r_associated | relid=0 | w=10
  4847. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fascia of individual abdominal organ
    n1=méningé (syndrome) | n2=en:fascia of individual abdominal organ | rel=r_associated | relid=0 | w=10
  4848. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fascia of individual muscle
    n1=méningé (syndrome) | n2=en:fascia of individual muscle | rel=r_associated | relid=0 | w=10
  4849. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fascia of individual organ
    n1=méningé (syndrome) | n2=en:fascia of individual organ | rel=r_associated | relid=0 | w=10
  4850. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fascia of individual pelvic organ
    n1=méningé (syndrome) | n2=en:fascia of individual pelvic organ | rel=r_associated | relid=0 | w=10
  4851. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fascia of limb
    n1=méningé (syndrome) | n2=en:fascia of limb | rel=r_associated | relid=0 | w=10
  4852. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fascia of muscle
    n1=méningé (syndrome) | n2=en:fascia of muscle | rel=r_associated | relid=0 | w=10
  4853. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fascicle
    n1=méningé (syndrome) | n2=en:fascicle | rel=r_associated | relid=0 | w=10
  4854. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibril - cell component
    n1=méningé (syndrome) | n2=en:fibril - cell component | rel=r_associated | relid=0 | w=10
  4855. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibroblastic/myofibroblastic tumors (all subtypes)
    n1=méningé (syndrome) | n2=en:fibroblastic/myofibroblastic tumors (all subtypes) | rel=r_associated | relid=0 | w=10
  4856. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibroelastic membrane larynx
    n1=méningé (syndrome) | n2=en:fibroelastic membrane larynx | rel=r_associated | relid=0 | w=10
  4857. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibroelastoma
    n1=méningé (syndrome) | n2=en:fibroelastoma | rel=r_associated | relid=0 | w=10
  4858. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibroepithelial neoplasm
    n1=méningé (syndrome) | n2=en:fibroepithelial neoplasm | rel=r_associated | relid=0 | w=10
  4859. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibrohistiocytic neoplasm
    n1=méningé (syndrome) | n2=en:fibrohistiocytic neoplasm | rel=r_associated | relid=0 | w=10
  4860. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibromatous neoplasm
    n1=méningé (syndrome) | n2=en:fibromatous neoplasm | rel=r_associated | relid=0 | w=10
  4861. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibrosarcoma
    n1=méningé (syndrome) | n2=en:fibrosarcoma | rel=r_associated | relid=0 | w=10
  4862. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibrous connective tissue neoplasm
    n1=méningé (syndrome) | n2=en:fibrous connective tissue neoplasm | rel=r_associated | relid=0 | w=10
  4863. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibrous layer
    n1=méningé (syndrome) | n2=en:fibrous layer | rel=r_associated | relid=0 | w=10
  4864. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibrous layer in or on deep aspect of fatty layer of subcutaneous tissue
    n1=méningé (syndrome) | n2=en:fibrous layer in or on deep aspect of fatty layer of subcutaneous tissue | rel=r_associated | relid=0 | w=10
  4865. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibrous membrane
    n1=méningé (syndrome) | n2=en:fibrous membrane | rel=r_associated | relid=0 | w=10
  4866. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fibrous sheath
    n1=méningé (syndrome) | n2=en:fibrous sheath | rel=r_associated | relid=0 | w=10
  4867. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fimbria of fallopian tube
    n1=méningé (syndrome) | n2=en:fimbria of fallopian tube | rel=r_associated | relid=0 | w=10
  4868. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:finger
    n1=méningé (syndrome) | n2=en:finger | rel=r_associated | relid=0 | w=10
  4869. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fissure
    n1=méningé (syndrome) | n2=en:fissure | rel=r_associated | relid=0 | w=10
  4870. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fixed end
    n1=méningé (syndrome) | n2=en:fixed end | rel=r_associated | relid=0 | w=10
  4871. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:follicular lymphoma
    n1=méningé (syndrome) | n2=en:follicular lymphoma | rel=r_associated | relid=0 | w=10
  4872. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:follicular neoplasm
    n1=méningé (syndrome) | n2=en:follicular neoplasm | rel=r_associated | relid=0 | w=10
  4873. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fontanelle
    n1=méningé (syndrome) | n2=en:fontanelle | rel=r_associated | relid=0 | w=10
  4874. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:foramen magnum meningioma
    n1=méningé (syndrome) | n2=en:foramen magnum meningioma | rel=r_associated | relid=0 | w=10
  4875. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fossa
    n1=méningé (syndrome) | n2=en:fossa | rel=r_associated | relid=0 | w=10
  4876. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:foveola
    n1=méningé (syndrome) | n2=en:foveola | rel=r_associated | relid=0 | w=10
  4877. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:foveolar cell
    n1=méningé (syndrome) | n2=en:foveolar cell | rel=r_associated | relid=0 | w=10
  4878. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:frenulum
    n1=méningé (syndrome) | n2=en:frenulum | rel=r_associated | relid=0 | w=10
  4879. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:frequent skin cancer
    n1=méningé (syndrome) | n2=en:frequent skin cancer | rel=r_associated | relid=0 | w=10
  4880. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:frontal convexity meningioma
    n1=méningé (syndrome) | n2=en:frontal convexity meningioma | rel=r_associated | relid=0 | w=10
  4881. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:funiculus
    n1=méningé (syndrome) | n2=en:funiculus | rel=r_associated | relid=0 | w=10
  4882. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:fusiform cell
    n1=méningé (syndrome) | n2=en:fusiform cell | rel=r_associated | relid=0 | w=10
  4883. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gain of chromosome 12q
    n1=méningé (syndrome) | n2=en:gain of chromosome 12q | rel=r_associated | relid=0 | w=10
  4884. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gain of chromosome 15q
    n1=méningé (syndrome) | n2=en:gain of chromosome 15q | rel=r_associated | relid=0 | w=10
  4885. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gain of chromosome 17q
    n1=méningé (syndrome) | n2=en:gain of chromosome 17q | rel=r_associated | relid=0 | w=10
  4886. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gain of chromosome 1q
    n1=méningé (syndrome) | n2=en:gain of chromosome 1q | rel=r_associated | relid=0 | w=10
  4887. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gain of chromosome 20q
    n1=méningé (syndrome) | n2=en:gain of chromosome 20q | rel=r_associated | relid=0 | w=10
  4888. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gain of chromosome 9q
    n1=méningé (syndrome) | n2=en:gain of chromosome 9q | rel=r_associated | relid=0 | w=10
  4889. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ganglioglioma
    n1=méningé (syndrome) | n2=en:ganglioglioma | rel=r_associated | relid=0 | w=10
  4890. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ganglion cell
    n1=méningé (syndrome) | n2=en:ganglion cell | rel=r_associated | relid=0 | w=10
  4891. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ganglioneuroblastoma
    n1=méningé (syndrome) | n2=en:ganglioneuroblastoma | rel=r_associated | relid=0 | w=10
  4892. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ganglioneuroma
    n1=méningé (syndrome) | n2=en:ganglioneuroma | rel=r_associated | relid=0 | w=10
  4893. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gasserian meningioma
    n1=méningé (syndrome) | n2=en:gasserian meningioma | rel=r_associated | relid=0 | w=10
  4894. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gastric adenocarcinoma
    n1=méningé (syndrome) | n2=en:gastric adenocarcinoma | rel=r_associated | relid=0 | w=10
  4895. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gastric cancer, diffuse type, poorly differentiated, high-grade submucosal lesions
    n1=méningé (syndrome) | n2=en:gastric cancer, diffuse type, poorly differentiated, high-grade submucosal lesions | rel=r_associated | relid=0 | w=10
  4896. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gastric hemangioma
    n1=méningé (syndrome) | n2=en:gastric hemangioma | rel=r_associated | relid=0 | w=10
  4897. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gastric rugae
    n1=méningé (syndrome) | n2=en:gastric rugae | rel=r_associated | relid=0 | w=10
  4898. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gastrointestinal neoplasms malignant and unspecified
    n1=méningé (syndrome) | n2=en:gastrointestinal neoplasms malignant and unspecified | rel=r_associated | relid=0 | w=10
  4899. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gastrointestinal stromal tumor
    n1=méningé (syndrome) | n2=en:gastrointestinal stromal tumor | rel=r_associated | relid=0 | w=10
  4900. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gastrointestinal stromal tumors (less common)
    n1=méningé (syndrome) | n2=en:gastrointestinal stromal tumors (less common) | rel=r_associated | relid=0 | w=10
  4901. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:general anatomy
    n1=méningé (syndrome) | n2=en:general anatomy | rel=r_associated | relid=0 | w=10
  4902. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:genetic aspects
    n1=méningé (syndrome) | n2=en:genetic aspects | rel=r_associated | relid=0 | w=10
  4903. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:genital
    n1=méningé (syndrome) | n2=en:genital | rel=r_associated | relid=0 | w=10
  4904. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:genome - anatomical entity
    n1=méningé (syndrome) | n2=en:genome - anatomical entity | rel=r_associated | relid=0 | w=10
  4905. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:germ cell and gonadal stromal cell neoplasms (all subtypes)
    n1=méningé (syndrome) | n2=en:germ cell and gonadal stromal cell neoplasms (all subtypes) | rel=r_associated | relid=0 | w=10
  4906. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:germ cell tumor
    n1=méningé (syndrome) | n2=en:germ cell tumor | rel=r_associated | relid=0 | w=10
  4907. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gestational trophoblastic tumor
    n1=méningé (syndrome) | n2=en:gestational trophoblastic tumor | rel=r_associated | relid=0 | w=10
  4908. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:giant cell
    n1=méningé (syndrome) | n2=en:giant cell | rel=r_associated | relid=0 | w=10
  4909. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:giant cell astrocytoma
    n1=méningé (syndrome) | n2=en:giant cell astrocytoma | rel=r_associated | relid=0 | w=10
  4910. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:giant cell lesion of small bones
    n1=méningé (syndrome) | n2=en:giant cell lesion of small bones | rel=r_associated | relid=0 | w=10
  4911. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:giant cell tumor
    n1=méningé (syndrome) | n2=en:giant cell tumor | rel=r_associated | relid=0 | w=10
  4912. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gland
    n1=méningé (syndrome) | n2=en:gland | rel=r_associated | relid=0 | w=10
  4913. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gland of littre
    n1=méningé (syndrome) | n2=en:gland of littre | rel=r_associated | relid=0 | w=10
  4914. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:glandular cell
    n1=méningé (syndrome) | n2=en:glandular cell | rel=r_associated | relid=0 | w=10
  4915. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:glioblastoma
    n1=méningé (syndrome) | n2=en:glioblastoma | rel=r_associated | relid=0 | w=10
  4916. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:glioma
    n1=méningé (syndrome) | n2=en:glioma | rel=r_associated | relid=0 | w=10
  4917. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:glioneuronal tumour
    n1=méningé (syndrome) | n2=en:glioneuronal tumour | rel=r_associated | relid=0 | w=10
  4918. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:glomus tumor
    n1=méningé (syndrome) | n2=en:glomus tumor | rel=r_associated | relid=0 | w=10
  4919. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:glomus tympanicum paraganglioma
    n1=méningé (syndrome) | n2=en:glomus tympanicum paraganglioma | rel=r_associated | relid=0 | w=10
  4920. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gonad
    n1=méningé (syndrome) | n2=en:gonad | rel=r_associated | relid=0 | w=10
  4921. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gonadoblastoma
    n1=méningé (syndrome) | n2=en:gonadoblastoma | rel=r_associated | relid=0 | w=10
  4922. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:grade 1
    n1=méningé (syndrome) | n2=en:grade 1 | rel=r_associated | relid=0 | w=10
  4923. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:granular cell tumor and/or alveolar soft part sarcoma
    n1=méningé (syndrome) | n2=en:granular cell tumor and/or alveolar soft part sarcoma | rel=r_associated | relid=0 | w=10
  4924. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:granular cell tumors and alveolar soft part sarcomas
    n1=méningé (syndrome) | n2=en:granular cell tumors and alveolar soft part sarcomas | rel=r_associated | relid=0 | w=10
  4925. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:greater pelvis
    n1=méningé (syndrome) | n2=en:greater pelvis | rel=r_associated | relid=0 | w=10
  4926. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:growth hormone-producing pituitary gland neoplasm
    n1=méningé (syndrome) | n2=en:growth hormone-producing pituitary gland neoplasm | rel=r_associated | relid=0 | w=10
  4927. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gustatory system
    n1=méningé (syndrome) | n2=en:gustatory system | rel=r_associated | relid=0 | w=10
  4928. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:gynecoid pelvis
    n1=méningé (syndrome) | n2=en:gynecoid pelvis | rel=r_associated | relid=0 | w=10
  4929. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:haematopoietic neoplasms (excl leukaemias and lymphomas)
    n1=méningé (syndrome) | n2=en:haematopoietic neoplasms (excl leukaemias and lymphomas) | rel=r_associated | relid=0 | w=10
  4930. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hair
    n1=méningé (syndrome) | n2=en:hair | rel=r_associated | relid=0 | w=10
  4931. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hair of tragus
    n1=méningé (syndrome) | n2=en:hair of tragus | rel=r_associated | relid=0 | w=10
  4932. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hair whorls
    n1=méningé (syndrome) | n2=en:hair whorls | rel=r_associated | relid=0 | w=10
  4933. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hamartoma
    n1=méningé (syndrome) | n2=en:hamartoma | rel=r_associated | relid=0 | w=10
  4934. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:head and neck lymph node
    n1=méningé (syndrome) | n2=en:head and neck lymph node | rel=r_associated | relid=0 | w=10
  4935. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:head and neck paraganglioma
    n1=méningé (syndrome) | n2=en:head and neck paraganglioma | rel=r_associated | relid=0 | w=10
  4936. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:heart cell
    n1=méningé (syndrome) | n2=en:heart cell | rel=r_associated | relid=0 | w=10
  4937. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:heart dimension/size
    n1=méningé (syndrome) | n2=en:heart dimension/size | rel=r_associated | relid=0 | w=10
  4938. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hemangioblastic meningioma
    n1=méningé (syndrome) | n2=en:hemangioblastic meningioma | rel=r_associated | relid=0 | w=10
  4939. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hemangioblastoma
    n1=méningé (syndrome) | n2=en:hemangioblastoma | rel=r_associated | relid=0 | w=10
  4940. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hemangioblastoma, sporadic cerebellar (e.g., 193300.0007)
    n1=méningé (syndrome) | n2=en:hemangioblastoma, sporadic cerebellar (e.g., 193300.0007) | rel=r_associated | relid=0 | w=10
  4941. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hemangioma
    n1=méningé (syndrome) | n2=en:hemangioma | rel=r_associated | relid=0 | w=10
  4942. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hemangioma of eyelid
    n1=méningé (syndrome) | n2=en:hemangioma of eyelid | rel=r_associated | relid=0 | w=10
  4943. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hemangiopericytoma
    n1=méningé (syndrome) | n2=en:hemangiopericytoma | rel=r_associated | relid=0 | w=10
  4944. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hematopoietic and lymphoid cell neoplasm
    n1=méningé (syndrome) | n2=en:hematopoietic and lymphoid cell neoplasm | rel=r_associated | relid=0 | w=10
  4945. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hemocytes (cell)
    n1=méningé (syndrome) | n2=en:hemocytes (cell) | rel=r_associated | relid=0 | w=10
  4946. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hemophagocytic lymphohistiocytosis
    n1=méningé (syndrome) | n2=en:hemophagocytic lymphohistiocytosis | rel=r_associated | relid=0 | w=10
  4947. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hemophagocytic lymphohistiocytosis (in some patients)
    n1=méningé (syndrome) | n2=en:hemophagocytic lymphohistiocytosis (in some patients) | rel=r_associated | relid=0 | w=10
  4948. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hepatic and biliary neoplasms benign
    n1=méningé (syndrome) | n2=en:hepatic and biliary neoplasms benign | rel=r_associated | relid=0 | w=10
  4949. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hepatic haemangioma rupture
    n1=méningé (syndrome) | n2=en:hepatic haemangioma rupture | rel=r_associated | relid=0 | w=10
  4950. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hepatic lobule
    n1=méningé (syndrome) | n2=en:hepatic lobule | rel=r_associated | relid=0 | w=10
  4951. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hepatobiliary neoplasms malignant and unspecified
    n1=méningé (syndrome) | n2=en:hepatobiliary neoplasms malignant and unspecified | rel=r_associated | relid=0 | w=10
  4952. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hepatoblastoma
    n1=méningé (syndrome) | n2=en:hepatoblastoma | rel=r_associated | relid=0 | w=10
  4953. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hepatocyte
    n1=méningé (syndrome) | n2=en:hepatocyte | rel=r_associated | relid=0 | w=10
  4954. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hereditary neoplastic syndrome
    n1=méningé (syndrome) | n2=en:hereditary neoplastic syndrome | rel=r_associated | relid=0 | w=10
  4955. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hidden part of duodenum
    n1=méningé (syndrome) | n2=en:hidden part of duodenum | rel=r_associated | relid=0 | w=10
  4956. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hilum
    n1=méningé (syndrome) | n2=en:hilum | rel=r_associated | relid=0 | w=10
  4957. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:histological internal os
    n1=méningé (syndrome) | n2=en:histological internal os | rel=r_associated | relid=0 | w=10
  4958. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:historical aspects qualifier
    n1=méningé (syndrome) | n2=en:historical aspects qualifier | rel=r_associated | relid=0 | w=10
  4959. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hodgkin lymphoma
    n1=méningé (syndrome) | n2=en:hodgkin lymphoma | rel=r_associated | relid=0 | w=10
  4960. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hunter-macdonald syndrome
    n1=méningé (syndrome) | n2=en:hunter-macdonald syndrome | rel=r_associated | relid=0 | w=10
  4961. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hypersensitivity to chemotherapy
    n1=méningé (syndrome) | n2=en:hypersensitivity to chemotherapy | rel=r_associated | relid=0 | w=10
  4962. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:hypothalamic neoplasm
    n1=méningé (syndrome) | n2=en:hypothalamic neoplasm | rel=r_associated | relid=0 | w=10
  4963. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ileal, cecal, ovarian, and breast tumors, occasionally (endemic form)
    n1=méningé (syndrome) | n2=en:ileal, cecal, ovarian, and breast tumors, occasionally (endemic form) | rel=r_associated | relid=0 | w=10
  4964. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:imaginal discs
    n1=méningé (syndrome) | n2=en:imaginal discs | rel=r_associated | relid=0 | w=10
  4965. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:immunoproliferative disorders
    n1=méningé (syndrome) | n2=en:immunoproliferative disorders | rel=r_associated | relid=0 | w=10
  4966. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:in blood
    n1=méningé (syndrome) | n2=en:in blood | rel=r_associated | relid=0 | w=10
  4967. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:in cerebrospinal fluid
    n1=méningé (syndrome) | n2=en:in cerebrospinal fluid | rel=r_associated | relid=0 | w=10
  4968. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:in situ neoplasm (morphology)
    n1=méningé (syndrome) | n2=en:in situ neoplasm (morphology) | rel=r_associated | relid=0 | w=10
  4969. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:in urine
    n1=méningé (syndrome) | n2=en:in urine | rel=r_associated | relid=0 | w=10
  4970. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:inappropriate anatomical term
    n1=méningé (syndrome) | n2=en:inappropriate anatomical term | rel=r_associated | relid=0 | w=10
  4971. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased hepatocellular carcinoma risk
    n1=méningé (syndrome) | n2=en:increased hepatocellular carcinoma risk | rel=r_associated | relid=0 | w=10
  4972. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased incidence of hepatocellular carcinoma
    n1=méningé (syndrome) | n2=en:increased incidence of hepatocellular carcinoma | rel=r_associated | relid=0 | w=10
  4973. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased incidence of rectosigmoid cancer
    n1=méningé (syndrome) | n2=en:increased incidence of rectosigmoid cancer | rel=r_associated | relid=0 | w=10
  4974. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased malignancy risk, especially lymphoma and skin neoplasm
    n1=méningé (syndrome) | n2=en:increased malignancy risk, especially lymphoma and skin neoplasm | rel=r_associated | relid=0 | w=10
  4975. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk for cancer
    n1=méningé (syndrome) | n2=en:increased risk for cancer | rel=r_associated | relid=0 | w=10
  4976. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk for embryonal tumors
    n1=méningé (syndrome) | n2=en:increased risk for embryonal tumors | rel=r_associated | relid=0 | w=10
  4977. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk for hematologic cancer, particularly acute myeloid leukemia
    n1=méningé (syndrome) | n2=en:increased risk for hematologic cancer, particularly acute myeloid leukemia | rel=r_associated | relid=0 | w=10
  4978. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk for lymphoma hodgkin disease
    n1=méningé (syndrome) | n2=en:increased risk for lymphoma hodgkin disease | rel=r_associated | relid=0 | w=10
  4979. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk for monoclonal gammopathy
    n1=méningé (syndrome) | n2=en:increased risk for monoclonal gammopathy | rel=r_associated | relid=0 | w=10
  4980. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk for multiple myeloma
    n1=méningé (syndrome) | n2=en:increased risk for multiple myeloma | rel=r_associated | relid=0 | w=10
  4981. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk for wilms tumor
    n1=méningé (syndrome) | n2=en:increased risk for wilms tumor | rel=r_associated | relid=0 | w=10
  4982. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk in heterozygotes
    n1=méningé (syndrome) | n2=en:increased risk in heterozygotes | rel=r_associated | relid=0 | w=10
  4983. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of breast cancer in women
    n1=méningé (syndrome) | n2=en:increased risk of breast cancer in women | rel=r_associated | relid=0 | w=10
  4984. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of chondrosarcoma
    n1=méningé (syndrome) | n2=en:increased risk of chondrosarcoma | rel=r_associated | relid=0 | w=10
  4985. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of chondrosarcoma (mean age of onset 31 years)
    n1=méningé (syndrome) | n2=en:increased risk of chondrosarcoma (mean age of onset 31 years) | rel=r_associated | relid=0 | w=10
  4986. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of gastrointestinal cancer
    n1=méningé (syndrome) | n2=en:increased risk of gastrointestinal cancer | rel=r_associated | relid=0 | w=10
  4987. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of hematologic malignancy (1 patient)
    n1=méningé (syndrome) | n2=en:increased risk of hematologic malignancy (1 patient) | rel=r_associated | relid=0 | w=10
  4988. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of leukemia
    n1=méningé (syndrome) | n2=en:increased risk of leukemia | rel=r_associated | relid=0 | w=10
  4989. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of malignancy
    n1=méningé (syndrome) | n2=en:increased risk of malignancy | rel=r_associated | relid=0 | w=10
  4990. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of malignancy (classic feature)
    n1=méningé (syndrome) | n2=en:increased risk of malignancy (classic feature) | rel=r_associated | relid=0 | w=10
  4991. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of malignant lymphoma
    n1=méningé (syndrome) | n2=en:increased risk of malignant lymphoma | rel=r_associated | relid=0 | w=10
  4992. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of medulloblastoma (rare)
    n1=méningé (syndrome) | n2=en:increased risk of medulloblastoma (rare) | rel=r_associated | relid=0 | w=10
  4993. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of meningioma
    n1=méningé (syndrome) | n2=en:increased risk of meningioma | rel=r_associated | relid=0 | w=10
  4994. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of myelodysplastic syndrome or leukemia (in some patients)
    n1=méningé (syndrome) | n2=en:increased risk of myelodysplastic syndrome or leukemia (in some patients) | rel=r_associated | relid=0 | w=10
  4995. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of myelodysplastic syndromes
    n1=méningé (syndrome) | n2=en:increased risk of myelodysplastic syndromes | rel=r_associated | relid=0 | w=10
  4996. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of pancreatic cancer
    n1=méningé (syndrome) | n2=en:increased risk of pancreatic cancer | rel=r_associated | relid=0 | w=10
  4997. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of testicular cancer
    n1=méningé (syndrome) | n2=en:increased risk of testicular cancer | rel=r_associated | relid=0 | w=10
  4998. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased risk of tumor formation, especially of the head
    n1=méningé (syndrome) | n2=en:increased risk of tumor formation, especially of the head | rel=r_associated | relid=0 | w=10
  4999. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased susceptibility to b-cell lymphoma
    n1=méningé (syndrome) | n2=en:increased susceptibility to b-cell lymphoma | rel=r_associated | relid=0 | w=10
  5000. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased susceptibility to cancer
    n1=méningé (syndrome) | n2=en:increased susceptibility to cancer | rel=r_associated | relid=0 | w=10
  5001. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased susceptibility to carcinomas, especially cancers related to cutaneous viral infections
    n1=méningé (syndrome) | n2=en:increased susceptibility to carcinomas, especially cancers related to cutaneous viral infections | rel=r_associated | relid=0 | w=10
  5002. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased susceptibility to hematologic malignancies
    n1=méningé (syndrome) | n2=en:increased susceptibility to hematologic malignancies | rel=r_associated | relid=0 | w=10
  5003. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:increased susceptibility to large granular lymphocytic t-cell leukemia
    n1=méningé (syndrome) | n2=en:increased susceptibility to large granular lymphocytic t-cell leukemia | rel=r_associated | relid=0 | w=10
  5004. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:index tumor
    n1=méningé (syndrome) | n2=en:index tumor | rel=r_associated | relid=0 | w=10
  5005. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:infantile hemangioma
    n1=méningé (syndrome) | n2=en:infantile hemangioma | rel=r_associated | relid=0 | w=10
  5006. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:infectious meningitis
    n1=méningé (syndrome) | n2=en:infectious meningitis | rel=r_associated | relid=0 | w=10
  5007. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:infectious meningoencephalitis
    n1=méningé (syndrome) | n2=en:infectious meningoencephalitis | rel=r_associated | relid=0 | w=10
  5008. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:inferior synovial membrane of temporomandibular joint
    n1=méningé (syndrome) | n2=en:inferior synovial membrane of temporomandibular joint | rel=r_associated | relid=0 | w=10
  5009. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:inferior tarsal plate of eyelid
    n1=méningé (syndrome) | n2=en:inferior tarsal plate of eyelid | rel=r_associated | relid=0 | w=10
  5010. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:inserting periodontium
    n1=méningé (syndrome) | n2=en:inserting periodontium | rel=r_associated | relid=0 | w=10
  5011. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intermediate vascular neoplasm
    n1=méningé (syndrome) | n2=en:intermediate vascular neoplasm | rel=r_associated | relid=0 | w=10
  5012. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:internal auditory canal meningioma
    n1=méningé (syndrome) | n2=en:internal auditory canal meningioma | rel=r_associated | relid=0 | w=10
  5013. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:interosseous membrane
    n1=méningé (syndrome) | n2=en:interosseous membrane | rel=r_associated | relid=0 | w=10
  5014. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:interphalangeal joint
    n1=méningé (syndrome) | n2=en:interphalangeal joint | rel=r_associated | relid=0 | w=10
  5015. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:interstitial cell
    n1=méningé (syndrome) | n2=en:interstitial cell | rel=r_associated | relid=0 | w=10
  5016. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intestinal angioma
    n1=méningé (syndrome) | n2=en:intestinal angioma | rel=r_associated | relid=0 | w=10
  5017. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intestinal cell
    n1=méningé (syndrome) | n2=en:intestinal cell | rel=r_associated | relid=0 | w=10
  5018. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intra-abdominal hemangioma
    n1=méningé (syndrome) | n2=en:intra-abdominal hemangioma | rel=r_associated | relid=0 | w=10
  5019. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intracerebral cystic meningioma
    n1=méningé (syndrome) | n2=en:intracerebral cystic meningioma | rel=r_associated | relid=0 | w=10
  5020. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intracranial hemangioma
    n1=méningé (syndrome) | n2=en:intracranial hemangioma | rel=r_associated | relid=0 | w=10
  5021. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intracranial neoplasm
    n1=méningé (syndrome) | n2=en:intracranial neoplasm | rel=r_associated | relid=0 | w=10
  5022. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intracranial pressure observable
    n1=méningé (syndrome) | n2=en:intracranial pressure observable | rel=r_associated | relid=0 | w=10
  5023. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intraosseous angioma
    n1=méningé (syndrome) | n2=en:intraosseous angioma | rel=r_associated | relid=0 | w=10
  5024. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intrapulmonary part of pulmonary venous tree organ
    n1=méningé (syndrome) | n2=en:intrapulmonary part of pulmonary venous tree organ | rel=r_associated | relid=0 | w=10
  5025. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intraspinal meningioma
    n1=méningé (syndrome) | n2=en:intraspinal meningioma | rel=r_associated | relid=0 | w=10
  5026. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:intravascular lipoma
    n1=méningé (syndrome) | n2=en:intravascular lipoma | rel=r_associated | relid=0 | w=10
  5027. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:invertebrate cuticle
    n1=méningé (syndrome) | n2=en:invertebrate cuticle | rel=r_associated | relid=0 | w=10
  5028. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:investing layer
    n1=méningé (syndrome) | n2=en:investing layer | rel=r_associated | relid=0 | w=10
  5029. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:islet cell tumor
    n1=méningé (syndrome) | n2=en:islet cell tumor | rel=r_associated | relid=0 | w=10
  5030. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:islet of langerhans
    n1=méningé (syndrome) | n2=en:islet of langerhans | rel=r_associated | relid=0 | w=10
  5031. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:jaw and kidney tumor (endemic form)
    n1=méningé (syndrome) | n2=en:jaw and kidney tumor (endemic form) | rel=r_associated | relid=0 | w=10
  5032. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:joint
    n1=méningé (syndrome) | n2=en:joint | rel=r_associated | relid=0 | w=10
  5033. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:joint capsule
    n1=méningé (syndrome) | n2=en:joint capsule | rel=r_associated | relid=0 | w=10
  5034. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:joint of cervical vertebral column
    n1=méningé (syndrome) | n2=en:joint of cervical vertebral column | rel=r_associated | relid=0 | w=10
  5035. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:joint of lumbar vertebra
    n1=méningé (syndrome) | n2=en:joint of lumbar vertebra | rel=r_associated | relid=0 | w=10
  5036. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:joint structure of pelvis
    n1=méningé (syndrome) | n2=en:joint structure of pelvis | rel=r_associated | relid=0 | w=10
  5037. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:joint structure of spine
    n1=méningé (syndrome) | n2=en:joint structure of spine | rel=r_associated | relid=0 | w=10
  5038. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:jugular foramen
    n1=méningé (syndrome) | n2=en:jugular foramen | rel=r_associated | relid=0 | w=10
  5039. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:jugular foramen meningioma
    n1=méningé (syndrome) | n2=en:jugular foramen meningioma | rel=r_associated | relid=0 | w=10
  5040. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:jugulotympanic paraganglioma
    n1=méningé (syndrome) | n2=en:jugulotympanic paraganglioma | rel=r_associated | relid=0 | w=10
  5041. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:juvenile ovarian granulosa cell tumor
    n1=méningé (syndrome) | n2=en:juvenile ovarian granulosa cell tumor | rel=r_associated | relid=0 | w=10
  5042. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:juxta-oral organ
    n1=méningé (syndrome) | n2=en:juxta-oral organ | rel=r_associated | relid=0 | w=10
  5043. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:kaposi sarcoma
    n1=méningé (syndrome) | n2=en:kaposi sarcoma | rel=r_associated | relid=0 | w=10
  5044. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:kaposi sarcoma (1 patient)
    n1=méningé (syndrome) | n2=en:kaposi sarcoma (1 patient) | rel=r_associated | relid=0 | w=10
  5045. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:kidney lobe
    n1=méningé (syndrome) | n2=en:kidney lobe | rel=r_associated | relid=0 | w=10
  5046. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:kidney wilms tumor
    n1=méningé (syndrome) | n2=en:kidney wilms tumor | rel=r_associated | relid=0 | w=10
  5047. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:labrum
    n1=méningé (syndrome) | n2=en:labrum | rel=r_associated | relid=0 | w=10
  5048. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lacrimal pathway
    n1=méningé (syndrome) | n2=en:lacrimal pathway | rel=r_associated | relid=0 | w=10
  5049. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:large cell medulloblastoma
    n1=méningé (syndrome) | n2=en:large cell medulloblastoma | rel=r_associated | relid=0 | w=10
  5050. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:large cell/anaplastic medulloblastoma
    n1=méningé (syndrome) | n2=en:large cell/anaplastic medulloblastoma | rel=r_associated | relid=0 | w=10
  5051. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:large neuron
    n1=méningé (syndrome) | n2=en:large neuron | rel=r_associated | relid=0 | w=10
  5052. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:laryngeal carcinoma
    n1=méningé (syndrome) | n2=en:laryngeal carcinoma | rel=r_associated | relid=0 | w=10
  5053. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lateral lacuna
    n1=méningé (syndrome) | n2=en:lateral lacuna | rel=r_associated | relid=0 | w=10
  5054. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lateral ventricle meningioma
    n1=méningé (syndrome) | n2=en:lateral ventricle meningioma | rel=r_associated | relid=0 | w=10
  5055. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:layer
    n1=méningé (syndrome) | n2=en:layer | rel=r_associated | relid=0 | w=10
  5056. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:left side of jaw
    n1=méningé (syndrome) | n2=en:left side of jaw | rel=r_associated | relid=0 | w=10
  5057. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lemniscus
    n1=méningé (syndrome) | n2=en:lemniscus | rel=r_associated | relid=0 | w=10
  5058. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lens fiber
    n1=méningé (syndrome) | n2=en:lens fiber | rel=r_associated | relid=0 | w=10
  5059. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:leptomeningeal sarcoma
    n1=méningé (syndrome) | n2=en:leptomeningeal sarcoma | rel=r_associated | relid=0 | w=10
  5060. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:leptomeninges
    n1=méningé (syndrome) | n2=en:leptomeninges | rel=r_associated | relid=0 | w=10
  5061. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lesser pelvis
    n1=méningé (syndrome) | n2=en:lesser pelvis | rel=r_associated | relid=0 | w=10
  5062. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:leukemia
    n1=méningé (syndrome) | n2=en:leukemia | rel=r_associated | relid=0 | w=10
  5063. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:leukemia (both all and aml)
    n1=méningé (syndrome) | n2=en:leukemia (both all and aml) | rel=r_associated | relid=0 | w=10
  5064. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ligament
    n1=méningé (syndrome) | n2=en:ligament | rel=r_associated | relid=0 | w=10
  5065. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ligamentum flavum
    n1=méningé (syndrome) | n2=en:ligamentum flavum | rel=r_associated | relid=0 | w=10
  5066. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:limb
    n1=méningé (syndrome) | n2=en:limb | rel=r_associated | relid=0 | w=10
  5067. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lipoma
    n1=méningé (syndrome) | n2=en:lipoma | rel=r_associated | relid=0 | w=10
  5068. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lipomas of the central neryous system
    n1=méningé (syndrome) | n2=en:lipomas of the central neryous system | rel=r_associated | relid=0 | w=10
  5069. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lipomatous neoplasm
    n1=méningé (syndrome) | n2=en:lipomatous neoplasm | rel=r_associated | relid=0 | w=10
  5070. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:liver angiosarcoma
    n1=méningé (syndrome) | n2=en:liver angiosarcoma | rel=r_associated | relid=0 | w=10
  5071. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:liver carcinoma
    n1=méningé (syndrome) | n2=en:liver carcinoma | rel=r_associated | relid=0 | w=10
  5072. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:liver hemangioma
    n1=méningé (syndrome) | n2=en:liver hemangioma | rel=r_associated | relid=0 | w=10
  5073. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lobular hemangioma
    n1=méningé (syndrome) | n2=en:lobular hemangioma | rel=r_associated | relid=0 | w=10
  5074. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:longitudinal fiber of ciliary muscle
    n1=méningé (syndrome) | n2=en:longitudinal fiber of ciliary muscle | rel=r_associated | relid=0 | w=10
  5075. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:loss of chromosome 14
    n1=méningé (syndrome) | n2=en:loss of chromosome 14 | rel=r_associated | relid=0 | w=10
  5076. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:loss of chromosome 1p
    n1=méningé (syndrome) | n2=en:loss of chromosome 1p | rel=r_associated | relid=0 | w=10
  5077. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:loss of chromosome 22
    n1=méningé (syndrome) | n2=en:loss of chromosome 22 | rel=r_associated | relid=0 | w=10
  5078. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:loss of chromosome 3p
    n1=méningé (syndrome) | n2=en:loss of chromosome 3p | rel=r_associated | relid=0 | w=10
  5079. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:low incidence of plexiform neurofibromas
    n1=méningé (syndrome) | n2=en:low incidence of plexiform neurofibromas | rel=r_associated | relid=0 | w=10
  5080. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:low-grade neuroendocrine carcinoma (submandibular glands, salivary glands, maxillary sinus, nasal cavity)
    n1=méningé (syndrome) | n2=en:low-grade neuroendocrine carcinoma (submandibular glands, salivary glands, maxillary sinus, nasal cavity) | rel=r_associated | relid=0 | w=10
  5081. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lower clivus meningioma
    n1=méningé (syndrome) | n2=en:lower clivus meningioma | rel=r_associated | relid=0 | w=10
  5082. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lumbar intraspinal meningioma
    n1=méningé (syndrome) | n2=en:lumbar intraspinal meningioma | rel=r_associated | relid=0 | w=10
  5083. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lund
    n1=méningé (syndrome) | n2=en:lund | rel=r_associated | relid=0 | w=10
  5084. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lung
    n1=méningé (syndrome) | n2=en:lung | rel=r_associated | relid=0 | w=10
  5085. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lung adenocarcinoma
    n1=méningé (syndrome) | n2=en:lung adenocarcinoma | rel=r_associated | relid=0 | w=10
  5086. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymph node group
    n1=méningé (syndrome) | n2=en:lymph node group | rel=r_associated | relid=0 | w=10
  5087. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymph node trabecula
    n1=méningé (syndrome) | n2=en:lymph node trabecula | rel=r_associated | relid=0 | w=10
  5088. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphangiosarcoma
    n1=méningé (syndrome) | n2=en:lymphangiosarcoma | rel=r_associated | relid=0 | w=10
  5089. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphatic group of abdomen
    n1=méningé (syndrome) | n2=en:lymphatic group of abdomen | rel=r_associated | relid=0 | w=10
  5090. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphatic group of axilla
    n1=méningé (syndrome) | n2=en:lymphatic group of axilla | rel=r_associated | relid=0 | w=10
  5091. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphatic vessel
    n1=méningé (syndrome) | n2=en:lymphatic vessel | rel=r_associated | relid=0 | w=10
  5092. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphatic vessel neoplasm
    n1=méningé (syndrome) | n2=en:lymphatic vessel neoplasm | rel=r_associated | relid=0 | w=10
  5093. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphoid organ structure
    n1=méningé (syndrome) | n2=en:lymphoid organ structure | rel=r_associated | relid=0 | w=10
  5094. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphoma
    n1=méningé (syndrome) | n2=en:lymphoma | rel=r_associated | relid=0 | w=10
  5095. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphoma (in some patients)
    n1=méningé (syndrome) | n2=en:lymphoma (in some patients) | rel=r_associated | relid=0 | w=10
  5096. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphomas nec
    n1=méningé (syndrome) | n2=en:lymphomas nec | rel=r_associated | relid=0 | w=10
  5097. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphoproliferative disorder
    n1=méningé (syndrome) | n2=en:lymphoproliferative disorder | rel=r_associated | relid=0 | w=10
  5098. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphoproliferative disorder (in some patients)
    n1=méningé (syndrome) | n2=en:lymphoproliferative disorder (in some patients) | rel=r_associated | relid=0 | w=10
  5099. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:lymphosarcoma
    n1=méningé (syndrome) | n2=en:lymphosarcoma | rel=r_associated | relid=0 | w=10
  5100. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:major fissure
    n1=méningé (syndrome) | n2=en:major fissure | rel=r_associated | relid=0 | w=10
  5101. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:male germ cell tumors (gct), 2 subtypes -
    n1=méningé (syndrome) | n2=en:male germ cell tumors (gct), 2 subtypes - | rel=r_associated | relid=0 | w=10
  5102. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignancy (34%)
    n1=méningé (syndrome) | n2=en:malignancy (34%) | rel=r_associated | relid=0 | w=10
  5103. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignancy in approximately 10%
    n1=méningé (syndrome) | n2=en:malignancy in approximately 10% | rel=r_associated | relid=0 | w=10
  5104. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant brain neoplasm
    n1=méningé (syndrome) | n2=en:malignant brain neoplasm | rel=r_associated | relid=0 | w=10
  5105. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant breast neoplasm
    n1=méningé (syndrome) | n2=en:malignant breast neoplasm | rel=r_associated | relid=0 | w=10
  5106. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant cell
    n1=méningé (syndrome) | n2=en:malignant cell | rel=r_associated | relid=0 | w=10
  5107. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant central nervous system germ cell tumor
    n1=méningé (syndrome) | n2=en:malignant central nervous system germ cell tumor | rel=r_associated | relid=0 | w=10
  5108. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant central nervous system mesenchymal, non-meningothelial neoplasm
    n1=méningé (syndrome) | n2=en:malignant central nervous system mesenchymal, non-meningothelial neoplasm | rel=r_associated | relid=0 | w=10
  5109. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant central nervous system neoplasm
    n1=méningé (syndrome) | n2=en:malignant central nervous system neoplasm | rel=r_associated | relid=0 | w=10
  5110. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant cerebral neoplasm
    n1=méningé (syndrome) | n2=en:malignant cerebral neoplasm | rel=r_associated | relid=0 | w=10
  5111. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant digestive system neoplasm
    n1=méningé (syndrome) | n2=en:malignant digestive system neoplasm | rel=r_associated | relid=0 | w=10
  5112. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant epithelial neoplasms (all subtypes)
    n1=méningé (syndrome) | n2=en:malignant epithelial neoplasms (all subtypes) | rel=r_associated | relid=0 | w=10
  5113. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant esophageal neoplasm
    n1=méningé (syndrome) | n2=en:malignant esophageal neoplasm | rel=r_associated | relid=0 | w=10
  5114. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant fibrous histiocytoma (in about 35% of patients)
    n1=méningé (syndrome) | n2=en:malignant fibrous histiocytoma (in about 35% of patients) | rel=r_associated | relid=0 | w=10
  5115. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant genitourinary tract tumor
    n1=méningé (syndrome) | n2=en:malignant genitourinary tract tumor | rel=r_associated | relid=0 | w=10
  5116. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant giant cell neoplasm
    n1=méningé (syndrome) | n2=en:malignant giant cell neoplasm | rel=r_associated | relid=0 | w=10
  5117. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant glioma
    n1=méningé (syndrome) | n2=en:malignant glioma | rel=r_associated | relid=0 | w=10
  5118. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant hemangiopericytoma
    n1=méningé (syndrome) | n2=en:malignant hemangiopericytoma | rel=r_associated | relid=0 | w=10
  5119. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant intracranial neoplasm
    n1=méningé (syndrome) | n2=en:malignant intracranial neoplasm | rel=r_associated | relid=0 | w=10
  5120. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant leptomeningeal neoplasm
    n1=méningé (syndrome) | n2=en:malignant leptomeningeal neoplasm | rel=r_associated | relid=0 | w=10
  5121. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant meningioma
    n1=méningé (syndrome) | n2=en:malignant meningioma | rel=r_associated | relid=0 | w=10
  5122. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant neoplasm
    n1=méningé (syndrome) | n2=en:malignant neoplasm | rel=r_associated | relid=0 | w=10
  5123. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant neoplasm (morphology)
    n1=méningé (syndrome) | n2=en:malignant neoplasm (morphology) | rel=r_associated | relid=0 | w=10
  5124. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant neoplasm of bone, connective tissue, skin and breast
    n1=méningé (syndrome) | n2=en:malignant neoplasm of bone, connective tissue, skin and breast | rel=r_associated | relid=0 | w=10
  5125. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant neoplasm of digestive organs and peritoneum
    n1=méningé (syndrome) | n2=en:malignant neoplasm of digestive organs and peritoneum | rel=r_associated | relid=0 | w=10
  5126. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant neoplasm of genitourinary organ
    n1=méningé (syndrome) | n2=en:malignant neoplasm of genitourinary organ | rel=r_associated | relid=0 | w=10
  5127. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant neoplasm of lip, oral cavity and pharynx
    n1=méningé (syndrome) | n2=en:malignant neoplasm of lip, oral cavity and pharynx | rel=r_associated | relid=0 | w=10
  5128. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant neoplasm of other and unspecified sites
    n1=méningé (syndrome) | n2=en:malignant neoplasm of other and unspecified sites | rel=r_associated | relid=0 | w=10
  5129. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant neoplasm, uncertain whether primary or metastatic
    n1=méningé (syndrome) | n2=en:malignant neoplasm, uncertain whether primary or metastatic | rel=r_associated | relid=0 | w=10
  5130. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant neoplasms of respiratory and intrathoracic organs
    n1=méningé (syndrome) | n2=en:malignant neoplasms of respiratory and intrathoracic organs | rel=r_associated | relid=0 | w=10
  5131. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant ovarian neoplasm
    n1=méningé (syndrome) | n2=en:malignant ovarian neoplasm | rel=r_associated | relid=0 | w=10
  5132. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant pancreatic neoplasm
    n1=méningé (syndrome) | n2=en:malignant pancreatic neoplasm | rel=r_associated | relid=0 | w=10
  5133. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant peripheral nerve sheath tumor
    n1=méningé (syndrome) | n2=en:malignant peripheral nerve sheath tumor | rel=r_associated | relid=0 | w=10
  5134. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant peripheral nerve sheath tumors (21%)
    n1=méningé (syndrome) | n2=en:malignant peripheral nerve sheath tumors (21%) | rel=r_associated | relid=0 | w=10
  5135. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant pharyngeal neoplasm
    n1=méningé (syndrome) | n2=en:malignant pharyngeal neoplasm | rel=r_associated | relid=0 | w=10
  5136. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant sex cord-stromal tumor
    n1=méningé (syndrome) | n2=en:malignant sex cord-stromal tumor | rel=r_associated | relid=0 | w=10
  5137. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant skin neoplasm
    n1=méningé (syndrome) | n2=en:malignant skin neoplasm | rel=r_associated | relid=0 | w=10
  5138. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant spinal cord neoplasm
    n1=méningé (syndrome) | n2=en:malignant spinal cord neoplasm | rel=r_associated | relid=0 | w=10
  5139. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant spindle cell neoplasm
    n1=méningé (syndrome) | n2=en:malignant spindle cell neoplasm | rel=r_associated | relid=0 | w=10
  5140. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant thyroid gland neoplasm
    n1=méningé (syndrome) | n2=en:malignant thyroid gland neoplasm | rel=r_associated | relid=0 | w=10
  5141. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant tumor of lymphoid hemopoietic and related tissue
    n1=méningé (syndrome) | n2=en:malignant tumor of lymphoid hemopoietic and related tissue | rel=r_associated | relid=0 | w=10
  5142. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant tumor of optic nerve
    n1=méningé (syndrome) | n2=en:malignant tumor of optic nerve | rel=r_associated | relid=0 | w=10
  5143. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant tumor of optic nerve and sheath
    n1=méningé (syndrome) | n2=en:malignant tumor of optic nerve and sheath | rel=r_associated | relid=0 | w=10
  5144. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant tumor, clear cell type
    n1=méningé (syndrome) | n2=en:malignant tumor, clear cell type | rel=r_associated | relid=0 | w=10
  5145. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant tumor, small cell type
    n1=méningé (syndrome) | n2=en:malignant tumor, small cell type | rel=r_associated | relid=0 | w=10
  5146. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant uterine neoplasm
    n1=méningé (syndrome) | n2=en:malignant uterine neoplasm | rel=r_associated | relid=0 | w=10
  5147. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:malignant vascular neoplasm
    n1=méningé (syndrome) | n2=en:malignant vascular neoplasm | rel=r_associated | relid=0 | w=10
  5148. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mammary ductal fibroadenoma
    n1=méningé (syndrome) | n2=en:mammary ductal fibroadenoma | rel=r_associated | relid=0 | w=10
  5149. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mammilla
    n1=méningé (syndrome) | n2=en:mammilla | rel=r_associated | relid=0 | w=10
  5150. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:massive osteolyses
    n1=méningé (syndrome) | n2=en:massive osteolyses | rel=r_associated | relid=0 | w=10
  5151. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mast cell neoplasm
    n1=méningé (syndrome) | n2=en:mast cell neoplasm | rel=r_associated | relid=0 | w=10
  5152. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mature b-cell neoplasms (all subtypes)
    n1=méningé (syndrome) | n2=en:mature b-cell neoplasms (all subtypes) | rel=r_associated | relid=0 | w=10
  5153. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mature t- and nk-cell neoplasms (all subtypes)
    n1=méningé (syndrome) | n2=en:mature t- and nk-cell neoplasms (all subtypes) | rel=r_associated | relid=0 | w=10
  5154. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:medium sized neuron
    n1=méningé (syndrome) | n2=en:medium sized neuron | rel=r_associated | relid=0 | w=10
  5155. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:medulloblastoma of cerebellum
    n1=méningé (syndrome) | n2=en:medulloblastoma of cerebellum | rel=r_associated | relid=0 | w=10
  5156. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:medulloblastoma with extensive nodularity
    n1=méningé (syndrome) | n2=en:medulloblastoma with extensive nodularity | rel=r_associated | relid=0 | w=10
  5157. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:medulloblastoma with melanotic differentiation
    n1=méningé (syndrome) | n2=en:medulloblastoma with melanotic differentiation | rel=r_associated | relid=0 | w=10
  5158. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:medulloblastoma, genetically defined
    n1=méningé (syndrome) | n2=en:medulloblastoma, genetically defined | rel=r_associated | relid=0 | w=10
  5159. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:medulloblastoma, not otherwise specified
    n1=méningé (syndrome) | n2=en:medulloblastoma, not otherwise specified | rel=r_associated | relid=0 | w=10
  5160. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:medullomyoblastoma with myogenic differentiation
    n1=méningé (syndrome) | n2=en:medullomyoblastoma with myogenic differentiation | rel=r_associated | relid=0 | w=10
  5161. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:melanocytic neoplasm
    n1=méningé (syndrome) | n2=en:melanocytic neoplasm | rel=r_associated | relid=0 | w=10
  5162. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:melanoma
    n1=méningé (syndrome) | n2=en:melanoma | rel=r_associated | relid=0 | w=10
  5163. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:membrane
    n1=méningé (syndrome) | n2=en:membrane | rel=r_associated | relid=0 | w=10
  5164. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:membrane of reissner
    n1=méningé (syndrome) | n2=en:membrane of reissner | rel=r_associated | relid=0 | w=10
  5165. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:membranous layer of subcutaneous tissue
    n1=méningé (syndrome) | n2=en:membranous layer of subcutaneous tissue | rel=r_associated | relid=0 | w=10
  5166. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:membranous wall
    n1=méningé (syndrome) | n2=en:membranous wall | rel=r_associated | relid=0 | w=10
  5167. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal branch
    n1=méningé (syndrome) | n2=en:meningeal branch | rel=r_associated | relid=0 | w=10
  5168. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal chronic myelogenous leukemia, bcr-abl1 positive
    n1=méningé (syndrome) | n2=en:meningeal chronic myelogenous leukemia, bcr-abl1 positive | rel=r_associated | relid=0 | w=10
  5169. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal cluster
    n1=méningé (syndrome) | n2=en:meningeal cluster | rel=r_associated | relid=0 | w=10
  5170. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal gliomatosis
    n1=méningé (syndrome) | n2=en:meningeal gliomatosis | rel=r_associated | relid=0 | w=10
  5171. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal leukemia
    n1=méningé (syndrome) | n2=en:meningeal leukemia | rel=r_associated | relid=0 | w=10
  5172. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal lymphoma
    n1=méningé (syndrome) | n2=en:meningeal lymphoma | rel=r_associated | relid=0 | w=10
  5173. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal melanocytosis
    n1=méningé (syndrome) | n2=en:meningeal melanocytosis | rel=r_associated | relid=0 | w=10
  5174. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal melanoma
    n1=méningé (syndrome) | n2=en:meningeal melanoma | rel=r_associated | relid=0 | w=10
  5175. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal melanomatosis
    n1=méningé (syndrome) | n2=en:meningeal melanomatosis | rel=r_associated | relid=0 | w=10
  5176. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal neoplasm, uncertain whether benign or malignant
    n1=méningé (syndrome) | n2=en:meningeal neoplasm, uncertain whether benign or malignant | rel=r_associated | relid=0 | w=10
  5177. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal sarcoma
    n1=méningé (syndrome) | n2=en:meningeal sarcoma | rel=r_associated | relid=0 | w=10
  5178. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal solitary fibrous tumor/hemangiopericytoma, grade 3
    n1=méningé (syndrome) | n2=en:meningeal solitary fibrous tumor/hemangiopericytoma, grade 3 | rel=r_associated | relid=0 | w=10
  5179. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningeal tuberculosis
    n1=méningé (syndrome) | n2=en:meningeal tuberculosis | rel=r_associated | relid=0 | w=10
  5180. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meninges operation
    n1=méningé (syndrome) | n2=en:meninges operation | rel=r_associated | relid=0 | w=10
  5181. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meninges, meningeal interspace
    n1=méningé (syndrome) | n2=en:meninges, meningeal interspace | rel=r_associated | relid=0 | w=10
  5182. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningioma, familial, susceptibility to
    n1=méningé (syndrome) | n2=en:meningioma, familial, susceptibility to | rel=r_associated | relid=0 | w=10
  5183. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningiomas, hemangiopericytic
    n1=méningé (syndrome) | n2=en:meningiomas, hemangiopericytic | rel=r_associated | relid=0 | w=10
  5184. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningism
    n1=méningé (syndrome) | n2=en:meningism | rel=r_associated | relid=0 | w=10
  5185. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningitis due to other and unspecified causes
    n1=méningé (syndrome) | n2=en:meningitis due to other and unspecified causes | rel=r_associated | relid=0 | w=10
  5186. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meningothelial cell
    n1=méningé (syndrome) | n2=en:meningothelial cell | rel=r_associated | relid=0 | w=10
  5187. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meninx
    n1=méningé (syndrome) | n2=en:meninx | rel=r_associated | relid=0 | w=10
  5188. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meniscus
    n1=méningé (syndrome) | n2=en:meniscus | rel=r_associated | relid=0 | w=10
  5189. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:meridional fibers of ciliary muscle
    n1=méningé (syndrome) | n2=en:meridional fibers of ciliary muscle | rel=r_associated | relid=0 | w=10
  5190. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mesenchymal tumor, nos
    n1=méningé (syndrome) | n2=en:mesenchymal tumor, nos | rel=r_associated | relid=0 | w=10
  5191. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mesenchymal tumor, special type
    n1=méningé (syndrome) | n2=en:mesenchymal tumor, special type | rel=r_associated | relid=0 | w=10
  5192. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mesoblastic nephroma
    n1=méningé (syndrome) | n2=en:mesoblastic nephroma | rel=r_associated | relid=0 | w=10
  5193. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mesonephric neoplasm
    n1=méningé (syndrome) | n2=en:mesonephric neoplasm | rel=r_associated | relid=0 | w=10
  5194. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mesotendon
    n1=méningé (syndrome) | n2=en:mesotendon | rel=r_associated | relid=0 | w=10
  5195. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mesothelial neoplasm
    n1=méningé (syndrome) | n2=en:mesothelial neoplasm | rel=r_associated | relid=0 | w=10
  5196. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mesothelioma
    n1=méningé (syndrome) | n2=en:mesothelioma | rel=r_associated | relid=0 | w=10
  5197. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mesothelioma, malignant, after asbestos exposure
    n1=méningé (syndrome) | n2=en:mesothelioma, malignant, after asbestos exposure | rel=r_associated | relid=0 | w=10
  5198. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:metastases to peripheral vascular system
    n1=méningé (syndrome) | n2=en:metastases to peripheral vascular system | rel=r_associated | relid=0 | w=10
  5199. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:metastatic angiosarcoma
    n1=méningé (syndrome) | n2=en:metastatic angiosarcoma | rel=r_associated | relid=0 | w=10
  5200. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:metastatic malignant hemangiopericytoma
    n1=méningé (syndrome) | n2=en:metastatic malignant hemangiopericytoma | rel=r_associated | relid=0 | w=10
  5201. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:metastatic malignant neoplasm in the central nervous system
    n1=méningé (syndrome) | n2=en:metastatic malignant neoplasm in the central nervous system | rel=r_associated | relid=0 | w=10
  5202. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:metastatic neoplasm
    n1=méningé (syndrome) | n2=en:metastatic neoplasm | rel=r_associated | relid=0 | w=10
  5203. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:metastatic qualifier
    n1=méningé (syndrome) | n2=en:metastatic qualifier | rel=r_associated | relid=0 | w=10
  5204. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:middle cranial fossa meningioma
    n1=méningé (syndrome) | n2=en:middle cranial fossa meningioma | rel=r_associated | relid=0 | w=10
  5205. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:miscellaneous and site unspecified neoplasms benign
    n1=méningé (syndrome) | n2=en:miscellaneous and site unspecified neoplasms benign | rel=r_associated | relid=0 | w=10
  5206. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:miscellaneous and site unspecified neoplasms malignant and unspecified
    n1=méningé (syndrome) | n2=en:miscellaneous and site unspecified neoplasms malignant and unspecified | rel=r_associated | relid=0 | w=10
  5207. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:miscellaneous bone tumors
    n1=méningé (syndrome) | n2=en:miscellaneous bone tumors | rel=r_associated | relid=0 | w=10
  5208. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:miscellaneous mesenchymal tumors (all subtypes)
    n1=méningé (syndrome) | n2=en:miscellaneous mesenchymal tumors (all subtypes) | rel=r_associated | relid=0 | w=10
  5209. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:miscellaneous soft tissue tumors (all subtypes)
    n1=méningé (syndrome) | n2=en:miscellaneous soft tissue tumors (all subtypes) | rel=r_associated | relid=0 | w=10
  5210. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:miscellaneous tumors
    n1=méningé (syndrome) | n2=en:miscellaneous tumors | rel=r_associated | relid=0 | w=10
  5211. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mixed glioma
    n1=méningé (syndrome) | n2=en:mixed glioma | rel=r_associated | relid=0 | w=10
  5212. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mixed nerve
    n1=méningé (syndrome) | n2=en:mixed nerve | rel=r_associated | relid=0 | w=10
  5213. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mobile end
    n1=méningé (syndrome) | n2=en:mobile end | rel=r_associated | relid=0 | w=10
  5214. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:molecule
    n1=méningé (syndrome) | n2=en:molecule | rel=r_associated | relid=0 | w=10
  5215. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:monomorphic cells, medium-sized, with round nuclei, multiple nucleoli, and moderate amount of cytoplasm
    n1=méningé (syndrome) | n2=en:monomorphic cells, medium-sized, with round nuclei, multiple nucleoli, and moderate amount of cytoplasm | rel=r_associated | relid=0 | w=10
  5216. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:montgomery tubercle
    n1=méningé (syndrome) | n2=en:montgomery tubercle | rel=r_associated | relid=0 | w=10
  5217. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:morphology
    n1=méningé (syndrome) | n2=en:morphology | rel=r_associated | relid=0 | w=10
  5218. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:motor nerve
    n1=méningé (syndrome) | n2=en:motor nerve | rel=r_associated | relid=0 | w=10
  5219. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:motor root
    n1=méningé (syndrome) | n2=en:motor root | rel=r_associated | relid=0 | w=10
  5220. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mouse angiomatous meningioma
    n1=méningé (syndrome) | n2=en:mouse angiomatous meningioma | rel=r_associated | relid=0 | w=10
  5221. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mouse meninges
    n1=méningé (syndrome) | n2=en:mouse meninges | rel=r_associated | relid=0 | w=10
  5222. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mouse meningioma
    n1=méningé (syndrome) | n2=en:mouse meningioma | rel=r_associated | relid=0 | w=10
  5223. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mucoepidermoid tumor
    n1=méningé (syndrome) | n2=en:mucoepidermoid tumor | rel=r_associated | relid=0 | w=10
  5224. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:mucosal neuromas
    n1=méningé (syndrome) | n2=en:mucosal neuromas | rel=r_associated | relid=0 | w=10
  5225. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multiform cell layer of the cerebral cortex
    n1=méningé (syndrome) | n2=en:multiform cell layer of the cerebral cortex | rel=r_associated | relid=0 | w=10
  5226. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multinucleate cell angiohistiocytoma
    n1=méningé (syndrome) | n2=en:multinucleate cell angiohistiocytoma | rel=r_associated | relid=0 | w=10
  5227. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multiple bilateral renal angiomyolipoma
    n1=méningé (syndrome) | n2=en:multiple bilateral renal angiomyolipoma | rel=r_associated | relid=0 | w=10
  5228. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multiple giant cell granulomas (bones, joints, soft tissues)
    n1=méningé (syndrome) | n2=en:multiple giant cell granulomas (bones, joints, soft tissues) | rel=r_associated | relid=0 | w=10
  5229. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multiple intraspinal meningiomas
    n1=méningé (syndrome) | n2=en:multiple intraspinal meningiomas | rel=r_associated | relid=0 | w=10
  5230. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multiple schwannomas
    n1=méningé (syndrome) | n2=en:multiple schwannomas | rel=r_associated | relid=0 | w=10
  5231. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multiple skull base meningiomas
    n1=méningé (syndrome) | n2=en:multiple skull base meningiomas | rel=r_associated | relid=0 | w=10
  5232. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multiple tumors
    n1=méningé (syndrome) | n2=en:multiple tumors | rel=r_associated | relid=0 | w=10
  5233. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multiple tumors in 28% of patients
    n1=méningé (syndrome) | n2=en:multiple tumors in 28% of patients | rel=r_associated | relid=0 | w=10
  5234. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:multiple tumors in 74% of patients
    n1=méningé (syndrome) | n2=en:multiple tumors in 74% of patients | rel=r_associated | relid=0 | w=10
  5235. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:muscle
    n1=méningé (syndrome) | n2=en:muscle | rel=r_associated | relid=0 | w=10
  5236. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:muscle tumors (all subtypes)
    n1=méningé (syndrome) | n2=en:muscle tumors (all subtypes) | rel=r_associated | relid=0 | w=10
  5237. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:muscular branch
    n1=méningé (syndrome) | n2=en:muscular branch | rel=r_associated | relid=0 | w=10
  5238. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:muscular trochlea
    n1=méningé (syndrome) | n2=en:muscular trochlea | rel=r_associated | relid=0 | w=10
  5239. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:musculi pectinati of right atrium
    n1=méningé (syndrome) | n2=en:musculi pectinati of right atrium | rel=r_associated | relid=0 | w=10
  5240. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:myelodysplastic syndrome
    n1=méningé (syndrome) | n2=en:myelodysplastic syndrome | rel=r_associated | relid=0 | w=10
  5241. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:myeloproliferative neoplasm
    n1=méningé (syndrome) | n2=en:myeloproliferative neoplasm | rel=r_associated | relid=0 | w=10
  5242. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:myocardial rhabdomyoma
    n1=méningé (syndrome) | n2=en:myocardial rhabdomyoma | rel=r_associated | relid=0 | w=10
  5243. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:myomatous neoplasm
    n1=méningé (syndrome) | n2=en:myomatous neoplasm | rel=r_associated | relid=0 | w=10
  5244. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:myone
    n1=méningé (syndrome) | n2=en:myone | rel=r_associated | relid=0 | w=10
  5245. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:myxoid subcutaneous tumors
    n1=méningé (syndrome) | n2=en:myxoid subcutaneous tumors | rel=r_associated | relid=0 | w=10
  5246. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:myxoma
    n1=méningé (syndrome) | n2=en:myxoma | rel=r_associated | relid=0 | w=10
  5247. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:myxomatous neoplasm
    n1=méningé (syndrome) | n2=en:myxomatous neoplasm | rel=r_associated | relid=0 | w=10
  5248. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nci ctep sdc meningeal tumors sub-category terminology
    n1=méningé (syndrome) | n2=en:nci ctep sdc meningeal tumors sub-category terminology | rel=r_associated | relid=0 | w=10
  5249. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nci ctep simplified disease classification terminology
    n1=méningé (syndrome) | n2=en:nci ctep simplified disease classification terminology | rel=r_associated | relid=0 | w=10
  5250. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ncit neoplasm core terminology
    n1=méningé (syndrome) | n2=en:ncit neoplasm core terminology | rel=r_associated | relid=0 | w=10
  5251. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neck of glans
    n1=méningé (syndrome) | n2=en:neck of glans | rel=r_associated | relid=0 | w=10
  5252. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm
    n1=méningé (syndrome) | n2=en:neoplasm | rel=r_associated | relid=0 | w=10
  5253. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm by morphology
    n1=méningé (syndrome) | n2=en:neoplasm by morphology | rel=r_associated | relid=0 | w=10
  5254. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm by site
    n1=méningé (syndrome) | n2=en:neoplasm by site | rel=r_associated | relid=0 | w=10
  5255. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm by special category
    n1=méningé (syndrome) | n2=en:neoplasm by special category | rel=r_associated | relid=0 | w=10
  5256. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of cerebral meninges
    n1=méningé (syndrome) | n2=en:neoplasm of cerebral meninges | rel=r_associated | relid=0 | w=10
  5257. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of perivascular myoid type - category
    n1=méningé (syndrome) | n2=en:neoplasm of perivascular myoid type - category | rel=r_associated | relid=0 | w=10
  5258. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of uncertain behavior of brain and spinal cord
    n1=méningé (syndrome) | n2=en:neoplasm of uncertain behavior of brain and spinal cord | rel=r_associated | relid=0 | w=10
  5259. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of uncertain behavior of central nervous system
    n1=méningé (syndrome) | n2=en:neoplasm of uncertain behavior of central nervous system | rel=r_associated | relid=0 | w=10
  5260. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of uncertain behavior of endocrine glands and nervous system
    n1=méningé (syndrome) | n2=en:neoplasm of uncertain behavior of endocrine glands and nervous system | rel=r_associated | relid=0 | w=10
  5261. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of uncertain behavior of meninges
    n1=méningé (syndrome) | n2=en:neoplasm of uncertain behavior of meninges | rel=r_associated | relid=0 | w=10
  5262. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of uncertain behavior of other and unspecified sites and tissues
    n1=méningé (syndrome) | n2=en:neoplasm of uncertain behavior of other and unspecified sites and tissues | rel=r_associated | relid=0 | w=10
  5263. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of uncertain behavior of other specified sites
    n1=méningé (syndrome) | n2=en:neoplasm of uncertain behavior of other specified sites | rel=r_associated | relid=0 | w=10
  5264. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of uncertain behavior, site unspecified
    n1=méningé (syndrome) | n2=en:neoplasm of uncertain behavior, site unspecified | rel=r_associated | relid=0 | w=10
  5265. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of uncertain malignant potential
    n1=méningé (syndrome) | n2=en:neoplasm of uncertain malignant potential | rel=r_associated | relid=0 | w=10
  5266. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of unspecified nature of bone, soft tissue, and skin
    n1=méningé (syndrome) | n2=en:neoplasm of unspecified nature of bone, soft tissue, and skin | rel=r_associated | relid=0 | w=10
  5267. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of unspecified nature of endocrine glands and other parts of nervous system
    n1=méningé (syndrome) | n2=en:neoplasm of unspecified nature of endocrine glands and other parts of nervous system | rel=r_associated | relid=0 | w=10
  5268. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of unspecified nature of other genitourinary organs
    n1=méningé (syndrome) | n2=en:neoplasm of unspecified nature of other genitourinary organs | rel=r_associated | relid=0 | w=10
  5269. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of unspecified nature of other specified sites
    n1=méningé (syndrome) | n2=en:neoplasm of unspecified nature of other specified sites | rel=r_associated | relid=0 | w=10
  5270. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm of unspecified nature of respiratory system
    n1=méningé (syndrome) | n2=en:neoplasm of unspecified nature of respiratory system | rel=r_associated | relid=0 | w=10
  5271. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm related morbidities
    n1=méningé (syndrome) | n2=en:neoplasm related morbidities | rel=r_associated | relid=0 | w=10
  5272. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm, uncertain whether benign or malignant
    n1=méningé (syndrome) | n2=en:neoplasm, uncertain whether benign or malignant | rel=r_associated | relid=0 | w=10
  5273. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasm/cancer invasiveness
    n1=méningé (syndrome) | n2=en:neoplasm/cancer invasiveness | rel=r_associated | relid=0 | w=10
  5274. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms by histologic type
    n1=méningé (syndrome) | n2=en:neoplasms by histologic type | rel=r_associated | relid=0 | w=10
  5275. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms of histiocytes and accessory lymphoid cells
    n1=méningé (syndrome) | n2=en:neoplasms of histiocytes and accessory lymphoid cells | rel=r_associated | relid=0 | w=10
  5276. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms of uncertain or unknown behaviour
    n1=méningé (syndrome) | n2=en:neoplasms of uncertain or unknown behaviour | rel=r_associated | relid=0 | w=10
  5277. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms, adnexal and skin appendage
    n1=méningé (syndrome) | n2=en:neoplasms, adnexal and skin appendage | rel=r_associated | relid=0 | w=10
  5278. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms, cystic, mucinous, and serous
    n1=méningé (syndrome) | n2=en:neoplasms, cystic, mucinous, and serous | rel=r_associated | relid=0 | w=10
  5279. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms, experimental
    n1=méningé (syndrome) | n2=en:neoplasms, experimental | rel=r_associated | relid=0 | w=10
  5280. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms, hormone-dependent
    n1=méningé (syndrome) | n2=en:neoplasms, hormone-dependent | rel=r_associated | relid=0 | w=10
  5281. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms, multiple primary
    n1=méningé (syndrome) | n2=en:neoplasms, multiple primary | rel=r_associated | relid=0 | w=10
  5282. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms, nerve tissue
    n1=méningé (syndrome) | n2=en:neoplasms, nerve tissue | rel=r_associated | relid=0 | w=10
  5283. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms, post-traumatic
    n1=méningé (syndrome) | n2=en:neoplasms, post-traumatic | rel=r_associated | relid=0 | w=10
  5284. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplasms, second primary
    n1=méningé (syndrome) | n2=en:neoplasms, second primary | rel=r_associated | relid=0 | w=10
  5285. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplastic cell
    n1=méningé (syndrome) | n2=en:neoplastic cell | rel=r_associated | relid=0 | w=10
  5286. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplastic meningothelial cell
    n1=méningé (syndrome) | n2=en:neoplastic meningothelial cell | rel=r_associated | relid=0 | w=10
  5287. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neoplastic processes
    n1=méningé (syndrome) | n2=en:neoplastic processes | rel=r_associated | relid=0 | w=10
  5288. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nephrocyte
    n1=méningé (syndrome) | n2=en:nephrocyte | rel=r_associated | relid=0 | w=10
  5289. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nerve endings
    n1=méningé (syndrome) | n2=en:nerve endings | rel=r_associated | relid=0 | w=10
  5290. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nerve sheath neoplasm
    n1=méningé (syndrome) | n2=en:nerve sheath neoplasm | rel=r_associated | relid=0 | w=10
  5291. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nervous system neoplasm
    n1=méningé (syndrome) | n2=en:nervous system neoplasm | rel=r_associated | relid=0 | w=10
  5292. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nervous system neoplasms malignant and unspecified nec
    n1=méningé (syndrome) | n2=en:nervous system neoplasms malignant and unspecified nec | rel=r_associated | relid=0 | w=10
  5293. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nervous system neoplasms unspecified malignancy nec
    n1=méningé (syndrome) | n2=en:nervous system neoplasms unspecified malignancy nec | rel=r_associated | relid=0 | w=10
  5294. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nervous system of cardinal body part
    n1=méningé (syndrome) | n2=en:nervous system of cardinal body part | rel=r_associated | relid=0 | w=10
  5295. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nervous system of subdivision of cardinal body part
    n1=méningé (syndrome) | n2=en:nervous system of subdivision of cardinal body part | rel=r_associated | relid=0 | w=10
  5296. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neural tissue tumors
    n1=méningé (syndrome) | n2=en:neural tissue tumors | rel=r_associated | relid=0 | w=10
  5297. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neuroblastic tumor
    n1=méningé (syndrome) | n2=en:neuroblastic tumor | rel=r_associated | relid=0 | w=10
  5298. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neuroblastoma
    n1=méningé (syndrome) | n2=en:neuroblastoma | rel=r_associated | relid=0 | w=10
  5299. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neuroblastoma (less common)
    n1=méningé (syndrome) | n2=en:neuroblastoma (less common) | rel=r_associated | relid=0 | w=10
  5300. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neuroblastoma, arises anywhere along the sympathetic chain (including intracranially)
    n1=méningé (syndrome) | n2=en:neuroblastoma, arises anywhere along the sympathetic chain (including intracranially) | rel=r_associated | relid=0 | w=10
  5301. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neuroectodermal tumors
    n1=méningé (syndrome) | n2=en:neuroectodermal tumors | rel=r_associated | relid=0 | w=10
  5302. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neuroendocrine neoplasm
    n1=méningé (syndrome) | n2=en:neuroendocrine neoplasm | rel=r_associated | relid=0 | w=10
  5303. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neuroepitheliomatous neoplasm
    n1=méningé (syndrome) | n2=en:neuroepitheliomatous neoplasm | rel=r_associated | relid=0 | w=10
  5304. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neurofibroma
    n1=méningé (syndrome) | n2=en:neurofibroma | rel=r_associated | relid=0 | w=10
  5305. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neurofibromatosis type 2
    n1=méningé (syndrome) | n2=en:neurofibromatosis type 2 | rel=r_associated | relid=0 | w=10
  5306. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neuronal and mixed neuronal-glial tumors
    n1=méningé (syndrome) | n2=en:neuronal and mixed neuronal-glial tumors | rel=r_associated | relid=0 | w=10
  5307. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:neuronal or mixed neuronal-glial neoplasm
    n1=méningé (syndrome) | n2=en:neuronal or mixed neuronal-glial neoplasm | rel=r_associated | relid=0 | w=10
  5308. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nevi and melanomas
    n1=méningé (syndrome) | n2=en:nevi and melanomas | rel=r_associated | relid=0 | w=10
  5309. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nevoid basal cell carcinoma syndrome associated medulloblastoma
    n1=méningé (syndrome) | n2=en:nevoid basal cell carcinoma syndrome associated medulloblastoma | rel=r_associated | relid=0 | w=10
  5310. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nevus and/or melanoma
    n1=méningé (syndrome) | n2=en:nevus and/or melanoma | rel=r_associated | relid=0 | w=10
  5311. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nf2 gene inactivation
    n1=méningé (syndrome) | n2=en:nf2 gene inactivation | rel=r_associated | relid=0 | w=10
  5312. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:no cancer despite harboring complete deletions of the tp53 gene
    n1=méningé (syndrome) | n2=en:no cancer despite harboring complete deletions of the tp53 gene | rel=r_associated | relid=0 | w=10
  5313. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:no progression to cancer
    n1=méningé (syndrome) | n2=en:no progression to cancer | rel=r_associated | relid=0 | w=10
  5314. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:non-hodgkin lymphoma
    n1=méningé (syndrome) | n2=en:non-hodgkin lymphoma | rel=r_associated | relid=0 | w=10
  5315. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:non-polyposis turcot syndrome
    n1=méningé (syndrome) | n2=en:non-polyposis turcot syndrome | rel=r_associated | relid=0 | w=10
  5316. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nonmelanoma skin cancer (in some patients)
    n1=méningé (syndrome) | n2=en:nonmelanoma skin cancer (in some patients) | rel=r_associated | relid=0 | w=10
  5317. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nonneoplastic disorders/lesions (all subtypes)
    n1=méningé (syndrome) | n2=en:nonneoplastic disorders/lesions (all subtypes) | rel=r_associated | relid=0 | w=10
  5318. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nonseminoma (embryonal carcinoma, teratoma, choriocarcinoma, endodermal sinus tumor)
    n1=méningé (syndrome) | n2=en:nonseminoma (embryonal carcinoma, teratoma, choriocarcinoma, endodermal sinus tumor) | rel=r_associated | relid=0 | w=10
  5319. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nursing therapy
    n1=méningé (syndrome) | n2=en:nursing therapy | rel=r_associated | relid=0 | w=10
  5320. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:nutritional management
    n1=méningé (syndrome) | n2=en:nutritional management | rel=r_associated | relid=0 | w=10
  5321. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:obturator membrane
    n1=méningé (syndrome) | n2=en:obturator membrane | rel=r_associated | relid=0 | w=10
  5322. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ocular haemangiopericytoma
    n1=méningé (syndrome) | n2=en:ocular haemangiopericytoma | rel=r_associated | relid=0 | w=10
  5323. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ocular muscle
    n1=méningé (syndrome) | n2=en:ocular muscle | rel=r_associated | relid=0 | w=10
  5324. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:odontogenic neoplasm
    n1=méningé (syndrome) | n2=en:odontogenic neoplasm | rel=r_associated | relid=0 | w=10
  5325. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:olfactory organ
    n1=méningé (syndrome) | n2=en:olfactory organ | rel=r_associated | relid=0 | w=10
  5326. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:olfactory system
    n1=méningé (syndrome) | n2=en:olfactory system | rel=r_associated | relid=0 | w=10
  5327. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:oligodendroglial tumor
    n1=méningé (syndrome) | n2=en:oligodendroglial tumor | rel=r_associated | relid=0 | w=10
  5328. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:oligodendroglioma
    n1=méningé (syndrome) | n2=en:oligodendroglioma | rel=r_associated | relid=0 | w=10
  5329. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:oncocytic adenoma
    n1=méningé (syndrome) | n2=en:oncocytic adenoma | rel=r_associated | relid=0 | w=10
  5330. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:oncogene sis
    n1=méningé (syndrome) | n2=en:oncogene sis | rel=r_associated | relid=0 | w=10
  5331. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:optic glioma (19%)
    n1=méningé (syndrome) | n2=en:optic glioma (19%) | rel=r_associated | relid=0 | w=10
  5332. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:optic nerve glioma
    n1=méningé (syndrome) | n2=en:optic nerve glioma | rel=r_associated | relid=0 | w=10
  5333. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:optic nerve meningioma
    n1=méningé (syndrome) | n2=en:optic nerve meningioma | rel=r_associated | relid=0 | w=10
  5334. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:optic nerve neoplasm
    n1=méningé (syndrome) | n2=en:optic nerve neoplasm | rel=r_associated | relid=0 | w=10
  5335. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:oral haemangioma
    n1=méningé (syndrome) | n2=en:oral haemangioma | rel=r_associated | relid=0 | w=10
  5336. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:orbit
    n1=méningé (syndrome) | n2=en:orbit | rel=r_associated | relid=0 | w=10
  5337. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:organ of special sense
    n1=méningé (syndrome) | n2=en:organ of special sense | rel=r_associated | relid=0 | w=10
  5338. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:oropharyngeal carcinoma
    n1=méningé (syndrome) | n2=en:oropharyngeal carcinoma | rel=r_associated | relid=0 | w=10
  5339. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:oropharyngeal squamous cell carcinoma
    n1=méningé (syndrome) | n2=en:oropharyngeal squamous cell carcinoma | rel=r_associated | relid=0 | w=10
  5340. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:os centrale
    n1=méningé (syndrome) | n2=en:os centrale | rel=r_associated | relid=0 | w=10
  5341. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:osseous and chondromatous neoplasms
    n1=méningé (syndrome) | n2=en:osseous and chondromatous neoplasms | rel=r_associated | relid=0 | w=10
  5342. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:osseous and/or chondromatous neoplasm
    n1=méningé (syndrome) | n2=en:osseous and/or chondromatous neoplasm | rel=r_associated | relid=0 | w=10
  5343. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:osteogenic/miscellaneous bone tumors (all subtypes)
    n1=méningé (syndrome) | n2=en:osteogenic/miscellaneous bone tumors (all subtypes) | rel=r_associated | relid=0 | w=10
  5344. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:osteosarcoma
    n1=méningé (syndrome) | n2=en:osteosarcoma | rel=r_associated | relid=0 | w=10
  5345. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:osteosarcoma and meningioma especially
    n1=méningé (syndrome) | n2=en:osteosarcoma and meningioma especially | rel=r_associated | relid=0 | w=10
  5346. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:other hematologic disorders
    n1=méningé (syndrome) | n2=en:other hematologic disorders | rel=r_associated | relid=0 | w=10
  5347. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ovarian carcinoma
    n1=méningé (syndrome) | n2=en:ovarian carcinoma | rel=r_associated | relid=0 | w=10
  5348. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ovarian cystadenoma
    n1=méningé (syndrome) | n2=en:ovarian cystadenoma | rel=r_associated | relid=0 | w=10
  5349. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ovarian sex cord-stromal tumor
    n1=méningé (syndrome) | n2=en:ovarian sex cord-stromal tumor | rel=r_associated | relid=0 | w=10
  5350. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:oxyphil cell
    n1=méningé (syndrome) | n2=en:oxyphil cell | rel=r_associated | relid=0 | w=10
  5351. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pancreatic adenocarcinoma
    n1=méningé (syndrome) | n2=en:pancreatic adenocarcinoma | rel=r_associated | relid=0 | w=10
  5352. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pancreatic carcinoma
    n1=méningé (syndrome) | n2=en:pancreatic carcinoma | rel=r_associated | relid=0 | w=10
  5353. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pancreatic squamous cell carcinoma
    n1=méningé (syndrome) | n2=en:pancreatic squamous cell carcinoma | rel=r_associated | relid=0 | w=10
  5354. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:papilla of the tongue
    n1=méningé (syndrome) | n2=en:papilla of the tongue | rel=r_associated | relid=0 | w=10
  5355. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:papillary endothelial hyperplasia
    n1=méningé (syndrome) | n2=en:papillary endothelial hyperplasia | rel=r_associated | relid=0 | w=10
  5356. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:papillary neoplasm
    n1=méningé (syndrome) | n2=en:papillary neoplasm | rel=r_associated | relid=0 | w=10
  5357. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:papillary renal cell carcinoma
    n1=méningé (syndrome) | n2=en:papillary renal cell carcinoma | rel=r_associated | relid=0 | w=10
  5358. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:papillary thyroid carcinoma (rare)
    n1=méningé (syndrome) | n2=en:papillary thyroid carcinoma (rare) | rel=r_associated | relid=0 | w=10
  5359. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:paraganglioma
    n1=méningé (syndrome) | n2=en:paraganglioma | rel=r_associated | relid=0 | w=10
  5360. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:paraganglioma and/or glomus tumor
    n1=méningé (syndrome) | n2=en:paraganglioma and/or glomus tumor | rel=r_associated | relid=0 | w=10
  5361. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:paraganglioma, catecholamine-secreting
    n1=méningé (syndrome) | n2=en:paraganglioma, catecholamine-secreting | rel=r_associated | relid=0 | w=10
  5362. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:paragangliomas, head and neck (31%)
    n1=méningé (syndrome) | n2=en:paragangliomas, head and neck (31%) | rel=r_associated | relid=0 | w=10
  5363. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:paragangliomas, head and neck (79%)
    n1=méningé (syndrome) | n2=en:paragangliomas, head and neck (79%) | rel=r_associated | relid=0 | w=10
  5364. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:paranasal sinus
    n1=méningé (syndrome) | n2=en:paranasal sinus | rel=r_associated | relid=0 | w=10
  5365. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:paraneoplastic sps is associated with autoantibodies to amphiphysin (amph, 600418)
    n1=méningé (syndrome) | n2=en:paraneoplastic sps is associated with autoantibodies to amphiphysin (amph, 600418) | rel=r_associated | relid=0 | w=10
  5366. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:paraneoplastic sps is associated with breast cancer and other malignancies
    n1=méningé (syndrome) | n2=en:paraneoplastic sps is associated with breast cancer and other malignancies | rel=r_associated | relid=0 | w=10
  5367. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:parathyroid disease rare
    n1=méningé (syndrome) | n2=en:parathyroid disease rare | rel=r_associated | relid=0 | w=10
  5368. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:parathyroid gland adenoma
    n1=méningé (syndrome) | n2=en:parathyroid gland adenoma | rel=r_associated | relid=0 | w=10
  5369. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:parathyroid gland carcinoma
    n1=méningé (syndrome) | n2=en:parathyroid gland carcinoma | rel=r_associated | relid=0 | w=10
  5370. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:paratracheal region
    n1=méningé (syndrome) | n2=en:paratracheal region | rel=r_associated | relid=0 | w=10
  5371. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:parenchyma of left lung
    n1=méningé (syndrome) | n2=en:parenchyma of left lung | rel=r_associated | relid=0 | w=10
  5372. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:parenchyma of right lung
    n1=méningé (syndrome) | n2=en:parenchyma of right lung | rel=r_associated | relid=0 | w=10
  5373. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:parenchymal cell
    n1=méningé (syndrome) | n2=en:parenchymal cell | rel=r_associated | relid=0 | w=10
  5374. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:parotid gland adenoma and adenocarcinoma
    n1=méningé (syndrome) | n2=en:parotid gland adenoma and adenocarcinoma | rel=r_associated | relid=0 | w=10
  5375. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:parotid gland monomorphic adenoma
    n1=méningé (syndrome) | n2=en:parotid gland monomorphic adenoma | rel=r_associated | relid=0 | w=10
  5376. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:parotid oncocytomas
    n1=méningé (syndrome) | n2=en:parotid oncocytomas | rel=r_associated | relid=0 | w=10
  5377. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pdgfb gene
    n1=méningé (syndrome) | n2=en:pdgfb gene | rel=r_associated | relid=0 | w=10
  5378. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pdgfb wt allele
    n1=méningé (syndrome) | n2=en:pdgfb wt allele | rel=r_associated | relid=0 | w=10
  5379. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pdgfb, 135-bp del, ivs5
    n1=méningé (syndrome) | n2=en:pdgfb, 135-bp del, ivs5 | rel=r_associated | relid=0 | w=10
  5380. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pectinate muscle of left atrium
    n1=méningé (syndrome) | n2=en:pectinate muscle of left atrium | rel=r_associated | relid=0 | w=10
  5381. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pediatric adverse events terminology
    n1=méningé (syndrome) | n2=en:pediatric adverse events terminology | rel=r_associated | relid=0 | w=10
  5382. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pelvic diaphragm
    n1=méningé (syndrome) | n2=en:pelvic diaphragm | rel=r_associated | relid=0 | w=10
  5383. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pelvic lateral wall triangle
    n1=méningé (syndrome) | n2=en:pelvic lateral wall triangle | rel=r_associated | relid=0 | w=10
  5384. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:penicillus of spleen
    n1=méningé (syndrome) | n2=en:penicillus of spleen | rel=r_associated | relid=0 | w=10
  5385. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:periampullary carcinoma nos
    n1=méningé (syndrome) | n2=en:periampullary carcinoma nos | rel=r_associated | relid=0 | w=10
  5386. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pericyte
    n1=méningé (syndrome) | n2=en:pericyte | rel=r_associated | relid=0 | w=10
  5387. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:peridural membrane
    n1=méningé (syndrome) | n2=en:peridural membrane | rel=r_associated | relid=0 | w=10
  5388. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:perineal membrane
    n1=méningé (syndrome) | n2=en:perineal membrane | rel=r_associated | relid=0 | w=10
  5389. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:periocular meningioma
    n1=méningé (syndrome) | n2=en:periocular meningioma | rel=r_associated | relid=0 | w=10
  5390. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:periorbital body
    n1=méningé (syndrome) | n2=en:periorbital body | rel=r_associated | relid=0 | w=10
  5391. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:periosteal cell
    n1=méningé (syndrome) | n2=en:periosteal cell | rel=r_associated | relid=0 | w=10
  5392. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:peripheral blood cell
    n1=méningé (syndrome) | n2=en:peripheral blood cell | rel=r_associated | relid=0 | w=10
  5393. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:peripheral nervous system neoplasm
    n1=méningé (syndrome) | n2=en:peripheral nervous system neoplasm | rel=r_associated | relid=0 | w=10
  5394. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:permanent tooth
    n1=méningé (syndrome) | n2=en:permanent tooth | rel=r_associated | relid=0 | w=10
  5395. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:petroclival meningioma
    n1=méningé (syndrome) | n2=en:petroclival meningioma | rel=r_associated | relid=0 | w=10
  5396. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:petrous apex meningioma
    n1=méningé (syndrome) | n2=en:petrous apex meningioma | rel=r_associated | relid=0 | w=10
  5397. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:peyer patch
    n1=méningé (syndrome) | n2=en:peyer patch | rel=r_associated | relid=0 | w=10
  5398. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:phaces syndrome
    n1=méningé (syndrome) | n2=en:phaces syndrome | rel=r_associated | relid=0 | w=10
  5399. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:phagocytic cell
    n1=méningé (syndrome) | n2=en:phagocytic cell | rel=r_associated | relid=0 | w=10
  5400. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pharmacotherapeutic
    n1=méningé (syndrome) | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=10
  5401. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pheochromocytoma, adrenal (53%)
    n1=méningé (syndrome) | n2=en:pheochromocytoma, adrenal (53%) | rel=r_associated | relid=0 | w=10
  5402. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pheochromocytoma, extraadrenal (21%)
    n1=méningé (syndrome) | n2=en:pheochromocytoma, extraadrenal (21%) | rel=r_associated | relid=0 | w=10
  5403. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pheochromocytomas, adrenal (28%)
    n1=méningé (syndrome) | n2=en:pheochromocytomas, adrenal (28%) | rel=r_associated | relid=0 | w=10
  5404. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pheochromocytomas, extraadrenal (48%)
    n1=méningé (syndrome) | n2=en:pheochromocytomas, extraadrenal (48%) | rel=r_associated | relid=0 | w=10
  5405. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:photoreceptor cell
    n1=méningé (syndrome) | n2=en:photoreceptor cell | rel=r_associated | relid=0 | w=10
  5406. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:phyllodes tumor
    n1=méningé (syndrome) | n2=en:phyllodes tumor | rel=r_associated | relid=0 | w=10
  5407. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:physiological aspects
    n1=méningé (syndrome) | n2=en:physiological aspects | rel=r_associated | relid=0 | w=10
  5408. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:physiological cup
    n1=méningé (syndrome) | n2=en:physiological cup | rel=r_associated | relid=0 | w=10
  5409. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pia mater
    n1=méningé (syndrome) | n2=en:pia mater | rel=r_associated | relid=0 | w=10
  5410. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pigmentation
    n1=méningé (syndrome) | n2=en:pigmentation | rel=r_associated | relid=0 | w=10
  5411. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pilocytic astrocytoma
    n1=méningé (syndrome) | n2=en:pilocytic astrocytoma | rel=r_associated | relid=0 | w=10
  5412. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pineal region meningioma
    n1=méningé (syndrome) | n2=en:pineal region meningioma | rel=r_associated | relid=0 | w=10
  5413. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pinealoma (trilateral retinoblastoma)
    n1=méningé (syndrome) | n2=en:pinealoma (trilateral retinoblastoma) | rel=r_associated | relid=0 | w=10
  5414. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pituitary cell
    n1=méningé (syndrome) | n2=en:pituitary cell | rel=r_associated | relid=0 | w=10
  5415. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pituitary gland neoplasm
    n1=méningé (syndrome) | n2=en:pituitary gland neoplasm | rel=r_associated | relid=0 | w=10
  5416. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pituitary stalk meningioma
    n1=méningé (syndrome) | n2=en:pituitary stalk meningioma | rel=r_associated | relid=0 | w=10
  5417. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:plant morphology
    n1=méningé (syndrome) | n2=en:plant morphology | rel=r_associated | relid=0 | w=10
  5418. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:plasma cell myeloma
    n1=méningé (syndrome) | n2=en:plasma cell myeloma | rel=r_associated | relid=0 | w=10
  5419. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:plasma cell neoplasm
    n1=méningé (syndrome) | n2=en:plasma cell neoplasm | rel=r_associated | relid=0 | w=10
  5420. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:plasma cell neoplasms (all subtypes)
    n1=méningé (syndrome) | n2=en:plasma cell neoplasms (all subtypes) | rel=r_associated | relid=0 | w=10
  5421. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:plasmacytoma
    n1=méningé (syndrome) | n2=en:plasmacytoma | rel=r_associated | relid=0 | w=10
  5422. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:platypelloid pelvis
    n1=méningé (syndrome) | n2=en:platypelloid pelvis | rel=r_associated | relid=0 | w=10
  5423. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pleocytosis
    n1=méningé (syndrome) | n2=en:pleocytosis | rel=r_associated | relid=0 | w=10
  5424. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:plexus
    n1=méningé (syndrome) | n2=en:plexus | rel=r_associated | relid=0 | w=10
  5425. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:possible increased risk of germ-cell tumors
    n1=méningé (syndrome) | n2=en:possible increased risk of germ-cell tumors | rel=r_associated | relid=0 | w=10
  5426. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:possibly increased risk for other cancers
    n1=méningé (syndrome) | n2=en:possibly increased risk for other cancers | rel=r_associated | relid=0 | w=10
  5427. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:possibly increased risk of cancer
    n1=méningé (syndrome) | n2=en:possibly increased risk of cancer | rel=r_associated | relid=0 | w=10
  5428. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:posterior cranial fossa meningioma
    n1=méningé (syndrome) | n2=en:posterior cranial fossa meningioma | rel=r_associated | relid=0 | w=10
  5429. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:posterior foramen magnum meningioma
    n1=méningé (syndrome) | n2=en:posterior foramen magnum meningioma | rel=r_associated | relid=0 | w=10
  5430. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:posterior fossa meningiomas
    n1=méningé (syndrome) | n2=en:posterior fossa meningiomas | rel=r_associated | relid=0 | w=10
  5431. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:posterior root
    n1=méningé (syndrome) | n2=en:posterior root | rel=r_associated | relid=0 | w=10
  5432. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:precancerous condition
    n1=méningé (syndrome) | n2=en:precancerous condition | rel=r_associated | relid=0 | w=10
  5433. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:precursor lymphoblastic leukemia/lymphoma (all subtypes)
    n1=méningé (syndrome) | n2=en:precursor lymphoblastic leukemia/lymphoma (all subtypes) | rel=r_associated | relid=0 | w=10
  5434. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:predisposition to uv-induced malignancies
    n1=méningé (syndrome) | n2=en:predisposition to uv-induced malignancies | rel=r_associated | relid=0 | w=10
  5435. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pregnancy complications, neoplastic
    n1=méningé (syndrome) | n2=en:pregnancy complications, neoplastic | rel=r_associated | relid=0 | w=10
  5436. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:primary adrenocortical nodular hyperplasia
    n1=méningé (syndrome) | n2=en:primary adrenocortical nodular hyperplasia | rel=r_associated | relid=0 | w=10
  5437. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:primary angiosarcoma
    n1=méningé (syndrome) | n2=en:primary angiosarcoma | rel=r_associated | relid=0 | w=10
  5438. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:primary central nervous system neoplasm
    n1=méningé (syndrome) | n2=en:primary central nervous system neoplasm | rel=r_associated | relid=0 | w=10
  5439. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:primary malignant liver neoplasm
    n1=méningé (syndrome) | n2=en:primary malignant liver neoplasm | rel=r_associated | relid=0 | w=10
  5440. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:primary malignant neoplasm of central nervous system
    n1=méningé (syndrome) | n2=en:primary malignant neoplasm of central nervous system | rel=r_associated | relid=0 | w=10
  5441. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:primary meningeal sarcomatosis
    n1=méningé (syndrome) | n2=en:primary meningeal sarcomatosis | rel=r_associated | relid=0 | w=10
  5442. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:projection fibre
    n1=méningé (syndrome) | n2=en:projection fibre | rel=r_associated | relid=0 | w=10
  5443. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:prolactin-producing pituitary gland adenoma
    n1=méningé (syndrome) | n2=en:prolactin-producing pituitary gland adenoma | rel=r_associated | relid=0 | w=10
  5444. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:propensity to tumor development
    n1=méningé (syndrome) | n2=en:propensity to tumor development | rel=r_associated | relid=0 | w=10
  5445. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:prostate carcinoma
    n1=méningé (syndrome) | n2=en:prostate carcinoma | rel=r_associated | relid=0 | w=10
  5446. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:protozoal cyst
    n1=méningé (syndrome) | n2=en:protozoal cyst | rel=r_associated | relid=0 | w=10
  5447. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:proximal interphalangeal joint
    n1=méningé (syndrome) | n2=en:proximal interphalangeal joint | rel=r_associated | relid=0 | w=10
  5448. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:psammomatous melanotic schwannomas
    n1=méningé (syndrome) | n2=en:psammomatous melanotic schwannomas | rel=r_associated | relid=0 | w=10
  5449. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:psychology qualifier
    n1=méningé (syndrome) | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=10
  5450. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pten gene
    n1=méningé (syndrome) | n2=en:pten gene | rel=r_associated | relid=0 | w=10
  5451. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pten wt allele
    n1=méningé (syndrome) | n2=en:pten wt allele | rel=r_associated | relid=0 | w=10
  5452. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pten, arg234gln
    n1=méningé (syndrome) | n2=en:pten, arg234gln | rel=r_associated | relid=0 | w=10
  5453. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:purkinje fiber
    n1=méningé (syndrome) | n2=en:purkinje fiber | rel=r_associated | relid=0 | w=10
  5454. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:pyramid of ferrein
    n1=méningé (syndrome) | n2=en:pyramid of ferrein | rel=r_associated | relid=0 | w=10
  5455. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:radiation induced meningioma
    n1=méningé (syndrome) | n2=en:radiation induced meningioma | rel=r_associated | relid=0 | w=10
  5456. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:radiation-induced intracranial meningioma
    n1=méningé (syndrome) | n2=en:radiation-induced intracranial meningioma | rel=r_associated | relid=0 | w=10
  5457. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:radiation-related neoplasm
    n1=méningé (syndrome) | n2=en:radiation-related neoplasm | rel=r_associated | relid=0 | w=10
  5458. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:radiotherapeutic
    n1=méningé (syndrome) | n2=en:radiotherapeutic | rel=r_associated | relid=0 | w=10
  5459. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:rarely malignant
    n1=méningé (syndrome) | n2=en:rarely malignant | rel=r_associated | relid=0 | w=10
  5460. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:recurrent angiosarcoma
    n1=méningé (syndrome) | n2=en:recurrent angiosarcoma | rel=r_associated | relid=0 | w=10
  5461. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:recurrent central nervous system neoplasm
    n1=méningé (syndrome) | n2=en:recurrent central nervous system neoplasm | rel=r_associated | relid=0 | w=10
  5462. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:recurrent malignant hemangiopericytoma
    n1=méningé (syndrome) | n2=en:recurrent malignant hemangiopericytoma | rel=r_associated | relid=0 | w=10
  5463. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:recurrent medulloblastoma
    n1=méningé (syndrome) | n2=en:recurrent medulloblastoma | rel=r_associated | relid=0 | w=10
  5464. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:refractory central nervous system neoplasm
    n1=méningé (syndrome) | n2=en:refractory central nervous system neoplasm | rel=r_associated | relid=0 | w=10
  5465. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:region 17p13 allelic loss associated medulloblastoma
    n1=méningé (syndrome) | n2=en:region 17p13 allelic loss associated medulloblastoma | rel=r_associated | relid=0 | w=10
  5466. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:rehabilitation aspects
    n1=méningé (syndrome) | n2=en:rehabilitation aspects | rel=r_associated | relid=0 | w=10
  5467. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal and urinary tract neoplasms benign
    n1=méningé (syndrome) | n2=en:renal and urinary tract neoplasms benign | rel=r_associated | relid=0 | w=10
  5468. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal and urinary tract neoplasms malignant and unspecified
    n1=méningé (syndrome) | n2=en:renal and urinary tract neoplasms malignant and unspecified | rel=r_associated | relid=0 | w=10
  5469. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal cell carcinoma
    n1=méningé (syndrome) | n2=en:renal cell carcinoma | rel=r_associated | relid=0 | w=10
  5470. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal cell carcinoma (less common)
    n1=méningé (syndrome) | n2=en:renal cell carcinoma (less common) | rel=r_associated | relid=0 | w=10
  5471. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal cell carcinoma, solitary papillary type 2 (about 20% of patients)
    n1=méningé (syndrome) | n2=en:renal cell carcinoma, solitary papillary type 2 (about 20% of patients) | rel=r_associated | relid=0 | w=10
  5472. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal cell carcinoma, usually clear cell type
    n1=méningé (syndrome) | n2=en:renal cell carcinoma, usually clear cell type | rel=r_associated | relid=0 | w=10
  5473. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal cortical adenoma
    n1=méningé (syndrome) | n2=en:renal cortical adenoma | rel=r_associated | relid=0 | w=10
  5474. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal haemangioma
    n1=méningé (syndrome) | n2=en:renal haemangioma | rel=r_associated | relid=0 | w=10
  5475. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal interstitial cell
    n1=méningé (syndrome) | n2=en:renal interstitial cell | rel=r_associated | relid=0 | w=10
  5476. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:renal pyramid
    n1=méningé (syndrome) | n2=en:renal pyramid | rel=r_associated | relid=0 | w=10
  5477. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:reported colon and other abdominal cancer in relatives
    n1=méningé (syndrome) | n2=en:reported colon and other abdominal cancer in relatives | rel=r_associated | relid=0 | w=10
  5478. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:reproductive and genitourinary neoplasms gender unspecified nec
    n1=méningé (syndrome) | n2=en:reproductive and genitourinary neoplasms gender unspecified nec | rel=r_associated | relid=0 | w=10
  5479. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:reproductive neoplasms female malignant and unspecified
    n1=méningé (syndrome) | n2=en:reproductive neoplasms female malignant and unspecified | rel=r_associated | relid=0 | w=10
  5480. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:reproductive neoplasms male malignant and unspecified
    n1=méningé (syndrome) | n2=en:reproductive neoplasms male malignant and unspecified | rel=r_associated | relid=0 | w=10
  5481. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:respiratory and mediastinal neoplasms benign (excl mesotheliomas)
    n1=méningé (syndrome) | n2=en:respiratory and mediastinal neoplasms benign (excl mesotheliomas) | rel=r_associated | relid=0 | w=10
  5482. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:respiratory and mediastinal neoplasms malignant and unspecified
    n1=méningé (syndrome) | n2=en:respiratory and mediastinal neoplasms malignant and unspecified | rel=r_associated | relid=0 | w=10
  5483. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:rete mirabile
    n1=méningé (syndrome) | n2=en:rete mirabile | rel=r_associated | relid=0 | w=10
  5484. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:reticuloendothelial cell
    n1=méningé (syndrome) | n2=en:reticuloendothelial cell | rel=r_associated | relid=0 | w=10
  5485. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:retinal hemangioma
    n1=méningé (syndrome) | n2=en:retinal hemangioma | rel=r_associated | relid=0 | w=10
  5486. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:retinoblastoma
    n1=méningé (syndrome) | n2=en:retinoblastoma | rel=r_associated | relid=0 | w=10
  5487. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:rhabdoid tumor
    n1=méningé (syndrome) | n2=en:rhabdoid tumor | rel=r_associated | relid=0 | w=10
  5488. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:rhabdoid tumors, malignant (renal or extrarenal)
    n1=méningé (syndrome) | n2=en:rhabdoid tumors, malignant (renal or extrarenal) | rel=r_associated | relid=0 | w=10
  5489. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:rhabdomyosarcoma
    n1=méningé (syndrome) | n2=en:rhabdomyosarcoma | rel=r_associated | relid=0 | w=10
  5490. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:right border of heart viewed radiologically
    n1=méningé (syndrome) | n2=en:right border of heart viewed radiologically | rel=r_associated | relid=0 | w=10
  5491. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:right side of jaw
    n1=méningé (syndrome) | n2=en:right side of jaw | rel=r_associated | relid=0 | w=10
  5492. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:root of brachial plexus
    n1=méningé (syndrome) | n2=en:root of brachial plexus | rel=r_associated | relid=0 | w=10
  5493. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:root of cervical plexus
    n1=méningé (syndrome) | n2=en:root of cervical plexus | rel=r_associated | relid=0 | w=10
  5494. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:root of lumbar plexus
    n1=méningé (syndrome) | n2=en:root of lumbar plexus | rel=r_associated | relid=0 | w=10
  5495. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:root of sacral plexus
    n1=méningé (syndrome) | n2=en:root of sacral plexus | rel=r_associated | relid=0 | w=10
  5496. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sacral intraspinal meningioma
    n1=méningé (syndrome) | n2=en:sacral intraspinal meningioma | rel=r_associated | relid=0 | w=10
  5497. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sacrococcygeal teratoma
    n1=méningé (syndrome) | n2=en:sacrococcygeal teratoma | rel=r_associated | relid=0 | w=10
  5498. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sarcoma
    n1=méningé (syndrome) | n2=en:sarcoma | rel=r_associated | relid=0 | w=10
  5499. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:satellite cell
    n1=méningé (syndrome) | n2=en:satellite cell | rel=r_associated | relid=0 | w=10
  5500. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:scapulothoracic joint
    n1=méningé (syndrome) | n2=en:scapulothoracic joint | rel=r_associated | relid=0 | w=10
  5501. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:schwannoma
    n1=méningé (syndrome) | n2=en:schwannoma | rel=r_associated | relid=0 | w=10
  5502. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:schwannomatosis 1
    n1=méningé (syndrome) | n2=en:schwannomatosis 1 | rel=r_associated | relid=0 | w=10
  5503. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sebaceous adenoma
    n1=méningé (syndrome) | n2=en:sebaceous adenoma | rel=r_associated | relid=0 | w=10
  5504. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sebaceous carcinoma
    n1=méningé (syndrome) | n2=en:sebaceous carcinoma | rel=r_associated | relid=0 | w=10
  5505. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sebaceous epithelioma
    n1=méningé (syndrome) | n2=en:sebaceous epithelioma | rel=r_associated | relid=0 | w=10
  5506. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:secondary central nervous system lymphoma
    n1=méningé (syndrome) | n2=en:secondary central nervous system lymphoma | rel=r_associated | relid=0 | w=10
  5507. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:secondary tympanic membrane
    n1=méningé (syndrome) | n2=en:secondary tympanic membrane | rel=r_associated | relid=0 | w=10
  5508. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:secretory cell
    n1=méningé (syndrome) | n2=en:secretory cell | rel=r_associated | relid=0 | w=10
  5509. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:seminiferous tubule
    n1=méningé (syndrome) | n2=en:seminiferous tubule | rel=r_associated | relid=0 | w=10
  5510. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:seminoma
    n1=méningé (syndrome) | n2=en:seminoma | rel=r_associated | relid=0 | w=10
  5511. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sense organs
    n1=méningé (syndrome) | n2=en:sense organs | rel=r_associated | relid=0 | w=10
  5512. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sensitivity to genotoxic agents
    n1=méningé (syndrome) | n2=en:sensitivity to genotoxic agents | rel=r_associated | relid=0 | w=10
  5513. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sensory root
    n1=méningé (syndrome) | n2=en:sensory root | rel=r_associated | relid=0 | w=10
  5514. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:septum - general anatomical term
    n1=méningé (syndrome) | n2=en:septum - general anatomical term | rel=r_associated | relid=0 | w=10
  5515. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:septum of glans
    n1=méningé (syndrome) | n2=en:septum of glans | rel=r_associated | relid=0 | w=10
  5516. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:serrated suture structure
    n1=méningé (syndrome) | n2=en:serrated suture structure | rel=r_associated | relid=0 | w=10
  5517. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sertoli cell tumor
    n1=méningé (syndrome) | n2=en:sertoli cell tumor | rel=r_associated | relid=0 | w=10
  5518. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sertoli-leydig cell ovarian tumors may occur
    n1=méningé (syndrome) | n2=en:sertoli-leydig cell ovarian tumors may occur | rel=r_associated | relid=0 | w=10
  5519. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of accessory thymic lobules
    n1=méningé (syndrome) | n2=en:set of accessory thymic lobules | rel=r_associated | relid=0 | w=10
  5520. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of accessory visual structures
    n1=méningé (syndrome) | n2=en:set of accessory visual structures | rel=r_associated | relid=0 | w=10
  5521. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of acoustic teeth
    n1=méningé (syndrome) | n2=en:set of acoustic teeth | rel=r_associated | relid=0 | w=10
  5522. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of aggregated lymphoid nodules
    n1=méningé (syndrome) | n2=en:set of aggregated lymphoid nodules | rel=r_associated | relid=0 | w=10
  5523. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of ampullary bony limbs
    n1=méningé (syndrome) | n2=en:set of ampullary bony limbs | rel=r_associated | relid=0 | w=10
  5524. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of anatomical canals
    n1=méningé (syndrome) | n2=en:set of anatomical canals | rel=r_associated | relid=0 | w=10
  5525. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of anatomical features
    n1=méningé (syndrome) | n2=en:set of anatomical features | rel=r_associated | relid=0 | w=10
  5526. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of anatomical folds
    n1=méningé (syndrome) | n2=en:set of anatomical folds | rel=r_associated | relid=0 | w=10
  5527. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of anterior rami of sacral nerves and coccygeal nerve
    n1=méningé (syndrome) | n2=en:set of anterior rami of sacral nerves and coccygeal nerve | rel=r_associated | relid=0 | w=10
  5528. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of apud cells
    n1=méningé (syndrome) | n2=en:set of apud cells | rel=r_associated | relid=0 | w=10
  5529. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of arachnoid trabeculae
    n1=méningé (syndrome) | n2=en:set of arachnoid trabeculae | rel=r_associated | relid=0 | w=10
  5530. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of choroid blood vessels
    n1=méningé (syndrome) | n2=en:set of choroid blood vessels | rel=r_associated | relid=0 | w=10
  5531. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of commissural cusps of mitral valve
    n1=méningé (syndrome) | n2=en:set of commissural cusps of mitral valve | rel=r_associated | relid=0 | w=10
  5532. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of commissures of semilunar cusps of pulmonary valve
    n1=méningé (syndrome) | n2=en:set of commissures of semilunar cusps of pulmonary valve | rel=r_associated | relid=0 | w=10
  5533. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of cruveilhier's plexuses
    n1=méningé (syndrome) | n2=en:set of cruveilhier's plexuses | rel=r_associated | relid=0 | w=10
  5534. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of cytoplasmic organelles
    n1=méningé (syndrome) | n2=en:set of cytoplasmic organelles | rel=r_associated | relid=0 | w=10
  5535. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of dorsal parts of intertransversarii laterales lumborum
    n1=méningé (syndrome) | n2=en:set of dorsal parts of intertransversarii laterales lumborum | rel=r_associated | relid=0 | w=10
  5536. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of dorsal rami of sacral nerves and coccygeal nerve
    n1=méningé (syndrome) | n2=en:set of dorsal rami of sacral nerves and coccygeal nerve | rel=r_associated | relid=0 | w=10
  5537. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of false chordae tendineae of heart
    n1=méningé (syndrome) | n2=en:set of false chordae tendineae of heart | rel=r_associated | relid=0 | w=10
  5538. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of gastrohepatic branches
    n1=méningé (syndrome) | n2=en:set of gastrohepatic branches | rel=r_associated | relid=0 | w=10
  5539. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of hair crosses
    n1=méningé (syndrome) | n2=en:set of hair crosses | rel=r_associated | relid=0 | w=10
  5540. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of hair streams
    n1=méningé (syndrome) | n2=en:set of hair streams | rel=r_associated | relid=0 | w=10
  5541. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of heterogeneous clusters
    n1=méningé (syndrome) | n2=en:set of heterogeneous clusters | rel=r_associated | relid=0 | w=10
  5542. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of intermuscular gluteal bursae
    n1=méningé (syndrome) | n2=en:set of intermuscular gluteal bursae | rel=r_associated | relid=0 | w=10
  5543. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of intertendinous connections of extensor digitorum
    n1=méningé (syndrome) | n2=en:set of intertendinous connections of extensor digitorum | rel=r_associated | relid=0 | w=10
  5544. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of intestinal villi of small intestine
    n1=méningé (syndrome) | n2=en:set of intestinal villi of small intestine | rel=r_associated | relid=0 | w=10
  5545. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of intrapulmonary blood vessels
    n1=méningé (syndrome) | n2=en:set of intrapulmonary blood vessels | rel=r_associated | relid=0 | w=10
  5546. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of intrasegmental bronchi
    n1=méningé (syndrome) | n2=en:set of intrasegmental bronchi | rel=r_associated | relid=0 | w=10
  5547. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of laryngeal cartilages and joints
    n1=méningé (syndrome) | n2=en:set of laryngeal cartilages and joints | rel=r_associated | relid=0 | w=10
  5548. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of lobar and segmental bronchi
    n1=méningé (syndrome) | n2=en:set of lobar and segmental bronchi | rel=r_associated | relid=0 | w=10
  5549. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of lobules of thyroid gland
    n1=méningé (syndrome) | n2=en:set of lobules of thyroid gland | rel=r_associated | relid=0 | w=10
  5550. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of lunules of semilunar cusps of aortic valve
    n1=méningé (syndrome) | n2=en:set of lunules of semilunar cusps of aortic valve | rel=r_associated | relid=0 | w=10
  5551. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of lunules of semilunar cusps of pulmonary valve
    n1=méningé (syndrome) | n2=en:set of lunules of semilunar cusps of pulmonary valve | rel=r_associated | relid=0 | w=10
  5552. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of lymphoid aggregates
    n1=méningé (syndrome) | n2=en:set of lymphoid aggregates | rel=r_associated | relid=0 | w=10
  5553. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of lymphoid nodules of lingual tonsil
    n1=méningé (syndrome) | n2=en:set of lymphoid nodules of lingual tonsil | rel=r_associated | relid=0 | w=10
  5554. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of maculae utriculosaccularis
    n1=méningé (syndrome) | n2=en:set of maculae utriculosaccularis | rel=r_associated | relid=0 | w=10
  5555. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of medullary rays
    n1=méningé (syndrome) | n2=en:set of medullary rays | rel=r_associated | relid=0 | w=10
  5556. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of muscles
    n1=méningé (syndrome) | n2=en:set of muscles | rel=r_associated | relid=0 | w=10
  5557. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of muscles of urogenital triangle
    n1=méningé (syndrome) | n2=en:set of muscles of urogenital triangle | rel=r_associated | relid=0 | w=10
  5558. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of nerves
    n1=méningé (syndrome) | n2=en:set of nerves | rel=r_associated | relid=0 | w=10
  5559. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of neuraxis fibers
    n1=méningé (syndrome) | n2=en:set of neuraxis fibers | rel=r_associated | relid=0 | w=10
  5560. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of nodes around cardia
    n1=méningé (syndrome) | n2=en:set of nodes around cardia | rel=r_associated | relid=0 | w=10
  5561. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of nodules of semilunar cusps of aortic valve
    n1=méningé (syndrome) | n2=en:set of nodules of semilunar cusps of aortic valve | rel=r_associated | relid=0 | w=10
  5562. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of nodules of semilunar cusps of pulmonary valve
    n1=méningé (syndrome) | n2=en:set of nodules of semilunar cusps of pulmonary valve | rel=r_associated | relid=0 | w=10
  5563. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of oblique fibers of pyloric sphincter
    n1=méningé (syndrome) | n2=en:set of oblique fibers of pyloric sphincter | rel=r_associated | relid=0 | w=10
  5564. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of olfactory islets
    n1=méningé (syndrome) | n2=en:set of olfactory islets | rel=r_associated | relid=0 | w=10
  5565. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of organ parts
    n1=méningé (syndrome) | n2=en:set of organ parts | rel=r_associated | relid=0 | w=10
  5566. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of organ system subdivisions
    n1=méningé (syndrome) | n2=en:set of organ system subdivisions | rel=r_associated | relid=0 | w=10
  5567. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of organ zones
    n1=méningé (syndrome) | n2=en:set of organ zones | rel=r_associated | relid=0 | w=10
  5568. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of organs
    n1=méningé (syndrome) | n2=en:set of organs | rel=r_associated | relid=0 | w=10
  5569. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of papillae of dermis
    n1=méningé (syndrome) | n2=en:set of papillae of dermis | rel=r_associated | relid=0 | w=10
  5570. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of papillary muscles of heart
    n1=méningé (syndrome) | n2=en:set of papillary muscles of heart | rel=r_associated | relid=0 | w=10
  5571. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of parts of human body
    n1=méningé (syndrome) | n2=en:set of parts of human body | rel=r_associated | relid=0 | w=10
  5572. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of peripheral autonomic plexuses and ganglia
    n1=méningé (syndrome) | n2=en:set of peripheral autonomic plexuses and ganglia | rel=r_associated | relid=0 | w=10
  5573. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of peripheral fibers
    n1=méningé (syndrome) | n2=en:set of peripheral fibers | rel=r_associated | relid=0 | w=10
  5574. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of peritoneal attachments of liver
    n1=méningé (syndrome) | n2=en:set of peritoneal attachments of liver | rel=r_associated | relid=0 | w=10
  5575. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of pharyngeal lymphoid nodules
    n1=méningé (syndrome) | n2=en:set of pharyngeal lymphoid nodules | rel=r_associated | relid=0 | w=10
  5576. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of primary lymphoid organs
    n1=méningé (syndrome) | n2=en:set of primary lymphoid organs | rel=r_associated | relid=0 | w=10
  5577. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of puboperineales
    n1=méningé (syndrome) | n2=en:set of puboperineales | rel=r_associated | relid=0 | w=10
  5578. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of radial fibers of ciliary muscle
    n1=méningé (syndrome) | n2=en:set of radial fibers of ciliary muscle | rel=r_associated | relid=0 | w=10
  5579. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of recesses, fossae and folds
    n1=méningé (syndrome) | n2=en:set of recesses, fossae and folds | rel=r_associated | relid=0 | w=10
  5580. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of right and left lobes of prostate
    n1=méningé (syndrome) | n2=en:set of right and left lobes of prostate | rel=r_associated | relid=0 | w=10
  5581. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of sacral nerves and coccygeal nerve [s1-s5, co]
    n1=méningé (syndrome) | n2=en:set of sacral nerves and coccygeal nerve [s1-s5, co] | rel=r_associated | relid=0 | w=10
  5582. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of sacral parasympathetic nuclei
    n1=méningé (syndrome) | n2=en:set of sacral parasympathetic nuclei | rel=r_associated | relid=0 | w=10
  5583. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of secondary lymphoid organs
    n1=méningé (syndrome) | n2=en:set of secondary lymphoid organs | rel=r_associated | relid=0 | w=10
  5584. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of sheaths
    n1=méningé (syndrome) | n2=en:set of sheaths | rel=r_associated | relid=0 | w=10
  5585. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of solid abdominal organs
    n1=méningé (syndrome) | n2=en:set of solid abdominal organs | rel=r_associated | relid=0 | w=10
  5586. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of spinal ganglia
    n1=méningé (syndrome) | n2=en:set of spinal ganglia | rel=r_associated | relid=0 | w=10
  5587. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of subarachnoid spaces
    n1=méningé (syndrome) | n2=en:set of subarachnoid spaces | rel=r_associated | relid=0 | w=10
  5588. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of subdivisions of cardinal body part
    n1=méningé (syndrome) | n2=en:set of subdivisions of cardinal body part | rel=r_associated | relid=0 | w=10
  5589. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of tendon sheaths and bursae
    n1=méningé (syndrome) | n2=en:set of tendon sheaths and bursae | rel=r_associated | relid=0 | w=10
  5590. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of thoracic joints
    n1=méningé (syndrome) | n2=en:set of thoracic joints | rel=r_associated | relid=0 | w=10
  5591. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of transverse ductules of epoophoron
    n1=méningé (syndrome) | n2=en:set of transverse ductules of epoophoron | rel=r_associated | relid=0 | w=10
  5592. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of vascular bundles of renal medulla
    n1=méningé (syndrome) | n2=en:set of vascular bundles of renal medulla | rel=r_associated | relid=0 | w=10
  5593. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of ventral parts of intertransversarii laterales lumborum
    n1=méningé (syndrome) | n2=en:set of ventral parts of intertransversarii laterales lumborum | rel=r_associated | relid=0 | w=10
  5594. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:set of vessels of internal ear
    n1=méningé (syndrome) | n2=en:set of vessels of internal ear | rel=r_associated | relid=0 | w=10
  5595. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sex cord-stromal tumor
    n1=méningé (syndrome) | n2=en:sex cord-stromal tumor | rel=r_associated | relid=0 | w=10
  5596. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:signet ring cell carcinoma
    n1=méningé (syndrome) | n2=en:signet ring cell carcinoma | rel=r_associated | relid=0 | w=10
  5597. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sinonasal undifferentiated carcinoma
    n1=méningé (syndrome) | n2=en:sinonasal undifferentiated carcinoma | rel=r_associated | relid=0 | w=10
  5598. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sinus
    n1=méningé (syndrome) | n2=en:sinus | rel=r_associated | relid=0 | w=10
  5599. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sinus of venae cavae
    n1=méningé (syndrome) | n2=en:sinus of venae cavae | rel=r_associated | relid=0 | w=10
  5600. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skeletal neoplasms benign
    n1=méningé (syndrome) | n2=en:skeletal neoplasms benign | rel=r_associated | relid=0 | w=10
  5601. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skeletal neoplasms malignant and unspecified
    n1=méningé (syndrome) | n2=en:skeletal neoplasms malignant and unspecified | rel=r_associated | relid=0 | w=10
  5602. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skeletal tissue
    n1=méningé (syndrome) | n2=en:skeletal tissue | rel=r_associated | relid=0 | w=10
  5603. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skeleton
    n1=méningé (syndrome) | n2=en:skeleton | rel=r_associated | relid=0 | w=10
  5604. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skin angiosarcoma
    n1=méningé (syndrome) | n2=en:skin angiosarcoma | rel=r_associated | relid=0 | w=10
  5605. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skin appendage tumors may show malignant transformation
    n1=méningé (syndrome) | n2=en:skin appendage tumors may show malignant transformation | rel=r_associated | relid=0 | w=10
  5606. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skin basal cell carcinoma
    n1=méningé (syndrome) | n2=en:skin basal cell carcinoma | rel=r_associated | relid=0 | w=10
  5607. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skin cancer susceptibility
    n1=méningé (syndrome) | n2=en:skin cancer susceptibility | rel=r_associated | relid=0 | w=10
  5608. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skin cell
    n1=méningé (syndrome) | n2=en:skin cell | rel=r_associated | relid=0 | w=10
  5609. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skin hemangioma
    n1=méningé (syndrome) | n2=en:skin hemangioma | rel=r_associated | relid=0 | w=10
  5610. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skin lymphangiosarcoma
    n1=méningé (syndrome) | n2=en:skin lymphangiosarcoma | rel=r_associated | relid=0 | w=10
  5611. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skin squamous cell carcinoma
    n1=méningé (syndrome) | n2=en:skin squamous cell carcinoma | rel=r_associated | relid=0 | w=10
  5612. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:skull base meningioma
    n1=méningé (syndrome) | n2=en:skull base meningioma | rel=r_associated | relid=0 | w=10
  5613. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:small cell carcinoma of the ovary, hypercalcemic type
    n1=méningé (syndrome) | n2=en:small cell carcinoma of the ovary, hypercalcemic type | rel=r_associated | relid=0 | w=10
  5614. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:small intestinal carcinoma
    n1=méningé (syndrome) | n2=en:small intestinal carcinoma | rel=r_associated | relid=0 | w=10
  5615. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:small intestine carcinoid
    n1=méningé (syndrome) | n2=en:small intestine carcinoid | rel=r_associated | relid=0 | w=10
  5616. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:small neuron
    n1=méningé (syndrome) | n2=en:small neuron | rel=r_associated | relid=0 | w=10
  5617. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:soft tissue neoplasms malignant and unspecified
    n1=méningé (syndrome) | n2=en:soft tissue neoplasms malignant and unspecified | rel=r_associated | relid=0 | w=10
  5618. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:soft tissue sarcoma
    n1=méningé (syndrome) | n2=en:soft tissue sarcoma | rel=r_associated | relid=0 | w=10
  5619. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:soft tissue tumor and/or sarcoma
    n1=méningé (syndrome) | n2=en:soft tissue tumor and/or sarcoma | rel=r_associated | relid=0 | w=10
  5620. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:solid neoplasm
    n1=méningé (syndrome) | n2=en:solid neoplasm | rel=r_associated | relid=0 | w=10
  5621. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:somatic nerve
    n1=méningé (syndrome) | n2=en:somatic nerve | rel=r_associated | relid=0 | w=10
  5622. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:somatostatin-producing neuroendocrine tumor
    n1=méningé (syndrome) | n2=en:somatostatin-producing neuroendocrine tumor | rel=r_associated | relid=0 | w=10
  5623. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:special sense organ system
    n1=méningé (syndrome) | n2=en:special sense organ system | rel=r_associated | relid=0 | w=10
  5624. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:specialized epithelial cell
    n1=méningé (syndrome) | n2=en:specialized epithelial cell | rel=r_associated | relid=0 | w=10
  5625. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:specimen from meninges
    n1=méningé (syndrome) | n2=en:specimen from meninges | rel=r_associated | relid=0 | w=10
  5626. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:specimen from meninges obtained by biopsy
    n1=méningé (syndrome) | n2=en:specimen from meninges obtained by biopsy | rel=r_associated | relid=0 | w=10
  5627. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sphenocavernous meningioma
    n1=méningé (syndrome) | n2=en:sphenocavernous meningioma | rel=r_associated | relid=0 | w=10
  5628. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sphenoorbital meningioma
    n1=méningé (syndrome) | n2=en:sphenoorbital meningioma | rel=r_associated | relid=0 | w=10
  5629. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:sphincter of common bile duct
    n1=méningé (syndrome) | n2=en:sphincter of common bile duct | rel=r_associated | relid=0 | w=10
  5630. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:spinal cord
    n1=méningé (syndrome) | n2=en:spinal cord | rel=r_associated | relid=0 | w=10
  5631. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:spinal cord neoplasm
    n1=méningé (syndrome) | n2=en:spinal cord neoplasm | rel=r_associated | relid=0 | w=10
  5632. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:spinal cord, cranial nerves, and other parts of central nervous system
    n1=méningé (syndrome) | n2=en:spinal cord, cranial nerves, and other parts of central nervous system | rel=r_associated | relid=0 | w=10
  5633. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:spinal meningeal neoplasm
    n1=méningé (syndrome) | n2=en:spinal meningeal neoplasm | rel=r_associated | relid=0 | w=10
  5634. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:spinal meninges
    n1=méningé (syndrome) | n2=en:spinal meninges | rel=r_associated | relid=0 | w=10
  5635. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:spinal multifocal clear cell meningioma
    n1=méningé (syndrome) | n2=en:spinal multifocal clear cell meningioma | rel=r_associated | relid=0 | w=10
  5636. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:spinal veins
    n1=méningé (syndrome) | n2=en:spinal veins | rel=r_associated | relid=0 | w=10
  5637. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:splenic hemangioma
    n1=méningé (syndrome) | n2=en:splenic hemangioma | rel=r_associated | relid=0 | w=10
  5638. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:splenic trabecula
    n1=méningé (syndrome) | n2=en:splenic trabecula | rel=r_associated | relid=0 | w=10
  5639. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:splenic white pulp
    n1=méningé (syndrome) | n2=en:splenic white pulp | rel=r_associated | relid=0 | w=10
  5640. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:squamous cell carcinoma
    n1=méningé (syndrome) | n2=en:squamous cell carcinoma | rel=r_associated | relid=0 | w=10
  5641. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:squamous cell carcinoma (1 patient)
    n1=méningé (syndrome) | n2=en:squamous cell carcinoma (1 patient) | rel=r_associated | relid=0 | w=10
  5642. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:squamous cell carcinoma (skin and tongue)
    n1=méningé (syndrome) | n2=en:squamous cell carcinoma (skin and tongue) | rel=r_associated | relid=0 | w=10
  5643. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:squamous cell carcinoma (skin or mucosa)
    n1=méningé (syndrome) | n2=en:squamous cell carcinoma (skin or mucosa) | rel=r_associated | relid=0 | w=10
  5644. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:squamous cell carcinoma in area of palmoplantar keratoderma (rare)
    n1=méningé (syndrome) | n2=en:squamous cell carcinoma in area of palmoplantar keratoderma (rare) | rel=r_associated | relid=0 | w=10
  5645. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:squamous cell neoplasm
    n1=méningé (syndrome) | n2=en:squamous cell neoplasm | rel=r_associated | relid=0 | w=10
  5646. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:squamous epitheliomas, multiple
    n1=méningé (syndrome) | n2=en:squamous epitheliomas, multiple | rel=r_associated | relid=0 | w=10
  5647. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:starry sky pattern
    n1=méningé (syndrome) | n2=en:starry sky pattern | rel=r_associated | relid=0 | w=10
  5648. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:statistical association of extensive metabolism (em, wildtype) and malignancy, especially smoking-induced lung cancer
    n1=méningé (syndrome) | n2=en:statistical association of extensive metabolism (em, wildtype) and malignancy, especially smoking-induced lung cancer | rel=r_associated | relid=0 | w=10
  5649. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:stem cell
    n1=méningé (syndrome) | n2=en:stem cell | rel=r_associated | relid=0 | w=10
  5650. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:stomach cell
    n1=méningé (syndrome) | n2=en:stomach cell | rel=r_associated | relid=0 | w=10
  5651. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:striae
    n1=méningé (syndrome) | n2=en:striae | rel=r_associated | relid=0 | w=10
  5652. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:striola
    n1=méningé (syndrome) | n2=en:striola | rel=r_associated | relid=0 | w=10
  5653. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:stromal cell
    n1=méningé (syndrome) | n2=en:stromal cell | rel=r_associated | relid=0 | w=10
  5654. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of anal valves
    n1=méningé (syndrome) | n2=en:structure of anal valves | rel=r_associated | relid=0 | w=10
  5655. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of anulus fibrosus of intervertebral disc
    n1=méningé (syndrome) | n2=en:structure of anulus fibrosus of intervertebral disc | rel=r_associated | relid=0 | w=10
  5656. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of blood vessel of retina
    n1=méningé (syndrome) | n2=en:structure of blood vessel of retina | rel=r_associated | relid=0 | w=10
  5657. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of carunculae hymenales
    n1=méningé (syndrome) | n2=en:structure of carunculae hymenales | rel=r_associated | relid=0 | w=10
  5658. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of circular fibers of ciliary muscle
    n1=méningé (syndrome) | n2=en:structure of circular fibers of ciliary muscle | rel=r_associated | relid=0 | w=10
  5659. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of crura of antihelix
    n1=méningé (syndrome) | n2=en:structure of crura of antihelix | rel=r_associated | relid=0 | w=10
  5660. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of deep vein of upper extremity
    n1=méningé (syndrome) | n2=en:structure of deep vein of upper extremity | rel=r_associated | relid=0 | w=10
  5661. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of diverticula of ampulla of vas deferens
    n1=méningé (syndrome) | n2=en:structure of diverticula of ampulla of vas deferens | rel=r_associated | relid=0 | w=10
  5662. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of fibrous portion of pericardium
    n1=méningé (syndrome) | n2=en:structure of fibrous portion of pericardium | rel=r_associated | relid=0 | w=10
  5663. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of fila radicularia of spinal nerve
    n1=méningé (syndrome) | n2=en:structure of fila radicularia of spinal nerve | rel=r_associated | relid=0 | w=10
  5664. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of gluteus medius muscle trochanteric bursa
    n1=méningé (syndrome) | n2=en:structure of gluteus medius muscle trochanteric bursa | rel=r_associated | relid=0 | w=10
  5665. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of inferior orbital fissure
    n1=méningé (syndrome) | n2=en:structure of inferior orbital fissure | rel=r_associated | relid=0 | w=10
  5666. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of intercrural fibers of superficial inguinal ring
    n1=méningé (syndrome) | n2=en:structure of intercrural fibers of superficial inguinal ring | rel=r_associated | relid=0 | w=10
  5667. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of intervertebral vein
    n1=méningé (syndrome) | n2=en:structure of intervertebral vein | rel=r_associated | relid=0 | w=10
  5668. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of joint cavity
    n1=méningé (syndrome) | n2=en:structure of joint cavity | rel=r_associated | relid=0 | w=10
  5669. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of lobule of epididymis
    n1=méningé (syndrome) | n2=en:structure of lobule of epididymis | rel=r_associated | relid=0 | w=10
  5670. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of lobule of testis
    n1=méningé (syndrome) | n2=en:structure of lobule of testis | rel=r_associated | relid=0 | w=10
  5671. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of macula cribrosa
    n1=méningé (syndrome) | n2=en:structure of macula cribrosa | rel=r_associated | relid=0 | w=10
  5672. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of major calyx
    n1=méningé (syndrome) | n2=en:structure of major calyx | rel=r_associated | relid=0 | w=10
  5673. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of minor calyx
    n1=méningé (syndrome) | n2=en:structure of minor calyx | rel=r_associated | relid=0 | w=10
  5674. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of nucleus pulposus of intervertebral disc
    n1=méningé (syndrome) | n2=en:structure of nucleus pulposus of intervertebral disc | rel=r_associated | relid=0 | w=10
  5675. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of orbital septum
    n1=méningé (syndrome) | n2=en:structure of orbital septum | rel=r_associated | relid=0 | w=10
  5676. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of pneumatic bone
    n1=méningé (syndrome) | n2=en:structure of pneumatic bone | rel=r_associated | relid=0 | w=10
  5677. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of premaxillary bone
    n1=méningé (syndrome) | n2=en:structure of premaxillary bone | rel=r_associated | relid=0 | w=10
  5678. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of radius of lens
    n1=méningé (syndrome) | n2=en:structure of radius of lens | rel=r_associated | relid=0 | w=10
  5679. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of renal segment
    n1=méningé (syndrome) | n2=en:structure of renal segment | rel=r_associated | relid=0 | w=10
  5680. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of serous cavity
    n1=méningé (syndrome) | n2=en:structure of serous cavity | rel=r_associated | relid=0 | w=10
  5681. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of solitary lymphoid nodule of small intestine
    n1=méningé (syndrome) | n2=en:structure of solitary lymphoid nodule of small intestine | rel=r_associated | relid=0 | w=10
  5682. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of sternal membrane
    n1=méningé (syndrome) | n2=en:structure of sternal membrane | rel=r_associated | relid=0 | w=10
  5683. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of straight seminiferous tubule
    n1=méningé (syndrome) | n2=en:structure of straight seminiferous tubule | rel=r_associated | relid=0 | w=10
  5684. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of sulci cutis
    n1=méningé (syndrome) | n2=en:structure of sulci cutis | rel=r_associated | relid=0 | w=10
  5685. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of superficial vein of upper extremity
    n1=méningé (syndrome) | n2=en:structure of superficial vein of upper extremity | rel=r_associated | relid=0 | w=10
  5686. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of superior orbital fissure
    n1=méningé (syndrome) | n2=en:structure of superior orbital fissure | rel=r_associated | relid=0 | w=10
  5687. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of superior urogenital diaphragmatic fascia
    n1=méningé (syndrome) | n2=en:structure of superior urogenital diaphragmatic fascia | rel=r_associated | relid=0 | w=10
  5688. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of tendinous arch
    n1=méningé (syndrome) | n2=en:structure of tendinous arch | rel=r_associated | relid=0 | w=10
  5689. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of tendinous intersection
    n1=méningé (syndrome) | n2=en:structure of tendinous intersection | rel=r_associated | relid=0 | w=10
  5690. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of trabecula carnea of left ventricle
    n1=méningé (syndrome) | n2=en:structure of trabecula carnea of left ventricle | rel=r_associated | relid=0 | w=10
  5691. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of trabecula carnea of right ventricle
    n1=méningé (syndrome) | n2=en:structure of trabecula carnea of right ventricle | rel=r_associated | relid=0 | w=10
  5692. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of trabeculae of corpus cavernosum
    n1=méningé (syndrome) | n2=en:structure of trabeculae of corpus cavernosum | rel=r_associated | relid=0 | w=10
  5693. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of trabeculae of corpus spongiosum
    n1=méningé (syndrome) | n2=en:structure of trabeculae of corpus spongiosum | rel=r_associated | relid=0 | w=10
  5694. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of transverse fascicles of plantar aponeurosis
    n1=méningé (syndrome) | n2=en:structure of transverse fascicles of plantar aponeurosis | rel=r_associated | relid=0 | w=10
  5695. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of vaginal rugae
    n1=méningé (syndrome) | n2=en:structure of vaginal rugae | rel=r_associated | relid=0 | w=10
  5696. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of vestibular system
    n1=méningé (syndrome) | n2=en:structure of vestibular system | rel=r_associated | relid=0 | w=10
  5697. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of vincula tendinum of foot
    n1=méningé (syndrome) | n2=en:structure of vincula tendinum of foot | rel=r_associated | relid=0 | w=10
  5698. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of vincula tendinum of tendons of fingers
    n1=méningé (syndrome) | n2=en:structure of vincula tendinum of tendons of fingers | rel=r_associated | relid=0 | w=10
  5699. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:structure of zonular fibers
    n1=méningé (syndrome) | n2=en:structure of zonular fibers | rel=r_associated | relid=0 | w=10
  5700. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:subarachnoid cistern
    n1=méningé (syndrome) | n2=en:subarachnoid cistern | rel=r_associated | relid=0 | w=10
  5701. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:subarachnoid space
    n1=méningé (syndrome) | n2=en:subarachnoid space | rel=r_associated | relid=0 | w=10
  5702. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:subdivision of skeleton
    n1=méningé (syndrome) | n2=en:subdivision of skeleton | rel=r_associated | relid=0 | w=10
  5703. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:subdural hematoma
    n1=méningé (syndrome) | n2=en:subdural hematoma | rel=r_associated | relid=0 | w=10
  5704. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:subependymoma
    n1=méningé (syndrome) | n2=en:subependymoma | rel=r_associated | relid=0 | w=10
  5705. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:superficial vein
    n1=méningé (syndrome) | n2=en:superficial vein | rel=r_associated | relid=0 | w=10
  5706. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:superior synovial membrane of temporomandibular joint
    n1=méningé (syndrome) | n2=en:superior synovial membrane of temporomandibular joint | rel=r_associated | relid=0 | w=10
  5707. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:superior tarsal plate of eyelid
    n1=méningé (syndrome) | n2=en:superior tarsal plate of eyelid | rel=r_associated | relid=0 | w=10
  5708. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:supporting cell
    n1=méningé (syndrome) | n2=en:supporting cell | rel=r_associated | relid=0 | w=10
  5709. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:suprasellar meningioma
    n1=méningé (syndrome) | n2=en:suprasellar meningioma | rel=r_associated | relid=0 | w=10
  5710. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:supratentorial meningioma
    n1=méningé (syndrome) | n2=en:supratentorial meningioma | rel=r_associated | relid=0 | w=10
  5711. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:susceptibility to malignant melanoma
    n1=méningé (syndrome) | n2=en:susceptibility to malignant melanoma | rel=r_associated | relid=0 | w=10
  5712. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:susceptibility to myelodysplasia
    n1=méningé (syndrome) | n2=en:susceptibility to myelodysplasia | rel=r_associated | relid=0 | w=10
  5713. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:susceptibility to myeloid leukemia
    n1=méningé (syndrome) | n2=en:susceptibility to myeloid leukemia | rel=r_associated | relid=0 | w=10
  5714. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:synovial bursa
    n1=méningé (syndrome) | n2=en:synovial bursa | rel=r_associated | relid=0 | w=10
  5715. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:synovial neoplasm
    n1=méningé (syndrome) | n2=en:synovial neoplasm | rel=r_associated | relid=0 | w=10
  5716. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:synovial sheath
    n1=méningé (syndrome) | n2=en:synovial sheath | rel=r_associated | relid=0 | w=10
  5717. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:synovial villus of joint
    n1=méningé (syndrome) | n2=en:synovial villus of joint | rel=r_associated | relid=0 | w=10
  5718. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:synovial-like neoplasm
    n1=méningé (syndrome) | n2=en:synovial-like neoplasm | rel=r_associated | relid=0 | w=10
  5719. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:syringocystadenoma papilliferum
    n1=méningé (syndrome) | n2=en:syringocystadenoma papilliferum | rel=r_associated | relid=0 | w=10
  5720. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:system term
    n1=méningé (syndrome) | n2=en:system term | rel=r_associated | relid=0 | w=10
  5721. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:t-cell non-hodgkin lymphoma
    n1=méningé (syndrome) | n2=en:t-cell non-hodgkin lymphoma | rel=r_associated | relid=0 | w=10
  5722. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:taenia coli
    n1=méningé (syndrome) | n2=en:taenia coli | rel=r_associated | relid=0 | w=10
  5723. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tarsal plate
    n1=méningé (syndrome) | n2=en:tarsal plate | rel=r_associated | relid=0 | w=10
  5724. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:taxonomic
    n1=méningé (syndrome) | n2=en:taxonomic | rel=r_associated | relid=0 | w=10
  5725. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:temporary tooth
    n1=méningé (syndrome) | n2=en:temporary tooth | rel=r_associated | relid=0 | w=10
  5726. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tendon sheath
    n1=méningé (syndrome) | n2=en:tendon sheath | rel=r_associated | relid=0 | w=10
  5727. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:teratoid tumor, atypical
    n1=méningé (syndrome) | n2=en:teratoid tumor, atypical | rel=r_associated | relid=0 | w=10
  5728. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:teratologic
    n1=méningé (syndrome) | n2=en:teratologic | rel=r_associated | relid=0 | w=10
  5729. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:terminal ganglion
    n1=méningé (syndrome) | n2=en:terminal ganglion | rel=r_associated | relid=0 | w=10
  5730. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:terminal nerve [0]
    n1=méningé (syndrome) | n2=en:terminal nerve [0] | rel=r_associated | relid=0 | w=10
  5731. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:testicular sertoli cell tumor
    n1=méningé (syndrome) | n2=en:testicular sertoli cell tumor | rel=r_associated | relid=0 | w=10
  5732. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:testicular sertoli cell tumor, calcified
    n1=méningé (syndrome) | n2=en:testicular sertoli cell tumor, calcified | rel=r_associated | relid=0 | w=10
  5733. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:therapeutic aspects
    n1=méningé (syndrome) | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=10
  5734. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thoracic intraspinal meningioma
    n1=méningé (syndrome) | n2=en:thoracic intraspinal meningioma | rel=r_associated | relid=0 | w=10
  5735. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thymic lobule
    n1=méningé (syndrome) | n2=en:thymic lobule | rel=r_associated | relid=0 | w=10
  5736. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thymoma
    n1=méningé (syndrome) | n2=en:thymoma | rel=r_associated | relid=0 | w=10
  5737. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thymus epithelial neoplasm
    n1=méningé (syndrome) | n2=en:thymus epithelial neoplasm | rel=r_associated | relid=0 | w=10
  5738. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thyrohyoid membrane
    n1=méningé (syndrome) | n2=en:thyrohyoid membrane | rel=r_associated | relid=0 | w=10
  5739. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thyroid cancer (follicular cell)
    n1=méningé (syndrome) | n2=en:thyroid cancer (follicular cell) | rel=r_associated | relid=0 | w=10
  5740. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thyroid follicular cell tumor
    n1=méningé (syndrome) | n2=en:thyroid follicular cell tumor | rel=r_associated | relid=0 | w=10
  5741. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thyroid gland carcinoma
    n1=méningé (syndrome) | n2=en:thyroid gland carcinoma | rel=r_associated | relid=0 | w=10
  5742. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thyroid gland medullary carcinoma
    n1=méningé (syndrome) | n2=en:thyroid gland medullary carcinoma | rel=r_associated | relid=0 | w=10
  5743. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thyroid gland oncocytic adenoma
    n1=méningé (syndrome) | n2=en:thyroid gland oncocytic adenoma | rel=r_associated | relid=0 | w=10
  5744. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thyroid gland oncocytic neoplasm
    n1=méningé (syndrome) | n2=en:thyroid gland oncocytic neoplasm | rel=r_associated | relid=0 | w=10
  5745. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:thyroid gland papillary carcinoma
    n1=méningé (syndrome) | n2=en:thyroid gland papillary carcinoma | rel=r_associated | relid=0 | w=10
  5746. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tissue fiber
    n1=méningé (syndrome) | n2=en:tissue fiber | rel=r_associated | relid=0 | w=10
  5747. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:toe
    n1=méningé (syndrome) | n2=en:toe | rel=r_associated | relid=0 | w=10
  5748. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tooth
    n1=méningé (syndrome) | n2=en:tooth | rel=r_associated | relid=0 | w=10
  5749. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:toruli tactiles
    n1=méningé (syndrome) | n2=en:toruli tactiles | rel=r_associated | relid=0 | w=10
  5750. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:trabeculae carneae cordis
    n1=méningé (syndrome) | n2=en:trabeculae carneae cordis | rel=r_associated | relid=0 | w=10
  5751. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tract
    n1=méningé (syndrome) | n2=en:tract | rel=r_associated | relid=0 | w=10
  5752. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tragal lamina
    n1=méningé (syndrome) | n2=en:tragal lamina | rel=r_associated | relid=0 | w=10
  5753. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tram track sign of optic nerve
    n1=méningé (syndrome) | n2=en:tram track sign of optic nerve | rel=r_associated | relid=0 | w=10
  5754. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:transition zone of prostate
    n1=méningé (syndrome) | n2=en:transition zone of prostate | rel=r_associated | relid=0 | w=10
  5755. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:transitional cell
    n1=méningé (syndrome) | n2=en:transitional cell | rel=r_associated | relid=0 | w=10
  5756. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:transitional cell papilloma and/or carcinoma
    n1=méningé (syndrome) | n2=en:transitional cell papilloma and/or carcinoma | rel=r_associated | relid=0 | w=10
  5757. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:transplantation aspects
    n1=méningé (syndrome) | n2=en:transplantation aspects | rel=r_associated | relid=0 | w=10
  5758. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:trapezoid area below prostate
    n1=méningé (syndrome) | n2=en:trapezoid area below prostate | rel=r_associated | relid=0 | w=10
  5759. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:trauma qualifier
    n1=méningé (syndrome) | n2=en:trauma qualifier | rel=r_associated | relid=0 | w=10
  5760. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:trichoblastoma
    n1=méningé (syndrome) | n2=en:trichoblastoma | rel=r_associated | relid=0 | w=10
  5761. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:trichoepitheliomas may rarely show malignant transformation to basal cell carcinoma
    n1=méningé (syndrome) | n2=en:trichoepitheliomas may rarely show malignant transformation to basal cell carcinoma | rel=r_associated | relid=0 | w=10
  5762. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:trophoblastic tumor
    n1=méningé (syndrome) | n2=en:trophoblastic tumor | rel=r_associated | relid=0 | w=10
  5763. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:trunk of brachial plexus
    n1=méningé (syndrome) | n2=en:trunk of brachial plexus | rel=r_associated | relid=0 | w=10
  5764. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tuberculum sellae meningioma
    n1=méningé (syndrome) | n2=en:tuberculum sellae meningioma | rel=r_associated | relid=0 | w=10
  5765. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tumor cells, benign
    n1=méningé (syndrome) | n2=en:tumor cells, benign | rel=r_associated | relid=0 | w=10
  5766. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tumor in vein
    n1=méningé (syndrome) | n2=en:tumor in vein | rel=r_associated | relid=0 | w=10
  5767. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tumor predisposition syndrome
    n1=méningé (syndrome) | n2=en:tumor predisposition syndrome | rel=r_associated | relid=0 | w=10
  5768. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tumors at multiple other sites including cns
    n1=méningé (syndrome) | n2=en:tumors at multiple other sites including cns | rel=r_associated | relid=0 | w=10
  5769. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tumors of the sympathetic nervous system (5 to 10%)
    n1=méningé (syndrome) | n2=en:tumors of the sympathetic nervous system (5 to 10%) | rel=r_associated | relid=0 | w=10
  5770. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tunica adventitia
    n1=méningé (syndrome) | n2=en:tunica adventitia | rel=r_associated | relid=0 | w=10
  5771. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tunica intima
    n1=méningé (syndrome) | n2=en:tunica intima | rel=r_associated | relid=0 | w=10
  5772. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tunica media
    n1=méningé (syndrome) | n2=en:tunica media | rel=r_associated | relid=0 | w=10
  5773. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:tympanic membrane
    n1=méningé (syndrome) | n2=en:tympanic membrane | rel=r_associated | relid=0 | w=10
  5774. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ulcerated haemangioma
    n1=méningé (syndrome) | n2=en:ulcerated haemangioma | rel=r_associated | relid=0 | w=10
  5775. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:undifferentiated and biphenotypic leukemia (all subtypes)
    n1=méningé (syndrome) | n2=en:undifferentiated and biphenotypic leukemia (all subtypes) | rel=r_associated | relid=0 | w=10
  5776. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:unilateral vestibular schwannoma
    n1=méningé (syndrome) | n2=en:unilateral vestibular schwannoma | rel=r_associated | relid=0 | w=10
  5777. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:upper clivus meningioma
    n1=méningé (syndrome) | n2=en:upper clivus meningioma | rel=r_associated | relid=0 | w=10
  5778. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:uriniferous tubule
    n1=méningé (syndrome) | n2=en:uriniferous tubule | rel=r_associated | relid=0 | w=10
  5779. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:urogenital diaphragm
    n1=méningé (syndrome) | n2=en:urogenital diaphragm | rel=r_associated | relid=0 | w=10
  5780. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:uterine leiomyosarcoma (less common)
    n1=méningé (syndrome) | n2=en:uterine leiomyosarcoma (less common) | rel=r_associated | relid=0 | w=10
  5781. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:uveal melanoma
    n1=méningé (syndrome) | n2=en:uveal melanoma | rel=r_associated | relid=0 | w=10
  5782. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vagus nerve paraganglioma
    n1=méningé (syndrome) | n2=en:vagus nerve paraganglioma | rel=r_associated | relid=0 | w=10
  5783. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vasa nervorum
    n1=méningé (syndrome) | n2=en:vasa nervorum | rel=r_associated | relid=0 | w=10
  5784. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vascular and perivascular tumors (all subtypes)
    n1=méningé (syndrome) | n2=en:vascular and perivascular tumors (all subtypes) | rel=r_associated | relid=0 | w=10
  5785. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vascular bone neoplasm
    n1=méningé (syndrome) | n2=en:vascular bone neoplasm | rel=r_associated | relid=0 | w=10
  5786. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vascular breast neoplasm
    n1=méningé (syndrome) | n2=en:vascular breast neoplasm | rel=r_associated | relid=0 | w=10
  5787. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vascular circle
    n1=méningé (syndrome) | n2=en:vascular circle | rel=r_associated | relid=0 | w=10
  5788. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vascular neoplasm
    n1=méningé (syndrome) | n2=en:vascular neoplasm | rel=r_associated | relid=0 | w=10
  5789. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vasculature of organ
    n1=méningé (syndrome) | n2=en:vasculature of organ | rel=r_associated | relid=0 | w=10
  5790. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vein
    n1=méningé (syndrome) | n2=en:vein | rel=r_associated | relid=0 | w=10
  5791. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vena comitans
    n1=méningé (syndrome) | n2=en:vena comitans | rel=r_associated | relid=0 | w=10
  5792. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:venous angioma of brain
    n1=méningé (syndrome) | n2=en:venous angioma of brain | rel=r_associated | relid=0 | w=10
  5793. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ventral nerve root
    n1=méningé (syndrome) | n2=en:ventral nerve root | rel=r_associated | relid=0 | w=10
  5794. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:ventricle
    n1=méningé (syndrome) | n2=en:ventricle | rel=r_associated | relid=0 | w=10
  5795. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vertebral region
    n1=méningé (syndrome) | n2=en:vertebral region | rel=r_associated | relid=0 | w=10
  5796. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vestibular schwannoma (over 90% of patients)
    n1=méningé (syndrome) | n2=en:vestibular schwannoma (over 90% of patients) | rel=r_associated | relid=0 | w=10
  5797. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:veterinary aspects
    n1=méningé (syndrome) | n2=en:veterinary aspects | rel=r_associated | relid=0 | w=10
  5798. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vinculum breve of digits of hand
    n1=méningé (syndrome) | n2=en:vinculum breve of digits of hand | rel=r_associated | relid=0 | w=10
  5799. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vinculum longum of digits of hand
    n1=méningé (syndrome) | n2=en:vinculum longum of digits of hand | rel=r_associated | relid=0 | w=10
  5800. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:viral meningitis
    n1=méningé (syndrome) | n2=en:viral meningitis | rel=r_associated | relid=0 | w=10
  5801. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:viscera
    n1=méningé (syndrome) | n2=en:viscera | rel=r_associated | relid=0 | w=10
  5802. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:visual pathway meningioma
    n1=méningé (syndrome) | n2=en:visual pathway meningioma | rel=r_associated | relid=0 | w=10
  5803. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:visual system
    n1=méningé (syndrome) | n2=en:visual system | rel=r_associated | relid=0 | w=10
  5804. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:vitreous membrane
    n1=méningé (syndrome) | n2=en:vitreous membrane | rel=r_associated | relid=0 | w=10
  5805. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:waldeyer's tonsillar ring
    n1=méningé (syndrome) | n2=en:waldeyer's tonsillar ring | rel=r_associated | relid=0 | w=10
  5806. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:werner syndrome
    n1=méningé (syndrome) | n2=en:werner syndrome | rel=r_associated | relid=0 | w=10
  5807. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:wing meningiomas, sphenoid
    n1=méningé (syndrome) | n2=en:wing meningiomas, sphenoid | rel=r_associated | relid=0 | w=10
  5808. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> en:xanthomatous meningiomas
    n1=méningé (syndrome) | n2=en:xanthomatous meningiomas | rel=r_associated | relid=0 | w=10
  5809. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> endothéliome méningé
    n1=méningé (syndrome) | n2=endothéliome méningé | rel=r_associated | relid=0 | w=10
  5810. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> esprit
    n1=méningé (syndrome) | n2=esprit | rel=r_associated | relid=0 | w=10
  5811. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> externe
    n1=méningé (syndrome) | n2=externe | rel=r_associated | relid=0 | w=10
  5812. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> familier
    n1=méningé (syndrome) | n2=familier | rel=r_associated | relid=0 | w=10
  5813. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> gadolinium
    n1=méningé (syndrome) | n2=gadolinium | rel=r_associated | relid=0 | w=10
  5814. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> grade I
    n1=méningé (syndrome) | n2=grade I | rel=r_associated | relid=0 | w=10
  5815. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> granulation arachnoïdienne
    n1=méningé (syndrome) | n2=granulation arachnoïdienne | rel=r_associated | relid=0 | w=10
  5816. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> hémangiopéricytome méningé
    n1=méningé (syndrome) | n2=hémangiopéricytome méningé | rel=r_associated | relid=0 | w=10
  5817. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> histologie
    n1=méningé (syndrome) | n2=histologie | rel=r_associated | relid=0 | w=10
  5818. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> hypersignal T2
    n1=méningé (syndrome) | n2=hypersignal T2 | rel=r_associated | relid=0 | w=10
  5819. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> imagerie par résonance magnétique
    n1=méningé (syndrome) | n2=imagerie par résonance magnétique | rel=r_associated | relid=0 | w=10
  5820. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> intelligence
    n1=méningé (syndrome) | n2=intelligence | rel=r_associated | relid=0 | w=10
  5821. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> IRM
    n1=méningé (syndrome) | n2=IRM | rel=r_associated | relid=0 | w=10
  5822. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> irritation méningée
    n1=méningé (syndrome) | n2=irritation méningée | rel=r_associated | relid=0 | w=10
  5823. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> isosignal par rapport à la substance grise
    n1=méningé (syndrome) | n2=isosignal par rapport à la substance grise | rel=r_associated | relid=0 | w=10
  5824. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> lésion
    n1=méningé (syndrome) | n2=lésion | rel=r_associated | relid=0 | w=10
  5825. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> lipome
    n1=méningé (syndrome) | n2=lipome | rel=r_associated | relid=0 | w=10
  5826. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> maladie neurologique
    n1=méningé (syndrome) | n2=maladie neurologique | rel=r_associated | relid=0 | w=10
  5827. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> masse
    n1=méningé (syndrome) | n2=masse | rel=r_associated | relid=0 | w=10
  5828. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> masse
    (médecine)
    n1=méningé (syndrome) | n2=masse
    (médecine)
    | rel=r_associated | relid=0 | w=10
  5829. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> Médecine
    n1=méningé (syndrome) | n2=Médecine | rel=r_associated | relid=0 | w=10
  5830. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> membrane
    (anatomie)
    n1=méningé (syndrome) | n2=membrane
    (anatomie)
    | rel=r_associated | relid=0 | w=10
  5831. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> membranes
    n1=méningé (syndrome) | n2=membranes | rel=r_associated | relid=0 | w=10
  5832. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> membranes autour du cerveau
    n1=méningé (syndrome) | n2=membranes autour du cerveau | rel=r_associated | relid=0 | w=10
  5833. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningés
    n1=méningé (syndrome) | n2=méningés | rel=r_associated | relid=0 | w=10
  5834. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome à cellules claires
    n1=méningé (syndrome) | n2=méningiome à cellules claires | rel=r_associated | relid=0 | w=10
  5835. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome à double composante
    n1=méningé (syndrome) | n2=méningiome à double composante | rel=r_associated | relid=0 | w=10
  5836. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome anaplasique
    n1=méningé (syndrome) | n2=méningiome anaplasique | rel=r_associated | relid=0 | w=10
  5837. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome angioblastique
    n1=méningé (syndrome) | n2=méningiome angioblastique | rel=r_associated | relid=0 | w=10
  5838. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome angioblastique (obs)
    n1=méningé (syndrome) | n2=méningiome angioblastique (obs) | rel=r_associated | relid=0 | w=10
  5839. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome bénin
    n1=méningé (syndrome) | n2=méningiome bénin | rel=r_associated | relid=0 | w=10
  5840. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome bénin, sai
    n1=méningé (syndrome) | n2=méningiome bénin, sai | rel=r_associated | relid=0 | w=10
  5841. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome de l'aile du sphénoïde
    n1=méningé (syndrome) | n2=méningiome de l'aile du sphénoïde | rel=r_associated | relid=0 | w=10
  5842. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome de la colonne vertébrale
    n1=méningé (syndrome) | n2=méningiome de la colonne vertébrale | rel=r_associated | relid=0 | w=10
  5843. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome de la convexité cérébrale
    n1=méningé (syndrome) | n2=méningiome de la convexité cérébrale | rel=r_associated | relid=0 | w=10
  5844. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome de la fosse postérieure
    n1=méningé (syndrome) | n2=méningiome de la fosse postérieure | rel=r_associated | relid=0 | w=10
  5845. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome de la gaine du nerf optique
    n1=méningé (syndrome) | n2=méningiome de la gaine du nerf optique | rel=r_associated | relid=0 | w=10
  5846. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome de la grande aile du sphénoïde
    n1=méningé (syndrome) | n2=méningiome de la grande aile du sphénoïde | rel=r_associated | relid=0 | w=10
  5847. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome de la petite aile du sphénoïde
    n1=méningé (syndrome) | n2=méningiome de la petite aile du sphénoïde | rel=r_associated | relid=0 | w=10
  5848. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome du sillon olfactif
    n1=méningé (syndrome) | n2=méningiome du sillon olfactif | rel=r_associated | relid=0 | w=10
  5849. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome endothélial
    n1=méningé (syndrome) | n2=méningiome endothélial | rel=r_associated | relid=0 | w=10
  5850. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome fibreux
    n1=méningé (syndrome) | n2=méningiome fibreux | rel=r_associated | relid=0 | w=10
  5851. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome fibroblastique
    n1=méningé (syndrome) | n2=méningiome fibroblastique | rel=r_associated | relid=0 | w=10
  5852. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome hémangioblastique
    n1=méningé (syndrome) | n2=méningiome hémangioblastique | rel=r_associated | relid=0 | w=10
  5853. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome hémangioblastique (obs)
    n1=méningé (syndrome) | n2=méningiome hémangioblastique (obs) | rel=r_associated | relid=0 | w=10
  5854. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome intra-orbitaire
    n1=méningé (syndrome) | n2=méningiome intra-orbitaire | rel=r_associated | relid=0 | w=10
  5855. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome intracrânien
    n1=méningé (syndrome) | n2=méningiome intracrânien | rel=r_associated | relid=0 | w=10
  5856. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome intraorbitaire
    n1=méningé (syndrome) | n2=méningiome intraorbitaire | rel=r_associated | relid=0 | w=10
  5857. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome intraventriculaire
    n1=méningé (syndrome) | n2=méningiome intraventriculaire | rel=r_associated | relid=0 | w=10
  5858. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome malin
    n1=méningé (syndrome) | n2=méningiome malin | rel=r_associated | relid=0 | w=10
  5859. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome méningothélial
    n1=méningé (syndrome) | n2=méningiome méningothélial | rel=r_associated | relid=0 | w=10
  5860. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome métaplasique
    n1=méningé (syndrome) | n2=méningiome métaplasique | rel=r_associated | relid=0 | w=10
  5861. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome microkystique
    n1=méningé (syndrome) | n2=méningiome microkystique | rel=r_associated | relid=0 | w=10
  5862. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome mixte
    n1=méningé (syndrome) | n2=méningiome mixte | rel=r_associated | relid=0 | w=10
  5863. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome papillaire
    n1=méningé (syndrome) | n2=méningiome papillaire | rel=r_associated | relid=0 | w=10
  5864. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome parasagittal
    n1=méningé (syndrome) | n2=méningiome parasagittal | rel=r_associated | relid=0 | w=10
  5865. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome psammomateux
    n1=méningé (syndrome) | n2=méningiome psammomateux | rel=r_associated | relid=0 | w=10
  5866. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome riche en lymphoplasmacytes
    n1=méningé (syndrome) | n2=méningiome riche en lymphoplasmacytes | rel=r_associated | relid=0 | w=10
  5867. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome sécrétoire
    n1=méningé (syndrome) | n2=méningiome sécrétoire | rel=r_associated | relid=0 | w=10
  5868. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome secrétoire
    n1=méningé (syndrome) | n2=méningiome secrétoire | rel=r_associated | relid=0 | w=10
  5869. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome spinal
    n1=méningé (syndrome) | n2=méningiome spinal | rel=r_associated | relid=0 | w=10
  5870. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome syncytial
    n1=méningé (syndrome) | n2=méningiome syncytial | rel=r_associated | relid=0 | w=10
  5871. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome transitionnel
    n1=méningé (syndrome) | n2=méningiome transitionnel | rel=r_associated | relid=0 | w=10
  5872. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome xanthomateux
    n1=méningé (syndrome) | n2=méningiome xanthomateux | rel=r_associated | relid=0 | w=10
  5873. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiome, sai
    n1=méningé (syndrome) | n2=méningiome, sai | rel=r_associated | relid=0 | w=10
  5874. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiomes bénins
    n1=méningé (syndrome) | n2=méningiomes bénins | rel=r_associated | relid=0 | w=10
  5875. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiomes malins
    n1=méningé (syndrome) | n2=méningiomes malins | rel=r_associated | relid=0 | w=10
  5876. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiomes méningothéliaux
    n1=méningé (syndrome) | n2=méningiomes méningothéliaux | rel=r_associated | relid=0 | w=10
  5877. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiomes parasagittaux
    n1=méningé (syndrome) | n2=méningiomes parasagittaux | rel=r_associated | relid=0 | w=10
  5878. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningiomes spinaux
    n1=méningé (syndrome) | n2=méningiomes spinaux | rel=r_associated | relid=0 | w=10
  5879. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> méningothéliome
    n1=méningé (syndrome) | n2=méningothéliome | rel=r_associated | relid=0 | w=10
  5880. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> nerf optique
    n1=méningé (syndrome) | n2=nerf optique | rel=r_associated | relid=0 | w=10
  5881. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> nerfs
    n1=méningé (syndrome) | n2=nerfs | rel=r_associated | relid=0 | w=10
  5882. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> neurofibromatose de type 2
    n1=méningé (syndrome) | n2=neurofibromatose de type 2 | rel=r_associated | relid=0 | w=10
  5883. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> névraxe
    n1=méningé (syndrome) | n2=névraxe | rel=r_associated | relid=0 | w=10
  5884. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> opération
    n1=méningé (syndrome) | n2=opération | rel=r_associated | relid=0 | w=10
  5885. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> opération
    (intervention chirurgicale)
    n1=méningé (syndrome) | n2=opération
    (intervention chirurgicale)
    | rel=r_associated | relid=0 | w=10
  5886. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> phacomatose
    n1=méningé (syndrome) | n2=phacomatose | rel=r_associated | relid=0 | w=10
  5887. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> prise de contraste
    n1=méningé (syndrome) | n2=prise de contraste | rel=r_associated | relid=0 | w=10
  5888. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> psammome méningé
    n1=méningé (syndrome) | n2=psammome méningé | rel=r_associated | relid=0 | w=10
  5889. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> pseudo-méningite
    n1=méningé (syndrome) | n2=pseudo-méningite | rel=r_associated | relid=0 | w=10
  5890. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> quatrième ventricule (tumeur du)
    n1=méningé (syndrome) | n2=quatrième ventricule (tumeur du) | rel=r_associated | relid=0 | w=10
  5891. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> réaction de type méningite
    n1=méningé (syndrome) | n2=réaction de type méningite | rel=r_associated | relid=0 | w=10
  5892. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> rehaussement
    n1=méningé (syndrome) | n2=rehaussement | rel=r_associated | relid=0 | w=10
  5893. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> rehaussement
    (médecine)
    n1=méningé (syndrome) | n2=rehaussement
    (médecine)
    | rel=r_associated | relid=0 | w=10
  5894. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> revêtement
    n1=méningé (syndrome) | n2=revêtement | rel=r_associated | relid=0 | w=10
  5895. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> sarcome
    n1=méningé (syndrome) | n2=sarcome | rel=r_associated | relid=0 | w=10
  5896. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> sarcome leptoméningé
    n1=méningé (syndrome) | n2=sarcome leptoméningé | rel=r_associated | relid=0 | w=10
  5897. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> sarcome méningé
    n1=méningé (syndrome) | n2=sarcome méningé | rel=r_associated | relid=0 | w=10
  5898. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> sarcome méningothélial
    n1=méningé (syndrome) | n2=sarcome méningothélial | rel=r_associated | relid=0 | w=10
  5899. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> sarcome primitif des méninges
    n1=méningé (syndrome) | n2=sarcome primitif des méninges | rel=r_associated | relid=0 | w=10
  5900. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> scanner
    n1=méningé (syndrome) | n2=scanner | rel=r_associated | relid=0 | w=10
  5901. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> scanner
    (médecine)
    n1=méningé (syndrome) | n2=scanner
    (médecine)
    | rel=r_associated | relid=0 | w=10
  5902. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> se trouver
    n1=méningé (syndrome) | n2=se trouver | rel=r_associated | relid=0 | w=10
  5903. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> se trouver dans
    n1=méningé (syndrome) | n2=se trouver dans | rel=r_associated | relid=0 | w=10
  5904. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> SNC
    n1=méningé (syndrome) | n2=SNC | rel=r_associated | relid=0 | w=10
  5905. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> syndrome de Dupré
    n1=méningé (syndrome) | n2=syndrome de Dupré | rel=r_associated | relid=0 | w=10
  5906. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> syndrome de dupré
    n1=méningé (syndrome) | n2=syndrome de dupré | rel=r_associated | relid=0 | w=10
  5907. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> syndrome de Foster-Kennedy
    n1=méningé (syndrome) | n2=syndrome de Foster-Kennedy | rel=r_associated | relid=0 | w=10
  5908. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> syndrome méningé
    n1=méningé (syndrome) | n2=syndrome méningé | rel=r_associated | relid=0 | w=10
  5909. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> syndromes méningés
    n1=méningé (syndrome) | n2=syndromes méningés | rel=r_associated | relid=0 | w=10
  5910. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tête
    n1=méningé (syndrome) | n2=tête | rel=r_associated | relid=0 | w=10
  5911. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> trabécule arachnoïdienne
    n1=méningé (syndrome) | n2=trabécule arachnoïdienne | rel=r_associated | relid=0 | w=10
  5912. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur bénigne
    n1=méningé (syndrome) | n2=tumeur bénigne | rel=r_associated | relid=0 | w=10
  5913. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur bénigne de la moelle épinière
    n1=méningé (syndrome) | n2=tumeur bénigne de la moelle épinière | rel=r_associated | relid=0 | w=10
  5914. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur bénigne des méninges
    n1=méningé (syndrome) | n2=tumeur bénigne des méninges | rel=r_associated | relid=0 | w=10
  5915. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur bénigne du cerveau
    n1=méningé (syndrome) | n2=tumeur bénigne du cerveau | rel=r_associated | relid=0 | w=10
  5916. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur bénigne du système nerveux
    n1=méningé (syndrome) | n2=tumeur bénigne du système nerveux | rel=r_associated | relid=0 | w=10
  5917. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur bénigne du système nerveux central
    n1=méningé (syndrome) | n2=tumeur bénigne du système nerveux central | rel=r_associated | relid=0 | w=10
  5918. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur cérébrale
    n1=méningé (syndrome) | n2=tumeur cérébrale | rel=r_associated | relid=0 | w=10
  5919. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur cérébrale bénigne
    n1=méningé (syndrome) | n2=tumeur cérébrale bénigne | rel=r_associated | relid=0 | w=10
  5920. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur de la faux du cerveau
    n1=méningé (syndrome) | n2=tumeur de la faux du cerveau | rel=r_associated | relid=0 | w=10
  5921. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur de la moelle épinière
    n1=méningé (syndrome) | n2=tumeur de la moelle épinière | rel=r_associated | relid=0 | w=10
  5922. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur des méninges
    n1=méningé (syndrome) | n2=tumeur des méninges | rel=r_associated | relid=0 | w=10
  5923. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur du cerveau
    n1=méningé (syndrome) | n2=tumeur du cerveau | rel=r_associated | relid=0 | w=10
  5924. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur du système nerveux
    n1=méningé (syndrome) | n2=tumeur du système nerveux | rel=r_associated | relid=0 | w=10
  5925. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur du système nerveux central
    n1=méningé (syndrome) | n2=tumeur du système nerveux central | rel=r_associated | relid=0 | w=10
  5926. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur extra axiale
    n1=méningé (syndrome) | n2=tumeur extra axiale | rel=r_associated | relid=0 | w=10
  5927. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur extra-axiale
    n1=méningé (syndrome) | n2=tumeur extra-axiale | rel=r_associated | relid=0 | w=10
  5928. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur intra-crânienne
    n1=méningé (syndrome) | n2=tumeur intra-crânienne | rel=r_associated | relid=0 | w=10
  5929. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur intracrânienne
    n1=méningé (syndrome) | n2=tumeur intracrânienne | rel=r_associated | relid=0 | w=10
  5930. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur maligne
    n1=méningé (syndrome) | n2=tumeur maligne | rel=r_associated | relid=0 | w=10
  5931. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeur maligne du système nerveux central
    n1=méningé (syndrome) | n2=tumeur maligne du système nerveux central | rel=r_associated | relid=0 | w=10
  5932. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeurs bénignes des méninges
    n1=méningé (syndrome) | n2=tumeurs bénignes des méninges | rel=r_associated | relid=0 | w=10
  5933. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeurs cérébrales
    n1=méningé (syndrome) | n2=tumeurs cérébrales | rel=r_associated | relid=0 | w=10
  5934. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeurs des méninges
    n1=méningé (syndrome) | n2=tumeurs des méninges | rel=r_associated | relid=0 | w=10
  5935. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> tumeurs méningées bénignes
    n1=méningé (syndrome) | n2=tumeurs méningées bénignes | rel=r_associated | relid=0 | w=10
  5936. méningé (syndrome) -- r_associated #0: 10 / 0.12 -> vaisseau sanguin
    n1=méningé (syndrome) | n2=vaisseau sanguin | rel=r_associated | relid=0 | w=10
  5937. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> cellule arachnoïdienne
    n1=méningé (syndrome) | n2=cellule arachnoïdienne | rel=r_associated | relid=0 | w=5
  5938. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> cervelet
    n1=méningé (syndrome) | n2=cervelet | rel=r_associated | relid=0 | w=5
  5939. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> cortex
    n1=méningé (syndrome) | n2=cortex | rel=r_associated | relid=0 | w=5
  5940. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> Cuisine
    n1=méningé (syndrome) | n2=Cuisine | rel=r_associated | relid=0 | w=5
  5941. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> dirigeant
    n1=méningé (syndrome) | n2=dirigeant | rel=r_associated | relid=0 | w=5
  5942. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:angiomatous
    n1=méningé (syndrome) | n2=en:angiomatous | rel=r_associated | relid=0 | w=5
  5943. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:arachnida
    n1=méningé (syndrome) | n2=en:arachnida | rel=r_associated | relid=0 | w=5
  5944. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:arachnoid
    n1=méningé (syndrome) | n2=en:arachnoid | rel=r_associated | relid=0 | w=5
  5945. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:arachnoidea
    n1=méningé (syndrome) | n2=en:arachnoidea | rel=r_associated | relid=0 | w=5
  5946. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:arachnoidea mater
    n1=méningé (syndrome) | n2=en:arachnoidea mater | rel=r_associated | relid=0 | w=5
  5947. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:benign dermal schwannoma
    n1=méningé (syndrome) | n2=en:benign dermal schwannoma | rel=r_associated | relid=0 | w=5
  5948. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:cutaneous ganglioneuroma
    n1=méningé (syndrome) | n2=en:cutaneous ganglioneuroma | rel=r_associated | relid=0 | w=5
  5949. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:cutaneous granular cell tumor
    n1=méningé (syndrome) | n2=en:cutaneous granular cell tumor | rel=r_associated | relid=0 | w=5
  5950. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:cutaneous neurofibroma
    n1=méningé (syndrome) | n2=en:cutaneous neurofibroma | rel=r_associated | relid=0 | w=5
  5951. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:cutaneous neuroma
    n1=méningé (syndrome) | n2=en:cutaneous neuroma | rel=r_associated | relid=0 | w=5
  5952. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:dermal nerve sheath myxoma
    n1=méningé (syndrome) | n2=en:dermal nerve sheath myxoma | rel=r_associated | relid=0 | w=5
  5953. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:medicine
    n1=méningé (syndrome) | n2=en:medicine | rel=r_associated | relid=0 | w=5
  5954. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:meninx serosa
    n1=méningé (syndrome) | n2=en:meninx serosa | rel=r_associated | relid=0 | w=5
  5955. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> en:peripheral primitive neuroectodermal tumor
    n1=méningé (syndrome) | n2=en:peripheral primitive neuroectodermal tumor | rel=r_associated | relid=0 | w=5
  5956. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> espace sous-arachnoïdien
    n1=méningé (syndrome) | n2=espace sous-arachnoïdien | rel=r_associated | relid=0 | w=5
  5957. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> figuré
    n1=méningé (syndrome) | n2=figuré | rel=r_associated | relid=0 | w=5
  5958. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> foramen
    n1=méningé (syndrome) | n2=foramen | rel=r_associated | relid=0 | w=5
  5959. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> oeil
    n1=méningé (syndrome) | n2=oeil | rel=r_associated | relid=0 | w=5
  5960. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> ophtalmologie
    n1=méningé (syndrome) | n2=ophtalmologie | rel=r_associated | relid=0 | w=5
  5961. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> péjoratif
    n1=méningé (syndrome) | n2=péjoratif | rel=r_associated | relid=0 | w=5
  5962. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> plat
    n1=méningé (syndrome) | n2=plat | rel=r_associated | relid=0 | w=5
  5963. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> tête pensante
    n1=méningé (syndrome) | n2=tête pensante | rel=r_associated | relid=0 | w=5
  5964. méningé (syndrome) -- r_associated #0: 5 / 0.06 -> tissu
    n1=méningé (syndrome) | n2=tissu | rel=r_associated | relid=0 | w=5
≈ 2392 relations entrantes

  1. méningiomes --- r_associated #0: 75 --> méningé (syndrome)
    n1=méningiomes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=75
  2. chirurgie --- r_associated #0: 72 --> méningé (syndrome)
    n1=chirurgie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=72
  3. en:angiomatous meningioma --- r_associated #0: 70 --> méningé (syndrome)
    n1=en:angiomatous meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=70
  4. en:meningioma --- r_associated #0: 57 --> méningé (syndrome)
    n1=en:meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=57
  5. méningiome --- r_associated #0: 55 --> méningé (syndrome)
    n1=méningiome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=55
  6. méningiome angiomateux --- r_associated #0: 45 --> méningé (syndrome)
    n1=méningiome angiomateux | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=45
  7. Méningiomes --- r_associated #0: 36 --> méningé (syndrome)
    n1=Méningiomes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=36
  8. Méningite --- r_associated #0: 35 --> méningé (syndrome)
    n1=Méningite | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=35
  9. en:meningitis --- r_associated #0: 35 --> méningé (syndrome)
    n1=en:meningitis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=35
  10. méningite --- r_associated #0: 35 --> méningé (syndrome)
    n1=méningite | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=35
  11. méningite cérébrospinale épidémique --- r_associated #0: 35 --> méningé (syndrome)
    n1=méningite cérébrospinale épidémique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=35
  12. en:epidemic cerebrospinal meningitis --- r_associated #0: 32 --> méningé (syndrome)
    n1=en:epidemic cerebrospinal meningitis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=32
  13. Brudzi?ski (signe de) --- r_associated #0: 30 --> méningé (syndrome)
    n1=Brudzi?ski (signe de) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=30
  14. Kernig (signe de) --- r_associated #0: 30 --> méningé (syndrome)
    n1=Kernig (signe de) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=30
  15. en:meningeal syndrome --- r_associated #0: 29 --> méningé (syndrome)
    n1=en:meningeal syndrome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=29
  16. arachnoïde --- r_associated #0: 26 --> méningé (syndrome)
    n1=arachnoïde | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=26
  17. en:arachnoid mater --- r_associated #0: 25 --> méningé (syndrome)
    n1=en:arachnoid mater | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=25
  18. maladie de trousseau --- r_associated #0: 25 --> méningé (syndrome)
    n1=maladie de trousseau | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=25
  19. neuralgie trigéminale --- r_associated #0: 25 --> méningé (syndrome)
    n1=neuralgie trigéminale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=25
  20. névralgie du nerf trijumeau --- r_associated #0: 25 --> méningé (syndrome)
    n1=névralgie du nerf trijumeau | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=25
  21. tics douloureux de la face --- r_associated #0: 25 --> méningé (syndrome)
    n1=tics douloureux de la face | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=25
  22. méninge arachnoïdienne --- r_associated #0: 22 --> méningé (syndrome)
    n1=méninge arachnoïdienne | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=22
  23. signe de Kernig --- r_associated #0: 22 --> méningé (syndrome)
    n1=signe de Kernig | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=22
  24. Méninges --- r_associated #0: 20 --> méningé (syndrome)
    n1=Méninges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  25. Spécialités médicales --- r_associated #0: 20 --> méningé (syndrome)
    n1=Spécialités médicales | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  26. anatomie --- r_associated #0: 20 --> méningé (syndrome)
    n1=anatomie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  27. ataxie appendiculaire --- r_associated #0: 20 --> méningé (syndrome)
    n1=ataxie appendiculaire | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  28. cancer --- r_associated #0: 20 --> méningé (syndrome)
    n1=cancer | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  29. cancérologie --- r_associated #0: 20 --> méningé (syndrome)
    n1=cancérologie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  30. carcinologie --- r_associated #0: 20 --> méningé (syndrome)
    n1=carcinologie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  31. carcinologie
    (oncologie)
     --- r_associated #0: 20 --> méningé (syndrome)
    n1=carcinologie
    (oncologie)
    | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  32. cerveau --- r_associated #0: 20 --> méningé (syndrome)
    n1=cerveau | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  33. en:'ballooned' neurons with autofluorescent fine granular material --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:'ballooned' neurons with autofluorescent fine granular material | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  34. en:'dragonfly' pattern on imaging --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:'dragonfly' pattern on imaging | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  35. en:'eye of the tiger' sign on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:'eye of the tiger' sign on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  36. en:'globoid multinucleated cells' in brain tissue --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:'globoid multinucleated cells' in brain tissue | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  37. en:'spheroid' inclusions in axons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:'spheroid' inclusions in axons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  38. en:3-4 hz slow sharp waves seen on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:3-4 hz slow sharp waves seen on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  39. en:3-6 hz polyspike eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:3-6 hz polyspike eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  40. en:abducens nerve palsy (cn vi) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abducens nerve palsy (cn vi) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  41. en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  42. en:abnormal cell orientation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal cell orientation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  43. en:abnormal cortical lamination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal cortical lamination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  44. en:abnormal cortical layering --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal cortical layering | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  45. en:abnormal corticospinal tract decussation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal corticospinal tract decussation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  46. en:abnormal eeg (abnormal slowing of background activity) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal eeg (abnormal slowing of background activity) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  47. en:abnormal eeg (poor alpha rhythms) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal eeg (poor alpha rhythms) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  48. en:abnormal eeg with epileptiform changes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal eeg with epileptiform changes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  49. en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  50. en:abnormal gyral pattern --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal gyral pattern | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  51. en:abnormal gyri (in 1 of 2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal gyri (in 1 of 2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  52. en:abnormal involuntary movement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal involuntary movement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  53. en:abnormal lower motor neuron morphology --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal lower motor neuron morphology | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  54. en:abnormal myelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal myelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  55. en:abnormal ocular motility --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal ocular motility | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  56. en:abnormal primitive reflexes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal primitive reflexes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  57. en:abnormal rapid eye movement sleep --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal rapid eye movement sleep | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  58. en:abnormal septum pellucidum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal septum pellucidum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  59. en:abnormal signals in the thalami seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal signals in the thalami seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  60. en:abnormal sleep pattern --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal sleep pattern | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  61. en:abnormal spike waves --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal spike waves | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  62. en:abnormal t2-weighted signals in the occipital white and gray matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal t2-weighted signals in the occipital white and gray matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  63. en:abnormal visual evoked potential --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormal visual evoked potential | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  64. en:abnormality of brainstem morphology --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormality of brainstem morphology | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  65. en:abnormality of ocular smooth pursuit --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormality of ocular smooth pursuit | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  66. en:abnormality of the corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormality of the corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  67. en:abnormality of the posterior cranial fossa --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:abnormality of the posterior cranial fossa | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  68. en:absence of balloon cells (in type iia) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of balloon cells (in type iia) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  69. en:absence of lower motor neuron involvement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of lower motor neuron involvement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  70. en:absence of myelin in the posterior column of the spinal cord (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of myelin in the posterior column of the spinal cord (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  71. en:absence of neuropathologic findings in the brainstem and anterior horn cells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of neuropathologic findings in the brainstem and anterior horn cells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  72. en:absence of septum pellucidum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of septum pellucidum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  73. en:absence of the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  74. en:absence of the cerebellar vermis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of the cerebellar vermis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  75. en:absence of the inferior olives --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of the inferior olives | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  76. en:absence of the olfactory bulbs and tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of the olfactory bulbs and tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  77. en:absence of transverse pontine fibers --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence of transverse pontine fibers | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  78. en:absence or atrophy of the putamen --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence or atrophy of the putamen | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  79. en:absence seizures (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absence seizures (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  80. en:absent cisterna magna --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absent cisterna magna | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  81. en:absent development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absent development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  82. en:absent olfactory bulbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absent olfactory bulbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  83. en:absent olfactory tract or bulbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absent olfactory tract or bulbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  84. en:absent optic nerves, chiasm, and tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absent optic nerves, chiasm, and tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  85. en:absent or limited speech development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absent or limited speech development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  86. en:absent or poor expressive speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absent or poor expressive speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  87. en:absent pituitary --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absent pituitary | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  88. en:absent primitive reflexes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:absent primitive reflexes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  89. en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  90. en:action myoclonus (triggered by voluntary movements) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:action myoclonus (triggered by voluntary movements) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  91. en:acute cerebrovascular accidents --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:acute cerebrovascular accidents | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  92. en:acute encephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:acute encephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  93. en:acute episodes of neuropathic symptoms --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:acute episodes of neuropathic symptoms | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  94. en:acute episodes of neuropathic symptoms (hcp) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:acute episodes of neuropathic symptoms (hcp) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  95. en:adult grade i meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:adult grade i meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  96. en:adult meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:adult meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  97. en:affected arteries show loss of smooth muscle cells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:affected arteries show loss of smooth muscle cells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  98. en:affected children are unable to sit without support --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:affected children are unable to sit without support | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  99. en:agenesis of pineal gland --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agenesis of pineal gland | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  100. en:agenesis of the corpus callosum (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agenesis of the corpus callosum (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  101. en:agenesis of the corpus callosum (in 1 of 2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agenesis of the corpus callosum (in 1 of 2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  102. en:agenesis of the corpus callosum (in 2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agenesis of the corpus callosum (in 2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  103. en:agenesis of the corpus callosum (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agenesis of the corpus callosum (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  104. en:agenesis of the corpus callosum (variable) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agenesis of the corpus callosum (variable) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  105. en:agenesis of the occipital lobes (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agenesis of the occipital lobes (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  106. en:agenesis or severe hypoplasia of cerebellar vermis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agenesis or severe hypoplasia of cerebellar vermis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  107. en:agitation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agitation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  108. en:agyria (posterior-to-anterior gradient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agyria (posterior-to-anterior gradient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  109. en:agyria (wws) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:agyria (wws) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  110. en:alobar holoprosencephaly (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:alobar holoprosencephaly (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  111. en:alpha-synuclein-containing inclusions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:alpha-synuclein-containing inclusions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  112. en:alpha-synuclein-immunoreactive lewy neurites --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:alpha-synuclein-immunoreactive lewy neurites | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  113. en:alzheimer disease, early onset --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:alzheimer disease, early onset | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  114. en:alzheimer's disease --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:alzheimer's disease | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  115. en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  116. en:amyotrophy, distal, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:amyotrophy, distal, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  117. en:anaplastic (malignant) meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anaplastic (malignant) meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  118. en:angiitis, cerebral --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:angiitis, cerebral | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  119. en:angiographically 'silent' --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:angiographically 'silent' | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  120. en:angulation of the frontal horns --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:angulation of the frontal horns | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  121. en:anisocoria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anisocoria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  122. en:ankle clonus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ankle clonus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  123. en:ankle clonus (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ankle clonus (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  124. en:anomalies of the temporal area --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anomalies of the temporal area | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  125. en:anosmia (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anosmia (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  126. en:anosmia (in contiguous gene syndrome patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anosmia (in contiguous gene syndrome patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  127. en:antenatal intracerebral hemorrhage --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:antenatal intracerebral hemorrhage | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  128. en:anterior basal encephalocele --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anterior basal encephalocele | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  129. en:anterior horn atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anterior horn atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  130. en:anterior horn cell impairment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anterior horn cell impairment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  131. en:anterior pituitary hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anterior pituitary hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  132. en:anterior temporal lobe subcortical cysts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:anterior temporal lobe subcortical cysts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  133. en:aplasia of corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:aplasia of corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  134. en:aplasia of olfactory bulbs, bilateral --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:aplasia of olfactory bulbs, bilateral | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  135. en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  136. en:aplasia of the vermis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:aplasia of the vermis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  137. en:aplasia/hypoplasia of the cerebellar vermis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:aplasia/hypoplasia of the cerebellar vermis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  138. en:aplasia/hypoplasia of the cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:aplasia/hypoplasia of the cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  139. en:aplasia/hypoplasia of the corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:aplasia/hypoplasia of the corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  140. en:appendicular hypertonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:appendicular hypertonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  141. en:apraxia, verbal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:apraxia, verbal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  142. en:arachnoid cysts (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:arachnoid cysts (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  143. en:arachnoid cysts of the cerebellopontine angle (reported in 1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:arachnoid cysts of the cerebellopontine angle (reported in 1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  144. en:arachnoid hemangiomata --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:arachnoid hemangiomata | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  145. en:arachnoidal cysts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:arachnoidal cysts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  146. en:areflexia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:areflexia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  147. en:arhinencephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:arhinencephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  148. en:arnold-chiari malformation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:arnold-chiari malformation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  149. en:arrested hydrocephalus (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:arrested hydrocephalus (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  150. en:articulatory defect --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:articulatory defect | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  151. en:asperger syndrome (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:asperger syndrome (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  152. en:associated with paresthesias and dysesthesias --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:associated with paresthesias and dysesthesias | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  153. en:associated with syringomyelia (186700) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:associated with syringomyelia (186700) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  154. en:astrocytes show reactive changes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:astrocytes show reactive changes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  155. en:astrocytosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:astrocytosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  156. en:asymmetry at onset (74%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:asymmetry at onset (74%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  157. en:asymmetry of symptoms --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:asymmetry of symptoms | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  158. en:ataxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  159. en:ataxia (cvs+) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia (cvs+) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  160. en:ataxia (deletion patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia (deletion patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  161. en:ataxia (early-onset form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia (early-onset form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  162. en:ataxia (if untreated) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia (if untreated) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  163. en:ataxia (type i and type ii, infantile and juvenile) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia (type i and type ii, infantile and juvenile) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  164. en:ataxia (uncommon) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia (uncommon) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  165. en:ataxia in those who survive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia in those who survive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  166. en:ataxia may develop in middle age (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia may develop in middle age (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  167. en:ataxia with febrile episodes (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia with febrile episodes (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  168. en:ataxia worsens in the dark --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia worsens in the dark | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  169. en:ataxia, cerebellar (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia, cerebellar (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  170. en:ataxia, episodic, occurring after febrile illness or stress --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia, episodic, occurring after febrile illness or stress | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  171. en:ataxia, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxia, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  172. en:ataxias, appendicular --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxias, appendicular | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  173. en:ataxias, truncal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxias, truncal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  174. en:ataxic gait (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxic gait (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  175. en:ataxic gait (juvenile form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxic gait (juvenile form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  176. en:ataxic movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ataxic movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  177. en:athetoid and dystonic hand movements (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:athetoid and dystonic hand movements (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  178. en:athetosis (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:athetosis (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  179. en:atrophic pons (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atrophic pons (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  180. en:atrophy and weakness of limb musculature --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atrophy and weakness of limb musculature | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  181. en:atrophy and weakness of the tongue, jaw, and throat muscles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atrophy and weakness of the tongue, jaw, and throat muscles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  182. en:atrophy of hippocampal dentate gyrus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atrophy of hippocampal dentate gyrus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  183. en:atrophy of pyramids --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atrophy of pyramids | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  184. en:atrophy of the motor cortex in older patients seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atrophy of the motor cortex in older patients seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  185. en:atrophy of the pituitary (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atrophy of the pituitary (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  186. en:atrophy of the pons (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atrophy of the pons (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  187. en:atrophy of the posterior columns and spinocerebellar tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atrophy of the posterior columns and spinocerebellar tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  188. en:attacks characterized by lethargy, incoordination, loss of motor skills --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:attacks characterized by lethargy, incoordination, loss of motor skills | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  189. en:attention deficit disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:attention deficit disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  190. en:atypical absence seizure --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atypical absence seizure | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  191. en:atypical absence, atonic/tonic, or tonic-clonic seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atypical absence, atonic/tonic, or tonic-clonic seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  192. en:atypical meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:atypical meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  193. en:auditory auras --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:auditory auras | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  194. en:aura (in some instances) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:aura (in some instances) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  195. en:aura may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:aura may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  196. en:autism or autistic features --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:autism or autistic features | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  197. en:autofluorescent pigment in microglia and macrophages --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:autofluorescent pigment in microglia and macrophages | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  198. en:automatism --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:automatism | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  199. en:autonomic dysfunction (in patients with hsan2d) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:autonomic dysfunction (in patients with hsan2d) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  200. en:autonomic dysregulation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:autonomic dysregulation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  201. en:autonomic features may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:autonomic features may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  202. en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  203. en:autonomic involvement may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:autonomic involvement may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  204. en:autonomic manifestations --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:autonomic manifestations | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  205. en:autonomic signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:autonomic signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  206. en:axial dystonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:axial dystonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  207. en:axial rigidity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:axial rigidity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  208. en:axonal 'spheroid' inclusions in the cns --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:axonal 'spheroid' inclusions in the cns | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  209. en:axonal dystrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:axonal dystrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  210. en:axonal dystrophy (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:axonal dystrophy (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  211. en:axonal loss and gliosis in the corticospinal tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:axonal loss and gliosis in the corticospinal tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  212. en:axonal spheroids --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:axonal spheroids | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  213. en:axonal spheroids in the dorsal column --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:axonal spheroids in the dorsal column | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  214. en:axonal swelling or thickening in the cns --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:axonal swelling or thickening in the cns | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  215. en:back pain --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:back pain | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  216. en:band heterotopia (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:band heterotopia (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  217. en:basal ganglia calcifications (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:basal ganglia calcifications (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  218. en:basal ganglia cysts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:basal ganglia cysts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  219. en:basal ganglia dysfunction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:basal ganglia dysfunction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  220. en:basal ganglia lesions seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:basal ganglia lesions seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  221. en:behavioral variant of frontotemporal dementia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:behavioral variant of frontotemporal dementia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  222. en:benign meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:benign meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  223. en:bilateral calcification of basal ganglia and cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bilateral calcification of basal ganglia and cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  224. en:bilateral convulsive seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bilateral convulsive seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  225. en:bilateral schizencephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bilateral schizencephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  226. en:bilateral striatal necrosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bilateral striatal necrosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  227. en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  228. en:biopsy shows white matter hypomyelination, demyelination, gliosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:biopsy shows white matter hypomyelination, demyelination, gliosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  229. en:blake's pouch (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:blake's pouch (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  230. en:blood supply aspects --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:blood supply aspects | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  231. en:blurring of the gray-white junction (in type iib) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:blurring of the gray-white junction (in type iib) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  232. en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  233. en:borderline intelligence --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:borderline intelligence | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  234. en:brain abscess --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain abscess | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  235. en:brain atrophy (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain atrophy (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  236. en:brain atrophy, particularly of the frontal and temporal lobes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain atrophy, particularly of the frontal and temporal lobes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  237. en:brain calcification (if left untreated) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain calcification (if left untreated) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  238. en:brain circuit --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain circuit | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  239. en:brain edema --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain edema | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  240. en:brain edema following head injury (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain edema following head injury (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  241. en:brain imaging shows cortical atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain imaging shows cortical atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  242. en:brain imaging shows functional defects in the cortical and subcortical motor-related areas of the frontal lobe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain imaging shows functional defects in the cortical and subcortical motor-related areas of the frontal lobe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  243. en:brain injury --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain injury | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  244. en:brain iron accumulation (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain iron accumulation (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  245. en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  246. en:brain mri shows arrest in myelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows arrest in myelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  247. en:brain mri shows cerebellar hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows cerebellar hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  248. en:brain mri shows diffusion abnormalities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows diffusion abnormalities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  249. en:brain mri shows flattening of the ventral pons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows flattening of the ventral pons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  250. en:brain mri shows hyperintensities in the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows hyperintensities in the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  251. en:brain mri shows hypoplastic pituitary --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows hypoplastic pituitary | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  252. en:brain mri shows lesions consistent with epileptic episodes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows lesions consistent with epileptic episodes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  253. en:brain mri shows lesions in the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows lesions in the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  254. en:brain mri shows signal abnormalities in the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows signal abnormalities in the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  255. en:brain mri shows t2-weighted hyperintensities (17%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mri shows t2-weighted hyperintensities (17%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  256. en:brain mrs shows decreased creatine content --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain mrs shows decreased creatine content | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  257. en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  258. en:brain small vessel disease with hemorrhage --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain small vessel disease with hemorrhage | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  259. en:brain stem --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain stem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  260. en:brain stem atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain stem atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  261. en:brain stem atrophy, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brain stem atrophy, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  262. en:brainstem atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brainstem atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  263. en:brainstem concavity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brainstem concavity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  264. en:brainstem hypoplasia (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brainstem hypoplasia (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  265. en:brainstem hypoplasia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brainstem hypoplasia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  266. en:brainstem may show neuronal loss --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brainstem may show neuronal loss | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  267. en:brainstem white matter lesions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brainstem white matter lesions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  268. en:brief involuntary movements of upper extremities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brief involuntary movements of upper extremities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  269. en:brisk knee reflexes (early-on) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brisk knee reflexes (early-on) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  270. en:brisk lower limb reflexes (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brisk lower limb reflexes (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  271. en:brisk reflexes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brisk reflexes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  272. en:brisk reflexes (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brisk reflexes (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  273. en:brisk tendon reflex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:brisk tendon reflex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  274. en:broad gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:broad gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  275. en:broad-based gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:broad-based gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  276. en:broad-based gait (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:broad-based gait (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  277. en:bulbar and upper limb symptoms more severe than lower limb symptoms --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bulbar and upper limb symptoms more severe than lower limb symptoms | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  278. en:bulbar dysfunction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bulbar dysfunction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  279. en:bulbar dysfunction (e.g. dysarthria and dysphagia) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bulbar dysfunction (e.g. dysarthria and dysphagia) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  280. en:bulbar dysfunction (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bulbar dysfunction (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  281. en:bulbar involvement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bulbar involvement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  282. en:bulging of the caudate nuclei --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:bulging of the caudate nuclei | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  283. en:burning or tingling of plantar surface of foot (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:burning or tingling of plantar surface of foot (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  284. en:burst suppression pattern seen on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:burst suppression pattern seen on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  285. en:c3hex, decreased ability to smell --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:c3hex, decreased ability to smell | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  286. en:calcification in the pons and cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:calcification in the pons and cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  287. en:calcification of the amygdala and the amygdala-hippocampal transition area --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:calcification of the amygdala and the amygdala-hippocampal transition area | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  288. en:calcification of the falx --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:calcification of the falx | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  289. en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  290. en:calicification of the falx cerebri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:calicification of the falx cerebri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  291. en:candidal meningitis (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:candidal meningitis (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  292. en:cataplexy often triggered by strong emotions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cataplexy often triggered by strong emotions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  293. en:caudate atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:caudate atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  294. en:cavitating leukoencephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cavitating leukoencephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  295. en:cavum vergae --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cavum vergae | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  296. en:ccerebellar ataxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ccerebellar ataxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  297. en:cell loss and gliosis in the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cell loss and gliosis in the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  298. en:central canal malformation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:central canal malformation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  299. en:central facial nerve paralysis (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:central facial nerve paralysis (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  300. en:central hypotonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:central hypotonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  301. en:central nervous system demyelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:central nervous system demyelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  302. en:central nervous system involvement (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:central nervous system involvement (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  303. en:central nervous system space --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:central nervous system space | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  304. en:cerebellar ataxia (in 1 of 3 families) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar ataxia (in 1 of 3 families) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  305. en:cerebellar ataxia (may be permanent in 50% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar ataxia (may be permanent in 50% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  306. en:cerebellar ataxia during episodes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar ataxia during episodes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  307. en:cerebellar ataxia, gait and stance --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar ataxia, gait and stance | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  308. en:cerebellar ataxia, mild, late-onset --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar ataxia, mild, late-onset | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  309. en:cerebellar ataxia, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar ataxia, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  310. en:cerebellar ataxia, slowly progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar ataxia, slowly progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  311. en:cerebellar atrophy (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  312. en:cerebellar atrophy (especially in the superior cerebellar vermis) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy (especially in the superior cerebellar vermis) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  313. en:cerebellar atrophy (especially of the vermis) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy (especially of the vermis) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  314. en:cerebellar atrophy (in 1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy (in 1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  315. en:cerebellar atrophy (in adulthood) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy (in adulthood) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  316. en:cerebellar atrophy (juvenile form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy (juvenile form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  317. en:cerebellar atrophy in older patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy in older patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  318. en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  319. en:cerebellar atrophy, diffuse, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy, diffuse, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  320. en:cerebellar atrophy, mild (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy, mild (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  321. en:cerebellar atrophy, particularly of the hemispheres --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy, particularly of the hemispheres | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  322. en:cerebellar atrophy, progressive (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar atrophy, progressive (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  323. en:cerebellar calcifications --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar calcifications | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  324. en:cerebellar cell paucity, more marked in vermis than hemispheres --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar cell paucity, more marked in vermis than hemispheres | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  325. en:cerebellar cyst --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar cyst | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  326. en:cerebellar degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  327. en:cerebellar dysfunction, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar dysfunction, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  328. en:cerebellar enlargement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar enlargement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  329. en:cerebellar gangliocytoma manifesting as seizure and tremor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar gangliocytoma manifesting as seizure and tremor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  330. en:cerebellar hemorrhage (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar hemorrhage (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  331. en:cerebellar hypoplasia (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar hypoplasia (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  332. en:cerebellar hypoplasia (male) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar hypoplasia (male) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  333. en:cerebellar hypoplasia (reported in 1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar hypoplasia (reported in 1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  334. en:cerebellar hypoplasia (seen in hhs variant) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar hypoplasia (seen in hhs variant) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  335. en:cerebellar hypoplasia due to enlarged foramen magnum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar hypoplasia due to enlarged foramen magnum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  336. en:cerebellar medulloblastoma (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar medulloblastoma (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  337. en:cerebellar signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  338. en:cerebellar signs (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar signs (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  339. en:cerebellar signs during episodes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar signs during episodes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  340. en:cerebellar signs may develop --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar signs may develop | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  341. en:cerebellar stroke --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar stroke | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  342. en:cerebellar tonsil herniation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar tonsil herniation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  343. en:cerebellar tonsillar herniation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar tonsillar herniation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  344. en:cerebellar vermis aplasia or hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar vermis aplasia or hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  345. en:cerebellar vermis atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar vermis atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  346. en:cerebellar vermis hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar vermis hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  347. en:cerebellar vermis hypoplasia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar vermis hypoplasia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  348. en:cerebellar white matter lesions on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebellar white matter lesions on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  349. en:cerebral and cerebellar atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral and cerebellar atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  350. en:cerebral atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  351. en:cerebral atrophy (in severe cases) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral atrophy (in severe cases) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  352. en:cerebral atrophy, diffuse, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral atrophy, diffuse, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  353. en:cerebral atrophy, frontotemporal, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral atrophy, frontotemporal, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  354. en:cerebral atrophy, generalized mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral atrophy, generalized mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  355. en:cerebral atrophy, mild, diffuse --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral atrophy, mild, diffuse | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  356. en:cerebral atrophy, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral atrophy, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  357. en:cerebral cavernous malformation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral cavernous malformation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  358. en:cerebral convexity meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral convexity meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  359. en:cerebral cortex with spongiform changes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral cortex with spongiform changes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  360. en:cerebral hypomyelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral hypomyelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  361. en:cerebral infarction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral infarction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  362. en:cerebral malformations --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral malformations | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  363. en:cerebral oligogyria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral oligogyria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  364. en:cerebral palsy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral palsy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  365. en:cerebral thrombosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral thrombosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  366. en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  367. en:cerebral vasculitis or vasculopathy (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral vasculitis or vasculopathy (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  368. en:cerebral white matter atrophy, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral white matter atrophy, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  369. en:cerebral white matter lesions (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebral white matter lesions (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  370. en:cerebrovascular accident (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cerebrovascular accident (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  371. en:characteristic arm position with wrist and elbow flexion --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:characteristic arm position with wrist and elbow flexion | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  372. en:characteristic findings on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:characteristic findings on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  373. en:chiari i malformation of the cerebellum (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chiari i malformation of the cerebellum (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  374. en:chiari i malformation on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chiari i malformation on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  375. en:chiari i malformation on mri (some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chiari i malformation on mri (some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  376. en:chiari malformation (uncommon) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chiari malformation (uncommon) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  377. en:chiari type i --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chiari type i | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  378. en:chiari type i malformation (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chiari type i malformation (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  379. en:childhood grade i meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:childhood grade i meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  380. en:childhood meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:childhood meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  381. en:childhood polyphagia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:childhood polyphagia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  382. en:chorea of all limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chorea of all limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  383. en:chorea of hands --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chorea of hands | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  384. en:choreoathetoid movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:choreoathetoid movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  385. en:choreoathetosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:choreoathetosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  386. en:choreoathetosis (2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:choreoathetosis (2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  387. en:choreoathetosis (in a subset of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:choreoathetosis (in a subset of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  388. en:choreoathetosis of the face, trunk, extremities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:choreoathetosis of the face, trunk, extremities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  389. en:choristoma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:choristoma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  390. en:choroid plexus meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:choroid plexus meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  391. en:chronic headaches --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chronic headaches | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  392. en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  393. en:clonus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:clonus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  394. en:closed-lip schizencephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:closed-lip schizencephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  395. en:clumsiness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:clumsiness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  396. en:clumsiness (82%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:clumsiness (82%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  397. en:clumsiness (mild) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:clumsiness (mild) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  398. en:clumsiness in childhood --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:clumsiness in childhood | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  399. en:cns component --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cns component | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  400. en:coarsened pattern of sulci and gyri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:coarsened pattern of sulci and gyri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  401. en:cobblestone lissencephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cobblestone lissencephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  402. en:cobblestone lissencephaly (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cobblestone lissencephaly (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  403. en:cobblestone lissencephaly, type ii --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cobblestone lissencephaly, type ii | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  404. en:cobblestone lissencephaly, type ii (wws) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cobblestone lissencephaly, type ii (wws) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  405. en:cognition is spared --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognition is spared | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  406. en:cognitive decline (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive decline (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  407. en:cognitive decline (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive decline (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  408. en:cognitive decline in adulthood --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive decline in adulthood | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  409. en:cognitive decline in older patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive decline in older patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  410. en:cognitive decline, rapid --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive decline, rapid | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  411. en:cognitive defects in executive function and attention --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive defects in executive function and attention | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  412. en:cognitive delay, mild (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive delay, mild (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  413. en:cognitive delay, mild to severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive delay, mild to severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  414. en:cognitive deterioration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive deterioration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  415. en:cognitive dysfunction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive dysfunction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  416. en:cognitive dysfunction (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive dysfunction (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  417. en:cognitive impairment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive impairment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  418. en:cognitive impairment (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive impairment (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  419. en:cognitive impairment (3 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive impairment (3 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  420. en:cognitive impairment (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive impairment (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  421. en:cognitive impairment, mild (in 2 of 3 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive impairment, mild (in 2 of 3 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  422. en:cognitive impairment, mild to severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive impairment, mild to severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  423. en:cognitive regression, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cognitive regression, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  424. en:cogwheel rigidities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cogwheel rigidities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  425. en:colpocephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:colpocephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  426. en:coma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:coma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  427. en:coma (in up to 33% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:coma (in up to 33% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  428. en:coma (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:coma (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  429. en:complete or partial absence of the corpus callosum (wws) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:complete or partial absence of the corpus callosum (wws) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  430. en:complex motor behavior such as sleep walking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:complex motor behavior such as sleep walking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  431. en:complex partial seizures (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:complex partial seizures (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  432. en:complex partial seizures, often with secondary generalization, are the most common type --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:complex partial seizures, often with secondary generalization, are the most common type | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  433. en:concentration impairment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:concentration impairment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  434. en:confusion, paroxysmal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:confusion, paroxysmal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  435. en:congenital absence of the vermis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:congenital absence of the vermis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  436. en:congenital anomaly of brain --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:congenital anomaly of brain | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  437. en:congenital cerebellar hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:congenital cerebellar hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  438. en:congenital hyperextension of limb --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:congenital hyperextension of limb | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  439. en:congenital hypotonia, axial or generalized --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:congenital hypotonia, axial or generalized | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  440. en:congenital hypotonia, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:congenital hypotonia, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  441. en:convulsions, febrile (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:convulsions, febrile (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  442. en:corprolalia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:corprolalia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  443. en:corpus callosum lipoma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:corpus callosum lipoma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  444. en:corpus callosum, thin (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:corpus callosum, thin (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  445. en:cortical and subcortical hyperintensities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical and subcortical hyperintensities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  446. en:cortical atrophy (43%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical atrophy (43%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  447. en:cortical cytotoxic edema --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical cytotoxic edema | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  448. en:cortical degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  449. en:cortical dysplasia (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical dysplasia (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  450. en:cortical dysplasia (2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical dysplasia (2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  451. en:cortical dysplasia, focal (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical dysplasia, focal (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  452. en:cortical malformations --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical malformations | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  453. en:cortical myoclonic tremors characterized by 8 to 10-hz discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical myoclonic tremors characterized by 8 to 10-hz discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  454. en:cortical origin of the tremor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical origin of the tremor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  455. en:cortical simplification --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical simplification | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  456. en:cortical venous thromboses --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cortical venous thromboses | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  457. en:corticobasal degeneration (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:corticobasal degeneration (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  458. en:corticospinal tract atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:corticospinal tract atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  459. en:corticospinal tracts with decreased myelin staining --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:corticospinal tracts with decreased myelin staining | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  460. en:cranial nerve anomalies --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cranial nerve anomalies | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  461. en:cranial nerve dysfunction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cranial nerve dysfunction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  462. en:cranial nerve palsies can arise with head and neck paragangliomas --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cranial nerve palsies can arise with head and neck paragangliomas | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  463. en:cranial nerve palsy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cranial nerve palsy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  464. en:crawling and standing not achieved --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:crawling and standing not achieved | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  465. en:crowding of the posterior fossa --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:crowding of the posterior fossa | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  466. en:ct scan shows dense calcifications in the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ct scan shows dense calcifications in the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  467. en:cyst of septum pellucidum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cyst of septum pellucidum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  468. en:cyst of septum pellucidum (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cyst of septum pellucidum (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  469. en:cystic cavitation of the white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cystic cavitation of the white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  470. en:cystic degeneration of cerebral white matter with preserved cortex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cystic degeneration of cerebral white matter with preserved cortex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  471. en:cystic degeneration of the white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cystic degeneration of the white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  472. en:cystic lysis of the deep white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cystic lysis of the deep white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  473. en:cysts tend to enlarge with age --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cysts tend to enlarge with age | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  474. en:cytopathic effect --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:cytopathic effect | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  475. en:dandy-walker malformation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dandy-walker malformation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  476. en:dandy-walker malformation (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dandy-walker malformation (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  477. en:dandy-walker malformation (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dandy-walker malformation (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  478. en:dandy-walker malformation (variable) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dandy-walker malformation (variable) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  479. en:dandy-walker malformation (wws) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dandy-walker malformation (wws) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  480. en:decerebrate or decorticate posturing late --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decerebrate or decorticate posturing late | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  481. en:decerebrate posturings --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decerebrate posturings | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  482. en:decrease in abstract thinking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decrease in abstract thinking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  483. en:decreased active movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased active movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  484. en:decreased brain volume (female) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased brain volume (female) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  485. en:decreased brain weight --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased brain weight | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  486. en:decreased core body temperature --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased core body temperature | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  487. en:decreased delineation of the basal ganglia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased delineation of the basal ganglia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  488. en:decreased fine motor coordination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased fine motor coordination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  489. en:decreased iron content in the substantia nigra --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased iron content in the substantia nigra | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  490. en:decreased mitochondrial respiratory chain complex activity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased mitochondrial respiratory chain complex activity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  491. en:decreased motor nerve conduction velocity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased motor nerve conduction velocity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  492. en:decreased myelination seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased myelination seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  493. en:decreased nonverbal iq --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased nonverbal iq | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  494. en:decreased pyramidal cells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased pyramidal cells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  495. en:decreased rapid automatized naming (ran) speed --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased rapid automatized naming (ran) speed | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  496. en:decreased sleep latency --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased sleep latency | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  497. en:decreased somatosensory-evoked potentials --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased somatosensory-evoked potentials | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  498. en:decreased spontaneous movements at birth --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased spontaneous movements at birth | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  499. en:decreased vibratory sense --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreased vibratory sense | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  500. en:decreasing responsiveness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:decreasing responsiveness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  501. en:deep hypointensities (mri, t2) suggestive of past microbleeds --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:deep hypointensities (mri, t2) suggestive of past microbleeds | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  502. en:deep white matter hypodensities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:deep white matter hypodensities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  503. en:defects in visual cue processing --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:defects in visual cue processing | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  504. en:deficit in basic reading --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:deficit in basic reading | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  505. en:deficit in expressive language --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:deficit in expressive language | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  506. en:deficit in reading comprehension --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:deficit in reading comprehension | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  507. en:deficits in abstraction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:deficits in abstraction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  508. en:deficits in language expression --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:deficits in language expression | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  509. en:degeneration of anterior horn cells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:degeneration of anterior horn cells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  510. en:degeneration of purkinje cells in the cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:degeneration of purkinje cells in the cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  511. en:degeneration of the dentatorubral and pallidoluysian systems --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:degeneration of the dentatorubral and pallidoluysian systems | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  512. en:degeneration of the lateral corticospinal tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:degeneration of the lateral corticospinal tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  513. en:deja vu feeling --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:deja vu feeling | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  514. en:delayed ambulation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed ambulation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  515. en:delayed cerebral myelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed cerebral myelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  516. en:delayed cognitive development, mild (reported in 1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed cognitive development, mild (reported in 1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  517. en:delayed cognitive development/learning disabilities (93%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed cognitive development/learning disabilities (93%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  518. en:delayed development (about 25%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed development (about 25%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  519. en:delayed development (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed development (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  520. en:delayed development (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed development (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  521. en:delayed development in early childhood (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed development in early childhood (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  522. en:delayed development, after 8-15 months --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed development, after 8-15 months | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  523. en:delayed development, ranging from mild to severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed development, ranging from mild to severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  524. en:delayed development, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed development, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  525. en:delayed development, variable (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed development, variable (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  526. en:delayed developmental milestones --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed developmental milestones | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  527. en:delayed intellectual development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed intellectual development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  528. en:delayed motor development (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed motor development (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  529. en:delayed motor development due to muscle weakness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed motor development due to muscle weakness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  530. en:delayed motor development, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed motor development, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  531. en:delayed myelination (1/4 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed myelination (1/4 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  532. en:delayed myelination (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed myelination (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  533. en:delayed myelination seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed myelination seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  534. en:delayed myelinization (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed myelinization (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  535. en:delayed onset of phrase speech (> 36 months) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed onset of phrase speech (> 36 months) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  536. en:delayed opercularization --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed opercularization | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  537. en:delayed or absent independent walking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed or absent independent walking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  538. en:delayed psychomotor development (in most patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development (in most patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  539. en:delayed psychomotor development (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  540. en:delayed psychomotor development (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  541. en:delayed psychomotor development (stops at development levels of 1-2 years) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development (stops at development levels of 1-2 years) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  542. en:delayed psychomotor development, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  543. en:delayed psychomotor development, moderate to severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development, moderate to severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  544. en:delayed psychomotor development, profound --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development, profound | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  545. en:delayed psychomotor development, profound (patient a) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development, profound (patient a) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  546. en:delayed psychomotor development, severe (in 2 of 6 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development, severe (in 2 of 6 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  547. en:delayed psychomotor development, severe to profound --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development, severe to profound | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  548. en:delayed psychomotor development, variable --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed psychomotor development, variable | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  549. en:delayed speech and language development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed speech and language development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  550. en:delayed speech development, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed speech development, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  551. en:delayed walking (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delayed walking (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  552. en:deletion of chromosome 3p associated meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:deletion of chromosome 3p associated meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  553. en:delirium (later-onset) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:delirium (later-onset) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  554. en:dementia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dementia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  555. en:dementia (5%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dementia (5%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  556. en:dementia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dementia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  557. en:dementia (later-onset) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dementia (later-onset) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  558. en:dementia (subtype 3a) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dementia (subtype 3a) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  559. en:dementia in a subset of patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dementia in a subset of patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  560. en:dementia of frontal lobe type --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dementia of frontal lobe type | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  561. en:dementia, progressive (more common in males) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dementia, progressive (more common in males) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  562. en:demyelination of the posterior and lateral columns of the spinal cord --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:demyelination of the posterior and lateral columns of the spinal cord | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  563. en:demyelination with white matter disease in internal capsule, external capsule, genu of corpus callosum, subcortical white matter, and posterior fossa --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:demyelination with white matter disease in internal capsule, external capsule, genu of corpus callosum, subcortical white matter, and posterior fossa | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  564. en:demyelination, symmetric --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:demyelination, symmetric | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  565. en:denervation seen on emg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:denervation seen on emg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  566. en:dense calcifications in the cerebellar dentate nucleus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dense calcifications in the cerebellar dentate nucleus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  567. en:depression --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:depression | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  568. en:development varies from normal to retarded --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:development varies from normal to retarded | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  569. en:developmental arrest, 2nd year of life --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental arrest, 2nd year of life | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  570. en:developmental delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  571. en:developmental delay (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  572. en:developmental delay (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  573. en:developmental delay (100%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay (100%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  574. en:developmental delay (20%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay (20%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  575. en:developmental delay (in most patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay (in most patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  576. en:developmental delay (microdeletion patients only) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay (microdeletion patients only) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  577. en:developmental delay (seen in recessive form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay (seen in recessive form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  578. en:developmental delay if undiagnosed or untreated --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay if undiagnosed or untreated | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  579. en:developmental delay or regression --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay or regression | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  580. en:developmental delay, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  581. en:developmental delay, mild to moderate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay, mild to moderate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  582. en:developmental delay, primarily motor, resolves in childhood --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay, primarily motor, resolves in childhood | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  583. en:developmental delay, profound --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay, profound | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  584. en:developmental delay, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  585. en:developmental delay, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  586. en:developmental delay, severe (2p21del) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay, severe (2p21del) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  587. en:developmental delay, significant --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental delay, significant | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  588. en:developmental regression --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental regression | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  589. en:developmental regression (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental regression (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  590. en:developmental regression after onset of seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental regression after onset of seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  591. en:developmental regression after the first year --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental regression after the first year | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  592. en:developmental regression before age 6 months --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental regression before age 6 months | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  593. en:developmental regression in about 50% of patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental regression in about 50% of patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  594. en:developmental regression, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental regression, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  595. en:developmental stagnation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental stagnation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  596. en:developmental stagnation at onset of seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:developmental stagnation at onset of seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  597. en:difficulties in fine movement of the hands --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulties in fine movement of the hands | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  598. en:difficulties with equilibrium --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulties with equilibrium | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  599. en:difficulties with fine motor skills and coordination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulties with fine motor skills and coordination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  600. en:difficulty in phonologic coding --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulty in phonologic coding | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  601. en:difficulty reading --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulty reading | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  602. en:difficulty running --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulty running | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  603. en:difficulty speaking during seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulty speaking during seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  604. en:difficulty standing --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulty standing | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  605. en:difficulty standing alone --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulty standing alone | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  606. en:difficulty walking, running --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulty walking, running | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  607. en:difficulty writing --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:difficulty writing | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  608. en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  609. en:diffuse axonal swelling --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse axonal swelling | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  610. en:diffuse brain and spinal cord atrophy on brain ct/mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse brain and spinal cord atrophy on brain ct/mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  611. en:diffuse cerebral atrophy on ct and mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse cerebral atrophy on ct and mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  612. en:diffuse cerebral atrophy seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse cerebral atrophy seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  613. en:diffuse cerebral gliosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse cerebral gliosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  614. en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  615. en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  616. en:diffuse fibrillar astrocytosis (in type iib) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse fibrillar astrocytosis (in type iib) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  617. en:diffuse hyperintense signal abnormalities in the white matter (in children) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse hyperintense signal abnormalities in the white matter (in children) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  618. en:diffuse hyporeflexia (later) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse hyporeflexia (later) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  619. en:diffuse hypotonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse hypotonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  620. en:diffuse leptomeningeal enhancement seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse leptomeningeal enhancement seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  621. en:diffuse paroxysmal discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse paroxysmal discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  622. en:diffuse signal abnormality of central white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse signal abnormality of central white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  623. en:diffuse white matter dysmyelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse white matter dysmyelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  624. en:diffuse white matter hyperintensities on t2-weighed imaging --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diffuse white matter hyperintensities on t2-weighed imaging | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  625. en:dilatation of the 3rd ventricle (in one family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dilatation of the 3rd ventricle (in one family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  626. en:dilatation of the lateral and third ventricles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dilatation of the lateral and third ventricles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  627. en:dilatation of the lateral ventricles (in one family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dilatation of the lateral ventricles (in one family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  628. en:dilated fourth ventricle --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dilated fourth ventricle | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  629. en:dilated lateral ventricles (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dilated lateral ventricles (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  630. en:dilated venous sinuses --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dilated venous sinuses | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  631. en:disdiadochokinesia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disdiadochokinesia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  632. en:disordered myelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disordered myelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  633. en:disordered sleep pattern (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disordered sleep pattern (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  634. en:disorganized brain cytoarchitecture --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disorganized brain cytoarchitecture | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  635. en:disorganized eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disorganized eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  636. en:disorientation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disorientation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  637. en:disproportionately small cerebral cortex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disproportionately small cerebral cortex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  638. en:distal amyotrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:distal amyotrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  639. en:disturbance of attention --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disturbance of attention | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  640. en:disturbance of consciousness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disturbance of consciousness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  641. en:disturbed gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disturbed gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  642. en:disturbed sleep-wake cycle --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:disturbed sleep-wake cycle | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  643. en:diurnal fluctuations of symptoms (in a subset of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:diurnal fluctuations of symptoms (in a subset of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  644. en:dizziness may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dizziness may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  645. en:double cortex syndrome --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:double cortex syndrome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  646. en:dream enactment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dream enactment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  647. en:drooling --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:drooling | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  648. en:dural and choroid plexus calcifications --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dural and choroid plexus calcifications | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  649. en:dysarthria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  650. en:dysarthria (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthria (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  651. en:dysarthria (74%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthria (74%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  652. en:dysarthria (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthria (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  653. en:dysarthria (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthria (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  654. en:dysarthria (most common presenting symptom) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthria (most common presenting symptom) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  655. en:dysarthria (onset in third decade) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthria (onset in third decade) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  656. en:dysarthria, mild (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthria, mild (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  657. en:dysarthria, slowly progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthria, slowly progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  658. en:dysarthrias, spastic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysarthrias, spastic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  659. en:dysautonomia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysautonomia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  660. en:dyscalculia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dyscalculia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  661. en:dysdiadochokinesis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysdiadochokinesis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  662. en:dysdiadochokinesis (63%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysdiadochokinesis (63%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  663. en:dysfunction of the autonomic nervous system --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysfunction of the autonomic nervous system | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  664. en:dysgenesis of the anterior commissure (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysgenesis of the anterior commissure (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  665. en:dysgenesis or agenesis of the corpus callosum (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysgenesis or agenesis of the corpus callosum (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  666. en:dysgraphias --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysgraphias | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  667. en:dyskinesia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dyskinesia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  668. en:dysmetria (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysmetria (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  669. en:dysmetria (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysmetria (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  670. en:dysmetria (type i) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysmetria (type i) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  671. en:dysmorphic basal ganglia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysmorphic basal ganglia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  672. en:dysmorphic basal ganglia (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysmorphic basal ganglia (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  673. en:dysmyelination of the brain and spinal cord --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysmyelination of the brain and spinal cord | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  674. en:dysphonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysphonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  675. en:dysplasia of the cerebellar hemispheres --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysplasia of the cerebellar hemispheres | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  676. en:dysplastic basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysplastic basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  677. en:dysplastic c-shaped inferior olivary nuclei --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysplastic c-shaped inferior olivary nuclei | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  678. en:dysplastic cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysplastic cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  679. en:dysplastic pons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysplastic pons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  680. en:dysplastic superior cerebellar vermis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dysplastic superior cerebellar vermis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  681. en:dystonia (in 2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonia (in 2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  682. en:dystonia (may spontaneously remit in childhood or adolescence) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonia (may spontaneously remit in childhood or adolescence) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  683. en:dystonia 18 (disorder) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonia 18 (disorder) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  684. en:dystonia with diurnal variation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonia with diurnal variation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  685. en:dystonia, episodic, primary affects hands and feet --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonia, episodic, primary affects hands and feet | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  686. en:dystonia, focal (at onset) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonia, focal (at onset) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  687. en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  688. en:dystonia, generalized, dopa-unresponsive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonia, generalized, dopa-unresponsive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  689. en:dystonia, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonia, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  690. en:dystonic tongue protrusion --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonic tongue protrusion | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  691. en:dystonic vocal tremor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonic vocal tremor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  692. en:dystonic writer's cramp --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystonic writer's cramp | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  693. en:dystrophic neurites --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:dystrophic neurites | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  694. en:earlier sleep-offset time (earlier awakening) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:earlier sleep-offset time (earlier awakening) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  695. en:echolalia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:echolalia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  696. en:ectopic posterior pituitary --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ectopic posterior pituitary | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  697. en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  698. en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  699. en:eeg abnormalities in 20-50% impaired language development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg abnormalities in 20-50% impaired language development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  700. en:eeg is slowed with polyspike wave discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg is slowed with polyspike wave discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  701. en:eeg may be normal at first --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg may be normal at first | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  702. en:eeg may show migrating focal or multifocal origin (in severe cases) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg may show migrating focal or multifocal origin (in severe cases) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  703. en:eeg shows 3-hz spike-wave discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows 3-hz spike-wave discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  704. en:eeg shows epileptiform activity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows epileptiform activity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  705. en:eeg shows epileptiform discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows epileptiform discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  706. en:eeg shows generalized polyspike and wave discharges (4-6 hz) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows generalized polyspike and wave discharges (4-6 hz) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  707. en:eeg shows generalized, bilateral, synchronous, symmetrical discharge --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows generalized, bilateral, synchronous, symmetrical discharge | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  708. en:eeg shows nonspecific slow-wave paroxysms --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows nonspecific slow-wave paroxysms | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  709. en:eeg shows rolandic sharp waves and spikes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows rolandic sharp waves and spikes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  710. en:eeg shows slow frequency high amplitude waves with high frequency polyspikes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows slow frequency high amplitude waves with high frequency polyspikes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  711. en:eeg shows slowed dysrhythmia and multifocal discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows slowed dysrhythmia and multifocal discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  712. en:eeg shows spike and wave or polyspike and wave discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows spike and wave or polyspike and wave discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  713. en:eeg shows suppression with ictal burst activities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows suppression with ictal burst activities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  714. en:eeg shows with a multifocal pattern with spikes and sharp waves --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg shows with a multifocal pattern with spikes and sharp waves | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  715. en:eeg with focal discharge --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eeg with focal discharge | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  716. en:effaced gyral pattern --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:effaced gyral pattern | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  717. en:electrophysiologic studies indicate cortical origin --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:electrophysiologic studies indicate cortical origin | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  718. en:elevated interferon levels in cerebrospinal fluid --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:elevated interferon levels in cerebrospinal fluid | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  719. en:elongated superior cerebellar peduncles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:elongated superior cerebellar peduncles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  720. en:embryologic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:embryologic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  721. en:emg shows bursts of activity originating in the masseter muscle and spreading to the orbicularis oris and oculi muscles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:emg shows bursts of activity originating in the masseter muscle and spreading to the orbicularis oris and oculi muscles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  722. en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  723. en:emg shows involuntary continuous motor activity at rest --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:emg shows involuntary continuous motor activity at rest | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  724. en:emg shows neurogenic changes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:emg shows neurogenic changes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  725. en:emg shows neurogenic changes and denervation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:emg shows neurogenic changes and denervation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  726. en:emg with spontaneous discharge of normal motor unit potentials --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:emg with spontaneous discharge of normal motor unit potentials | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  727. en:encephalitis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalitis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  728. en:encephalocele --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalocele | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  729. en:encephalocele (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalocele (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  730. en:encephalocele (single case) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalocele (single case) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  731. en:encephalocele of orbit --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalocele of orbit | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  732. en:encephaloceles, frontal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephaloceles, frontal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  733. en:encephalomyelopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalomyelopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  734. en:encephalomyopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalomyopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  735. en:encephalopathic episodes, often associated with infection --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalopathic episodes, often associated with infection | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  736. en:encephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  737. en:encephalopathy, acute, sudden-onset during febrile illness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalopathy, acute, sudden-onset during febrile illness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  738. en:encephalopathy, acute-onset --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:encephalopathy, acute-onset | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  739. en:end-position nystagmus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:end-position nystagmus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  740. en:endothelial intracytoplasmic globular inclusions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:endothelial intracytoplasmic globular inclusions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  741. en:enhancement of the c-reflex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:enhancement of the c-reflex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  742. en:enlarged cerebellar cistern --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:enlarged cerebellar cistern | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  743. en:enlarged cisterna magna --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:enlarged cisterna magna | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  744. en:enlarged fourth ventricle, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:enlarged fourth ventricle, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  745. en:enlarged lateral and third ventricles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:enlarged lateral and third ventricles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  746. en:enlarged or prominent ventricles (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:enlarged or prominent ventricles (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  747. en:enlarged ventricles (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:enlarged ventricles (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  748. en:enlarged white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:enlarged white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  749. en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  750. en:epilepsia partialis continua --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:epilepsia partialis continua | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  751. en:epilepsy (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:epilepsy (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  752. en:epilepsy, frontal lobe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:epilepsy, frontal lobe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  753. en:epilepsy, multifocal, intractable --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:epilepsy, multifocal, intractable | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  754. en:epilepsy, myoclonic astatic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:epilepsy, myoclonic astatic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  755. en:epilepsy, refractory (onset in adolescence or young adulthood) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:epilepsy, refractory (onset in adolescence or young adulthood) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  756. en:epileptic encephalopathy with psychomotor retardation (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:epileptic encephalopathy with psychomotor retardation (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  757. en:episodes begin with muscle tightening --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:episodes begin with muscle tightening | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  758. en:episodes last up to 2 minutes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:episodes last up to 2 minutes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  759. en:episodes typically occur several times a week --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:episodes typically occur several times a week | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  760. en:episodic absence-like spells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:episodic absence-like spells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  761. en:episodic confusion --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:episodic confusion | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  762. en:episodic generalized skeletal muscle contractions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:episodic generalized skeletal muscle contractions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  763. en:episodic sudden headache --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:episodic sudden headache | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  764. en:equivocal plantar response --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:equivocal plantar response | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  765. en:essential tremor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:essential tremor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  766. en:exaggerated acoustic startle response --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:exaggerated acoustic startle response | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  767. en:exaggerated moro reflex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:exaggerated moro reflex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  768. en:excessive daytime somnolence --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:excessive daytime somnolence | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  769. en:expressive aphasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:expressive aphasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  770. en:expressive language delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:expressive language delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  771. en:expressive language disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:expressive language disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  772. en:expressive speech deficit --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:expressive speech deficit | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  773. en:extensor plantar responses (early-on) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extensor plantar responses (early-on) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  774. en:extensor plantar responses (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extensor plantar responses (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  775. en:extensor plantar responses (reported in 1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extensor plantar responses (reported in 1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  776. en:extensor posturing --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extensor posturing | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  777. en:external capsule and claustrum may be involved --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:external capsule and claustrum may be involved | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  778. en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  779. en:extrapyramidal disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extrapyramidal disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  780. en:extrapyramidal features --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extrapyramidal features | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  781. en:extrapyramidal muscular rigidity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extrapyramidal muscular rigidity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  782. en:extrapyramidal signs (in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extrapyramidal signs (in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  783. en:extrapyramidal signs (in some patients) thinning of the corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extrapyramidal signs (in some patients) thinning of the corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  784. en:extrapyramidal signs (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extrapyramidal signs (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  785. en:extrapyramidal signs may develop --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extrapyramidal signs may develop | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  786. en:extrapyramidal symptoms may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extrapyramidal symptoms may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  787. en:extremity ataxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:extremity ataxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  788. en:facial muscle weakness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:facial muscle weakness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  789. en:facial myokymia, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:facial myokymia, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  790. en:facial myokymias --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:facial myokymias | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  791. en:facial neuralgia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:facial neuralgia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  792. en:facial palsy secondary to cranial hyperostosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:facial palsy secondary to cranial hyperostosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  793. en:facial paralysis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:facial paralysis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  794. en:facial, pharyngeal, and masticatory muscle diplegia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:facial, pharyngeal, and masticatory muscle diplegia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  795. en:facial-lingual fasciculations --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:facial-lingual fasciculations | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  796. en:fall --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fall | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  797. en:fatal subacute encephalopathy (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fatal subacute encephalopathy (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  798. en:fatigue --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fatigue | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  799. en:febrile seizures (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:febrile seizures (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  800. en:febrile seizures (reported in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:febrile seizures (reported in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  801. en:febrile seizures (usually remit by age 6 years) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:febrile seizures (usually remit by age 6 years) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  802. en:febrile seizures may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:febrile seizures may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  803. en:feeding problem --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:feeding problem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  804. en:fenestrated basilar artery --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fenestrated basilar artery | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  805. en:fibrillary plaques in the cerebellar cortex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fibrillary plaques in the cerebellar cortex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  806. en:fifth ventricle --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fifth ventricle | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  807. en:fine motor delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fine motor delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  808. en:fine motor impairment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fine motor impairment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  809. en:fine tremors --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fine tremors | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  810. en:finger dysmetria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:finger dysmetria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  811. en:first dorsal interossei muscle atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:first dorsal interossei muscle atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  812. en:flaccidity, episodic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:flaccidity, episodic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  813. en:flat pons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:flat pons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  814. en:flattening of the pons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:flattening of the pons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  815. en:floppiness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:floppiness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  816. en:fluctuating neurologic signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fluctuating neurologic signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  817. en:fluid filled posterior fossa --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:fluid filled posterior fossa | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  818. en:focal cortical dysplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal cortical dysplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  819. en:focal discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  820. en:focal dyscognitive seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal dyscognitive seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  821. en:focal dystonia (adult onset) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal dystonia (adult onset) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  822. en:focal dystonia (e.g., writer's cramp) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal dystonia (e.g., writer's cramp) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  823. en:focal dystonia (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal dystonia (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  824. en:focal dystonias --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal dystonias | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  825. en:focal lissencephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal lissencephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  826. en:focal neurologic deficits (i.e., hemiparesis) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal neurologic deficits (i.e., hemiparesis) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  827. en:focal neurologic signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal neurologic signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  828. en:focal nodular heterotopia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal nodular heterotopia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  829. en:focal pachygyria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal pachygyria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  830. en:focal parietal pachygyria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal parietal pachygyria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  831. en:focal thickening of the cortex on mri (in type iib) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal thickening of the cortex on mri (in type iib) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  832. en:focal white matter lesions (in type iib) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal white matter lesions (in type iib) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  833. en:focal, segmental or multifocal dystonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:focal, segmental or multifocal dystonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  834. en:foot-drop --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:foot-drop | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  835. en:forebrain defects --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:forebrain defects | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  836. en:four-repeat tau plaques in the striatum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:four-repeat tau plaques in the striatum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  837. en:frequency 3.5 hz in midline --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frequency 3.5 hz in midline | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  838. en:frequency 6 hz in lateral gaze --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frequency 6 hz in lateral gaze | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  839. en:frequent falls --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frequent falls | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  840. en:frequent falls with preservation of consciousness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frequent falls with preservation of consciousness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  841. en:frequent headache --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frequent headache | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  842. en:frontal lobe origin --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontal lobe origin | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  843. en:frontal lobe syndrome --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontal lobe syndrome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  844. en:frontal release signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontal release signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  845. en:frontolimbic dementia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontolimbic dementia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  846. en:frontoparietal polymicrogyria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontoparietal polymicrogyria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  847. en:frontotemporal atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontotemporal atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  848. en:frontotemporal dementia (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontotemporal dementia (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  849. en:frontotemporal dementia (in 30% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontotemporal dementia (in 30% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  850. en:frontotemporal leukoencephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontotemporal leukoencephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  851. en:frontotemporal lobar atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontotemporal lobar atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  852. en:frontotemporal pachygyria (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontotemporal pachygyria (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  853. en:frontotemporal polymicrogyria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontotemporal polymicrogyria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  854. en:frontotemporal/subcortical dementia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:frontotemporal/subcortical dementia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  855. en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  856. en:gait abnormalities (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait abnormalities (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  857. en:gait abnormalities (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait abnormalities (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  858. en:gait abnormalities may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait abnormalities may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  859. en:gait and limb ataxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait and limb ataxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  860. en:gait ataxia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait ataxia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  861. en:gait ataxias, cerebellar --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait ataxias, cerebellar | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  862. en:gait difficulties, late-onset --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait difficulties, late-onset | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  863. en:gait disturbance --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait disturbance | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  864. en:gait imbalance --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait imbalance | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  865. en:gait instability, worse in the dark --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait instability, worse in the dark | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  866. en:gait unsteady --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait unsteady | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  867. en:gait, drop foot --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait, drop foot | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  868. en:gait, rigid --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gait, rigid | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  869. en:gaze deviation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gaze deviation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  870. en:generalized amyotrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized amyotrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  871. en:generalized and focal spike and wave complexes seen on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized and focal spike and wave complexes seen on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  872. en:generalized clonic or tonic-clonic seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized clonic or tonic-clonic seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  873. en:generalized cortical atrophy (in one patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized cortical atrophy (in one patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  874. en:generalized dystonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized dystonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  875. en:generalized hypotonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized hypotonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  876. en:generalized myelin loss --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized myelin loss | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  877. en:generalized seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  878. en:generalized slowing --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized slowing | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  879. en:generalized spike wave discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized spike wave discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  880. en:generalized spike-wave activity seen on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized spike-wave activity seen on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  881. en:generalized tonic-clonic seizures (gtcs) (in most patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized tonic-clonic seizures (gtcs) (in most patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  882. en:generalized tonic-clonic seizures (gtcs) on awakening --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized tonic-clonic seizures (gtcs) on awakening | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  883. en:generalized tonic-clonic seizures in 50% --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:generalized tonic-clonic seizures in 50% | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  884. en:giant cortical somatosensory evoked potentials (seps) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:giant cortical somatosensory evoked potentials (seps) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  885. en:gilles de la tourette syndrome (reported in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gilles de la tourette syndrome (reported in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  886. en:glial activation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:glial activation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  887. en:gliosis of the white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gliosis of the white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  888. en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  889. en:global and focal neurologic abnormalities (less than 30%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:global and focal neurologic abnormalities (less than 30%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  890. en:global cerebral atrophy, mild (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:global cerebral atrophy, mild (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  891. en:global developmental delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:global developmental delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  892. en:global developmental delay, variable severity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:global developmental delay, variable severity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  893. en:glomeruloid vascular proliferation in brain and spinal cord --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:glomeruloid vascular proliferation in brain and spinal cord | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  894. en:grade i meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:grade i meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  895. en:grade ii meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:grade ii meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  896. en:grade iii meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:grade iii meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  897. en:granular material in neurons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:granular material in neurons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  898. en:gray matter heterotopia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gray matter heterotopia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  899. en:gray matter structure of central nervous system --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gray matter structure of central nervous system | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  900. en:grimaces --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:grimaces | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  901. en:gross motor delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gross motor delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  902. en:gross motor delay (in one family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gross motor delay (in one family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  903. en:gross motor skill delay (infancy) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gross motor skill delay (infancy) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  904. en:gurgling or drooling during seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gurgling or drooling during seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  905. en:gyral disorganization --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:gyral disorganization | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  906. en:hallucination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hallucination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  907. en:head 'tilt' in infancy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:head 'tilt' in infancy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  908. en:head bobbing --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:head bobbing | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  909. en:head movements abnormal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:head movements abnormal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  910. en:head titubation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:head titubation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  911. en:head titubations --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:head titubations | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  912. en:head tremor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:head tremor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  913. en:head tremor (14% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:head tremor (14% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  914. en:head tremor (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:head tremor (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  915. en:head tremor, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:head tremor, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  916. en:headache (with pheochromocytoma) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:headache (with pheochromocytoma) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  917. en:headache is usually not a symptom --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:headache is usually not a symptom | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  918. en:headaches, severe, unilateral --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:headaches, severe, unilateral | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  919. en:heightened sensitivity to external stimuli --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:heightened sensitivity to external stimuli | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  920. en:hemiclonic seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hemiclonic seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  921. en:hemimegalencephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hemimegalencephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  922. en:hemiparesis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hemiparesis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  923. en:hemiparesis, paroxysmal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hemiparesis, paroxysmal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  924. en:hemiplegia (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hemiplegia (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  925. en:hemiplegic migraine --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hemiplegic migraine | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  926. en:hemispheric atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hemispheric atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  927. en:hemorrhage --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hemorrhage | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  928. en:hemorrhagic cerebrovascular accident --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hemorrhagic cerebrovascular accident | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  929. en:hepatic encephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hepatic encephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  930. en:herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  931. en:high intensity area in white matter on head mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:high intensity area in white matter on head mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  932. en:high signal intensities at gray/white matter junction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:high signal intensities at gray/white matter junction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  933. en:high voltage spikes over the temporal and central regions seen on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:high voltage spikes over the temporal and central regions seen on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  934. en:high-steppage gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:high-steppage gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  935. en:hippocampal atrophy (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hippocampal atrophy (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  936. en:hippocampal hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hippocampal hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  937. en:holoprosencephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:holoprosencephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  938. en:holoprosencephaly (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:holoprosencephaly (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  939. en:holoprosencephaly (100%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:holoprosencephaly (100%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  940. en:holoprosencephaly (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:holoprosencephaly (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  941. en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  942. en:horner syndrome --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:horner syndrome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  943. en:hunger and thirst disturbances (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hunger and thirst disturbances (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  944. en:hydrocephalus (11%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hydrocephalus (11%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  945. en:hydrocephalus (12%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hydrocephalus (12%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  946. en:hydrocephalus (in 2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hydrocephalus (in 2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  947. en:hydrocephalus (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hydrocephalus (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  948. en:hydrocephalus (uncommon) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hydrocephalus (uncommon) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  949. en:hydrocephaly, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hydrocephaly, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  950. en:hyperactive brainstem reflexes (head retraction, palmomental, snout) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperactive brainstem reflexes (head retraction, palmomental, snout) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  951. en:hyperactivity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperactivity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  952. en:hyperekplexia (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperekplexia (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  953. en:hyperintense lesions in the basal ganglia on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperintense lesions in the basal ganglia on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  954. en:hyperirritability --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperirritability | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  955. en:hyperkinetic involuntary movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperkinetic involuntary movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  956. en:hyperreflexia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperreflexia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  957. en:hyperreflexia (2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperreflexia (2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  958. en:hyperreflexia (33%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperreflexia (33%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  959. en:hyperreflexia (70%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperreflexia (70%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  960. en:hyperreflexia (early) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperreflexia (early) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  961. en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  962. en:hyperreflexia (type i) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperreflexia (type i) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  963. en:hyperreflexia in some --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperreflexia in some | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  964. en:hyperreflexia, lower limbs more than upper limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperreflexia, lower limbs more than upper limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  965. en:hypersomnolent --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypersomnolent | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  966. en:hyperthermia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyperthermia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  967. en:hypertonia (childhood) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypertonia (childhood) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  968. en:hypertonia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypertonia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  969. en:hypertonia (older children and adolescents) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypertonia (older children and adolescents) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  970. en:hypertonia (type ii) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypertonia (type ii) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  971. en:hypertonia and rigidity during seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypertonia and rigidity during seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  972. en:hypertonia in neonatal period --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypertonia in neonatal period | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  973. en:hypertonia late --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypertonia late | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  974. en:hypertonia, peripheral dystonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypertonia, peripheral dystonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  975. en:hypertonic seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypertonic seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  976. en:hypnagogic hallucinations --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypnagogic hallucinations | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  977. en:hypnapompic hallucinations --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypnapompic hallucinations | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  978. en:hypo- and demyelination of the brain --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypo- and demyelination of the brain | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  979. en:hypocalcemic tetany --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypocalcemic tetany | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  980. en:hypodensity of caudate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypodensity of caudate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  981. en:hypodensity of lenticular nuclei --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypodensity of lenticular nuclei | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  982. en:hypodysplasia of the corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypodysplasia of the corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  983. en:hypogenesis of the corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypogenesis of the corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  984. en:hypoglycemic coma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoglycemic coma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  985. en:hypoglycemic encephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoglycemic encephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  986. en:hypokinesia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypokinesia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  987. en:hypokinetic movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypokinetic movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  988. en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  989. en:hypomyelination of the brain white matter, diffuse --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypomyelination of the brain white matter, diffuse | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  990. en:hypoplasia of anterior or entire pituitary gland (frequent) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of anterior or entire pituitary gland (frequent) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  991. en:hypoplasia of corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  992. en:hypoplasia of olfactory tract --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of olfactory tract | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  993. en:hypoplasia of septum pellucidum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of septum pellucidum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  994. en:hypoplasia of the corpus callosum (2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of the corpus callosum (2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  995. en:hypoplasia of the hypothalamus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of the hypothalamus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  996. en:hypoplasia of the medulla oblongata --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of the medulla oblongata | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  997. en:hypoplasia of the mesencephalic tectum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of the mesencephalic tectum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  998. en:hypoplasia of the optic tract --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of the optic tract | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  999. en:hypoplasia of the pons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of the pons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1000. en:hypoplasia of the pyramidal tract --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of the pyramidal tract | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1001. en:hypoplasia of the ventral pons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplasia of the ventral pons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1002. en:hypoplastic anterior pituitary (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplastic anterior pituitary (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1003. en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1004. en:hypoplastic cerebellar vermis (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplastic cerebellar vermis (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1005. en:hypoplastic corpus callosum (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplastic corpus callosum (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1006. en:hypoplastic corpus callosum (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplastic corpus callosum (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1007. en:hypoplastic internal capsule (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplastic internal capsule (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1008. en:hypoplastic olfactory lobes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplastic olfactory lobes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1009. en:hypoplastic pituitary gland (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplastic pituitary gland (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1010. en:hypoplastic/atrophic corpus callosum (55%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypoplastic/atrophic corpus callosum (55%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1011. en:hyporeflexia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyporeflexia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1012. en:hyporeflexia (occurs later) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyporeflexia (occurs later) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1013. en:hyporeflexia of lower limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hyporeflexia of lower limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1014. en:hypothalamic hamartoma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypothalamic hamartoma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1015. en:hypothalamus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypothalamus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1016. en:hypotonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1017. en:hypotonia (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1018. en:hypotonia (congenital form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia (congenital form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1019. en:hypotonia (early-onset form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia (early-onset form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1020. en:hypotonia (hcs and 2p21del) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia (hcs and 2p21del) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1021. en:hypotonia (in 1/4 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia (in 1/4 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1022. en:hypotonia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1023. en:hypotonia (newborn) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia (newborn) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1024. en:hypotonia (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1025. en:hypotonia (type i and type ii, infantile) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia (type i and type ii, infantile) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1026. en:hypotonia changing to hypertonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia changing to hypertonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1027. en:hypotonia in later stages --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia in later stages | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1028. en:hypotonia progressing to hypertonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia progressing to hypertonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1029. en:hypotonia, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1030. en:hypotonia, mild, transient --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia, mild, transient | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1031. en:hypotonia, proximal, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonia, proximal, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1032. en:hypotonic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1033. en:hypotonic seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypotonic seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1034. en:hypsarrhythmia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypsarrhythmia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1035. en:hypsarrhythmia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypsarrhythmia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1036. en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1037. en:ictal eeg showed partial seizures with frontal lobe origin --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ictal eeg showed partial seizures with frontal lobe origin | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1038. en:ictal eeg shows focal onset in central, parietal, or temporal regions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ictal eeg shows focal onset in central, parietal, or temporal regions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1039. en:idiopathic generalized epilepsy in childhood (homozygous patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:idiopathic generalized epilepsy in childhood (homozygous patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1040. en:illegible handwriting --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:illegible handwriting | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1041. en:immature brain with no gyral development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:immature brain with no gyral development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1042. en:immature myelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:immature myelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1043. en:immobile --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:immobile | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1044. en:immunology aspects --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:immunology aspects | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1045. en:impaired ambulation due to muscle weakness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:impaired ambulation due to muscle weakness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1046. en:impaired cognition (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:impaired cognition (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1047. en:impaired expression of language --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:impaired expression of language | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1048. en:impaired expressive speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:impaired expressive speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1049. en:impaired gait due to peripheral neuropathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:impaired gait due to peripheral neuropathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1050. en:impaired motor control, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:impaired motor control, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1051. en:impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1052. en:impaired voluntary movement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:impaired voluntary movement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1053. en:impairment of gross and fine motor coordination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:impairment of gross and fine motor coordination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1054. en:inability to communicate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inability to communicate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1055. en:inability to hold head --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inability to hold head | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1056. en:inability to hold neck up ('limber neck') onset at 6 months --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inability to hold neck up ('limber neck') onset at 6 months | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1057. en:inability to run --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inability to run | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1058. en:inability to sit or control head --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inability to sit or control head | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1059. en:inability to sit or stand independently --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inability to sit or stand independently | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1060. en:inability to walk independently --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inability to walk independently | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1061. en:inability to walk unsupported --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inability to walk unsupported | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1062. en:incomprehensible speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:incomprehensible speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1063. en:incoordination of trunk and limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:incoordination of trunk and limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1064. en:increased activity period --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:increased activity period | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1065. en:increased cerebral lactate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:increased cerebral lactate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1066. en:increased csf lactate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:increased csf lactate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1067. en:increased csf protein --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:increased csf protein | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1068. en:increased csf protein with normal cell count --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:increased csf protein with normal cell count | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1069. en:increased iron deposition in the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:increased iron deposition in the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1070. en:increased iron deposition in the basal ganglia (40%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:increased iron deposition in the basal ganglia (40%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1071. en:increased neurologic sequelae of infections (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:increased neurologic sequelae of infections (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1072. en:increased subdural space around frontal lobes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:increased subdural space around frontal lobes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1073. en:individuals can stand or walk with support by 4 to 6 years of age --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:individuals can stand or walk with support by 4 to 6 years of age | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1074. en:infantile encephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:infantile encephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1075. en:infantile encephalopathy, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:infantile encephalopathy, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1076. en:infantile seizures (approximately 80% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:infantile seizures (approximately 80% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1077. en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1078. en:infantile spasm --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:infantile spasm | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1079. en:inferior vermis hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inferior vermis hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1080. en:inflexible adherence to routines or rituals --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:inflexible adherence to routines or rituals | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1081. en:intellectual disabilities (in 1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intellectual disabilities (in 1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1082. en:intellectual disability --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intellectual disability | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1083. en:intellectual disability, mild (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intellectual disability, mild (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1084. en:intellectual disability, mild (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intellectual disability, mild (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1085. en:intellectual disability, mild to moderate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intellectual disability, mild to moderate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1086. en:intellectual disability, mild to moderate (in homozygotes) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intellectual disability, mild to moderate (in homozygotes) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1087. en:intellectual disability, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intellectual disability, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1088. en:intellectual impairment, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intellectual impairment, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1089. en:intellectual impairment, mild (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intellectual impairment, mild (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1090. en:intention tremor (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intention tremor (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1091. en:interhemispheric cysts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:interhemispheric cysts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1092. en:interictal ataxia may occur later in disease course --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:interictal ataxia may occur later in disease course | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1093. en:interictal eeg is usually normal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:interictal eeg is usually normal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1094. en:interictal eeg may be normal or abnormal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:interictal eeg may be normal or abnormal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1095. en:interictal eeg may show nonspecific changes in 15 to 20% --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:interictal eeg may show nonspecific changes in 15 to 20% | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1096. en:interictal eeg shows 3-4 hz general spike-wave complexes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:interictal eeg shows 3-4 hz general spike-wave complexes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1097. en:intermittent wheelchair dependence (stage 3) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intermittent wheelchair dependence (stage 3) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1098. en:interventricular cysts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:interventricular cysts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1099. en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1100. en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1101. en:intracellular lewy bodies --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracellular lewy bodies | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1102. en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1103. en:intracerebral calcifications (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracerebral calcifications (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1104. en:intracranial calcification affecting the basal ganglia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracranial calcification affecting the basal ganglia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1105. en:intracranial calcifications (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracranial calcifications (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1106. en:intracranial hemorrhage --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracranial hemorrhage | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1107. en:intracranial lipoma (cerebello-pontine) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracranial lipoma (cerebello-pontine) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1108. en:intracranial meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intracranial meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1109. en:intractable epilepsy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intractable epilepsy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1110. en:intraorbital meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intraorbital meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1111. en:intraventricular meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:intraventricular meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1112. en:involuntary dystonic or choreiform movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:involuntary dystonic or choreiform movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1113. en:involuntary movements may be precipitated by exertion or anxiety --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:involuntary movements may be precipitated by exertion or anxiety | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1114. en:involuntary repetitive movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:involuntary repetitive movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1115. en:involuntary writhing movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:involuntary writhing movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1116. en:ipsilateral cranial nerve hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ipsilateral cranial nerve hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1117. en:iq 85-115 (female) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:iq 85-115 (female) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1118. en:iron deposition in pallidal nuclei --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:iron deposition in pallidal nuclei | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1119. en:iron deposition in the globus pallidus and substantia nigra seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:iron deposition in the globus pallidus and substantia nigra seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1120. en:iron deposits in the globus pallidus, caudate, and substantia nigra --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:iron deposits in the globus pallidus, caudate, and substantia nigra | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1121. en:irregular cortical ribbon --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:irregular cortical ribbon | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1122. en:irregular folding of the cortex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:irregular folding of the cortex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1123. en:irregular spike and slow waves --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:irregular spike and slow waves | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1124. en:irresistible desire to move the legs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:irresistible desire to move the legs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1125. en:ischemic cerebrovascular accident --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ischemic cerebrovascular accident | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1126. en:ischemic infarct of brain --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ischemic infarct of brain | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1127. en:ischemic infarction (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ischemic infarction (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1128. en:ischemic necrotic lesions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ischemic necrotic lesions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1129. en:ischemic stroke (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ischemic stroke (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1130. en:jerk-locked premyoclonus spikes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:jerk-locked premyoclonus spikes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1131. en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1132. en:jerky movements in infancy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:jerky movements in infancy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1133. en:kearns-sayre syndrome (530000), in a subset of patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:kearns-sayre syndrome (530000), in a subset of patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1134. en:kernicterus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:kernicterus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1135. en:lack of bunina bodies --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of bunina bodies | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1136. en:lack of development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1137. en:lack of developmental development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of developmental development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1138. en:lack of developmental milestones --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of developmental milestones | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1139. en:lack of expressive speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of expressive speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1140. en:lack of head control --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of head control | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1141. en:lack of independent ambulation (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of independent ambulation (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1142. en:lack of independent sitting or walking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of independent sitting or walking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1143. en:lack of inflammatory infiltrate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of inflammatory infiltrate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1144. en:lack of neurologic development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of neurologic development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1145. en:lack of psychomotor development (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of psychomotor development (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1146. en:lack of speech or only a few words --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of speech or only a few words | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1147. en:lack of speech or poor speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of speech or poor speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1148. en:lack of spontaneous movement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of spontaneous movement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1149. en:lack of spontaneous play --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of spontaneous play | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1150. en:lack of upper motor neuron signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of upper motor neuron signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1151. en:lack of verbal communication --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of verbal communication | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1152. en:lack of visual attention --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of visual attention | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1153. en:lack of volitional movement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lack of volitional movement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1154. en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1155. en:laminar necrosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:laminar necrosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1156. en:language acquisition difficulties (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:language acquisition difficulties (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1157. en:language development limited to a few words --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:language development limited to a few words | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1158. en:large cavum vergae --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:large cavum vergae | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1159. en:large cerebellum, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:large cerebellum, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1160. en:large sella turcica --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:large sella turcica | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1161. en:lateral corticospinal tracts show atrophy, pallor, and degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lateral corticospinal tracts show atrophy, pallor, and degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1162. en:learning and developmental delay (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:learning and developmental delay (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1163. en:learning difficulties --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:learning difficulties | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1164. en:learning difficulties (in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:learning difficulties (in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1165. en:learning difficulties (seen in recessive form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:learning difficulties (seen in recessive form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1166. en:learning disabilities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:learning disabilities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1167. en:learning disabilities (30%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:learning disabilities (30%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1168. en:learning disabilities (in females) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:learning disabilities (in females) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1169. en:learning disabilities (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:learning disabilities (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1170. en:leg cramp --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leg cramp | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1171. en:leg pain --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leg pain | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1172. en:leigh disease --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leigh disease | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1173. en:leptomeningeal melanocytosis (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leptomeningeal melanocytosis (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1174. en:leptomeningeal neoplasm --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leptomeningeal neoplasm | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1175. en:leptomeningeal thickening --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leptomeningeal thickening | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1176. en:lesions are symmetrical --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lesions are symmetrical | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1177. en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1178. en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1179. en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1180. en:lesions in the anterior pituitary (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lesions in the anterior pituitary (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1181. en:lethargy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lethargy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1182. en:lethargy associated with hypoglycemia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lethargy associated with hypoglycemia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1183. en:leukoaraiosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leukoaraiosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1184. en:leukodystrophy (in 1 of 2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leukodystrophy (in 1 of 2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1185. en:leukodystrophy, hypomyelinating --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leukodystrophy, hypomyelinating | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1186. en:leukoencephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leukoencephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1187. en:leukoencephalopathy, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:leukoencephalopathy, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1188. en:lewy bodies (not always present) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lewy bodies (not always present) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1189. en:lewy bodies in the substantia nigra --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lewy bodies in the substantia nigra | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1190. en:lightheadedness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lightheadedness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1191. en:limb dysmetria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:limb dysmetria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1192. en:limb dystonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:limb dystonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1193. en:limb posturing (if left untreated) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:limb posturing (if left untreated) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1194. en:limb spasticity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:limb spasticity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1195. en:limbic malformations --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:limbic malformations | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1196. en:limited memory, attention, language --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:limited memory, attention, language | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1197. en:lipomyelocystoceles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lipomyelocystoceles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1198. en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1199. en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1200. en:lissencephaly (reported in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lissencephaly (reported in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1201. en:lissencephaly, posterior to anterior gradient --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lissencephaly, posterior to anterior gradient | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1202. en:little polarity in remaining neurons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:little polarity in remaining neurons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1203. en:little spontaneous limb movement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:little spontaneous limb movement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1204. en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1205. en:locomotor delay (early-onset form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:locomotor delay (early-onset form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1206. en:long-tract signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:long-tract signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1207. en:loss of ability to walk --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of ability to walk | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1208. en:loss of anterior horn cells and gliosis in the spinal cord --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of anterior horn cells and gliosis in the spinal cord | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1209. en:loss of any acquired abilities in early childhood --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of any acquired abilities in early childhood | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1210. en:loss of cerebellar granular cells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of cerebellar granular cells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1211. en:loss of cerebellar purkinje cells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of cerebellar purkinje cells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1212. en:loss of consciousness (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of consciousness (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1213. en:loss of coordination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of coordination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1214. en:loss of developmental milestones --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of developmental milestones | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1215. en:loss of dopaminergic neurons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of dopaminergic neurons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1216. en:loss of dopaminergic neurons in the substantia nigra --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of dopaminergic neurons in the substantia nigra | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1217. en:loss of executive functions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of executive functions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1218. en:loss of gait (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of gait (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1219. en:loss of independent ambulation (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of independent ambulation (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1220. en:loss of language ability --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of language ability | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1221. en:loss of lower alpha-motor neurons in the anterior horn of the spinal cord and lower brainstem --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of lower alpha-motor neurons in the anterior horn of the spinal cord and lower brainstem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1222. en:loss of motor functions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of motor functions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1223. en:loss of motor milestones --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of motor milestones | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1224. en:loss of motor skills --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of motor skills | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1225. en:loss of myelin and oligodendroglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of myelin and oligodendroglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1226. en:loss of myelin in the descending lateral spinal cord tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of myelin in the descending lateral spinal cord tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1227. en:loss of myelin in the pyramidal tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of myelin in the pyramidal tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1228. en:loss of myelinated fibers with regenerative clusters on biopsy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of myelinated fibers with regenerative clusters on biopsy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1229. en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1230. en:loss of pigmented neurons in the substantia nigra --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of pigmented neurons in the substantia nigra | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1231. en:loss of postural tone --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of postural tone | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1232. en:loss of purkinje cells in the cerebellar vermis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of purkinje cells in the cerebellar vermis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1233. en:loss of purkinje cells in the cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of purkinje cells in the cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1234. en:loss of purposeful hand movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of purposeful hand movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1235. en:loss of spontaneous movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of spontaneous movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1236. en:loss of white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:loss of white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1237. en:low apparent diffusion coefficient (adc) values --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:low apparent diffusion coefficient (adc) values | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1238. en:low densities in the basal ganglia similar to leigh syndrome (256000) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:low densities in the basal ganglia similar to leigh syndrome (256000) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1239. en:low iq --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:low iq | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1240. en:low-lying cerebellar tonsils --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:low-lying cerebellar tonsils | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1241. en:low-normal iq --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:low-normal iq | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1242. en:lower extremity weakness with febrile episodes (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower extremity weakness with febrile episodes (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1243. en:lower limb hyperreflexia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower limb hyperreflexia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1244. en:lower limb hypotrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower limb hypotrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1245. en:lower limb muscle weakness (occurs later) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower limb muscle weakness (occurs later) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1246. en:lower limb weakness, proximal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower limb weakness, proximal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1247. en:lower limbs weakness and atrophy, distal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower limbs weakness and atrophy, distal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1248. en:lower motor neuron degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower motor neuron degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1249. en:lower motor neuron involvement after long disease duration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower motor neuron involvement after long disease duration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1250. en:lower motor neuron involvement, mild, seen on emg (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower motor neuron involvement, mild, seen on emg (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1251. en:lower motor neuron signs, later --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower motor neuron signs, later | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1252. en:lower motor neuron symptoms --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower motor neuron symptoms | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1253. en:lower motor signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lower motor signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1254. en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1255. en:lumbosacral meningocele --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lumbosacral meningocele | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1256. en:lymphocytic infiltration of the brain --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:lymphocytic infiltration of the brain | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1257. en:macrocephaly (due to dandy-walker malformation) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:macrocephaly (due to dandy-walker malformation) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1258. en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1259. en:magnetic resonance spectroscopy shows increased lactate in white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:magnetic resonance spectroscopy shows increased lactate in white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1260. en:major developmental milestones are not attained --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:major developmental milestones are not attained | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1261. en:malformations of cortical development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:malformations of cortical development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1262. en:mask-like facies --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mask-like facies | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1263. en:mega cisterna magna --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mega cisterna magna | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1264. en:megacisterna magna (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:megacisterna magna (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1265. en:memory loss --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:memory loss | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1266. en:meningeal carcinomatosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningeal carcinomatosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1267. en:meningeal disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningeal disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1268. en:meningeal neoplasm --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningeal neoplasm | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1269. en:meningeal sarcomatosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningeal sarcomatosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1270. en:meningioma by site --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningioma by site | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1271. en:meningiomatosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningiomatosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1272. en:meningoceles, multiple, lateral --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningoceles, multiple, lateral | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1273. en:meningoencephalitis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningoencephalitis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1274. en:meningoencephalocele (wws) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningoencephalocele (wws) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1275. en:meningothelial meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:meningothelial meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1276. en:mental deterioration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental deterioration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1277. en:mental deterioration beginning 2 to 5 years after onset of seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental deterioration beginning 2 to 5 years after onset of seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1278. en:mental impairment may develop with repeated acute episodes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental impairment may develop with repeated acute episodes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1279. en:mental impairment, mild to moderate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental impairment, mild to moderate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1280. en:mental lethargy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental lethargy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1281. en:mental retardation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1282. en:mental retardation (15%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (15%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1283. en:mental retardation (20%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (20%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1284. en:mental retardation (30%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (30%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1285. en:mental retardation (50% patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (50% patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1286. en:mental retardation (6%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (6%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1287. en:mental retardation (70%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (70%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1288. en:mental retardation (cvs+) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (cvs+) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1289. en:mental retardation (develops later) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (develops later) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1290. en:mental retardation (if untreated in infancy) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (if untreated in infancy) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1291. en:mental retardation (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1292. en:mental retardation (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1293. en:mental retardation (in type iia) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (in type iia) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1294. en:mental retardation (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1295. en:mental retardation (moderate to severe in males) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (moderate to severe in males) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1296. en:mental retardation (one-third) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (one-third) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1297. en:mental retardation (range mild to severe) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (range mild to severe) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1298. en:mental retardation (rare less than 1% of cases) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (rare less than 1% of cases) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1299. en:mental retardation (secondary to intracranial bleed) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (secondary to intracranial bleed) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1300. en:mental retardation (seen in hhs variant) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (seen in hhs variant) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1301. en:mental retardation (type i) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (type i) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1302. en:mental retardation (uncommon) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (uncommon) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1303. en:mental retardation (untreated hypothyroidism) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation (untreated hypothyroidism) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1304. en:mental retardation can occur in patients with repeated episodes of dehydration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation can occur in patients with repeated episodes of dehydration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1305. en:mental retardation has been reported --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation has been reported | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1306. en:mental retardation in 5-13% --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation in 5-13% | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1307. en:mental retardation, borderline to severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, borderline to severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1308. en:mental retardation, borderline-mild in carrier females --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, borderline-mild in carrier females | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1309. en:mental retardation, mild (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1310. en:mental retardation, mild (18%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild (18%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1311. en:mental retardation, mild (carrier females) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild (carrier females) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1312. en:mental retardation, mild (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1313. en:mental retardation, mild (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1314. en:mental retardation, mild to moderate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild to moderate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1315. en:mental retardation, mild to moderate (iq 30-76) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild to moderate (iq 30-76) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1316. en:mental retardation, mild to profound --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild to profound | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1317. en:mental retardation, mild, some patients (iq 70-80) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild, some patients (iq 70-80) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1318. en:mental retardation, mild-moderate (28%, usually in males) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, mild-moderate (28%, usually in males) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1319. en:mental retardation, moderate (in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, moderate (in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1320. en:mental retardation, moderate (in sister) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, moderate (in sister) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1321. en:mental retardation, moderate to profound --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, moderate to profound | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1322. en:mental retardation, moderate to severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, moderate to severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1323. en:mental retardation, moderate to severe (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, moderate to severe (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1324. en:mental retardation, moderate to severe (iq 40 to 60) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, moderate to severe (iq 40 to 60) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1325. en:mental retardation, moderate-severe (2p21del) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, moderate-severe (2p21del) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1326. en:mental retardation, progressive (50% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, progressive (50% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1327. en:mental retardation, residual mild-to-severe (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, residual mild-to-severe (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1328. en:mental retardation, severe in some patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, severe in some patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1329. en:mental retardation, severe, profound --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mental retardation, severe, profound | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1330. en:mesial temporal brain malformations --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mesial temporal brain malformations | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1331. en:mesial temporal sclerosis (in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mesial temporal sclerosis (in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1332. en:metastatic malignant neoplasm in the leptomeninges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:metastatic malignant neoplasm in the leptomeninges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1333. en:microbiological --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:microbiological | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1334. en:microbleeds --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:microbleeds | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1335. en:microcephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:microcephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1336. en:microcystic degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:microcystic degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1337. en:microcystic meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:microcystic meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1338. en:micrographia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:micrographia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1339. en:microlissencephalies --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:microlissencephalies | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1340. en:microvacuolation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:microvacuolation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1341. en:microvascular spaces, dilated --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:microvascular spaces, dilated | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1342. en:midbrain atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:midbrain atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1343. en:midline brain calcifications --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:midline brain calcifications | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1344. en:migraine --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:migraine | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1345. en:migraine (uncommon) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:migraine (uncommon) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1346. en:migraine headache (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:migraine headache (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1347. en:migraine headaches (ipsilateral to facial hemangioma) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:migraine headaches (ipsilateral to facial hemangioma) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1348. en:migraine headaches (onset in adolescence) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:migraine headaches (onset in adolescence) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1349. en:migraines (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:migraines (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1350. en:migrating focal discharges from one cortical region to another seen on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:migrating focal discharges from one cortical region to another seen on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1351. en:migrating partial seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:migrating partial seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1352. en:mild cerebellar hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild cerebellar hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1353. en:mild cognitive deterioration in adults --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild cognitive deterioration in adults | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1354. en:mild cognitive impairment (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild cognitive impairment (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1355. en:mild cortical atrophy (in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild cortical atrophy (in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1356. en:mild cortical atrophy on ct or mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild cortical atrophy on ct or mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1357. en:mild distal sensory deficits --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild distal sensory deficits | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1358. en:mild global developmental delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild global developmental delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1359. en:mild memory loss --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild memory loss | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1360. en:mild mental decline --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild mental decline | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1361. en:mild mental retardation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild mental retardation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1362. en:mild mental retardation (39%) feeding problems/weak suck (43%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild mental retardation (39%) feeding problems/weak suck (43%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1363. en:mild motor development delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild motor development delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1364. en:mild paraparesis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild paraparesis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1365. en:mild pyramidal signs (variable expression) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild pyramidal signs (variable expression) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1366. en:mild sensorimotor neuropathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild sensorimotor neuropathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1367. en:mild spasticity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild spasticity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1368. en:mild structural abnormalities seen mri (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild structural abnormalities seen mri (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1369. en:mild to moderate learning difficulties --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild to moderate learning difficulties | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1370. en:mild upper limb involvement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild upper limb involvement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1371. en:mild-moderate mental retardation (80% affected males) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild-moderate mental retardation (80% affected males) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1372. en:mild-moderate ventricular dilatation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild-moderate ventricular dilatation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1373. en:mild-severe mental retardation (20%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mild-severe mental retardation (20%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1374. en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1375. en:mildly decreased intelligence has been reported --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mildly decreased intelligence has been reported | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1376. en:mildly delayed developmental milestones --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mildly delayed developmental milestones | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1377. en:mildly delayed motor development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mildly delayed motor development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1378. en:minimal gliosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:minimal gliosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1379. en:minimal or lack of speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:minimal or lack of speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1380. en:minor motor impairment (stage 2) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:minor motor impairment (stage 2) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1381. en:mirror hand movements (bimanual synkinesis, in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mirror hand movements (bimanual synkinesis, in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1382. en:mirror movements, involuntary, affecting the hand and fingers --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mirror movements, involuntary, affecting the hand and fingers | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1383. en:misorientation of pyramidal fibers --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:misorientation of pyramidal fibers | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1384. en:mitochondrial encephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mitochondrial encephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1385. en:mobility poor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mobility poor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1386. en:moderate cortical atrophy (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:moderate cortical atrophy (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1387. en:molar tooth sign on brain mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:molar tooth sign on brain mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1388. en:molar tooth sign on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:molar tooth sign on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1389. en:mood lability --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mood lability | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1390. en:most patients achieve walking with aid --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:most patients achieve walking with aid | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1391. en:most patients are wheelchair-bound --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:most patients are wheelchair-bound | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1392. en:most patients do not achieve independent sitting or walking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:most patients do not achieve independent sitting or walking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1393. en:mosy patients become wheelchair-bound after 10 years --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mosy patients become wheelchair-bound after 10 years | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1394. en:motor abnormalities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor abnormalities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1395. en:motor and intellectual disability, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor and intellectual disability, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1396. en:motor and vocal tics --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor and vocal tics | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1397. en:motor automatisms --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor automatisms | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1398. en:motor delay (in one patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor delay (in one patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1399. en:motor development delay (83%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor development delay (83%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1400. en:motor development delayed (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor development delayed (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1401. en:motor developmental delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor developmental delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1402. en:motor developmental delay, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor developmental delay, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1403. en:motor disturbances --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor disturbances | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1404. en:motor dysfunction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor dysfunction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1405. en:motor dyspraxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor dyspraxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1406. en:motor incoordination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor incoordination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1407. en:motor neuron disease --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor neuron disease | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1408. en:motor regression --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor regression | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1409. en:motor retardation, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor retardation, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1410. en:motor seizures, nocturnal, usually occur in clusters (up to 8 per night) during dozing or on awakening --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor seizures, nocturnal, usually occur in clusters (up to 8 per night) during dozing or on awakening | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1411. en:motor tic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:motor tic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1412. en:mouth movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mouth movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1413. en:movement of visual image - finding --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:movement of visual image - finding | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1414. en:movements are exacerbated by anxiety --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:movements are exacerbated by anxiety | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1415. en:moyamoya disease --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:moyamoya disease | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1416. en:mr spectroscopy shows decreased n-acetyl aspartate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mr spectroscopy shows decreased n-acetyl aspartate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1417. en:mri imaging shows cavitation of the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri imaging shows cavitation of the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1418. en:mri is best imaging modality to detect lesions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri is best imaging modality to detect lesions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1419. en:mri may show lesions in basal ganglia, thalamus, and white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri may show lesions in basal ganglia, thalamus, and white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1420. en:mri shows absence of the facial nerve --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows absence of the facial nerve | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1421. en:mri shows brain asymmetry --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows brain asymmetry | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1422. en:mri shows cerebellar atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows cerebellar atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1423. en:mri shows congenital abnormalities of the posterior fossa --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows congenital abnormalities of the posterior fossa | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1424. en:mri shows decreased signal intensity in the pallidal nuclei with central hyperintensity ('eye of the tiger' sign) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows decreased signal intensity in the pallidal nuclei with central hyperintensity ('eye of the tiger' sign) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1425. en:mri shows delayed myelination (1 of 6 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows delayed myelination (1 of 6 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1426. en:mri shows frontal and temporal cortical atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows frontal and temporal cortical atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1427. en:mri shows generalized atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows generalized atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1428. en:mri shows globus pallidus signal abnormalities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows globus pallidus signal abnormalities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1429. en:mri shows high signal intensity of the white matter later --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows high signal intensity of the white matter later | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1430. en:mri shows hypointensity of the thalami early-on --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows hypointensity of the thalami early-on | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1431. en:mri shows leukoencephalopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows leukoencephalopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1432. en:mri shows symmetric, diffuse lesions with csf-like signal intensity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mri shows symmetric, diffuse lesions with csf-like signal intensity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1433. en:mrs shows decreased choline in affected white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mrs shows decreased choline in affected white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1434. en:mrs shows decreased creatine in white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mrs shows decreased creatine in white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1435. en:multifocal areas of laminar dysmorphic neurons (in type iia) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal areas of laminar dysmorphic neurons (in type iia) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1436. en:multifocal discharges associated with contralateral jerky movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal discharges associated with contralateral jerky movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1437. en:multifocal discharges seen on eeg (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal discharges seen on eeg (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1438. en:multifocal epileptic activity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal epileptic activity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1439. en:multifocal epileptiform discharges on diffuse slow background --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal epileptiform discharges on diffuse slow background | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1440. en:multifocal seizure --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal seizure | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1441. en:multifocal spike waves --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal spike waves | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1442. en:multifocal spikes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal spikes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1443. en:multifocal spikes and progressive slowing of background activity seen on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal spikes and progressive slowing of background activity seen on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1444. en:multifocal white matter lesions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multifocal white matter lesions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1445. en:multiple independent spike foci --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multiple independent spike foci | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1446. en:multiple lesions in the white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multiple lesions in the white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1447. en:multiple sclerosis-like illness (516003.0001) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:multiple sclerosis-like illness (516003.0001) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1448. en:muscle cramp --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:muscle cramp | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1449. en:musician's cramp --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:musician's cramp | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1450. en:mutism --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:mutism | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1451. en:myclonus (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myclonus (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1452. en:myelin loss in the corticospinal tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myelin loss in the corticospinal tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1453. en:myelin-like lamellar structures in schwann cells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myelin-like lamellar structures in schwann cells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1454. en:myelination defect --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myelination defect | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1455. en:myelomeningocele --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myelomeningocele | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1456. en:myelomeningocele (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myelomeningocele (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1457. en:myoclonic epilepsy (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonic epilepsy (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1458. en:myoclonic jerk --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonic jerk | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1459. en:myoclonic jerks (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonic jerks (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1460. en:myoclonic jerks (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonic jerks (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1461. en:myoclonic seizures (subtype 3a) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonic seizures (subtype 3a) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1462. en:myoclonic seizures, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonic seizures, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1463. en:myoclonic spasms, superimposed episodic, severe, painful (characterized by activation of antagonistic muscle pairs, may involve facial muscles) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonic spasms, superimposed episodic, severe, painful (characterized by activation of antagonistic muscle pairs, may involve facial muscles) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1464. en:myoclonus (in 1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonus (in 1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1465. en:myoclonus (in a subset of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonus (in a subset of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1466. en:myoclonus (subtype 3a) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonus (subtype 3a) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1467. en:myoclonus (type i and type ii, infantile and juvenile) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonus (type i and type ii, infantile and juvenile) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1468. en:myoclonus, cortical, multifocal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonus, cortical, multifocal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1469. en:myoclonus, paroxysmal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myoclonus, paroxysmal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1470. en:myokymia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myokymia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1471. en:myotonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myotonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1472. en:myotonia (in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myotonia (in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1473. en:myotonic seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:myotonic seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1474. en:necrotic process --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:necrotic process | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1475. en:necrotic white matter lesions throughout the brain and brainstem --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:necrotic white matter lesions throughout the brain and brainstem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1476. en:neocortical dysplasia (27%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neocortical dysplasia (27%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1477. en:neonatal irritability --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neonatal irritability | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1478. en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1479. en:nerve degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nerve degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1480. en:nervousness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nervousness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1481. en:neural tube defect (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neural tube defect (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1482. en:neural tube defects (4%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neural tube defects (4%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1483. en:neurobehavioral changes associated with hyperammonemia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurobehavioral changes associated with hyperammonemia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1484. en:neurodegeneration in the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurodegeneration in the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1485. en:neurodegeneration in the cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurodegeneration in the cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1486. en:neurodevelopmental regression --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurodevelopmental regression | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1487. en:neurofibrillary degeneration (morphologic abnormality) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurofibrillary degeneration (morphologic abnormality) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1488. en:neurofibrillary mapt (tau)-positive tangles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurofibrillary mapt (tau)-positive tangles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1489. en:neurofibrillary tangles may be present --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurofibrillary tangles may be present | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1490. en:neurogenic bladder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurogenic bladder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1491. en:neuroimaging shows cortical atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuroimaging shows cortical atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1492. en:neurologic abnormalities in about 7% --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurologic abnormalities in about 7% | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1493. en:neurologic decompensation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurologic decompensation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1494. en:neurologic degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurologic degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1495. en:neurologic deterioration in longterm survivors --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurologic deterioration in longterm survivors | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1496. en:neurologic involvement (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurologic involvement (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1497. en:neurologic regression around age 3 months --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurologic regression around age 3 months | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1498. en:neurologic regression following seizure onset --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurologic regression following seizure onset | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1499. en:neurologic sequelae not always present --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurologic sequelae not always present | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1500. en:neurologic symptoms, if present, usually result from associated syringomyelia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurologic symptoms, if present, usually result from associated syringomyelia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1501. en:neuromuscular disturbances, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuromuscular disturbances, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1502. en:neuron apoptotic process --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuron apoptotic process | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1503. en:neuron loss --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuron loss | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1504. en:neuronal heterotopia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal heterotopia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1505. en:neuronal inclusion bodies stain for neuroserpin --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal inclusion bodies stain for neuroserpin | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1506. en:neuronal loss (patient a) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal loss (patient a) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1507. en:neuronal loss and gliosis in caudate and putamen --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal loss and gliosis in caudate and putamen | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1508. en:neuronal loss and gliosis in the cerebral cortex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal loss and gliosis in the cerebral cortex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1509. en:neuronal loss and gliosis in the substantia nigra pars compacta --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal loss and gliosis in the substantia nigra pars compacta | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1510. en:neuronal loss in the brainstem --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal loss in the brainstem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1511. en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1512. en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1513. en:neuronal loss, diffuse --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal loss, diffuse | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1514. en:neuronal loss, particularly of cerebellar purkinje cells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal loss, particularly of cerebellar purkinje cells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1515. en:neuronal migration defect --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal migration defect | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1516. en:neuronal migration disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuronal migration disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1517. en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1518. en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1519. en:neuropathology shows diffuse demyelination of the cerebral white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuropathology shows diffuse demyelination of the cerebral white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1520. en:neuropathology shows neuronal degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuropathology shows neuronal degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1521. en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1522. en:neurophysiologic abnormalities (eeg, sep, vep) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurophysiologic abnormalities (eeg, sep, vep) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1523. en:neuropil --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuropil | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1524. en:neuropsychologic cognitive abnormalities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuropsychologic cognitive abnormalities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1525. en:neuropsychologic impairment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neuropsychologic impairment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1526. en:neurosarcoidosis (5-16% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:neurosarcoidosis (5-16% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1527. en:no amyloid plaques --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no amyloid plaques | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1528. en:no autistic features --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no autistic features | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1529. en:no cerebellar signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no cerebellar signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1530. en:no language development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no language development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1531. en:no lewy bodies --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no lewy bodies | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1532. en:no mental retardation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no mental retardation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1533. en:no motor skills acquired (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no motor skills acquired (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1534. en:no neurofibromas --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no neurofibromas | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1535. en:no other neurologic deficits --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no other neurologic deficits | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1536. en:no other neurologic disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no other neurologic disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1537. en:no pick bodies or lewy bodies --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no pick bodies or lewy bodies | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1538. en:no response to l-dopa treatment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no response to l-dopa treatment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1539. en:no seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1540. en:no sensory symptoms --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no sensory symptoms | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1541. en:no speech acquisition --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no speech acquisition | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1542. en:no speech development (in most patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no speech development (in most patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1543. en:no speech problem --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no speech problem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1544. en:no spontaneous movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no spontaneous movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1545. en:no structural brain abnormalities seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no structural brain abnormalities seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1546. en:no structural brain anomalies --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no structural brain anomalies | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1547. en:no tremor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no tremor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1548. en:no visual fixation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no visual fixation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1549. en:no voluntary movement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:no voluntary movement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1550. en:nocturnal occurrence --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nocturnal occurrence | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1551. en:nocturnal occurrence, usually during light sleep --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nocturnal occurrence, usually during light sleep | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1552. en:nocturnal sleep disruption --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nocturnal sleep disruption | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1553. en:nodding of head --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nodding of head | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1554. en:nodular heterotopia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nodular heterotopia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1555. en:nodular heterotopia (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nodular heterotopia (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1556. en:nodular heterotopia of the grey matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nodular heterotopia of the grey matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1557. en:non-febrile seizures later --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:non-febrile seizures later | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1558. en:non-purposeful arm movements, choreoathetoid-like --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:non-purposeful arm movements, choreoathetoid-like | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1559. en:nonspecific leukoencephalopathy (52%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nonspecific leukoencephalopathy (52%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1560. en:nonspecific spongiform degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nonspecific spongiform degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1561. en:normal brain mri or ct scan --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal brain mri or ct scan | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1562. en:normal cognition (reported in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal cognition (reported in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1563. en:normal development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1564. en:normal development in some patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal development in some patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1565. en:normal development until 6-18 months --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal development until 6-18 months | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1566. en:normal early development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal early development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1567. en:normal initial psychomotor development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal initial psychomotor development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1568. en:normal intellectual development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal intellectual development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1569. en:normal intellectual function --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal intellectual function | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1570. en:normal intelligence (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal intelligence (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1571. en:normal intelligence (majority) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal intelligence (majority) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1572. en:normal intelligence in carrier females --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal intelligence in carrier females | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1573. en:normal intelligence in iib --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal intelligence in iib | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1574. en:normal intelligence in majority --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal intelligence in majority | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1575. en:normal intelligence in most cases --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal intelligence in most cases | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1576. en:normal interictal neurologic examination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal interictal neurologic examination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1577. en:normal motor conduction studies (initially) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal motor conduction studies (initially) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1578. en:normal muscle strength --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal muscle strength | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1579. en:normal neurologic development in most cases --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal neurologic development in most cases | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1580. en:normal neurological development is possible --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal neurological development is possible | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1581. en:normal psychomotor development until age 2 to 3 years --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal psychomotor development until age 2 to 3 years | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1582. en:normal sleep-onset time (normal time of falling asleep) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal sleep-onset time (normal time of falling asleep) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1583. en:normal to mild mental retardation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal to mild mental retardation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1584. en:normal to mildly delayed development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal to mildly delayed development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1585. en:normal, timely language development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:normal, timely language development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1586. en:nystagmus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nystagmus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1587. en:nystagmus decreases on convergence --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nystagmus decreases on convergence | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1588. en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1589. en:nystagmus, jerky, horizontal, congenital --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nystagmus, jerky, horizontal, congenital | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1590. en:nystagmus, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:nystagmus, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1591. en:occipital dermal sinus tract --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:occipital dermal sinus tract | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1592. en:occipital encephalocele (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:occipital encephalocele (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1593. en:occipital encephalocele (wws) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:occipital encephalocele (wws) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1594. en:occipital encephaloceles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:occipital encephaloceles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1595. en:occipital lobe atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:occipital lobe atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1596. en:occipital lobe infarct (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:occipital lobe infarct (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1597. en:occipital meningocele (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:occipital meningocele (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1598. en:occipital myelomeningocele (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:occipital myelomeningocele (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1599. en:occlusive hydrocephalus, congenital --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:occlusive hydrocephalus, congenital | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1600. en:ocular motility spared --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ocular motility spared | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1601. en:oculomotor apraxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:oculomotor apraxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1602. en:olfactory groove meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:olfactory groove meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1603. en:olfactory lobe agenesis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:olfactory lobe agenesis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1604. en:oligodendrocytes with foamy cytoplasm --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:oligodendrocytes with foamy cytoplasm | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1605. en:olivopontocerebellar hypoplasia, fetal-onset --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:olivopontocerebellar hypoplasia, fetal-onset | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1606. en:only walking achieved --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:only walking achieved | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1607. en:onset may be triggered by emotional stress, fever, exercise, exposure to heat --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:onset may be triggered by emotional stress, fever, exercise, exposure to heat | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1608. en:open operculum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:open operculum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1609. en:open spina bifida (myelomeningocele, 182940) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:open spina bifida (myelomeningocele, 182940) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1610. en:opisthotonos (type ii) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:opisthotonos (type ii) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1611. en:opsoclonus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:opsoclonus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1612. en:optic nerve hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:optic nerve hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1613. en:optic nerve sheath meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:optic nerve sheath meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1614. en:optic tract agenesis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:optic tract agenesis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1615. en:ossification of the faux cerebri (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ossification of the faux cerebri (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1616. en:other auras may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:other auras may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1617. en:over time, white matter vanishes and is replaced by csf --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:over time, white matter vanishes and is replaced by csf | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1618. en:pachygyria (posterior-to-anterior gradient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pachygyria (posterior-to-anterior gradient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1619. en:pachygyria with preferential frontoparietal involvement (meb) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pachygyria with preferential frontoparietal involvement (meb) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1620. en:pachygyria, bilateral frontotemporal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pachygyria, bilateral frontotemporal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1621. en:pachygyria, most prominent in the frontal lobes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pachygyria, most prominent in the frontal lobes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1622. en:pachygyrias --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pachygyrias | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1623. en:pachymeningitis cervicalis (cervical cord compression due to thickened dura) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pachymeningitis cervicalis (cervical cord compression due to thickened dura) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1624. en:pain affects upper body --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pain affects upper body | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1625. en:pallidal degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pallidal degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1626. en:papillary meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:papillary meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1627. en:paralysis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paralysis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1628. en:paralysis, episodic, after strenuous exercise --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paralysis, episodic, after strenuous exercise | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1629. en:paraparesis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paraparesis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1630. en:paraplegia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paraplegia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1631. en:paraplegia secondary to spinal cord compression due to severe kyphosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paraplegia secondary to spinal cord compression due to severe kyphosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1632. en:parasagittal meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:parasagittal meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1633. en:parenchymal neuromelanosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:parenchymal neuromelanosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1634. en:paresis (hcp) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paresis (hcp) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1635. en:paresis of extensor muscles of the big toe is presenting symptom --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paresis of extensor muscles of the big toe is presenting symptom | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1636. en:parietal lobe epilepsy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:parietal lobe epilepsy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1637. en:parkinsonism (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:parkinsonism (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1638. en:parkinsonism (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:parkinsonism (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1639. en:parkinsonism (later onset) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:parkinsonism (later onset) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1640. en:parkinsonism (later) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:parkinsonism (later) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1641. en:parkinsonism, early-onset --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:parkinsonism, early-onset | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1642. en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1643. en:paroxysmal choreoathetosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paroxysmal choreoathetosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1644. en:paroxysmal dystonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paroxysmal dystonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1645. en:paroxysmal lethargy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paroxysmal lethargy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1646. en:paroxysmal nonkinesigenic dyskinesia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paroxysmal nonkinesigenic dyskinesia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1647. en:partial absence of the corpus callosum (in one patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:partial absence of the corpus callosum (in one patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1648. en:partial agenesis of corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:partial agenesis of corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1649. en:partial agenesis of the corpus callosum (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:partial agenesis of the corpus callosum (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1650. en:partial or complete agenesis of corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:partial or complete agenesis of corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1651. en:partial or total agenesis of the corpus callosum (33%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:partial or total agenesis of the corpus callosum (33%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1652. en:partial pachygyria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:partial pachygyria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1653. en:partial response to pyridoxine --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:partial response to pyridoxine | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1654. en:partial seizure --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:partial seizure | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1655. en:partial seizures, simple and complex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:partial seizures, simple and complex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1656. en:patchy demyelination of subcortical white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:patchy demyelination of subcortical white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1657. en:patellar and ankle clonus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:patellar and ankle clonus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1658. en:pathologic calcification, calcified structure --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pathologic calcification, calcified structure | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1659. en:pathological aspects --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pathological aspects | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1660. en:patients may develop a seizure disorder later in life --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:patients may develop a seizure disorder later in life | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1661. en:patients may have no structural abnormalities in the central nervous system --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:patients may have no structural abnormalities in the central nervous system | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1662. en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1663. en:patients show normal psychomotor development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:patients show normal psychomotor development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1664. en:paucity of anterior horn motor neurons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:paucity of anterior horn motor neurons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1665. en:pediatric terminology --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pediatric terminology | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1666. en:periodic paralysis, usually hypokalemic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:periodic paralysis, usually hypokalemic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1667. en:periodic stiffness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:periodic stiffness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1668. en:peripheral motor neuropathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:peripheral motor neuropathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1669. en:perivascular spaces --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:perivascular spaces | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1670. en:periventricular calcifications --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:periventricular calcifications | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1671. en:periventricular gray matter heterotopia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:periventricular gray matter heterotopia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1672. en:periventricular hemorrhagic infarction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:periventricular hemorrhagic infarction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1673. en:periventricular white matter abnormalities (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:periventricular white matter abnormalities (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1674. en:periventricular white matter gliosis (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:periventricular white matter gliosis (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1675. en:periventricular white matter hyperintensities, bilateral --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:periventricular white matter hyperintensities, bilateral | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1676. en:periventricular white matter lesions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:periventricular white matter lesions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1677. en:persistent falcine venous sinus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:persistent falcine venous sinus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1678. en:photoparoxysmal and photomyoclonic responses --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:photoparoxysmal and photomyoclonic responses | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1679. en:photoparoxysmal response (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:photoparoxysmal response (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1680. en:photophobia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:photophobia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1681. en:physiopathological --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:physiopathological | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1682. en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1683. en:pigmentary loss in the substantia nigra --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pigmentary loss in the substantia nigra | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1684. en:pineal gland --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pineal gland | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1685. en:pituitary agenesis (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pituitary agenesis (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1686. en:pituitary gland hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pituitary gland hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1687. en:pituitary hypoplasia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pituitary hypoplasia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1688. en:polymicrogyria (64%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:polymicrogyria (64%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1689. en:polymicrogyria (meb) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:polymicrogyria (meb) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1690. en:polymicrogyria, asymmetric or symmetric --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:polymicrogyria, asymmetric or symmetric | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1691. en:polymicrogyria, bilateral frontoparietal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:polymicrogyria, bilateral frontoparietal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1692. en:polymicrogyria, predominantly frontal and perisylvian --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:polymicrogyria, predominantly frontal and perisylvian | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1693. en:polymicrogyria, temporo-occipital --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:polymicrogyria, temporo-occipital | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1694. en:polyneuropathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:polyneuropathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1695. en:pontine dysraphia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pontine dysraphia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1696. en:pontine hypoplasia (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pontine hypoplasia (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1697. en:pontocerebellar arachnoid cyst (reported in 2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pontocerebellar arachnoid cyst (reported in 2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1698. en:pontoneocerebellar hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pontoneocerebellar hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1699. en:poor balance (finding) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor balance (finding) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1700. en:poor cognition --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor cognition | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1701. en:poor concentration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor concentration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1702. en:poor coordination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor coordination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1703. en:poor delineation of cerebral cortical regions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor delineation of cerebral cortical regions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1704. en:poor dendritic maturation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor dendritic maturation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1705. en:poor feeding (congenital form form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor feeding (congenital form form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1706. en:poor fine and gross motor coordination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor fine and gross motor coordination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1707. en:poor gross motor coordination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor gross motor coordination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1708. en:poor head and trunk control in infancy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor head and trunk control in infancy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1709. en:poor head control --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor head control | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1710. en:poor language --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor language | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1711. en:poor motor coordination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor motor coordination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1712. en:poor motor development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor motor development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1713. en:poor myelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor myelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1714. en:poor neonatal suck and swallow reflexes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor neonatal suck and swallow reflexes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1715. en:poor or absent independent walking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor or absent independent walking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1716. en:poor or absent speech development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor or absent speech development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1717. en:poor school performance --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor school performance | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1718. en:poor speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1719. en:poor spontaneous movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor spontaneous movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1720. en:poor vestibuloocular reflex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor vestibuloocular reflex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1721. en:poor visual-spatial construction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:poor visual-spatial construction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1722. en:porencephaly (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:porencephaly (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1723. en:posterior column sensory loss --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:posterior column sensory loss | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1724. en:posterior fossa arachnoid cyst --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:posterior fossa arachnoid cyst | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1725. en:posterior fossa cyst continuous with the fourth ventricle --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:posterior fossa cyst continuous with the fourth ventricle | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1726. en:posterior fossa cysts (wws) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:posterior fossa cysts (wws) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1727. en:posterior pachygyria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:posterior pachygyria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1728. en:postnatal development of hypertonic extremities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:postnatal development of hypertonic extremities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1729. en:postural hand tremor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:postural hand tremor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1730. en:postural instability --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:postural instability | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1731. en:postural instability (63%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:postural instability (63%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1732. en:postural tremor (later onset, spreads to all limbs and neck) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:postural tremor (later onset, spreads to all limbs and neck) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1733. en:posturing --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:posturing | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1734. en:praxis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:praxis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1735. en:pre-senile dementia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pre-senile dementia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1736. en:premature stroke --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:premature stroke | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1737. en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1738. en:presenile and senile dementia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:presenile and senile dementia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1739. en:primitive reflex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:primitive reflex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1740. en:primitive reflexes (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:primitive reflexes (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1741. en:primitive sylvian fissures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:primitive sylvian fissures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1742. en:prion protein-positive senile plaques --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:prion protein-positive senile plaques | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1743. en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1744. en:profound intellectual disabilities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:profound intellectual disabilities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1745. en:progressive bulbar palsy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive bulbar palsy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1746. en:progressive cerebellar degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive cerebellar degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1747. en:progressive cerebral atrophy seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive cerebral atrophy seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1748. en:progressive cognitive decline following normal development in childhood (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive cognitive decline following normal development in childhood (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1749. en:progressive extrapyramidal movement disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive extrapyramidal movement disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1750. en:progressive gait ataxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive gait ataxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1751. en:progressive impairment of gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive impairment of gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1752. en:progressive intellectual decline --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive intellectual decline | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1753. en:progressive myoclonus epilepsy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive myoclonus epilepsy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1754. en:progressive neurologic deterioration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive neurologic deterioration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1755. en:progressive psychomotor deterioration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive psychomotor deterioration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1756. en:progressive spastic diplegia to quadriplegia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive spastic diplegia to quadriplegia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1757. en:progressive spastic paraplegia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive spastic paraplegia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1758. en:progressive spastic quadriplegia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive spastic quadriplegia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1759. en:progressive, symmetric degeneration of the caudate and putamen --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:progressive, symmetric degeneration of the caudate and putamen | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1760. en:prolonged seizure --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:prolonged seizure | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1761. en:prolonged somatosensory evoked potentials (seps) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:prolonged somatosensory evoked potentials (seps) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1762. en:prominent cortical sulci --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:prominent cortical sulci | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1763. en:prominent perivascular spaces --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:prominent perivascular spaces | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1764. en:prominent perivascular spaces with surrounding gliosis in periatrial white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:prominent perivascular spaces with surrounding gliosis in periatrial white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1765. en:prominent sulci --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:prominent sulci | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1766. en:proximal amyotrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:proximal amyotrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1767. en:proximal muscle weakness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:proximal muscle weakness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1768. en:psammomatous meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psammomatous meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1769. en:pseudobulbar palsy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pseudobulbar palsy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1770. en:pseudobulbar signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pseudobulbar signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1771. en:pseudobulbar symptoms (uncontrolled laughter, weeping) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pseudobulbar symptoms (uncontrolled laughter, weeping) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1772. en:pseudotumor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pseudotumor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1773. en:psychiatric disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychiatric disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1774. en:psychomotor agitation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor agitation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1775. en:psychomotor delay (evident at 3 months) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor delay (evident at 3 months) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1776. en:psychomotor delay after second year --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor delay after second year | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1777. en:psychomotor delay, mild to moderate --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor delay, mild to moderate | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1778. en:psychomotor delay, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor delay, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1779. en:psychomotor deterioration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor deterioration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1780. en:psychomotor deterioration (classical form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor deterioration (classical form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1781. en:psychomotor impairments --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor impairments | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1782. en:psychomotor regression --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor regression | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1783. en:psychomotor regression (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor regression (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1784. en:psychomotor regression (onset within first year of life) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor regression (onset within first year of life) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1785. en:psychomotor regression may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor regression may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1786. en:psychomotor regression, episodic, often associated with common childhood infections --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor regression, episodic, often associated with common childhood infections | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1787. en:psychomotor regression, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor regression, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1788. en:psychomotor regression, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor regression, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1789. en:psychomotor retardation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor retardation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1790. en:psychomotor retardation (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor retardation (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1791. en:psychomotor retardation, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor retardation, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1792. en:psychomotor retardation, profound --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor retardation, profound | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1793. en:psychomotor retardation, profound, in those who survive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor retardation, profound, in those who survive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1794. en:psychomotor retardation, severe to profound --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:psychomotor retardation, severe to profound | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1795. en:purposeless movements (if left untreated) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:purposeless movements (if left untreated) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1796. en:pyramidal features (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pyramidal features (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1797. en:pyramidal hypertonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pyramidal hypertonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1798. en:pyramidal signs (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pyramidal signs (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1799. en:pyramidal signs (21% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pyramidal signs (21% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1800. en:pyramidal signs (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pyramidal signs (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1801. en:pyramidal signs, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pyramidal signs, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1802. en:pyramidal syndrome of the lower limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pyramidal syndrome of the lower limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1803. en:pyramidal system --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pyramidal system | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1804. en:pyramidal tract signs (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:pyramidal tract signs (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1805. en:quadriplegia, flaccid --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:quadriplegia, flaccid | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1806. en:quadriplegic dyskinesia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:quadriplegic dyskinesia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1807. en:quadrupedal gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:quadrupedal gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1808. en:quadrupedal gait (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:quadrupedal gait (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1809. en:quadrupedal gait (palm of hands, legs straight) with diagonal walking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:quadrupedal gait (palm of hands, legs straight) with diagonal walking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1810. en:rapid initial onset of symptoms (hours to weeks) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:rapid initial onset of symptoms (hours to weeks) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1811. en:rare secondary generalization --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:rare secondary generalization | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1812. en:reactive gliosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reactive gliosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1813. en:reduced consciousness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reduced consciousness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1814. en:reduced consciousness, hypoglycemia-related --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reduced consciousness, hypoglycemia-related | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1815. en:reduced posterior white matter volume (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reduced posterior white matter volume (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1816. en:reduced sleep latency --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reduced sleep latency | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1817. en:reduced tendon reflexes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reduced tendon reflexes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1818. en:reduction of white matter, generalized --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reduction of white matter, generalized | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1819. en:reflex epilepsy, photosensitive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reflex epilepsy, photosensitive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1820. en:reflex, deep tendon, absent --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reflex, deep tendon, absent | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1821. en:regression of development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:regression of development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1822. en:regression of motor development --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:regression of motor development | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1823. en:relative preservation of purkinje cells, but they are deformed and disaligned --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:relative preservation of purkinje cells, but they are deformed and disaligned | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1824. en:relative preservation of the cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:relative preservation of the cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1825. en:rem sleep behavior disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:rem sleep behavior disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1826. en:resting tremor (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:resting tremor (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1827. en:resting tremors --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:resting tremors | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1828. en:restlessness at birth --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:restlessness at birth | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1829. en:restrictive behavior, interests, and activities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:restrictive behavior, interests, and activities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1830. en:results in nocturnal insomnia and chronic sleep deprivation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:results in nocturnal insomnia and chronic sleep deprivation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1831. en:retrocerebellar cyst --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:retrocerebellar cyst | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1832. en:retrocerebellar cyst (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:retrocerebellar cyst (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1833. en:retrocerebellar cyst (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:retrocerebellar cyst (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1834. en:retrocollis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:retrocollis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1835. en:retroflexion of the neck --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:retroflexion of the neck | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1836. en:reye syndrome --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:reye syndrome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1837. en:rhabdoid meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:rhabdoid meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1838. en:rhombencephalosynapsis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:rhombencephalosynapsis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1839. en:rigidity during seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:rigidity during seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1840. en:rigidity, axial and limb --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:rigidity, axial and limb | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1841. en:roentgenographic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:roentgenographic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1842. en:roving eye movements (infancy) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:roving eye movements (infancy) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1843. en:rudimentary white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:rudimentary white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1844. en:sagittal sinus thrombosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sagittal sinus thrombosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1845. en:scanning speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:scanning speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1846. en:scant iron deposition in the brain (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:scant iron deposition in the brain (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1847. en:scattered cns demyelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:scattered cns demyelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1848. en:schizencephaly --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:schizencephaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1849. en:schizophrenia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:schizophrenia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1850. en:school problem (finding) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:school problem (finding) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1851. en:scissoring --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:scissoring | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1852. en:scissors gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:scissors gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1853. en:secondary generalization --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secondary generalization | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1854. en:secondary generalization may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secondary generalization may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1855. en:secondary generalization occurs in about 33% of patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secondary generalization occurs in about 33% of patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1856. en:secondary generalized tonic-clonic seizures may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secondary generalized tonic-clonic seizures may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1857. en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1858. en:secondary hypertonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secondary hypertonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1859. en:secondary involvement of proximal and trunk muscles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secondary involvement of proximal and trunk muscles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1860. en:secondary seizures (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secondary seizures (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1861. en:secondary spinal cord compression may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secondary spinal cord compression may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1862. en:secretory meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:secretory meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1863. en:see spg5a (270800) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:see spg5a (270800) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1864. en:segmental sensory loss, especially of pain and temperature --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:segmental sensory loss, especially of pain and temperature | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1865. en:seizure --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizure | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1866. en:seizure (in a subset of patients in infancy) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizure (in a subset of patients in infancy) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1867. en:seizure including seizure-like activity in utero starting around 18 weeks gestation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizure including seizure-like activity in utero starting around 18 weeks gestation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1868. en:seizure, febrile (2/3 children) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizure, febrile (2/3 children) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1869. en:seizures (40%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (40%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1870. en:seizures (50%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (50%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1871. en:seizures (> 90%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (> 90%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1872. en:seizures (adult) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (adult) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1873. en:seizures (cvs+) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (cvs+) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1874. en:seizures (eclampsia) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (eclampsia) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1875. en:seizures (in 1 of 3 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (in 1 of 3 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1876. en:seizures (in 2 of 9 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (in 2 of 9 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1877. en:seizures (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1878. en:seizures (juvenile form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (juvenile form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1879. en:seizures (mean onset 4-5 months) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (mean onset 4-5 months) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1880. en:seizures (meb) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (meb) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1881. en:seizures (onset <2 years) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (onset <2 years) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1882. en:seizures (rare, in males) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (rare, in males) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1883. en:seizures (reported in 2 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (reported in 2 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1884. en:seizures (type i and type ii, juvenile) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (type i and type ii, juvenile) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1885. en:seizures (uncommon) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures (uncommon) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1886. en:seizures affect the vocal cords, lips, mouth, and face --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures affect the vocal cords, lips, mouth, and face | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1887. en:seizures are poorly controlled --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures are poorly controlled | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1888. en:seizures may occur during hypotensive episodes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures may occur during hypotensive episodes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1889. en:seizures occur in clusters over 1 or several days --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures occur in clusters over 1 or several days | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1890. en:seizures occur multiple times per day --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures occur multiple times per day | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1891. en:seizures often associated with infections --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures often associated with infections | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1892. en:seizures provoked by tactile stimulation or extreme emotion --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures provoked by tactile stimulation or extreme emotion | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1893. en:seizures recur in 33% of patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures recur in 33% of patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1894. en:seizures, focal, partial, motor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, focal, partial, motor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1895. en:seizures, generalized, afebrile --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, generalized, afebrile | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1896. en:seizures, hypoglycemic (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, hypoglycemic (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1897. en:seizures, infantile-onset --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, infantile-onset | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1898. en:seizures, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1899. en:seizures, multiple types --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, multiple types | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1900. en:seizures, neonatal (2p21del) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, neonatal (2p21del) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1901. en:seizures, onset age 5 to 10 years --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, onset age 5 to 10 years | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1902. en:seizures, partial with secondary generalization, focal at onset, usually motor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, partial with secondary generalization, focal at onset, usually motor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1903. en:seizures, refractory to treatment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, refractory to treatment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1904. en:seizures, severe, drug-resistant, intractable --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, severe, drug-resistant, intractable | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1905. en:seizures, sudden-onset, drug-resistant --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, sudden-onset, drug-resistant | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1906. en:seizures, tonic, clonic, focal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, tonic, clonic, focal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1907. en:seizures, tonic-clonic or absence (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:seizures, tonic-clonic or absence (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1908. en:self mutilation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:self mutilation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1909. en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1910. en:sensitivity to neuroleptic medication --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sensitivity to neuroleptic medication | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1911. en:sensory ataxia (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sensory ataxia (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1912. en:septum pellucidum deficient or cavum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:septum pellucidum deficient or cavum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1913. en:severe brain damage --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe brain damage | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1914. en:severe cognitive deficits (develop later) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe cognitive deficits (develop later) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1915. en:severe cognitive impairment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe cognitive impairment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1916. en:severe delay in myelination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe delay in myelination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1917. en:severe developmental delay in survivors --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe developmental delay in survivors | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1918. en:severe expressive language delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe expressive language delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1919. en:severe mental retardation (congenital form) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe mental retardation (congenital form) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1920. en:severe mental retardation (iq 10-40) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe mental retardation (iq 10-40) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1921. en:severe muscular hypotonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe muscular hypotonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1922. en:severe psychomotor retardation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe psychomotor retardation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1923. en:severe psychomotor retardation from birth --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:severe psychomotor retardation from birth | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1924. en:shivering sensation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:shivering sensation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1925. en:short pons --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:short pons | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1926. en:shorter daily total sleep times compared to age-matched controls --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:shorter daily total sleep times compared to age-matched controls | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1927. en:simple partial seizures --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:simple partial seizures | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1928. en:simple partial seizures with secondary generalization --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:simple partial seizures with secondary generalization | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1929. en:simplified cortical gyration pattern --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:simplified cortical gyration pattern | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1930. en:simplified gyral pattern (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:simplified gyral pattern (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1931. en:simplified gyral pattern (in one patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:simplified gyral pattern (in one patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1932. en:simplified gyration pattern --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:simplified gyration pattern | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1933. en:sinus pericranii (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sinus pericranii (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1934. en:skin photosensitivity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:skin photosensitivity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1935. en:sleep abnormalities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep abnormalities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1936. en:sleep apnea (in 1/4 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep apnea (in 1/4 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1937. en:sleep disorder (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep disorder (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1938. en:sleep disturbances --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep disturbances | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1939. en:sleep disturbances (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep disturbances (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1940. en:sleep disturbances common --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep disturbances common | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1941. en:sleep impairment, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep impairment, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1942. en:sleep paralysis at beginning or end of sleep period (in 60% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep paralysis at beginning or end of sleep period (in 60% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1943. en:sleep pattern disturbance --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep pattern disturbance | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1944. en:sleep talking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep talking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1945. en:sleep-wake cycle disturbance --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sleep-wake cycle disturbance | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1946. en:slow reactions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:slow reactions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1947. en:slow spike-wave discharges --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:slow spike-wave discharges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1948. en:slow, broad-based gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:slow, broad-based gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1949. en:slowly progressive neurologic deterioration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:slowly progressive neurologic deterioration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1950. en:slurred speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:slurred speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1951. en:slurred speech, episodic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:slurred speech, episodic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1952. en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1953. en:small brain --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:small brain | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1954. en:small but structurally normal cerebral cortex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:small but structurally normal cerebral cortex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1955. en:small pituitary gland (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:small pituitary gland (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1956. en:small sella --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:small sella | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1957. en:small shrunken brain --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:small shrunken brain | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1958. en:small size of the left hippocampus gyri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:small size of the left hippocampus gyri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1959. en:small thalami --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:small thalami | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1960. en:small, thin cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:small, thin cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1961. en:smooth brain surface --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:smooth brain surface | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1962. en:smooth, thin cortical mantle (wws) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:smooth, thin cortical mantle (wws) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1963. en:social communication disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:social communication disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1964. en:somatosensory evoked potentials show prolonged latency --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:somatosensory evoked potentials show prolonged latency | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1965. en:some patients have neurologic involvement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:some patients have neurologic involvement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1966. en:somnolence --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:somnolence | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1967. en:sparing of optic tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sparing of optic tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1968. en:spastic ataxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic ataxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1969. en:spastic diplegia, symmetric --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic diplegia, symmetric | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1970. en:spastic dystonia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic dystonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1971. en:spastic paraparesis (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic paraparesis (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1972. en:spastic paraparesis (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic paraparesis (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1973. en:spastic paraplegia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic paraplegia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1974. en:spastic paraplegia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic paraplegia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1975. en:spastic paraplegia, later onset (in one patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic paraplegia, later onset (in one patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1976. en:spastic quadriplegia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic quadriplegia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1977. en:spastic quadriplegia (in one patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic quadriplegia (in one patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1978. en:spastic quadriplegia, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic quadriplegia, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1979. en:spastic tetraparesis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic tetraparesis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1980. en:spastic-ataxic gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spastic-ataxic gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1981. en:spasticity (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1982. en:spasticity (1 of 4 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity (1 of 4 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1983. en:spasticity (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1984. en:spasticity (later onset) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity (later onset) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1985. en:spasticity (later) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity (later) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1986. en:spasticity (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1987. en:spasticity in infancy (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity in infancy (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1988. en:spasticity may be present --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity may be present | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1989. en:spasticity of lower and upper limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity of lower and upper limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1990. en:spasticity, hyperreflexia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity, hyperreflexia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1991. en:spasticity, lower limbs greater than upper limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity, lower limbs greater than upper limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1992. en:spasticity, mainly in the lower limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity, mainly in the lower limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1993. en:spasticity, mild (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity, mild (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1994. en:spasticity, primarily lower limbs, but upper limbs may be involved --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity, primarily lower limbs, but upper limbs may be involved | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1995. en:spasticity, severe --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity, severe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1996. en:spasticity, severe, affecting lower limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity, severe, affecting lower limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1997. en:spasticity/paresis (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spasticity/paresis (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1998. en:specialized branches of medicine --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:specialized branches of medicine | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  1999. en:specific visual spatial processing defect --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:specific visual spatial processing defect | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2000. en:speech and language disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech and language disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2001. en:speech articulation defects --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech articulation defects | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2002. en:speech articulation problems --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech articulation problems | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2003. en:speech delay (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech delay (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2004. en:speech delay (10%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech delay (10%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2005. en:speech delay (59%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech delay (59%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2006. en:speech deterioration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech deterioration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2007. en:speech development delayed (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech development delayed (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2008. en:speech difficulties due to hypoglossia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech difficulties due to hypoglossia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2009. en:speech disorder (in 1 of 6 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech disorder (in 1 of 6 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2010. en:speech disorders (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech disorders (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2011. en:speech limited --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech limited | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2012. en:speech never acquired --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech never acquired | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2013. en:speech severely limited or absent --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech severely limited or absent | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2014. en:speech, limited or nonverbal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:speech, limited or nonverbal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2015. en:spina bifida --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spina bifida | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2016. en:spinal arteriovenous malformation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinal arteriovenous malformation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2017. en:spinal cord compression --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinal cord compression | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2018. en:spinal cord compression by tumor infiltration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinal cord compression by tumor infiltration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2019. en:spinal cord disorder --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinal cord disorder | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2020. en:spinal cord glial hyperplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinal cord glial hyperplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2021. en:spinal cord meningioma --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinal cord meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2022. en:spinal neurofibromas (64%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinal neurofibromas (64%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2023. en:spinocerebellar ataxia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinocerebellar ataxia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2024. en:spinocerebellar ataxia (upper and lower limb involvement) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinocerebellar ataxia (upper and lower limb involvement) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2025. en:spinocerebellar degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spinocerebellar degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2026. en:spongiform changes are mild or may not be present --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spongiform changes are mild or may not be present | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2027. en:spongiform encephalomyelopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spongiform encephalomyelopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2028. en:spongy degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:spongy degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2029. en:stance ataxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stance ataxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2030. en:staring --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:staring | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2031. en:staring spells --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:staring spells | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2032. en:start with tonic posturing --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:start with tonic posturing | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2033. en:startle myoclonus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:startle myoclonus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2034. en:status epilepticus (in 1 of 6 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:status epilepticus (in 1 of 6 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2035. en:stenosis of the aqueduct of sylvius (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stenosis of the aqueduct of sylvius (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2036. en:stereotypic movements --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stereotypic movements | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2037. en:stiff gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stiff gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2038. en:stiff limbs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stiff limbs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2039. en:stiffness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stiffness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2040. en:stiffness while walking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stiffness while walking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2041. en:stimulation sensitive segmental myoclonus (stage 2) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stimulation sensitive segmental myoclonus (stage 2) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2042. en:stoke-like lesions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stoke-like lesions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2043. en:stretched cerebellar peduncles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stretched cerebellar peduncles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2044. en:striatal atrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:striatal atrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2045. en:stroke-like episodes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stroke-like episodes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2046. en:stroke-like episodes (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:stroke-like episodes (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2047. en:strokes due to coagulopathy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:strokes due to coagulopathy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2048. en:structural abnormalities in the basal ganglia (especially caudate) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:structural abnormalities in the basal ganglia (especially caudate) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2049. en:structural abnormalities of cerebellum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:structural abnormalities of cerebellum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2050. en:structural brain abnormalities --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:structural brain abnormalities | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2051. en:structure of central sensory visual system --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:structure of central sensory visual system | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2052. en:structure of decussation of superior cerebellar peduncles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:structure of decussation of superior cerebellar peduncles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2053. en:sturge-weber syndrome --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sturge-weber syndrome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2054. en:subacute neurologic deterioration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subacute neurologic deterioration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2055. en:subarachnoid hemorrhage --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subarachnoid hemorrhage | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2056. en:subarachnoid hemorrhage (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subarachnoid hemorrhage (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2057. en:subcortical band or laminar heterotopia (in female carriers) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subcortical band or laminar heterotopia (in female carriers) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2058. en:subcortical lesions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subcortical lesions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2059. en:subcortical lesions with edema --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subcortical lesions with edema | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2060. en:subcortical leukodystrophy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subcortical leukodystrophy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2061. en:subcortical nodular grey matter heterotopia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subcortical nodular grey matter heterotopia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2062. en:subcortical nodular lesions in perivascular white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subcortical nodular lesions in perivascular white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2063. en:subcortical white matter abnormalities (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subcortical white matter abnormalities (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2064. en:subcortical white matter abnormalities seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subcortical white matter abnormalities seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2065. en:subependymal heterotopias --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subependymal heterotopias | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2066. en:subependymal nodules --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subependymal nodules | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2067. en:subnormal cognition --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subnormal cognition | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2068. en:subnormal intelligence (62%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:subnormal intelligence (62%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2069. en:sudden awakening --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sudden awakening | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2070. en:sudden onset of neuropsychiatric symptoms --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sudden onset of neuropsychiatric symptoms | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2071. en:superficial laminar spongiosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:superficial laminar spongiosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2072. en:suppression-burst pattern --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:suppression-burst pattern | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2073. en:suppression-burst pattern see on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:suppression-burst pattern see on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2074. en:supranuclear gaze palsy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:supranuclear gaze palsy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2075. en:supratentorial structures unformed or regressed --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:supratentorial structures unformed or regressed | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2076. en:sweating problem --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:sweating problem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2077. en:swelling of the cerebral white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:swelling of the cerebral white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2078. en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2079. en:symmetric spinal nerve root neurofibromas --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:symmetric spinal nerve root neurofibromas | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2080. en:symptoms are exacerbated during pregnancy --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:symptoms are exacerbated during pregnancy | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2081. en:syndrome screaming --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:syndrome screaming | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2082. en:synkinesia (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:synkinesia (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2083. en:syringomyelia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:syringomyelia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2084. en:syringomyelia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:syringomyelia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2085. en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2086. en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2087. en:t2-weighted hyperintensities in the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:t2-weighted hyperintensities in the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2088. en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2089. en:t2-weighted hyperintensities in the corticospinal tracts and posterior arms of the internal capsule in older patients seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:t2-weighted hyperintensities in the corticospinal tracts and posterior arms of the internal capsule in older patients seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2090. en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2091. en:t2-weighted hyperintensities in the putamen and caudate nuclei --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:t2-weighted hyperintensities in the putamen and caudate nuclei | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2092. en:t2-weighted mri shows hyperintensities in the thalamus, basal ganglia, and brainstem during acute illness (may later resolve) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:t2-weighted mri shows hyperintensities in the thalamus, basal ganglia, and brainstem during acute illness (may later resolve) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2093. en:t2-weighted signal abnormalities in the deep white matter --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:t2-weighted signal abnormalities in the deep white matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2094. en:tau-immunoreactive inclusions in neurons and astrocytes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tau-immunoreactive inclusions in neurons and astrocytes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2095. en:tau-positive inclusions may be found --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tau-positive inclusions may be found | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2096. en:tbp- and 1c2-immunoreactive neuronal inclusions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tbp- and 1c2-immunoreactive neuronal inclusions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2097. en:tdp43-positive inclusions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tdp43-positive inclusions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2098. en:tectal enlargement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tectal enlargement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2099. en:temporal epileptiform discharges seen on eeg --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:temporal epileptiform discharges seen on eeg | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2100. en:temporal lobe heterotopias --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:temporal lobe heterotopias | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2101. en:temporal lobe seizures (in 1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:temporal lobe seizures (in 1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2102. en:tendency to walk on toes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tendency to walk on toes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2103. en:tetany, hypocalcemic (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tetany, hypocalcemic (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2104. en:tetany, hypocalcemic, episodic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tetany, hypocalcemic, episodic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2105. en:tethered cord (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tethered cord (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2106. en:tethered spinal cord syndrome --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tethered spinal cord syndrome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2107. en:thalamic lesions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thalamic lesions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2108. en:thalamic neuronal loss, especially in the medial dorsal nucleus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thalamic neuronal loss, especially in the medial dorsal nucleus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2109. en:thick corpus callosum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thick corpus callosum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2110. en:thick, maloriented superior cerebellar peduncles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thick, maloriented superior cerebellar peduncles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2111. en:thickened frontal cortex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thickened frontal cortex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2112. en:thickened optic nerve sheath --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thickened optic nerve sheath | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2113. en:thickening of the skull (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thickening of the skull (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2114. en:thin bony cortex --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thin bony cortex | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2115. en:thin corpus callosum (1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thin corpus callosum (1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2116. en:thin corpus callosum (1/4 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thin corpus callosum (1/4 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2117. en:thin corpus callosum enlarged ventricles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thin corpus callosum enlarged ventricles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2118. en:thin cortical mantle (wws) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thin cortical mantle (wws) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2119. en:thin optic chiasm --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thin optic chiasm | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2120. en:thinning of the cerebellopontine tracts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thinning of the cerebellopontine tracts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2121. en:third ventricle subependymal focal gliosis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:third ventricle subependymal focal gliosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2122. en:thrombosis of cerebral veins --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:thrombosis of cerebral veins | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2123. en:toe-walking gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:toe-walking gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2124. en:toe-walking in early childhood --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:toe-walking in early childhood | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2125. en:tonic convulsion --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tonic convulsion | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2126. en:tonic seizures, refractory --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tonic seizures, refractory | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2127. en:tonic-clonic seizures (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tonic-clonic seizures (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2128. en:torticollis --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:torticollis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2129. en:touch, vibration, and limb position may or may not be affected --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:touch, vibration, and limb position may or may not be affected | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2130. en:tow-walking --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tow-walking | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2131. en:transitional facial palsy (15%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:transitional facial palsy (15%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2132. en:tremor --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2133. en:tremor (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2134. en:tremor (3 patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor (3 patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2135. en:tremor (30%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor (30%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2136. en:tremor (57% of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor (57% of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2137. en:tremor (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2138. en:tremor (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2139. en:tremor is exacerbated by stress and exercise --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor is exacerbated by stress and exercise | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2140. en:tremor of the upper limb --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor of the upper limb | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2141. en:tremor with febrile episodes (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor with febrile episodes (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2142. en:tremor, action (arms, tongue, head, legs and trunk) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor, action (arms, tongue, head, legs and trunk) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2143. en:tremor, action, progressive --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor, action, progressive | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2144. en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2145. en:tremor, static --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor, static | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2146. en:tremor, variable --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremor, variable | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2147. en:tremors, action --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:tremors, action | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2148. en:trigeminal neuralgia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:trigeminal neuralgia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2149. en:trismus (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:trismus (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2150. en:truncal arching --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:truncal arching | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2151. en:truncal ataxia, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:truncal ataxia, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2152. en:truncal instability --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:truncal instability | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2153. en:type i arnold chiari malformation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:type i arnold chiari malformation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2154. en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2155. en:type iii eeg response is parietooccipital spikes followed by biphasic slow waves and spreading to the frontal region --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:type iii eeg response is parietooccipital spikes followed by biphasic slow waves and spreading to the frontal region | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2156. en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2157. en:ubiquitin-positive intranuclear neuronal inclusions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ubiquitin-positive intranuclear neuronal inclusions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2158. en:ultrastructure --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ultrastructure | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2159. en:unable to walk --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:unable to walk | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2160. en:undersulcation of the frontal lobes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:undersulcation of the frontal lobes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2161. en:unilateral cerebellar hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:unilateral cerebellar hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2162. en:unintelligible speech, vocalizations, grunting --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:unintelligible speech, vocalizations, grunting | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2163. en:unstable, ataxic gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:unstable, ataxic gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2164. en:unsteadiness, episodic --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:unsteadiness, episodic | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2165. en:unsteady standing --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:unsteady standing | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2166. en:upper and lower motor neuron degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper and lower motor neuron degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2167. en:upper and lower motor neuron disease --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper and lower motor neuron disease | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2168. en:upper limb ataxia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb ataxia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2169. en:upper limb dysmetria --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb dysmetria | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2170. en:upper limb hyperreflexia (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb hyperreflexia (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2171. en:upper limb involvement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb involvement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2172. en:upper limb involvement (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb involvement (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2173. en:upper limb involvement (onset in the first decade) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb involvement (onset in the first decade) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2174. en:upper limb involvement may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb involvement may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2175. en:upper limb spasticity (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb spasticity (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2176. en:upper limb spasticity, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb spasticity, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2177. en:upper limb weakness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limb weakness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2178. en:upper limbs affected --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limbs affected | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2179. en:upper limbs may be affected --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limbs may be affected | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2180. en:upper limbs may show mild involvement --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper limbs may show mild involvement | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2181. en:upper motor neuron degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper motor neuron degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2182. en:upper motor neuron dysfunction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper motor neuron dysfunction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2183. en:upper motor neuron signs (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper motor neuron signs (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2184. en:upper motor neuron signs, early --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper motor neuron signs, early | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2185. en:upper motor signs --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper motor signs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2186. en:upper motor signs (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:upper motor signs (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2187. en:use of ultrasonography --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:use of ultrasonography | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2188. en:usually occurs at night --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:usually occurs at night | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2189. en:vacuolization (patient a) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vacuolization (patient a) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2190. en:variable delay (iq range 52-104) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:variable delay (iq range 52-104) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2191. en:variable mental retardation (40%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:variable mental retardation (40%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2192. en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2193. en:varying degree of mental retardation --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:varying degree of mental retardation | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2194. en:vcp-positive inclusions --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vcp-positive inclusions | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2195. en:ventricular asymmetry --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ventricular asymmetry | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2196. en:ventricular dilatation (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ventricular dilatation (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2197. en:ventricular enlargement, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ventricular enlargement, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2198. en:ventriculomegaly (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ventriculomegaly (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2199. en:ventriculomegaly (variable) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ventriculomegaly (variable) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2200. en:ventriculomegaly, mild (rare) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ventriculomegaly, mild (rare) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2201. en:ventriculomeglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:ventriculomeglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2202. en:verbal delay (in some patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:verbal delay (in some patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2203. en:vermian hypoplasia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vermian hypoplasia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2204. en:vertical orientation of hippocampus --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vertical orientation of hippocampus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2205. en:vertigo --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vertigo | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2206. en:vertigo, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vertigo, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2207. en:very poor expressive speech --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:very poor expressive speech | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2208. en:vestibular anomalies (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vestibular anomalies (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2209. en:vestibular dysfunction, mild --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vestibular dysfunction, mild | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2210. en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2211. en:vibrissae --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:vibrissae | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2212. en:visceroautonomic dysfunction --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:visceroautonomic dysfunction | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2213. en:visual acuity is normal --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:visual acuity is normal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2214. en:visual auras --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:visual auras | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2215. en:visual changes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:visual changes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2216. en:visual hallucination --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:visual hallucination | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2217. en:visual impairment --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:visual impairment | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2218. en:visuospatial agnosia (in a subset of patients) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:visuospatial agnosia (in a subset of patients) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2219. en:waddling gait --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:waddling gait | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2220. en:walking delay --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:walking delay | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2221. en:walking impairment due to myoclonus late in disease --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:walking impairment due to myoclonus late in disease | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2222. en:weakness --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:weakness | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2223. en:weakness of hip and ankle flexion --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:weakness of hip and ankle flexion | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2224. en:white matter abnormalities (in some) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter abnormalities (in some) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2225. en:white matter abnormalities (uncommon) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter abnormalities (uncommon) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2226. en:white matter abnormalities on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter abnormalities on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2227. en:white matter abnormalities seen on mri --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter abnormalities seen on mri | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2228. en:white matter changes --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter changes | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2229. en:white matter changes may occur (in adulthood) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter changes may occur (in adulthood) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2230. en:white matter changes on brain imaging (less common) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter changes on brain imaging (less common) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2231. en:white matter degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2232. en:white matter dysmyelination/demyelination (71%) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter dysmyelination/demyelination (71%) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2233. en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2234. en:white matter immaturity --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter immaturity | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2235. en:white matter lacks axons and myelin --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter lacks axons and myelin | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2236. en:white matter lesions (1 patient) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter lesions (1 patient) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2237. en:white matter lesions in the basal ganglia --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter lesions in the basal ganglia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2238. en:white matter lesions in the brainstem may occur --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter lesions in the brainstem may occur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2239. en:white matter lesions may occur in the thalami, basal ganglia, and periventricular white matter (see leigh syndrome, 256000) --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter lesions may occur in the thalami, basal ganglia, and periventricular white matter (see leigh syndrome, 256000) | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2240. en:white matter lesions seen on brain imaging --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter lesions seen on brain imaging | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2241. en:white matter rarefaction and cystic degeneration --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter rarefaction and cystic degeneration | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2242. en:white matter streaks --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter streaks | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2243. en:white matter vacuolization --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:white matter vacuolization | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2244. en:wide subarachnoid spaces --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:wide subarachnoid spaces | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2245. en:wide sylvian fissures with incomplete opercularization --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:wide sylvian fissures with incomplete opercularization | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2246. en:widened lateral ventricles --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:widened lateral ventricles | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2247. en:widened subarachnoid spaces --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:widened subarachnoid spaces | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2248. en:widening of the operculum --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:widening of the operculum | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2249. en:widespread neuronal loss --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:widespread neuronal loss | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2250. en:writing fatigability --- r_associated #0: 20 --> méningé (syndrome)
    n1=en:writing fatigability | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2251. maladies --- r_associated #0: 20 --> méningé (syndrome)
    n1=maladies | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2252. médecine --- r_associated #0: 20 --> méningé (syndrome)
    n1=médecine | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2253. médecine spécialisée --- r_associated #0: 20 --> méningé (syndrome)
    n1=médecine spécialisée | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2254. médecine
    (science)
     --- r_associated #0: 20 --> méningé (syndrome)
    n1=médecine
    (science)
    | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2255. méningiomatose, sai --- r_associated #0: 20 --> méningé (syndrome)
    n1=méningiomatose, sai | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2256. méningiome multiple --- r_associated #0: 20 --> méningé (syndrome)
    n1=méningiome multiple | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2257. méningiomes multiples --- r_associated #0: 20 --> méningé (syndrome)
    n1=méningiomes multiples | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2258. méningé --- r_associated #0: 20 --> méningé (syndrome)
    n1=méningé | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2259. neurologie --- r_associated #0: 20 --> méningé (syndrome)
    n1=neurologie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2260. nystagmus --- r_associated #0: 20 --> méningé (syndrome)
    n1=nystagmus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2261. oncologie --- r_associated #0: 20 --> méningé (syndrome)
    n1=oncologie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2262. pachyméninge --- r_associated #0: 20 --> méningé (syndrome)
    n1=pachyméninge | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2263. paralysis --- r_associated #0: 20 --> méningé (syndrome)
    n1=paralysis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2264. pie-mère --- r_associated #0: 20 --> méningé (syndrome)
    n1=pie-mère | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2265. processus pathologique --- r_associated #0: 20 --> méningé (syndrome)
    n1=processus pathologique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2266. spécialités médicales --- r_associated #0: 20 --> méningé (syndrome)
    n1=spécialités médicales | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2267. syndrome --- r_associated #0: 20 --> méningé (syndrome)
    n1=syndrome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2268. tronc cérébral --- r_associated #0: 20 --> méningé (syndrome)
    n1=tronc cérébral | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2269. trouble psychiatrique --- r_associated #0: 20 --> méningé (syndrome)
    n1=trouble psychiatrique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2270. tumeur --- r_associated #0: 20 --> méningé (syndrome)
    n1=tumeur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2271. tumeurs --- r_associated #0: 20 --> méningé (syndrome)
    n1=tumeurs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=20
  2272. Arachnoïde --- r_associated #0: 15 --> méningé (syndrome)
    n1=Arachnoïde | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2273. Pie-mère --- r_associated #0: 15 --> méningé (syndrome)
    n1=Pie-mère | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2274. coma hépatique --- r_associated #0: 15 --> méningé (syndrome)
    n1=coma hépatique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2275. coupant avec des ciseaux --- r_associated #0: 15 --> méningé (syndrome)
    n1=coupant avec des ciseaux | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2276. en:brains --- r_associated #0: 15 --> méningé (syndrome)
    n1=en:brains | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2277. en:cutaneous meningioma --- r_associated #0: 15 --> méningé (syndrome)
    n1=en:cutaneous meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2278. en:kernig's sign --- r_associated #0: 15 --> méningé (syndrome)
    n1=en:kernig's sign | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2279. en:meninges --- r_associated #0: 15 --> méningé (syndrome)
    n1=en:meninges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2280. en:meningism --- r_associated #0: 15 --> méningé (syndrome)
    n1=en:meningism | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2281. en:optic nerve meningioma --- r_associated #0: 15 --> méningé (syndrome)
    n1=en:optic nerve meningioma | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2282. en:primary meningeal sarcomatosis --- r_associated #0: 15 --> méningé (syndrome)
    n1=en:primary meningeal sarcomatosis | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2283. en:tumour --- r_associated #0: 15 --> méningé (syndrome)
    n1=en:tumour | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2284. encéphalopathie hépato-cérébrale --- r_associated #0: 15 --> méningé (syndrome)
    n1=encéphalopathie hépato-cérébrale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2285. encéphalopathie porto-cave --- r_associated #0: 15 --> méningé (syndrome)
    n1=encéphalopathie porto-cave | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2286. insuffisance hépatique transitoire --- r_associated #0: 15 --> méningé (syndrome)
    n1=insuffisance hépatique transitoire | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2287. leuco-encéphalopathie --- r_associated #0: 15 --> méningé (syndrome)
    n1=leuco-encéphalopathie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2288. leucoencéphalopathie --- r_associated #0: 15 --> méningé (syndrome)
    n1=leucoencéphalopathie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2289. malformation d'Arnold-Chiari --- r_associated #0: 15 --> méningé (syndrome)
    n1=malformation d'Arnold-Chiari | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2290. méninge --- r_associated #0: 15 --> méningé (syndrome)
    n1=méninge | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2291. méninge dure --- r_associated #0: 15 --> méningé (syndrome)
    n1=méninge dure | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2292. méninge externe --- r_associated #0: 15 --> méningé (syndrome)
    n1=méninge externe | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2293. méninges --- r_associated #0: 15 --> méningé (syndrome)
    n1=méninges | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2294. méningiomatose --- r_associated #0: 15 --> méningé (syndrome)
    n1=méningiomatose | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2295. méningiome cutané --- r_associated #0: 15 --> méningé (syndrome)
    n1=méningiome cutané | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2296. méningiome du nerf optique --- r_associated #0: 15 --> méningé (syndrome)
    n1=méningiome du nerf optique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2297. méningiome intracrânien --- r_associated #0: 15 --> méningé (syndrome)
    n1=méningiome intracrânien | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2298. méningisme --- r_associated #0: 15 --> méningé (syndrome)
    n1=méningisme | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2299. oedème de l'encéphale --- r_associated #0: 15 --> méningé (syndrome)
    n1=oedème de l'encéphale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2300. paraplégie --- r_associated #0: 15 --> méningé (syndrome)
    n1=paraplégie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2301. paraplégie spasmodique --- r_associated #0: 15 --> méningé (syndrome)
    n1=paraplégie spasmodique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2302. paraplégie spastique --- r_associated #0: 15 --> méningé (syndrome)
    n1=paraplégie spastique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2303. sommeil paradoxal (REM) anormal --- r_associated #0: 15 --> méningé (syndrome)
    n1=sommeil paradoxal (REM) anormal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2304. syndrome de Reye --- r_associated #0: 15 --> méningé (syndrome)
    n1=syndrome de Reye | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2305. évolution chronique-progressive avec épisodes de détérioration rapide après fièvre ou traumatisme crânien --- r_associated #0: 15 --> méningé (syndrome)
    n1=évolution chronique-progressive avec épisodes de détérioration rapide après fièvre ou traumatisme crânien | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=15
  2306. Fothergill --- r_associated #0: 10 --> méningé (syndrome)
    n1=Fothergill | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2307. Malformation d'Arnold-Chiari --- r_associated #0: 10 --> méningé (syndrome)
    n1=Malformation d'Arnold-Chiari | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2308. Méningiome --- r_associated #0: 10 --> méningé (syndrome)
    n1=Méningiome | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2309. Neurologie --- r_associated #0: 10 --> méningé (syndrome)
    n1=Neurologie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2310. Tumeurs --- r_associated #0: 10 --> méningé (syndrome)
    n1=Tumeurs | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2311. abcès du cerveau --- r_associated #0: 10 --> méningé (syndrome)
    n1=abcès du cerveau | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2312. affection extrapyramidale --- r_associated #0: 10 --> méningé (syndrome)
    n1=affection extrapyramidale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2313. algie rachidienne --- r_associated #0: 10 --> méningé (syndrome)
    n1=algie rachidienne | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2314. cerveaux --- r_associated #0: 10 --> méningé (syndrome)
    n1=cerveaux | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2315. clonus --- r_associated #0: 10 --> méningé (syndrome)
    n1=clonus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2316. colpocéphalie --- r_associated #0: 10 --> méningé (syndrome)
    n1=colpocéphalie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2317. compression de la moelle épinière par infiltration tumorale --- r_associated #0: 10 --> méningé (syndrome)
    n1=compression de la moelle épinière par infiltration tumorale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2318. demence --- r_associated #0: 10 --> méningé (syndrome)
    n1=demence | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2319. douleur de la face --- r_associated #0: 10 --> méningé (syndrome)
    n1=douleur de la face | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2320. dysplasie corticale focale --- r_associated #0: 10 --> méningé (syndrome)
    n1=dysplasie corticale focale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2321. détérioration mentale --- r_associated #0: 10 --> méningé (syndrome)
    n1=détérioration mentale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2322. en:Kernig's sign --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:Kernig's sign | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2323. en:arachnida --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:arachnida | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2324. en:arachnoid membrane --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:arachnoid membrane | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2325. en:arachnoidea --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:arachnoidea | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2326. en:arachnoidea mater --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:arachnoidea mater | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2327. en:brainstem --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:brainstem | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2328. en:cerebral ventriculomegaly --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:cerebral ventriculomegaly | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2329. en:gray matter --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:gray matter | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2330. en:meningeal --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:meningeal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2331. en:meninx --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:meninx | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2332. en:meninx serosa --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:meninx serosa | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2333. en:pia mater --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:pia mater | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2334. en:tenuis mater --- r_associated #0: 10 --> méningé (syndrome)
    n1=en:tenuis mater | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2335. encéphalocèle --- r_associated #0: 10 --> méningé (syndrome)
    n1=encéphalocèle | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2336. encéphalopathie --- r_associated #0: 10 --> méningé (syndrome)
    n1=encéphalopathie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2337. encéphalopathie hépatique --- r_associated #0: 10 --> méningé (syndrome)
    n1=encéphalopathie hépatique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2338. faiblesse du visage --- r_associated #0: 10 --> méningé (syndrome)
    n1=faiblesse du visage | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2339. grimaces --- r_associated #0: 10 --> méningé (syndrome)
    n1=grimaces | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2340. holoprosencéphalie --- r_associated #0: 10 --> méningé (syndrome)
    n1=holoprosencéphalie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2341. hypoplasie du nerf optique --- r_associated #0: 10 --> méningé (syndrome)
    n1=hypoplasie du nerf optique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2342. hémimégalencéphalie --- r_associated #0: 10 --> méningé (syndrome)
    n1=hémimégalencéphalie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2343. hémorragie intracranienne --- r_associated #0: 10 --> méningé (syndrome)
    n1=hémorragie intracranienne | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2344. hémorragie intracrânienne --- r_associated #0: 10 --> méningé (syndrome)
    n1=hémorragie intracrânienne | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2345. kérose --- r_associated #0: 10 --> méningé (syndrome)
    n1=kérose | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2346. myotonia --- r_associated #0: 10 --> méningé (syndrome)
    n1=myotonia | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2347. myéloméningocèle --- r_associated #0: 10 --> méningé (syndrome)
    n1=myéloméningocèle | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2348. névralgie du trijumeau --- r_associated #0: 10 --> méningé (syndrome)
    n1=névralgie du trijumeau | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2349. névralgie essentielle du trijumeau --- r_associated #0: 10 --> méningé (syndrome)
    n1=névralgie essentielle du trijumeau | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2350. névralgie faciale --- r_associated #0: 10 --> méningé (syndrome)
    n1=névralgie faciale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2351. névralgie trigéminale --- r_associated #0: 10 --> méningé (syndrome)
    n1=névralgie trigéminale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2352. oedème cytotoxique cortical --- r_associated #0: 10 --> méningé (syndrome)
    n1=oedème cytotoxique cortical | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2353. opsoclonus --- r_associated #0: 10 --> méningé (syndrome)
    n1=opsoclonus | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2354. parésie faciale --- r_associated #0: 10 --> méningé (syndrome)
    n1=parésie faciale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2355. polyneuropathie --- r_associated #0: 10 --> méningé (syndrome)
    n1=polyneuropathie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2356. pseudo-tumeur --- r_associated #0: 10 --> méningé (syndrome)
    n1=pseudo-tumeur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2357. schizencéphalie --- r_associated #0: 10 --> méningé (syndrome)
    n1=schizencéphalie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2358. signe de Brudzi?ski --- r_associated #0: 10 --> méningé (syndrome)
    n1=signe de Brudzi?ski | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2359. signe de kernig --- r_associated #0: 10 --> méningé (syndrome)
    n1=signe de kernig | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2360. spina bifida --- r_associated #0: 10 --> méningé (syndrome)
    n1=spina bifida | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2361. thrombose d'un sinus sagittal --- r_associated #0: 10 --> méningé (syndrome)
    n1=thrombose d'un sinus sagittal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2362. thrombose de sinus sagittaux --- r_associated #0: 10 --> méningé (syndrome)
    n1=thrombose de sinus sagittaux | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2363. thrombose des sinus sagittaux --- r_associated #0: 10 --> méningé (syndrome)
    n1=thrombose des sinus sagittaux | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2364. thrombose du sinus sagittal --- r_associated #0: 10 --> méningé (syndrome)
    n1=thrombose du sinus sagittal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2365. tic douloureux --- r_associated #0: 10 --> méningé (syndrome)
    n1=tic douloureux | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2366. tic douloureux de la face --- r_associated #0: 10 --> méningé (syndrome)
    n1=tic douloureux de la face | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2367. tête pensante --- r_associated #0: 10 --> méningé (syndrome)
    n1=tête pensante | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2368. ventriculomégalie cérébrale --- r_associated #0: 10 --> méningé (syndrome)
    n1=ventriculomégalie cérébrale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2369. vibrisses --- r_associated #0: 10 --> méningé (syndrome)
    n1=vibrisses | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=10
  2370. Effet cytopathique --- r_associated #0: 5 --> méningé (syndrome)
    n1=Effet cytopathique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2371. Médecine --- r_associated #0: 5 --> méningé (syndrome)
    n1=Médecine | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2372. Système pyramidal --- r_associated #0: 5 --> méningé (syndrome)
    n1=Système pyramidal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2373. Tronc cérébral --- r_associated #0: 5 --> méningé (syndrome)
    n1=Tronc cérébral | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2374. abcès cérébral --- r_associated #0: 5 --> méningé (syndrome)
    n1=abcès cérébral | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2375. altération de la conscience --- r_associated #0: 5 --> méningé (syndrome)
    n1=altération de la conscience | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2376. altération mentale --- r_associated #0: 5 --> méningé (syndrome)
    n1=altération mentale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2377. atteinte extrapyramidale --- r_associated #0: 5 --> méningé (syndrome)
    n1=atteinte extrapyramidale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2378. défaut articulatoire --- r_associated #0: 5 --> méningé (syndrome)
    n1=défaut articulatoire | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2379. dégénérescence cytopathique --- r_associated #0: 5 --> méningé (syndrome)
    n1=dégénérescence cytopathique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2380. dégénérescence spongieuse --- r_associated #0: 5 --> méningé (syndrome)
    n1=dégénérescence spongieuse | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2381. détérioration intellectuelle --- r_associated #0: 5 --> méningé (syndrome)
    n1=détérioration intellectuelle | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2382. effet cytopathique --- r_associated #0: 5 --> méningé (syndrome)
    n1=effet cytopathique | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2383. faiblesse musculaire du visage --- r_associated #0: 5 --> méningé (syndrome)
    n1=faiblesse musculaire du visage | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2384. hydrocéphalie --- r_associated #0: 5 --> méningé (syndrome)
    n1=hydrocéphalie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2385. méningiome intra-orbitaire --- r_associated #0: 5 --> méningé (syndrome)
    n1=méningiome intra-orbitaire | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2386. méningiome intraorbitaire --- r_associated #0: 5 --> méningé (syndrome)
    n1=méningiome intraorbitaire | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2387. paralysie cérébrale --- r_associated #0: 5 --> méningé (syndrome)
    n1=paralysie cérébrale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2388. pseudotumeur --- r_associated #0: 5 --> méningé (syndrome)
    n1=pseudotumeur | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2389. retardation mentale --- r_associated #0: 5 --> méningé (syndrome)
    n1=retardation mentale | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2390. système pyramidal --- r_associated #0: 5 --> méningé (syndrome)
    n1=système pyramidal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2391. trouble extrapyramidal --- r_associated #0: 5 --> méningé (syndrome)
    n1=trouble extrapyramidal | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
  2392. écholalie --- r_associated #0: 5 --> méningé (syndrome)
    n1=écholalie | n2=méningé (syndrome) | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr