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'DYNC2H1 gene'
(id=16837101 ; fe=DYNC2H1 gene ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1149 creation date=2021-07-24 touchdate=2025-08-31 22:49:23.000)
≈ 4654 relations sortantes

  1. DYNC2H1 gene -- r_associated #0: 72 / 1 -> médecine
    n1=DYNC2H1 gene | n2=médecine | rel=r_associated | relid=0 | w=72
  2. DYNC2H1 gene -- r_associated #0: 57 / 0.792 -> DYNC2H1
    n1=DYNC2H1 gene | n2=DYNC2H1 | rel=r_associated | relid=0 | w=57
  3. DYNC2H1 gene -- r_associated #0: 56 / 0.778 -> gene
    n1=DYNC2H1 gene | n2=gene | rel=r_associated | relid=0 | w=56
  4. DYNC2H1 gene -- r_associated #0: 40 / 0.556 -> dysplasie thoracique asphyxiante
    n1=DYNC2H1 gene | n2=dysplasie thoracique asphyxiante | rel=r_associated | relid=0 | w=40
  5. DYNC2H1 gene -- r_associated #0: 35 / 0.486 -> anatomie
    n1=DYNC2H1 gene | n2=anatomie | rel=r_associated | relid=0 | w=35
  6. DYNC2H1 gene -- r_associated #0: 35 / 0.486 -> pathologie
    n1=DYNC2H1 gene | n2=pathologie | rel=r_associated | relid=0 | w=35
  7. DYNC2H1 gene -- r_associated #0: 34 / 0.472 -> processus pathologique
    n1=DYNC2H1 gene | n2=processus pathologique | rel=r_associated | relid=0 | w=34
  8. DYNC2H1 gene -- r_associated #0: 30 / 0.417 -> dynamique (point de vue)
    n1=DYNC2H1 gene | n2=dynamique (point de vue) | rel=r_associated | relid=0 | w=30
  9. DYNC2H1 gene -- r_associated #0: 29 / 0.403 -> dysarthrie
    n1=DYNC2H1 gene | n2=dysarthrie | rel=r_associated | relid=0 | w=29
  10. DYNC2H1 gene -- r_associated #0: 25 / 0.347 -> en:anarthria speech disorder
    n1=DYNC2H1 gene | n2=en:anarthria speech disorder | rel=r_associated | relid=0 | w=25
  11. DYNC2H1 gene -- r_associated #0: 25 / 0.347 -> en:dysarthria
    n1=DYNC2H1 gene | n2=en:dysarthria | rel=r_associated | relid=0 | w=25
  12. DYNC2H1 gene -- r_associated #0: 25 / 0.347 -> en:dysarthrias, spastic
    n1=DYNC2H1 gene | n2=en:dysarthrias, spastic | rel=r_associated | relid=0 | w=25
  13. DYNC2H1 gene -- r_associated #0: 25 / 0.347 -> en:slurred speech
    n1=DYNC2H1 gene | n2=en:slurred speech | rel=r_associated | relid=0 | w=25
  14. DYNC2H1 gene -- r_associated #0: 25 / 0.347 -> maladie
    n1=DYNC2H1 gene | n2=maladie | rel=r_associated | relid=0 | w=25
  15. DYNC2H1 gene -- r_associated #0: 25 / 0.347 -> trouble
    n1=DYNC2H1 gene | n2=trouble | rel=r_associated | relid=0 | w=25
  16. DYNC2H1 gene -- r_associated #0: 24 / 0.333 -> dysautonomie
    n1=DYNC2H1 gene | n2=dysautonomie | rel=r_associated | relid=0 | w=24
  17. DYNC2H1 gene -- r_associated #0: 23 / 0.319 -> DEXA
    n1=DYNC2H1 gene | n2=DEXA | rel=r_associated | relid=0 | w=23
  18. DYNC2H1 gene -- r_associated #0: 23 / 0.319 -> fr.
    n1=DYNC2H1 gene | n2=fr. | rel=r_associated | relid=0 | w=23
  19. DYNC2H1 gene -- r_associated #0: 22 / 0.306 -> dynamique
    n1=DYNC2H1 gene | n2=dynamique | rel=r_associated | relid=0 | w=22
  20. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> biologie
    n1=DYNC2H1 gene | n2=biologie | rel=r_associated | relid=0 | w=15
  21. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> chimie
    n1=DYNC2H1 gene | n2=chimie | rel=r_associated | relid=0 | w=15
  22. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> cil vibratile
    n1=DYNC2H1 gene | n2=cil vibratile | rel=r_associated | relid=0 | w=15
  23. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> dynamométre
    n1=DYNC2H1 gene | n2=dynamométre | rel=r_associated | relid=0 | w=15
  24. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> dynamométrie
    n1=DYNC2H1 gene | n2=dynamométrie | rel=r_associated | relid=0 | w=15
  25. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> dynapénia
    n1=DYNC2H1 gene | n2=dynapénia | rel=r_associated | relid=0 | w=15
  26. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> dynéine
    n1=DYNC2H1 gene | n2=dynéine | rel=r_associated | relid=0 | w=15
  27. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> dynéines
    n1=DYNC2H1 gene | n2=dynéines | rel=r_associated | relid=0 | w=15
  28. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> dynode
    n1=DYNC2H1 gene | n2=dynode | rel=r_associated | relid=0 | w=15
  29. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> dynorphine
    n1=DYNC2H1 gene | n2=dynorphine | rel=r_associated | relid=0 | w=15
  30. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> DYS
    n1=DYNC2H1 gene | n2=DYS | rel=r_associated | relid=0 | w=15
  31. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> dysacousie
    n1=DYNC2H1 gene | n2=dysacousie | rel=r_associated | relid=0 | w=15
  32. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> dysarthrie de l'enfant
    n1=DYNC2H1 gene | n2=dysarthrie de l'enfant | rel=r_associated | relid=0 | w=15
  33. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> électricité
    n1=DYNC2H1 gene | n2=électricité | rel=r_associated | relid=0 | w=15
  34. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> électrode
    n1=DYNC2H1 gene | n2=électrode | rel=r_associated | relid=0 | w=15
  35. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> en:dynamic point of view
    n1=DYNC2H1 gene | n2=en:dynamic point of view | rel=r_associated | relid=0 | w=15
  36. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> en:dynein
    n1=DYNC2H1 gene | n2=en:dynein | rel=r_associated | relid=0 | w=15
  37. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> en:dynod
    n1=DYNC2H1 gene | n2=en:dynod | rel=r_associated | relid=0 | w=15
  38. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> en:dynorphin
    n1=DYNC2H1 gene | n2=en:dynorphin | rel=r_associated | relid=0 | w=15
  39. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> en:dynorphins
    n1=DYNC2H1 gene | n2=en:dynorphins | rel=r_associated | relid=0 | w=15
  40. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> en:dysacusis
    n1=DYNC2H1 gene | n2=en:dysacusis | rel=r_associated | relid=0 | w=15
  41. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> en:medicine
    n1=DYNC2H1 gene | n2=en:medicine | rel=r_associated | relid=0 | w=15
  42. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> molécule protéique
    n1=DYNC2H1 gene | n2=molécule protéique | rel=r_associated | relid=0 | w=15
  43. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> photomultiplicateur
    n1=DYNC2H1 gene | n2=photomultiplicateur | rel=r_associated | relid=0 | w=15
  44. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> point
    n1=DYNC2H1 gene | n2=point | rel=r_associated | relid=0 | w=15
  45. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> protéine
    n1=DYNC2H1 gene | n2=protéine | rel=r_associated | relid=0 | w=15
  46. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> sperme
    n1=DYNC2H1 gene | n2=sperme | rel=r_associated | relid=0 | w=15
  47. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> syndrome de Young
    n1=DYNC2H1 gene | n2=syndrome de Young | rel=r_associated | relid=0 | w=15
  48. DYNC2H1 gene -- r_associated #0: 15 / 0.208 -> vue
    n1=DYNC2H1 gene | n2=vue | rel=r_associated | relid=0 | w=15
  49. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> a-48 affections du système nerveux autonome
    n1=DYNC2H1 gene | n2=a-48 affections du système nerveux autonome | rel=r_associated | relid=0 | w=10
  50. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> acouphènes
    n1=DYNC2H1 gene | n2=acouphènes | rel=r_associated | relid=0 | w=10
  51. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> acoustique
    n1=DYNC2H1 gene | n2=acoustique | rel=r_associated | relid=0 | w=10
  52. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> acoustique
    (science)
    n1=DYNC2H1 gene | n2=acoustique
    (science)
    | rel=r_associated | relid=0 | w=10
  53. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> affection du système nerveux autonome
    n1=DYNC2H1 gene | n2=affection du système nerveux autonome | rel=r_associated | relid=0 | w=10
  54. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> affection du système nerveux autonome périphérique
    n1=DYNC2H1 gene | n2=affection du système nerveux autonome périphérique | rel=r_associated | relid=0 | w=10
  55. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> affection du système neurovégétatif
    n1=DYNC2H1 gene | n2=affection du système neurovégétatif | rel=r_associated | relid=0 | w=10
  56. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> affection non précisée du système nerveux autonomique
    n1=DYNC2H1 gene | n2=affection non précisée du système nerveux autonomique | rel=r_associated | relid=0 | w=10
  57. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> affections du système nerveux autonome
    n1=DYNC2H1 gene | n2=affections du système nerveux autonome | rel=r_associated | relid=0 | w=10
  58. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> affections du système nerveux autonomique
    n1=DYNC2H1 gene | n2=affections du système nerveux autonomique | rel=r_associated | relid=0 | w=10
  59. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> allodynie auditive
    n1=DYNC2H1 gene | n2=allodynie auditive | rel=r_associated | relid=0 | w=10
  60. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> anarthrie
    n1=DYNC2H1 gene | n2=anarthrie | rel=r_associated | relid=0 | w=10
  61. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> anxiété
    n1=DYNC2H1 gene | n2=anxiété | rel=r_associated | relid=0 | w=10
  62. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> aphasie motrice
    n1=DYNC2H1 gene | n2=aphasie motrice | rel=r_associated | relid=0 | w=10
  63. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> apraxie
    n1=DYNC2H1 gene | n2=apraxie | rel=r_associated | relid=0 | w=10
  64. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> articulation
    n1=DYNC2H1 gene | n2=articulation | rel=r_associated | relid=0 | w=10
  65. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> articulation
    (langage)
    n1=DYNC2H1 gene | n2=articulation
    (langage)
    | rel=r_associated | relid=0 | w=10
  66. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> ataxie spinocérébelleuse type 1
    n1=DYNC2H1 gene | n2=ataxie spinocérébelleuse type 1 | rel=r_associated | relid=0 | w=10
  67. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> ataxophémie
    n1=DYNC2H1 gene | n2=ataxophémie | rel=r_associated | relid=0 | w=10
  68. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> atrophie multisystématisée
    n1=DYNC2H1 gene | n2=atrophie multisystématisée | rel=r_associated | relid=0 | w=10
  69. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> audition
    n1=DYNC2H1 gene | n2=audition | rel=r_associated | relid=0 | w=10
  70. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> audition déformée
    n1=DYNC2H1 gene | n2=audition déformée | rel=r_associated | relid=0 | w=10
  71. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> audition douloureuse
    n1=DYNC2H1 gene | n2=audition douloureuse | rel=r_associated | relid=0 | w=10
  72. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> audition
    (ouïe)
    n1=DYNC2H1 gene | n2=audition
    (ouïe)
    | rel=r_associated | relid=0 | w=10
  73. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> autonomie
    n1=DYNC2H1 gene | n2=autonomie | rel=r_associated | relid=0 | w=10
  74. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> botanique
    n1=DYNC2H1 gene | n2=botanique | rel=r_associated | relid=0 | w=10
  75. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> bruit
    n1=DYNC2H1 gene | n2=bruit | rel=r_associated | relid=0 | w=10
  76. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> céphalées
    n1=DYNC2H1 gene | n2=céphalées | rel=r_associated | relid=0 | w=10
  77. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> cerveau
    n1=DYNC2H1 gene | n2=cerveau | rel=r_associated | relid=0 | w=10
  78. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> cerveau
    (anatomie)
    n1=DYNC2H1 gene | n2=cerveau
    (anatomie)
    | rel=r_associated | relid=0 | w=10
  79. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> cheveu sur la langue
    n1=DYNC2H1 gene | n2=cheveu sur la langue | rel=r_associated | relid=0 | w=10
  80. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dégénérative
    n1=DYNC2H1 gene | n2=dégénérative | rel=r_associated | relid=0 | w=10
  81. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dépression
    n1=DYNC2H1 gene | n2=dépression | rel=r_associated | relid=0 | w=10
  82. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dépression
    (psychiatrie)
    n1=DYNC2H1 gene | n2=dépression
    (psychiatrie)
    | rel=r_associated | relid=0 | w=10
  83. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> déviation phonétique
    n1=DYNC2H1 gene | n2=déviation phonétique | rel=r_associated | relid=0 | w=10
  84. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> difficulté d'élocution
    n1=DYNC2H1 gene | n2=difficulté d'élocution | rel=r_associated | relid=0 | w=10
  85. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> DNV
    n1=DYNC2H1 gene | n2=DNV | rel=r_associated | relid=0 | w=10
  86. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> Dwyer (opération de)
    n1=DYNC2H1 gene | n2=Dwyer (opération de) | rel=r_associated | relid=0 | w=10
  87. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> Dyggve
    n1=DYNC2H1 gene | n2=Dyggve | rel=r_associated | relid=0 | w=10
  88. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> Dyggve -Melchior et Clausen ( syndrome de)
    n1=DYNC2H1 gene | n2=Dyggve -Melchior et Clausen ( syndrome de) | rel=r_associated | relid=0 | w=10
  89. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> Dyggve (syndrome de)
    n1=DYNC2H1 gene | n2=Dyggve (syndrome de) | rel=r_associated | relid=0 | w=10
  90. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dynamomètre
    n1=DYNC2H1 gene | n2=dynamomètre | rel=r_associated | relid=0 | w=10
  91. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysarthrie corticale
    n1=DYNC2H1 gene | n2=dysarthrie corticale | rel=r_associated | relid=0 | w=10
  92. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysarthrie mixte
    n1=DYNC2H1 gene | n2=dysarthrie mixte | rel=r_associated | relid=0 | w=10
  93. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysarthrie scandée
    n1=DYNC2H1 gene | n2=dysarthrie scandée | rel=r_associated | relid=0 | w=10
  94. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysarthrie spasmodique
    n1=DYNC2H1 gene | n2=dysarthrie spasmodique | rel=r_associated | relid=0 | w=10
  95. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysarthrie spastique
    n1=DYNC2H1 gene | n2=dysarthrie spastique | rel=r_associated | relid=0 | w=10
  96. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysarthries
    n1=DYNC2H1 gene | n2=dysarthries | rel=r_associated | relid=0 | w=10
  97. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysautonomie (anesthésie et)
    n1=DYNC2H1 gene | n2=dysautonomie (anesthésie et) | rel=r_associated | relid=0 | w=10
  98. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysautonomie alcoolique
    n1=DYNC2H1 gene | n2=dysautonomie alcoolique | rel=r_associated | relid=0 | w=10
  99. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysautonomie familiale dominante
    n1=DYNC2H1 gene | n2=dysautonomie familiale dominante | rel=r_associated | relid=0 | w=10
  100. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysautonomies primaires
    n1=DYNC2H1 gene | n2=dysautonomies primaires | rel=r_associated | relid=0 | w=10
  101. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysautonomies primitives
    n1=DYNC2H1 gene | n2=dysautonomies primitives | rel=r_associated | relid=0 | w=10
  102. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysesthésie auditive
    n1=DYNC2H1 gene | n2=dysesthésie auditive | rel=r_associated | relid=0 | w=10
  103. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dysfonction
    n1=DYNC2H1 gene | n2=dysfonction | rel=r_associated | relid=0 | w=10
  104. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dyslalie
    n1=DYNC2H1 gene | n2=dyslalie | rel=r_associated | relid=0 | w=10
  105. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dyspraxie articulatoire
    n1=DYNC2H1 gene | n2=dyspraxie articulatoire | rel=r_associated | relid=0 | w=10
  106. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dystonie neurovégétative
    n1=DYNC2H1 gene | n2=dystonie neurovégétative | rel=r_associated | relid=0 | w=10
  107. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> dystonie vagosympathique
    n1=DYNC2H1 gene | n2=dystonie vagosympathique | rel=r_associated | relid=0 | w=10
  108. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> empâté
    n1=DYNC2H1 gene | n2=empâté | rel=r_associated | relid=0 | w=10
  109. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> empâtement de la parole
    n1=DYNC2H1 gene | n2=empâtement de la parole | rel=r_associated | relid=0 | w=10
  110. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:'ballooned' neurons with autofluorescent fine granular material
    n1=DYNC2H1 gene | n2=en:'ballooned' neurons with autofluorescent fine granular material | rel=r_associated | relid=0 | w=10
  111. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:'double contour' convolutional calcification on ct scan
    n1=DYNC2H1 gene | n2=en:'double contour' convolutional calcification on ct scan | rel=r_associated | relid=0 | w=10
  112. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:'dragonfly-like' pattern
    n1=DYNC2H1 gene | n2=en:'dragonfly-like' pattern | rel=r_associated | relid=0 | w=10
  113. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:'dragonfly' pattern on imaging
    n1=DYNC2H1 gene | n2=en:'dragonfly' pattern on imaging | rel=r_associated | relid=0 | w=10
  114. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:'eye of the tiger' sign on mri
    n1=DYNC2H1 gene | n2=en:'eye of the tiger' sign on mri | rel=r_associated | relid=0 | w=10
  115. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:'globoid multinucleated cells' in brain tissue
    n1=DYNC2H1 gene | n2=en:'globoid multinucleated cells' in brain tissue | rel=r_associated | relid=0 | w=10
  116. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:'spheroid' inclusions in axons
    n1=DYNC2H1 gene | n2=en:'spheroid' inclusions in axons | rel=r_associated | relid=0 | w=10
  117. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:3-4 hz slow sharp waves seen on eeg
    n1=DYNC2H1 gene | n2=en:3-4 hz slow sharp waves seen on eeg | rel=r_associated | relid=0 | w=10
  118. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:3-6 hz polyspike eeg
    n1=DYNC2H1 gene | n2=en:3-6 hz polyspike eeg | rel=r_associated | relid=0 | w=10
  119. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:a subset of patients develop frontotemporal dementia
    n1=DYNC2H1 gene | n2=en:a subset of patients develop frontotemporal dementia | rel=r_associated | relid=0 | w=10
  120. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:a subset of patients have neurologic abnormalities
    n1=DYNC2H1 gene | n2=en:a subset of patients have neurologic abnormalities | rel=r_associated | relid=0 | w=10
  121. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abducens nerve palsy (cn vi)
    n1=DYNC2H1 gene | n2=en:abducens nerve palsy (cn vi) | rel=r_associated | relid=0 | w=10
  122. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle
    n1=DYNC2H1 gene | n2=en:abnormal 'cap' on the dorsal pons extending into the fourth ventricle | rel=r_associated | relid=0 | w=10
  123. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal 'hobby horse' ataxic gait
    n1=DYNC2H1 gene | n2=en:abnormal 'hobby horse' ataxic gait | rel=r_associated | relid=0 | w=10
  124. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal behavior
    n1=DYNC2H1 gene | n2=en:abnormal behavior | rel=r_associated | relid=0 | w=10
  125. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal brain myelination
    n1=DYNC2H1 gene | n2=en:abnormal brain myelination | rel=r_associated | relid=0 | w=10
  126. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal cell orientation
    n1=DYNC2H1 gene | n2=en:abnormal cell orientation | rel=r_associated | relid=0 | w=10
  127. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal coordination
    n1=DYNC2H1 gene | n2=en:abnormal coordination | rel=r_associated | relid=0 | w=10
  128. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal cortical eeg discharges triggered by intermittent light
    n1=DYNC2H1 gene | n2=en:abnormal cortical eeg discharges triggered by intermittent light | rel=r_associated | relid=0 | w=10
  129. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal cortical gyration
    n1=DYNC2H1 gene | n2=en:abnormal cortical gyration | rel=r_associated | relid=0 | w=10
  130. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal cortical lamination
    n1=DYNC2H1 gene | n2=en:abnormal cortical lamination | rel=r_associated | relid=0 | w=10
  131. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal cortical layering
    n1=DYNC2H1 gene | n2=en:abnormal cortical layering | rel=r_associated | relid=0 | w=10
  132. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal corticospinal tract decussation
    n1=DYNC2H1 gene | n2=en:abnormal corticospinal tract decussation | rel=r_associated | relid=0 | w=10
  133. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal eeg (abnormal slowing of background activity)
    n1=DYNC2H1 gene | n2=en:abnormal eeg (abnormal slowing of background activity) | rel=r_associated | relid=0 | w=10
  134. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal eeg (poor alpha rhythms)
    n1=DYNC2H1 gene | n2=en:abnormal eeg (poor alpha rhythms) | rel=r_associated | relid=0 | w=10
  135. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal eeg activity during sleep
    n1=DYNC2H1 gene | n2=en:abnormal eeg activity during sleep | rel=r_associated | relid=0 | w=10
  136. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal eeg with epileptiform changes
    n1=DYNC2H1 gene | n2=en:abnormal eeg with epileptiform changes | rel=r_associated | relid=0 | w=10
  137. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal gait (67%)
    n1=DYNC2H1 gene | n2=en:abnormal gait (67%) | rel=r_associated | relid=0 | w=10
  138. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal gait due to muscle weakness
    n1=DYNC2H1 gene | n2=en:abnormal gait due to muscle weakness | rel=r_associated | relid=0 | w=10
  139. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan
    n1=DYNC2H1 gene | n2=en:abnormal gray and white matter differentiation in frontal, occipital, and cerebellar regions on ct scan | rel=r_associated | relid=0 | w=10
  140. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal gyral pattern
    n1=DYNC2H1 gene | n2=en:abnormal gyral pattern | rel=r_associated | relid=0 | w=10
  141. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal gyri
    n1=DYNC2H1 gene | n2=en:abnormal gyri | rel=r_associated | relid=0 | w=10
  142. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal gyri (in 1 of 2 patients)
    n1=DYNC2H1 gene | n2=en:abnormal gyri (in 1 of 2 patients) | rel=r_associated | relid=0 | w=10
  143. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal hippocampus
    n1=DYNC2H1 gene | n2=en:abnormal hippocampus | rel=r_associated | relid=0 | w=10
  144. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal hypothalamo-pituitary axis
    n1=DYNC2H1 gene | n2=en:abnormal hypothalamo-pituitary axis | rel=r_associated | relid=0 | w=10
  145. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal interictal eeg (in some patients)
    n1=DYNC2H1 gene | n2=en:abnormal interictal eeg (in some patients) | rel=r_associated | relid=0 | w=10
  146. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal involuntary movement
    n1=DYNC2H1 gene | n2=en:abnormal involuntary movement | rel=r_associated | relid=0 | w=10
  147. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal lipid peak on brain mrs
    n1=DYNC2H1 gene | n2=en:abnormal lipid peak on brain mrs | rel=r_associated | relid=0 | w=10
  148. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal lower motor neuron morphology
    n1=DYNC2H1 gene | n2=en:abnormal lower motor neuron morphology | rel=r_associated | relid=0 | w=10
  149. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal movement
    n1=DYNC2H1 gene | n2=en:abnormal movement | rel=r_associated | relid=0 | w=10
  150. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal myelination
    n1=DYNC2H1 gene | n2=en:abnormal myelination | rel=r_associated | relid=0 | w=10
  151. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal ocular motility
    n1=DYNC2H1 gene | n2=en:abnormal ocular motility | rel=r_associated | relid=0 | w=10
  152. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal posture
    n1=DYNC2H1 gene | n2=en:abnormal posture | rel=r_associated | relid=0 | w=10
  153. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal primitive reflexes
    n1=DYNC2H1 gene | n2=en:abnormal primitive reflexes | rel=r_associated | relid=0 | w=10
  154. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal purkinje cells
    n1=DYNC2H1 gene | n2=en:abnormal purkinje cells | rel=r_associated | relid=0 | w=10
  155. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal rapid eye movement sleep
    n1=DYNC2H1 gene | n2=en:abnormal rapid eye movement sleep | rel=r_associated | relid=0 | w=10
  156. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal septum pellucidum
    n1=DYNC2H1 gene | n2=en:abnormal septum pellucidum | rel=r_associated | relid=0 | w=10
  157. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal signals in the thalami seen on mri
    n1=DYNC2H1 gene | n2=en:abnormal signals in the thalami seen on mri | rel=r_associated | relid=0 | w=10
  158. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal sleep pattern
    n1=DYNC2H1 gene | n2=en:abnormal sleep pattern | rel=r_associated | relid=0 | w=10
  159. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal sleep-wake cycles
    n1=DYNC2H1 gene | n2=en:abnormal sleep-wake cycles | rel=r_associated | relid=0 | w=10
  160. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal spike waves
    n1=DYNC2H1 gene | n2=en:abnormal spike waves | rel=r_associated | relid=0 | w=10
  161. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal sudomotor regulation
    n1=DYNC2H1 gene | n2=en:abnormal sudomotor regulation | rel=r_associated | relid=0 | w=10
  162. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal sulci
    n1=DYNC2H1 gene | n2=en:abnormal sulci | rel=r_associated | relid=0 | w=10
  163. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal t2-weighted signals in the occipital white and gray matter
    n1=DYNC2H1 gene | n2=en:abnormal t2-weighted signals in the occipital white and gray matter | rel=r_associated | relid=0 | w=10
  164. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal visual evoked potential
    n1=DYNC2H1 gene | n2=en:abnormal visual evoked potential | rel=r_associated | relid=0 | w=10
  165. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal visual evoked potential (vep)
    n1=DYNC2H1 gene | n2=en:abnormal visual evoked potential (vep) | rel=r_associated | relid=0 | w=10
  166. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal visual sensitivity of the brain in reaction to intermittent photic stimulation
    n1=DYNC2H1 gene | n2=en:abnormal visual sensitivity of the brain in reaction to intermittent photic stimulation | rel=r_associated | relid=0 | w=10
  167. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormal white matter signals, in the basal ganglia or cerebellum seen on brain mri
    n1=DYNC2H1 gene | n2=en:abnormal white matter signals, in the basal ganglia or cerebellum seen on brain mri | rel=r_associated | relid=0 | w=10
  168. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormality of brainstem morphology
    n1=DYNC2H1 gene | n2=en:abnormality of brainstem morphology | rel=r_associated | relid=0 | w=10
  169. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormality of ocular smooth pursuit
    n1=DYNC2H1 gene | n2=en:abnormality of ocular smooth pursuit | rel=r_associated | relid=0 | w=10
  170. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormality of the cerebellum
    n1=DYNC2H1 gene | n2=en:abnormality of the cerebellum | rel=r_associated | relid=0 | w=10
  171. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormality of the corpus callosum
    n1=DYNC2H1 gene | n2=en:abnormality of the corpus callosum | rel=r_associated | relid=0 | w=10
  172. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormality of the posterior cranial fossa
    n1=DYNC2H1 gene | n2=en:abnormality of the posterior cranial fossa | rel=r_associated | relid=0 | w=10
  173. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:abnormally marked pontobulbar sulcus
    n1=DYNC2H1 gene | n2=en:abnormally marked pontobulbar sulcus | rel=r_associated | relid=0 | w=10
  174. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of anterior pituitary
    n1=DYNC2H1 gene | n2=en:absence of anterior pituitary | rel=r_associated | relid=0 | w=10
  175. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of balloon cells (in type iia)
    n1=DYNC2H1 gene | n2=en:absence of balloon cells (in type iia) | rel=r_associated | relid=0 | w=10
  176. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of cerebral aneurysms
    n1=DYNC2H1 gene | n2=en:absence of cerebral aneurysms | rel=r_associated | relid=0 | w=10
  177. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of language development
    n1=DYNC2H1 gene | n2=en:absence of language development | rel=r_associated | relid=0 | w=10
  178. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of lower motor neuron involvement
    n1=DYNC2H1 gene | n2=en:absence of lower motor neuron involvement | rel=r_associated | relid=0 | w=10
  179. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of myelin in the posterior column of the spinal cord (1 patient)
    n1=DYNC2H1 gene | n2=en:absence of myelin in the posterior column of the spinal cord (1 patient) | rel=r_associated | relid=0 | w=10
  180. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of neurologic manifestations
    n1=DYNC2H1 gene | n2=en:absence of neurologic manifestations | rel=r_associated | relid=0 | w=10
  181. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of neuropathologic findings in the brainstem and anterior horn cells
    n1=DYNC2H1 gene | n2=en:absence of neuropathologic findings in the brainstem and anterior horn cells | rel=r_associated | relid=0 | w=10
  182. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of olfactory bulbs
    n1=DYNC2H1 gene | n2=en:absence of olfactory bulbs | rel=r_associated | relid=0 | w=10
  183. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of primitive reflexes
    n1=DYNC2H1 gene | n2=en:absence of primitive reflexes | rel=r_associated | relid=0 | w=10
  184. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of septum pellucidum
    n1=DYNC2H1 gene | n2=en:absence of septum pellucidum | rel=r_associated | relid=0 | w=10
  185. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of spontaneous movements
    n1=DYNC2H1 gene | n2=en:absence of spontaneous movements | rel=r_associated | relid=0 | w=10
  186. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of the basal ganglia
    n1=DYNC2H1 gene | n2=en:absence of the basal ganglia | rel=r_associated | relid=0 | w=10
  187. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of the cerebellar vermis
    n1=DYNC2H1 gene | n2=en:absence of the cerebellar vermis | rel=r_associated | relid=0 | w=10
  188. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of the inferior olives
    n1=DYNC2H1 gene | n2=en:absence of the inferior olives | rel=r_associated | relid=0 | w=10
  189. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of the olfactory bulbs and tracts
    n1=DYNC2H1 gene | n2=en:absence of the olfactory bulbs and tracts | rel=r_associated | relid=0 | w=10
  190. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of transverse pontine fibers
    n1=DYNC2H1 gene | n2=en:absence of transverse pontine fibers | rel=r_associated | relid=0 | w=10
  191. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence of vestibular schwannomas at age greater than 18 years
    n1=DYNC2H1 gene | n2=en:absence of vestibular schwannomas at age greater than 18 years | rel=r_associated | relid=0 | w=10
  192. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence or atrophy of the putamen
    n1=DYNC2H1 gene | n2=en:absence or atrophy of the putamen | rel=r_associated | relid=0 | w=10
  193. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence or hypoplasia of the anterior limb of the internal capsule
    n1=DYNC2H1 gene | n2=en:absence or hypoplasia of the anterior limb of the internal capsule | rel=r_associated | relid=0 | w=10
  194. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence seizures (in some)
    n1=DYNC2H1 gene | n2=en:absence seizures (in some) | rel=r_associated | relid=0 | w=10
  195. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence seizures (stage 2 and 3)
    n1=DYNC2H1 gene | n2=en:absence seizures (stage 2 and 3) | rel=r_associated | relid=0 | w=10
  196. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absence seizures may occur
    n1=DYNC2H1 gene | n2=en:absence seizures may occur | rel=r_associated | relid=0 | w=10
  197. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent cisterna magna
    n1=DYNC2H1 gene | n2=en:absent cisterna magna | rel=r_associated | relid=0 | w=10
  198. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent corpus callosum (variable)
    n1=DYNC2H1 gene | n2=en:absent corpus callosum (variable) | rel=r_associated | relid=0 | w=10
  199. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent cortical responses of somatosensory evoked potentials
    n1=DYNC2H1 gene | n2=en:absent cortical responses of somatosensory evoked potentials | rel=r_associated | relid=0 | w=10
  200. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent development
    n1=DYNC2H1 gene | n2=en:absent development | rel=r_associated | relid=0 | w=10
  201. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent myelination of the brain (severe connatal form)
    n1=DYNC2H1 gene | n2=en:absent myelination of the brain (severe connatal form) | rel=r_associated | relid=0 | w=10
  202. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent olfactory bulbs
    n1=DYNC2H1 gene | n2=en:absent olfactory bulbs | rel=r_associated | relid=0 | w=10
  203. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent olfactory tract or bulbs
    n1=DYNC2H1 gene | n2=en:absent olfactory tract or bulbs | rel=r_associated | relid=0 | w=10
  204. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent olfactory tracts and bulbs
    n1=DYNC2H1 gene | n2=en:absent olfactory tracts and bulbs | rel=r_associated | relid=0 | w=10
  205. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent optic nerves, chiasm, and tracts
    n1=DYNC2H1 gene | n2=en:absent optic nerves, chiasm, and tracts | rel=r_associated | relid=0 | w=10
  206. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent or delayed psychomotor development, severe
    n1=DYNC2H1 gene | n2=en:absent or delayed psychomotor development, severe | rel=r_associated | relid=0 | w=10
  207. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent or delayed speech development
    n1=DYNC2H1 gene | n2=en:absent or delayed speech development | rel=r_associated | relid=0 | w=10
  208. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent or immature dentate nuclei
    n1=DYNC2H1 gene | n2=en:absent or immature dentate nuclei | rel=r_associated | relid=0 | w=10
  209. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent or limited speech development
    n1=DYNC2H1 gene | n2=en:absent or limited speech development | rel=r_associated | relid=0 | w=10
  210. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent or poor expressive speech
    n1=DYNC2H1 gene | n2=en:absent or poor expressive speech | rel=r_associated | relid=0 | w=10
  211. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent pituitary
    n1=DYNC2H1 gene | n2=en:absent pituitary | rel=r_associated | relid=0 | w=10
  212. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent posterior pituitary bright spot
    n1=DYNC2H1 gene | n2=en:absent posterior pituitary bright spot | rel=r_associated | relid=0 | w=10
  213. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent primitive reflexes
    n1=DYNC2H1 gene | n2=en:absent primitive reflexes | rel=r_associated | relid=0 | w=10
  214. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent rem sleep
    n1=DYNC2H1 gene | n2=en:absent rem sleep | rel=r_associated | relid=0 | w=10
  215. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent speech
    n1=DYNC2H1 gene | n2=en:absent speech | rel=r_associated | relid=0 | w=10
  216. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:absent superior division of oculomotor nerve and corresponding alpha motor neurons
    n1=DYNC2H1 gene | n2=en:absent superior division of oculomotor nerve and corresponding alpha motor neurons | rel=r_associated | relid=0 | w=10
  217. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:accumulation of autofluorescent material in neurons
    n1=DYNC2H1 gene | n2=en:accumulation of autofluorescent material in neurons | rel=r_associated | relid=0 | w=10
  218. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:accumulation of pas-positive diastase-resistant neuronal inclusion bodies in the cerebral cortex (collins bodies)
    n1=DYNC2H1 gene | n2=en:accumulation of pas-positive diastase-resistant neuronal inclusion bodies in the cerebral cortex (collins bodies) | rel=r_associated | relid=0 | w=10
  219. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acontractile detrusor
    n1=DYNC2H1 gene | n2=en:acontractile detrusor | rel=r_associated | relid=0 | w=10
  220. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acoustic shock
    n1=DYNC2H1 gene | n2=en:acoustic shock | rel=r_associated | relid=0 | w=10
  221. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons
    n1=DYNC2H1 gene | n2=en:actin depolymerizing factor/cofilin-immunoreactive eosinophilic rod-like cytoplasmic inclusions in neocortical and thalamic neurons | rel=r_associated | relid=0 | w=10
  222. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:actin- and actin depolymerizing factor/cofilin-immunoreactive eosinophilic spherical structures in the striatum
    n1=DYNC2H1 gene | n2=en:actin- and actin depolymerizing factor/cofilin-immunoreactive eosinophilic spherical structures in the striatum | rel=r_associated | relid=0 | w=10
  223. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:action and postural tremor
    n1=DYNC2H1 gene | n2=en:action and postural tremor | rel=r_associated | relid=0 | w=10
  224. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:action dystonia
    n1=DYNC2H1 gene | n2=en:action dystonia | rel=r_associated | relid=0 | w=10
  225. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:action myoclonus
    n1=DYNC2H1 gene | n2=en:action myoclonus | rel=r_associated | relid=0 | w=10
  226. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:action myoclonus (triggered by voluntary movements)
    n1=DYNC2H1 gene | n2=en:action myoclonus (triggered by voluntary movements) | rel=r_associated | relid=0 | w=10
  227. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:actual effective cognition
    n1=DYNC2H1 gene | n2=en:actual effective cognition | rel=r_associated | relid=0 | w=10
  228. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acute cerebrovascular accidents
    n1=DYNC2H1 gene | n2=en:acute cerebrovascular accidents | rel=r_associated | relid=0 | w=10
  229. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acute encephalopathy
    n1=DYNC2H1 gene | n2=en:acute encephalopathy | rel=r_associated | relid=0 | w=10
  230. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acute episodes of neuropathic symptoms
    n1=DYNC2H1 gene | n2=en:acute episodes of neuropathic symptoms | rel=r_associated | relid=0 | w=10
  231. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acute episodes of neuropathic symptoms (hcp)
    n1=DYNC2H1 gene | n2=en:acute episodes of neuropathic symptoms (hcp) | rel=r_associated | relid=0 | w=10
  232. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acute necrotizing encephalopathy
    n1=DYNC2H1 gene | n2=en:acute necrotizing encephalopathy | rel=r_associated | relid=0 | w=10
  233. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acute neurologic decompensation (in later-onset cases)
    n1=DYNC2H1 gene | n2=en:acute neurologic decompensation (in later-onset cases) | rel=r_associated | relid=0 | w=10
  234. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acute neurologic deficits due to cerebrovascular disease
    n1=DYNC2H1 gene | n2=en:acute neurologic deficits due to cerebrovascular disease | rel=r_associated | relid=0 | w=10
  235. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acute pandysautonomia
    n1=DYNC2H1 gene | n2=en:acute pandysautonomia | rel=r_associated | relid=0 | w=10
  236. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:acute poliomyelitis
    n1=DYNC2H1 gene | n2=en:acute poliomyelitis | rel=r_associated | relid=0 | w=10
  237. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:adipose tissue in subarachnoid space
    n1=DYNC2H1 gene | n2=en:adipose tissue in subarachnoid space | rel=r_associated | relid=0 | w=10
  238. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:afebrile seizure
    n1=DYNC2H1 gene | n2=en:afebrile seizure | rel=r_associated | relid=0 | w=10
  239. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:affected arteries have electron-dense granular material close to vascular smooth muscle cell membranes
    n1=DYNC2H1 gene | n2=en:affected arteries have electron-dense granular material close to vascular smooth muscle cell membranes | rel=r_associated | relid=0 | w=10
  240. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:affected arteries show loss of smooth muscle cells
    n1=DYNC2H1 gene | n2=en:affected arteries show loss of smooth muscle cells | rel=r_associated | relid=0 | w=10
  241. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:affected children are unable to sit without support
    n1=DYNC2H1 gene | n2=en:affected children are unable to sit without support | rel=r_associated | relid=0 | w=10
  242. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of corpus callosum, partial or complete (rare)
    n1=DYNC2H1 gene | n2=en:agenesis of corpus callosum, partial or complete (rare) | rel=r_associated | relid=0 | w=10
  243. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of pineal gland
    n1=DYNC2H1 gene | n2=en:agenesis of pineal gland | rel=r_associated | relid=0 | w=10
  244. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the anterior commissure
    n1=DYNC2H1 gene | n2=en:agenesis of the anterior commissure | rel=r_associated | relid=0 | w=10
  245. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the corpus callosum (1 patient)
    n1=DYNC2H1 gene | n2=en:agenesis of the corpus callosum (1 patient) | rel=r_associated | relid=0 | w=10
  246. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the corpus callosum (in 1 of 2 patients)
    n1=DYNC2H1 gene | n2=en:agenesis of the corpus callosum (in 1 of 2 patients) | rel=r_associated | relid=0 | w=10
  247. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the corpus callosum (in 2 patients)
    n1=DYNC2H1 gene | n2=en:agenesis of the corpus callosum (in 2 patients) | rel=r_associated | relid=0 | w=10
  248. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the corpus callosum (less common)
    n1=DYNC2H1 gene | n2=en:agenesis of the corpus callosum (less common) | rel=r_associated | relid=0 | w=10
  249. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the corpus callosum (patient a)
    n1=DYNC2H1 gene | n2=en:agenesis of the corpus callosum (patient a) | rel=r_associated | relid=0 | w=10
  250. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the corpus callosum (rare)
    n1=DYNC2H1 gene | n2=en:agenesis of the corpus callosum (rare) | rel=r_associated | relid=0 | w=10
  251. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the corpus callosum (variable)
    n1=DYNC2H1 gene | n2=en:agenesis of the corpus callosum (variable) | rel=r_associated | relid=0 | w=10
  252. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the occipital lobes (1 patient)
    n1=DYNC2H1 gene | n2=en:agenesis of the occipital lobes (1 patient) | rel=r_associated | relid=0 | w=10
  253. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis of the rostrum of corpus callosum
    n1=DYNC2H1 gene | n2=en:agenesis of the rostrum of corpus callosum | rel=r_associated | relid=0 | w=10
  254. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis or hypogenesis of the cerebellar vermis
    n1=DYNC2H1 gene | n2=en:agenesis or hypogenesis of the cerebellar vermis | rel=r_associated | relid=0 | w=10
  255. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis or hypoplasia of the corpus callosum
    n1=DYNC2H1 gene | n2=en:agenesis or hypoplasia of the corpus callosum | rel=r_associated | relid=0 | w=10
  256. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agenesis or severe hypoplasia of cerebellar vermis
    n1=DYNC2H1 gene | n2=en:agenesis or severe hypoplasia of cerebellar vermis | rel=r_associated | relid=0 | w=10
  257. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aggregation of snca-immunopositive inclusions
    n1=DYNC2H1 gene | n2=en:aggregation of snca-immunopositive inclusions | rel=r_associated | relid=0 | w=10
  258. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aggression
    n1=DYNC2H1 gene | n2=en:aggression | rel=r_associated | relid=0 | w=10
  259. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agitation
    n1=DYNC2H1 gene | n2=en:agitation | rel=r_associated | relid=0 | w=10
  260. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agnosia
    n1=DYNC2H1 gene | n2=en:agnosia | rel=r_associated | relid=0 | w=10
  261. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agyria (1 patient)
    n1=DYNC2H1 gene | n2=en:agyria (1 patient) | rel=r_associated | relid=0 | w=10
  262. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agyria (posterior-to-anterior gradient)
    n1=DYNC2H1 gene | n2=en:agyria (posterior-to-anterior gradient) | rel=r_associated | relid=0 | w=10
  263. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:agyria (wws)
    n1=DYNC2H1 gene | n2=en:agyria (wws) | rel=r_associated | relid=0 | w=10
  264. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:akinesia
    n1=DYNC2H1 gene | n2=en:akinesia | rel=r_associated | relid=0 | w=10
  265. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:akinetic mutism (in some patients)
    n1=DYNC2H1 gene | n2=en:akinetic mutism (in some patients) | rel=r_associated | relid=0 | w=10
  266. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:alobar holoprosencephaly (rare)
    n1=DYNC2H1 gene | n2=en:alobar holoprosencephaly (rare) | rel=r_associated | relid=0 | w=10
  267. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:alobar hpe shows absence of interhemispheric cleavage and single ventricle
    n1=DYNC2H1 gene | n2=en:alobar hpe shows absence of interhemispheric cleavage and single ventricle | rel=r_associated | relid=0 | w=10
  268. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:alpha-b-crystallin expression in oligodendrocytes
    n1=DYNC2H1 gene | n2=en:alpha-b-crystallin expression in oligodendrocytes | rel=r_associated | relid=0 | w=10
  269. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:alpha-synuclein immunoreactive neuronal and glial inclusions
    n1=DYNC2H1 gene | n2=en:alpha-synuclein immunoreactive neuronal and glial inclusions | rel=r_associated | relid=0 | w=10
  270. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:alpha-synuclein-containing inclusions
    n1=DYNC2H1 gene | n2=en:alpha-synuclein-containing inclusions | rel=r_associated | relid=0 | w=10
  271. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:alpha-synuclein-immunoreactive lewy neurites
    n1=DYNC2H1 gene | n2=en:alpha-synuclein-immunoreactive lewy neurites | rel=r_associated | relid=0 | w=10
  272. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:alpha-synuclein-immunreactive lewy bodies
    n1=DYNC2H1 gene | n2=en:alpha-synuclein-immunreactive lewy bodies | rel=r_associated | relid=0 | w=10
  273. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:altered breathing patterns
    n1=DYNC2H1 gene | n2=en:altered breathing patterns | rel=r_associated | relid=0 | w=10
  274. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:altered mental status
    n1=DYNC2H1 gene | n2=en:altered mental status | rel=r_associated | relid=0 | w=10
  275. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:alzheimer disease, early onset
    n1=DYNC2H1 gene | n2=en:alzheimer disease, early onset | rel=r_associated | relid=0 | w=10
  276. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:alzheimer's disease
    n1=DYNC2H1 gene | n2=en:alzheimer's disease | rel=r_associated | relid=0 | w=10
  277. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ambulation difficulty
    n1=DYNC2H1 gene | n2=en:ambulation difficulty | rel=r_associated | relid=0 | w=10
  278. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord
    n1=DYNC2H1 gene | n2=en:amyloid deposition in the leptomeningeal vessels, brainstem, spinal cord | rel=r_associated | relid=0 | w=10
  279. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:amyloid plaques may be present
    n1=DYNC2H1 gene | n2=en:amyloid plaques may be present | rel=r_associated | relid=0 | w=10
  280. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:amyloid-like plaques are not immunoreactive to app (104760)
    n1=DYNC2H1 gene | n2=en:amyloid-like plaques are not immunoreactive to app (104760) | rel=r_associated | relid=0 | w=10
  281. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:amyloid-like plaques, immunoreactive to prp, predominantly in the cerebellum
    n1=DYNC2H1 gene | n2=en:amyloid-like plaques, immunoreactive to prp, predominantly in the cerebellum | rel=r_associated | relid=0 | w=10
  282. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:amyotrophic lateral sclerosis
    n1=DYNC2H1 gene | n2=en:amyotrophic lateral sclerosis | rel=r_associated | relid=0 | w=10
  283. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:amyotrophy, distal, severe
    n1=DYNC2H1 gene | n2=en:amyotrophy, distal, severe | rel=r_associated | relid=0 | w=10
  284. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anencephaly
    n1=DYNC2H1 gene | n2=en:anencephaly | rel=r_associated | relid=0 | w=10
  285. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anencephaly (1 patient)
    n1=DYNC2H1 gene | n2=en:anencephaly (1 patient) | rel=r_associated | relid=0 | w=10
  286. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:angiitis, cerebral
    n1=DYNC2H1 gene | n2=en:angiitis, cerebral | rel=r_associated | relid=0 | w=10
  287. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:angiographically 'silent'
    n1=DYNC2H1 gene | n2=en:angiographically 'silent' | rel=r_associated | relid=0 | w=10
  288. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:angulation of the frontal horns
    n1=DYNC2H1 gene | n2=en:angulation of the frontal horns | rel=r_associated | relid=0 | w=10
  289. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anisocoria
    n1=DYNC2H1 gene | n2=en:anisocoria | rel=r_associated | relid=0 | w=10
  290. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ankle clonus
    n1=DYNC2H1 gene | n2=en:ankle clonus | rel=r_associated | relid=0 | w=10
  291. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ankle clonus (in some patients)
    n1=DYNC2H1 gene | n2=en:ankle clonus (in some patients) | rel=r_associated | relid=0 | w=10
  292. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ankle clonus (in some)
    n1=DYNC2H1 gene | n2=en:ankle clonus (in some) | rel=r_associated | relid=0 | w=10
  293. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ankle or knee clonus
    n1=DYNC2H1 gene | n2=en:ankle or knee clonus | rel=r_associated | relid=0 | w=10
  294. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ankle reflex absent
    n1=DYNC2H1 gene | n2=en:ankle reflex absent | rel=r_associated | relid=0 | w=10
  295. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anomalies of the folding of the right sylvian area
    n1=DYNC2H1 gene | n2=en:anomalies of the folding of the right sylvian area | rel=r_associated | relid=0 | w=10
  296. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anomalies of the temporal area
    n1=DYNC2H1 gene | n2=en:anomalies of the temporal area | rel=r_associated | relid=0 | w=10
  297. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anomia
    n1=DYNC2H1 gene | n2=en:anomia | rel=r_associated | relid=0 | w=10
  298. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anosmia
    n1=DYNC2H1 gene | n2=en:anosmia | rel=r_associated | relid=0 | w=10
  299. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anosmia (1 patient)
    n1=DYNC2H1 gene | n2=en:anosmia (1 patient) | rel=r_associated | relid=0 | w=10
  300. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anosmia (in contiguous gene syndrome patients)
    n1=DYNC2H1 gene | n2=en:anosmia (in contiguous gene syndrome patients) | rel=r_associated | relid=0 | w=10
  301. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anosmia (in some patients)
    n1=DYNC2H1 gene | n2=en:anosmia (in some patients) | rel=r_associated | relid=0 | w=10
  302. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:antenatal intracerebral hemorrhage
    n1=DYNC2H1 gene | n2=en:antenatal intracerebral hemorrhage | rel=r_associated | relid=0 | w=10
  303. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anterior basal encephalocele
    n1=DYNC2H1 gene | n2=en:anterior basal encephalocele | rel=r_associated | relid=0 | w=10
  304. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anterior commissure not evident
    n1=DYNC2H1 gene | n2=en:anterior commissure not evident | rel=r_associated | relid=0 | w=10
  305. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anterior horn atrophy
    n1=DYNC2H1 gene | n2=en:anterior horn atrophy | rel=r_associated | relid=0 | w=10
  306. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anterior horn cell impairment
    n1=DYNC2H1 gene | n2=en:anterior horn cell impairment | rel=r_associated | relid=0 | w=10
  307. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anterior pachygyria and posterior agyria
    n1=DYNC2H1 gene | n2=en:anterior pachygyria and posterior agyria | rel=r_associated | relid=0 | w=10
  308. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anterior pituitary adenoma
    n1=DYNC2H1 gene | n2=en:anterior pituitary adenoma | rel=r_associated | relid=0 | w=10
  309. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anterior pituitary hypoplasia
    n1=DYNC2H1 gene | n2=en:anterior pituitary hypoplasia | rel=r_associated | relid=0 | w=10
  310. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anterior sacral meningocele
    n1=DYNC2H1 gene | n2=en:anterior sacral meningocele | rel=r_associated | relid=0 | w=10
  311. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anterior temporal lobe subcortical cysts
    n1=DYNC2H1 gene | n2=en:anterior temporal lobe subcortical cysts | rel=r_associated | relid=0 | w=10
  312. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anticholinergic syndrome
    n1=DYNC2H1 gene | n2=en:anticholinergic syndrome | rel=r_associated | relid=0 | w=10
  313. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:anxiety
    n1=DYNC2H1 gene | n2=en:anxiety | rel=r_associated | relid=0 | w=10
  314. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:apathy
    n1=DYNC2H1 gene | n2=en:apathy | rel=r_associated | relid=0 | w=10
  315. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aphasia
    n1=DYNC2H1 gene | n2=en:aphasia | rel=r_associated | relid=0 | w=10
  316. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aplasia of corpus callosum
    n1=DYNC2H1 gene | n2=en:aplasia of corpus callosum | rel=r_associated | relid=0 | w=10
  317. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aplasia of olfactory bulbs, bilateral
    n1=DYNC2H1 gene | n2=en:aplasia of olfactory bulbs, bilateral | rel=r_associated | relid=0 | w=10
  318. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb)
    n1=DYNC2H1 gene | n2=en:aplasia of the corpus callosum (wws) encephalocele (1 patient, meb) | rel=r_associated | relid=0 | w=10
  319. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aplasia of the inferior half of the cerebellar vermis
    n1=DYNC2H1 gene | n2=en:aplasia of the inferior half of the cerebellar vermis | rel=r_associated | relid=0 | w=10
  320. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aplasia of the vermis
    n1=DYNC2H1 gene | n2=en:aplasia of the vermis | rel=r_associated | relid=0 | w=10
  321. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aplasia/hypoplasia of the cerebellar vermis
    n1=DYNC2H1 gene | n2=en:aplasia/hypoplasia of the cerebellar vermis | rel=r_associated | relid=0 | w=10
  322. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aplasia/hypoplasia of the cerebellum
    n1=DYNC2H1 gene | n2=en:aplasia/hypoplasia of the cerebellum | rel=r_associated | relid=0 | w=10
  323. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aplasia/hypoplasia of the corpus callosum
    n1=DYNC2H1 gene | n2=en:aplasia/hypoplasia of the corpus callosum | rel=r_associated | relid=0 | w=10
  324. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:apoptotic neurons
    n1=DYNC2H1 gene | n2=en:apoptotic neurons | rel=r_associated | relid=0 | w=10
  325. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:appendicular hypertonia
    n1=DYNC2H1 gene | n2=en:appendicular hypertonia | rel=r_associated | relid=0 | w=10
  326. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:approximately 30% of patients show normal early development
    n1=DYNC2H1 gene | n2=en:approximately 30% of patients show normal early development | rel=r_associated | relid=0 | w=10
  327. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:apraxia (in some patients)
    n1=DYNC2H1 gene | n2=en:apraxia (in some patients) | rel=r_associated | relid=0 | w=10
  328. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:apraxia, verbal
    n1=DYNC2H1 gene | n2=en:apraxia, verbal | rel=r_associated | relid=0 | w=10
  329. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:apraxias
    n1=DYNC2H1 gene | n2=en:apraxias | rel=r_associated | relid=0 | w=10
  330. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aqueductal stenosis
    n1=DYNC2H1 gene | n2=en:aqueductal stenosis | rel=r_associated | relid=0 | w=10
  331. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arachnoid cyst
    n1=DYNC2H1 gene | n2=en:arachnoid cyst | rel=r_associated | relid=0 | w=10
  332. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arachnoid cyst (in some patients)
    n1=DYNC2H1 gene | n2=en:arachnoid cyst (in some patients) | rel=r_associated | relid=0 | w=10
  333. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arachnoid cysts (1 patient)
    n1=DYNC2H1 gene | n2=en:arachnoid cysts (1 patient) | rel=r_associated | relid=0 | w=10
  334. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arachnoid cysts (in one family)
    n1=DYNC2H1 gene | n2=en:arachnoid cysts (in one family) | rel=r_associated | relid=0 | w=10
  335. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arachnoid cysts of the cerebellopontine angle (reported in 1 family)
    n1=DYNC2H1 gene | n2=en:arachnoid cysts of the cerebellopontine angle (reported in 1 family) | rel=r_associated | relid=0 | w=10
  336. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arachnoid hemangiomata
    n1=DYNC2H1 gene | n2=en:arachnoid hemangiomata | rel=r_associated | relid=0 | w=10
  337. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arachnoidal cysts
    n1=DYNC2H1 gene | n2=en:arachnoidal cysts | rel=r_associated | relid=0 | w=10
  338. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:areflexia
    n1=DYNC2H1 gene | n2=en:areflexia | rel=r_associated | relid=0 | w=10
  339. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:areflexia (30%)
    n1=DYNC2H1 gene | n2=en:areflexia (30%) | rel=r_associated | relid=0 | w=10
  340. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:areflexia of lower limbs
    n1=DYNC2H1 gene | n2=en:areflexia of lower limbs | rel=r_associated | relid=0 | w=10
  341. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:areflexia of upper limbs
    n1=DYNC2H1 gene | n2=en:areflexia of upper limbs | rel=r_associated | relid=0 | w=10
  342. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:argyrophilic hyperphosphorylated tau-positive inclusions (pick bodies)
    n1=DYNC2H1 gene | n2=en:argyrophilic hyperphosphorylated tau-positive inclusions (pick bodies) | rel=r_associated | relid=0 | w=10
  343. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arhinencephaly
    n1=DYNC2H1 gene | n2=en:arhinencephaly | rel=r_associated | relid=0 | w=10
  344. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arhinencephaly (1 patient)
    n1=DYNC2H1 gene | n2=en:arhinencephaly (1 patient) | rel=r_associated | relid=0 | w=10
  345. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arm flexion
    n1=DYNC2H1 gene | n2=en:arm flexion | rel=r_associated | relid=0 | w=10
  346. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arm pain
    n1=DYNC2H1 gene | n2=en:arm pain | rel=r_associated | relid=0 | w=10
  347. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arnold-chiari i malformation
    n1=DYNC2H1 gene | n2=en:arnold-chiari i malformation | rel=r_associated | relid=0 | w=10
  348. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arnold-chiari malformation
    n1=DYNC2H1 gene | n2=en:arnold-chiari malformation | rel=r_associated | relid=0 | w=10
  349. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arrest of psychomotor development after seizure onset
    n1=DYNC2H1 gene | n2=en:arrest of psychomotor development after seizure onset | rel=r_associated | relid=0 | w=10
  350. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:arrested hydrocephalus (rare)
    n1=DYNC2H1 gene | n2=en:arrested hydrocephalus (rare) | rel=r_associated | relid=0 | w=10
  351. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:articulation difficulties
    n1=DYNC2H1 gene | n2=en:articulation difficulties | rel=r_associated | relid=0 | w=10
  352. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:articulation, unintelligible
    n1=DYNC2H1 gene | n2=en:articulation, unintelligible | rel=r_associated | relid=0 | w=10
  353. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:articulatory defect
    n1=DYNC2H1 gene | n2=en:articulatory defect | rel=r_associated | relid=0 | w=10
  354. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:asperger syndrome (rare)
    n1=DYNC2H1 gene | n2=en:asperger syndrome (rare) | rel=r_associated | relid=0 | w=10
  355. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:associated with paresthesias and dysesthesias
    n1=DYNC2H1 gene | n2=en:associated with paresthesias and dysesthesias | rel=r_associated | relid=0 | w=10
  356. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:associated with syringomyelia (186700)
    n1=DYNC2H1 gene | n2=en:associated with syringomyelia (186700) | rel=r_associated | relid=0 | w=10
  357. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:association between poor metabolizers (pm) and parkinson disease
    n1=DYNC2H1 gene | n2=en:association between poor metabolizers (pm) and parkinson disease | rel=r_associated | relid=0 | w=10
  358. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:astrocyte
    n1=DYNC2H1 gene | n2=en:astrocyte | rel=r_associated | relid=0 | w=10
  359. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:astrocytes show reactive changes
    n1=DYNC2H1 gene | n2=en:astrocytes show reactive changes | rel=r_associated | relid=0 | w=10
  360. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:astrocytic gliosis
    n1=DYNC2H1 gene | n2=en:astrocytic gliosis | rel=r_associated | relid=0 | w=10
  361. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:astrocytosis
    n1=DYNC2H1 gene | n2=en:astrocytosis | rel=r_associated | relid=0 | w=10
  362. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:astrogliosis (in some patients)
    n1=DYNC2H1 gene | n2=en:astrogliosis (in some patients) | rel=r_associated | relid=0 | w=10
  363. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:asymmetric brain development
    n1=DYNC2H1 gene | n2=en:asymmetric brain development | rel=r_associated | relid=0 | w=10
  364. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:asymmetry at onset (74%)
    n1=DYNC2H1 gene | n2=en:asymmetry at onset (74%) | rel=r_associated | relid=0 | w=10
  365. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:asymmetry of symptoms
    n1=DYNC2H1 gene | n2=en:asymmetry of symptoms | rel=r_associated | relid=0 | w=10
  366. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia
    n1=DYNC2H1 gene | n2=en:ataxia | rel=r_associated | relid=0 | w=10
  367. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia (1 patient)
    n1=DYNC2H1 gene | n2=en:ataxia (1 patient) | rel=r_associated | relid=0 | w=10
  368. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia (cvs+)
    n1=DYNC2H1 gene | n2=en:ataxia (cvs+) | rel=r_associated | relid=0 | w=10
  369. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia (deletion patients)
    n1=DYNC2H1 gene | n2=en:ataxia (deletion patients) | rel=r_associated | relid=0 | w=10
  370. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia (early-onset form)
    n1=DYNC2H1 gene | n2=en:ataxia (early-onset form) | rel=r_associated | relid=0 | w=10
  371. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia (if untreated)
    n1=DYNC2H1 gene | n2=en:ataxia (if untreated) | rel=r_associated | relid=0 | w=10
  372. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia (in some patients)
    n1=DYNC2H1 gene | n2=en:ataxia (in some patients) | rel=r_associated | relid=0 | w=10
  373. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia (less common)
    n1=DYNC2H1 gene | n2=en:ataxia (less common) | rel=r_associated | relid=0 | w=10
  374. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia (type i and type ii, infantile and juvenile)
    n1=DYNC2H1 gene | n2=en:ataxia (type i and type ii, infantile and juvenile) | rel=r_associated | relid=0 | w=10
  375. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia (uncommon)
    n1=DYNC2H1 gene | n2=en:ataxia (uncommon) | rel=r_associated | relid=0 | w=10
  376. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia in those who survive
    n1=DYNC2H1 gene | n2=en:ataxia in those who survive | rel=r_associated | relid=0 | w=10
  377. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia may develop in middle age (less common)
    n1=DYNC2H1 gene | n2=en:ataxia may develop in middle age (less common) | rel=r_associated | relid=0 | w=10
  378. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia with febrile episodes (rare)
    n1=DYNC2H1 gene | n2=en:ataxia with febrile episodes (rare) | rel=r_associated | relid=0 | w=10
  379. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia with jerky arm movements
    n1=DYNC2H1 gene | n2=en:ataxia with jerky arm movements | rel=r_associated | relid=0 | w=10
  380. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia worsens in the dark
    n1=DYNC2H1 gene | n2=en:ataxia worsens in the dark | rel=r_associated | relid=0 | w=10
  381. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia, (1 family)
    n1=DYNC2H1 gene | n2=en:ataxia, (1 family) | rel=r_associated | relid=0 | w=10
  382. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia, cerebellar (in some patients)
    n1=DYNC2H1 gene | n2=en:ataxia, cerebellar (in some patients) | rel=r_associated | relid=0 | w=10
  383. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia, cerebellar (upper and lower limbs affected)
    n1=DYNC2H1 gene | n2=en:ataxia, cerebellar (upper and lower limbs affected) | rel=r_associated | relid=0 | w=10
  384. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia, cerebellar, limb and gait
    n1=DYNC2H1 gene | n2=en:ataxia, cerebellar, limb and gait | rel=r_associated | relid=0 | w=10
  385. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia, episodic (episodes last from hours to days)
    n1=DYNC2H1 gene | n2=en:ataxia, episodic (episodes last from hours to days) | rel=r_associated | relid=0 | w=10
  386. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia, episodic, occurring after febrile illness or stress
    n1=DYNC2H1 gene | n2=en:ataxia, episodic, occurring after febrile illness or stress | rel=r_associated | relid=0 | w=10
  387. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia, gait and appendicular
    n1=DYNC2H1 gene | n2=en:ataxia, gait and appendicular | rel=r_associated | relid=0 | w=10
  388. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxia, mild
    n1=DYNC2H1 gene | n2=en:ataxia, mild | rel=r_associated | relid=0 | w=10
  389. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxias, appendicular
    n1=DYNC2H1 gene | n2=en:ataxias, appendicular | rel=r_associated | relid=0 | w=10
  390. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxias, sensory
    n1=DYNC2H1 gene | n2=en:ataxias, sensory | rel=r_associated | relid=0 | w=10
  391. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxias, truncal
    n1=DYNC2H1 gene | n2=en:ataxias, truncal | rel=r_associated | relid=0 | w=10
  392. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxic gait
    n1=DYNC2H1 gene | n2=en:ataxic gait | rel=r_associated | relid=0 | w=10
  393. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxic gait (in some patients)
    n1=DYNC2H1 gene | n2=en:ataxic gait (in some patients) | rel=r_associated | relid=0 | w=10
  394. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxic gait (juvenile form)
    n1=DYNC2H1 gene | n2=en:ataxic gait (juvenile form) | rel=r_associated | relid=0 | w=10
  395. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ataxic movements
    n1=DYNC2H1 gene | n2=en:ataxic movements | rel=r_associated | relid=0 | w=10
  396. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atelencephaly
    n1=DYNC2H1 gene | n2=en:atelencephaly | rel=r_associated | relid=0 | w=10
  397. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:athetoid and dystonic hand movements (in some patients)
    n1=DYNC2H1 gene | n2=en:athetoid and dystonic hand movements (in some patients) | rel=r_associated | relid=0 | w=10
  398. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:athetosis
    n1=DYNC2H1 gene | n2=en:athetosis | rel=r_associated | relid=0 | w=10
  399. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:athetosis (in some patients)
    n1=DYNC2H1 gene | n2=en:athetosis (in some patients) | rel=r_associated | relid=0 | w=10
  400. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:athetosis (later)
    n1=DYNC2H1 gene | n2=en:athetosis (later) | rel=r_associated | relid=0 | w=10
  401. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:athetosis, mild (in one patient)
    n1=DYNC2H1 gene | n2=en:athetosis, mild (in one patient) | rel=r_associated | relid=0 | w=10
  402. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atlantoaxial instability
    n1=DYNC2H1 gene | n2=en:atlantoaxial instability | rel=r_associated | relid=0 | w=10
  403. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atretic occipital cephalocele
    n1=DYNC2H1 gene | n2=en:atretic occipital cephalocele | rel=r_associated | relid=0 | w=10
  404. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophic pons (in some)
    n1=DYNC2H1 gene | n2=en:atrophic pons (in some) | rel=r_associated | relid=0 | w=10
  405. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy and weakness of limb musculature
    n1=DYNC2H1 gene | n2=en:atrophy and weakness of limb musculature | rel=r_associated | relid=0 | w=10
  406. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy and weakness of the tongue, jaw, and throat muscles
    n1=DYNC2H1 gene | n2=en:atrophy and weakness of the tongue, jaw, and throat muscles | rel=r_associated | relid=0 | w=10
  407. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy may be more severe in the left hemisphere
    n1=DYNC2H1 gene | n2=en:atrophy may be more severe in the left hemisphere | rel=r_associated | relid=0 | w=10
  408. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of cerebellum, brainstem, cervical spinal cord
    n1=DYNC2H1 gene | n2=en:atrophy of cerebellum, brainstem, cervical spinal cord | rel=r_associated | relid=0 | w=10
  409. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of corpus callosum
    n1=DYNC2H1 gene | n2=en:atrophy of corpus callosum | rel=r_associated | relid=0 | w=10
  410. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of hippocampal dentate gyrus
    n1=DYNC2H1 gene | n2=en:atrophy of hippocampal dentate gyrus | rel=r_associated | relid=0 | w=10
  411. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of pyramids
    n1=DYNC2H1 gene | n2=en:atrophy of pyramids | rel=r_associated | relid=0 | w=10
  412. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the cerebellar vermis seen on mri
    n1=DYNC2H1 gene | n2=en:atrophy of the cerebellar vermis seen on mri | rel=r_associated | relid=0 | w=10
  413. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the dentate nucleus
    n1=DYNC2H1 gene | n2=en:atrophy of the dentate nucleus | rel=r_associated | relid=0 | w=10
  414. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the frontal and parietal cortex
    n1=DYNC2H1 gene | n2=en:atrophy of the frontal and parietal cortex | rel=r_associated | relid=0 | w=10
  415. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the granular cell layer of the cerebellum
    n1=DYNC2H1 gene | n2=en:atrophy of the granular cell layer of the cerebellum | rel=r_associated | relid=0 | w=10
  416. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the motor cortex in older patients seen on mri
    n1=DYNC2H1 gene | n2=en:atrophy of the motor cortex in older patients seen on mri | rel=r_associated | relid=0 | w=10
  417. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the pituitary (1 patient)
    n1=DYNC2H1 gene | n2=en:atrophy of the pituitary (1 patient) | rel=r_associated | relid=0 | w=10
  418. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the pons (in some patients)
    n1=DYNC2H1 gene | n2=en:atrophy of the pons (in some patients) | rel=r_associated | relid=0 | w=10
  419. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the posterior columns and spinocerebellar tracts
    n1=DYNC2H1 gene | n2=en:atrophy of the posterior columns and spinocerebellar tracts | rel=r_associated | relid=0 | w=10
  420. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the spinal cord
    n1=DYNC2H1 gene | n2=en:atrophy of the spinal cord | rel=r_associated | relid=0 | w=10
  421. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy of the spinal cord and cerebellar tracts
    n1=DYNC2H1 gene | n2=en:atrophy of the spinal cord and cerebellar tracts | rel=r_associated | relid=0 | w=10
  422. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy, thin hemisphere
    n1=DYNC2H1 gene | n2=en:atrophy, thin hemisphere | rel=r_associated | relid=0 | w=10
  423. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atrophy/degeneration involving the spinal cord
    n1=DYNC2H1 gene | n2=en:atrophy/degeneration involving the spinal cord | rel=r_associated | relid=0 | w=10
  424. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:attacks characterized by lethargy, incoordination, loss of motor skills
    n1=DYNC2H1 gene | n2=en:attacks characterized by lethargy, incoordination, loss of motor skills | rel=r_associated | relid=0 | w=10
  425. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:attacks of disabling daytime drowsiness and low alertness
    n1=DYNC2H1 gene | n2=en:attacks of disabling daytime drowsiness and low alertness | rel=r_associated | relid=0 | w=10
  426. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:attention deficit disorder
    n1=DYNC2H1 gene | n2=en:attention deficit disorder | rel=r_associated | relid=0 | w=10
  427. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:attention deficit hyperactivity disorder
    n1=DYNC2H1 gene | n2=en:attention deficit hyperactivity disorder | rel=r_associated | relid=0 | w=10
  428. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:attenuated gyri
    n1=DYNC2H1 gene | n2=en:attenuated gyri | rel=r_associated | relid=0 | w=10
  429. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atypical absence seizure
    n1=DYNC2H1 gene | n2=en:atypical absence seizure | rel=r_associated | relid=0 | w=10
  430. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:atypical absence, atonic/tonic, or tonic-clonic seizures
    n1=DYNC2H1 gene | n2=en:atypical absence, atonic/tonic, or tonic-clonic seizures | rel=r_associated | relid=0 | w=10
  431. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:auditory auras
    n1=DYNC2H1 gene | n2=en:auditory auras | rel=r_associated | relid=0 | w=10
  432. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:auditory neuropathy spectrum disorder
    n1=DYNC2H1 gene | n2=en:auditory neuropathy spectrum disorder | rel=r_associated | relid=0 | w=10
  433. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:auditory perseveration
    n1=DYNC2H1 gene | n2=en:auditory perseveration | rel=r_associated | relid=0 | w=10
  434. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:auditory recuitment disorder
    n1=DYNC2H1 gene | n2=en:auditory recuitment disorder | rel=r_associated | relid=0 | w=10
  435. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:auditory, olfactory, and visual auras
    n1=DYNC2H1 gene | n2=en:auditory, olfactory, and visual auras | rel=r_associated | relid=0 | w=10
  436. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aura
    n1=DYNC2H1 gene | n2=en:aura | rel=r_associated | relid=0 | w=10
  437. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aura (in some instances)
    n1=DYNC2H1 gene | n2=en:aura (in some instances) | rel=r_associated | relid=0 | w=10
  438. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:aura may occur
    n1=DYNC2H1 gene | n2=en:aura may occur | rel=r_associated | relid=0 | w=10
  439. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autism
    n1=DYNC2H1 gene | n2=en:autism | rel=r_associated | relid=0 | w=10
  440. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autism (rare)
    n1=DYNC2H1 gene | n2=en:autism (rare) | rel=r_associated | relid=0 | w=10
  441. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autism or autistic features
    n1=DYNC2H1 gene | n2=en:autism or autistic features | rel=r_associated | relid=0 | w=10
  442. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autofluorescent lipopigment in neurons
    n1=DYNC2H1 gene | n2=en:autofluorescent lipopigment in neurons | rel=r_associated | relid=0 | w=10
  443. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autofluorescent pigment in microglia and macrophages
    n1=DYNC2H1 gene | n2=en:autofluorescent pigment in microglia and macrophages | rel=r_associated | relid=0 | w=10
  444. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:automatism
    n1=DYNC2H1 gene | n2=en:automatism | rel=r_associated | relid=0 | w=10
  445. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic abnormalities
    n1=DYNC2H1 gene | n2=en:autonomic abnormalities | rel=r_associated | relid=0 | w=10
  446. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic disturbances
    n1=DYNC2H1 gene | n2=en:autonomic disturbances | rel=r_associated | relid=0 | w=10
  447. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic dysfunction (in patients with hsan2d)
    n1=DYNC2H1 gene | n2=en:autonomic dysfunction (in patients with hsan2d) | rel=r_associated | relid=0 | w=10
  448. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic dysfunction may occur
    n1=DYNC2H1 gene | n2=en:autonomic dysfunction may occur | rel=r_associated | relid=0 | w=10
  449. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic dysfunctions, segmental
    n1=DYNC2H1 gene | n2=en:autonomic dysfunctions, segmental | rel=r_associated | relid=0 | w=10
  450. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic dysreflexia
    n1=DYNC2H1 gene | n2=en:autonomic dysreflexia | rel=r_associated | relid=0 | w=10
  451. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic dysregulation
    n1=DYNC2H1 gene | n2=en:autonomic dysregulation | rel=r_associated | relid=0 | w=10
  452. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic failure syndrome
    n1=DYNC2H1 gene | n2=en:autonomic failure syndrome | rel=r_associated | relid=0 | w=10
  453. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic features may occur
    n1=DYNC2H1 gene | n2=en:autonomic features may occur | rel=r_associated | relid=0 | w=10
  454. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension)
    n1=DYNC2H1 gene | n2=en:autonomic features may occur (diaphoresis, tachycardia, hyperthermia, hypertension) | rel=r_associated | relid=0 | w=10
  455. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic ganglion
    n1=DYNC2H1 gene | n2=en:autonomic ganglion | rel=r_associated | relid=0 | w=10
  456. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic ganglion disorders
    n1=DYNC2H1 gene | n2=en:autonomic ganglion disorders | rel=r_associated | relid=0 | w=10
  457. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic hyperreflexia of bladder
    n1=DYNC2H1 gene | n2=en:autonomic hyperreflexia of bladder | rel=r_associated | relid=0 | w=10
  458. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic instability (22%)
    n1=DYNC2H1 gene | n2=en:autonomic instability (22%) | rel=r_associated | relid=0 | w=10
  459. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic involvement
    n1=DYNC2H1 gene | n2=en:autonomic involvement | rel=r_associated | relid=0 | w=10
  460. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic involvement affecting limbs during episodes
    n1=DYNC2H1 gene | n2=en:autonomic involvement affecting limbs during episodes | rel=r_associated | relid=0 | w=10
  461. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic involvement may occur
    n1=DYNC2H1 gene | n2=en:autonomic involvement may occur | rel=r_associated | relid=0 | w=10
  462. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic manifestations
    n1=DYNC2H1 gene | n2=en:autonomic manifestations | rel=r_associated | relid=0 | w=10
  463. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic nerve injury
    n1=DYNC2H1 gene | n2=en:autonomic nerve injury | rel=r_associated | relid=0 | w=10
  464. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic nervous system
    n1=DYNC2H1 gene | n2=en:autonomic nervous system | rel=r_associated | relid=0 | w=10
  465. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic nervous system disorders
    n1=DYNC2H1 gene | n2=en:autonomic nervous system disorders | rel=r_associated | relid=0 | w=10
  466. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic neuropathy
    n1=DYNC2H1 gene | n2=en:autonomic neuropathy | rel=r_associated | relid=0 | w=10
  467. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic pathways
    n1=DYNC2H1 gene | n2=en:autonomic pathways | rel=r_associated | relid=0 | w=10
  468. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic signs
    n1=DYNC2H1 gene | n2=en:autonomic signs | rel=r_associated | relid=0 | w=10
  469. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic symptoms
    n1=DYNC2H1 gene | n2=en:autonomic symptoms | rel=r_associated | relid=0 | w=10
  470. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autonomic vascular dystonia
    n1=DYNC2H1 gene | n2=en:autonomic vascular dystonia | rel=r_associated | relid=0 | w=10
  471. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:autophony
    n1=DYNC2H1 gene | n2=en:autophony | rel=r_associated | relid=0 | w=10
  472. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:average intellect
    n1=DYNC2H1 gene | n2=en:average intellect | rel=r_associated | relid=0 | w=10
  473. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axial dystonia
    n1=DYNC2H1 gene | n2=en:axial dystonia | rel=r_associated | relid=0 | w=10
  474. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axial hypotonia (1 patient)
    n1=DYNC2H1 gene | n2=en:axial hypotonia (1 patient) | rel=r_associated | relid=0 | w=10
  475. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axial hypotonia (rare)
    n1=DYNC2H1 gene | n2=en:axial hypotonia (rare) | rel=r_associated | relid=0 | w=10
  476. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axial imbalance (34%)
    n1=DYNC2H1 gene | n2=en:axial imbalance (34%) | rel=r_associated | relid=0 | w=10
  477. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axial muscle stiffness, symmetric
    n1=DYNC2H1 gene | n2=en:axial muscle stiffness, symmetric | rel=r_associated | relid=0 | w=10
  478. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axial rigidity
    n1=DYNC2H1 gene | n2=en:axial rigidity | rel=r_associated | relid=0 | w=10
  479. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal 'spheroid' inclusions
    n1=DYNC2H1 gene | n2=en:axonal 'spheroid' inclusions | rel=r_associated | relid=0 | w=10
  480. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal 'spheroid' inclusions in the cns
    n1=DYNC2H1 gene | n2=en:axonal 'spheroid' inclusions in the cns | rel=r_associated | relid=0 | w=10
  481. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal dystrophy
    n1=DYNC2H1 gene | n2=en:axonal dystrophy | rel=r_associated | relid=0 | w=10
  482. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal dystrophy (in some patients)
    n1=DYNC2H1 gene | n2=en:axonal dystrophy (in some patients) | rel=r_associated | relid=0 | w=10
  483. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal loss
    n1=DYNC2H1 gene | n2=en:axonal loss | rel=r_associated | relid=0 | w=10
  484. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal loss and gliosis in the corticospinal tracts
    n1=DYNC2H1 gene | n2=en:axonal loss and gliosis in the corticospinal tracts | rel=r_associated | relid=0 | w=10
  485. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal spheroids
    n1=DYNC2H1 gene | n2=en:axonal spheroids | rel=r_associated | relid=0 | w=10
  486. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal spheroids in the dorsal column
    n1=DYNC2H1 gene | n2=en:axonal spheroids in the dorsal column | rel=r_associated | relid=0 | w=10
  487. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal swelling of spinal nerve roots and cranial nerves
    n1=DYNC2H1 gene | n2=en:axonal swelling of spinal nerve roots and cranial nerves | rel=r_associated | relid=0 | w=10
  488. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal swelling or thickening
    n1=DYNC2H1 gene | n2=en:axonal swelling or thickening | rel=r_associated | relid=0 | w=10
  489. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal swelling or thickening in the cns
    n1=DYNC2H1 gene | n2=en:axonal swelling or thickening in the cns | rel=r_associated | relid=0 | w=10
  490. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:axonal swellings or spheroids
    n1=DYNC2H1 gene | n2=en:axonal swellings or spheroids | rel=r_associated | relid=0 | w=10
  491. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:babinski sign
    n1=DYNC2H1 gene | n2=en:babinski sign | rel=r_associated | relid=0 | w=10
  492. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:back pain
    n1=DYNC2H1 gene | n2=en:back pain | rel=r_associated | relid=0 | w=10
  493. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:background slowing
    n1=DYNC2H1 gene | n2=en:background slowing | rel=r_associated | relid=0 | w=10
  494. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:balloon cells (in type iib)
    n1=DYNC2H1 gene | n2=en:balloon cells (in type iib) | rel=r_associated | relid=0 | w=10
  495. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ballooned neurons
    n1=DYNC2H1 gene | n2=en:ballooned neurons | rel=r_associated | relid=0 | w=10
  496. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:band heterotopia (1 patient)
    n1=DYNC2H1 gene | n2=en:band heterotopia (1 patient) | rel=r_associated | relid=0 | w=10
  497. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:baroreflex failure syndrome
    n1=DYNC2H1 gene | n2=en:baroreflex failure syndrome | rel=r_associated | relid=0 | w=10
  498. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia atrophy
    n1=DYNC2H1 gene | n2=en:basal ganglia atrophy | rel=r_associated | relid=0 | w=10
  499. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia atrophy, progressive
    n1=DYNC2H1 gene | n2=en:basal ganglia atrophy, progressive | rel=r_associated | relid=0 | w=10
  500. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia calcification
    n1=DYNC2H1 gene | n2=en:basal ganglia calcification | rel=r_associated | relid=0 | w=10
  501. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia calcifications (in some patients)
    n1=DYNC2H1 gene | n2=en:basal ganglia calcifications (in some patients) | rel=r_associated | relid=0 | w=10
  502. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia calcifications (rare)
    n1=DYNC2H1 gene | n2=en:basal ganglia calcifications (rare) | rel=r_associated | relid=0 | w=10
  503. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia cysts
    n1=DYNC2H1 gene | n2=en:basal ganglia cysts | rel=r_associated | relid=0 | w=10
  504. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia dysfunction
    n1=DYNC2H1 gene | n2=en:basal ganglia dysfunction | rel=r_associated | relid=0 | w=10
  505. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia gliosis
    n1=DYNC2H1 gene | n2=en:basal ganglia gliosis | rel=r_associated | relid=0 | w=10
  506. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia lesions may be present before onset of clinical symptoms
    n1=DYNC2H1 gene | n2=en:basal ganglia lesions may be present before onset of clinical symptoms | rel=r_associated | relid=0 | w=10
  507. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia lesions seen on mri
    n1=DYNC2H1 gene | n2=en:basal ganglia lesions seen on mri | rel=r_associated | relid=0 | w=10
  508. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglia lucencies
    n1=DYNC2H1 gene | n2=en:basal ganglia lucencies | rel=r_associated | relid=0 | w=10
  509. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:basal ganglion degeneration
    n1=DYNC2H1 gene | n2=en:basal ganglion degeneration | rel=r_associated | relid=0 | w=10
  510. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:begins in limbs, later generalized (childhood onset)
    n1=DYNC2H1 gene | n2=en:begins in limbs, later generalized (childhood onset) | rel=r_associated | relid=0 | w=10
  511. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:behavioral variant of frontotemporal dementia
    n1=DYNC2H1 gene | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=10
  512. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:beta-amyloid-positive senile plaques
    n1=DYNC2H1 gene | n2=en:beta-amyloid-positive senile plaques | rel=r_associated | relid=0 | w=10
  513. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:between 2 and 7% of children will develop afebrile seizure disorders later in life
    n1=DYNC2H1 gene | n2=en:between 2 and 7% of children will develop afebrile seizure disorders later in life | rel=r_associated | relid=0 | w=10
  514. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bilateral calcification of basal ganglia and cerebellum
    n1=DYNC2H1 gene | n2=en:bilateral calcification of basal ganglia and cerebellum | rel=r_associated | relid=0 | w=10
  515. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bilateral convulsive seizures
    n1=DYNC2H1 gene | n2=en:bilateral convulsive seizures | rel=r_associated | relid=0 | w=10
  516. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bilateral perisylvian cortical malformations on mri
    n1=DYNC2H1 gene | n2=en:bilateral perisylvian cortical malformations on mri | rel=r_associated | relid=0 | w=10
  517. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bilateral schizencephaly
    n1=DYNC2H1 gene | n2=en:bilateral schizencephaly | rel=r_associated | relid=0 | w=10
  518. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bilateral signals in the basal ganglia
    n1=DYNC2H1 gene | n2=en:bilateral signals in the basal ganglia | rel=r_associated | relid=0 | w=10
  519. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bilateral striatal lucencies on imaging
    n1=DYNC2H1 gene | n2=en:bilateral striatal lucencies on imaging | rel=r_associated | relid=0 | w=10
  520. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bilateral striatal necrosis
    n1=DYNC2H1 gene | n2=en:bilateral striatal necrosis | rel=r_associated | relid=0 | w=10
  521. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bilateral thalamic lesions on mri
    n1=DYNC2H1 gene | n2=en:bilateral thalamic lesions on mri | rel=r_associated | relid=0 | w=10
  522. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas
    n1=DYNC2H1 gene | n2=en:bilateral, symmetric intracerebral calcifications, especially in the basal ganglia and periventricular areas | rel=r_associated | relid=0 | w=10
  523. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:biopsy in both types shows neuronal cytomegaly (large, bizarre, maloriented neurons) in the laminar cortex
    n1=DYNC2H1 gene | n2=en:biopsy in both types shows neuronal cytomegaly (large, bizarre, maloriented neurons) in the laminar cortex | rel=r_associated | relid=0 | w=10
  524. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:biopsy shows foamy lipid-laden macrophages
    n1=DYNC2H1 gene | n2=en:biopsy shows foamy lipid-laden macrophages | rel=r_associated | relid=0 | w=10
  525. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:biopsy shows white matter hypomyelination, demyelination, gliosis
    n1=DYNC2H1 gene | n2=en:biopsy shows white matter hypomyelination, demyelination, gliosis | rel=r_associated | relid=0 | w=10
  526. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bladder sphincter atony
    n1=DYNC2H1 gene | n2=en:bladder sphincter atony | rel=r_associated | relid=0 | w=10
  527. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:blake's pouch (rare)
    n1=DYNC2H1 gene | n2=en:blake's pouch (rare) | rel=r_associated | relid=0 | w=10
  528. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:blindness
    n1=DYNC2H1 gene | n2=en:blindness | rel=r_associated | relid=0 | w=10
  529. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:blurring of the gray-white junction (in type iib)
    n1=DYNC2H1 gene | n2=en:blurring of the gray-white junction (in type iib) | rel=r_associated | relid=0 | w=10
  530. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib)
    n1=DYNC2H1 gene | n2=en:blurry cortical-white matter junction due to spillover of abnormal neurons (in type iib) | rel=r_associated | relid=0 | w=10
  531. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:board and poorly defined gyri
    n1=DYNC2H1 gene | n2=en:board and poorly defined gyri | rel=r_associated | relid=0 | w=10
  532. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:borderline intelligence
    n1=DYNC2H1 gene | n2=en:borderline intelligence | rel=r_associated | relid=0 | w=10
  533. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brachial plexus neuritis
    n1=DYNC2H1 gene | n2=en:brachial plexus neuritis | rel=r_associated | relid=0 | w=10
  534. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bradykinesia
    n1=DYNC2H1 gene | n2=en:bradykinesia | rel=r_associated | relid=0 | w=10
  535. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bradykinesia (in severe cases)
    n1=DYNC2H1 gene | n2=en:bradykinesia (in severe cases) | rel=r_associated | relid=0 | w=10
  536. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain
    n1=DYNC2H1 gene | n2=en:brain | rel=r_associated | relid=0 | w=10
  537. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain abscess
    n1=DYNC2H1 gene | n2=en:brain abscess | rel=r_associated | relid=0 | w=10
  538. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain and spinal cord structure
    n1=DYNC2H1 gene | n2=en:brain and spinal cord structure | rel=r_associated | relid=0 | w=10
  539. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain atrophy (1 family)
    n1=DYNC2H1 gene | n2=en:brain atrophy (1 family) | rel=r_associated | relid=0 | w=10
  540. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain atrophy (1 patient)
    n1=DYNC2H1 gene | n2=en:brain atrophy (1 patient) | rel=r_associated | relid=0 | w=10
  541. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain atrophy (in some patients)
    n1=DYNC2H1 gene | n2=en:brain atrophy (in some patients) | rel=r_associated | relid=0 | w=10
  542. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain atrophy seen on mri
    n1=DYNC2H1 gene | n2=en:brain atrophy seen on mri | rel=r_associated | relid=0 | w=10
  543. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain atrophy, particularly of the frontal and temporal lobes
    n1=DYNC2H1 gene | n2=en:brain atrophy, particularly of the frontal and temporal lobes | rel=r_associated | relid=0 | w=10
  544. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain calcification (if left untreated)
    n1=DYNC2H1 gene | n2=en:brain calcification (if left untreated) | rel=r_associated | relid=0 | w=10
  545. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain circuit
    n1=DYNC2H1 gene | n2=en:brain circuit | rel=r_associated | relid=0 | w=10
  546. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain edema
    n1=DYNC2H1 gene | n2=en:brain edema | rel=r_associated | relid=0 | w=10
  547. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain edema following head injury (less common)
    n1=DYNC2H1 gene | n2=en:brain edema following head injury (less common) | rel=r_associated | relid=0 | w=10
  548. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain imaging shows calcification of the dentate nucleus
    n1=DYNC2H1 gene | n2=en:brain imaging shows calcification of the dentate nucleus | rel=r_associated | relid=0 | w=10
  549. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain imaging shows cortical atrophy
    n1=DYNC2H1 gene | n2=en:brain imaging shows cortical atrophy | rel=r_associated | relid=0 | w=10
  550. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain imaging shows decreased white matter density
    n1=DYNC2H1 gene | n2=en:brain imaging shows decreased white matter density | rel=r_associated | relid=0 | w=10
  551. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain imaging shows diffuse white matter abnormalities
    n1=DYNC2H1 gene | n2=en:brain imaging shows diffuse white matter abnormalities | rel=r_associated | relid=0 | w=10
  552. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain imaging shows functional defects in the cortical and subcortical motor-related areas of the frontal lobe
    n1=DYNC2H1 gene | 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=10
  553. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain imaging shows generalized atrophy
    n1=DYNC2H1 gene | n2=en:brain imaging shows generalized atrophy | rel=r_associated | relid=0 | w=10
  554. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain imaging shows hypomyelination
    n1=DYNC2H1 gene | n2=en:brain imaging shows hypomyelination | rel=r_associated | relid=0 | w=10
  555. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain imaging shows lesions in the thalami, brainstem, and cerebellum
    n1=DYNC2H1 gene | n2=en:brain imaging shows lesions in the thalami, brainstem, and cerebellum | rel=r_associated | relid=0 | w=10
  556. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain imaging shows white-matter hypodensities and demyelination
    n1=DYNC2H1 gene | n2=en:brain imaging shows white-matter hypodensities and demyelination | rel=r_associated | relid=0 | w=10
  557. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain injury
    n1=DYNC2H1 gene | n2=en:brain injury | rel=r_associated | relid=0 | w=10
  558. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain iron accumulation (in some patients)
    n1=DYNC2H1 gene | n2=en:brain iron accumulation (in some patients) | rel=r_associated | relid=0 | w=10
  559. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain iron accumulation in the basal ganglia (in some patients)
    n1=DYNC2H1 gene | n2=en:brain iron accumulation in the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=10
  560. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family)
    n1=DYNC2H1 gene | n2=en:brain mri shows abnormal cortical thickening in the anteromesial frontal areas (1 family) | rel=r_associated | relid=0 | w=10
  561. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows abnormal gyral pattern in frontal lobes
    n1=DYNC2H1 gene | n2=en:brain mri shows abnormal gyral pattern in frontal lobes | rel=r_associated | relid=0 | w=10
  562. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows arrest in myelination
    n1=DYNC2H1 gene | n2=en:brain mri shows arrest in myelination | rel=r_associated | relid=0 | w=10
  563. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows cerebellar atrophy
    n1=DYNC2H1 gene | n2=en:brain mri shows cerebellar atrophy | rel=r_associated | relid=0 | w=10
  564. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows cerebellar atrophy (1 patient)
    n1=DYNC2H1 gene | n2=en:brain mri shows cerebellar atrophy (1 patient) | rel=r_associated | relid=0 | w=10
  565. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows cerebellar hypoplasia
    n1=DYNC2H1 gene | n2=en:brain mri shows cerebellar hypoplasia | rel=r_associated | relid=0 | w=10
  566. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows cortical atrophy
    n1=DYNC2H1 gene | n2=en:brain mri shows cortical atrophy | rel=r_associated | relid=0 | w=10
  567. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows diffusion abnormalities
    n1=DYNC2H1 gene | n2=en:brain mri shows diffusion abnormalities | rel=r_associated | relid=0 | w=10
  568. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows flattening of the ventral pons
    n1=DYNC2H1 gene | n2=en:brain mri shows flattening of the ventral pons | rel=r_associated | relid=0 | w=10
  569. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows hyperintensities in the basal ganglia
    n1=DYNC2H1 gene | n2=en:brain mri shows hyperintensities in the basal ganglia | rel=r_associated | relid=0 | w=10
  570. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows hypoplasia of the corpus callosum
    n1=DYNC2H1 gene | n2=en:brain mri shows hypoplasia of the corpus callosum | rel=r_associated | relid=0 | w=10
  571. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows hypoplastic pituitary
    n1=DYNC2H1 gene | n2=en:brain mri shows hypoplastic pituitary | rel=r_associated | relid=0 | w=10
  572. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows lesions consistent with epileptic episodes
    n1=DYNC2H1 gene | n2=en:brain mri shows lesions consistent with epileptic episodes | rel=r_associated | relid=0 | w=10
  573. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows lesions in the basal ganglia
    n1=DYNC2H1 gene | n2=en:brain mri shows lesions in the basal ganglia | rel=r_associated | relid=0 | w=10
  574. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows molar tooth sign
    n1=DYNC2H1 gene | n2=en:brain mri shows molar tooth sign | rel=r_associated | relid=0 | w=10
  575. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows proportionate pontocerebellar hypoplasia
    n1=DYNC2H1 gene | n2=en:brain mri shows proportionate pontocerebellar hypoplasia | rel=r_associated | relid=0 | w=10
  576. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows signal abnormalities in the basal ganglia
    n1=DYNC2H1 gene | n2=en:brain mri shows signal abnormalities in the basal ganglia | rel=r_associated | relid=0 | w=10
  577. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mri shows t2-weighted hyperintensities (17%)
    n1=DYNC2H1 gene | n2=en:brain mri shows t2-weighted hyperintensities (17%) | rel=r_associated | relid=0 | w=10
  578. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mrs shows decreased creatine content
    n1=DYNC2H1 gene | n2=en:brain mrs shows decreased creatine content | rel=r_associated | relid=0 | w=10
  579. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain mrs shows reduced choline and inositol peaks in the parieto-occipital white matter
    n1=DYNC2H1 gene | n2=en:brain mrs shows reduced choline and inositol peaks in the parieto-occipital white matter | rel=r_associated | relid=0 | w=10
  580. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd)
    n1=DYNC2H1 gene | n2=en:brain prp-immunoreactive amyloid plaques (in 10% if patients with sporadic cjd and in variant cjd) | rel=r_associated | relid=0 | w=10
  581. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain small vessel disease with hemorrhage
    n1=DYNC2H1 gene | n2=en:brain small vessel disease with hemorrhage | rel=r_associated | relid=0 | w=10
  582. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain stem
    n1=DYNC2H1 gene | n2=en:brain stem | rel=r_associated | relid=0 | w=10
  583. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain stem atrophy
    n1=DYNC2H1 gene | n2=en:brain stem atrophy | rel=r_associated | relid=0 | w=10
  584. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain stem atrophy, progressive
    n1=DYNC2H1 gene | n2=en:brain stem atrophy, progressive | rel=r_associated | relid=0 | w=10
  585. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain tissue shows abnormal spherical aggregates of iron and ferritin in the basal ganglia, forebrain, and cerebellum
    n1=DYNC2H1 gene | 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=10
  586. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain tissue shows cavitation of the basal ganglia
    n1=DYNC2H1 gene | n2=en:brain tissue shows cavitation of the basal ganglia | rel=r_associated | relid=0 | w=10
  587. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain vascular anomalies (rare)
    n1=DYNC2H1 gene | n2=en:brain vascular anomalies (rare) | rel=r_associated | relid=0 | w=10
  588. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brain white matter hyperintensities on mri
    n1=DYNC2H1 gene | n2=en:brain white matter hyperintensities on mri | rel=r_associated | relid=0 | w=10
  589. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brainstem atrophy
    n1=DYNC2H1 gene | n2=en:brainstem atrophy | rel=r_associated | relid=0 | w=10
  590. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brainstem concavity
    n1=DYNC2H1 gene | n2=en:brainstem concavity | rel=r_associated | relid=0 | w=10
  591. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brainstem damage
    n1=DYNC2H1 gene | n2=en:brainstem damage | rel=r_associated | relid=0 | w=10
  592. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brainstem dysplasia
    n1=DYNC2H1 gene | n2=en:brainstem dysplasia | rel=r_associated | relid=0 | w=10
  593. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brainstem hypoplasia (1 patient)
    n1=DYNC2H1 gene | n2=en:brainstem hypoplasia (1 patient) | rel=r_associated | relid=0 | w=10
  594. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brainstem hypoplasia (in some patients)
    n1=DYNC2H1 gene | n2=en:brainstem hypoplasia (in some patients) | rel=r_associated | relid=0 | w=10
  595. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brainstem lesions, hyperintense on t2-weighted imaging
    n1=DYNC2H1 gene | n2=en:brainstem lesions, hyperintense on t2-weighted imaging | rel=r_associated | relid=0 | w=10
  596. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brainstem may show neuronal loss
    n1=DYNC2H1 gene | n2=en:brainstem may show neuronal loss | rel=r_associated | relid=0 | w=10
  597. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brainstem white matter lesions
    n1=DYNC2H1 gene | n2=en:brainstem white matter lesions | rel=r_associated | relid=0 | w=10
  598. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:breathing difficulty due to vocal cord paralysis
    n1=DYNC2H1 gene | n2=en:breathing difficulty due to vocal cord paralysis | rel=r_associated | relid=0 | w=10
  599. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brief involuntary movements of upper extremities
    n1=DYNC2H1 gene | n2=en:brief involuntary movements of upper extremities | rel=r_associated | relid=0 | w=10
  600. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brisk knee reflexes (early-on)
    n1=DYNC2H1 gene | n2=en:brisk knee reflexes (early-on) | rel=r_associated | relid=0 | w=10
  601. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brisk lower limb reflexes (in some patients)
    n1=DYNC2H1 gene | n2=en:brisk lower limb reflexes (in some patients) | rel=r_associated | relid=0 | w=10
  602. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brisk reflexes
    n1=DYNC2H1 gene | n2=en:brisk reflexes | rel=r_associated | relid=0 | w=10
  603. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brisk reflexes (1 patient)
    n1=DYNC2H1 gene | n2=en:brisk reflexes (1 patient) | rel=r_associated | relid=0 | w=10
  604. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:brisk tendon reflex
    n1=DYNC2H1 gene | n2=en:brisk tendon reflex | rel=r_associated | relid=0 | w=10
  605. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:broad gait
    n1=DYNC2H1 gene | n2=en:broad gait | rel=r_associated | relid=0 | w=10
  606. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:broad-based gait
    n1=DYNC2H1 gene | n2=en:broad-based gait | rel=r_associated | relid=0 | w=10
  607. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:broad-based gait (1 patient)
    n1=DYNC2H1 gene | n2=en:broad-based gait (1 patient) | rel=r_associated | relid=0 | w=10
  608. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:broca's aphasia
    n1=DYNC2H1 gene | n2=en:broca's aphasia | rel=r_associated | relid=0 | w=10
  609. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:buccolingofacial dyspraxia
    n1=DYNC2H1 gene | n2=en:buccolingofacial dyspraxia | rel=r_associated | relid=0 | w=10
  610. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar and upper limb symptoms more severe than lower limb symptoms
    n1=DYNC2H1 gene | n2=en:bulbar and upper limb symptoms more severe than lower limb symptoms | rel=r_associated | relid=0 | w=10
  611. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar dysfunction
    n1=DYNC2H1 gene | n2=en:bulbar dysfunction | rel=r_associated | relid=0 | w=10
  612. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar dysfunction (e.g. dysarthria and dysphagia)
    n1=DYNC2H1 gene | n2=en:bulbar dysfunction (e.g. dysarthria and dysphagia) | rel=r_associated | relid=0 | w=10
  613. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar dysfunction (in some patients)
    n1=DYNC2H1 gene | n2=en:bulbar dysfunction (in some patients) | rel=r_associated | relid=0 | w=10
  614. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar dysfunction (juvenile-onset, less common)
    n1=DYNC2H1 gene | n2=en:bulbar dysfunction (juvenile-onset, less common) | rel=r_associated | relid=0 | w=10
  615. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar involvement
    n1=DYNC2H1 gene | n2=en:bulbar involvement | rel=r_associated | relid=0 | w=10
  616. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar paresis
    n1=DYNC2H1 gene | n2=en:bulbar paresis | rel=r_associated | relid=0 | w=10
  617. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar signs
    n1=DYNC2H1 gene | n2=en:bulbar signs | rel=r_associated | relid=0 | w=10
  618. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar spasticity
    n1=DYNC2H1 gene | n2=en:bulbar spasticity | rel=r_associated | relid=0 | w=10
  619. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar symptoms may occur (less common)
    n1=DYNC2H1 gene | n2=en:bulbar symptoms may occur (less common) | rel=r_associated | relid=0 | w=10
  620. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulbar weakness
    n1=DYNC2H1 gene | n2=en:bulbar weakness | rel=r_associated | relid=0 | w=10
  621. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:bulging of the caudate nuclei
    n1=DYNC2H1 gene | n2=en:bulging of the caudate nuclei | rel=r_associated | relid=0 | w=10
  622. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:burning or tingling of plantar surface of foot (in some patients)
    n1=DYNC2H1 gene | n2=en:burning or tingling of plantar surface of foot (in some patients) | rel=r_associated | relid=0 | w=10
  623. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:burning pain in the limbs
    n1=DYNC2H1 gene | n2=en:burning pain in the limbs | rel=r_associated | relid=0 | w=10
  624. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:burst suppression pattern on neonatal eeg
    n1=DYNC2H1 gene | n2=en:burst suppression pattern on neonatal eeg | rel=r_associated | relid=0 | w=10
  625. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:burst suppression pattern seen on eeg
    n1=DYNC2H1 gene | n2=en:burst suppression pattern seen on eeg | rel=r_associated | relid=0 | w=10
  626. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:by 10-15 years after onset, postural dystonia spreads to all limbs
    n1=DYNC2H1 gene | n2=en:by 10-15 years after onset, postural dystonia spreads to all limbs | rel=r_associated | relid=0 | w=10
  627. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:c3hex, decreased ability to smell
    n1=DYNC2H1 gene | n2=en:c3hex, decreased ability to smell | rel=r_associated | relid=0 | w=10
  628. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:calcification in the pons and cerebellum
    n1=DYNC2H1 gene | n2=en:calcification in the pons and cerebellum | rel=r_associated | relid=0 | w=10
  629. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:calcification may occur in other brain regions, including cerebellum, thalamus, white matter
    n1=DYNC2H1 gene | n2=en:calcification may occur in other brain regions, including cerebellum, thalamus, white matter | rel=r_associated | relid=0 | w=10
  630. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:calcification of the amygdala and the amygdala-hippocampal transition area
    n1=DYNC2H1 gene | n2=en:calcification of the amygdala and the amygdala-hippocampal transition area | rel=r_associated | relid=0 | w=10
  631. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:calcification of the falx
    n1=DYNC2H1 gene | n2=en:calcification of the falx | rel=r_associated | relid=0 | w=10
  632. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord
    n1=DYNC2H1 gene | n2=en:calcifications in white matter, basal ganglia, brainstem, cerebellum, and spinal cord | rel=r_associated | relid=0 | w=10
  633. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:calcifications may be seen in the thalamus, hippocampus, subcortical white matter, and cortex
    n1=DYNC2H1 gene | n2=en:calcifications may be seen in the thalamus, hippocampus, subcortical white matter, and cortex | rel=r_associated | relid=0 | w=10
  634. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:calcifications of cerebral ventricles
    n1=DYNC2H1 gene | n2=en:calcifications of cerebral ventricles | rel=r_associated | relid=0 | w=10
  635. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:calicification of the falx cerebri
    n1=DYNC2H1 gene | n2=en:calicification of the falx cerebri | rel=r_associated | relid=0 | w=10
  636. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:candidal meningitis (in some patients)
    n1=DYNC2H1 gene | n2=en:candidal meningitis (in some patients) | rel=r_associated | relid=0 | w=10
  637. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cardiac autonomic neuropathy
    n1=DYNC2H1 gene | n2=en:cardiac autonomic neuropathy | rel=r_associated | relid=0 | w=10
  638. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cardiovascular somatic symptom disorder
    n1=DYNC2H1 gene | n2=en:cardiovascular somatic symptom disorder | rel=r_associated | relid=0 | w=10
  639. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:carotid sinus hypersensitivity
    n1=DYNC2H1 gene | n2=en:carotid sinus hypersensitivity | rel=r_associated | relid=0 | w=10
  640. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cataplexy
    n1=DYNC2H1 gene | n2=en:cataplexy | rel=r_associated | relid=0 | w=10
  641. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cataplexy often triggered by strong emotions
    n1=DYNC2H1 gene | n2=en:cataplexy often triggered by strong emotions | rel=r_associated | relid=0 | w=10
  642. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cataplexy, paroxysmal weakness or paralysis
    n1=DYNC2H1 gene | n2=en:cataplexy, paroxysmal weakness or paralysis | rel=r_associated | relid=0 | w=10
  643. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:catatonic behavior
    n1=DYNC2H1 gene | n2=en:catatonic behavior | rel=r_associated | relid=0 | w=10
  644. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cauda equina syndrome
    n1=DYNC2H1 gene | n2=en:cauda equina syndrome | rel=r_associated | relid=0 | w=10
  645. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cauda equina syndrome with neurogenic bladder
    n1=DYNC2H1 gene | n2=en:cauda equina syndrome with neurogenic bladder | rel=r_associated | relid=0 | w=10
  646. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:caudate atrophy
    n1=DYNC2H1 gene | n2=en:caudate atrophy | rel=r_associated | relid=0 | w=10
  647. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:caudate nuclei atrophy
    n1=DYNC2H1 gene | n2=en:caudate nuclei atrophy | rel=r_associated | relid=0 | w=10
  648. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cavitating leukoencephalopathy
    n1=DYNC2H1 gene | n2=en:cavitating leukoencephalopathy | rel=r_associated | relid=0 | w=10
  649. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cavitating white matter degeneration
    n1=DYNC2H1 gene | n2=en:cavitating white matter degeneration | rel=r_associated | relid=0 | w=10
  650. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cavum septum pellucidum atrophy
    n1=DYNC2H1 gene | n2=en:cavum septum pellucidum atrophy | rel=r_associated | relid=0 | w=10
  651. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cavum vergae
    n1=DYNC2H1 gene | n2=en:cavum vergae | rel=r_associated | relid=0 | w=10
  652. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ccerebellar ataxia
    n1=DYNC2H1 gene | n2=en:ccerebellar ataxia | rel=r_associated | relid=0 | w=10
  653. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cell loss and gliosis in the basal ganglia
    n1=DYNC2H1 gene | n2=en:cell loss and gliosis in the basal ganglia | rel=r_associated | relid=0 | w=10
  654. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central canal malformation
    n1=DYNC2H1 gene | n2=en:central canal malformation | rel=r_associated | relid=0 | w=10
  655. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central facial nerve paralysis (rare)
    n1=DYNC2H1 gene | n2=en:central facial nerve paralysis (rare) | rel=r_associated | relid=0 | w=10
  656. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central facial palsy (in some patients)
    n1=DYNC2H1 gene | n2=en:central facial palsy (in some patients) | rel=r_associated | relid=0 | w=10
  657. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central hypotonia
    n1=DYNC2H1 gene | n2=en:central hypotonia | rel=r_associated | relid=0 | w=10
  658. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central nervous system
    n1=DYNC2H1 gene | n2=en:central nervous system | rel=r_associated | relid=0 | w=10
  659. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central nervous system degeneration
    n1=DYNC2H1 gene | n2=en:central nervous system degeneration | rel=r_associated | relid=0 | w=10
  660. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central nervous system demyelination
    n1=DYNC2H1 gene | n2=en:central nervous system demyelination | rel=r_associated | relid=0 | w=10
  661. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central nervous system involvement (in some patients)
    n1=DYNC2H1 gene | n2=en:central nervous system involvement (in some patients) | rel=r_associated | relid=0 | w=10
  662. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central nervous system involvement in approximately 50% of patients
    n1=DYNC2H1 gene | n2=en:central nervous system involvement in approximately 50% of patients | rel=r_associated | relid=0 | w=10
  663. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central nervous system malformations (40%)
    n1=DYNC2H1 gene | n2=en:central nervous system malformations (40%) | rel=r_associated | relid=0 | w=10
  664. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central nervous system neoplasm
    n1=DYNC2H1 gene | n2=en:central nervous system neoplasm | rel=r_associated | relid=0 | w=10
  665. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central nervous system part
    n1=DYNC2H1 gene | n2=en:central nervous system part | rel=r_associated | relid=0 | w=10
  666. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central nervous system space
    n1=DYNC2H1 gene | n2=en:central nervous system space | rel=r_associated | relid=0 | w=10
  667. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:central neural pathway/tract
    n1=DYNC2H1 gene | n2=en:central neural pathway/tract | rel=r_associated | relid=0 | w=10
  668. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar and brainstem atrophy, mild (1 patient)
    n1=DYNC2H1 gene | n2=en:cerebellar and brainstem atrophy, mild (1 patient) | rel=r_associated | relid=0 | w=10
  669. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia | rel=r_associated | relid=0 | w=10
  670. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia (1 patient)
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia (1 patient) | rel=r_associated | relid=0 | w=10
  671. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia (in 1 of 3 families)
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia (in 1 of 3 families) | rel=r_associated | relid=0 | w=10
  672. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia (may be permanent in 50% of patients)
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia (may be permanent in 50% of patients) | rel=r_associated | relid=0 | w=10
  673. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia (rare)
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia (rare) | rel=r_associated | relid=0 | w=10
  674. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia (seen in hhs variant)
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia (seen in hhs variant) | rel=r_associated | relid=0 | w=10
  675. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia during episodes
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia during episodes | rel=r_associated | relid=0 | w=10
  676. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia, adult-onset (in 1 family)
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia, adult-onset (in 1 family) | rel=r_associated | relid=0 | w=10
  677. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia, gait and stance
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia, gait and stance | rel=r_associated | relid=0 | w=10
  678. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia, limb and trunk
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia, limb and trunk | rel=r_associated | relid=0 | w=10
  679. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia, mild, late-onset
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia, mild, late-onset | rel=r_associated | relid=0 | w=10
  680. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia, severe
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia, severe | rel=r_associated | relid=0 | w=10
  681. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar ataxia, slowly progressive
    n1=DYNC2H1 gene | n2=en:cerebellar ataxia, slowly progressive | rel=r_associated | relid=0 | w=10
  682. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy | rel=r_associated | relid=0 | w=10
  683. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy (1 patient)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy (1 patient) | rel=r_associated | relid=0 | w=10
  684. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy (96% of patients)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy (96% of patients) | rel=r_associated | relid=0 | w=10
  685. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy (especially in the superior cerebellar vermis)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy (especially in the superior cerebellar vermis) | rel=r_associated | relid=0 | w=10
  686. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy (especially of the vermis)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy (especially of the vermis) | rel=r_associated | relid=0 | w=10
  687. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy (in 1 family)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy (in 1 family) | rel=r_associated | relid=0 | w=10
  688. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy (in adulthood)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy (in adulthood) | rel=r_associated | relid=0 | w=10
  689. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy (in some patients)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy (in some patients) | rel=r_associated | relid=0 | w=10
  690. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy (juvenile form)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy (juvenile form) | rel=r_associated | relid=0 | w=10
  691. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  692. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy in most cases
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy in most cases | rel=r_associated | relid=0 | w=10
  693. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy in older patients
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy in older patients | rel=r_associated | relid=0 | w=10
  694. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy seen on mri
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy seen on mri | rel=r_associated | relid=0 | w=10
  695. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy with signal hyperintensity in the cerebellar cortex seen on t2-weighted mri | rel=r_associated | relid=0 | w=10
  696. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, diffuse, severe
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, diffuse, severe | rel=r_associated | relid=0 | w=10
  697. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, mild
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, mild | rel=r_associated | relid=0 | w=10
  698. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, mild (1 patient)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, mild (1 patient) | rel=r_associated | relid=0 | w=10
  699. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, mild (in 1 of 3 families)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, mild (in 1 of 3 families) | rel=r_associated | relid=0 | w=10
  700. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, particularly of the hemispheres
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, particularly of the hemispheres | rel=r_associated | relid=0 | w=10
  701. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, progressive
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, progressive | rel=r_associated | relid=0 | w=10
  702. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, progressive (1 patient)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, progressive (1 patient) | rel=r_associated | relid=0 | w=10
  703. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, progressive (cerebellar vermal atrophy before cerebral atrophy) | rel=r_associated | relid=0 | w=10
  704. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, progressive (in some patients)
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, progressive (in some patients) | rel=r_associated | relid=0 | w=10
  705. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar atrophy, severe
    n1=DYNC2H1 gene | n2=en:cerebellar atrophy, severe | rel=r_associated | relid=0 | w=10
  706. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar calcifications
    n1=DYNC2H1 gene | n2=en:cerebellar calcifications | rel=r_associated | relid=0 | w=10
  707. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar cell paucity, more marked in vermis than hemispheres
    n1=DYNC2H1 gene | n2=en:cerebellar cell paucity, more marked in vermis than hemispheres | rel=r_associated | relid=0 | w=10
  708. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar cortex shows normal layers
    n1=DYNC2H1 gene | n2=en:cerebellar cortex shows normal layers | rel=r_associated | relid=0 | w=10
  709. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar cortical degeneration
    n1=DYNC2H1 gene | n2=en:cerebellar cortical degeneration | rel=r_associated | relid=0 | w=10
  710. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar cyst
    n1=DYNC2H1 gene | n2=en:cerebellar cyst | rel=r_associated | relid=0 | w=10
  711. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar cyst (rare)
    n1=DYNC2H1 gene | n2=en:cerebellar cyst (rare) | rel=r_associated | relid=0 | w=10
  712. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar cysts (meb)
    n1=DYNC2H1 gene | n2=en:cerebellar cysts (meb) | rel=r_associated | relid=0 | w=10
  713. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar degeneration
    n1=DYNC2H1 gene | n2=en:cerebellar degeneration | rel=r_associated | relid=0 | w=10
  714. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar dysarthria
    n1=DYNC2H1 gene | n2=en:cerebellar dysarthria | rel=r_associated | relid=0 | w=10
  715. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar dysfunction, progressive
    n1=DYNC2H1 gene | n2=en:cerebellar dysfunction, progressive | rel=r_associated | relid=0 | w=10
  716. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar dysplasia
    n1=DYNC2H1 gene | n2=en:cerebellar dysplasia | rel=r_associated | relid=0 | w=10
  717. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar enlargement
    n1=DYNC2H1 gene | n2=en:cerebellar enlargement | rel=r_associated | relid=0 | w=10
  718. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar gangliocytoma manifesting as seizure and tremor
    n1=DYNC2H1 gene | n2=en:cerebellar gangliocytoma manifesting as seizure and tremor | rel=r_associated | relid=0 | w=10
  719. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hemangioblastoma
    n1=DYNC2H1 gene | n2=en:cerebellar hemangioblastoma | rel=r_associated | relid=0 | w=10
  720. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hemorrhage (rare)
    n1=DYNC2H1 gene | n2=en:cerebellar hemorrhage (rare) | rel=r_associated | relid=0 | w=10
  721. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar herniation (rare)
    n1=DYNC2H1 gene | n2=en:cerebellar herniation (rare) | rel=r_associated | relid=0 | w=10
  722. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar heterotopias
    n1=DYNC2H1 gene | n2=en:cerebellar heterotopias | rel=r_associated | relid=0 | w=10
  723. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (1 patient)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (1 patient) | rel=r_associated | relid=0 | w=10
  724. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (in 1 of 2 patients)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (in 1 of 2 patients) | rel=r_associated | relid=0 | w=10
  725. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (in 1 of 2 sibs)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=10
  726. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (in most patients)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (in most patients) | rel=r_associated | relid=0 | w=10
  727. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (in some patients)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (in some patients) | rel=r_associated | relid=0 | w=10
  728. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (in some)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (in some) | rel=r_associated | relid=0 | w=10
  729. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (male)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (male) | rel=r_associated | relid=0 | w=10
  730. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (reported in 1 family)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (reported in 1 family) | rel=r_associated | relid=0 | w=10
  731. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (seen in hhs variant)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (seen in hhs variant) | rel=r_associated | relid=0 | w=10
  732. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (seen in recessive form)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (seen in recessive form) | rel=r_associated | relid=0 | w=10
  733. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia (variable)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia (variable) | rel=r_associated | relid=0 | w=10
  734. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia due to enlarged foramen magnum
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia due to enlarged foramen magnum | rel=r_associated | relid=0 | w=10
  735. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia or agenesis
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia or agenesis | rel=r_associated | relid=0 | w=10
  736. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia predominantly affecting the vermis
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia predominantly affecting the vermis | rel=r_associated | relid=0 | w=10
  737. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia, mild (in some patients) | rel=r_associated | relid=0 | w=10
  738. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia, mild asymmetric (rare)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia, mild asymmetric (rare) | rel=r_associated | relid=0 | w=10
  739. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia, particularly of the hemispheres
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia, particularly of the hemispheres | rel=r_associated | relid=0 | w=10
  740. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia, severe (wws)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia, severe (wws) | rel=r_associated | relid=0 | w=10
  741. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar hypoplasia/atrophy (27%)
    n1=DYNC2H1 gene | n2=en:cerebellar hypoplasia/atrophy (27%) | rel=r_associated | relid=0 | w=10
  742. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar lesion nos
    n1=DYNC2H1 gene | n2=en:cerebellar lesion nos | rel=r_associated | relid=0 | w=10
  743. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar medulloblastoma (rare)
    n1=DYNC2H1 gene | n2=en:cerebellar medulloblastoma (rare) | rel=r_associated | relid=0 | w=10
  744. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar neuronal loss
    n1=DYNC2H1 gene | n2=en:cerebellar neuronal loss | rel=r_associated | relid=0 | w=10
  745. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar origin most likely
    n1=DYNC2H1 gene | n2=en:cerebellar origin most likely | rel=r_associated | relid=0 | w=10
  746. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar signs
    n1=DYNC2H1 gene | n2=en:cerebellar signs | rel=r_associated | relid=0 | w=10
  747. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar signs (in some patients)
    n1=DYNC2H1 gene | n2=en:cerebellar signs (in some patients) | rel=r_associated | relid=0 | w=10
  748. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar signs (less common)
    n1=DYNC2H1 gene | n2=en:cerebellar signs (less common) | rel=r_associated | relid=0 | w=10
  749. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar signs (may be permanent in 50% of patients)
    n1=DYNC2H1 gene | n2=en:cerebellar signs (may be permanent in 50% of patients) | rel=r_associated | relid=0 | w=10
  750. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar signs (more common in variant cjd)
    n1=DYNC2H1 gene | n2=en:cerebellar signs (more common in variant cjd) | rel=r_associated | relid=0 | w=10
  751. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar signs during episodes
    n1=DYNC2H1 gene | n2=en:cerebellar signs during episodes | rel=r_associated | relid=0 | w=10
  752. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar signs may develop
    n1=DYNC2H1 gene | n2=en:cerebellar signs may develop | rel=r_associated | relid=0 | w=10
  753. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar signs, mild (in 1 of 3 families)
    n1=DYNC2H1 gene | n2=en:cerebellar signs, mild (in 1 of 3 families) | rel=r_associated | relid=0 | w=10
  754. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar stroke
    n1=DYNC2H1 gene | n2=en:cerebellar stroke | rel=r_associated | relid=0 | w=10
  755. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar tonsil herniation
    n1=DYNC2H1 gene | n2=en:cerebellar tonsil herniation | rel=r_associated | relid=0 | w=10
  756. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar tonsillar herniation
    n1=DYNC2H1 gene | n2=en:cerebellar tonsillar herniation | rel=r_associated | relid=0 | w=10
  757. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar vermis aplasia or hypoplasia
    n1=DYNC2H1 gene | n2=en:cerebellar vermis aplasia or hypoplasia | rel=r_associated | relid=0 | w=10
  758. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar vermis atrophy
    n1=DYNC2H1 gene | n2=en:cerebellar vermis atrophy | rel=r_associated | relid=0 | w=10
  759. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar vermis hypoplasia
    n1=DYNC2H1 gene | n2=en:cerebellar vermis hypoplasia | rel=r_associated | relid=0 | w=10
  760. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar vermis hypoplasia (in 1 patient)
    n1=DYNC2H1 gene | n2=en:cerebellar vermis hypoplasia (in 1 patient) | rel=r_associated | relid=0 | w=10
  761. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar vermis hypoplasia (in some patients)
    n1=DYNC2H1 gene | n2=en:cerebellar vermis hypoplasia (in some patients) | rel=r_associated | relid=0 | w=10
  762. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellar white matter lesions on mri
    n1=DYNC2H1 gene | n2=en:cerebellar white matter lesions on mri | rel=r_associated | relid=0 | w=10
  763. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebellum
    n1=DYNC2H1 gene | n2=en:cerebellum | rel=r_associated | relid=0 | w=10
  764. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral and cerebellar atrophy
    n1=DYNC2H1 gene | n2=en:cerebral and cerebellar atrophy | rel=r_associated | relid=0 | w=10
  765. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral arterial hemorrhage
    n1=DYNC2H1 gene | n2=en:cerebral arterial hemorrhage | rel=r_associated | relid=0 | w=10
  766. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy
    n1=DYNC2H1 gene | n2=en:cerebral atrophy | rel=r_associated | relid=0 | w=10
  767. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy (1 patient)
    n1=DYNC2H1 gene | n2=en:cerebral atrophy (1 patient) | rel=r_associated | relid=0 | w=10
  768. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy (in 1 family)
    n1=DYNC2H1 gene | n2=en:cerebral atrophy (in 1 family) | rel=r_associated | relid=0 | w=10
  769. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy (in severe cases)
    n1=DYNC2H1 gene | n2=en:cerebral atrophy (in severe cases) | rel=r_associated | relid=0 | w=10
  770. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy (in some patients)
    n1=DYNC2H1 gene | n2=en:cerebral atrophy (in some patients) | rel=r_associated | relid=0 | w=10
  771. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy (rare)
    n1=DYNC2H1 gene | n2=en:cerebral atrophy (rare) | rel=r_associated | relid=0 | w=10
  772. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:cerebral atrophy (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  773. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy diffuse
    n1=DYNC2H1 gene | n2=en:cerebral atrophy diffuse | rel=r_associated | relid=0 | w=10
  774. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy, diffuse, severe
    n1=DYNC2H1 gene | n2=en:cerebral atrophy, diffuse, severe | rel=r_associated | relid=0 | w=10
  775. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy, frontotemporal, progressive
    n1=DYNC2H1 gene | n2=en:cerebral atrophy, frontotemporal, progressive | rel=r_associated | relid=0 | w=10
  776. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy, generalized mild
    n1=DYNC2H1 gene | n2=en:cerebral atrophy, generalized mild | rel=r_associated | relid=0 | w=10
  777. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy, mild
    n1=DYNC2H1 gene | n2=en:cerebral atrophy, mild | rel=r_associated | relid=0 | w=10
  778. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy, mild, diffuse
    n1=DYNC2H1 gene | n2=en:cerebral atrophy, mild, diffuse | rel=r_associated | relid=0 | w=10
  779. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy, progressive
    n1=DYNC2H1 gene | n2=en:cerebral atrophy, progressive | rel=r_associated | relid=0 | w=10
  780. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy, progressive, from anterior to posterior
    n1=DYNC2H1 gene | n2=en:cerebral atrophy, progressive, from anterior to posterior | rel=r_associated | relid=0 | w=10
  781. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral atrophy, severe
    n1=DYNC2H1 gene | n2=en:cerebral atrophy, severe | rel=r_associated | relid=0 | w=10
  782. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral calcification
    n1=DYNC2H1 gene | n2=en:cerebral calcification | rel=r_associated | relid=0 | w=10
  783. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral cavernous malformation
    n1=DYNC2H1 gene | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=10
  784. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral cortex myoclonus
    n1=DYNC2H1 gene | n2=en:cerebral cortex myoclonus | rel=r_associated | relid=0 | w=10
  785. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral cortex with spongiform changes
    n1=DYNC2H1 gene | n2=en:cerebral cortex with spongiform changes | rel=r_associated | relid=0 | w=10
  786. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral cortical and cerebellar atrophy (patient a)
    n1=DYNC2H1 gene | n2=en:cerebral cortical and cerebellar atrophy (patient a) | rel=r_associated | relid=0 | w=10
  787. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral cortical atrophy, diffuse
    n1=DYNC2H1 gene | n2=en:cerebral cortical atrophy, diffuse | rel=r_associated | relid=0 | w=10
  788. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral cortical atrophy, especially frontal lobes
    n1=DYNC2H1 gene | n2=en:cerebral cortical atrophy, especially frontal lobes | rel=r_associated | relid=0 | w=10
  789. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral cortical neurodegeneration
    n1=DYNC2H1 gene | n2=en:cerebral cortical neurodegeneration | rel=r_associated | relid=0 | w=10
  790. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral cyst
    n1=DYNC2H1 gene | n2=en:cerebral cyst | rel=r_associated | relid=0 | w=10
  791. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral degeneration
    n1=DYNC2H1 gene | n2=en:cerebral degeneration | rel=r_associated | relid=0 | w=10
  792. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral demyelination and inflammation
    n1=DYNC2H1 gene | n2=en:cerebral demyelination and inflammation | rel=r_associated | relid=0 | w=10
  793. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral dysmyelination
    n1=DYNC2H1 gene | n2=en:cerebral dysmyelination | rel=r_associated | relid=0 | w=10
  794. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral edema
    n1=DYNC2H1 gene | n2=en:cerebral edema | rel=r_associated | relid=0 | w=10
  795. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral hemorrhage
    n1=DYNC2H1 gene | n2=en:cerebral hemorrhage | rel=r_associated | relid=0 | w=10
  796. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral hypomyelination
    n1=DYNC2H1 gene | n2=en:cerebral hypomyelination | rel=r_associated | relid=0 | w=10
  797. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral hypoplasia
    n1=DYNC2H1 gene | n2=en:cerebral hypoplasia | rel=r_associated | relid=0 | w=10
  798. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral infarction
    n1=DYNC2H1 gene | n2=en:cerebral infarction | rel=r_associated | relid=0 | w=10
  799. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral infarction dandy-walker malformation
    n1=DYNC2H1 gene | n2=en:cerebral infarction dandy-walker malformation | rel=r_associated | relid=0 | w=10
  800. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral malformations
    n1=DYNC2H1 gene | n2=en:cerebral malformations | rel=r_associated | relid=0 | w=10
  801. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral oligogyria
    n1=DYNC2H1 gene | n2=en:cerebral oligogyria | rel=r_associated | relid=0 | w=10
  802. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral palsy
    n1=DYNC2H1 gene | n2=en:cerebral palsy | rel=r_associated | relid=0 | w=10
  803. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral spongiosis
    n1=DYNC2H1 gene | n2=en:cerebral spongiosis | rel=r_associated | relid=0 | w=10
  804. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral thrombosis
    n1=DYNC2H1 gene | n2=en:cerebral thrombosis | rel=r_associated | relid=0 | w=10
  805. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency)
    n1=DYNC2H1 gene | n2=en:cerebral thrombosis (e.g. 612283.0014 protein c deficiency) | rel=r_associated | relid=0 | w=10
  806. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral vasculitis or vasculopathy (rare)
    n1=DYNC2H1 gene | n2=en:cerebral vasculitis or vasculopathy (rare) | rel=r_associated | relid=0 | w=10
  807. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral white matter atrophy, progressive
    n1=DYNC2H1 gene | n2=en:cerebral white matter atrophy, progressive | rel=r_associated | relid=0 | w=10
  808. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral white matter lesion
    n1=DYNC2H1 gene | n2=en:cerebral white matter lesion | rel=r_associated | relid=0 | w=10
  809. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebral white matter lesions (1 patient)
    n1=DYNC2H1 gene | n2=en:cerebral white matter lesions (1 patient) | rel=r_associated | relid=0 | w=10
  810. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebrospinal fluid
    n1=DYNC2H1 gene | n2=en:cerebrospinal fluid | rel=r_associated | relid=0 | w=10
  811. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebrospinal fluid glucose decreased
    n1=DYNC2H1 gene | n2=en:cerebrospinal fluid glucose decreased | rel=r_associated | relid=0 | w=10
  812. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebrospinal fluid may show decreased levels of homovanillic acid (hva)
    n1=DYNC2H1 gene | n2=en:cerebrospinal fluid may show decreased levels of homovanillic acid (hva) | rel=r_associated | relid=0 | w=10
  813. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebrovascular accident
    n1=DYNC2H1 gene | n2=en:cerebrovascular accident | rel=r_associated | relid=0 | w=10
  814. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebrovascular accident (in some patients)
    n1=DYNC2H1 gene | n2=en:cerebrovascular accident (in some patients) | rel=r_associated | relid=0 | w=10
  815. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebrovascular ischemia
    n1=DYNC2H1 gene | n2=en:cerebrovascular ischemia | rel=r_associated | relid=0 | w=10
  816. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cerebrovascular ischemic attacks, transient (proceed secondary neurologic findings)
    n1=DYNC2H1 gene | n2=en:cerebrovascular ischemic attacks, transient (proceed secondary neurologic findings) | rel=r_associated | relid=0 | w=10
  817. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cervical cord compression
    n1=DYNC2H1 gene | n2=en:cervical cord compression | rel=r_associated | relid=0 | w=10
  818. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cervical myelopathy
    n1=DYNC2H1 gene | n2=en:cervical myelopathy | rel=r_associated | relid=0 | w=10
  819. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cervicocranial syndrome
    n1=DYNC2H1 gene | n2=en:cervicocranial syndrome | rel=r_associated | relid=0 | w=10
  820. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:characteristic arm position with wrist and elbow flexion
    n1=DYNC2H1 gene | n2=en:characteristic arm position with wrist and elbow flexion | rel=r_associated | relid=0 | w=10
  821. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:characteristic electroencephalogram (eeg) discharges
    n1=DYNC2H1 gene | n2=en:characteristic electroencephalogram (eeg) discharges | rel=r_associated | relid=0 | w=10
  822. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:characteristic findings on mri
    n1=DYNC2H1 gene | n2=en:characteristic findings on mri | rel=r_associated | relid=0 | w=10
  823. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:characteristic periodic eeg complexes (only in sporadic and familial cjd, not in variant cjd)
    n1=DYNC2H1 gene | n2=en:characteristic periodic eeg complexes (only in sporadic and familial cjd, not in variant cjd) | rel=r_associated | relid=0 | w=10
  824. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chiari i malformation of the cerebellum (in some patients)
    n1=DYNC2H1 gene | n2=en:chiari i malformation of the cerebellum (in some patients) | rel=r_associated | relid=0 | w=10
  825. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chiari i malformation on mri
    n1=DYNC2H1 gene | n2=en:chiari i malformation on mri | rel=r_associated | relid=0 | w=10
  826. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chiari i malformation on mri (some)
    n1=DYNC2H1 gene | n2=en:chiari i malformation on mri (some) | rel=r_associated | relid=0 | w=10
  827. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chiari malformation (uncommon)
    n1=DYNC2H1 gene | n2=en:chiari malformation (uncommon) | rel=r_associated | relid=0 | w=10
  828. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chiari malformation type ii
    n1=DYNC2H1 gene | n2=en:chiari malformation type ii | rel=r_associated | relid=0 | w=10
  829. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chiari type i
    n1=DYNC2H1 gene | n2=en:chiari type i | rel=r_associated | relid=0 | w=10
  830. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chiari type i malformation (in some patients)
    n1=DYNC2H1 gene | n2=en:chiari type i malformation (in some patients) | rel=r_associated | relid=0 | w=10
  831. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:child dysarthria
    n1=DYNC2H1 gene | n2=en:child dysarthria | rel=r_associated | relid=0 | w=10
  832. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:childhood polyphagia
    n1=DYNC2H1 gene | n2=en:childhood polyphagia | rel=r_associated | relid=0 | w=10
  833. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cholinesterase inhibition
    n1=DYNC2H1 gene | n2=en:cholinesterase inhibition | rel=r_associated | relid=0 | w=10
  834. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chorea
    n1=DYNC2H1 gene | n2=en:chorea | rel=r_associated | relid=0 | w=10
  835. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chorea (in some patients)
    n1=DYNC2H1 gene | n2=en:chorea (in some patients) | rel=r_associated | relid=0 | w=10
  836. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chorea of all limbs
    n1=DYNC2H1 gene | n2=en:chorea of all limbs | rel=r_associated | relid=0 | w=10
  837. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chorea of hands
    n1=DYNC2H1 gene | n2=en:chorea of hands | rel=r_associated | relid=0 | w=10
  838. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chorea-ballism
    n1=DYNC2H1 gene | n2=en:chorea-ballism | rel=r_associated | relid=0 | w=10
  839. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chorea, mild (in some)
    n1=DYNC2H1 gene | n2=en:chorea, mild (in some) | rel=r_associated | relid=0 | w=10
  840. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chorea, prominent (in some patients)
    n1=DYNC2H1 gene | n2=en:chorea, prominent (in some patients) | rel=r_associated | relid=0 | w=10
  841. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreic movements (10 to 22% of patients)
    n1=DYNC2H1 gene | n2=en:choreic movements (10 to 22% of patients) | rel=r_associated | relid=0 | w=10
  842. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreic movements, episodic
    n1=DYNC2H1 gene | n2=en:choreic movements, episodic | rel=r_associated | relid=0 | w=10
  843. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreoathetoid movements
    n1=DYNC2H1 gene | n2=en:choreoathetoid movements | rel=r_associated | relid=0 | w=10
  844. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreoathetosis
    n1=DYNC2H1 gene | n2=en:choreoathetosis | rel=r_associated | relid=0 | w=10
  845. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreoathetosis (2 patients)
    n1=DYNC2H1 gene | n2=en:choreoathetosis (2 patients) | rel=r_associated | relid=0 | w=10
  846. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreoathetosis (described in 1 patient)
    n1=DYNC2H1 gene | n2=en:choreoathetosis (described in 1 patient) | rel=r_associated | relid=0 | w=10
  847. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreoathetosis (in 79%), more frequent at disease onset
    n1=DYNC2H1 gene | n2=en:choreoathetosis (in 79%), more frequent at disease onset | rel=r_associated | relid=0 | w=10
  848. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreoathetosis (in a subset of patients)
    n1=DYNC2H1 gene | n2=en:choreoathetosis (in a subset of patients) | rel=r_associated | relid=0 | w=10
  849. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreoathetosis (in some patients)
    n1=DYNC2H1 gene | n2=en:choreoathetosis (in some patients) | rel=r_associated | relid=0 | w=10
  850. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreoathetosis of the face, trunk, extremities
    n1=DYNC2H1 gene | n2=en:choreoathetosis of the face, trunk, extremities | rel=r_associated | relid=0 | w=10
  851. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choreodystonia of the upper limbs
    n1=DYNC2H1 gene | n2=en:choreodystonia of the upper limbs | rel=r_associated | relid=0 | w=10
  852. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choristoma
    n1=DYNC2H1 gene | n2=en:choristoma | rel=r_associated | relid=0 | w=10
  853. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choroid plexus calcification
    n1=DYNC2H1 gene | n2=en:choroid plexus calcification | rel=r_associated | relid=0 | w=10
  854. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choroid plexus cyst
    n1=DYNC2H1 gene | n2=en:choroid plexus cyst | rel=r_associated | relid=0 | w=10
  855. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:choroid plexus papilloma (in some patients)
    n1=DYNC2H1 gene | n2=en:choroid plexus papilloma (in some patients) | rel=r_associated | relid=0 | w=10
  856. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chronic headaches
    n1=DYNC2H1 gene | n2=en:chronic headaches | rel=r_associated | relid=0 | w=10
  857. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chronic idiopathic anhidrosis
    n1=DYNC2H1 gene | n2=en:chronic idiopathic anhidrosis | rel=r_associated | relid=0 | w=10
  858. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chronic lymphocytic meningitis
    n1=DYNC2H1 gene | n2=en:chronic lymphocytic meningitis | rel=r_associated | relid=0 | w=10
  859. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chronic pain
    n1=DYNC2H1 gene | n2=en:chronic pain | rel=r_associated | relid=0 | w=10
  860. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chronic subtype, headaches occur without remission for 1 year
    n1=DYNC2H1 gene | n2=en:chronic subtype, headaches occur without remission for 1 year | rel=r_associated | relid=0 | w=10
  861. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma
    n1=DYNC2H1 gene | n2=en:chronic-progressive course with episodes of rapid deterioration following fever or head trauma | rel=r_associated | relid=0 | w=10
  862. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:clonic convulsion
    n1=DYNC2H1 gene | n2=en:clonic convulsion | rel=r_associated | relid=0 | w=10
  863. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:clonus
    n1=DYNC2H1 gene | n2=en:clonus | rel=r_associated | relid=0 | w=10
  864. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:clonus may occur
    n1=DYNC2H1 gene | n2=en:clonus may occur | rel=r_associated | relid=0 | w=10
  865. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:closed-lip schizencephaly
    n1=DYNC2H1 gene | n2=en:closed-lip schizencephaly | rel=r_associated | relid=0 | w=10
  866. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:clumsiness
    n1=DYNC2H1 gene | n2=en:clumsiness | rel=r_associated | relid=0 | w=10
  867. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:clumsiness (82%)
    n1=DYNC2H1 gene | n2=en:clumsiness (82%) | rel=r_associated | relid=0 | w=10
  868. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:clumsiness (mild)
    n1=DYNC2H1 gene | n2=en:clumsiness (mild) | rel=r_associated | relid=0 | w=10
  869. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:clumsiness in childhood
    n1=DYNC2H1 gene | n2=en:clumsiness in childhood | rel=r_associated | relid=0 | w=10
  870. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:clumsiness, unsteadiness
    n1=DYNC2H1 gene | n2=en:clumsiness, unsteadiness | rel=r_associated | relid=0 | w=10
  871. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:clumsy gait
    n1=DYNC2H1 gene | n2=en:clumsy gait | rel=r_associated | relid=0 | w=10
  872. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cns component
    n1=DYNC2H1 gene | n2=en:cns component | rel=r_associated | relid=0 | w=10
  873. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cns infarctions
    n1=DYNC2H1 gene | n2=en:cns infarctions | rel=r_associated | relid=0 | w=10
  874. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cns venous malformations
    n1=DYNC2H1 gene | n2=en:cns venous malformations | rel=r_associated | relid=0 | w=10
  875. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:coarse tremors
    n1=DYNC2H1 gene | n2=en:coarse tremors | rel=r_associated | relid=0 | w=10
  876. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:coarsened pattern of sulci and gyri
    n1=DYNC2H1 gene | n2=en:coarsened pattern of sulci and gyri | rel=r_associated | relid=0 | w=10
  877. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cobblestone lissencephaly
    n1=DYNC2H1 gene | n2=en:cobblestone lissencephaly | rel=r_associated | relid=0 | w=10
  878. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cobblestone lissencephaly (1 patient)
    n1=DYNC2H1 gene | n2=en:cobblestone lissencephaly (1 patient) | rel=r_associated | relid=0 | w=10
  879. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cobblestone lissencephaly (posterior brain regions more affected than anterior regions)
    n1=DYNC2H1 gene | n2=en:cobblestone lissencephaly (posterior brain regions more affected than anterior regions) | rel=r_associated | relid=0 | w=10
  880. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cobblestone lissencephaly, posterior frontal and parietal regions
    n1=DYNC2H1 gene | n2=en:cobblestone lissencephaly, posterior frontal and parietal regions | rel=r_associated | relid=0 | w=10
  881. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cobblestone lissencephaly, type ii
    n1=DYNC2H1 gene | n2=en:cobblestone lissencephaly, type ii | rel=r_associated | relid=0 | w=10
  882. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cobblestone lissencephaly, type ii (wws)
    n1=DYNC2H1 gene | n2=en:cobblestone lissencephaly, type ii (wws) | rel=r_associated | relid=0 | w=10
  883. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognition is preserved
    n1=DYNC2H1 gene | n2=en:cognition is preserved | rel=r_associated | relid=0 | w=10
  884. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognition is spared
    n1=DYNC2H1 gene | n2=en:cognition is spared | rel=r_associated | relid=0 | w=10
  885. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive decline (1 family)
    n1=DYNC2H1 gene | n2=en:cognitive decline (1 family) | rel=r_associated | relid=0 | w=10
  886. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive decline (1 patient)
    n1=DYNC2H1 gene | n2=en:cognitive decline (1 patient) | rel=r_associated | relid=0 | w=10
  887. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive decline (in some patients)
    n1=DYNC2H1 gene | n2=en:cognitive decline (in some patients) | rel=r_associated | relid=0 | w=10
  888. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive decline (later in life)
    n1=DYNC2H1 gene | n2=en:cognitive decline (later in life) | rel=r_associated | relid=0 | w=10
  889. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive decline (rare)
    n1=DYNC2H1 gene | n2=en:cognitive decline (rare) | rel=r_associated | relid=0 | w=10
  890. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive decline in adulthood
    n1=DYNC2H1 gene | n2=en:cognitive decline in adulthood | rel=r_associated | relid=0 | w=10
  891. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive decline in older patients
    n1=DYNC2H1 gene | n2=en:cognitive decline in older patients | rel=r_associated | relid=0 | w=10
  892. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive decline, rapid
    n1=DYNC2H1 gene | n2=en:cognitive decline, rapid | rel=r_associated | relid=0 | w=10
  893. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive defects (rare)
    n1=DYNC2H1 gene | n2=en:cognitive defects (rare) | rel=r_associated | relid=0 | w=10
  894. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive defects (variable from mild to severe)
    n1=DYNC2H1 gene | n2=en:cognitive defects (variable from mild to severe) | rel=r_associated | relid=0 | w=10
  895. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive defects develop later in the disease
    n1=DYNC2H1 gene | n2=en:cognitive defects develop later in the disease | rel=r_associated | relid=0 | w=10
  896. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive defects in executive function and attention
    n1=DYNC2H1 gene | n2=en:cognitive defects in executive function and attention | rel=r_associated | relid=0 | w=10
  897. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive deficits (less common)
    n1=DYNC2H1 gene | n2=en:cognitive deficits (less common) | rel=r_associated | relid=0 | w=10
  898. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive deficits may occur
    n1=DYNC2H1 gene | n2=en:cognitive deficits may occur | rel=r_associated | relid=0 | w=10
  899. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive deficits, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:cognitive deficits, mild (in some patients) | rel=r_associated | relid=0 | w=10
  900. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive delay
    n1=DYNC2H1 gene | n2=en:cognitive delay | rel=r_associated | relid=0 | w=10
  901. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive delay, mild (1 patient)
    n1=DYNC2H1 gene | n2=en:cognitive delay, mild (1 patient) | rel=r_associated | relid=0 | w=10
  902. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive delay, mild to severe
    n1=DYNC2H1 gene | n2=en:cognitive delay, mild to severe | rel=r_associated | relid=0 | w=10
  903. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive deterioration
    n1=DYNC2H1 gene | n2=en:cognitive deterioration | rel=r_associated | relid=0 | w=10
  904. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive dysfunction
    n1=DYNC2H1 gene | n2=en:cognitive dysfunction | rel=r_associated | relid=0 | w=10
  905. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive dysfunction (in some patients)
    n1=DYNC2H1 gene | n2=en:cognitive dysfunction (in some patients) | rel=r_associated | relid=0 | w=10
  906. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive dysfunction (rare)
    n1=DYNC2H1 gene | n2=en:cognitive dysfunction (rare) | rel=r_associated | relid=0 | w=10
  907. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive function, variable
    n1=DYNC2H1 gene | n2=en:cognitive function, variable | rel=r_associated | relid=0 | w=10
  908. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment
    n1=DYNC2H1 gene | n2=en:cognitive impairment | rel=r_associated | relid=0 | w=10
  909. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment (1 family)
    n1=DYNC2H1 gene | n2=en:cognitive impairment (1 family) | rel=r_associated | relid=0 | w=10
  910. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment (1 patient)
    n1=DYNC2H1 gene | n2=en:cognitive impairment (1 patient) | rel=r_associated | relid=0 | w=10
  911. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment (3 patients)
    n1=DYNC2H1 gene | n2=en:cognitive impairment (3 patients) | rel=r_associated | relid=0 | w=10
  912. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment (cvs+)
    n1=DYNC2H1 gene | n2=en:cognitive impairment (cvs+) | rel=r_associated | relid=0 | w=10
  913. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment (in 1 of 3 patients)
    n1=DYNC2H1 gene | n2=en:cognitive impairment (in 1 of 3 patients) | rel=r_associated | relid=0 | w=10
  914. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment (in some patients)
    n1=DYNC2H1 gene | n2=en:cognitive impairment (in some patients) | rel=r_associated | relid=0 | w=10
  915. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment (rare)
    n1=DYNC2H1 gene | n2=en:cognitive impairment (rare) | rel=r_associated | relid=0 | w=10
  916. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment, gradual onset
    n1=DYNC2H1 gene | n2=en:cognitive impairment, gradual onset | rel=r_associated | relid=0 | w=10
  917. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment, mild (1 patient)
    n1=DYNC2H1 gene | n2=en:cognitive impairment, mild (1 patient) | rel=r_associated | relid=0 | w=10
  918. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment, mild (44%)
    n1=DYNC2H1 gene | n2=en:cognitive impairment, mild (44%) | rel=r_associated | relid=0 | w=10
  919. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment, mild (in 2 of 3 patients)
    n1=DYNC2H1 gene | n2=en:cognitive impairment, mild (in 2 of 3 patients) | rel=r_associated | relid=0 | w=10
  920. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment, mild to moderate
    n1=DYNC2H1 gene | n2=en:cognitive impairment, mild to moderate | rel=r_associated | relid=0 | w=10
  921. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive impairment, mild to severe
    n1=DYNC2H1 gene | n2=en:cognitive impairment, mild to severe | rel=r_associated | relid=0 | w=10
  922. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive regression
    n1=DYNC2H1 gene | n2=en:cognitive regression | rel=r_associated | relid=0 | w=10
  923. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cognitive regression, mild
    n1=DYNC2H1 gene | n2=en:cognitive regression, mild | rel=r_associated | relid=0 | w=10
  924. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cogwheel rigidities
    n1=DYNC2H1 gene | n2=en:cogwheel rigidities | rel=r_associated | relid=0 | w=10
  925. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cogwheel rigidity (in some patients)
    n1=DYNC2H1 gene | n2=en:cogwheel rigidity (in some patients) | rel=r_associated | relid=0 | w=10
  926. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:colonic pseudo-obstruction
    n1=DYNC2H1 gene | n2=en:colonic pseudo-obstruction | rel=r_associated | relid=0 | w=10
  927. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:colpocephaly
    n1=DYNC2H1 gene | n2=en:colpocephaly | rel=r_associated | relid=0 | w=10
  928. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:coma
    n1=DYNC2H1 gene | n2=en:coma | rel=r_associated | relid=0 | w=10
  929. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:coma (if untreated)
    n1=DYNC2H1 gene | n2=en:coma (if untreated) | rel=r_associated | relid=0 | w=10
  930. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:coma (in up to 33% of patients)
    n1=DYNC2H1 gene | n2=en:coma (in up to 33% of patients) | rel=r_associated | relid=0 | w=10
  931. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:coma (less common)
    n1=DYNC2H1 gene | n2=en:coma (less common) | rel=r_associated | relid=0 | w=10
  932. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:coma during episodes (in some patients)
    n1=DYNC2H1 gene | n2=en:coma during episodes (in some patients) | rel=r_associated | relid=0 | w=10
  933. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:coma may occur after force feeding of high protein diet
    n1=DYNC2H1 gene | n2=en:coma may occur after force feeding of high protein diet | rel=r_associated | relid=0 | w=10
  934. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:communicating hydrocephalus
    n1=DYNC2H1 gene | n2=en:communicating hydrocephalus | rel=r_associated | relid=0 | w=10
  935. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:communication defects
    n1=DYNC2H1 gene | n2=en:communication defects | rel=r_associated | relid=0 | w=10
  936. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complete or partial absence of the corpus callosum
    n1=DYNC2H1 gene | n2=en:complete or partial absence of the corpus callosum | rel=r_associated | relid=0 | w=10
  937. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complete or partial absence of the corpus callosum (wws)
    n1=DYNC2H1 gene | n2=en:complete or partial absence of the corpus callosum (wws) | rel=r_associated | relid=0 | w=10
  938. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complex motor behavior such as sleep walking
    n1=DYNC2H1 gene | n2=en:complex motor behavior such as sleep walking | rel=r_associated | relid=0 | w=10
  939. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complex partial seizure with impairment of consciousness
    n1=DYNC2H1 gene | n2=en:complex partial seizure with impairment of consciousness | rel=r_associated | relid=0 | w=10
  940. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complex partial seizures
    n1=DYNC2H1 gene | n2=en:complex partial seizures | rel=r_associated | relid=0 | w=10
  941. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complex partial seizures (in some patients)
    n1=DYNC2H1 gene | n2=en:complex partial seizures (in some patients) | rel=r_associated | relid=0 | w=10
  942. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complex partial seizures, often with secondary generalization, are the most common type
    n1=DYNC2H1 gene | n2=en:complex partial seizures, often with secondary generalization, are the most common type | rel=r_associated | relid=0 | w=10
  943. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complex regional pain syndrome i
    n1=DYNC2H1 gene | n2=en:complex regional pain syndrome i | rel=r_associated | relid=0 | w=10
  944. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complex regional pain syndrome i, unspecified
    n1=DYNC2H1 gene | n2=en:complex regional pain syndrome i, unspecified | rel=r_associated | relid=0 | w=10
  945. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:complex regional pain syndromes
    n1=DYNC2H1 gene | n2=en:complex regional pain syndromes | rel=r_associated | relid=0 | w=10
  946. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:compromised expressive language development, severe
    n1=DYNC2H1 gene | n2=en:compromised expressive language development, severe | rel=r_associated | relid=0 | w=10
  947. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:concentration impairment
    n1=DYNC2H1 gene | n2=en:concentration impairment | rel=r_associated | relid=0 | w=10
  948. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:confusion
    n1=DYNC2H1 gene | n2=en:confusion | rel=r_associated | relid=0 | w=10
  949. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:confusion (later-onset)
    n1=DYNC2H1 gene | n2=en:confusion (later-onset) | rel=r_associated | relid=0 | w=10
  950. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:confusion, paroxysmal
    n1=DYNC2H1 gene | n2=en:confusion, paroxysmal | rel=r_associated | relid=0 | w=10
  951. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:congenital absence of the vermis
    n1=DYNC2H1 gene | n2=en:congenital absence of the vermis | rel=r_associated | relid=0 | w=10
  952. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:congenital anomaly of brain
    n1=DYNC2H1 gene | n2=en:congenital anomaly of brain | rel=r_associated | relid=0 | w=10
  953. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:congenital central hypoventilation
    n1=DYNC2H1 gene | n2=en:congenital central hypoventilation | rel=r_associated | relid=0 | w=10
  954. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:congenital cerebellar hypoplasia
    n1=DYNC2H1 gene | n2=en:congenital cerebellar hypoplasia | rel=r_associated | relid=0 | w=10
  955. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:congenital hyperextension of limb
    n1=DYNC2H1 gene | n2=en:congenital hyperextension of limb | rel=r_associated | relid=0 | w=10
  956. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:congenital hypotonia, axial or generalized
    n1=DYNC2H1 gene | n2=en:congenital hypotonia, axial or generalized | rel=r_associated | relid=0 | w=10
  957. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:congenital hypotonia, mild
    n1=DYNC2H1 gene | n2=en:congenital hypotonia, mild | rel=r_associated | relid=0 | w=10
  958. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:congenital porencephaly
    n1=DYNC2H1 gene | n2=en:congenital porencephaly | rel=r_associated | relid=0 | w=10
  959. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:consciousness fluctuating
    n1=DYNC2H1 gene | n2=en:consciousness fluctuating | rel=r_associated | relid=0 | w=10
  960. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:constructional apraxia (in a subset of patients)
    n1=DYNC2H1 gene | n2=en:constructional apraxia (in a subset of patients) | rel=r_associated | relid=0 | w=10
  961. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:continuous spike-wave discharges during sleep
    n1=DYNC2H1 gene | n2=en:continuous spike-wave discharges during sleep | rel=r_associated | relid=0 | w=10
  962. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:continuous spike-waves during slow-wave sleep
    n1=DYNC2H1 gene | n2=en:continuous spike-waves during slow-wave sleep | rel=r_associated | relid=0 | w=10
  963. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:contractures (older children and adolescents)
    n1=DYNC2H1 gene | n2=en:contractures (older children and adolescents) | rel=r_associated | relid=0 | w=10
  964. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:contralateral hemiparesis, congenital
    n1=DYNC2H1 gene | n2=en:contralateral hemiparesis, congenital | rel=r_associated | relid=0 | w=10
  965. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:convulsions, febrile (in some patients)
    n1=DYNC2H1 gene | n2=en:convulsions, febrile (in some patients) | rel=r_associated | relid=0 | w=10
  966. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:convulsive seizures
    n1=DYNC2H1 gene | n2=en:convulsive seizures | rel=r_associated | relid=0 | w=10
  967. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corprolalia
    n1=DYNC2H1 gene | n2=en:corprolalia | rel=r_associated | relid=0 | w=10
  968. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corpus callosum abnormalities (in some patients)
    n1=DYNC2H1 gene | n2=en:corpus callosum abnormalities (in some patients) | rel=r_associated | relid=0 | w=10
  969. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corpus callosum agenesis
    n1=DYNC2H1 gene | n2=en:corpus callosum agenesis | rel=r_associated | relid=0 | w=10
  970. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corpus callosum lipoma
    n1=DYNC2H1 gene | n2=en:corpus callosum lipoma | rel=r_associated | relid=0 | w=10
  971. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corpus callosum, agenesis of (in some patients)
    n1=DYNC2H1 gene | n2=en:corpus callosum, agenesis of (in some patients) | rel=r_associated | relid=0 | w=10
  972. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corpus callosum, thin (rare)
    n1=DYNC2H1 gene | n2=en:corpus callosum, thin (rare) | rel=r_associated | relid=0 | w=10
  973. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical and brainstem neuronal loss
    n1=DYNC2H1 gene | n2=en:cortical and brainstem neuronal loss | rel=r_associated | relid=0 | w=10
  974. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical and subcortical atrophy (1 patient)
    n1=DYNC2H1 gene | n2=en:cortical and subcortical atrophy (1 patient) | rel=r_associated | relid=0 | w=10
  975. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical and subcortical hyperintensities
    n1=DYNC2H1 gene | n2=en:cortical and subcortical hyperintensities | rel=r_associated | relid=0 | w=10
  976. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical and subcortical neuronal loss in the frontal and temporal regions
    n1=DYNC2H1 gene | n2=en:cortical and subcortical neuronal loss in the frontal and temporal regions | rel=r_associated | relid=0 | w=10
  977. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical and subcortical regions involved
    n1=DYNC2H1 gene | n2=en:cortical and subcortical regions involved | rel=r_associated | relid=0 | w=10
  978. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical atrophy (43%)
    n1=DYNC2H1 gene | n2=en:cortical atrophy (43%) | rel=r_associated | relid=0 | w=10
  979. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical atrophy (frontal area)
    n1=DYNC2H1 gene | n2=en:cortical atrophy (frontal area) | rel=r_associated | relid=0 | w=10
  980. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical atrophy (in 2 siblings)
    n1=DYNC2H1 gene | n2=en:cortical atrophy (in 2 siblings) | rel=r_associated | relid=0 | w=10
  981. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical atrophy (in some patients)
    n1=DYNC2H1 gene | n2=en:cortical atrophy (in some patients) | rel=r_associated | relid=0 | w=10
  982. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical atrophy (rare)
    n1=DYNC2H1 gene | n2=en:cortical atrophy (rare) | rel=r_associated | relid=0 | w=10
  983. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical atrophy with loss of pyramidal neurons in the motor cortex
    n1=DYNC2H1 gene | n2=en:cortical atrophy with loss of pyramidal neurons in the motor cortex | rel=r_associated | relid=0 | w=10
  984. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical atrophy, progressive
    n1=DYNC2H1 gene | n2=en:cortical atrophy, progressive | rel=r_associated | relid=0 | w=10
  985. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical blindness (in 1 moroccan patient)
    n1=DYNC2H1 gene | n2=en:cortical blindness (in 1 moroccan patient) | rel=r_associated | relid=0 | w=10
  986. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical cytotoxic edema
    n1=DYNC2H1 gene | n2=en:cortical cytotoxic edema | rel=r_associated | relid=0 | w=10
  987. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical degeneration
    n1=DYNC2H1 gene | n2=en:cortical degeneration | rel=r_associated | relid=0 | w=10
  988. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical dysgenesis
    n1=DYNC2H1 gene | n2=en:cortical dysgenesis | rel=r_associated | relid=0 | w=10
  989. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical dysgenesis, complex
    n1=DYNC2H1 gene | n2=en:cortical dysgenesis, complex | rel=r_associated | relid=0 | w=10
  990. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical dysplasia
    n1=DYNC2H1 gene | n2=en:cortical dysplasia | rel=r_associated | relid=0 | w=10
  991. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical dysplasia (1 patient)
    n1=DYNC2H1 gene | n2=en:cortical dysplasia (1 patient) | rel=r_associated | relid=0 | w=10
  992. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical dysplasia (2 patients)
    n1=DYNC2H1 gene | n2=en:cortical dysplasia (2 patients) | rel=r_associated | relid=0 | w=10
  993. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical dysplasia, focal (1 patient)
    n1=DYNC2H1 gene | n2=en:cortical dysplasia, focal (1 patient) | rel=r_associated | relid=0 | w=10
  994. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical dysplasia, focal (in some patients)
    n1=DYNC2H1 gene | n2=en:cortical dysplasia, focal (in some patients) | rel=r_associated | relid=0 | w=10
  995. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical gyral simplification
    n1=DYNC2H1 gene | n2=en:cortical gyral simplification | rel=r_associated | relid=0 | w=10
  996. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical hypergyria (in some patients)
    n1=DYNC2H1 gene | n2=en:cortical hypergyria (in some patients) | rel=r_associated | relid=0 | w=10
  997. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical malformations
    n1=DYNC2H1 gene | n2=en:cortical malformations | rel=r_associated | relid=0 | w=10
  998. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical myoclonic tremors characterized by 8 to 10-hz discharges
    n1=DYNC2H1 gene | n2=en:cortical myoclonic tremors characterized by 8 to 10-hz discharges | rel=r_associated | relid=0 | w=10
  999. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical neuronal loss
    n1=DYNC2H1 gene | n2=en:cortical neuronal loss | rel=r_associated | relid=0 | w=10
  1000. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical origin of the tremor
    n1=DYNC2H1 gene | n2=en:cortical origin of the tremor | rel=r_associated | relid=0 | w=10
  1001. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical reflex myoclonus
    n1=DYNC2H1 gene | n2=en:cortical reflex myoclonus | rel=r_associated | relid=0 | w=10
  1002. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical simplification
    n1=DYNC2H1 gene | n2=en:cortical simplification | rel=r_associated | relid=0 | w=10
  1003. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical thinning
    n1=DYNC2H1 gene | n2=en:cortical thinning | rel=r_associated | relid=0 | w=10
  1004. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical tubers
    n1=DYNC2H1 gene | n2=en:cortical tubers | rel=r_associated | relid=0 | w=10
  1005. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cortical venous thromboses
    n1=DYNC2H1 gene | n2=en:cortical venous thromboses | rel=r_associated | relid=0 | w=10
  1006. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corticobasal degeneration (in some patients)
    n1=DYNC2H1 gene | n2=en:corticobasal degeneration (in some patients) | rel=r_associated | relid=0 | w=10
  1007. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corticospinal signs (87% of patients in 1 report)
    n1=DYNC2H1 gene | n2=en:corticospinal signs (87% of patients in 1 report) | rel=r_associated | relid=0 | w=10
  1008. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corticospinal tract atrophy
    n1=DYNC2H1 gene | n2=en:corticospinal tract atrophy | rel=r_associated | relid=0 | w=10
  1009. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corticospinal tract disease in lower limbs (in adulthood)
    n1=DYNC2H1 gene | n2=en:corticospinal tract disease in lower limbs (in adulthood) | rel=r_associated | relid=0 | w=10
  1010. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corticospinal tract hypoplasia
    n1=DYNC2H1 gene | n2=en:corticospinal tract hypoplasia | rel=r_associated | relid=0 | w=10
  1011. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:corticospinal tracts with decreased myelin staining
    n1=DYNC2H1 gene | n2=en:corticospinal tracts with decreased myelin staining | rel=r_associated | relid=0 | w=10
  1012. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cranial nerve anomalies
    n1=DYNC2H1 gene | n2=en:cranial nerve anomalies | rel=r_associated | relid=0 | w=10
  1013. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cranial nerve dysfunction
    n1=DYNC2H1 gene | n2=en:cranial nerve dysfunction | rel=r_associated | relid=0 | w=10
  1014. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cranial nerve palsies can arise with head and neck paragangliomas
    n1=DYNC2H1 gene | n2=en:cranial nerve palsies can arise with head and neck paragangliomas | rel=r_associated | relid=0 | w=10
  1015. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cranial nerve palsy
    n1=DYNC2H1 gene | n2=en:cranial nerve palsy | rel=r_associated | relid=0 | w=10
  1016. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cranial nerve palsy, intermittent, transient
    n1=DYNC2H1 gene | n2=en:cranial nerve palsy, intermittent, transient | rel=r_associated | relid=0 | w=10
  1017. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:crawling and standing not achieved
    n1=DYNC2H1 gene | n2=en:crawling and standing not achieved | rel=r_associated | relid=0 | w=10
  1018. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:crisponi syndrome
    n1=DYNC2H1 gene | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=10
  1019. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:crowding of the posterior fossa
    n1=DYNC2H1 gene | n2=en:crowding of the posterior fossa | rel=r_associated | relid=0 | w=10
  1020. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ct scan shows dense calcifications in the basal ganglia
    n1=DYNC2H1 gene | n2=en:ct scan shows dense calcifications in the basal ganglia | rel=r_associated | relid=0 | w=10
  1021. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cyst of septum pellucidum
    n1=DYNC2H1 gene | n2=en:cyst of septum pellucidum | rel=r_associated | relid=0 | w=10
  1022. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cyst of septum pellucidum (in some patients)
    n1=DYNC2H1 gene | n2=en:cyst of septum pellucidum (in some patients) | rel=r_associated | relid=0 | w=10
  1023. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cystic cavitation of the white matter
    n1=DYNC2H1 gene | n2=en:cystic cavitation of the white matter | rel=r_associated | relid=0 | w=10
  1024. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cystic degeneration of cerebral white matter with preserved cortex
    n1=DYNC2H1 gene | n2=en:cystic degeneration of cerebral white matter with preserved cortex | rel=r_associated | relid=0 | w=10
  1025. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cystic degeneration of the white matter
    n1=DYNC2H1 gene | n2=en:cystic degeneration of the white matter | rel=r_associated | relid=0 | w=10
  1026. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cystic destruction of brain tissue, including basal ganglia
    n1=DYNC2H1 gene | n2=en:cystic destruction of brain tissue, including basal ganglia | rel=r_associated | relid=0 | w=10
  1027. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cystic lesions consistent with leigh syndrome (256000)
    n1=DYNC2H1 gene | n2=en:cystic lesions consistent with leigh syndrome (256000) | rel=r_associated | relid=0 | w=10
  1028. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cystic lesions in the basal ganglia, brainstem, and cerebral hemispheres similar to leigh syndrome (256000)
    n1=DYNC2H1 gene | n2=en:cystic lesions in the basal ganglia, brainstem, and cerebral hemispheres similar to leigh syndrome (256000) | rel=r_associated | relid=0 | w=10
  1029. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cystic lysis of the deep white matter
    n1=DYNC2H1 gene | n2=en:cystic lysis of the deep white matter | rel=r_associated | relid=0 | w=10
  1030. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cysts tend to enlarge with age
    n1=DYNC2H1 gene | n2=en:cysts tend to enlarge with age | rel=r_associated | relid=0 | w=10
  1031. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:cytopathic effect
    n1=DYNC2H1 gene | n2=en:cytopathic effect | rel=r_associated | relid=0 | w=10
  1032. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dandy walker variant
    n1=DYNC2H1 gene | n2=en:dandy walker variant | rel=r_associated | relid=0 | w=10
  1033. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dandy-walker malformation
    n1=DYNC2H1 gene | n2=en:dandy-walker malformation | rel=r_associated | relid=0 | w=10
  1034. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dandy-walker malformation (1 patient)
    n1=DYNC2H1 gene | n2=en:dandy-walker malformation (1 patient) | rel=r_associated | relid=0 | w=10
  1035. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dandy-walker malformation (in 1 of 4 patients)
    n1=DYNC2H1 gene | n2=en:dandy-walker malformation (in 1 of 4 patients) | rel=r_associated | relid=0 | w=10
  1036. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dandy-walker malformation (in some patients)
    n1=DYNC2H1 gene | n2=en:dandy-walker malformation (in some patients) | rel=r_associated | relid=0 | w=10
  1037. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dandy-walker malformation (rare)
    n1=DYNC2H1 gene | n2=en:dandy-walker malformation (rare) | rel=r_associated | relid=0 | w=10
  1038. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dandy-walker malformation (variable)
    n1=DYNC2H1 gene | n2=en:dandy-walker malformation (variable) | rel=r_associated | relid=0 | w=10
  1039. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dandy-walker malformation (wws)
    n1=DYNC2H1 gene | n2=en:dandy-walker malformation (wws) | rel=r_associated | relid=0 | w=10
  1040. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deafness
    n1=DYNC2H1 gene | n2=en:deafness | rel=r_associated | relid=0 | w=10
  1041. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decerebrate or decorticate posturing late
    n1=DYNC2H1 gene | n2=en:decerebrate or decorticate posturing late | rel=r_associated | relid=0 | w=10
  1042. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decerebrate posturings
    n1=DYNC2H1 gene | n2=en:decerebrate posturings | rel=r_associated | relid=0 | w=10
  1043. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decorticate posture
    n1=DYNC2H1 gene | n2=en:decorticate posture | rel=r_associated | relid=0 | w=10
  1044. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decrease in abstract thinking
    n1=DYNC2H1 gene | n2=en:decrease in abstract thinking | rel=r_associated | relid=0 | w=10
  1045. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased active movements
    n1=DYNC2H1 gene | n2=en:decreased active movements | rel=r_associated | relid=0 | w=10
  1046. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased amount of myelin-specific lipids
    n1=DYNC2H1 gene | n2=en:decreased amount of myelin-specific lipids | rel=r_associated | relid=0 | w=10
  1047. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased amount of myelin-specific proteins
    n1=DYNC2H1 gene | n2=en:decreased amount of myelin-specific proteins | rel=r_associated | relid=0 | w=10
  1048. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased brain volume (female)
    n1=DYNC2H1 gene | n2=en:decreased brain volume (female) | rel=r_associated | relid=0 | w=10
  1049. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased brain weight
    n1=DYNC2H1 gene | n2=en:decreased brain weight | rel=r_associated | relid=0 | w=10
  1050. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased cerebellar folia
    n1=DYNC2H1 gene | n2=en:decreased cerebellar folia | rel=r_associated | relid=0 | w=10
  1051. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased cerebral volume, especially of the frontal lobes
    n1=DYNC2H1 gene | n2=en:decreased cerebral volume, especially of the frontal lobes | rel=r_associated | relid=0 | w=10
  1052. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased cognition (later-onset)
    n1=DYNC2H1 gene | n2=en:decreased cognition (later-onset) | rel=r_associated | relid=0 | w=10
  1053. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased core body temperature
    n1=DYNC2H1 gene | n2=en:decreased core body temperature | rel=r_associated | relid=0 | w=10
  1054. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased creatine signal seen on magnetic resonance spectroscopy
    n1=DYNC2H1 gene | n2=en:decreased creatine signal seen on magnetic resonance spectroscopy | rel=r_associated | relid=0 | w=10
  1055. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased csf volume in posterior fossa
    n1=DYNC2H1 gene | n2=en:decreased csf volume in posterior fossa | rel=r_associated | relid=0 | w=10
  1056. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased delineation of the basal ganglia (in some patients)
    n1=DYNC2H1 gene | n2=en:decreased delineation of the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=10
  1057. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased fine motor coordination
    n1=DYNC2H1 gene | n2=en:decreased fine motor coordination | rel=r_associated | relid=0 | w=10
  1058. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased iq
    n1=DYNC2H1 gene | n2=en:decreased iq | rel=r_associated | relid=0 | w=10
  1059. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased iq (1 patient)
    n1=DYNC2H1 gene | n2=en:decreased iq (1 patient) | rel=r_associated | relid=0 | w=10
  1060. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased iq (some patients)
    n1=DYNC2H1 gene | n2=en:decreased iq (some patients) | rel=r_associated | relid=0 | w=10
  1061. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased iron content in the substantia nigra
    n1=DYNC2H1 gene | n2=en:decreased iron content in the substantia nigra | rel=r_associated | relid=0 | w=10
  1062. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased mental processing speed
    n1=DYNC2H1 gene | n2=en:decreased mental processing speed | rel=r_associated | relid=0 | w=10
  1063. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased mitochondrial respiratory chain complex activity
    n1=DYNC2H1 gene | n2=en:decreased mitochondrial respiratory chain complex activity | rel=r_associated | relid=0 | w=10
  1064. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased motor nerve conduction velocity
    n1=DYNC2H1 gene | n2=en:decreased motor nerve conduction velocity | rel=r_associated | relid=0 | w=10
  1065. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased myelin
    n1=DYNC2H1 gene | n2=en:decreased myelin | rel=r_associated | relid=0 | w=10
  1066. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased myelination seen on mri
    n1=DYNC2H1 gene | n2=en:decreased myelination seen on mri | rel=r_associated | relid=0 | w=10
  1067. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased n-acetylaspartate
    n1=DYNC2H1 gene | n2=en:decreased n-acetylaspartate | rel=r_associated | relid=0 | w=10
  1068. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased need for sleep
    n1=DYNC2H1 gene | n2=en:decreased need for sleep | rel=r_associated | relid=0 | w=10
  1069. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased nonverbal iq
    n1=DYNC2H1 gene | n2=en:decreased nonverbal iq | rel=r_associated | relid=0 | w=10
  1070. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased numbers of astrocytes
    n1=DYNC2H1 gene | n2=en:decreased numbers of astrocytes | rel=r_associated | relid=0 | w=10
  1071. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased or absent gyri (in some patients)
    n1=DYNC2H1 gene | n2=en:decreased or absent gyri (in some patients) | rel=r_associated | relid=0 | w=10
  1072. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased or absent motor evoked potentials (mep), indicating dysfunction of the corticospinal tracts
    n1=DYNC2H1 gene | n2=en:decreased or absent motor evoked potentials (mep), indicating dysfunction of the corticospinal tracts | rel=r_associated | relid=0 | w=10
  1073. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased pain response
    n1=DYNC2H1 gene | n2=en:decreased pain response | rel=r_associated | relid=0 | w=10
  1074. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased pyramidal cells
    n1=DYNC2H1 gene | n2=en:decreased pyramidal cells | rel=r_associated | relid=0 | w=10
  1075. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased rapid automatized naming (ran) speed
    n1=DYNC2H1 gene | n2=en:decreased rapid automatized naming (ran) speed | rel=r_associated | relid=0 | w=10
  1076. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased reflexes (in some patients)
    n1=DYNC2H1 gene | n2=en:decreased reflexes (in some patients) | rel=r_associated | relid=0 | w=10
  1077. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased sleep latency
    n1=DYNC2H1 gene | n2=en:decreased sleep latency | rel=r_associated | relid=0 | w=10
  1078. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased somatosensory-evoked potentials
    n1=DYNC2H1 gene | n2=en:decreased somatosensory-evoked potentials | rel=r_associated | relid=0 | w=10
  1079. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased speech
    n1=DYNC2H1 gene | n2=en:decreased speech | rel=r_associated | relid=0 | w=10
  1080. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased spontaneous movements at birth
    n1=DYNC2H1 gene | n2=en:decreased spontaneous movements at birth | rel=r_associated | relid=0 | w=10
  1081. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased supratentorial volume
    n1=DYNC2H1 gene | n2=en:decreased supratentorial volume | rel=r_associated | relid=0 | w=10
  1082. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased tendon reflex
    n1=DYNC2H1 gene | n2=en:decreased tendon reflex | rel=r_associated | relid=0 | w=10
  1083. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased upper extremity reflexes
    n1=DYNC2H1 gene | n2=en:decreased upper extremity reflexes | rel=r_associated | relid=0 | w=10
  1084. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased vibration sense, suggesting posterior column involvement
    n1=DYNC2H1 gene | n2=en:decreased vibration sense, suggesting posterior column involvement | rel=r_associated | relid=0 | w=10
  1085. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased vibratory sense
    n1=DYNC2H1 gene | n2=en:decreased vibratory sense | rel=r_associated | relid=0 | w=10
  1086. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased volume of the cerebral white matter
    n1=DYNC2H1 gene | n2=en:decreased volume of the cerebral white matter | rel=r_associated | relid=0 | w=10
  1087. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased volume of the posterior cranial fossa with normal hindbrain volume
    n1=DYNC2H1 gene | n2=en:decreased volume of the posterior cranial fossa with normal hindbrain volume | rel=r_associated | relid=0 | w=10
  1088. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased white matter
    n1=DYNC2H1 gene | n2=en:decreased white matter | rel=r_associated | relid=0 | w=10
  1089. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreased white matter volume
    n1=DYNC2H1 gene | n2=en:decreased white matter volume | rel=r_associated | relid=0 | w=10
  1090. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:decreasing responsiveness
    n1=DYNC2H1 gene | n2=en:decreasing responsiveness | rel=r_associated | relid=0 | w=10
  1091. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deep hypointensities (mri, t2) suggestive of past microbleeds
    n1=DYNC2H1 gene | n2=en:deep hypointensities (mri, t2) suggestive of past microbleeds | rel=r_associated | relid=0 | w=10
  1092. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deep interpeduncular fossa
    n1=DYNC2H1 gene | n2=en:deep interpeduncular fossa | rel=r_associated | relid=0 | w=10
  1093. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deep posterior interpeduncular fossa
    n1=DYNC2H1 gene | n2=en:deep posterior interpeduncular fossa | rel=r_associated | relid=0 | w=10
  1094. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deep white matter changes
    n1=DYNC2H1 gene | n2=en:deep white matter changes | rel=r_associated | relid=0 | w=10
  1095. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deep white matter hypodensities
    n1=DYNC2H1 gene | n2=en:deep white matter hypodensities | rel=r_associated | relid=0 | w=10
  1096. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deep white matter lesions, particularly affecting the frontal and parietal lobes
    n1=DYNC2H1 gene | n2=en:deep white matter lesions, particularly affecting the frontal and parietal lobes | rel=r_associated | relid=0 | w=10
  1097. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:defect in axonal guidance
    n1=DYNC2H1 gene | n2=en:defect in axonal guidance | rel=r_associated | relid=0 | w=10
  1098. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:defect in morphosyntactic rules
    n1=DYNC2H1 gene | n2=en:defect in morphosyntactic rules | rel=r_associated | relid=0 | w=10
  1099. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:defective myelination of the deep white matter
    n1=DYNC2H1 gene | n2=en:defective myelination of the deep white matter | rel=r_associated | relid=0 | w=10
  1100. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:defective opercularization
    n1=DYNC2H1 gene | n2=en:defective opercularization | rel=r_associated | relid=0 | w=10
  1101. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:defects in auditory cue processing
    n1=DYNC2H1 gene | n2=en:defects in auditory cue processing | rel=r_associated | relid=0 | w=10
  1102. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:defects in fine motor skills
    n1=DYNC2H1 gene | n2=en:defects in fine motor skills | rel=r_associated | relid=0 | w=10
  1103. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:defects in visual cue processing
    n1=DYNC2H1 gene | n2=en:defects in visual cue processing | rel=r_associated | relid=0 | w=10
  1104. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deficient myelination
    n1=DYNC2H1 gene | n2=en:deficient myelination | rel=r_associated | relid=0 | w=10
  1105. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deficit in basic reading
    n1=DYNC2H1 gene | n2=en:deficit in basic reading | rel=r_associated | relid=0 | w=10
  1106. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deficit in expressive language
    n1=DYNC2H1 gene | n2=en:deficit in expressive language | rel=r_associated | relid=0 | w=10
  1107. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deficit in nonword repetition (nwr)
    n1=DYNC2H1 gene | n2=en:deficit in nonword repetition (nwr) | rel=r_associated | relid=0 | w=10
  1108. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deficit in phonologic short-term memory
    n1=DYNC2H1 gene | n2=en:deficit in phonologic short-term memory | rel=r_associated | relid=0 | w=10
  1109. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deficit in reading comprehension
    n1=DYNC2H1 gene | n2=en:deficit in reading comprehension | rel=r_associated | relid=0 | w=10
  1110. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deficit in spelling
    n1=DYNC2H1 gene | n2=en:deficit in spelling | rel=r_associated | relid=0 | w=10
  1111. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deficits in abstraction
    n1=DYNC2H1 gene | n2=en:deficits in abstraction | rel=r_associated | relid=0 | w=10
  1112. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deficits in language expression
    n1=DYNC2H1 gene | n2=en:deficits in language expression | rel=r_associated | relid=0 | w=10
  1113. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deformed temporal lobes
    n1=DYNC2H1 gene | n2=en:deformed temporal lobes | rel=r_associated | relid=0 | w=10
  1114. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:degeneration of anterior horn cells
    n1=DYNC2H1 gene | n2=en:degeneration of anterior horn cells | rel=r_associated | relid=0 | w=10
  1115. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:degeneration of purkinje cells in the cerebellum
    n1=DYNC2H1 gene | n2=en:degeneration of purkinje cells in the cerebellum | rel=r_associated | relid=0 | w=10
  1116. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:degeneration of the dentatorubral and pallidoluysian systems
    n1=DYNC2H1 gene | n2=en:degeneration of the dentatorubral and pallidoluysian systems | rel=r_associated | relid=0 | w=10
  1117. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:degeneration of the lateral corticospinal tracts
    n1=DYNC2H1 gene | n2=en:degeneration of the lateral corticospinal tracts | rel=r_associated | relid=0 | w=10
  1118. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deja vu feeling
    n1=DYNC2H1 gene | n2=en:deja vu feeling | rel=r_associated | relid=0 | w=10
  1119. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delay in gross motor development due to weakness
    n1=DYNC2H1 gene | n2=en:delay in gross motor development due to weakness | rel=r_associated | relid=0 | w=10
  1120. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delay of gross motor function
    n1=DYNC2H1 gene | n2=en:delay of gross motor function | rel=r_associated | relid=0 | w=10
  1121. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed adaptive hand use
    n1=DYNC2H1 gene | n2=en:delayed adaptive hand use | rel=r_associated | relid=0 | w=10
  1122. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed ambulation
    n1=DYNC2H1 gene | n2=en:delayed ambulation | rel=r_associated | relid=0 | w=10
  1123. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed brainstem development (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed brainstem development (in some patients) | rel=r_associated | relid=0 | w=10
  1124. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed cerebellar development (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed cerebellar development (in some patients) | rel=r_associated | relid=0 | w=10
  1125. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed cerebral myelination
    n1=DYNC2H1 gene | n2=en:delayed cerebral myelination | rel=r_associated | relid=0 | w=10
  1126. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed cognitive development (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed cognitive development (in some patients) | rel=r_associated | relid=0 | w=10
  1127. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed cognitive development, mild (reported in 1 family)
    n1=DYNC2H1 gene | n2=en:delayed cognitive development, mild (reported in 1 family) | rel=r_associated | relid=0 | w=10
  1128. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed cognitive development/learning disabilities (93%)
    n1=DYNC2H1 gene | n2=en:delayed cognitive development/learning disabilities (93%) | rel=r_associated | relid=0 | w=10
  1129. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development (1 family)
    n1=DYNC2H1 gene | n2=en:delayed development (1 family) | rel=r_associated | relid=0 | w=10
  1130. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development (about 25%)
    n1=DYNC2H1 gene | n2=en:delayed development (about 25%) | rel=r_associated | relid=0 | w=10
  1131. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed development (in some patients) | rel=r_associated | relid=0 | w=10
  1132. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development (in some)
    n1=DYNC2H1 gene | n2=en:delayed development (in some) | rel=r_associated | relid=0 | w=10
  1133. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development if untreated
    n1=DYNC2H1 gene | n2=en:delayed development if untreated | rel=r_associated | relid=0 | w=10
  1134. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development in early childhood (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed development in early childhood (in some patients) | rel=r_associated | relid=0 | w=10
  1135. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development may occur
    n1=DYNC2H1 gene | n2=en:delayed development may occur | rel=r_associated | relid=0 | w=10
  1136. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development, after 8-15 months
    n1=DYNC2H1 gene | n2=en:delayed development, after 8-15 months | rel=r_associated | relid=0 | w=10
  1137. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development, ranging from mild to severe
    n1=DYNC2H1 gene | n2=en:delayed development, ranging from mild to severe | rel=r_associated | relid=0 | w=10
  1138. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development, severe
    n1=DYNC2H1 gene | n2=en:delayed development, severe | rel=r_associated | relid=0 | w=10
  1139. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development, variable (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed development, variable (in some patients) | rel=r_associated | relid=0 | w=10
  1140. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed development, variable severity, from birth in some patients
    n1=DYNC2H1 gene | n2=en:delayed development, variable severity, from birth in some patients | rel=r_associated | relid=0 | w=10
  1141. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed developmental milestones
    n1=DYNC2H1 gene | n2=en:delayed developmental milestones | rel=r_associated | relid=0 | w=10
  1142. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed gross motor development (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed gross motor development (in some patients) | rel=r_associated | relid=0 | w=10
  1143. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed gyration
    n1=DYNC2H1 gene | n2=en:delayed gyration | rel=r_associated | relid=0 | w=10
  1144. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed independent walking
    n1=DYNC2H1 gene | n2=en:delayed independent walking | rel=r_associated | relid=0 | w=10
  1145. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed intellectual development
    n1=DYNC2H1 gene | n2=en:delayed intellectual development | rel=r_associated | relid=0 | w=10
  1146. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed motor and speech development, mild (1 family)
    n1=DYNC2H1 gene | n2=en:delayed motor and speech development, mild (1 family) | rel=r_associated | relid=0 | w=10
  1147. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed motor development (1 patient)
    n1=DYNC2H1 gene | n2=en:delayed motor development (1 patient) | rel=r_associated | relid=0 | w=10
  1148. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed motor development (secondary to skeletal abnormalities)
    n1=DYNC2H1 gene | n2=en:delayed motor development (secondary to skeletal abnormalities) | rel=r_associated | relid=0 | w=10
  1149. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed motor development due to muscle weakness
    n1=DYNC2H1 gene | n2=en:delayed motor development due to muscle weakness | rel=r_associated | relid=0 | w=10
  1150. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed motor development, mild, transient
    n1=DYNC2H1 gene | n2=en:delayed motor development, mild, transient | rel=r_associated | relid=0 | w=10
  1151. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed motor development, severe
    n1=DYNC2H1 gene | n2=en:delayed motor development, severe | rel=r_associated | relid=0 | w=10
  1152. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed motor milestones due to muscle weakness
    n1=DYNC2H1 gene | n2=en:delayed motor milestones due to muscle weakness | rel=r_associated | relid=0 | w=10
  1153. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed myelination
    n1=DYNC2H1 gene | n2=en:delayed myelination | rel=r_associated | relid=0 | w=10
  1154. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed myelination (1 patient)
    n1=DYNC2H1 gene | n2=en:delayed myelination (1 patient) | rel=r_associated | relid=0 | w=10
  1155. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed myelination (1/4 patients)
    n1=DYNC2H1 gene | n2=en:delayed myelination (1/4 patients) | rel=r_associated | relid=0 | w=10
  1156. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed myelination (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed myelination (in some patients) | rel=r_associated | relid=0 | w=10
  1157. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed myelination (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:delayed myelination (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  1158. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed myelination on brain mri (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:delayed myelination on brain mri (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  1159. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed myelination seen on mri
    n1=DYNC2H1 gene | n2=en:delayed myelination seen on mri | rel=r_associated | relid=0 | w=10
  1160. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed myelination, mild
    n1=DYNC2H1 gene | n2=en:delayed myelination, mild | rel=r_associated | relid=0 | w=10
  1161. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed myelinization (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed myelinization (in some patients) | rel=r_associated | relid=0 | w=10
  1162. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed onset of phrase speech (> 36 months)
    n1=DYNC2H1 gene | n2=en:delayed onset of phrase speech (> 36 months) | rel=r_associated | relid=0 | w=10
  1163. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed opercularization
    n1=DYNC2H1 gene | n2=en:delayed opercularization | rel=r_associated | relid=0 | w=10
  1164. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed or absent independent walking
    n1=DYNC2H1 gene | n2=en:delayed or absent independent walking | rel=r_associated | relid=0 | w=10
  1165. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development (1 patient)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development (1 patient) | rel=r_associated | relid=0 | w=10
  1166. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development (in 1 family)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development (in 1 family) | rel=r_associated | relid=0 | w=10
  1167. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development (in most patients)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development (in most patients) | rel=r_associated | relid=0 | w=10
  1168. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development (in severe cases)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development (in severe cases) | rel=r_associated | relid=0 | w=10
  1169. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development (in some patients) | rel=r_associated | relid=0 | w=10
  1170. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development (in some)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development (in some) | rel=r_associated | relid=0 | w=10
  1171. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development (mild to severe)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development (mild to severe) | rel=r_associated | relid=0 | w=10
  1172. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development (stops at development levels of 1-2 years)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development (stops at development levels of 1-2 years) | rel=r_associated | relid=0 | w=10
  1173. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development after onset of seizures
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development after onset of seizures | rel=r_associated | relid=0 | w=10
  1174. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, mild
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, mild | rel=r_associated | relid=0 | w=10
  1175. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, mild (in 3 of 5 patients)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, mild (in 3 of 5 patients) | rel=r_associated | relid=0 | w=10
  1176. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, mild (in some patients) | rel=r_associated | relid=0 | w=10
  1177. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, moderate to severe
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, moderate to severe | rel=r_associated | relid=0 | w=10
  1178. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, profound
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, profound | rel=r_associated | relid=0 | w=10
  1179. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, profound (1 patient)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, profound (1 patient) | rel=r_associated | relid=0 | w=10
  1180. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, profound (patient a)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, profound (patient a) | rel=r_associated | relid=0 | w=10
  1181. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, severe
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, severe | rel=r_associated | relid=0 | w=10
  1182. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, severe (> 90%)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, severe (> 90%) | rel=r_associated | relid=0 | w=10
  1183. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, severe (in 2 of 6 patients)
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, severe (in 2 of 6 patients) | rel=r_associated | relid=0 | w=10
  1184. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, severe to profound
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, severe to profound | rel=r_associated | relid=0 | w=10
  1185. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed psychomotor development, variable
    n1=DYNC2H1 gene | n2=en:delayed psychomotor development, variable | rel=r_associated | relid=0 | w=10
  1186. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed speech and language development
    n1=DYNC2H1 gene | n2=en:delayed speech and language development | rel=r_associated | relid=0 | w=10
  1187. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed speech development, severe
    n1=DYNC2H1 gene | n2=en:delayed speech development, severe | rel=r_associated | relid=0 | w=10
  1188. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed walking (1 family)
    n1=DYNC2H1 gene | n2=en:delayed walking (1 family) | rel=r_associated | relid=0 | w=10
  1189. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed walking (less common)
    n1=DYNC2H1 gene | n2=en:delayed walking (less common) | rel=r_associated | relid=0 | w=10
  1190. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed walking (rare)
    n1=DYNC2H1 gene | n2=en:delayed walking (rare) | rel=r_associated | relid=0 | w=10
  1191. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed walking and running in early childhood
    n1=DYNC2H1 gene | n2=en:delayed walking and running in early childhood | rel=r_associated | relid=0 | w=10
  1192. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delayed walking, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:delayed walking, mild (in some patients) | rel=r_associated | relid=0 | w=10
  1193. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delirium (later-onset)
    n1=DYNC2H1 gene | n2=en:delirium (later-onset) | rel=r_associated | relid=0 | w=10
  1194. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:delusion
    n1=DYNC2H1 gene | n2=en:delusion | rel=r_associated | relid=0 | w=10
  1195. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia
    n1=DYNC2H1 gene | n2=en:dementia | rel=r_associated | relid=0 | w=10
  1196. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia (<20%)
    n1=DYNC2H1 gene | n2=en:dementia (<20%) | rel=r_associated | relid=0 | w=10
  1197. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia (1 family)
    n1=DYNC2H1 gene | n2=en:dementia (1 family) | rel=r_associated | relid=0 | w=10
  1198. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia (5%)
    n1=DYNC2H1 gene | n2=en:dementia (5%) | rel=r_associated | relid=0 | w=10
  1199. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia (in some patients)
    n1=DYNC2H1 gene | n2=en:dementia (in some patients) | rel=r_associated | relid=0 | w=10
  1200. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia (later-onset)
    n1=DYNC2H1 gene | n2=en:dementia (later-onset) | rel=r_associated | relid=0 | w=10
  1201. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia (onset in fifth decade)
    n1=DYNC2H1 gene | n2=en:dementia (onset in fifth decade) | rel=r_associated | relid=0 | w=10
  1202. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia (subtype 3a)
    n1=DYNC2H1 gene | n2=en:dementia (subtype 3a) | rel=r_associated | relid=0 | w=10
  1203. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia in a subset of patients
    n1=DYNC2H1 gene | n2=en:dementia in a subset of patients | rel=r_associated | relid=0 | w=10
  1204. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia may occur
    n1=DYNC2H1 gene | n2=en:dementia may occur | rel=r_associated | relid=0 | w=10
  1205. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia of frontal lobe type
    n1=DYNC2H1 gene | n2=en:dementia of frontal lobe type | rel=r_associated | relid=0 | w=10
  1206. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia, presenile, progressive, beginning around age 30 years
    n1=DYNC2H1 gene | n2=en:dementia, presenile, progressive, beginning around age 30 years | rel=r_associated | relid=0 | w=10
  1207. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia, progressive (more common in males)
    n1=DYNC2H1 gene | n2=en:dementia, progressive (more common in males) | rel=r_associated | relid=0 | w=10
  1208. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia, progressive, with onset of disease
    n1=DYNC2H1 gene | n2=en:dementia, progressive, with onset of disease | rel=r_associated | relid=0 | w=10
  1209. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dementia, rapidly progressive
    n1=DYNC2H1 gene | n2=en:dementia, rapidly progressive | rel=r_associated | relid=0 | w=10
  1210. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:demyelination
    n1=DYNC2H1 gene | n2=en:demyelination | rel=r_associated | relid=0 | w=10
  1211. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:demyelination of the posterior and lateral columns of the spinal cord
    n1=DYNC2H1 gene | n2=en:demyelination of the posterior and lateral columns of the spinal cord | rel=r_associated | relid=0 | w=10
  1212. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:demyelination with white matter disease in internal capsule, external capsule, genu of corpus callosum, subcortical white matter, and posterior fossa
    n1=DYNC2H1 gene | 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=10
  1213. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:demyelination, symmetric
    n1=DYNC2H1 gene | n2=en:demyelination, symmetric | rel=r_associated | relid=0 | w=10
  1214. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:demyelinization
    n1=DYNC2H1 gene | n2=en:demyelinization | rel=r_associated | relid=0 | w=10
  1215. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:denervation seen on emg
    n1=DYNC2H1 gene | n2=en:denervation seen on emg | rel=r_associated | relid=0 | w=10
  1216. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dense calcifications in the cerebellar dentate nucleus
    n1=DYNC2H1 gene | n2=en:dense calcifications in the cerebellar dentate nucleus | rel=r_associated | relid=0 | w=10
  1217. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:depression
    n1=DYNC2H1 gene | n2=en:depression | rel=r_associated | relid=0 | w=10
  1218. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dermoid cyst
    n1=DYNC2H1 gene | n2=en:dermoid cyst | rel=r_associated | relid=0 | w=10
  1219. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:deterioration of motor development
    n1=DYNC2H1 gene | n2=en:deterioration of motor development | rel=r_associated | relid=0 | w=10
  1220. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:development varies from normal to retarded
    n1=DYNC2H1 gene | n2=en:development varies from normal to retarded | rel=r_associated | relid=0 | w=10
  1221. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental arrest, 2nd year of life
    n1=DYNC2H1 gene | n2=en:developmental arrest, 2nd year of life | rel=r_associated | relid=0 | w=10
  1222. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay
    n1=DYNC2H1 gene | n2=en:developmental delay | rel=r_associated | relid=0 | w=10
  1223. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (1 family)
    n1=DYNC2H1 gene | n2=en:developmental delay (1 family) | rel=r_associated | relid=0 | w=10
  1224. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (1 patient)
    n1=DYNC2H1 gene | n2=en:developmental delay (1 patient) | rel=r_associated | relid=0 | w=10
  1225. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (100%)
    n1=DYNC2H1 gene | n2=en:developmental delay (100%) | rel=r_associated | relid=0 | w=10
  1226. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (20%)
    n1=DYNC2H1 gene | n2=en:developmental delay (20%) | rel=r_associated | relid=0 | w=10
  1227. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (apparent after the first year of life)
    n1=DYNC2H1 gene | n2=en:developmental delay (apparent after the first year of life) | rel=r_associated | relid=0 | w=10
  1228. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (female)
    n1=DYNC2H1 gene | n2=en:developmental delay (female) | rel=r_associated | relid=0 | w=10
  1229. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (homozygote)
    n1=DYNC2H1 gene | n2=en:developmental delay (homozygote) | rel=r_associated | relid=0 | w=10
  1230. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (in most patients)
    n1=DYNC2H1 gene | n2=en:developmental delay (in most patients) | rel=r_associated | relid=0 | w=10
  1231. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (in some patients who survive infancy)
    n1=DYNC2H1 gene | n2=en:developmental delay (in some patients who survive infancy) | rel=r_associated | relid=0 | w=10
  1232. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (in some patients)
    n1=DYNC2H1 gene | n2=en:developmental delay (in some patients) | rel=r_associated | relid=0 | w=10
  1233. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (in some)
    n1=DYNC2H1 gene | n2=en:developmental delay (in some) | rel=r_associated | relid=0 | w=10
  1234. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (microdeletion patients only)
    n1=DYNC2H1 gene | n2=en:developmental delay (microdeletion patients only) | rel=r_associated | relid=0 | w=10
  1235. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (mild-severe)
    n1=DYNC2H1 gene | n2=en:developmental delay (mild-severe) | rel=r_associated | relid=0 | w=10
  1236. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (rare)
    n1=DYNC2H1 gene | n2=en:developmental delay (rare) | rel=r_associated | relid=0 | w=10
  1237. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (seen in recessive form)
    n1=DYNC2H1 gene | n2=en:developmental delay (seen in recessive form) | rel=r_associated | relid=0 | w=10
  1238. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (type ii)
    n1=DYNC2H1 gene | n2=en:developmental delay (type ii) | rel=r_associated | relid=0 | w=10
  1239. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay (uncommon)
    n1=DYNC2H1 gene | n2=en:developmental delay (uncommon) | rel=r_associated | relid=0 | w=10
  1240. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay evident by 12-24 months of age
    n1=DYNC2H1 gene | n2=en:developmental delay evident by 12-24 months of age | rel=r_associated | relid=0 | w=10
  1241. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay if undiagnosed or untreated
    n1=DYNC2H1 gene | n2=en:developmental delay if undiagnosed or untreated | rel=r_associated | relid=0 | w=10
  1242. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay or regression
    n1=DYNC2H1 gene | n2=en:developmental delay or regression | rel=r_associated | relid=0 | w=10
  1243. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, mild
    n1=DYNC2H1 gene | n2=en:developmental delay, mild | rel=r_associated | relid=0 | w=10
  1244. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:developmental delay, mild (in some patients) | rel=r_associated | relid=0 | w=10
  1245. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, mild (in some)
    n1=DYNC2H1 gene | n2=en:developmental delay, mild (in some) | rel=r_associated | relid=0 | w=10
  1246. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, mild to moderate
    n1=DYNC2H1 gene | n2=en:developmental delay, mild to moderate | rel=r_associated | relid=0 | w=10
  1247. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, moderate (in some patients)
    n1=DYNC2H1 gene | n2=en:developmental delay, moderate (in some patients) | rel=r_associated | relid=0 | w=10
  1248. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, primarily motor, resolves in childhood
    n1=DYNC2H1 gene | n2=en:developmental delay, primarily motor, resolves in childhood | rel=r_associated | relid=0 | w=10
  1249. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, profound
    n1=DYNC2H1 gene | n2=en:developmental delay, profound | rel=r_associated | relid=0 | w=10
  1250. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, progressive
    n1=DYNC2H1 gene | n2=en:developmental delay, progressive | rel=r_associated | relid=0 | w=10
  1251. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, severe
    n1=DYNC2H1 gene | n2=en:developmental delay, severe | rel=r_associated | relid=0 | w=10
  1252. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, severe (2p21del)
    n1=DYNC2H1 gene | n2=en:developmental delay, severe (2p21del) | rel=r_associated | relid=0 | w=10
  1253. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, significant
    n1=DYNC2H1 gene | n2=en:developmental delay, significant | rel=r_associated | relid=0 | w=10
  1254. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, variable
    n1=DYNC2H1 gene | n2=en:developmental delay, variable | rel=r_associated | relid=0 | w=10
  1255. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental delay, variable severity
    n1=DYNC2H1 gene | n2=en:developmental delay, variable severity | rel=r_associated | relid=0 | w=10
  1256. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression
    n1=DYNC2H1 gene | n2=en:developmental regression | rel=r_associated | relid=0 | w=10
  1257. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression (in some patients)
    n1=DYNC2H1 gene | n2=en:developmental regression (in some patients) | rel=r_associated | relid=0 | w=10
  1258. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression after age 2 years
    n1=DYNC2H1 gene | n2=en:developmental regression after age 2 years | rel=r_associated | relid=0 | w=10
  1259. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression after onset of seizures
    n1=DYNC2H1 gene | n2=en:developmental regression after onset of seizures | rel=r_associated | relid=0 | w=10
  1260. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression after the first year
    n1=DYNC2H1 gene | n2=en:developmental regression after the first year | rel=r_associated | relid=0 | w=10
  1261. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression before age 6 months
    n1=DYNC2H1 gene | n2=en:developmental regression before age 6 months | rel=r_associated | relid=0 | w=10
  1262. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression in about 50% of patients
    n1=DYNC2H1 gene | n2=en:developmental regression in about 50% of patients | rel=r_associated | relid=0 | w=10
  1263. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression in affected children
    n1=DYNC2H1 gene | n2=en:developmental regression in affected children | rel=r_associated | relid=0 | w=10
  1264. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression, after age 2 years (some)
    n1=DYNC2H1 gene | n2=en:developmental regression, after age 2 years (some) | rel=r_associated | relid=0 | w=10
  1265. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental regression, severe
    n1=DYNC2H1 gene | n2=en:developmental regression, severe | rel=r_associated | relid=0 | w=10
  1266. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental retardation (in some patients)
    n1=DYNC2H1 gene | n2=en:developmental retardation (in some patients) | rel=r_associated | relid=0 | w=10
  1267. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental retardation, profound
    n1=DYNC2H1 gene | n2=en:developmental retardation, profound | rel=r_associated | relid=0 | w=10
  1268. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental retardation, severe
    n1=DYNC2H1 gene | n2=en:developmental retardation, severe | rel=r_associated | relid=0 | w=10
  1269. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental stagnation
    n1=DYNC2H1 gene | n2=en:developmental stagnation | rel=r_associated | relid=0 | w=10
  1270. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:developmental stagnation at onset of seizures
    n1=DYNC2H1 gene | n2=en:developmental stagnation at onset of seizures | rel=r_associated | relid=0 | w=10
  1271. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diabetic autonomic neuropathy
    n1=DYNC2H1 gene | n2=en:diabetic autonomic neuropathy | rel=r_associated | relid=0 | w=10
  1272. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulties in fine bimanual activities
    n1=DYNC2H1 gene | n2=en:difficulties in fine bimanual activities | rel=r_associated | relid=0 | w=10
  1273. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulties in fine movement of the hands
    n1=DYNC2H1 gene | n2=en:difficulties in fine movement of the hands | rel=r_associated | relid=0 | w=10
  1274. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulties with equilibrium
    n1=DYNC2H1 gene | n2=en:difficulties with equilibrium | rel=r_associated | relid=0 | w=10
  1275. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulties with fine motor skills and coordination
    n1=DYNC2H1 gene | n2=en:difficulties with fine motor skills and coordination | rel=r_associated | relid=0 | w=10
  1276. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty in phonologic coding
    n1=DYNC2H1 gene | n2=en:difficulty in phonologic coding | rel=r_associated | relid=0 | w=10
  1277. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty in spelling
    n1=DYNC2H1 gene | n2=en:difficulty in spelling | rel=r_associated | relid=0 | w=10
  1278. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty reading
    n1=DYNC2H1 gene | n2=en:difficulty reading | rel=r_associated | relid=0 | w=10
  1279. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty running
    n1=DYNC2H1 gene | n2=en:difficulty running | rel=r_associated | relid=0 | w=10
  1280. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty running and climbing stairs
    n1=DYNC2H1 gene | n2=en:difficulty running and climbing stairs | rel=r_associated | relid=0 | w=10
  1281. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty sleeping
    n1=DYNC2H1 gene | n2=en:difficulty sleeping | rel=r_associated | relid=0 | w=10
  1282. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty speaking during seizures
    n1=DYNC2H1 gene | n2=en:difficulty speaking during seizures | rel=r_associated | relid=0 | w=10
  1283. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty standing
    n1=DYNC2H1 gene | n2=en:difficulty standing | rel=r_associated | relid=0 | w=10
  1284. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty standing alone
    n1=DYNC2H1 gene | n2=en:difficulty standing alone | rel=r_associated | relid=0 | w=10
  1285. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty walking and climbing stairs
    n1=DYNC2H1 gene | n2=en:difficulty walking and climbing stairs | rel=r_associated | relid=0 | w=10
  1286. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty walking in childhood
    n1=DYNC2H1 gene | n2=en:difficulty walking in childhood | rel=r_associated | relid=0 | w=10
  1287. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty walking, running
    n1=DYNC2H1 gene | n2=en:difficulty walking, running | rel=r_associated | relid=0 | w=10
  1288. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty with writing and drawing
    n1=DYNC2H1 gene | n2=en:difficulty with writing and drawing | rel=r_associated | relid=0 | w=10
  1289. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:difficulty writing
    n1=DYNC2H1 gene | n2=en:difficulty writing | rel=r_associated | relid=0 | w=10
  1290. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem
    n1=DYNC2H1 gene | n2=en:diffuse atrophy of cerebral hemispheres, corpus callosum, and brainstem | rel=r_associated | relid=0 | w=10
  1291. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse axonal swelling
    n1=DYNC2H1 gene | n2=en:diffuse axonal swelling | rel=r_associated | relid=0 | w=10
  1292. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse brain and spinal cord atrophy on brain ct/mri
    n1=DYNC2H1 gene | n2=en:diffuse brain and spinal cord atrophy on brain ct/mri | rel=r_associated | relid=0 | w=10
  1293. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse brain swelling occurs during coma
    n1=DYNC2H1 gene | n2=en:diffuse brain swelling occurs during coma | rel=r_associated | relid=0 | w=10
  1294. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse cerebellar atrophy
    n1=DYNC2H1 gene | n2=en:diffuse cerebellar atrophy | rel=r_associated | relid=0 | w=10
  1295. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse cerebral atrophy on ct and mri
    n1=DYNC2H1 gene | n2=en:diffuse cerebral atrophy on ct and mri | rel=r_associated | relid=0 | w=10
  1296. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse cerebral atrophy seen on mri
    n1=DYNC2H1 gene | n2=en:diffuse cerebral atrophy seen on mri | rel=r_associated | relid=0 | w=10
  1297. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse cerebral gliosis
    n1=DYNC2H1 gene | n2=en:diffuse cerebral gliosis | rel=r_associated | relid=0 | w=10
  1298. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes)
    n1=DYNC2H1 gene | n2=en:diffuse demyelination (increased signal intensity in t2-weighted images, especially frontal lobes) | rel=r_associated | relid=0 | w=10
  1299. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare)
    n1=DYNC2H1 gene | n2=en:diffuse enlargement of subarachnoid spaces and lateral ventricles (rare) | rel=r_associated | relid=0 | w=10
  1300. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse fibrillar astrocytosis (in type iib)
    n1=DYNC2H1 gene | n2=en:diffuse fibrillar astrocytosis (in type iib) | rel=r_associated | relid=0 | w=10
  1301. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse hyperintense signal abnormalities in the white matter (in children)
    n1=DYNC2H1 gene | n2=en:diffuse hyperintense signal abnormalities in the white matter (in children) | rel=r_associated | relid=0 | w=10
  1302. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse hypomyelination
    n1=DYNC2H1 gene | n2=en:diffuse hypomyelination | rel=r_associated | relid=0 | w=10
  1303. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse hyporeflexia (later)
    n1=DYNC2H1 gene | n2=en:diffuse hyporeflexia (later) | rel=r_associated | relid=0 | w=10
  1304. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse hypotonia
    n1=DYNC2H1 gene | n2=en:diffuse hypotonia | rel=r_associated | relid=0 | w=10
  1305. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse leptomeningeal enhancement seen on mri
    n1=DYNC2H1 gene | n2=en:diffuse leptomeningeal enhancement seen on mri | rel=r_associated | relid=0 | w=10
  1306. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse leukoencephalopathy
    n1=DYNC2H1 gene | n2=en:diffuse leukoencephalopathy | rel=r_associated | relid=0 | w=10
  1307. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse lewy bodies throughout the brain (cortical and subcortical regions)
    n1=DYNC2H1 gene | n2=en:diffuse lewy bodies throughout the brain (cortical and subcortical regions) | rel=r_associated | relid=0 | w=10
  1308. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse lewy body pathology
    n1=DYNC2H1 gene | n2=en:diffuse lewy body pathology | rel=r_associated | relid=0 | w=10
  1309. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse paroxysmal discharges
    n1=DYNC2H1 gene | n2=en:diffuse paroxysmal discharges | rel=r_associated | relid=0 | w=10
  1310. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse periventricular leukoencephalopathy
    n1=DYNC2H1 gene | n2=en:diffuse periventricular leukoencephalopathy | rel=r_associated | relid=0 | w=10
  1311. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse signal abnormality of central white matter
    n1=DYNC2H1 gene | n2=en:diffuse signal abnormality of central white matter | rel=r_associated | relid=0 | w=10
  1312. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse slowing
    n1=DYNC2H1 gene | n2=en:diffuse slowing | rel=r_associated | relid=0 | w=10
  1313. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse slowing of background
    n1=DYNC2H1 gene | n2=en:diffuse slowing of background | rel=r_associated | relid=0 | w=10
  1314. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse spongiform leukoencephalopathy
    n1=DYNC2H1 gene | n2=en:diffuse spongiform leukoencephalopathy | rel=r_associated | relid=0 | w=10
  1315. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse swelling of cerebral white matter
    n1=DYNC2H1 gene | n2=en:diffuse swelling of cerebral white matter | rel=r_associated | relid=0 | w=10
  1316. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse white matter abnormalities on brain mri
    n1=DYNC2H1 gene | n2=en:diffuse white matter abnormalities on brain mri | rel=r_associated | relid=0 | w=10
  1317. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse white matter abnormalities seen on brain mri
    n1=DYNC2H1 gene | n2=en:diffuse white matter abnormalities seen on brain mri | rel=r_associated | relid=0 | w=10
  1318. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse white matter changes (meb)
    n1=DYNC2H1 gene | n2=en:diffuse white matter changes (meb) | rel=r_associated | relid=0 | w=10
  1319. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse white matter dysmyelination
    n1=DYNC2H1 gene | n2=en:diffuse white matter dysmyelination | rel=r_associated | relid=0 | w=10
  1320. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse white matter hyperintensities on t2-weighed imaging
    n1=DYNC2H1 gene | n2=en:diffuse white matter hyperintensities on t2-weighed imaging | rel=r_associated | relid=0 | w=10
  1321. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse white matter loss
    n1=DYNC2H1 gene | n2=en:diffuse white matter loss | rel=r_associated | relid=0 | w=10
  1322. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diffuse, severe neuronal loss
    n1=DYNC2H1 gene | n2=en:diffuse, severe neuronal loss | rel=r_associated | relid=0 | w=10
  1323. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilatation of the 3rd ventricle (in one family)
    n1=DYNC2H1 gene | n2=en:dilatation of the 3rd ventricle (in one family) | rel=r_associated | relid=0 | w=10
  1324. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilatation of the lateral and third ventricles
    n1=DYNC2H1 gene | n2=en:dilatation of the lateral and third ventricles | rel=r_associated | relid=0 | w=10
  1325. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilatation of the lateral ventricles (in one family)
    n1=DYNC2H1 gene | n2=en:dilatation of the lateral ventricles (in one family) | rel=r_associated | relid=0 | w=10
  1326. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilated fourth ventricle
    n1=DYNC2H1 gene | n2=en:dilated fourth ventricle | rel=r_associated | relid=0 | w=10
  1327. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilated lateral ventricles (1 patient)
    n1=DYNC2H1 gene | n2=en:dilated lateral ventricles (1 patient) | rel=r_associated | relid=0 | w=10
  1328. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilated perivascular spaces
    n1=DYNC2H1 gene | n2=en:dilated perivascular spaces | rel=r_associated | relid=0 | w=10
  1329. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilated venous sinuses
    n1=DYNC2H1 gene | n2=en:dilated venous sinuses | rel=r_associated | relid=0 | w=10
  1330. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilated ventricles (finding)
    n1=DYNC2H1 gene | n2=en:dilated ventricles (finding) | rel=r_associated | relid=0 | w=10
  1331. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilation of cerebral ventricles
    n1=DYNC2H1 gene | n2=en:dilation of cerebral ventricles | rel=r_associated | relid=0 | w=10
  1332. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilation of lateral ventricles
    n1=DYNC2H1 gene | n2=en:dilation of lateral ventricles | rel=r_associated | relid=0 | w=10
  1333. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dilation of lateral ventricles (in some patients)
    n1=DYNC2H1 gene | n2=en:dilation of lateral ventricles (in some patients) | rel=r_associated | relid=0 | w=10
  1334. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diminished visual activity
    n1=DYNC2H1 gene | n2=en:diminished visual activity | rel=r_associated | relid=0 | w=10
  1335. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diplacusis
    n1=DYNC2H1 gene | n2=en:diplacusis | rel=r_associated | relid=0 | w=10
  1336. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diplegia
    n1=DYNC2H1 gene | n2=en:diplegia | rel=r_associated | relid=0 | w=10
  1337. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:discrepancy between verbal and nonverbal abilities
    n1=DYNC2H1 gene | n2=en:discrepancy between verbal and nonverbal abilities | rel=r_associated | relid=0 | w=10
  1338. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disdiadochokinesia
    n1=DYNC2H1 gene | n2=en:disdiadochokinesia | rel=r_associated | relid=0 | w=10
  1339. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorder of parasympathetic nervous system
    n1=DYNC2H1 gene | n2=en:disorder of parasympathetic nervous system | rel=r_associated | relid=0 | w=10
  1340. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorder of peripheral autonomic nervous system
    n1=DYNC2H1 gene | n2=en:disorder of peripheral autonomic nervous system | rel=r_associated | relid=0 | w=10
  1341. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorder of sympathetic nervous system
    n1=DYNC2H1 gene | n2=en:disorder of sympathetic nervous system | rel=r_associated | relid=0 | w=10
  1342. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disordered myelination
    n1=DYNC2H1 gene | n2=en:disordered myelination | rel=r_associated | relid=0 | w=10
  1343. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disordered sleep pattern (in some patients)
    n1=DYNC2H1 gene | n2=en:disordered sleep pattern (in some patients) | rel=r_associated | relid=0 | w=10
  1344. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorganised speech
    n1=DYNC2H1 gene | n2=en:disorganised speech | rel=r_associated | relid=0 | w=10
  1345. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorganization of the anterior cerebellar vermis
    n1=DYNC2H1 gene | n2=en:disorganization of the anterior cerebellar vermis | rel=r_associated | relid=0 | w=10
  1346. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorganized brain cytoarchitecture
    n1=DYNC2H1 gene | n2=en:disorganized brain cytoarchitecture | rel=r_associated | relid=0 | w=10
  1347. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorganized cortical architecture
    n1=DYNC2H1 gene | n2=en:disorganized cortical architecture | rel=r_associated | relid=0 | w=10
  1348. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorganized eeg
    n1=DYNC2H1 gene | n2=en:disorganized eeg | rel=r_associated | relid=0 | w=10
  1349. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorganized slow background activity seen on eeg
    n1=DYNC2H1 gene | n2=en:disorganized slow background activity seen on eeg | rel=r_associated | relid=0 | w=10
  1350. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disorientation
    n1=DYNC2H1 gene | n2=en:disorientation | rel=r_associated | relid=0 | w=10
  1351. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disproportionately small cerebral cortex
    n1=DYNC2H1 gene | n2=en:disproportionately small cerebral cortex | rel=r_associated | relid=0 | w=10
  1352. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:distal amyotrophy
    n1=DYNC2H1 gene | n2=en:distal amyotrophy | rel=r_associated | relid=0 | w=10
  1353. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:distal muscle weakness
    n1=DYNC2H1 gene | n2=en:distal muscle weakness | rel=r_associated | relid=0 | w=10
  1354. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:distal muscle weakness and atrophy due to motor neuronopathy
    n1=DYNC2H1 gene | n2=en:distal muscle weakness and atrophy due to motor neuronopathy | rel=r_associated | relid=0 | w=10
  1355. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:distal muscle weakness, upper and lower limbs
    n1=DYNC2H1 gene | n2=en:distal muscle weakness, upper and lower limbs | rel=r_associated | relid=0 | w=10
  1356. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:distal sensory impairment
    n1=DYNC2H1 gene | n2=en:distal sensory impairment | rel=r_associated | relid=0 | w=10
  1357. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:distal sensory loss to all modalities, lower limbs more affected than upper limbs
    n1=DYNC2H1 gene | n2=en:distal sensory loss to all modalities, lower limbs more affected than upper limbs | rel=r_associated | relid=0 | w=10
  1358. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:distal tapering of the carotid, cerebellar, and meningeal arteries
    n1=DYNC2H1 gene | n2=en:distal tapering of the carotid, cerebellar, and meningeal arteries | rel=r_associated | relid=0 | w=10
  1359. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:distal weakness occurs later
    n1=DYNC2H1 gene | n2=en:distal weakness occurs later | rel=r_associated | relid=0 | w=10
  1360. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:distorted hearing
    n1=DYNC2H1 gene | n2=en:distorted hearing | rel=r_associated | relid=0 | w=10
  1361. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disturbance of attention
    n1=DYNC2H1 gene | n2=en:disturbance of attention | rel=r_associated | relid=0 | w=10
  1362. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disturbance of consciousness
    n1=DYNC2H1 gene | n2=en:disturbance of consciousness | rel=r_associated | relid=0 | w=10
  1363. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disturbed equilibrium
    n1=DYNC2H1 gene | n2=en:disturbed equilibrium | rel=r_associated | relid=0 | w=10
  1364. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disturbed gait
    n1=DYNC2H1 gene | n2=en:disturbed gait | rel=r_associated | relid=0 | w=10
  1365. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disturbed myelination affecting the periventricular and subcortical white matter
    n1=DYNC2H1 gene | n2=en:disturbed myelination affecting the periventricular and subcortical white matter | rel=r_associated | relid=0 | w=10
  1366. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:disturbed sleep-wake cycle
    n1=DYNC2H1 gene | n2=en:disturbed sleep-wake cycle | rel=r_associated | relid=0 | w=10
  1367. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:diurnal fluctuations of symptoms (in a subset of patients)
    n1=DYNC2H1 gene | n2=en:diurnal fluctuations of symptoms (in a subset of patients) | rel=r_associated | relid=0 | w=10
  1368. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dizziness
    n1=DYNC2H1 gene | n2=en:dizziness | rel=r_associated | relid=0 | w=10
  1369. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dizziness may occur
    n1=DYNC2H1 gene | n2=en:dizziness may occur | rel=r_associated | relid=0 | w=10
  1370. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dizziness, episodic
    n1=DYNC2H1 gene | n2=en:dizziness, episodic | rel=r_associated | relid=0 | w=10
  1371. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dopamine-responsive parkinsonism
    n1=DYNC2H1 gene | n2=en:dopamine-responsive parkinsonism | rel=r_associated | relid=0 | w=10
  1372. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:double cortex syndrome
    n1=DYNC2H1 gene | n2=en:double cortex syndrome | rel=r_associated | relid=0 | w=10
  1373. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dream enactment
    n1=DYNC2H1 gene | n2=en:dream enactment | rel=r_associated | relid=0 | w=10
  1374. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:drooling
    n1=DYNC2H1 gene | n2=en:drooling | rel=r_associated | relid=0 | w=10
  1375. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:drop attack
    n1=DYNC2H1 gene | n2=en:drop attack | rel=r_associated | relid=0 | w=10
  1376. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:drug-induced autonomic dysfunction
    n1=DYNC2H1 gene | n2=en:drug-induced autonomic dysfunction | rel=r_associated | relid=0 | w=10
  1377. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:drug-resistent seizures (rare)
    n1=DYNC2H1 gene | n2=en:drug-resistent seizures (rare) | rel=r_associated | relid=0 | w=10
  1378. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dural and choroid plexus calcifications
    n1=DYNC2H1 gene | n2=en:dural and choroid plexus calcifications | rel=r_associated | relid=0 | w=10
  1379. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dural ectasia
    n1=DYNC2H1 gene | n2=en:dural ectasia | rel=r_associated | relid=0 | w=10
  1380. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:Dyggve's syndrome
    n1=DYNC2H1 gene | n2=en:Dyggve's syndrome | rel=r_associated | relid=0 | w=10
  1381. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysacousia
    n1=DYNC2H1 gene | n2=en:dysacousia | rel=r_associated | relid=0 | w=10
  1382. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysacousiadysacousis
    n1=DYNC2H1 gene | n2=en:dysacousiadysacousis | rel=r_associated | relid=0 | w=10
  1383. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysacousma
    n1=DYNC2H1 gene | n2=en:dysacousma | rel=r_associated | relid=0 | w=10
  1384. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria (1 family)
    n1=DYNC2H1 gene | n2=en:dysarthria (1 family) | rel=r_associated | relid=0 | w=10
  1385. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria (1 patient)
    n1=DYNC2H1 gene | n2=en:dysarthria (1 patient) | rel=r_associated | relid=0 | w=10
  1386. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria (74%)
    n1=DYNC2H1 gene | n2=en:dysarthria (74%) | rel=r_associated | relid=0 | w=10
  1387. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria (in some patients)
    n1=DYNC2H1 gene | n2=en:dysarthria (in some patients) | rel=r_associated | relid=0 | w=10
  1388. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria (less common)
    n1=DYNC2H1 gene | n2=en:dysarthria (less common) | rel=r_associated | relid=0 | w=10
  1389. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria (mild)
    n1=DYNC2H1 gene | n2=en:dysarthria (mild) | rel=r_associated | relid=0 | w=10
  1390. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria (most common presenting symptom)
    n1=DYNC2H1 gene | n2=en:dysarthria (most common presenting symptom) | rel=r_associated | relid=0 | w=10
  1391. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria (onset in third decade)
    n1=DYNC2H1 gene | n2=en:dysarthria (onset in third decade) | rel=r_associated | relid=0 | w=10
  1392. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria may occur
    n1=DYNC2H1 gene | n2=en:dysarthria may occur | rel=r_associated | relid=0 | w=10
  1393. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria, mild (1 family)
    n1=DYNC2H1 gene | n2=en:dysarthria, mild (1 family) | rel=r_associated | relid=0 | w=10
  1394. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:dysarthria, mild (in some patients) | rel=r_associated | relid=0 | w=10
  1395. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthria, slowly progressive
    n1=DYNC2H1 gene | n2=en:dysarthria, slowly progressive | rel=r_associated | relid=0 | w=10
  1396. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthrias, guttural
    n1=DYNC2H1 gene | n2=en:dysarthrias, guttural | rel=r_associated | relid=0 | w=10
  1397. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthrias, mixed
    n1=DYNC2H1 gene | n2=en:dysarthrias, mixed | rel=r_associated | relid=0 | w=10
  1398. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysarthrias, scanning
    n1=DYNC2H1 gene | n2=en:dysarthrias, scanning | rel=r_associated | relid=0 | w=10
  1399. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysautonomia
    n1=DYNC2H1 gene | n2=en:dysautonomia | rel=r_associated | relid=0 | w=10
  1400. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysautonomia like disorder
    n1=DYNC2H1 gene | n2=en:dysautonomia like disorder | rel=r_associated | relid=0 | w=10
  1401. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysautonomia may occur
    n1=DYNC2H1 gene | n2=en:dysautonomia may occur | rel=r_associated | relid=0 | w=10
  1402. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dyscalculia
    n1=DYNC2H1 gene | n2=en:dyscalculia | rel=r_associated | relid=0 | w=10
  1403. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysdiadochokinesis
    n1=DYNC2H1 gene | n2=en:dysdiadochokinesis | rel=r_associated | relid=0 | w=10
  1404. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysdiadochokinesis (1 family)
    n1=DYNC2H1 gene | n2=en:dysdiadochokinesis (1 family) | rel=r_associated | relid=0 | w=10
  1405. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysdiadochokinesis (63%)
    n1=DYNC2H1 gene | n2=en:dysdiadochokinesis (63%) | rel=r_associated | relid=0 | w=10
  1406. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysfunction of lateral corticospinal tracts
    n1=DYNC2H1 gene | n2=en:dysfunction of lateral corticospinal tracts | rel=r_associated | relid=0 | w=10
  1407. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysfunction of the autonomic nervous system
    n1=DYNC2H1 gene | n2=en:dysfunction of the autonomic nervous system | rel=r_associated | relid=0 | w=10
  1408. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysgenesis of corpus callosum
    n1=DYNC2H1 gene | n2=en:dysgenesis of corpus callosum | rel=r_associated | relid=0 | w=10
  1409. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysgenesis of the anterior commissure (in some)
    n1=DYNC2H1 gene | n2=en:dysgenesis of the anterior commissure (in some) | rel=r_associated | relid=0 | w=10
  1410. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysgenesis of the corpus callosum (1 patient)
    n1=DYNC2H1 gene | n2=en:dysgenesis of the corpus callosum (1 patient) | rel=r_associated | relid=0 | w=10
  1411. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysgenesis or agenesis of the cerebellar vermis
    n1=DYNC2H1 gene | n2=en:dysgenesis or agenesis of the cerebellar vermis | rel=r_associated | relid=0 | w=10
  1412. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysgenesis or agenesis of the corpus callosum (in some)
    n1=DYNC2H1 gene | n2=en:dysgenesis or agenesis of the corpus callosum (in some) | rel=r_associated | relid=0 | w=10
  1413. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysgraphias
    n1=DYNC2H1 gene | n2=en:dysgraphias | rel=r_associated | relid=0 | w=10
  1414. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dyskinesia
    n1=DYNC2H1 gene | n2=en:dyskinesia | rel=r_associated | relid=0 | w=10
  1415. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dyskinesia, episodic
    n1=DYNC2H1 gene | n2=en:dyskinesia, episodic | rel=r_associated | relid=0 | w=10
  1416. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dyskinesia, limb, exertion-induced
    n1=DYNC2H1 gene | n2=en:dyskinesia, limb, exertion-induced | rel=r_associated | relid=0 | w=10
  1417. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dyskinetic movements
    n1=DYNC2H1 gene | n2=en:dyskinetic movements | rel=r_associated | relid=0 | w=10
  1418. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dyslexia
    n1=DYNC2H1 gene | n2=en:dyslexia | rel=r_associated | relid=0 | w=10
  1419. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmetria (1 family)
    n1=DYNC2H1 gene | n2=en:dysmetria (1 family) | rel=r_associated | relid=0 | w=10
  1420. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmetria (1 patient)
    n1=DYNC2H1 gene | n2=en:dysmetria (1 patient) | rel=r_associated | relid=0 | w=10
  1421. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmetria (in 1 of 3 families)
    n1=DYNC2H1 gene | n2=en:dysmetria (in 1 of 3 families) | rel=r_associated | relid=0 | w=10
  1422. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmetria (in some patients)
    n1=DYNC2H1 gene | n2=en:dysmetria (in some patients) | rel=r_associated | relid=0 | w=10
  1423. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmetria (type i)
    n1=DYNC2H1 gene | n2=en:dysmetria (type i) | rel=r_associated | relid=0 | w=10
  1424. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmetria, mild
    n1=DYNC2H1 gene | n2=en:dysmetria, mild | rel=r_associated | relid=0 | w=10
  1425. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmetrias, cerebellar
    n1=DYNC2H1 gene | n2=en:dysmetrias, cerebellar | rel=r_associated | relid=0 | w=10
  1426. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmetric saccades
    n1=DYNC2H1 gene | n2=en:dysmetric saccades | rel=r_associated | relid=0 | w=10
  1427. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmorphic basal ganglia
    n1=DYNC2H1 gene | n2=en:dysmorphic basal ganglia | rel=r_associated | relid=0 | w=10
  1428. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmorphic basal ganglia (1 patient)
    n1=DYNC2H1 gene | n2=en:dysmorphic basal ganglia (1 patient) | rel=r_associated | relid=0 | w=10
  1429. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmorphic basal ganglia (in some patients)
    n1=DYNC2H1 gene | n2=en:dysmorphic basal ganglia (in some patients) | rel=r_associated | relid=0 | w=10
  1430. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmorphic basal ganglia (in some)
    n1=DYNC2H1 gene | n2=en:dysmorphic basal ganglia (in some) | rel=r_associated | relid=0 | w=10
  1431. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmorphic corpus callosum
    n1=DYNC2H1 gene | n2=en:dysmorphic corpus callosum | rel=r_associated | relid=0 | w=10
  1432. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmyelinating leukodystrophy
    n1=DYNC2H1 gene | n2=en:dysmyelinating leukodystrophy | rel=r_associated | relid=0 | w=10
  1433. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmyelination of the brain and spinal cord
    n1=DYNC2H1 gene | n2=en:dysmyelination of the brain and spinal cord | rel=r_associated | relid=0 | w=10
  1434. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysmyelination of the brain, myelin is not formed properly
    n1=DYNC2H1 gene | n2=en:dysmyelination of the brain, myelin is not formed properly | rel=r_associated | relid=0 | w=10
  1435. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysphagia
    n1=DYNC2H1 gene | n2=en:dysphagia | rel=r_associated | relid=0 | w=10
  1436. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysphasia
    n1=DYNC2H1 gene | n2=en:dysphasia | rel=r_associated | relid=0 | w=10
  1437. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysphonia
    n1=DYNC2H1 gene | n2=en:dysphonia | rel=r_associated | relid=0 | w=10
  1438. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysplasia of the cerebellar hemispheres
    n1=DYNC2H1 gene | n2=en:dysplasia of the cerebellar hemispheres | rel=r_associated | relid=0 | w=10
  1439. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysplastic basal ganglia
    n1=DYNC2H1 gene | n2=en:dysplastic basal ganglia | rel=r_associated | relid=0 | w=10
  1440. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysplastic c-shaped inferior olivary nuclei
    n1=DYNC2H1 gene | n2=en:dysplastic c-shaped inferior olivary nuclei | rel=r_associated | relid=0 | w=10
  1441. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysplastic cerebellar gangliocytoma
    n1=DYNC2H1 gene | n2=en:dysplastic cerebellar gangliocytoma | rel=r_associated | relid=0 | w=10
  1442. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysplastic cerebellar vermis
    n1=DYNC2H1 gene | n2=en:dysplastic cerebellar vermis | rel=r_associated | relid=0 | w=10
  1443. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysplastic cerebellum
    n1=DYNC2H1 gene | n2=en:dysplastic cerebellum | rel=r_associated | relid=0 | w=10
  1444. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysplastic pons
    n1=DYNC2H1 gene | n2=en:dysplastic pons | rel=r_associated | relid=0 | w=10
  1445. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dysplastic superior cerebellar vermis
    n1=DYNC2H1 gene | n2=en:dysplastic superior cerebellar vermis | rel=r_associated | relid=0 | w=10
  1446. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia
    n1=DYNC2H1 gene | n2=en:dystonia | rel=r_associated | relid=0 | w=10
  1447. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (<20%) (finding)
    n1=DYNC2H1 gene | n2=en:dystonia (<20%) (finding) | rel=r_associated | relid=0 | w=10
  1448. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (1 family)
    n1=DYNC2H1 gene | n2=en:dystonia (1 family) | rel=r_associated | relid=0 | w=10
  1449. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (1 patient)
    n1=DYNC2H1 gene | n2=en:dystonia (1 patient) | rel=r_associated | relid=0 | w=10
  1450. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (14% of patients)
    n1=DYNC2H1 gene | n2=en:dystonia (14% of patients) | rel=r_associated | relid=0 | w=10
  1451. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (57%)
    n1=DYNC2H1 gene | n2=en:dystonia (57%) | rel=r_associated | relid=0 | w=10
  1452. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (in 2 patients)
    n1=DYNC2H1 gene | n2=en:dystonia (in 2 patients) | rel=r_associated | relid=0 | w=10
  1453. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (in severe cases)
    n1=DYNC2H1 gene | n2=en:dystonia (in severe cases) | rel=r_associated | relid=0 | w=10
  1454. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (in some patients)
    n1=DYNC2H1 gene | n2=en:dystonia (in some patients) | rel=r_associated | relid=0 | w=10
  1455. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (less common)
    n1=DYNC2H1 gene | n2=en:dystonia (less common) | rel=r_associated | relid=0 | w=10
  1456. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia (may spontaneously remit in childhood or adolescence)
    n1=DYNC2H1 gene | n2=en:dystonia (may spontaneously remit in childhood or adolescence) | rel=r_associated | relid=0 | w=10
  1457. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia 18 (disorder)
    n1=DYNC2H1 gene | n2=en:dystonia 18 (disorder) | rel=r_associated | relid=0 | w=10
  1458. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia at onset (16%)
    n1=DYNC2H1 gene | n2=en:dystonia at onset (16%) | rel=r_associated | relid=0 | w=10
  1459. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia disorders
    n1=DYNC2H1 gene | n2=en:dystonia disorders | rel=r_associated | relid=0 | w=10
  1460. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia may become generalized
    n1=DYNC2H1 gene | n2=en:dystonia may become generalized | rel=r_associated | relid=0 | w=10
  1461. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia with diurnal variation
    n1=DYNC2H1 gene | n2=en:dystonia with diurnal variation | rel=r_associated | relid=0 | w=10
  1462. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia, episodic, primary affects hands and feet
    n1=DYNC2H1 gene | n2=en:dystonia, episodic, primary affects hands and feet | rel=r_associated | relid=0 | w=10
  1463. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia, focal (at onset)
    n1=DYNC2H1 gene | n2=en:dystonia, focal (at onset) | rel=r_associated | relid=0 | w=10
  1464. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm)
    n1=DYNC2H1 gene | n2=en:dystonia, focal, limited to orbicularis oculi muscle (blepharospasm) | rel=r_associated | relid=0 | w=10
  1465. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia, generalized, dopa-unresponsive
    n1=DYNC2H1 gene | n2=en:dystonia, generalized, dopa-unresponsive | rel=r_associated | relid=0 | w=10
  1466. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia, limb, exercise-induced
    n1=DYNC2H1 gene | n2=en:dystonia, limb, exercise-induced | rel=r_associated | relid=0 | w=10
  1467. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia, progressive
    n1=DYNC2H1 gene | n2=en:dystonia, progressive | rel=r_associated | relid=0 | w=10
  1468. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia, severe (in all limbs)
    n1=DYNC2H1 gene | n2=en:dystonia, severe (in all limbs) | rel=r_associated | relid=0 | w=10
  1469. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonia, trunk and limbs (upper and lower)
    n1=DYNC2H1 gene | n2=en:dystonia, trunk and limbs (upper and lower) | rel=r_associated | relid=0 | w=10
  1470. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonic hand posturing (44% of patients)
    n1=DYNC2H1 gene | n2=en:dystonic hand posturing (44% of patients) | rel=r_associated | relid=0 | w=10
  1471. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonic movements (in 1 of 6 patients)
    n1=DYNC2H1 gene | n2=en:dystonic movements (in 1 of 6 patients) | rel=r_associated | relid=0 | w=10
  1472. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonic posture
    n1=DYNC2H1 gene | n2=en:dystonic posture | rel=r_associated | relid=0 | w=10
  1473. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonic posturing (rare)
    n1=DYNC2H1 gene | n2=en:dystonic posturing (rare) | rel=r_associated | relid=0 | w=10
  1474. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonic posturing of the hands
    n1=DYNC2H1 gene | n2=en:dystonic posturing of the hands | rel=r_associated | relid=0 | w=10
  1475. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonic tongue protrusion
    n1=DYNC2H1 gene | n2=en:dystonic tongue protrusion | rel=r_associated | relid=0 | w=10
  1476. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonic tremor
    n1=DYNC2H1 gene | n2=en:dystonic tremor | rel=r_associated | relid=0 | w=10
  1477. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonic vocal tremor
    n1=DYNC2H1 gene | n2=en:dystonic vocal tremor | rel=r_associated | relid=0 | w=10
  1478. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystonic writer's cramp
    n1=DYNC2H1 gene | n2=en:dystonic writer's cramp | rel=r_associated | relid=0 | w=10
  1479. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:dystrophic neurites
    n1=DYNC2H1 gene | n2=en:dystrophic neurites | rel=r_associated | relid=0 | w=10
  1480. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:earlier sleep-offset time (earlier awakening)
    n1=DYNC2H1 gene | n2=en:earlier sleep-offset time (earlier awakening) | rel=r_associated | relid=0 | w=10
  1481. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:early and severe foot extensor muscle involvement
    n1=DYNC2H1 gene | n2=en:early and severe foot extensor muscle involvement | rel=r_associated | relid=0 | w=10
  1482. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:early involvement of the corticospinal pathways
    n1=DYNC2H1 gene | n2=en:early involvement of the corticospinal pathways | rel=r_associated | relid=0 | w=10
  1483. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:early severe fetal akinesia sequence
    n1=DYNC2H1 gene | n2=en:early severe fetal akinesia sequence | rel=r_associated | relid=0 | w=10
  1484. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:early-onset myoclonic seizures
    n1=DYNC2H1 gene | n2=en:early-onset myoclonic seizures | rel=r_associated | relid=0 | w=10
  1485. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:echoacousia
    n1=DYNC2H1 gene | n2=en:echoacousia | rel=r_associated | relid=0 | w=10
  1486. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:echolalia
    n1=DYNC2H1 gene | n2=en:echolalia | rel=r_associated | relid=0 | w=10
  1487. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ectopic dorsal pontine transverse bundle of fibers forms the 'cap'
    n1=DYNC2H1 gene | n2=en:ectopic dorsal pontine transverse bundle of fibers forms the 'cap' | rel=r_associated | relid=0 | w=10
  1488. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ectopic posterior pituitary
    n1=DYNC2H1 gene | n2=en:ectopic posterior pituitary | rel=r_associated | relid=0 | w=10
  1489. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ectopic posterior pituitary (in some patients)
    n1=DYNC2H1 gene | n2=en:ectopic posterior pituitary (in some patients) | rel=r_associated | relid=0 | w=10
  1490. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3)
    n1=DYNC2H1 gene | n2=en:eeg - alpha abolished, continuous spike waves, intense myoclonus on photic stimulation (stage 3) | rel=r_associated | relid=0 | w=10
  1491. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg - alpha slowing, 4-6 hz spike waves, myoclonus on photic stimulation (stage 2)
    n1=DYNC2H1 gene | n2=en:eeg - alpha slowing, 4-6 hz spike waves, myoclonus on photic stimulation (stage 2) | rel=r_associated | relid=0 | w=10
  1492. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg - polyspike on photic stimulation (stage 1)
    n1=DYNC2H1 gene | n2=en:eeg - polyspike on photic stimulation (stage 1) | rel=r_associated | relid=0 | w=10
  1493. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges
    n1=DYNC2H1 gene | n2=en:eeg abnormalities - slow waking background, intermittent rhythmical slowing (3-5hz), epileptiform discharges | rel=r_associated | relid=0 | w=10
  1494. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg abnormalities in 20-50%
    n1=DYNC2H1 gene | n2=en:eeg abnormalities in 20-50% | rel=r_associated | relid=0 | w=10
  1495. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg abnormalities in 20-50% impaired language development
    n1=DYNC2H1 gene | n2=en:eeg abnormalities in 20-50% impaired language development | rel=r_associated | relid=0 | w=10
  1496. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg and symptomatology suggest mesial temporal origin
    n1=DYNC2H1 gene | n2=en:eeg and symptomatology suggest mesial temporal origin | rel=r_associated | relid=0 | w=10
  1497. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg during episodes shows desynchronization
    n1=DYNC2H1 gene | n2=en:eeg during episodes shows desynchronization | rel=r_associated | relid=0 | w=10
  1498. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg is slowed with polyspike wave discharges
    n1=DYNC2H1 gene | n2=en:eeg is slowed with polyspike wave discharges | rel=r_associated | relid=0 | w=10
  1499. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg is usually normal
    n1=DYNC2H1 gene | n2=en:eeg is usually normal | rel=r_associated | relid=0 | w=10
  1500. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg later shows generalized spike or polyspike waves and focal spikes
    n1=DYNC2H1 gene | n2=en:eeg later shows generalized spike or polyspike waves and focal spikes | rel=r_associated | relid=0 | w=10
  1501. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg may be normal at first
    n1=DYNC2H1 gene | n2=en:eeg may be normal at first | rel=r_associated | relid=0 | w=10
  1502. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg may show migrating focal or multifocal origin (in severe cases)
    n1=DYNC2H1 gene | n2=en:eeg may show migrating focal or multifocal origin (in severe cases) | rel=r_associated | relid=0 | w=10
  1503. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows 3-4-hz spike and multispike slow wave complexes
    n1=DYNC2H1 gene | n2=en:eeg shows 3-4-hz spike and multispike slow wave complexes | rel=r_associated | relid=0 | w=10
  1504. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows 3-4-hz spike waves
    n1=DYNC2H1 gene | n2=en:eeg shows 3-4-hz spike waves | rel=r_associated | relid=0 | w=10
  1505. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows 3-hz spike-wave discharges
    n1=DYNC2H1 gene | n2=en:eeg shows 3-hz spike-wave discharges | rel=r_associated | relid=0 | w=10
  1506. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows abundant slow waves and fast spike activity
    n1=DYNC2H1 gene | n2=en:eeg shows abundant slow waves and fast spike activity | rel=r_associated | relid=0 | w=10
  1507. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows active generalized spike and wave and polyspike pattern
    n1=DYNC2H1 gene | n2=en:eeg shows active generalized spike and wave and polyspike pattern | rel=r_associated | relid=0 | w=10
  1508. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows burst suppression
    n1=DYNC2H1 gene | n2=en:eeg shows burst suppression | rel=r_associated | relid=0 | w=10
  1509. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows centrotemporal spike-wave discharges
    n1=DYNC2H1 gene | n2=en:eeg shows centrotemporal spike-wave discharges | rel=r_associated | relid=0 | w=10
  1510. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows epileptiform activity
    n1=DYNC2H1 gene | n2=en:eeg shows epileptiform activity | rel=r_associated | relid=0 | w=10
  1511. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows epileptiform discharges
    n1=DYNC2H1 gene | n2=en:eeg shows epileptiform discharges | rel=r_associated | relid=0 | w=10
  1512. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows frontal lobe origin
    n1=DYNC2H1 gene | n2=en:eeg shows frontal lobe origin | rel=r_associated | relid=0 | w=10
  1513. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows generalized polyspike and wave discharges (4-5 hz)
    n1=DYNC2H1 gene | n2=en:eeg shows generalized polyspike and wave discharges (4-5 hz) | rel=r_associated | relid=0 | w=10
  1514. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows generalized polyspike and wave discharges (4-6 hz)
    n1=DYNC2H1 gene | n2=en:eeg shows generalized polyspike and wave discharges (4-6 hz) | rel=r_associated | relid=0 | w=10
  1515. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows generalized, bilateral, synchronous, symmetrical discharge
    n1=DYNC2H1 gene | n2=en:eeg shows generalized, bilateral, synchronous, symmetrical discharge | rel=r_associated | relid=0 | w=10
  1516. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows hypsarrhythmia
    n1=DYNC2H1 gene | n2=en:eeg shows hypsarrhythmia | rel=r_associated | relid=0 | w=10
  1517. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows hypsarrhythmia (in 1 of 6 patients)
    n1=DYNC2H1 gene | n2=en:eeg shows hypsarrhythmia (in 1 of 6 patients) | rel=r_associated | relid=0 | w=10
  1518. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows multifocal discharges
    n1=DYNC2H1 gene | n2=en:eeg shows multifocal discharges | rel=r_associated | relid=0 | w=10
  1519. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows multifocal epileptic activity
    n1=DYNC2H1 gene | n2=en:eeg shows multifocal epileptic activity | rel=r_associated | relid=0 | w=10
  1520. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows nonspecific slow-wave paroxysms
    n1=DYNC2H1 gene | n2=en:eeg shows nonspecific slow-wave paroxysms | rel=r_associated | relid=0 | w=10
  1521. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows photosensitivity
    n1=DYNC2H1 gene | n2=en:eeg shows photosensitivity | rel=r_associated | relid=0 | w=10
  1522. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows rolandic sharp waves and spikes
    n1=DYNC2H1 gene | n2=en:eeg shows rolandic sharp waves and spikes | rel=r_associated | relid=0 | w=10
  1523. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows slow frequency high amplitude waves with high frequency polyspikes
    n1=DYNC2H1 gene | n2=en:eeg shows slow frequency high amplitude waves with high frequency polyspikes | rel=r_associated | relid=0 | w=10
  1524. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows slowed dysrhythmia and multifocal discharges
    n1=DYNC2H1 gene | n2=en:eeg shows slowed dysrhythmia and multifocal discharges | rel=r_associated | relid=0 | w=10
  1525. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows spike and multispike waves, 3-4 hz
    n1=DYNC2H1 gene | n2=en:eeg shows spike and multispike waves, 3-4 hz | rel=r_associated | relid=0 | w=10
  1526. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows spike and wave or polyspike and wave discharges
    n1=DYNC2H1 gene | n2=en:eeg shows spike and wave or polyspike and wave discharges | rel=r_associated | relid=0 | w=10
  1527. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows suppression with ictal burst activities
    n1=DYNC2H1 gene | n2=en:eeg shows suppression with ictal burst activities | rel=r_associated | relid=0 | w=10
  1528. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows suppression-burst pattern
    n1=DYNC2H1 gene | n2=en:eeg shows suppression-burst pattern | rel=r_associated | relid=0 | w=10
  1529. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows unilateral centrotemporal spikes
    n1=DYNC2H1 gene | n2=en:eeg shows unilateral centrotemporal spikes | rel=r_associated | relid=0 | w=10
  1530. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg shows with a multifocal pattern with spikes and sharp waves
    n1=DYNC2H1 gene | n2=en:eeg shows with a multifocal pattern with spikes and sharp waves | rel=r_associated | relid=0 | w=10
  1531. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg with burst suppression
    n1=DYNC2H1 gene | n2=en:eeg with burst suppression | rel=r_associated | relid=0 | w=10
  1532. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg with focal discharge
    n1=DYNC2H1 gene | n2=en:eeg with focal discharge | rel=r_associated | relid=0 | w=10
  1533. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg with paroxysmal activity
    n1=DYNC2H1 gene | n2=en:eeg with paroxysmal activity | rel=r_associated | relid=0 | w=10
  1534. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eeg with photoparoxysmal response
    n1=DYNC2H1 gene | n2=en:eeg with photoparoxysmal response | rel=r_associated | relid=0 | w=10
  1535. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:effaced gyral pattern
    n1=DYNC2H1 gene | n2=en:effaced gyral pattern | rel=r_associated | relid=0 | w=10
  1536. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:effect, sympathomimetic
    n1=DYNC2H1 gene | n2=en:effect, sympathomimetic | rel=r_associated | relid=0 | w=10
  1537. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:electroencephalogram (eeg) abnormalities
    n1=DYNC2H1 gene | n2=en:electroencephalogram (eeg) abnormalities | rel=r_associated | relid=0 | w=10
  1538. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:electroencephalogram abnormal
    n1=DYNC2H1 gene | n2=en:electroencephalogram abnormal | rel=r_associated | relid=0 | w=10
  1539. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:electrophysiologic studies indicate cortical origin
    n1=DYNC2H1 gene | n2=en:electrophysiologic studies indicate cortical origin | rel=r_associated | relid=0 | w=10
  1540. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:elevated interferon levels in cerebrospinal fluid
    n1=DYNC2H1 gene | n2=en:elevated interferon levels in cerebrospinal fluid | rel=r_associated | relid=0 | w=10
  1541. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:elevated pterin levels (tetrahydrobiopterin, neopterin) in cerebrospinal fluid
    n1=DYNC2H1 gene | n2=en:elevated pterin levels (tetrahydrobiopterin, neopterin) in cerebrospinal fluid | rel=r_associated | relid=0 | w=10
  1542. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:elevated white cell count in cerebrospinal fluid
    n1=DYNC2H1 gene | n2=en:elevated white cell count in cerebrospinal fluid | rel=r_associated | relid=0 | w=10
  1543. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:elevation and splaying of the superior cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:elevation and splaying of the superior cerebellar peduncles | rel=r_associated | relid=0 | w=10
  1544. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:elongated superior cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:elongated superior cerebellar peduncles | rel=r_associated | relid=0 | w=10
  1545. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows bursts of activity originating in the masseter muscle and spreading to the orbicularis oris and oculi muscles
    n1=DYNC2H1 gene | 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=10
  1546. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows continuous motor unit firing at rest
    n1=DYNC2H1 gene | n2=en:emg shows continuous motor unit firing at rest | rel=r_associated | relid=0 | w=10
  1547. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows evidence of denervation
    n1=DYNC2H1 gene | n2=en:emg shows evidence of denervation | rel=r_associated | relid=0 | w=10
  1548. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials
    n1=DYNC2H1 gene | n2=en:emg shows fibrillation potentials and mixed myopathic and neurogenic motor unit potentials | rel=r_associated | relid=0 | w=10
  1549. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows fibrillations and fasiculations
    n1=DYNC2H1 gene | n2=en:emg shows fibrillations and fasiculations | rel=r_associated | relid=0 | w=10
  1550. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows involuntary continuous motor activity at rest
    n1=DYNC2H1 gene | n2=en:emg shows involuntary continuous motor activity at rest | rel=r_associated | relid=0 | w=10
  1551. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows neurogenic abnormalities
    n1=DYNC2H1 gene | n2=en:emg shows neurogenic abnormalities | rel=r_associated | relid=0 | w=10
  1552. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows neurogenic changes
    n1=DYNC2H1 gene | n2=en:emg shows neurogenic changes | rel=r_associated | relid=0 | w=10
  1553. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows neurogenic changes and denervation
    n1=DYNC2H1 gene | n2=en:emg shows neurogenic changes and denervation | rel=r_associated | relid=0 | w=10
  1554. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg shows neurogenic findings
    n1=DYNC2H1 gene | n2=en:emg shows neurogenic findings | rel=r_associated | relid=0 | w=10
  1555. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:emg with spontaneous discharge of normal motor unit potentials
    n1=DYNC2H1 gene | n2=en:emg with spontaneous discharge of normal motor unit potentials | rel=r_associated | relid=0 | w=10
  1556. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:empty sella syndrome
    n1=DYNC2H1 gene | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=10
  1557. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalitis
    n1=DYNC2H1 gene | n2=en:encephalitis | rel=r_associated | relid=0 | w=10
  1558. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalocele
    n1=DYNC2H1 gene | n2=en:encephalocele | rel=r_associated | relid=0 | w=10
  1559. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalocele (1 patient)
    n1=DYNC2H1 gene | n2=en:encephalocele (1 patient) | rel=r_associated | relid=0 | w=10
  1560. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalocele (rare)
    n1=DYNC2H1 gene | n2=en:encephalocele (rare) | rel=r_associated | relid=0 | w=10
  1561. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalocele (single case)
    n1=DYNC2H1 gene | n2=en:encephalocele (single case) | rel=r_associated | relid=0 | w=10
  1562. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalocele (uncommon)
    n1=DYNC2H1 gene | n2=en:encephalocele (uncommon) | rel=r_associated | relid=0 | w=10
  1563. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalocele of orbit
    n1=DYNC2H1 gene | n2=en:encephalocele of orbit | rel=r_associated | relid=0 | w=10
  1564. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephaloceles, frontal
    n1=DYNC2H1 gene | n2=en:encephaloceles, frontal | rel=r_associated | relid=0 | w=10
  1565. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalomyelopathy
    n1=DYNC2H1 gene | n2=en:encephalomyelopathy | rel=r_associated | relid=0 | w=10
  1566. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalomyopathy
    n1=DYNC2H1 gene | n2=en:encephalomyopathy | rel=r_associated | relid=0 | w=10
  1567. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathic attacks, episodic, associated with infection
    n1=DYNC2H1 gene | n2=en:encephalopathic attacks, episodic, associated with infection | rel=r_associated | relid=0 | w=10
  1568. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathic episodes, often associated with infection
    n1=DYNC2H1 gene | n2=en:encephalopathic episodes, often associated with infection | rel=r_associated | relid=0 | w=10
  1569. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy
    n1=DYNC2H1 gene | n2=en:encephalopathy | rel=r_associated | relid=0 | w=10
  1570. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy (in 1 patient)
    n1=DYNC2H1 gene | n2=en:encephalopathy (in 1 patient) | rel=r_associated | relid=0 | w=10
  1571. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy (in some patients)
    n1=DYNC2H1 gene | n2=en:encephalopathy (in some patients) | rel=r_associated | relid=0 | w=10
  1572. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy associated with hypoglycemia
    n1=DYNC2H1 gene | n2=en:encephalopathy associated with hypoglycemia | rel=r_associated | relid=0 | w=10
  1573. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy during episodes
    n1=DYNC2H1 gene | n2=en:encephalopathy during episodes | rel=r_associated | relid=0 | w=10
  1574. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy, acute-onset
    n1=DYNC2H1 gene | n2=en:encephalopathy, acute-onset | rel=r_associated | relid=0 | w=10
  1575. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy, acute, episodic
    n1=DYNC2H1 gene | n2=en:encephalopathy, acute, episodic | rel=r_associated | relid=0 | w=10
  1576. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy, acute, sudden-onset after febrile illness
    n1=DYNC2H1 gene | n2=en:encephalopathy, acute, sudden-onset after febrile illness | rel=r_associated | relid=0 | w=10
  1577. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy, acute, sudden-onset during febrile illness
    n1=DYNC2H1 gene | n2=en:encephalopathy, acute, sudden-onset during febrile illness | rel=r_associated | relid=0 | w=10
  1578. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy, episodic
    n1=DYNC2H1 gene | n2=en:encephalopathy, episodic | rel=r_associated | relid=0 | w=10
  1579. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy, episodic, associated with febrile illnesses
    n1=DYNC2H1 gene | n2=en:encephalopathy, episodic, associated with febrile illnesses | rel=r_associated | relid=0 | w=10
  1580. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:encephalopathy, severe, neonatal
    n1=DYNC2H1 gene | n2=en:encephalopathy, severe, neonatal | rel=r_associated | relid=0 | w=10
  1581. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:end-position nystagmus
    n1=DYNC2H1 gene | n2=en:end-position nystagmus | rel=r_associated | relid=0 | w=10
  1582. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:endothelial intracytoplasmic globular inclusions
    n1=DYNC2H1 gene | n2=en:endothelial intracytoplasmic globular inclusions | rel=r_associated | relid=0 | w=10
  1583. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enhancement of the c-reflex
    n1=DYNC2H1 gene | n2=en:enhancement of the c-reflex | rel=r_associated | relid=0 | w=10
  1584. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged cerebellar cistern
    n1=DYNC2H1 gene | n2=en:enlarged cerebellar cistern | rel=r_associated | relid=0 | w=10
  1585. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged cerebellum
    n1=DYNC2H1 gene | n2=en:enlarged cerebellum | rel=r_associated | relid=0 | w=10
  1586. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged cisterna magna
    n1=DYNC2H1 gene | n2=en:enlarged cisterna magna | rel=r_associated | relid=0 | w=10
  1587. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged cisterna magna (in some patients)
    n1=DYNC2H1 gene | n2=en:enlarged cisterna magna (in some patients) | rel=r_associated | relid=0 | w=10
  1588. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged corpus callosum
    n1=DYNC2H1 gene | n2=en:enlarged corpus callosum | rel=r_associated | relid=0 | w=10
  1589. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged extraaxial space on brain imaging
    n1=DYNC2H1 gene | n2=en:enlarged extraaxial space on brain imaging | rel=r_associated | relid=0 | w=10
  1590. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged fourth ventricle, mild
    n1=DYNC2H1 gene | n2=en:enlarged fourth ventricle, mild | rel=r_associated | relid=0 | w=10
  1591. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged lateral and third ventricles
    n1=DYNC2H1 gene | n2=en:enlarged lateral and third ventricles | rel=r_associated | relid=0 | w=10
  1592. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged lateral ventricles (occipital>frontal)
    n1=DYNC2H1 gene | n2=en:enlarged lateral ventricles (occipital>frontal) | rel=r_associated | relid=0 | w=10
  1593. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged motor unit action potentials
    n1=DYNC2H1 gene | n2=en:enlarged motor unit action potentials | rel=r_associated | relid=0 | w=10
  1594. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged or prominent ventricles (in some patients)
    n1=DYNC2H1 gene | n2=en:enlarged or prominent ventricles (in some patients) | rel=r_associated | relid=0 | w=10
  1595. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged ventricles (1 patient)
    n1=DYNC2H1 gene | n2=en:enlarged ventricles (1 patient) | rel=r_associated | relid=0 | w=10
  1596. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged ventricles (in some patients)
    n1=DYNC2H1 gene | n2=en:enlarged ventricles (in some patients) | rel=r_associated | relid=0 | w=10
  1597. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged ventricles (in some)
    n1=DYNC2H1 gene | n2=en:enlarged ventricles (in some) | rel=r_associated | relid=0 | w=10
  1598. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enlarged white matter
    n1=DYNC2H1 gene | n2=en:enlarged white matter | rel=r_associated | relid=0 | w=10
  1599. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:enteric nervous system
    n1=DYNC2H1 gene | n2=en:enteric nervous system | rel=r_associated | relid=0 | w=10
  1600. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:entire autonomic nervous system
    n1=DYNC2H1 gene | n2=en:entire autonomic nervous system | rel=r_associated | relid=0 | w=10
  1601. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:entire central nervous system
    n1=DYNC2H1 gene | n2=en:entire central nervous system | rel=r_associated | relid=0 | w=10
  1602. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions
    n1=DYNC2H1 gene | n2=en:eosinophilic 'cotton wool' plaques without dense congophilic core in various brain regions | rel=r_associated | relid=0 | w=10
  1603. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsia partialis continua
    n1=DYNC2H1 gene | n2=en:epilepsia partialis continua | rel=r_associated | relid=0 | w=10
  1604. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsies, myoclonic
    n1=DYNC2H1 gene | n2=en:epilepsies, myoclonic | rel=r_associated | relid=0 | w=10
  1605. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsy (in 2 of 3 patients)
    n1=DYNC2H1 gene | n2=en:epilepsy (in 2 of 3 patients) | rel=r_associated | relid=0 | w=10
  1606. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsy (in some patients)
    n1=DYNC2H1 gene | n2=en:epilepsy (in some patients) | rel=r_associated | relid=0 | w=10
  1607. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsy, frontal lobe
    n1=DYNC2H1 gene | n2=en:epilepsy, frontal lobe | rel=r_associated | relid=0 | w=10
  1608. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsy, multifocal, intractable
    n1=DYNC2H1 gene | n2=en:epilepsy, multifocal, intractable | rel=r_associated | relid=0 | w=10
  1609. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsy, myoclonic astatic
    n1=DYNC2H1 gene | n2=en:epilepsy, myoclonic astatic | rel=r_associated | relid=0 | w=10
  1610. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsy, refractory (onset in adolescence or young adulthood)
    n1=DYNC2H1 gene | n2=en:epilepsy, refractory (onset in adolescence or young adulthood) | rel=r_associated | relid=0 | w=10
  1611. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsy, rolandic
    n1=DYNC2H1 gene | n2=en:epilepsy, rolandic | rel=r_associated | relid=0 | w=10
  1612. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epilepsy, temporal lobe
    n1=DYNC2H1 gene | n2=en:epilepsy, temporal lobe | rel=r_associated | relid=0 | w=10
  1613. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epileptic drop attack
    n1=DYNC2H1 gene | n2=en:epileptic drop attack | rel=r_associated | relid=0 | w=10
  1614. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epileptic encephalopathy
    n1=DYNC2H1 gene | n2=en:epileptic encephalopathy | rel=r_associated | relid=0 | w=10
  1615. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epileptic encephalopathy (in 2 of 3 patients)
    n1=DYNC2H1 gene | n2=en:epileptic encephalopathy (in 2 of 3 patients) | rel=r_associated | relid=0 | w=10
  1616. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epileptic encephalopathy (in some patients)
    n1=DYNC2H1 gene | n2=en:epileptic encephalopathy (in some patients) | rel=r_associated | relid=0 | w=10
  1617. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:epileptic encephalopathy with psychomotor retardation (rare)
    n1=DYNC2H1 gene | n2=en:epileptic encephalopathy with psychomotor retardation (rare) | rel=r_associated | relid=0 | w=10
  1618. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodes begin with muscle tightening
    n1=DYNC2H1 gene | n2=en:episodes begin with muscle tightening | rel=r_associated | relid=0 | w=10
  1619. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodes last up to 2 minutes
    n1=DYNC2H1 gene | n2=en:episodes last up to 2 minutes | rel=r_associated | relid=0 | w=10
  1620. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodes may last less than 30 minutes or greater than several hours
    n1=DYNC2H1 gene | n2=en:episodes may last less than 30 minutes or greater than several hours | rel=r_associated | relid=0 | w=10
  1621. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodes of decreased alertness, hypotonia, and poor respiration requiring mechanical ventilation
    n1=DYNC2H1 gene | n2=en:episodes of decreased alertness, hypotonia, and poor respiration requiring mechanical ventilation | rel=r_associated | relid=0 | w=10
  1622. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodes of weakness can last 1 day to several weeks and can occur 1-3 times per month
    n1=DYNC2H1 gene | 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=10
  1623. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodes typically occur several times a week
    n1=DYNC2H1 gene | n2=en:episodes typically occur several times a week | rel=r_associated | relid=0 | w=10
  1624. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodic absence-like spells
    n1=DYNC2H1 gene | n2=en:episodic absence-like spells | rel=r_associated | relid=0 | w=10
  1625. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodic acute neurologic deterioration/encephalopathy, recurrent
    n1=DYNC2H1 gene | n2=en:episodic acute neurologic deterioration/encephalopathy, recurrent | rel=r_associated | relid=0 | w=10
  1626. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodic ataxia
    n1=DYNC2H1 gene | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=10
  1627. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodic confusion
    n1=DYNC2H1 gene | n2=en:episodic confusion | rel=r_associated | relid=0 | w=10
  1628. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodic generalized skeletal muscle contractions
    n1=DYNC2H1 gene | n2=en:episodic generalized skeletal muscle contractions | rel=r_associated | relid=0 | w=10
  1629. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodic hemiplegia
    n1=DYNC2H1 gene | n2=en:episodic hemiplegia | rel=r_associated | relid=0 | w=10
  1630. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodic subtype, headaches occur in clusters
    n1=DYNC2H1 gene | n2=en:episodic subtype, headaches occur in clusters | rel=r_associated | relid=0 | w=10
  1631. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodic sudden headache
    n1=DYNC2H1 gene | n2=en:episodic sudden headache | rel=r_associated | relid=0 | w=10
  1632. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:episodic vomiting
    n1=DYNC2H1 gene | n2=en:episodic vomiting | rel=r_associated | relid=0 | w=10
  1633. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:equivocal plantar response
    n1=DYNC2H1 gene | n2=en:equivocal plantar response | rel=r_associated | relid=0 | w=10
  1634. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:essential tremor
    n1=DYNC2H1 gene | n2=en:essential tremor | rel=r_associated | relid=0 | w=10
  1635. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:essential tremor (1 family)
    n1=DYNC2H1 gene | n2=en:essential tremor (1 family) | rel=r_associated | relid=0 | w=10
  1636. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:evolution to severe encephalopathy
    n1=DYNC2H1 gene | n2=en:evolution to severe encephalopathy | rel=r_associated | relid=0 | w=10
  1637. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:exaggerated acoustic startle response
    n1=DYNC2H1 gene | n2=en:exaggerated acoustic startle response | rel=r_associated | relid=0 | w=10
  1638. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:exaggerated moro reflex
    n1=DYNC2H1 gene | n2=en:exaggerated moro reflex | rel=r_associated | relid=0 | w=10
  1639. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:exaggerated startle response
    n1=DYNC2H1 gene | n2=en:exaggerated startle response | rel=r_associated | relid=0 | w=10
  1640. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:exaggerated startle response to tactile or acoustic stimuli
    n1=DYNC2H1 gene | n2=en:exaggerated startle response to tactile or acoustic stimuli | rel=r_associated | relid=0 | w=10
  1641. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:excessive daytime somnolence
    n1=DYNC2H1 gene | n2=en:excessive daytime somnolence | rel=r_associated | relid=0 | w=10
  1642. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:expressive aphasia
    n1=DYNC2H1 gene | n2=en:expressive aphasia | rel=r_associated | relid=0 | w=10
  1643. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:expressive language delay
    n1=DYNC2H1 gene | n2=en:expressive language delay | rel=r_associated | relid=0 | w=10
  1644. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:expressive language disorder
    n1=DYNC2H1 gene | n2=en:expressive language disorder | rel=r_associated | relid=0 | w=10
  1645. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:expressive speech absent
    n1=DYNC2H1 gene | n2=en:expressive speech absent | rel=r_associated | relid=0 | w=10
  1646. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:expressive speech deficit
    n1=DYNC2H1 gene | n2=en:expressive speech deficit | rel=r_associated | relid=0 | w=10
  1647. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensive melanosis of leptomeninges, amygdala, and cerebellar hemispheres
    n1=DYNC2H1 gene | n2=en:extensive melanosis of leptomeninges, amygdala, and cerebellar hemispheres | rel=r_associated | relid=0 | w=10
  1648. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensor plantar responses (1 family)
    n1=DYNC2H1 gene | n2=en:extensor plantar responses (1 family) | rel=r_associated | relid=0 | w=10
  1649. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensor plantar responses (1 patient)
    n1=DYNC2H1 gene | n2=en:extensor plantar responses (1 patient) | rel=r_associated | relid=0 | w=10
  1650. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensor plantar responses (early-on)
    n1=DYNC2H1 gene | n2=en:extensor plantar responses (early-on) | rel=r_associated | relid=0 | w=10
  1651. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensor plantar responses (in some patients)
    n1=DYNC2H1 gene | n2=en:extensor plantar responses (in some patients) | rel=r_associated | relid=0 | w=10
  1652. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensor plantar responses (later)
    n1=DYNC2H1 gene | n2=en:extensor plantar responses (later) | rel=r_associated | relid=0 | w=10
  1653. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensor plantar responses (reported in 1 family)
    n1=DYNC2H1 gene | n2=en:extensor plantar responses (reported in 1 family) | rel=r_associated | relid=0 | w=10
  1654. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensor plantar responses (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:extensor plantar responses (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  1655. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensor plantar responses (variable)
    n1=DYNC2H1 gene | n2=en:extensor plantar responses (variable) | rel=r_associated | relid=0 | w=10
  1656. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extensor posturing
    n1=DYNC2H1 gene | n2=en:extensor posturing | rel=r_associated | relid=0 | w=10
  1657. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:external capsule and claustrum may be involved
    n1=DYNC2H1 gene | n2=en:external capsule and claustrum may be involved | rel=r_associated | relid=0 | w=10
  1658. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extra superior temporal gyrus (female)
    n1=DYNC2H1 gene | n2=en:extra superior temporal gyrus (female) | rel=r_associated | relid=0 | w=10
  1659. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions
    n1=DYNC2H1 gene | n2=en:extraneuronal accumulation of autofluorescent pigmented material in various brain regions | rel=r_associated | relid=0 | w=10
  1660. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal disorder
    n1=DYNC2H1 gene | n2=en:extrapyramidal disorder | rel=r_associated | relid=0 | w=10
  1661. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal dyskinesia
    n1=DYNC2H1 gene | n2=en:extrapyramidal dyskinesia | rel=r_associated | relid=0 | w=10
  1662. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal dyskinesias (1 patient)
    n1=DYNC2H1 gene | n2=en:extrapyramidal dyskinesias (1 patient) | rel=r_associated | relid=0 | w=10
  1663. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal features
    n1=DYNC2H1 gene | n2=en:extrapyramidal features | rel=r_associated | relid=0 | w=10
  1664. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal muscular rigidity
    n1=DYNC2H1 gene | n2=en:extrapyramidal muscular rigidity | rel=r_associated | relid=0 | w=10
  1665. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal sign
    n1=DYNC2H1 gene | n2=en:extrapyramidal sign | rel=r_associated | relid=0 | w=10
  1666. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal signs (in 1 patient)
    n1=DYNC2H1 gene | n2=en:extrapyramidal signs (in 1 patient) | rel=r_associated | relid=0 | w=10
  1667. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal signs (in some patients) thinning of the corpus callosum
    n1=DYNC2H1 gene | n2=en:extrapyramidal signs (in some patients) thinning of the corpus callosum | rel=r_associated | relid=0 | w=10
  1668. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal signs (less common)
    n1=DYNC2H1 gene | n2=en:extrapyramidal signs (less common) | rel=r_associated | relid=0 | w=10
  1669. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal signs may develop
    n1=DYNC2H1 gene | n2=en:extrapyramidal signs may develop | rel=r_associated | relid=0 | w=10
  1670. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal signs, mild
    n1=DYNC2H1 gene | n2=en:extrapyramidal signs, mild | rel=r_associated | relid=0 | w=10
  1671. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal symptoms (later-onset)
    n1=DYNC2H1 gene | n2=en:extrapyramidal symptoms (later-onset) | rel=r_associated | relid=0 | w=10
  1672. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extrapyramidal symptoms may occur
    n1=DYNC2H1 gene | n2=en:extrapyramidal symptoms may occur | rel=r_associated | relid=0 | w=10
  1673. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:extremity ataxia
    n1=DYNC2H1 gene | n2=en:extremity ataxia | rel=r_associated | relid=0 | w=10
  1674. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:eye
    n1=DYNC2H1 gene | n2=en:eye | rel=r_associated | relid=0 | w=10
  1675. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial muscle sparing
    n1=DYNC2H1 gene | n2=en:facial muscle sparing | rel=r_associated | relid=0 | w=10
  1676. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial muscle weakness
    n1=DYNC2H1 gene | n2=en:facial muscle weakness | rel=r_associated | relid=0 | w=10
  1677. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial muscle weakness of muscles innervated by cn vii
    n1=DYNC2H1 gene | n2=en:facial muscle weakness of muscles innervated by cn vii | rel=r_associated | relid=0 | w=10
  1678. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial myokymia, mild
    n1=DYNC2H1 gene | n2=en:facial myokymia, mild | rel=r_associated | relid=0 | w=10
  1679. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial myokymias
    n1=DYNC2H1 gene | n2=en:facial myokymias | rel=r_associated | relid=0 | w=10
  1680. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial nerve palsy
    n1=DYNC2H1 gene | n2=en:facial nerve palsy | rel=r_associated | relid=0 | w=10
  1681. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial nerve weakness
    n1=DYNC2H1 gene | n2=en:facial nerve weakness | rel=r_associated | relid=0 | w=10
  1682. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial palsy secondary to cranial hyperostosis
    n1=DYNC2H1 gene | n2=en:facial palsy secondary to cranial hyperostosis | rel=r_associated | relid=0 | w=10
  1683. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial paralysis
    n1=DYNC2H1 gene | n2=en:facial paralysis | rel=r_associated | relid=0 | w=10
  1684. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial paresis, congenital bilateral
    n1=DYNC2H1 gene | n2=en:facial paresis, congenital bilateral | rel=r_associated | relid=0 | w=10
  1685. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial-faucial-finger mini-myoclonus (fff)
    n1=DYNC2H1 gene | n2=en:facial-faucial-finger mini-myoclonus (fff) | rel=r_associated | relid=0 | w=10
  1686. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial-lingual fasciculations
    n1=DYNC2H1 gene | n2=en:facial-lingual fasciculations | rel=r_associated | relid=0 | w=10
  1687. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:facial, pharyngeal, and masticatory muscle diplegia
    n1=DYNC2H1 gene | n2=en:facial, pharyngeal, and masticatory muscle diplegia | rel=r_associated | relid=0 | w=10
  1688. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:faciomandibular myoclonus, nocturnal
    n1=DYNC2H1 gene | n2=en:faciomandibular myoclonus, nocturnal | rel=r_associated | relid=0 | w=10
  1689. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:failure of opercularization of the frontal and temporal lobes on ct
    n1=DYNC2H1 gene | n2=en:failure of opercularization of the frontal and temporal lobes on ct | rel=r_associated | relid=0 | w=10
  1690. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:failure to achieve sitting or walking (severe form)
    n1=DYNC2H1 gene | n2=en:failure to achieve sitting or walking (severe form) | rel=r_associated | relid=0 | w=10
  1691. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fall
    n1=DYNC2H1 gene | n2=en:fall | rel=r_associated | relid=0 | w=10
  1692. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:falx cerebri, precocious calcification of
    n1=DYNC2H1 gene | n2=en:falx cerebri, precocious calcification of | rel=r_associated | relid=0 | w=10
  1693. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:familial dysautonomia
    n1=DYNC2H1 gene | n2=en:familial dysautonomia | rel=r_associated | relid=0 | w=10
  1694. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fasciculation
    n1=DYNC2H1 gene | n2=en:fasciculation | rel=r_associated | relid=0 | w=10
  1695. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fasciculation-like movements
    n1=DYNC2H1 gene | n2=en:fasciculation-like movements | rel=r_associated | relid=0 | w=10
  1696. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fasciculations (after long disease duration)
    n1=DYNC2H1 gene | n2=en:fasciculations (after long disease duration) | rel=r_associated | relid=0 | w=10
  1697. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fasciculations, tongue
    n1=DYNC2H1 gene | n2=en:fasciculations, tongue | rel=r_associated | relid=0 | w=10
  1698. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fatal familial insomnia
    n1=DYNC2H1 gene | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=10
  1699. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fatal subacute encephalopathy (1 family)
    n1=DYNC2H1 gene | n2=en:fatal subacute encephalopathy (1 family) | rel=r_associated | relid=0 | w=10
  1700. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fatigue
    n1=DYNC2H1 gene | n2=en:fatigue | rel=r_associated | relid=0 | w=10
  1701. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:favorable response to levodopa
    n1=DYNC2H1 gene | n2=en:favorable response to levodopa | rel=r_associated | relid=0 | w=10
  1702. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fearful expression
    n1=DYNC2H1 gene | n2=en:fearful expression | rel=r_associated | relid=0 | w=10
  1703. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:febrile seizure
    n1=DYNC2H1 gene | n2=en:febrile seizure | rel=r_associated | relid=0 | w=10
  1704. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:febrile seizures (1 patient)
    n1=DYNC2H1 gene | n2=en:febrile seizures (1 patient) | rel=r_associated | relid=0 | w=10
  1705. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:febrile seizures (in some)
    n1=DYNC2H1 gene | n2=en:febrile seizures (in some) | rel=r_associated | relid=0 | w=10
  1706. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:febrile seizures (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:febrile seizures (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  1707. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:febrile seizures (usually remit by age 6 years)
    n1=DYNC2H1 gene | n2=en:febrile seizures (usually remit by age 6 years) | rel=r_associated | relid=0 | w=10
  1708. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:febrile seizures in infancy
    n1=DYNC2H1 gene | n2=en:febrile seizures in infancy | rel=r_associated | relid=0 | w=10
  1709. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:febrile seizures may occur
    n1=DYNC2H1 gene | n2=en:febrile seizures may occur | rel=r_associated | relid=0 | w=10
  1710. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fecal incontinence
    n1=DYNC2H1 gene | n2=en:fecal incontinence | rel=r_associated | relid=0 | w=10
  1711. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:feeding problem
    n1=DYNC2H1 gene | n2=en:feeding problem | rel=r_associated | relid=0 | w=10
  1712. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fenestrated basilar artery
    n1=DYNC2H1 gene | n2=en:fenestrated basilar artery | rel=r_associated | relid=0 | w=10
  1713. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:festinating (parkinsonian) gait
    n1=DYNC2H1 gene | n2=en:festinating (parkinsonian) gait | rel=r_associated | relid=0 | w=10
  1714. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fetal akinesia deformation sequence
    n1=DYNC2H1 gene | n2=en:fetal akinesia deformation sequence | rel=r_associated | relid=0 | w=10
  1715. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fibrillary plaques in the cerebellar cortex
    n1=DYNC2H1 gene | n2=en:fibrillary plaques in the cerebellar cortex | rel=r_associated | relid=0 | w=10
  1716. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fibrillation
    n1=DYNC2H1 gene | n2=en:fibrillation | rel=r_associated | relid=0 | w=10
  1717. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fibrous astrocyte
    n1=DYNC2H1 gene | n2=en:fibrous astrocyte | rel=r_associated | relid=0 | w=10
  1718. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fifth ventricle
    n1=DYNC2H1 gene | n2=en:fifth ventricle | rel=r_associated | relid=0 | w=10
  1719. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fine motor delay
    n1=DYNC2H1 gene | n2=en:fine motor delay | rel=r_associated | relid=0 | w=10
  1720. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fine motor impairment
    n1=DYNC2H1 gene | n2=en:fine motor impairment | rel=r_associated | relid=0 | w=10
  1721. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fine motor skills delayed
    n1=DYNC2H1 gene | n2=en:fine motor skills delayed | rel=r_associated | relid=0 | w=10
  1722. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fine motor task disruption
    n1=DYNC2H1 gene | n2=en:fine motor task disruption | rel=r_associated | relid=0 | w=10
  1723. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fine motor/coordination problems (12%)
    n1=DYNC2H1 gene | n2=en:fine motor/coordination problems (12%) | rel=r_associated | relid=0 | w=10
  1724. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fine rapid hand tremor, 4-12 hz
    n1=DYNC2H1 gene | n2=en:fine rapid hand tremor, 4-12 hz | rel=r_associated | relid=0 | w=10
  1725. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fine tremors
    n1=DYNC2H1 gene | n2=en:fine tremors | rel=r_associated | relid=0 | w=10
  1726. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:finger dysmetria
    n1=DYNC2H1 gene | n2=en:finger dysmetria | rel=r_associated | relid=0 | w=10
  1727. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:finger twitching
    n1=DYNC2H1 gene | n2=en:finger twitching | rel=r_associated | relid=0 | w=10
  1728. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:first bite syndrome
    n1=DYNC2H1 gene | n2=en:first bite syndrome | rel=r_associated | relid=0 | w=10
  1729. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:first dorsal interossei muscle atrophy
    n1=DYNC2H1 gene | n2=en:first dorsal interossei muscle atrophy | rel=r_associated | relid=0 | w=10
  1730. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:first dorsal interossei muscle weakness
    n1=DYNC2H1 gene | n2=en:first dorsal interossei muscle weakness | rel=r_associated | relid=0 | w=10
  1731. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:flaccid dysarthrias
    n1=DYNC2H1 gene | n2=en:flaccid dysarthrias | rel=r_associated | relid=0 | w=10
  1732. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:flaccidity, episodic
    n1=DYNC2H1 gene | n2=en:flaccidity, episodic | rel=r_associated | relid=0 | w=10
  1733. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:flat pons
    n1=DYNC2H1 gene | n2=en:flat pons | rel=r_associated | relid=0 | w=10
  1734. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:flattening of the caudate
    n1=DYNC2H1 gene | n2=en:flattening of the caudate | rel=r_associated | relid=0 | w=10
  1735. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:flattening of the pons
    n1=DYNC2H1 gene | n2=en:flattening of the pons | rel=r_associated | relid=0 | w=10
  1736. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:flexor plantar response
    n1=DYNC2H1 gene | n2=en:flexor plantar response | rel=r_associated | relid=0 | w=10
  1737. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:floppiness
    n1=DYNC2H1 gene | n2=en:floppiness | rel=r_associated | relid=0 | w=10
  1738. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:floppy infant
    n1=DYNC2H1 gene | n2=en:floppy infant | rel=r_associated | relid=0 | w=10
  1739. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fluctuating neurologic signs
    n1=DYNC2H1 gene | n2=en:fluctuating neurologic signs | rel=r_associated | relid=0 | w=10
  1740. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fluctuations in consciousness
    n1=DYNC2H1 gene | n2=en:fluctuations in consciousness | rel=r_associated | relid=0 | w=10
  1741. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fluid filled posterior fossa
    n1=DYNC2H1 gene | n2=en:fluid filled posterior fossa | rel=r_associated | relid=0 | w=10
  1742. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> 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=DYNC2H1 gene | 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=10
  1743. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal cerebellar dysplasia
    n1=DYNC2H1 gene | n2=en:focal cerebellar dysplasia | rel=r_associated | relid=0 | w=10
  1744. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal clonic seizure
    n1=DYNC2H1 gene | n2=en:focal clonic seizure | rel=r_associated | relid=0 | w=10
  1745. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal cortical dysplasia
    n1=DYNC2H1 gene | n2=en:focal cortical dysplasia | rel=r_associated | relid=0 | w=10
  1746. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal discharges
    n1=DYNC2H1 gene | n2=en:focal discharges | rel=r_associated | relid=0 | w=10
  1747. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal dyscognitive seizures
    n1=DYNC2H1 gene | n2=en:focal dyscognitive seizures | rel=r_associated | relid=0 | w=10
  1748. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal dystonia (adult onset)
    n1=DYNC2H1 gene | n2=en:focal dystonia (adult onset) | rel=r_associated | relid=0 | w=10
  1749. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal dystonia (e.g., writer's cramp)
    n1=DYNC2H1 gene | n2=en:focal dystonia (e.g., writer's cramp) | rel=r_associated | relid=0 | w=10
  1750. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal dystonia (rare)
    n1=DYNC2H1 gene | n2=en:focal dystonia (rare) | rel=r_associated | relid=0 | w=10
  1751. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal dystonia, upper limb
    n1=DYNC2H1 gene | n2=en:focal dystonia, upper limb | rel=r_associated | relid=0 | w=10
  1752. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal dystonia, usually of the hands
    n1=DYNC2H1 gene | n2=en:focal dystonia, usually of the hands | rel=r_associated | relid=0 | w=10
  1753. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal dystonias
    n1=DYNC2H1 gene | n2=en:focal dystonias | rel=r_associated | relid=0 | w=10
  1754. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal hyperplasia of the choroid plexus
    n1=DYNC2H1 gene | n2=en:focal hyperplasia of the choroid plexus | rel=r_associated | relid=0 | w=10
  1755. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal interhemispheric fusion
    n1=DYNC2H1 gene | n2=en:focal interhemispheric fusion | rel=r_associated | relid=0 | w=10
  1756. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal lissencephaly
    n1=DYNC2H1 gene | n2=en:focal lissencephaly | rel=r_associated | relid=0 | w=10
  1757. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal microgyria
    n1=DYNC2H1 gene | n2=en:focal microgyria | rel=r_associated | relid=0 | w=10
  1758. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal neurologic deficit
    n1=DYNC2H1 gene | n2=en:focal neurologic deficit | rel=r_associated | relid=0 | w=10
  1759. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal neurologic deficits (i.e., hemiparesis)
    n1=DYNC2H1 gene | n2=en:focal neurologic deficits (i.e., hemiparesis) | rel=r_associated | relid=0 | w=10
  1760. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal neurologic signs
    n1=DYNC2H1 gene | n2=en:focal neurologic signs | rel=r_associated | relid=0 | w=10
  1761. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal nodular heterotopia
    n1=DYNC2H1 gene | n2=en:focal nodular heterotopia | rel=r_associated | relid=0 | w=10
  1762. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal pachygyria
    n1=DYNC2H1 gene | n2=en:focal pachygyria | rel=r_associated | relid=0 | w=10
  1763. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal parietal pachygyria
    n1=DYNC2H1 gene | n2=en:focal parietal pachygyria | rel=r_associated | relid=0 | w=10
  1764. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal paroxysmal discharges
    n1=DYNC2H1 gene | n2=en:focal paroxysmal discharges | rel=r_associated | relid=0 | w=10
  1765. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal thickening of the cortex on mri (in type iib)
    n1=DYNC2H1 gene | n2=en:focal thickening of the cortex on mri (in type iib) | rel=r_associated | relid=0 | w=10
  1766. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal tremor
    n1=DYNC2H1 gene | n2=en:focal tremor | rel=r_associated | relid=0 | w=10
  1767. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal white matter lesions (in type iib)
    n1=DYNC2H1 gene | n2=en:focal white matter lesions (in type iib) | rel=r_associated | relid=0 | w=10
  1768. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:focal, segmental or multifocal dystonia
    n1=DYNC2H1 gene | n2=en:focal, segmental or multifocal dystonia | rel=r_associated | relid=0 | w=10
  1769. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:foot-drop
    n1=DYNC2H1 gene | n2=en:foot-drop | rel=r_associated | relid=0 | w=10
  1770. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:forebrain defects
    n1=DYNC2H1 gene | n2=en:forebrain defects | rel=r_associated | relid=0 | w=10
  1771. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:four-repeat tau plaques in the striatum
    n1=DYNC2H1 gene | n2=en:four-repeat tau plaques in the striatum | rel=r_associated | relid=0 | w=10
  1772. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frequency 3.5 hz in midline
    n1=DYNC2H1 gene | n2=en:frequency 3.5 hz in midline | rel=r_associated | relid=0 | w=10
  1773. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frequency 6 hz in lateral gaze
    n1=DYNC2H1 gene | n2=en:frequency 6 hz in lateral gaze | rel=r_associated | relid=0 | w=10
  1774. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frequency of 1 to 20 episodes per day
    n1=DYNC2H1 gene | n2=en:frequency of 1 to 20 episodes per day | rel=r_associated | relid=0 | w=10
  1775. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frequent falls
    n1=DYNC2H1 gene | n2=en:frequent falls | rel=r_associated | relid=0 | w=10
  1776. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frequent falls with preservation of consciousness
    n1=DYNC2H1 gene | n2=en:frequent falls with preservation of consciousness | rel=r_associated | relid=0 | w=10
  1777. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frequent headache
    n1=DYNC2H1 gene | n2=en:frequent headache | rel=r_associated | relid=0 | w=10
  1778. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frightening sensation
    n1=DYNC2H1 gene | n2=en:frightening sensation | rel=r_associated | relid=0 | w=10
  1779. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontal cortical atophy
    n1=DYNC2H1 gene | n2=en:frontal cortical atophy | rel=r_associated | relid=0 | w=10
  1780. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontal lobe atrophy
    n1=DYNC2H1 gene | n2=en:frontal lobe atrophy | rel=r_associated | relid=0 | w=10
  1781. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontal lobe hypoplasia
    n1=DYNC2H1 gene | n2=en:frontal lobe hypoplasia | rel=r_associated | relid=0 | w=10
  1782. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontal lobe origin
    n1=DYNC2H1 gene | n2=en:frontal lobe origin | rel=r_associated | relid=0 | w=10
  1783. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontal lobe syndrome
    n1=DYNC2H1 gene | n2=en:frontal lobe syndrome | rel=r_associated | relid=0 | w=10
  1784. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontal release signs
    n1=DYNC2H1 gene | n2=en:frontal release signs | rel=r_associated | relid=0 | w=10
  1785. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontolimbic dementia
    n1=DYNC2H1 gene | n2=en:frontolimbic dementia | rel=r_associated | relid=0 | w=10
  1786. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontoparietal polymicrogyria
    n1=DYNC2H1 gene | n2=en:frontoparietal polymicrogyria | rel=r_associated | relid=0 | w=10
  1787. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal atrophy
    n1=DYNC2H1 gene | n2=en:frontotemporal atrophy | rel=r_associated | relid=0 | w=10
  1788. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal atrophy, mild, seen on mri
    n1=DYNC2H1 gene | n2=en:frontotemporal atrophy, mild, seen on mri | rel=r_associated | relid=0 | w=10
  1789. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal dementia
    n1=DYNC2H1 gene | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=10
  1790. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal dementia (1 patient)
    n1=DYNC2H1 gene | n2=en:frontotemporal dementia (1 patient) | rel=r_associated | relid=0 | w=10
  1791. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal dementia (in 30% of patients)
    n1=DYNC2H1 gene | n2=en:frontotemporal dementia (in 30% of patients) | rel=r_associated | relid=0 | w=10
  1792. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal dementia, variable severity
    n1=DYNC2H1 gene | n2=en:frontotemporal dementia, variable severity | rel=r_associated | relid=0 | w=10
  1793. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal hypoplasia
    n1=DYNC2H1 gene | n2=en:frontotemporal hypoplasia | rel=r_associated | relid=0 | w=10
  1794. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal leukoencephalopathy
    n1=DYNC2H1 gene | n2=en:frontotemporal leukoencephalopathy | rel=r_associated | relid=0 | w=10
  1795. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal lobar atrophy
    n1=DYNC2H1 gene | n2=en:frontotemporal lobar atrophy | rel=r_associated | relid=0 | w=10
  1796. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal lobar atrophy with 'knife-edge' distinction
    n1=DYNC2H1 gene | n2=en:frontotemporal lobar atrophy with 'knife-edge' distinction | rel=r_associated | relid=0 | w=10
  1797. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal pachygyria (1 patient)
    n1=DYNC2H1 gene | n2=en:frontotemporal pachygyria (1 patient) | rel=r_associated | relid=0 | w=10
  1798. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal polymicrogyria
    n1=DYNC2H1 gene | n2=en:frontotemporal polymicrogyria | rel=r_associated | relid=0 | w=10
  1799. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporal/subcortical dementia
    n1=DYNC2H1 gene | n2=en:frontotemporal/subcortical dementia | rel=r_associated | relid=0 | w=10
  1800. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:frontotemporoparietal cortical dysplasia
    n1=DYNC2H1 gene | n2=en:frontotemporoparietal cortical dysplasia | rel=r_associated | relid=0 | w=10
  1801. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients)
    n1=DYNC2H1 gene | n2=en:funnel-shaped signal tapering from subcortical white matter to ventricle (in some type iib patients) | rel=r_associated | relid=0 | w=10
  1802. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fused hemispheres (wws)
    n1=DYNC2H1 gene | n2=en:fused hemispheres (wws) | rel=r_associated | relid=0 | w=10
  1803. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fusion of the basal ganglia
    n1=DYNC2H1 gene | n2=en:fusion of the basal ganglia | rel=r_associated | relid=0 | w=10
  1804. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fusion of the cerebellar hemispheres
    n1=DYNC2H1 gene | n2=en:fusion of the cerebellar hemispheres | rel=r_associated | relid=0 | w=10
  1805. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fusion of the dentate nuclei and the superior cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:fusion of the dentate nuclei and the superior cerebellar peduncles | rel=r_associated | relid=0 | w=10
  1806. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:fusion of the left and right thalami
    n1=DYNC2H1 gene | n2=en:fusion of the left and right thalami | rel=r_associated | relid=0 | w=10
  1807. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait abnormalities (in some patients)
    n1=DYNC2H1 gene | n2=en:gait abnormalities (in some patients) | rel=r_associated | relid=0 | w=10
  1808. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait abnormalities (less common)
    n1=DYNC2H1 gene | n2=en:gait abnormalities (less common) | rel=r_associated | relid=0 | w=10
  1809. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait abnormalities due to muscle weakness
    n1=DYNC2H1 gene | n2=en:gait abnormalities due to muscle weakness | rel=r_associated | relid=0 | w=10
  1810. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait abnormalities may occur
    n1=DYNC2H1 gene | n2=en:gait abnormalities may occur | rel=r_associated | relid=0 | w=10
  1811. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait and limb ataxia
    n1=DYNC2H1 gene | n2=en:gait and limb ataxia | rel=r_associated | relid=0 | w=10
  1812. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait apraxia
    n1=DYNC2H1 gene | n2=en:gait apraxia | rel=r_associated | relid=0 | w=10
  1813. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait ataxia (in some patients)
    n1=DYNC2H1 gene | n2=en:gait ataxia (in some patients) | rel=r_associated | relid=0 | w=10
  1814. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait ataxias, cerebellar
    n1=DYNC2H1 gene | n2=en:gait ataxias, cerebellar | rel=r_associated | relid=0 | w=10
  1815. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait difficulties due to contractures of the lower limbs
    n1=DYNC2H1 gene | n2=en:gait difficulties due to contractures of the lower limbs | rel=r_associated | relid=0 | w=10
  1816. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait difficulties, late-onset
    n1=DYNC2H1 gene | n2=en:gait difficulties, late-onset | rel=r_associated | relid=0 | w=10
  1817. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait disability
    n1=DYNC2H1 gene | n2=en:gait disability | rel=r_associated | relid=0 | w=10
  1818. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait disturbance
    n1=DYNC2H1 gene | n2=en:gait disturbance | rel=r_associated | relid=0 | w=10
  1819. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait disturbance (ataxia)
    n1=DYNC2H1 gene | n2=en:gait disturbance (ataxia) | rel=r_associated | relid=0 | w=10
  1820. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait imbalance
    n1=DYNC2H1 gene | n2=en:gait imbalance | rel=r_associated | relid=0 | w=10
  1821. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait impairment
    n1=DYNC2H1 gene | n2=en:gait impairment | rel=r_associated | relid=0 | w=10
  1822. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait impairment (55%)
    n1=DYNC2H1 gene | n2=en:gait impairment (55%) | rel=r_associated | relid=0 | w=10
  1823. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait instability, worse in the dark
    n1=DYNC2H1 gene | n2=en:gait instability, worse in the dark | rel=r_associated | relid=0 | w=10
  1824. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait unsteady
    n1=DYNC2H1 gene | n2=en:gait unsteady | rel=r_associated | relid=0 | w=10
  1825. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait, drop foot
    n1=DYNC2H1 gene | n2=en:gait, drop foot | rel=r_associated | relid=0 | w=10
  1826. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gait, rigid
    n1=DYNC2H1 gene | n2=en:gait, rigid | rel=r_associated | relid=0 | w=10
  1827. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gastroparesis due to diabetes mellitus
    n1=DYNC2H1 gene | n2=en:gastroparesis due to diabetes mellitus | rel=r_associated | relid=0 | w=10
  1828. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gaze deviation
    n1=DYNC2H1 gene | n2=en:gaze deviation | rel=r_associated | relid=0 | w=10
  1829. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized amyotrophy
    n1=DYNC2H1 gene | n2=en:generalized amyotrophy | rel=r_associated | relid=0 | w=10
  1830. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized and focal spike and wave complexes seen on eeg
    n1=DYNC2H1 gene | n2=en:generalized and focal spike and wave complexes seen on eeg | rel=r_associated | relid=0 | w=10
  1831. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized cerebral hypoplasia/atrophy (45%)
    n1=DYNC2H1 gene | n2=en:generalized cerebral hypoplasia/atrophy (45%) | rel=r_associated | relid=0 | w=10
  1832. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized cerebral, cerebellar, and brainstem atrophy, progressive
    n1=DYNC2H1 gene | n2=en:generalized cerebral, cerebellar, and brainstem atrophy, progressive | rel=r_associated | relid=0 | w=10
  1833. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized clonic or tonic-clonic seizures
    n1=DYNC2H1 gene | n2=en:generalized clonic or tonic-clonic seizures | rel=r_associated | relid=0 | w=10
  1834. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized cortical atrophy (in one patient)
    n1=DYNC2H1 gene | n2=en:generalized cortical atrophy (in one patient) | rel=r_associated | relid=0 | w=10
  1835. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized cortical atrophy, most prominent in the frontal and parietal lobes
    n1=DYNC2H1 gene | n2=en:generalized cortical atrophy, most prominent in the frontal and parietal lobes | rel=r_associated | relid=0 | w=10
  1836. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized dystonia
    n1=DYNC2H1 gene | n2=en:generalized dystonia | rel=r_associated | relid=0 | w=10
  1837. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized hypotonia
    n1=DYNC2H1 gene | n2=en:generalized hypotonia | rel=r_associated | relid=0 | w=10
  1838. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized myelin loss
    n1=DYNC2H1 gene | n2=en:generalized myelin loss | rel=r_associated | relid=0 | w=10
  1839. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized seizures
    n1=DYNC2H1 gene | n2=en:generalized seizures | rel=r_associated | relid=0 | w=10
  1840. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized slowing
    n1=DYNC2H1 gene | n2=en:generalized slowing | rel=r_associated | relid=0 | w=10
  1841. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized slowing seen on eeg
    n1=DYNC2H1 gene | n2=en:generalized slowing seen on eeg | rel=r_associated | relid=0 | w=10
  1842. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized spike wave discharges
    n1=DYNC2H1 gene | n2=en:generalized spike wave discharges | rel=r_associated | relid=0 | w=10
  1843. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized spike-wave activity seen on eeg
    n1=DYNC2H1 gene | n2=en:generalized spike-wave activity seen on eeg | rel=r_associated | relid=0 | w=10
  1844. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized spike-wave discharges see on eeg
    n1=DYNC2H1 gene | n2=en:generalized spike-wave discharges see on eeg | rel=r_associated | relid=0 | w=10
  1845. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized stiffening
    n1=DYNC2H1 gene | n2=en:generalized stiffening | rel=r_associated | relid=0 | w=10
  1846. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized tonic-clonic seizures (gtcs) (in most patients)
    n1=DYNC2H1 gene | n2=en:generalized tonic-clonic seizures (gtcs) (in most patients) | rel=r_associated | relid=0 | w=10
  1847. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized tonic-clonic seizures (gtcs) on awakening
    n1=DYNC2H1 gene | n2=en:generalized tonic-clonic seizures (gtcs) on awakening | rel=r_associated | relid=0 | w=10
  1848. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized tonic-clonic seizures (often develop in adolescence)
    n1=DYNC2H1 gene | n2=en:generalized tonic-clonic seizures (often develop in adolescence) | rel=r_associated | relid=0 | w=10
  1849. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized tonic-clonic seizures (rare)
    n1=DYNC2H1 gene | n2=en:generalized tonic-clonic seizures (rare) | rel=r_associated | relid=0 | w=10
  1850. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized tonic-clonic seizures (stage 2 and 3)
    n1=DYNC2H1 gene | n2=en:generalized tonic-clonic seizures (stage 2 and 3) | rel=r_associated | relid=0 | w=10
  1851. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized tonic-clonic seizures in 50%
    n1=DYNC2H1 gene | n2=en:generalized tonic-clonic seizures in 50% | rel=r_associated | relid=0 | w=10
  1852. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:generalized tonic-clonic seizures on awakening
    n1=DYNC2H1 gene | n2=en:generalized tonic-clonic seizures on awakening | rel=r_associated | relid=0 | w=10
  1853. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:germinal cysts over the caudate
    n1=DYNC2H1 gene | n2=en:germinal cysts over the caudate | rel=r_associated | relid=0 | w=10
  1854. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:giant cortical somatosensory evoked potentials (seps)
    n1=DYNC2H1 gene | n2=en:giant cortical somatosensory evoked potentials (seps) | rel=r_associated | relid=0 | w=10
  1855. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:giant granules in schwann cells
    n1=DYNC2H1 gene | n2=en:giant granules in schwann cells | rel=r_associated | relid=0 | w=10
  1856. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gilles de la tourette syndrome (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:gilles de la tourette syndrome (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  1857. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:glial activation
    n1=DYNC2H1 gene | n2=en:glial activation | rel=r_associated | relid=0 | w=10
  1858. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:glial cell
    n1=DYNC2H1 gene | n2=en:glial cell | rel=r_associated | relid=0 | w=10
  1859. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:glial inclusions
    n1=DYNC2H1 gene | n2=en:glial inclusions | rel=r_associated | relid=0 | w=10
  1860. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gliosis
    n1=DYNC2H1 gene | n2=en:gliosis | rel=r_associated | relid=0 | w=10
  1861. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gliosis (27%)
    n1=DYNC2H1 gene | n2=en:gliosis (27%) | rel=r_associated | relid=0 | w=10
  1862. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gliosis (patient a)
    n1=DYNC2H1 gene | n2=en:gliosis (patient a) | rel=r_associated | relid=0 | w=10
  1863. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gliosis in the brainstem
    n1=DYNC2H1 gene | n2=en:gliosis in the brainstem | rel=r_associated | relid=0 | w=10
  1864. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gliosis in the striatum, medial thalamic nuclei, and inferior olives
    n1=DYNC2H1 gene | n2=en:gliosis in the striatum, medial thalamic nuclei, and inferior olives | rel=r_associated | relid=0 | w=10
  1865. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gliosis of the white matter
    n1=DYNC2H1 gene | n2=en:gliosis of the white matter | rel=r_associated | relid=0 | w=10
  1866. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord
    n1=DYNC2H1 gene | n2=en:gliosis, necrosis, neuronal loss in basal ganglia, brainstem, and spinal cord | rel=r_associated | relid=0 | w=10
  1867. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:global and focal neurologic abnormalities (less than 30%)
    n1=DYNC2H1 gene | n2=en:global and focal neurologic abnormalities (less than 30%) | rel=r_associated | relid=0 | w=10
  1868. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:global brain atrophy
    n1=DYNC2H1 gene | n2=en:global brain atrophy | rel=r_associated | relid=0 | w=10
  1869. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:global cerebral atrophy, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:global cerebral atrophy, mild (in some patients) | rel=r_associated | relid=0 | w=10
  1870. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:global developmental delay
    n1=DYNC2H1 gene | n2=en:global developmental delay | rel=r_associated | relid=0 | w=10
  1871. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:global developmental delay if untreated
    n1=DYNC2H1 gene | n2=en:global developmental delay if untreated | rel=r_associated | relid=0 | w=10
  1872. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:global developmental delay, variable severity
    n1=DYNC2H1 gene | n2=en:global developmental delay, variable severity | rel=r_associated | relid=0 | w=10
  1873. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:global hypotonia
    n1=DYNC2H1 gene | n2=en:global hypotonia | rel=r_associated | relid=0 | w=10
  1874. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:global reduction in cerebral blood flow on pet scan
    n1=DYNC2H1 gene | n2=en:global reduction in cerebral blood flow on pet scan | rel=r_associated | relid=0 | w=10
  1875. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:globally delayed development
    n1=DYNC2H1 gene | n2=en:globally delayed development | rel=r_associated | relid=0 | w=10
  1876. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:globular basal ganglia (1 patient)
    n1=DYNC2H1 gene | n2=en:globular basal ganglia (1 patient) | rel=r_associated | relid=0 | w=10
  1877. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:globular thalamus (1 patient)
    n1=DYNC2H1 gene | n2=en:globular thalamus (1 patient) | rel=r_associated | relid=0 | w=10
  1878. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:glomeruloid vascular proliferation in brain and spinal cord
    n1=DYNC2H1 gene | n2=en:glomeruloid vascular proliferation in brain and spinal cord | rel=r_associated | relid=0 | w=10
  1879. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gowers sign
    n1=DYNC2H1 gene | n2=en:gowers sign | rel=r_associated | relid=0 | w=10
  1880. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:grand mal seizure
    n1=DYNC2H1 gene | n2=en:grand mal seizure | rel=r_associated | relid=0 | w=10
  1881. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:granular material in neurons
    n1=DYNC2H1 gene | n2=en:granular material in neurons | rel=r_associated | relid=0 | w=10
  1882. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:granular osmiophilic cytoplasmic deposits in schwann cells
    n1=DYNC2H1 gene | n2=en:granular osmiophilic cytoplasmic deposits in schwann cells | rel=r_associated | relid=0 | w=10
  1883. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:granulovacuolar degeneration
    n1=DYNC2H1 gene | n2=en:granulovacuolar degeneration | rel=r_associated | relid=0 | w=10
  1884. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gray matter
    n1=DYNC2H1 gene | n2=en:gray matter | rel=r_associated | relid=0 | w=10
  1885. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gray matter appears relatively unaffected
    n1=DYNC2H1 gene | n2=en:gray matter appears relatively unaffected | rel=r_associated | relid=0 | w=10
  1886. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gray matter heterotopia (in some patients)
    n1=DYNC2H1 gene | n2=en:gray matter heterotopia (in some patients) | rel=r_associated | relid=0 | w=10
  1887. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gray matter structure of central nervous system
    n1=DYNC2H1 gene | n2=en:gray matter structure of central nervous system | rel=r_associated | relid=0 | w=10
  1888. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:grimaces
    n1=DYNC2H1 gene | n2=en:grimaces | rel=r_associated | relid=0 | w=10
  1889. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gross motor delay
    n1=DYNC2H1 gene | n2=en:gross motor delay | rel=r_associated | relid=0 | w=10
  1890. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gross motor delay (in one family)
    n1=DYNC2H1 gene | n2=en:gross motor delay (in one family) | rel=r_associated | relid=0 | w=10
  1891. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gross motor delay, mild
    n1=DYNC2H1 gene | n2=en:gross motor delay, mild | rel=r_associated | relid=0 | w=10
  1892. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gross motor skill delay (infancy)
    n1=DYNC2H1 gene | n2=en:gross motor skill delay (infancy) | rel=r_associated | relid=0 | w=10
  1893. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gtcs during 'leisure' time (evening)
    n1=DYNC2H1 gene | n2=en:gtcs during 'leisure' time (evening) | rel=r_associated | relid=0 | w=10
  1894. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gurgling or drooling during seizures
    n1=DYNC2H1 gene | n2=en:gurgling or drooling during seizures | rel=r_associated | relid=0 | w=10
  1895. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gyral disorganization
    n1=DYNC2H1 gene | n2=en:gyral disorganization | rel=r_associated | relid=0 | w=10
  1896. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:gyral simplification
    n1=DYNC2H1 gene | n2=en:gyral simplification | rel=r_associated | relid=0 | w=10
  1897. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hallucination
    n1=DYNC2H1 gene | n2=en:hallucination | rel=r_associated | relid=0 | w=10
  1898. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hallucinations (rare)
    n1=DYNC2H1 gene | n2=en:hallucinations (rare) | rel=r_associated | relid=0 | w=10
  1899. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hamartomatous lesions of the brain
    n1=DYNC2H1 gene | n2=en:hamartomatous lesions of the brain | rel=r_associated | relid=0 | w=10
  1900. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hand muscle atrophy
    n1=DYNC2H1 gene | n2=en:hand muscle atrophy | rel=r_associated | relid=0 | w=10
  1901. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hand muscle weakness
    n1=DYNC2H1 gene | n2=en:hand muscle weakness | rel=r_associated | relid=0 | w=10
  1902. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hand tremor (in some patients)
    n1=DYNC2H1 gene | n2=en:hand tremor (in some patients) | rel=r_associated | relid=0 | w=10
  1903. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:harlequin syndrome
    n1=DYNC2H1 gene | n2=en:harlequin syndrome | rel=r_associated | relid=0 | w=10
  1904. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:has tingling sensation
    n1=DYNC2H1 gene | n2=en:has tingling sensation | rel=r_associated | relid=0 | w=10
  1905. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head 'tilt' in infancy
    n1=DYNC2H1 gene | n2=en:head 'tilt' in infancy | rel=r_associated | relid=0 | w=10
  1906. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head bobbing
    n1=DYNC2H1 gene | n2=en:head bobbing | rel=r_associated | relid=0 | w=10
  1907. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head lag
    n1=DYNC2H1 gene | n2=en:head lag | rel=r_associated | relid=0 | w=10
  1908. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head movements abnormal
    n1=DYNC2H1 gene | n2=en:head movements abnormal | rel=r_associated | relid=0 | w=10
  1909. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head oscillations
    n1=DYNC2H1 gene | n2=en:head oscillations | rel=r_associated | relid=0 | w=10
  1910. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head titubation
    n1=DYNC2H1 gene | n2=en:head titubation | rel=r_associated | relid=0 | w=10
  1911. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head titubations
    n1=DYNC2H1 gene | n2=en:head titubations | rel=r_associated | relid=0 | w=10
  1912. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head tremor
    n1=DYNC2H1 gene | n2=en:head tremor | rel=r_associated | relid=0 | w=10
  1913. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head tremor (14% of patients)
    n1=DYNC2H1 gene | n2=en:head tremor (14% of patients) | rel=r_associated | relid=0 | w=10
  1914. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head tremor (in some patients)
    n1=DYNC2H1 gene | n2=en:head tremor (in some patients) | rel=r_associated | relid=0 | w=10
  1915. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head tremor, mild
    n1=DYNC2H1 gene | n2=en:head tremor, mild | rel=r_associated | relid=0 | w=10
  1916. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:head-rolling movements
    n1=DYNC2H1 gene | n2=en:head-rolling movements | rel=r_associated | relid=0 | w=10
  1917. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:headache
    n1=DYNC2H1 gene | n2=en:headache | rel=r_associated | relid=0 | w=10
  1918. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:headache (with pheochromocytoma)
    n1=DYNC2H1 gene | n2=en:headache (with pheochromocytoma) | rel=r_associated | relid=0 | w=10
  1919. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:headache is unilateral
    n1=DYNC2H1 gene | n2=en:headache is unilateral | rel=r_associated | relid=0 | w=10
  1920. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:headache is usually not a symptom
    n1=DYNC2H1 gene | n2=en:headache is usually not a symptom | rel=r_associated | relid=0 | w=10
  1921. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:headache recurrent
    n1=DYNC2H1 gene | n2=en:headache recurrent | rel=r_associated | relid=0 | w=10
  1922. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:headache, episodic
    n1=DYNC2H1 gene | n2=en:headache, episodic | rel=r_associated | relid=0 | w=10
  1923. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:headache, suboccipital, migraine-like (most common symptom) precipitated by coughing, sneezing, bending forward, lifting, neck extension
    n1=DYNC2H1 gene | n2=en:headache, suboccipital, migraine-like (most common symptom) precipitated by coughing, sneezing, bending forward, lifting, neck extension | rel=r_associated | relid=0 | w=10
  1924. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:headaches, severe, unilateral
    n1=DYNC2H1 gene | n2=en:headaches, severe, unilateral | rel=r_associated | relid=0 | w=10
  1925. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hearing disorder
    n1=DYNC2H1 gene | n2=en:hearing disorder | rel=r_associated | relid=0 | w=10
  1926. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:heart innervation
    n1=DYNC2H1 gene | n2=en:heart innervation | rel=r_associated | relid=0 | w=10
  1927. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:heightened sensitivity to external stimuli
    n1=DYNC2H1 gene | n2=en:heightened sensitivity to external stimuli | rel=r_associated | relid=0 | w=10
  1928. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemiclonic seizures
    n1=DYNC2H1 gene | n2=en:hemiclonic seizures | rel=r_associated | relid=0 | w=10
  1929. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemifacial anhidrosis
    n1=DYNC2H1 gene | n2=en:hemifacial anhidrosis | rel=r_associated | relid=0 | w=10
  1930. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemihypoasthesia
    n1=DYNC2H1 gene | n2=en:hemihypoasthesia | rel=r_associated | relid=0 | w=10
  1931. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemimegalencephaly
    n1=DYNC2H1 gene | n2=en:hemimegalencephaly | rel=r_associated | relid=0 | w=10
  1932. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemiparesis
    n1=DYNC2H1 gene | n2=en:hemiparesis | rel=r_associated | relid=0 | w=10
  1933. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemiparesis (in some patients)
    n1=DYNC2H1 gene | n2=en:hemiparesis (in some patients) | rel=r_associated | relid=0 | w=10
  1934. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemiparesis, paroxysmal
    n1=DYNC2H1 gene | n2=en:hemiparesis, paroxysmal | rel=r_associated | relid=0 | w=10
  1935. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemiplegia
    n1=DYNC2H1 gene | n2=en:hemiplegia | rel=r_associated | relid=0 | w=10
  1936. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemiplegia (rare)
    n1=DYNC2H1 gene | n2=en:hemiplegia (rare) | rel=r_associated | relid=0 | w=10
  1937. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemiplegic migraine
    n1=DYNC2H1 gene | n2=en:hemiplegic migraine | rel=r_associated | relid=0 | w=10
  1938. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemiplegic migraine in some patients
    n1=DYNC2H1 gene | n2=en:hemiplegic migraine in some patients | rel=r_associated | relid=0 | w=10
  1939. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemisensory attacks
    n1=DYNC2H1 gene | n2=en:hemisensory attacks | rel=r_associated | relid=0 | w=10
  1940. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemispheric atrophy
    n1=DYNC2H1 gene | n2=en:hemispheric atrophy | rel=r_associated | relid=0 | w=10
  1941. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemorrhage
    n1=DYNC2H1 gene | n2=en:hemorrhage | rel=r_associated | relid=0 | w=10
  1942. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemorrhagic cerebrovascular accident
    n1=DYNC2H1 gene | n2=en:hemorrhagic cerebrovascular accident | rel=r_associated | relid=0 | w=10
  1943. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hemosiderin deposition
    n1=DYNC2H1 gene | n2=en:hemosiderin deposition | rel=r_associated | relid=0 | w=10
  1944. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hepatic encephalopathy
    n1=DYNC2H1 gene | n2=en:hepatic encephalopathy | rel=r_associated | relid=0 | w=10
  1945. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hereditary sensory and autonomic neuropathies
    n1=DYNC2H1 gene | n2=en:hereditary sensory and autonomic neuropathies | rel=r_associated | relid=0 | w=10
  1946. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:herniation and elongation of the cerebellar tonsils, cerebellar vermis, brainstem, and fourth ventricle through the foramen magnum
    n1=DYNC2H1 gene | 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=10
  1947. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:herniation of the cerebellar tonsils through the foramen magnum 5 mm or greater
    n1=DYNC2H1 gene | n2=en:herniation of the cerebellar tonsils through the foramen magnum 5 mm or greater | rel=r_associated | relid=0 | w=10
  1948. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:heterotopic neurons in the white matter (36%)
    n1=DYNC2H1 gene | n2=en:heterotopic neurons in the white matter (36%) | rel=r_associated | relid=0 | w=10
  1949. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hiccough
    n1=DYNC2H1 gene | n2=en:hiccough | rel=r_associated | relid=0 | w=10
  1950. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:high intensity area in white matter on head mri
    n1=DYNC2H1 gene | n2=en:high intensity area in white matter on head mri | rel=r_associated | relid=0 | w=10
  1951. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:high pain threshold
    n1=DYNC2H1 gene | n2=en:high pain threshold | rel=r_associated | relid=0 | w=10
  1952. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:high signal intensities at gray/white matter junction
    n1=DYNC2H1 gene | n2=en:high signal intensities at gray/white matter junction | rel=r_associated | relid=0 | w=10
  1953. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:high signal intensities in periventricular white matter
    n1=DYNC2H1 gene | n2=en:high signal intensities in periventricular white matter | rel=r_associated | relid=0 | w=10
  1954. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:high voltage spikes over the temporal and central regions seen on eeg
    n1=DYNC2H1 gene | n2=en:high voltage spikes over the temporal and central regions seen on eeg | rel=r_associated | relid=0 | w=10
  1955. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:high voltage, fast rhythms seen on eeg
    n1=DYNC2H1 gene | n2=en:high voltage, fast rhythms seen on eeg | rel=r_associated | relid=0 | w=10
  1956. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:high-steppage gait
    n1=DYNC2H1 gene | n2=en:high-steppage gait | rel=r_associated | relid=0 | w=10
  1957. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:high-stepping gait
    n1=DYNC2H1 gene | n2=en:high-stepping gait | rel=r_associated | relid=0 | w=10
  1958. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hippocampal atrophy (1 patient)
    n1=DYNC2H1 gene | n2=en:hippocampal atrophy (1 patient) | rel=r_associated | relid=0 | w=10
  1959. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hippocampal atrophy (in 2 siblings)
    n1=DYNC2H1 gene | n2=en:hippocampal atrophy (in 2 siblings) | rel=r_associated | relid=0 | w=10
  1960. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hippocampal hypoplasia
    n1=DYNC2H1 gene | n2=en:hippocampal hypoplasia | rel=r_associated | relid=0 | w=10
  1961. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:holmes-adie syndrome
    n1=DYNC2H1 gene | n2=en:holmes-adie syndrome | rel=r_associated | relid=0 | w=10
  1962. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:holoprosencephaly
    n1=DYNC2H1 gene | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=10
  1963. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:holoprosencephaly (1 patient)
    n1=DYNC2H1 gene | n2=en:holoprosencephaly (1 patient) | rel=r_associated | relid=0 | w=10
  1964. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:holoprosencephaly (100%)
    n1=DYNC2H1 gene | n2=en:holoprosencephaly (100%) | rel=r_associated | relid=0 | w=10
  1965. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:holoprosencephaly (less common)
    n1=DYNC2H1 gene | n2=en:holoprosencephaly (less common) | rel=r_associated | relid=0 | w=10
  1966. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:holoprosencephaly (variable)
    n1=DYNC2H1 gene | n2=en:holoprosencephaly (variable) | rel=r_associated | relid=0 | w=10
  1967. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia
    n1=DYNC2H1 gene | n2=en:hooked aspect of the frontal horn of the lateral ventricles due to abnormally shaped basal ganglia | rel=r_associated | relid=0 | w=10
  1968. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:horner syndrome
    n1=DYNC2H1 gene | n2=en:horner syndrome | rel=r_associated | relid=0 | w=10
  1969. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hunger and thirst disturbances (in some patients)
    n1=DYNC2H1 gene | n2=en:hunger and thirst disturbances (in some patients) | rel=r_associated | relid=0 | w=10
  1970. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydranencephaly
    n1=DYNC2H1 gene | n2=en:hydranencephaly | rel=r_associated | relid=0 | w=10
  1971. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus
    n1=DYNC2H1 gene | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=10
  1972. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus (11%)
    n1=DYNC2H1 gene | n2=en:hydrocephalus (11%) | rel=r_associated | relid=0 | w=10
  1973. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus (12%)
    n1=DYNC2H1 gene | n2=en:hydrocephalus (12%) | rel=r_associated | relid=0 | w=10
  1974. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus (in 1 patient)
    n1=DYNC2H1 gene | n2=en:hydrocephalus (in 1 patient) | rel=r_associated | relid=0 | w=10
  1975. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus (in 2 patients)
    n1=DYNC2H1 gene | n2=en:hydrocephalus (in 2 patients) | rel=r_associated | relid=0 | w=10
  1976. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus (in some patients)
    n1=DYNC2H1 gene | n2=en:hydrocephalus (in some patients) | rel=r_associated | relid=0 | w=10
  1977. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus (less common)
    n1=DYNC2H1 gene | n2=en:hydrocephalus (less common) | rel=r_associated | relid=0 | w=10
  1978. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus (rare)
    n1=DYNC2H1 gene | n2=en:hydrocephalus (rare) | rel=r_associated | relid=0 | w=10
  1979. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus (uncommon)
    n1=DYNC2H1 gene | n2=en:hydrocephalus (uncommon) | rel=r_associated | relid=0 | w=10
  1980. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus (variable)
    n1=DYNC2H1 gene | n2=en:hydrocephalus (variable) | rel=r_associated | relid=0 | w=10
  1981. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus, normal pressure
    n1=DYNC2H1 gene | n2=en:hydrocephalus, normal pressure | rel=r_associated | relid=0 | w=10
  1982. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephalus, occasional
    n1=DYNC2H1 gene | n2=en:hydrocephalus, occasional | rel=r_associated | relid=0 | w=10
  1983. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hydrocephaly, mild
    n1=DYNC2H1 gene | n2=en:hydrocephaly, mild | rel=r_associated | relid=0 | w=10
  1984. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperactive brainstem reflexes (head retraction, palmomental, snout)
    n1=DYNC2H1 gene | n2=en:hyperactive brainstem reflexes (head retraction, palmomental, snout) | rel=r_associated | relid=0 | w=10
  1985. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperactive deep tendon reflexes
    n1=DYNC2H1 gene | n2=en:hyperactive deep tendon reflexes | rel=r_associated | relid=0 | w=10
  1986. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperactive deep tendon reflexes in early stage
    n1=DYNC2H1 gene | n2=en:hyperactive deep tendon reflexes in early stage | rel=r_associated | relid=0 | w=10
  1987. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperactive startle reflex
    n1=DYNC2H1 gene | n2=en:hyperactive startle reflex | rel=r_associated | relid=0 | w=10
  1988. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperactivity
    n1=DYNC2H1 gene | n2=en:hyperactivity | rel=r_associated | relid=0 | w=10
  1989. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperacusis
    n1=DYNC2H1 gene | n2=en:hyperacusis | rel=r_associated | relid=0 | w=10
  1990. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperekplexia (rare)
    n1=DYNC2H1 gene | n2=en:hyperekplexia (rare) | rel=r_associated | relid=0 | w=10
  1991. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperexplexia
    n1=DYNC2H1 gene | n2=en:hyperexplexia | rel=r_associated | relid=0 | w=10
  1992. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperextension of the neck
    n1=DYNC2H1 gene | n2=en:hyperextension of the neck | rel=r_associated | relid=0 | w=10
  1993. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperintense lesions in the basal ganglia on mri
    n1=DYNC2H1 gene | n2=en:hyperintense lesions in the basal ganglia on mri | rel=r_associated | relid=0 | w=10
  1994. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperintense lesions of the globi pallidi
    n1=DYNC2H1 gene | n2=en:hyperintense lesions of the globi pallidi | rel=r_associated | relid=0 | w=10
  1995. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperintensities in the basal ganglia (rare)
    n1=DYNC2H1 gene | n2=en:hyperintensities in the basal ganglia (rare) | rel=r_associated | relid=0 | w=10
  1996. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperintensities in the basal ganglia and/or thalamus
    n1=DYNC2H1 gene | n2=en:hyperintensities in the basal ganglia and/or thalamus | rel=r_associated | relid=0 | w=10
  1997. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperirritability
    n1=DYNC2H1 gene | n2=en:hyperirritability | rel=r_associated | relid=0 | w=10
  1998. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperkinesia
    n1=DYNC2H1 gene | n2=en:hyperkinesia | rel=r_associated | relid=0 | w=10
  1999. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperkinetic involuntary movements
    n1=DYNC2H1 gene | n2=en:hyperkinetic involuntary movements | rel=r_associated | relid=0 | w=10
  2000. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypermetric saccades
    n1=DYNC2H1 gene | n2=en:hypermetric saccades | rel=r_associated | relid=0 | w=10
  2001. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypermotor automatisms
    n1=DYNC2H1 gene | n2=en:hypermotor automatisms | rel=r_associated | relid=0 | w=10
  2002. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypermotor behavior
    n1=DYNC2H1 gene | n2=en:hypermotor behavior | rel=r_associated | relid=0 | w=10
  2003. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia
    n1=DYNC2H1 gene | n2=en:hyperreflexia | rel=r_associated | relid=0 | w=10
  2004. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia (2 patients)
    n1=DYNC2H1 gene | n2=en:hyperreflexia (2 patients) | rel=r_associated | relid=0 | w=10
  2005. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia (33%)
    n1=DYNC2H1 gene | n2=en:hyperreflexia (33%) | rel=r_associated | relid=0 | w=10
  2006. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia (70%)
    n1=DYNC2H1 gene | n2=en:hyperreflexia (70%) | rel=r_associated | relid=0 | w=10
  2007. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia (early)
    n1=DYNC2H1 gene | n2=en:hyperreflexia (early) | rel=r_associated | relid=0 | w=10
  2008. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia (later)
    n1=DYNC2H1 gene | n2=en:hyperreflexia (later) | rel=r_associated | relid=0 | w=10
  2009. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia (less common)
    n1=DYNC2H1 gene | n2=en:hyperreflexia (less common) | rel=r_associated | relid=0 | w=10
  2010. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults)
    n1=DYNC2H1 gene | n2=en:hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults) | rel=r_associated | relid=0 | w=10
  2011. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia (some patients)
    n1=DYNC2H1 gene | n2=en:hyperreflexia (some patients) | rel=r_associated | relid=0 | w=10
  2012. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia (type i)
    n1=DYNC2H1 gene | n2=en:hyperreflexia (type i) | rel=r_associated | relid=0 | w=10
  2013. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia in some
    n1=DYNC2H1 gene | n2=en:hyperreflexia in some | rel=r_associated | relid=0 | w=10
  2014. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia in the lower limbs (in some patients)
    n1=DYNC2H1 gene | n2=en:hyperreflexia in the lower limbs (in some patients) | rel=r_associated | relid=0 | w=10
  2015. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia may occur
    n1=DYNC2H1 gene | n2=en:hyperreflexia may occur | rel=r_associated | relid=0 | w=10
  2016. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia proximally
    n1=DYNC2H1 gene | n2=en:hyperreflexia proximally | rel=r_associated | relid=0 | w=10
  2017. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia, especially of the lower limbs
    n1=DYNC2H1 gene | n2=en:hyperreflexia, especially of the lower limbs | rel=r_associated | relid=0 | w=10
  2018. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia, lower limbs more than upper limbs
    n1=DYNC2H1 gene | n2=en:hyperreflexia, lower limbs more than upper limbs | rel=r_associated | relid=0 | w=10
  2019. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperreflexia, lower limbs, mild
    n1=DYNC2H1 gene | n2=en:hyperreflexia, lower limbs, mild | rel=r_associated | relid=0 | w=10
  2020. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypersensitive to stimuli
    n1=DYNC2H1 gene | n2=en:hypersensitive to stimuli | rel=r_associated | relid=0 | w=10
  2021. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypersensitivity to sound
    n1=DYNC2H1 gene | n2=en:hypersensitivity to sound | rel=r_associated | relid=0 | w=10
  2022. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypersomnolent
    n1=DYNC2H1 gene | n2=en:hypersomnolent | rel=r_associated | relid=0 | w=10
  2023. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyperthermia
    n1=DYNC2H1 gene | n2=en:hyperthermia | rel=r_associated | relid=0 | w=10
  2024. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia
    n1=DYNC2H1 gene | n2=en:hypertonia | rel=r_associated | relid=0 | w=10
  2025. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia (after age 2 years)
    n1=DYNC2H1 gene | n2=en:hypertonia (after age 2 years) | rel=r_associated | relid=0 | w=10
  2026. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia (childhood)
    n1=DYNC2H1 gene | n2=en:hypertonia (childhood) | rel=r_associated | relid=0 | w=10
  2027. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia (in some patients)
    n1=DYNC2H1 gene | n2=en:hypertonia (in some patients) | rel=r_associated | relid=0 | w=10
  2028. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia (older children and adolescents)
    n1=DYNC2H1 gene | n2=en:hypertonia (older children and adolescents) | rel=r_associated | relid=0 | w=10
  2029. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia (type ii)
    n1=DYNC2H1 gene | n2=en:hypertonia (type ii) | rel=r_associated | relid=0 | w=10
  2030. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia and rigidity during seizures
    n1=DYNC2H1 gene | n2=en:hypertonia and rigidity during seizures | rel=r_associated | relid=0 | w=10
  2031. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia in early stage
    n1=DYNC2H1 gene | n2=en:hypertonia in early stage | rel=r_associated | relid=0 | w=10
  2032. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia in neonatal period
    n1=DYNC2H1 gene | n2=en:hypertonia in neonatal period | rel=r_associated | relid=0 | w=10
  2033. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia late
    n1=DYNC2H1 gene | n2=en:hypertonia late | rel=r_associated | relid=0 | w=10
  2034. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia of lower limbs, later
    n1=DYNC2H1 gene | n2=en:hypertonia of lower limbs, later | rel=r_associated | relid=0 | w=10
  2035. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia of the extremities
    n1=DYNC2H1 gene | n2=en:hypertonia of the extremities | rel=r_associated | relid=0 | w=10
  2036. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia, mild, transient
    n1=DYNC2H1 gene | n2=en:hypertonia, mild, transient | rel=r_associated | relid=0 | w=10
  2037. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonia, peripheral dystonia
    n1=DYNC2H1 gene | n2=en:hypertonia, peripheral dystonia | rel=r_associated | relid=0 | w=10
  2038. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonic seizures
    n1=DYNC2H1 gene | n2=en:hypertonic seizures | rel=r_associated | relid=0 | w=10
  2039. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypertonicity
    n1=DYNC2H1 gene | n2=en:hypertonicity | rel=r_associated | relid=0 | w=10
  2040. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypnagogic hallucinations
    n1=DYNC2H1 gene | n2=en:hypnagogic hallucinations | rel=r_associated | relid=0 | w=10
  2041. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypnapompic hallucinations
    n1=DYNC2H1 gene | n2=en:hypnapompic hallucinations | rel=r_associated | relid=0 | w=10
  2042. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypo- and demyelination of the brain
    n1=DYNC2H1 gene | n2=en:hypo- and demyelination of the brain | rel=r_associated | relid=0 | w=10
  2043. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypocalcemic seizures
    n1=DYNC2H1 gene | n2=en:hypocalcemic seizures | rel=r_associated | relid=0 | w=10
  2044. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypocalcemic tetany
    n1=DYNC2H1 gene | n2=en:hypocalcemic tetany | rel=r_associated | relid=0 | w=10
  2045. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypodensity of caudate
    n1=DYNC2H1 gene | n2=en:hypodensity of caudate | rel=r_associated | relid=0 | w=10
  2046. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypodensity of cerebral white matter seen on mri
    n1=DYNC2H1 gene | n2=en:hypodensity of cerebral white matter seen on mri | rel=r_associated | relid=0 | w=10
  2047. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypodensity of lenticular nuclei
    n1=DYNC2H1 gene | n2=en:hypodensity of lenticular nuclei | rel=r_associated | relid=0 | w=10
  2048. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypodensity of the white matter
    n1=DYNC2H1 gene | n2=en:hypodensity of the white matter | rel=r_associated | relid=0 | w=10
  2049. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypodysplasia of the corpus callosum
    n1=DYNC2H1 gene | n2=en:hypodysplasia of the corpus callosum | rel=r_associated | relid=0 | w=10
  2050. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypogenesis of the corpus callosum
    n1=DYNC2H1 gene | n2=en:hypogenesis of the corpus callosum | rel=r_associated | relid=0 | w=10
  2051. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoglycemia-related seizures
    n1=DYNC2H1 gene | n2=en:hypoglycemia-related seizures | rel=r_associated | relid=0 | w=10
  2052. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoglycemic coma
    n1=DYNC2H1 gene | n2=en:hypoglycemic coma | rel=r_associated | relid=0 | w=10
  2053. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoglycemic encephalopathy
    n1=DYNC2H1 gene | n2=en:hypoglycemic encephalopathy | rel=r_associated | relid=0 | w=10
  2054. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoglycemic seizures
    n1=DYNC2H1 gene | n2=en:hypoglycemic seizures | rel=r_associated | relid=0 | w=10
  2055. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypokinesia
    n1=DYNC2H1 gene | n2=en:hypokinesia | rel=r_associated | relid=0 | w=10
  2056. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypokinesia in infancy
    n1=DYNC2H1 gene | n2=en:hypokinesia in infancy | rel=r_associated | relid=0 | w=10
  2057. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypokinetic movements
    n1=DYNC2H1 gene | n2=en:hypokinetic movements | rel=r_associated | relid=0 | w=10
  2058. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypometabolism of the frontal lobe and thalamic regions
    n1=DYNC2H1 gene | n2=en:hypometabolism of the frontal lobe and thalamic regions | rel=r_associated | relid=0 | w=10
  2059. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypomimia
    n1=DYNC2H1 gene | n2=en:hypomimia | rel=r_associated | relid=0 | w=10
  2060. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypomyelinating leukoencephalopathy
    n1=DYNC2H1 gene | n2=en:hypomyelinating leukoencephalopathy | rel=r_associated | relid=0 | w=10
  2061. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypomyelination
    n1=DYNC2H1 gene | n2=en:hypomyelination | rel=r_associated | relid=0 | w=10
  2062. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypomyelination (1 patient)
    n1=DYNC2H1 gene | n2=en:hypomyelination (1 patient) | rel=r_associated | relid=0 | w=10
  2063. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a)
    n1=DYNC2H1 gene | n2=en:hypomyelination (patient a) metabolic : hypochloremia metabolic alkalosis (patient a) | rel=r_associated | relid=0 | w=10
  2064. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypomyelination of the brain white matter, diffuse
    n1=DYNC2H1 gene | n2=en:hypomyelination of the brain white matter, diffuse | rel=r_associated | relid=0 | w=10
  2065. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia and displacement of the corticospinal fibers within the brainstem
    n1=DYNC2H1 gene | n2=en:hypoplasia and displacement of the corticospinal fibers within the brainstem | rel=r_associated | relid=0 | w=10
  2066. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of anterior or entire pituitary gland (frequent)
    n1=DYNC2H1 gene | n2=en:hypoplasia of anterior or entire pituitary gland (frequent) | rel=r_associated | relid=0 | w=10
  2067. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of corpus callosum
    n1=DYNC2H1 gene | n2=en:hypoplasia of corpus callosum | rel=r_associated | relid=0 | w=10
  2068. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of corpus callosum and cerebellar vermis
    n1=DYNC2H1 gene | n2=en:hypoplasia of corpus callosum and cerebellar vermis | rel=r_associated | relid=0 | w=10
  2069. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of dentate nucleus
    n1=DYNC2H1 gene | n2=en:hypoplasia of dentate nucleus | rel=r_associated | relid=0 | w=10
  2070. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of olfactory tract
    n1=DYNC2H1 gene | n2=en:hypoplasia of olfactory tract | rel=r_associated | relid=0 | w=10
  2071. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of septum pellucidum
    n1=DYNC2H1 gene | n2=en:hypoplasia of septum pellucidum | rel=r_associated | relid=0 | w=10
  2072. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the brainstem
    n1=DYNC2H1 gene | n2=en:hypoplasia of the brainstem | rel=r_associated | relid=0 | w=10
  2073. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the corpus callosum (2 patients)
    n1=DYNC2H1 gene | n2=en:hypoplasia of the corpus callosum (2 patients) | rel=r_associated | relid=0 | w=10
  2074. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the hypothalamus
    n1=DYNC2H1 gene | n2=en:hypoplasia of the hypothalamus | rel=r_associated | relid=0 | w=10
  2075. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the medulla oblongata
    n1=DYNC2H1 gene | n2=en:hypoplasia of the medulla oblongata | rel=r_associated | relid=0 | w=10
  2076. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the mesencephalic tectum
    n1=DYNC2H1 gene | n2=en:hypoplasia of the mesencephalic tectum | rel=r_associated | relid=0 | w=10
  2077. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the optic chiasm
    n1=DYNC2H1 gene | n2=en:hypoplasia of the optic chiasm | rel=r_associated | relid=0 | w=10
  2078. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the optic tract
    n1=DYNC2H1 gene | n2=en:hypoplasia of the optic tract | rel=r_associated | relid=0 | w=10
  2079. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the pons
    n1=DYNC2H1 gene | n2=en:hypoplasia of the pons | rel=r_associated | relid=0 | w=10
  2080. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the posterior corpus callosum (in some patients)
    n1=DYNC2H1 gene | n2=en:hypoplasia of the posterior corpus callosum (in some patients) | rel=r_associated | relid=0 | w=10
  2081. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the pyramidal tract
    n1=DYNC2H1 gene | n2=en:hypoplasia of the pyramidal tract | rel=r_associated | relid=0 | w=10
  2082. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia of the ventral pons
    n1=DYNC2H1 gene | n2=en:hypoplasia of the ventral pons | rel=r_associated | relid=0 | w=10
  2083. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplasia or dysgenesis of the corpus callosum (in some patients)
    n1=DYNC2H1 gene | n2=en:hypoplasia or dysgenesis of the corpus callosum (in some patients) | rel=r_associated | relid=0 | w=10
  2084. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic anterior pituitary (in some patients)
    n1=DYNC2H1 gene | n2=en:hypoplastic anterior pituitary (in some patients) | rel=r_associated | relid=0 | w=10
  2085. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic anterior pituitary gland
    n1=DYNC2H1 gene | n2=en:hypoplastic anterior pituitary gland | rel=r_associated | relid=0 | w=10
  2086. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction
    n1=DYNC2H1 gene | n2=en:hypoplastic brainstem with loss of demarcation at the pontomedullary junction | rel=r_associated | relid=0 | w=10
  2087. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic cerebellar vermis (rare)
    n1=DYNC2H1 gene | n2=en:hypoplastic cerebellar vermis (rare) | rel=r_associated | relid=0 | w=10
  2088. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic cerebrum
    n1=DYNC2H1 gene | n2=en:hypoplastic cerebrum | rel=r_associated | relid=0 | w=10
  2089. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic corpus callosum (1 patient)
    n1=DYNC2H1 gene | n2=en:hypoplastic corpus callosum (1 patient) | rel=r_associated | relid=0 | w=10
  2090. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic corpus callosum (in some patients)
    n1=DYNC2H1 gene | n2=en:hypoplastic corpus callosum (in some patients) | rel=r_associated | relid=0 | w=10
  2091. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic corpus callosum (in some)
    n1=DYNC2H1 gene | n2=en:hypoplastic corpus callosum (in some) | rel=r_associated | relid=0 | w=10
  2092. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic corpus callosum (rare)
    n1=DYNC2H1 gene | n2=en:hypoplastic corpus callosum (rare) | rel=r_associated | relid=0 | w=10
  2093. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic internal capsule (in some)
    n1=DYNC2H1 gene | n2=en:hypoplastic internal capsule (in some) | rel=r_associated | relid=0 | w=10
  2094. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic olfactory lobes
    n1=DYNC2H1 gene | n2=en:hypoplastic olfactory lobes | rel=r_associated | relid=0 | w=10
  2095. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic or absent middle cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:hypoplastic or absent middle cerebellar peduncles | rel=r_associated | relid=0 | w=10
  2096. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic or absent optic chiasm
    n1=DYNC2H1 gene | n2=en:hypoplastic or absent optic chiasm | rel=r_associated | relid=0 | w=10
  2097. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic pituitary gland (in some patients)
    n1=DYNC2H1 gene | n2=en:hypoplastic pituitary gland (in some patients) | rel=r_associated | relid=0 | w=10
  2098. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic pons
    n1=DYNC2H1 gene | n2=en:hypoplastic pons | rel=r_associated | relid=0 | w=10
  2099. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoplastic/atrophic corpus callosum (55%)
    n1=DYNC2H1 gene | n2=en:hypoplastic/atrophic corpus callosum (55%) | rel=r_associated | relid=0 | w=10
  2100. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyporeflexia
    n1=DYNC2H1 gene | n2=en:hyporeflexia | rel=r_associated | relid=0 | w=10
  2101. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyporeflexia (early)
    n1=DYNC2H1 gene | n2=en:hyporeflexia (early) | rel=r_associated | relid=0 | w=10
  2102. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyporeflexia (occurs later)
    n1=DYNC2H1 gene | n2=en:hyporeflexia (occurs later) | rel=r_associated | relid=0 | w=10
  2103. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyporeflexia of lower limbs
    n1=DYNC2H1 gene | n2=en:hyporeflexia of lower limbs | rel=r_associated | relid=0 | w=10
  2104. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyporeflexia or areflexia
    n1=DYNC2H1 gene | n2=en:hyporeflexia or areflexia | rel=r_associated | relid=0 | w=10
  2105. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyporeflexia to hyperreflexia
    n1=DYNC2H1 gene | n2=en:hyporeflexia to hyperreflexia | rel=r_associated | relid=0 | w=10
  2106. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyposmia/anosmia
    n1=DYNC2H1 gene | n2=en:hyposmia/anosmia | rel=r_associated | relid=0 | w=10
  2107. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hyposmia/anosmia (in some patients)
    n1=DYNC2H1 gene | n2=en:hyposmia/anosmia (in some patients) | rel=r_associated | relid=0 | w=10
  2108. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypothalamic hamartoma
    n1=DYNC2H1 gene | n2=en:hypothalamic hamartoma | rel=r_associated | relid=0 | w=10
  2109. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypothalamus
    n1=DYNC2H1 gene | n2=en:hypothalamus | rel=r_associated | relid=0 | w=10
  2110. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia
    n1=DYNC2H1 gene | n2=en:hypotonia | rel=r_associated | relid=0 | w=10
  2111. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (1 patient)
    n1=DYNC2H1 gene | n2=en:hypotonia (1 patient) | rel=r_associated | relid=0 | w=10
  2112. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (93%)
    n1=DYNC2H1 gene | n2=en:hypotonia (93%) | rel=r_associated | relid=0 | w=10
  2113. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (96%)
    n1=DYNC2H1 gene | n2=en:hypotonia (96%) | rel=r_associated | relid=0 | w=10
  2114. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (congenital form)
    n1=DYNC2H1 gene | n2=en:hypotonia (congenital form) | rel=r_associated | relid=0 | w=10
  2115. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (early infancy)
    n1=DYNC2H1 gene | n2=en:hypotonia (early infancy) | rel=r_associated | relid=0 | w=10
  2116. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (early-onset form)
    n1=DYNC2H1 gene | n2=en:hypotonia (early-onset form) | rel=r_associated | relid=0 | w=10
  2117. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (hcs and 2p21del)
    n1=DYNC2H1 gene | n2=en:hypotonia (hcs and 2p21del) | rel=r_associated | relid=0 | w=10
  2118. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (in 1/4 patients)
    n1=DYNC2H1 gene | n2=en:hypotonia (in 1/4 patients) | rel=r_associated | relid=0 | w=10
  2119. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (in males)
    n1=DYNC2H1 gene | n2=en:hypotonia (in males) | rel=r_associated | relid=0 | w=10
  2120. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (in some patients)
    n1=DYNC2H1 gene | n2=en:hypotonia (in some patients) | rel=r_associated | relid=0 | w=10
  2121. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (less common)
    n1=DYNC2H1 gene | n2=en:hypotonia (less common) | rel=r_associated | relid=0 | w=10
  2122. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (newborn)
    n1=DYNC2H1 gene | n2=en:hypotonia (newborn) | rel=r_associated | relid=0 | w=10
  2123. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (rare)
    n1=DYNC2H1 gene | n2=en:hypotonia (rare) | rel=r_associated | relid=0 | w=10
  2124. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia (type i and type ii, infantile)
    n1=DYNC2H1 gene | n2=en:hypotonia (type i and type ii, infantile) | rel=r_associated | relid=0 | w=10
  2125. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia at birth
    n1=DYNC2H1 gene | n2=en:hypotonia at birth | rel=r_associated | relid=0 | w=10
  2126. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia changing to hypertonia
    n1=DYNC2H1 gene | n2=en:hypotonia changing to hypertonia | rel=r_associated | relid=0 | w=10
  2127. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia in infancy and early childhood
    n1=DYNC2H1 gene | n2=en:hypotonia in infancy and early childhood | rel=r_associated | relid=0 | w=10
  2128. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia in later stages
    n1=DYNC2H1 gene | n2=en:hypotonia in later stages | rel=r_associated | relid=0 | w=10
  2129. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia progressing to hypertonia
    n1=DYNC2H1 gene | n2=en:hypotonia progressing to hypertonia | rel=r_associated | relid=0 | w=10
  2130. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia, axial, severe
    n1=DYNC2H1 gene | n2=en:hypotonia, axial, severe | rel=r_associated | relid=0 | w=10
  2131. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia, global, severe
    n1=DYNC2H1 gene | n2=en:hypotonia, global, severe | rel=r_associated | relid=0 | w=10
  2132. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia, mild
    n1=DYNC2H1 gene | n2=en:hypotonia, mild | rel=r_associated | relid=0 | w=10
  2133. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia, mild, transient
    n1=DYNC2H1 gene | n2=en:hypotonia, mild, transient | rel=r_associated | relid=0 | w=10
  2134. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia, neonatal (> 90%)
    n1=DYNC2H1 gene | n2=en:hypotonia, neonatal (> 90%) | rel=r_associated | relid=0 | w=10
  2135. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia, poor moro reflex
    n1=DYNC2H1 gene | n2=en:hypotonia, poor moro reflex | rel=r_associated | relid=0 | w=10
  2136. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia, profound muscular (in some patients)
    n1=DYNC2H1 gene | n2=en:hypotonia, profound muscular (in some patients) | rel=r_associated | relid=0 | w=10
  2137. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia, proximal, severe
    n1=DYNC2H1 gene | n2=en:hypotonia, proximal, severe | rel=r_associated | relid=0 | w=10
  2138. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonia, severe (rare)
    n1=DYNC2H1 gene | n2=en:hypotonia, severe (rare) | rel=r_associated | relid=0 | w=10
  2139. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonic
    n1=DYNC2H1 gene | n2=en:hypotonic | rel=r_associated | relid=0 | w=10
  2140. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonic seizures
    n1=DYNC2H1 gene | n2=en:hypotonic seizures | rel=r_associated | relid=0 | w=10
  2141. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonic urinary bladder
    n1=DYNC2H1 gene | n2=en:hypotonic urinary bladder | rel=r_associated | relid=0 | w=10
  2142. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotonicity (in some patients)
    n1=DYNC2H1 gene | n2=en:hypotonicity (in some patients) | rel=r_associated | relid=0 | w=10
  2143. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypotrophic brainstem
    n1=DYNC2H1 gene | n2=en:hypotrophic brainstem | rel=r_associated | relid=0 | w=10
  2144. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypoxic convulsions
    n1=DYNC2H1 gene | n2=en:hypoxic convulsions | rel=r_associated | relid=0 | w=10
  2145. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypperreflexia
    n1=DYNC2H1 gene | n2=en:hypperreflexia | rel=r_associated | relid=0 | w=10
  2146. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypsarrhythmia
    n1=DYNC2H1 gene | n2=en:hypsarrhythmia | rel=r_associated | relid=0 | w=10
  2147. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypsarrhythmia (1 patient)
    n1=DYNC2H1 gene | n2=en:hypsarrhythmia (1 patient) | rel=r_associated | relid=0 | w=10
  2148. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypsarrhythmia (in some patients)
    n1=DYNC2H1 gene | n2=en:hypsarrhythmia (in some patients) | rel=r_associated | relid=0 | w=10
  2149. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg
    n1=DYNC2H1 gene | n2=en:hypsarrhythmia or severe multifocal epileptic abnormalities with poor background activity on eeg | rel=r_associated | relid=0 | w=10
  2150. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:hypsarrhythmia seen on eeg
    n1=DYNC2H1 gene | n2=en:hypsarrhythmia seen on eeg | rel=r_associated | relid=0 | w=10
  2151. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ictal eeg showed partial seizures with frontal lobe origin
    n1=DYNC2H1 gene | n2=en:ictal eeg showed partial seizures with frontal lobe origin | rel=r_associated | relid=0 | w=10
  2152. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ictal eeg shows diffuse slow delta and theta activity
    n1=DYNC2H1 gene | n2=en:ictal eeg shows diffuse slow delta and theta activity | rel=r_associated | relid=0 | w=10
  2153. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ictal eeg shows focal onset in central, parietal, or temporal regions
    n1=DYNC2H1 gene | n2=en:ictal eeg shows focal onset in central, parietal, or temporal regions | rel=r_associated | relid=0 | w=10
  2154. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ictal eeg shows focal onset, often posterior region of brain
    n1=DYNC2H1 gene | n2=en:ictal eeg shows focal onset, often posterior region of brain | rel=r_associated | relid=0 | w=10
  2155. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ictal eeg shows focal, temporal, unilateral, rhythmic slow wave activity of high amplitude
    n1=DYNC2H1 gene | n2=en:ictal eeg shows focal, temporal, unilateral, rhythmic slow wave activity of high amplitude | rel=r_associated | relid=0 | w=10
  2156. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ictal eeg with bisynchronous spike waves
    n1=DYNC2H1 gene | n2=en:ictal eeg with bisynchronous spike waves | rel=r_associated | relid=0 | w=10
  2157. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:idiopathic diffuse hyperhidrosis
    n1=DYNC2H1 gene | n2=en:idiopathic diffuse hyperhidrosis | rel=r_associated | relid=0 | w=10
  2158. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:idiopathic generalized epilepsy in childhood (homozygous patient)
    n1=DYNC2H1 gene | n2=en:idiopathic generalized epilepsy in childhood (homozygous patient) | rel=r_associated | relid=0 | w=10
  2159. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:idiopathic peripheral autonomic neuropathy
    n1=DYNC2H1 gene | n2=en:idiopathic peripheral autonomic neuropathy | rel=r_associated | relid=0 | w=10
  2160. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:idiopathic torsion dystonia
    n1=DYNC2H1 gene | n2=en:idiopathic torsion dystonia | rel=r_associated | relid=0 | w=10
  2161. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:illegible handwriting
    n1=DYNC2H1 gene | n2=en:illegible handwriting | rel=r_associated | relid=0 | w=10
  2162. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:imaging shows noncalcified subependymal periventricular heterotopic nodules of gray matter
    n1=DYNC2H1 gene | n2=en:imaging shows noncalcified subependymal periventricular heterotopic nodules of gray matter | rel=r_associated | relid=0 | w=10
  2163. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:imaging shows signal abnormalities in basal ganglia
    n1=DYNC2H1 gene | n2=en:imaging shows signal abnormalities in basal ganglia | rel=r_associated | relid=0 | w=10
  2164. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:imbalance
    n1=DYNC2H1 gene | n2=en:imbalance | rel=r_associated | relid=0 | w=10
  2165. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:imbalance autonomic nervous system
    n1=DYNC2H1 gene | n2=en:imbalance autonomic nervous system | rel=r_associated | relid=0 | w=10
  2166. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:immature autonomic system
    n1=DYNC2H1 gene | n2=en:immature autonomic system | rel=r_associated | relid=0 | w=10
  2167. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:immature brain with no gyral development
    n1=DYNC2H1 gene | n2=en:immature brain with no gyral development | rel=r_associated | relid=0 | w=10
  2168. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:immature myelination
    n1=DYNC2H1 gene | n2=en:immature myelination | rel=r_associated | relid=0 | w=10
  2169. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:immobile
    n1=DYNC2H1 gene | n2=en:immobile | rel=r_associated | relid=0 | w=10
  2170. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired ambulation due to muscle weakness
    n1=DYNC2H1 gene | n2=en:impaired ambulation due to muscle weakness | rel=r_associated | relid=0 | w=10
  2171. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired balance
    n1=DYNC2H1 gene | n2=en:impaired balance | rel=r_associated | relid=0 | w=10
  2172. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired balance (2 patients)
    n1=DYNC2H1 gene | n2=en:impaired balance (2 patients) | rel=r_associated | relid=0 | w=10
  2173. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired cognition (in some patients)
    n1=DYNC2H1 gene | n2=en:impaired cognition (in some patients) | rel=r_associated | relid=0 | w=10
  2174. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired executive function (in some patients)
    n1=DYNC2H1 gene | n2=en:impaired executive function (in some patients) | rel=r_associated | relid=0 | w=10
  2175. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired expression of language
    n1=DYNC2H1 gene | n2=en:impaired expression of language | rel=r_associated | relid=0 | w=10
  2176. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired expressive speech
    n1=DYNC2H1 gene | n2=en:impaired expressive speech | rel=r_associated | relid=0 | w=10
  2177. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired fine motor skills
    n1=DYNC2H1 gene | n2=en:impaired fine motor skills | rel=r_associated | relid=0 | w=10
  2178. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired gait due to peripheral neuropathy
    n1=DYNC2H1 gene | n2=en:impaired gait due to peripheral neuropathy | rel=r_associated | relid=0 | w=10
  2179. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired horizontal smooth pursuit
    n1=DYNC2H1 gene | n2=en:impaired horizontal smooth pursuit | rel=r_associated | relid=0 | w=10
  2180. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired language development
    n1=DYNC2H1 gene | n2=en:impaired language development | rel=r_associated | relid=0 | w=10
  2181. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired long-term verbal memory
    n1=DYNC2H1 gene | n2=en:impaired long-term verbal memory | rel=r_associated | relid=0 | w=10
  2182. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired motor control, mild
    n1=DYNC2H1 gene | n2=en:impaired motor control, mild | rel=r_associated | relid=0 | w=10
  2183. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired processing of language
    n1=DYNC2H1 gene | n2=en:impaired processing of language | rel=r_associated | relid=0 | w=10
  2184. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired proprioception
    n1=DYNC2H1 gene | n2=en:impaired proprioception | rel=r_associated | relid=0 | w=10
  2185. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired psychomotor development
    n1=DYNC2H1 gene | n2=en:impaired psychomotor development | rel=r_associated | relid=0 | w=10
  2186. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired tandem gait
    n1=DYNC2H1 gene | n2=en:impaired tandem gait | rel=r_associated | relid=0 | w=10
  2187. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures
    n1=DYNC2H1 gene | 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=10
  2188. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired vertical visual pursuit
    n1=DYNC2H1 gene | n2=en:impaired vertical visual pursuit | rel=r_associated | relid=0 | w=10
  2189. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired vibration sensation at ankles
    n1=DYNC2H1 gene | n2=en:impaired vibration sensation at ankles | rel=r_associated | relid=0 | w=10
  2190. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired vibration sensation in the lower limbs
    n1=DYNC2H1 gene | n2=en:impaired vibration sensation in the lower limbs | rel=r_associated | relid=0 | w=10
  2191. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired visuospatial skills
    n1=DYNC2H1 gene | n2=en:impaired visuospatial skills | rel=r_associated | relid=0 | w=10
  2192. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired voluntary movement
    n1=DYNC2H1 gene | n2=en:impaired voluntary movement | rel=r_associated | relid=0 | w=10
  2193. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impaired walking ability (in some patients)
    n1=DYNC2H1 gene | n2=en:impaired walking ability (in some patients) | rel=r_associated | relid=0 | w=10
  2194. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impairment of balance
    n1=DYNC2H1 gene | n2=en:impairment of balance | rel=r_associated | relid=0 | w=10
  2195. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:impairment of gross and fine motor coordination
    n1=DYNC2H1 gene | n2=en:impairment of gross and fine motor coordination | rel=r_associated | relid=0 | w=10
  2196. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to communicate
    n1=DYNC2H1 gene | n2=en:inability to communicate | rel=r_associated | relid=0 | w=10
  2197. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to generate syntactic grammar rules (i.e., tense, gender, number)
    n1=DYNC2H1 gene | n2=en:inability to generate syntactic grammar rules (i.e., tense, gender, number) | rel=r_associated | relid=0 | w=10
  2198. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to hold head
    n1=DYNC2H1 gene | n2=en:inability to hold head | rel=r_associated | relid=0 | w=10
  2199. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to hold head up
    n1=DYNC2H1 gene | n2=en:inability to hold head up | rel=r_associated | relid=0 | w=10
  2200. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to hold neck up ('limber neck') onset at 6 months
    n1=DYNC2H1 gene | n2=en:inability to hold neck up ('limber neck') onset at 6 months | rel=r_associated | relid=0 | w=10
  2201. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to reach
    n1=DYNC2H1 gene | n2=en:inability to reach | rel=r_associated | relid=0 | w=10
  2202. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to run
    n1=DYNC2H1 gene | n2=en:inability to run | rel=r_associated | relid=0 | w=10
  2203. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to run (in some patients)
    n1=DYNC2H1 gene | n2=en:inability to run (in some patients) | rel=r_associated | relid=0 | w=10
  2204. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to sit
    n1=DYNC2H1 gene | n2=en:inability to sit | rel=r_associated | relid=0 | w=10
  2205. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to sit or control head
    n1=DYNC2H1 gene | n2=en:inability to sit or control head | rel=r_associated | relid=0 | w=10
  2206. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to sit or stand independently
    n1=DYNC2H1 gene | n2=en:inability to sit or stand independently | rel=r_associated | relid=0 | w=10
  2207. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to sit or walk independently
    n1=DYNC2H1 gene | n2=en:inability to sit or walk independently | rel=r_associated | relid=0 | w=10
  2208. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to stand on toes
    n1=DYNC2H1 gene | n2=en:inability to stand on toes | rel=r_associated | relid=0 | w=10
  2209. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to stand without assistance
    n1=DYNC2H1 gene | n2=en:inability to stand without assistance | rel=r_associated | relid=0 | w=10
  2210. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to walk independently
    n1=DYNC2H1 gene | n2=en:inability to walk independently | rel=r_associated | relid=0 | w=10
  2211. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to walk unaided
    n1=DYNC2H1 gene | n2=en:inability to walk unaided | rel=r_associated | relid=0 | w=10
  2212. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inability to walk unsupported
    n1=DYNC2H1 gene | n2=en:inability to walk unsupported | rel=r_associated | relid=0 | w=10
  2213. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inarticulate speech delayed gross motor skills
    n1=DYNC2H1 gene | n2=en:inarticulate speech delayed gross motor skills | rel=r_associated | relid=0 | w=10
  2214. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:incomplete myelination
    n1=DYNC2H1 gene | n2=en:incomplete myelination | rel=r_associated | relid=0 | w=10
  2215. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:incomprehensible speech
    n1=DYNC2H1 gene | n2=en:incomprehensible speech | rel=r_associated | relid=0 | w=10
  2216. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:incontinence
    n1=DYNC2H1 gene | n2=en:incontinence | rel=r_associated | relid=0 | w=10
  2217. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:incoordination of the hands
    n1=DYNC2H1 gene | n2=en:incoordination of the hands | rel=r_associated | relid=0 | w=10
  2218. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:incoordination of trunk and limbs
    n1=DYNC2H1 gene | n2=en:incoordination of trunk and limbs | rel=r_associated | relid=0 | w=10
  2219. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased activity period
    n1=DYNC2H1 gene | n2=en:increased activity period | rel=r_associated | relid=0 | w=10
  2220. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased cerebral lactate
    n1=DYNC2H1 gene | n2=en:increased cerebral lactate | rel=r_associated | relid=0 | w=10
  2221. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased csf lactate
    n1=DYNC2H1 gene | n2=en:increased csf lactate | rel=r_associated | relid=0 | w=10
  2222. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased csf protein
    n1=DYNC2H1 gene | n2=en:increased csf protein | rel=r_associated | relid=0 | w=10
  2223. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased csf protein with normal cell count
    n1=DYNC2H1 gene | n2=en:increased csf protein with normal cell count | rel=r_associated | relid=0 | w=10
  2224. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased deep tendon reflexes (if left untreated)
    n1=DYNC2H1 gene | n2=en:increased deep tendon reflexes (if left untreated) | rel=r_associated | relid=0 | w=10
  2225. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased falls
    n1=DYNC2H1 gene | n2=en:increased falls | rel=r_associated | relid=0 | w=10
  2226. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased intracranial pressure preoperatively (in some patients)
    n1=DYNC2H1 gene | n2=en:increased intracranial pressure preoperatively (in some patients) | rel=r_associated | relid=0 | w=10
  2227. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased iron deposition in the basal ganglia
    n1=DYNC2H1 gene | n2=en:increased iron deposition in the basal ganglia | rel=r_associated | relid=0 | w=10
  2228. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased iron deposition in the basal ganglia (40%)
    n1=DYNC2H1 gene | n2=en:increased iron deposition in the basal ganglia (40%) | rel=r_associated | relid=0 | w=10
  2229. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased lactate in the brain
    n1=DYNC2H1 gene | n2=en:increased lactate in the brain | rel=r_associated | relid=0 | w=10
  2230. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased muscle tone in the lower limbs
    n1=DYNC2H1 gene | n2=en:increased muscle tone in the lower limbs | rel=r_associated | relid=0 | w=10
  2231. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased neurologic sequelae of infections (rare)
    n1=DYNC2H1 gene | n2=en:increased neurologic sequelae of infections (rare) | rel=r_associated | relid=0 | w=10
  2232. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased risk of seizures in childhood or adulthood (11-16%)
    n1=DYNC2H1 gene | n2=en:increased risk of seizures in childhood or adulthood (11-16%) | rel=r_associated | relid=0 | w=10
  2233. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased signal intensity on t(2)-weighted scans in the periventricular and centrum ovale area
    n1=DYNC2H1 gene | n2=en:increased signal intensity on t(2)-weighted scans in the periventricular and centrum ovale area | rel=r_associated | relid=0 | w=10
  2234. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased startle response
    n1=DYNC2H1 gene | n2=en:increased startle response | rel=r_associated | relid=0 | w=10
  2235. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased subdural space around frontal lobes
    n1=DYNC2H1 gene | n2=en:increased subdural space around frontal lobes | rel=r_associated | relid=0 | w=10
  2236. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased t2 signal intensities in the middle cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:increased t2 signal intensities in the middle cerebellar peduncles | rel=r_associated | relid=0 | w=10
  2237. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased tone in the upper limbs (occur later)
    n1=DYNC2H1 gene | n2=en:increased tone in the upper limbs (occur later) | rel=r_associated | relid=0 | w=10
  2238. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:increased white matter abnormalities on t2 signalling (in type iib)
    n1=DYNC2H1 gene | n2=en:increased white matter abnormalities on t2 signalling (in type iib) | rel=r_associated | relid=0 | w=10
  2239. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:independent walking never achieved
    n1=DYNC2H1 gene | n2=en:independent walking never achieved | rel=r_associated | relid=0 | w=10
  2240. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:individuals can stand or walk with support by 4 to 6 years of age
    n1=DYNC2H1 gene | n2=en:individuals can stand or walk with support by 4 to 6 years of age | rel=r_associated | relid=0 | w=10
  2241. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:individuals require less sleep in a 24-hour period compared to age-matched controls
    n1=DYNC2H1 gene | n2=en:individuals require less sleep in a 24-hour period compared to age-matched controls | rel=r_associated | relid=0 | w=10
  2242. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile encephalopathy
    n1=DYNC2H1 gene | n2=en:infantile encephalopathy | rel=r_associated | relid=0 | w=10
  2243. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile encephalopathy, progressive
    n1=DYNC2H1 gene | n2=en:infantile encephalopathy, progressive | rel=r_associated | relid=0 | w=10
  2244. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile hemiplegias
    n1=DYNC2H1 gene | n2=en:infantile hemiplegias | rel=r_associated | relid=0 | w=10
  2245. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile irritability (if left untreated)
    n1=DYNC2H1 gene | n2=en:infantile irritability (if left untreated) | rel=r_associated | relid=0 | w=10
  2246. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile muscular hypotonia
    n1=DYNC2H1 gene | n2=en:infantile muscular hypotonia | rel=r_associated | relid=0 | w=10
  2247. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile nystagmus
    n1=DYNC2H1 gene | n2=en:infantile nystagmus | rel=r_associated | relid=0 | w=10
  2248. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile seizures
    n1=DYNC2H1 gene | n2=en:infantile seizures | rel=r_associated | relid=0 | w=10
  2249. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile seizures (approximately 80% of patients)
    n1=DYNC2H1 gene | n2=en:infantile seizures (approximately 80% of patients) | rel=r_associated | relid=0 | w=10
  2250. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients)
    n1=DYNC2H1 gene | n2=en:infantile seizures, afebrile, with no neurologic sequelae (in 40% of patients) | rel=r_associated | relid=0 | w=10
  2251. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infantile spasm
    n1=DYNC2H1 gene | n2=en:infantile spasm | rel=r_associated | relid=0 | w=10
  2252. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infarction
    n1=DYNC2H1 gene | n2=en:infarction | rel=r_associated | relid=0 | w=10
  2253. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inferior olivary nuclei show fetal pattern
    n1=DYNC2H1 gene | n2=en:inferior olivary nuclei show fetal pattern | rel=r_associated | relid=0 | w=10
  2254. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inferior vermis hypoplasia
    n1=DYNC2H1 gene | n2=en:inferior vermis hypoplasia | rel=r_associated | relid=0 | w=10
  2255. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:inflexible adherence to routines or rituals
    n1=DYNC2H1 gene | n2=en:inflexible adherence to routines or rituals | rel=r_associated | relid=0 | w=10
  2256. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:infrequent generalized seizures
    n1=DYNC2H1 gene | n2=en:infrequent generalized seizures | rel=r_associated | relid=0 | w=10
  2257. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:initial hypotonia, followed by spasticity
    n1=DYNC2H1 gene | n2=en:initial hypotonia, followed by spasticity | rel=r_associated | relid=0 | w=10
  2258. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:initial normal development
    n1=DYNC2H1 gene | n2=en:initial normal development | rel=r_associated | relid=0 | w=10
  2259. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:insomnia
    n1=DYNC2H1 gene | n2=en:insomnia | rel=r_associated | relid=0 | w=10
  2260. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:insomnia, refractory
    n1=DYNC2H1 gene | n2=en:insomnia, refractory | rel=r_associated | relid=0 | w=10
  2261. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:instability vasomotor
    n1=DYNC2H1 gene | n2=en:instability vasomotor | rel=r_associated | relid=0 | w=10
  2262. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellect high (in some patients)
    n1=DYNC2H1 gene | n2=en:intellect high (in some patients) | rel=r_associated | relid=0 | w=10
  2263. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual delay
    n1=DYNC2H1 gene | n2=en:intellectual delay | rel=r_associated | relid=0 | w=10
  2264. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disabilities (in 1 family)
    n1=DYNC2H1 gene | n2=en:intellectual disabilities (in 1 family) | rel=r_associated | relid=0 | w=10
  2265. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability
    n1=DYNC2H1 gene | n2=en:intellectual disability | rel=r_associated | relid=0 | w=10
  2266. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability (in 1 ashkenazi patient)
    n1=DYNC2H1 gene | n2=en:intellectual disability (in 1 ashkenazi patient) | rel=r_associated | relid=0 | w=10
  2267. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability (in most patients)
    n1=DYNC2H1 gene | n2=en:intellectual disability (in most patients) | rel=r_associated | relid=0 | w=10
  2268. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability (in some patients)
    n1=DYNC2H1 gene | n2=en:intellectual disability (in some patients) | rel=r_associated | relid=0 | w=10
  2269. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability, mild (1 patient)
    n1=DYNC2H1 gene | n2=en:intellectual disability, mild (1 patient) | rel=r_associated | relid=0 | w=10
  2270. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:intellectual disability, mild (in some patients) | rel=r_associated | relid=0 | w=10
  2271. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability, mild (uncommon)
    n1=DYNC2H1 gene | n2=en:intellectual disability, mild (uncommon) | rel=r_associated | relid=0 | w=10
  2272. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability, mild to moderate
    n1=DYNC2H1 gene | n2=en:intellectual disability, mild to moderate | rel=r_associated | relid=0 | w=10
  2273. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability, mild to moderate (in homozygotes)
    n1=DYNC2H1 gene | n2=en:intellectual disability, mild to moderate (in homozygotes) | rel=r_associated | relid=0 | w=10
  2274. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability, mild to severe
    n1=DYNC2H1 gene | n2=en:intellectual disability, mild to severe | rel=r_associated | relid=0 | w=10
  2275. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability, moderate (in some patients)
    n1=DYNC2H1 gene | n2=en:intellectual disability, moderate (in some patients) | rel=r_associated | relid=0 | w=10
  2276. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability, moderate to severe
    n1=DYNC2H1 gene | n2=en:intellectual disability, moderate to severe | rel=r_associated | relid=0 | w=10
  2277. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual disability, progressive
    n1=DYNC2H1 gene | n2=en:intellectual disability, progressive | rel=r_associated | relid=0 | w=10
  2278. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual function may be high in milder cases
    n1=DYNC2H1 gene | n2=en:intellectual function may be high in milder cases | rel=r_associated | relid=0 | w=10
  2279. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual impairment (rare)
    n1=DYNC2H1 gene | n2=en:intellectual impairment (rare) | rel=r_associated | relid=0 | w=10
  2280. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual impairment, mild
    n1=DYNC2H1 gene | n2=en:intellectual impairment, mild | rel=r_associated | relid=0 | w=10
  2281. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intellectual impairment, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:intellectual impairment, mild (in some patients) | rel=r_associated | relid=0 | w=10
  2282. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intention tremor (1 patient)
    n1=DYNC2H1 gene | n2=en:intention tremor (1 patient) | rel=r_associated | relid=0 | w=10
  2283. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intention tremor (in some patients)
    n1=DYNC2H1 gene | n2=en:intention tremor (in some patients) | rel=r_associated | relid=0 | w=10
  2284. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intention tremor in those who survive
    n1=DYNC2H1 gene | n2=en:intention tremor in those who survive | rel=r_associated | relid=0 | w=10
  2285. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interhemispheric cysts
    n1=DYNC2H1 gene | n2=en:interhemispheric cysts | rel=r_associated | relid=0 | w=10
  2286. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interhemispheric lipoma
    n1=DYNC2H1 gene | n2=en:interhemispheric lipoma | rel=r_associated | relid=0 | w=10
  2287. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interictal ataxia may occur later in disease course
    n1=DYNC2H1 gene | n2=en:interictal ataxia may occur later in disease course | rel=r_associated | relid=0 | w=10
  2288. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interictal downbeat nystagmus
    n1=DYNC2H1 gene | n2=en:interictal downbeat nystagmus | rel=r_associated | relid=0 | w=10
  2289. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interictal dystonia may occur later in disease course
    n1=DYNC2H1 gene | n2=en:interictal dystonia may occur later in disease course | rel=r_associated | relid=0 | w=10
  2290. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interictal eeg is usually normal
    n1=DYNC2H1 gene | n2=en:interictal eeg is usually normal | rel=r_associated | relid=0 | w=10
  2291. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interictal eeg may be normal or abnormal
    n1=DYNC2H1 gene | n2=en:interictal eeg may be normal or abnormal | rel=r_associated | relid=0 | w=10
  2292. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interictal eeg may show nonspecific changes in 15 to 20%
    n1=DYNC2H1 gene | n2=en:interictal eeg may show nonspecific changes in 15 to 20% | rel=r_associated | relid=0 | w=10
  2293. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interictal eeg shows 3-4 hz general spike-wave complexes
    n1=DYNC2H1 gene | n2=en:interictal eeg shows 3-4 hz general spike-wave complexes | rel=r_associated | relid=0 | w=10
  2294. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interictal neurologic impairment
    n1=DYNC2H1 gene | n2=en:interictal neurologic impairment | rel=r_associated | relid=0 | w=10
  2295. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interictal periods of normal health
    n1=DYNC2H1 gene | n2=en:interictal periods of normal health | rel=r_associated | relid=0 | w=10
  2296. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intermediate syndrome
    n1=DYNC2H1 gene | n2=en:intermediate syndrome | rel=r_associated | relid=0 | w=10
  2297. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intermittent episodes associated with lethargy, vomiting
    n1=DYNC2H1 gene | n2=en:intermittent episodes associated with lethargy, vomiting | rel=r_associated | relid=0 | w=10
  2298. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intermittent migraine headaches
    n1=DYNC2H1 gene | n2=en:intermittent migraine headaches | rel=r_associated | relid=0 | w=10
  2299. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intermittent wheelchair dependence (stage 3)
    n1=DYNC2H1 gene | n2=en:intermittent wheelchair dependence (stage 3) | rel=r_associated | relid=0 | w=10
  2300. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intermittent, transient episodes of worsening of ataxia
    n1=DYNC2H1 gene | n2=en:intermittent, transient episodes of worsening of ataxia | rel=r_associated | relid=0 | w=10
  2301. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interosseus muscle atrophy
    n1=DYNC2H1 gene | n2=en:interosseus muscle atrophy | rel=r_associated | relid=0 | w=10
  2302. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:interventricular cysts
    n1=DYNC2H1 gene | n2=en:interventricular cysts | rel=r_associated | relid=0 | w=10
  2303. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis
    n1=DYNC2H1 gene | n2=en:intracellular accumulation of material resulting in curvilinear profiles on ultrastructural analysis | rel=r_associated | relid=0 | w=10
  2304. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracellular accumulation of material resulting in fingerprint profiles on ultrastructural analysis
    n1=DYNC2H1 gene | n2=en:intracellular accumulation of material resulting in fingerprint profiles on ultrastructural analysis | rel=r_associated | relid=0 | w=10
  2305. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis
    n1=DYNC2H1 gene | n2=en:intracellular accumulation of material resulting in rectilinear profiles on ultrastructural analysis | rel=r_associated | relid=0 | w=10
  2306. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracellular lewy bodies
    n1=DYNC2H1 gene | n2=en:intracellular lewy bodies | rel=r_associated | relid=0 | w=10
  2307. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies)
    n1=DYNC2H1 gene | n2=en:intracellular pas-positive polyglucosan inclusion bodies ('lafora' bodies) | rel=r_associated | relid=0 | w=10
  2308. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracerebral calcifications (in some patients)
    n1=DYNC2H1 gene | n2=en:intracerebral calcifications (in some patients) | rel=r_associated | relid=0 | w=10
  2309. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracerebral cysts (in some patients)
    n1=DYNC2H1 gene | n2=en:intracerebral cysts (in some patients) | rel=r_associated | relid=0 | w=10
  2310. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracerebral periventricular calcifications
    n1=DYNC2H1 gene | n2=en:intracerebral periventricular calcifications | rel=r_associated | relid=0 | w=10
  2311. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial bleeding (1 patient)
    n1=DYNC2H1 gene | n2=en:intracranial bleeding (1 patient) | rel=r_associated | relid=0 | w=10
  2312. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial calcification affecting the basal ganglia (in some patients)
    n1=DYNC2H1 gene | n2=en:intracranial calcification affecting the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=10
  2313. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial calcification by x-ray or ct
    n1=DYNC2H1 gene | n2=en:intracranial calcification by x-ray or ct | rel=r_associated | relid=0 | w=10
  2314. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial calcifications (1 patient)
    n1=DYNC2H1 gene | n2=en:intracranial calcifications (1 patient) | rel=r_associated | relid=0 | w=10
  2315. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial calcifications (in some patients)
    n1=DYNC2H1 gene | n2=en:intracranial calcifications (in some patients) | rel=r_associated | relid=0 | w=10
  2316. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial calcifications in the anterior mesial temporal lobes
    n1=DYNC2H1 gene | n2=en:intracranial calcifications in the anterior mesial temporal lobes | rel=r_associated | relid=0 | w=10
  2317. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial calcifications, band-like, particularly periventricular and in the basal ganglia and thalamus
    n1=DYNC2H1 gene | n2=en:intracranial calcifications, band-like, particularly periventricular and in the basal ganglia and thalamus | rel=r_associated | relid=0 | w=10
  2318. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial cysts
    n1=DYNC2H1 gene | n2=en:intracranial cysts | rel=r_associated | relid=0 | w=10
  2319. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial hemorrhage
    n1=DYNC2H1 gene | n2=en:intracranial hemorrhage | rel=r_associated | relid=0 | w=10
  2320. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial hypertension
    n1=DYNC2H1 gene | n2=en:intracranial hypertension | rel=r_associated | relid=0 | w=10
  2321. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial lipoma (cerebello-pontine)
    n1=DYNC2H1 gene | n2=en:intracranial lipoma (cerebello-pontine) | rel=r_associated | relid=0 | w=10
  2322. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intracranial thin-walled sinusoidal vessel (cavernous) malformations
    n1=DYNC2H1 gene | n2=en:intracranial thin-walled sinusoidal vessel (cavernous) malformations | rel=r_associated | relid=0 | w=10
  2323. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intractable epilepsy
    n1=DYNC2H1 gene | n2=en:intractable epilepsy | rel=r_associated | relid=0 | w=10
  2324. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intraneuronal inclusions
    n1=DYNC2H1 gene | n2=en:intraneuronal inclusions | rel=r_associated | relid=0 | w=10
  2325. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intraparenchymal brain hemorrhage, multifocal
    n1=DYNC2H1 gene | n2=en:intraparenchymal brain hemorrhage, multifocal | rel=r_associated | relid=0 | w=10
  2326. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:intraspinal neoplasm
    n1=DYNC2H1 gene | n2=en:intraspinal neoplasm | rel=r_associated | relid=0 | w=10
  2327. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary dystonic or choreiform movements
    n1=DYNC2H1 gene | n2=en:involuntary dystonic or choreiform movements | rel=r_associated | relid=0 | w=10
  2328. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary jerking movements
    n1=DYNC2H1 gene | n2=en:involuntary jerking movements | rel=r_associated | relid=0 | w=10
  2329. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary movements
    n1=DYNC2H1 gene | n2=en:involuntary movements | rel=r_associated | relid=0 | w=10
  2330. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary movements may be precipitated by exertion or anxiety
    n1=DYNC2H1 gene | n2=en:involuntary movements may be precipitated by exertion or anxiety | rel=r_associated | relid=0 | w=10
  2331. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary movements of extremities, neck, trunk, and/or face
    n1=DYNC2H1 gene | n2=en:involuntary movements of extremities, neck, trunk, and/or face | rel=r_associated | relid=0 | w=10
  2332. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary movements, asymmetric
    n1=DYNC2H1 gene | n2=en:involuntary movements, asymmetric | rel=r_associated | relid=0 | w=10
  2333. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary repetitive movements
    n1=DYNC2H1 gene | n2=en:involuntary repetitive movements | rel=r_associated | relid=0 | w=10
  2334. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary rhythmic myoclonic movements ('tremor') of the distal extremities, usually fingers
    n1=DYNC2H1 gene | n2=en:involuntary rhythmic myoclonic movements ('tremor') of the distal extremities, usually fingers | rel=r_associated | relid=0 | w=10
  2335. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary rhythmic myoclonic movements ('tremor'), upper extremities
    n1=DYNC2H1 gene | n2=en:involuntary rhythmic myoclonic movements ('tremor'), upper extremities | rel=r_associated | relid=0 | w=10
  2336. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:involuntary writhing movements
    n1=DYNC2H1 gene | n2=en:involuntary writhing movements | rel=r_associated | relid=0 | w=10
  2337. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ipsilateral brain hypoplasia
    n1=DYNC2H1 gene | n2=en:ipsilateral brain hypoplasia | rel=r_associated | relid=0 | w=10
  2338. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ipsilateral cranial nerve hypoplasia
    n1=DYNC2H1 gene | n2=en:ipsilateral cranial nerve hypoplasia | rel=r_associated | relid=0 | w=10
  2339. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:iq 85-115 (female)
    n1=DYNC2H1 gene | n2=en:iq 85-115 (female) | rel=r_associated | relid=0 | w=10
  2340. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:iron accumulation in the basal ganglia seen on mri
    n1=DYNC2H1 gene | n2=en:iron accumulation in the basal ganglia seen on mri | rel=r_associated | relid=0 | w=10
  2341. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:iron accumulation in the globus pallidus and substantia nigra seen on mri
    n1=DYNC2H1 gene | n2=en:iron accumulation in the globus pallidus and substantia nigra seen on mri | rel=r_associated | relid=0 | w=10
  2342. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:iron deposition in pallidal nuclei
    n1=DYNC2H1 gene | n2=en:iron deposition in pallidal nuclei | rel=r_associated | relid=0 | w=10
  2343. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:iron deposition in the basal ganglia (in some patients)
    n1=DYNC2H1 gene | n2=en:iron deposition in the basal ganglia (in some patients) | rel=r_associated | relid=0 | w=10
  2344. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:iron deposition in the globus pallidus (variable)
    n1=DYNC2H1 gene | n2=en:iron deposition in the globus pallidus (variable) | rel=r_associated | relid=0 | w=10
  2345. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:iron deposition in the globus pallidus and substantia nigra seen on mri
    n1=DYNC2H1 gene | n2=en:iron deposition in the globus pallidus and substantia nigra seen on mri | rel=r_associated | relid=0 | w=10
  2346. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:iron deposits in the globus pallidus, caudate, and substantia nigra
    n1=DYNC2H1 gene | n2=en:iron deposits in the globus pallidus, caudate, and substantia nigra | rel=r_associated | relid=0 | w=10
  2347. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:iron-containing deposits in various brain regions
    n1=DYNC2H1 gene | n2=en:iron-containing deposits in various brain regions | rel=r_associated | relid=0 | w=10
  2348. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:irregular cortical ribbon
    n1=DYNC2H1 gene | n2=en:irregular cortical ribbon | rel=r_associated | relid=0 | w=10
  2349. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:irregular folding of the cortex
    n1=DYNC2H1 gene | n2=en:irregular folding of the cortex | rel=r_associated | relid=0 | w=10
  2350. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:irregular spike and slow waves
    n1=DYNC2H1 gene | n2=en:irregular spike and slow waves | rel=r_associated | relid=0 | w=10
  2351. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:irresistible desire to move the legs
    n1=DYNC2H1 gene | n2=en:irresistible desire to move the legs | rel=r_associated | relid=0 | w=10
  2352. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:irritation
    n1=DYNC2H1 gene | n2=en:irritation | rel=r_associated | relid=0 | w=10
  2353. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ischemic cerebrovascular accident
    n1=DYNC2H1 gene | n2=en:ischemic cerebrovascular accident | rel=r_associated | relid=0 | w=10
  2354. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ischemic infarct of brain
    n1=DYNC2H1 gene | n2=en:ischemic infarct of brain | rel=r_associated | relid=0 | w=10
  2355. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ischemic infarction (rare)
    n1=DYNC2H1 gene | n2=en:ischemic infarction (rare) | rel=r_associated | relid=0 | w=10
  2356. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ischemic necrotic lesions
    n1=DYNC2H1 gene | n2=en:ischemic necrotic lesions | rel=r_associated | relid=0 | w=10
  2357. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ischemic stroke (in some patients)
    n1=DYNC2H1 gene | n2=en:ischemic stroke (in some patients) | rel=r_associated | relid=0 | w=10
  2358. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ischemic stroke in the basal ganglia (rare)
    n1=DYNC2H1 gene | n2=en:ischemic stroke in the basal ganglia (rare) | rel=r_associated | relid=0 | w=10
  2359. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:isolated absence of pain sensation
    n1=DYNC2H1 gene | n2=en:isolated absence of pain sensation | rel=r_associated | relid=0 | w=10
  2360. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:isolated focal dystonia may occur
    n1=DYNC2H1 gene | n2=en:isolated focal dystonia may occur | rel=r_associated | relid=0 | w=10
  2361. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:jacksonian seizure
    n1=DYNC2H1 gene | n2=en:jacksonian seizure | rel=r_associated | relid=0 | w=10
  2362. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:jerk-locked premyoclonus spikes
    n1=DYNC2H1 gene | n2=en:jerk-locked premyoclonus spikes | rel=r_associated | relid=0 | w=10
  2363. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like
    n1=DYNC2H1 gene | n2=en:jerking may be unidirectional, periodically alternating, or mixed pendular and jerk-like | rel=r_associated | relid=0 | w=10
  2364. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:jerking movements
    n1=DYNC2H1 gene | n2=en:jerking movements | rel=r_associated | relid=0 | w=10
  2365. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:jerky head movements
    n1=DYNC2H1 gene | n2=en:jerky head movements | rel=r_associated | relid=0 | w=10
  2366. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:jerky limb movements
    n1=DYNC2H1 gene | n2=en:jerky limb movements | rel=r_associated | relid=0 | w=10
  2367. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:jerky movements in infancy
    n1=DYNC2H1 gene | n2=en:jerky movements in infancy | rel=r_associated | relid=0 | w=10
  2368. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:joubert syndrome
    n1=DYNC2H1 gene | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=10
  2369. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:kearns-sayre syndrome (530000), in a subset of patients
    n1=DYNC2H1 gene | n2=en:kearns-sayre syndrome (530000), in a subset of patients | rel=r_associated | relid=0 | w=10
  2370. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:kernicterus
    n1=DYNC2H1 gene | n2=en:kernicterus | rel=r_associated | relid=0 | w=10
  2371. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:knee and ankle clonus
    n1=DYNC2H1 gene | n2=en:knee and ankle clonus | rel=r_associated | relid=0 | w=10
  2372. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of bunina bodies
    n1=DYNC2H1 gene | n2=en:lack of bunina bodies | rel=r_associated | relid=0 | w=10
  2373. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of communication
    n1=DYNC2H1 gene | n2=en:lack of communication | rel=r_associated | relid=0 | w=10
  2374. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of development
    n1=DYNC2H1 gene | n2=en:lack of development | rel=r_associated | relid=0 | w=10
  2375. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of developmental development
    n1=DYNC2H1 gene | n2=en:lack of developmental development | rel=r_associated | relid=0 | w=10
  2376. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of developmental milestones
    n1=DYNC2H1 gene | n2=en:lack of developmental milestones | rel=r_associated | relid=0 | w=10
  2377. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of ependymal cells
    n1=DYNC2H1 gene | n2=en:lack of ependymal cells | rel=r_associated | relid=0 | w=10
  2378. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of expressive speech
    n1=DYNC2H1 gene | n2=en:lack of expressive speech | rel=r_associated | relid=0 | w=10
  2379. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of head control
    n1=DYNC2H1 gene | n2=en:lack of head control | rel=r_associated | relid=0 | w=10
  2380. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of head or postural control (in severe cases)
    n1=DYNC2H1 gene | n2=en:lack of head or postural control (in severe cases) | rel=r_associated | relid=0 | w=10
  2381. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of independent ambulation
    n1=DYNC2H1 gene | n2=en:lack of independent ambulation | rel=r_associated | relid=0 | w=10
  2382. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of independent ambulation (1 patient)
    n1=DYNC2H1 gene | n2=en:lack of independent ambulation (1 patient) | rel=r_associated | relid=0 | w=10
  2383. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of independent sitting or walking
    n1=DYNC2H1 gene | n2=en:lack of independent sitting or walking | rel=r_associated | relid=0 | w=10
  2384. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of independent walking (in some patients)
    n1=DYNC2H1 gene | n2=en:lack of independent walking (in some patients) | rel=r_associated | relid=0 | w=10
  2385. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of inflammatory infiltrate
    n1=DYNC2H1 gene | n2=en:lack of inflammatory infiltrate | rel=r_associated | relid=0 | w=10
  2386. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of motor development
    n1=DYNC2H1 gene | n2=en:lack of motor development | rel=r_associated | relid=0 | w=10
  2387. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of motor development (wws)
    n1=DYNC2H1 gene | n2=en:lack of motor development (wws) | rel=r_associated | relid=0 | w=10
  2388. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of motor milestones
    n1=DYNC2H1 gene | n2=en:lack of motor milestones | rel=r_associated | relid=0 | w=10
  2389. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of neurologic development
    n1=DYNC2H1 gene | n2=en:lack of neurologic development | rel=r_associated | relid=0 | w=10
  2390. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of peer relationships
    n1=DYNC2H1 gene | n2=en:lack of peer relationships | rel=r_associated | relid=0 | w=10
  2391. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of psychomotor development (1 patient)
    n1=DYNC2H1 gene | n2=en:lack of psychomotor development (1 patient) | rel=r_associated | relid=0 | w=10
  2392. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of psychomotor development (severe connatal form)
    n1=DYNC2H1 gene | n2=en:lack of psychomotor development (severe connatal form) | rel=r_associated | relid=0 | w=10
  2393. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of skein-like inclusions
    n1=DYNC2H1 gene | n2=en:lack of skein-like inclusions | rel=r_associated | relid=0 | w=10
  2394. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of speech (in severe cases)
    n1=DYNC2H1 gene | n2=en:lack of speech (in severe cases) | rel=r_associated | relid=0 | w=10
  2395. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of speech acquisition
    n1=DYNC2H1 gene | n2=en:lack of speech acquisition | rel=r_associated | relid=0 | w=10
  2396. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of speech development
    n1=DYNC2H1 gene | n2=en:lack of speech development | rel=r_associated | relid=0 | w=10
  2397. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of speech development (some patients)
    n1=DYNC2H1 gene | n2=en:lack of speech development (some patients) | rel=r_associated | relid=0 | w=10
  2398. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of speech or only a few words
    n1=DYNC2H1 gene | n2=en:lack of speech or only a few words | rel=r_associated | relid=0 | w=10
  2399. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of speech or poor speech
    n1=DYNC2H1 gene | n2=en:lack of speech or poor speech | rel=r_associated | relid=0 | w=10
  2400. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of spontaneous movement
    n1=DYNC2H1 gene | n2=en:lack of spontaneous movement | rel=r_associated | relid=0 | w=10
  2401. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of spontaneous play
    n1=DYNC2H1 gene | n2=en:lack of spontaneous play | rel=r_associated | relid=0 | w=10
  2402. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of upper motor neuron signs
    n1=DYNC2H1 gene | n2=en:lack of upper motor neuron signs | rel=r_associated | relid=0 | w=10
  2403. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of verbal communication
    n1=DYNC2H1 gene | n2=en:lack of verbal communication | rel=r_associated | relid=0 | w=10
  2404. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of visual attention
    n1=DYNC2H1 gene | n2=en:lack of visual attention | rel=r_associated | relid=0 | w=10
  2405. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lack of volitional movement
    n1=DYNC2H1 gene | n2=en:lack of volitional movement | rel=r_associated | relid=0 | w=10
  2406. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lacunar infarcts develop after age 40 years
    n1=DYNC2H1 gene | n2=en:lacunar infarcts develop after age 40 years | rel=r_associated | relid=0 | w=10
  2407. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging
    n1=DYNC2H1 gene | n2=en:lacunar infarcts in the deep-brain nuclei, brainstem, internal capsule seen on imaging | rel=r_associated | relid=0 | w=10
  2408. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:laminar necrosis
    n1=DYNC2H1 gene | n2=en:laminar necrosis | rel=r_associated | relid=0 | w=10
  2409. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:language acquisition difficulties (in some patients)
    n1=DYNC2H1 gene | n2=en:language acquisition difficulties (in some patients) | rel=r_associated | relid=0 | w=10
  2410. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:language delay
    n1=DYNC2H1 gene | n2=en:language delay | rel=r_associated | relid=0 | w=10
  2411. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:language delay (55%)
    n1=DYNC2H1 gene | n2=en:language delay (55%) | rel=r_associated | relid=0 | w=10
  2412. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:language delay/disorder
    n1=DYNC2H1 gene | n2=en:language delay/disorder | rel=r_associated | relid=0 | w=10
  2413. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:language development limited to a few words
    n1=DYNC2H1 gene | n2=en:language development limited to a few words | rel=r_associated | relid=0 | w=10
  2414. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:language disorder
    n1=DYNC2H1 gene | n2=en:language disorder | rel=r_associated | relid=0 | w=10
  2415. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:large basal ganglia
    n1=DYNC2H1 gene | n2=en:large basal ganglia | rel=r_associated | relid=0 | w=10
  2416. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:large cavum vergae
    n1=DYNC2H1 gene | n2=en:large cavum vergae | rel=r_associated | relid=0 | w=10
  2417. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:large cerebellum, progressive
    n1=DYNC2H1 gene | n2=en:large cerebellum, progressive | rel=r_associated | relid=0 | w=10
  2418. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:large sella turcica
    n1=DYNC2H1 gene | n2=en:large sella turcica | rel=r_associated | relid=0 | w=10
  2419. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:large subcortical cysts in frontal and temporal lobes
    n1=DYNC2H1 gene | n2=en:large subcortical cysts in frontal and temporal lobes | rel=r_associated | relid=0 | w=10
  2420. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:laryngeal nerve paralysis
    n1=DYNC2H1 gene | n2=en:laryngeal nerve paralysis | rel=r_associated | relid=0 | w=10
  2421. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:late ambulation
    n1=DYNC2H1 gene | n2=en:late ambulation | rel=r_associated | relid=0 | w=10
  2422. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:late diaphragmatic involvement
    n1=DYNC2H1 gene | n2=en:late diaphragmatic involvement | rel=r_associated | relid=0 | w=10
  2423. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:late-onset spinocerebellar degeneration
    n1=DYNC2H1 gene | n2=en:late-onset spinocerebellar degeneration | rel=r_associated | relid=0 | w=10
  2424. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lateral corticospinal tracts show atrophy, pallor, and degeneration
    n1=DYNC2H1 gene | n2=en:lateral corticospinal tracts show atrophy, pallor, and degeneration | rel=r_associated | relid=0 | w=10
  2425. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning and developmental delay (in some patients)
    n1=DYNC2H1 gene | n2=en:learning and developmental delay (in some patients) | rel=r_associated | relid=0 | w=10
  2426. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning difficulties
    n1=DYNC2H1 gene | n2=en:learning difficulties | rel=r_associated | relid=0 | w=10
  2427. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning difficulties (in 1 patient)
    n1=DYNC2H1 gene | n2=en:learning difficulties (in 1 patient) | rel=r_associated | relid=0 | w=10
  2428. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning difficulties (in some patients)
    n1=DYNC2H1 gene | n2=en:learning difficulties (in some patients) | rel=r_associated | relid=0 | w=10
  2429. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning difficulties (less common)
    n1=DYNC2H1 gene | n2=en:learning difficulties (less common) | rel=r_associated | relid=0 | w=10
  2430. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning difficulties (seen in recessive form)
    n1=DYNC2H1 gene | n2=en:learning difficulties (seen in recessive form) | rel=r_associated | relid=0 | w=10
  2431. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning difficulties in affected females
    n1=DYNC2H1 gene | n2=en:learning difficulties in affected females | rel=r_associated | relid=0 | w=10
  2432. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning difficulties, mild (1 family)
    n1=DYNC2H1 gene | n2=en:learning difficulties, mild (1 family) | rel=r_associated | relid=0 | w=10
  2433. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning disabilities
    n1=DYNC2H1 gene | n2=en:learning disabilities | rel=r_associated | relid=0 | w=10
  2434. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning disabilities (1 family)
    n1=DYNC2H1 gene | n2=en:learning disabilities (1 family) | rel=r_associated | relid=0 | w=10
  2435. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning disabilities (30%)
    n1=DYNC2H1 gene | n2=en:learning disabilities (30%) | rel=r_associated | relid=0 | w=10
  2436. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning disabilities (in females)
    n1=DYNC2H1 gene | n2=en:learning disabilities (in females) | rel=r_associated | relid=0 | w=10
  2437. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning disabilities (in some patients)
    n1=DYNC2H1 gene | n2=en:learning disabilities (in some patients) | rel=r_associated | relid=0 | w=10
  2438. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning disabilities (in some)
    n1=DYNC2H1 gene | n2=en:learning disabilities (in some) | rel=r_associated | relid=0 | w=10
  2439. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning disabilities (major)
    n1=DYNC2H1 gene | n2=en:learning disabilities (major) | rel=r_associated | relid=0 | w=10
  2440. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning disability (90% patients)
    n1=DYNC2H1 gene | n2=en:learning disability (90% patients) | rel=r_associated | relid=0 | w=10
  2441. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning disability (early in life)
    n1=DYNC2H1 gene | n2=en:learning disability (early in life) | rel=r_associated | relid=0 | w=10
  2442. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:learning problems
    n1=DYNC2H1 gene | n2=en:learning problems | rel=r_associated | relid=0 | w=10
  2443. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leg cramp
    n1=DYNC2H1 gene | n2=en:leg cramp | rel=r_associated | relid=0 | w=10
  2444. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leg pain
    n1=DYNC2H1 gene | n2=en:leg pain | rel=r_associated | relid=0 | w=10
  2445. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leg stiffness
    n1=DYNC2H1 gene | n2=en:leg stiffness | rel=r_associated | relid=0 | w=10
  2446. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leigh disease
    n1=DYNC2H1 gene | n2=en:leigh disease | rel=r_associated | relid=0 | w=10
  2447. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leigh syndrome (245000), in a subset of patients
    n1=DYNC2H1 gene | n2=en:leigh syndrome (245000), in a subset of patients | rel=r_associated | relid=0 | w=10
  2448. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leigh syndrome (in some patients)
    n1=DYNC2H1 gene | n2=en:leigh syndrome (in some patients) | rel=r_associated | relid=0 | w=10
  2449. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leptomeningeal melanocytosis (in some patients)
    n1=DYNC2H1 gene | n2=en:leptomeningeal melanocytosis (in some patients) | rel=r_associated | relid=0 | w=10
  2450. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leptomeningeal thickening
    n1=DYNC2H1 gene | n2=en:leptomeningeal thickening | rel=r_associated | relid=0 | w=10
  2451. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions are symmetrical
    n1=DYNC2H1 gene | n2=en:lesions are symmetrical | rel=r_associated | relid=0 | w=10
  2452. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation
    n1=DYNC2H1 gene | n2=en:lesions characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation | rel=r_associated | relid=0 | w=10
  2453. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord
    n1=DYNC2H1 gene | n2=en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord | rel=r_associated | relid=0 | w=10
  2454. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions in basal ganglia, brainstem, cerebellum, thalamus, spinal cord characterized by demyelination, necrosis, gliosis, spongiosis, and capillary proliferation
    n1=DYNC2H1 gene | 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=10
  2455. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions in the anterior pituitary (less common)
    n1=DYNC2H1 gene | n2=en:lesions in the anterior pituitary (less common) | rel=r_associated | relid=0 | w=10
  2456. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions in the basal ganglia
    n1=DYNC2H1 gene | n2=en:lesions in the basal ganglia | rel=r_associated | relid=0 | w=10
  2457. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions in the caudate and putamen
    n1=DYNC2H1 gene | n2=en:lesions in the caudate and putamen | rel=r_associated | relid=0 | w=10
  2458. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions in the caudate and putamen seen on mri
    n1=DYNC2H1 gene | n2=en:lesions in the caudate and putamen seen on mri | rel=r_associated | relid=0 | w=10
  2459. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions in the internal capsule after age 40 years
    n1=DYNC2H1 gene | n2=en:lesions in the internal capsule after age 40 years | rel=r_associated | relid=0 | w=10
  2460. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lesions show signal increase on t2- and signal decrease on t1-weighted images
    n1=DYNC2H1 gene | n2=en:lesions show signal increase on t2- and signal decrease on t1-weighted images | rel=r_associated | relid=0 | w=10
  2461. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lethargy
    n1=DYNC2H1 gene | n2=en:lethargy | rel=r_associated | relid=0 | w=10
  2462. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lethargy associated with hypoglycemia
    n1=DYNC2H1 gene | n2=en:lethargy associated with hypoglycemia | rel=r_associated | relid=0 | w=10
  2463. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lethargy, neonatal
    n1=DYNC2H1 gene | n2=en:lethargy, neonatal | rel=r_associated | relid=0 | w=10
  2464. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukoaraiosis
    n1=DYNC2H1 gene | n2=en:leukoaraiosis | rel=r_associated | relid=0 | w=10
  2465. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukodystrophy
    n1=DYNC2H1 gene | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=10
  2466. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukodystrophy (in 1 of 2 patients)
    n1=DYNC2H1 gene | n2=en:leukodystrophy (in 1 of 2 patients) | rel=r_associated | relid=0 | w=10
  2467. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukodystrophy (in some patients)
    n1=DYNC2H1 gene | n2=en:leukodystrophy (in some patients) | rel=r_associated | relid=0 | w=10
  2468. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukodystrophy and white matter changes, which improve with age
    n1=DYNC2H1 gene | n2=en:leukodystrophy and white matter changes, which improve with age | rel=r_associated | relid=0 | w=10
  2469. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukodystrophy, demyelinating
    n1=DYNC2H1 gene | n2=en:leukodystrophy, demyelinating | rel=r_associated | relid=0 | w=10
  2470. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukodystrophy, hypomyelinating
    n1=DYNC2H1 gene | n2=en:leukodystrophy, hypomyelinating | rel=r_associated | relid=0 | w=10
  2471. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukoencephalopathy
    n1=DYNC2H1 gene | n2=en:leukoencephalopathy | rel=r_associated | relid=0 | w=10
  2472. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukoencephalopathy in the frontal and parietal lobes (later)
    n1=DYNC2H1 gene | n2=en:leukoencephalopathy in the frontal and parietal lobes (later) | rel=r_associated | relid=0 | w=10
  2473. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukoencephalopathy in the periventricular and deep white matter and brainstem, cerebellum, and spinal cord tracts
    n1=DYNC2H1 gene | n2=en:leukoencephalopathy in the periventricular and deep white matter and brainstem, cerebellum, and spinal cord tracts | rel=r_associated | relid=0 | w=10
  2474. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukoencephalopathy on ct and mri
    n1=DYNC2H1 gene | n2=en:leukoencephalopathy on ct and mri | rel=r_associated | relid=0 | w=10
  2475. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukoencephalopathy, severe
    n1=DYNC2H1 gene | n2=en:leukoencephalopathy, severe | rel=r_associated | relid=0 | w=10
  2476. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:leukomalacia (rare)
    n1=DYNC2H1 gene | n2=en:leukomalacia (rare) | rel=r_associated | relid=0 | w=10
  2477. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lewy bodies
    n1=DYNC2H1 gene | n2=en:lewy bodies | rel=r_associated | relid=0 | w=10
  2478. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lewy bodies (not always present)
    n1=DYNC2H1 gene | n2=en:lewy bodies (not always present) | rel=r_associated | relid=0 | w=10
  2479. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lewy bodies in the substantia nigra
    n1=DYNC2H1 gene | n2=en:lewy bodies in the substantia nigra | rel=r_associated | relid=0 | w=10
  2480. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lewy bodies throughout the brain
    n1=DYNC2H1 gene | n2=en:lewy bodies throughout the brain | rel=r_associated | relid=0 | w=10
  2481. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:light-induced sneezing
    n1=DYNC2H1 gene | n2=en:light-induced sneezing | rel=r_associated | relid=0 | w=10
  2482. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lightheadedness
    n1=DYNC2H1 gene | n2=en:lightheadedness | rel=r_associated | relid=0 | w=10
  2483. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb ataxia, progressive
    n1=DYNC2H1 gene | n2=en:limb ataxia, progressive | rel=r_associated | relid=0 | w=10
  2484. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb dysmetria
    n1=DYNC2H1 gene | n2=en:limb dysmetria | rel=r_associated | relid=0 | w=10
  2485. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb dystonia
    n1=DYNC2H1 gene | n2=en:limb dystonia | rel=r_associated | relid=0 | w=10
  2486. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb dystonia (18%)
    n1=DYNC2H1 gene | n2=en:limb dystonia (18%) | rel=r_associated | relid=0 | w=10
  2487. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb fasciculations
    n1=DYNC2H1 gene | n2=en:limb fasciculations | rel=r_associated | relid=0 | w=10
  2488. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb hypertonia
    n1=DYNC2H1 gene | n2=en:limb hypertonia | rel=r_associated | relid=0 | w=10
  2489. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb hypertonia (in some patients)
    n1=DYNC2H1 gene | n2=en:limb hypertonia (in some patients) | rel=r_associated | relid=0 | w=10
  2490. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb incoordination (in some patients)
    n1=DYNC2H1 gene | n2=en:limb incoordination (in some patients) | rel=r_associated | relid=0 | w=10
  2491. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb muscle stiffness is often asymmetric
    n1=DYNC2H1 gene | n2=en:limb muscle stiffness is often asymmetric | rel=r_associated | relid=0 | w=10
  2492. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb muscle weakness (distal greater than proximal)
    n1=DYNC2H1 gene | n2=en:limb muscle weakness (distal greater than proximal) | rel=r_associated | relid=0 | w=10
  2493. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb posturing (if left untreated)
    n1=DYNC2H1 gene | n2=en:limb posturing (if left untreated) | rel=r_associated | relid=0 | w=10
  2494. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limb spasticity
    n1=DYNC2H1 gene | n2=en:limb spasticity | rel=r_associated | relid=0 | w=10
  2495. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limbic malformations
    n1=DYNC2H1 gene | n2=en:limbic malformations | rel=r_associated | relid=0 | w=10
  2496. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limited expressive language
    n1=DYNC2H1 gene | n2=en:limited expressive language | rel=r_associated | relid=0 | w=10
  2497. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limited memory, attention, language
    n1=DYNC2H1 gene | n2=en:limited memory, attention, language | rel=r_associated | relid=0 | w=10
  2498. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limited verbal comprehension
    n1=DYNC2H1 gene | n2=en:limited verbal comprehension | rel=r_associated | relid=0 | w=10
  2499. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:limited walking ability
    n1=DYNC2H1 gene | n2=en:limited walking ability | rel=r_associated | relid=0 | w=10
  2500. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lingual-facial-buccal dyskinesia
    n1=DYNC2H1 gene | n2=en:lingual-facial-buccal dyskinesia | rel=r_associated | relid=0 | w=10
  2501. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lipoma, anterior sacral
    n1=DYNC2H1 gene | n2=en:lipoma, anterior sacral | rel=r_associated | relid=0 | w=10
  2502. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lipomyelocystoceles
    n1=DYNC2H1 gene | n2=en:lipomyelocystoceles | rel=r_associated | relid=0 | w=10
  2503. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lissencephaly
    n1=DYNC2H1 gene | n2=en:lissencephaly | rel=r_associated | relid=0 | w=10
  2504. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions)
    n1=DYNC2H1 gene | n2=en:lissencephaly (anterior to posterior decreasing gradient of severity, more prominent in anterior brain regions) | rel=r_associated | relid=0 | w=10
  2505. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions)
    n1=DYNC2H1 gene | n2=en:lissencephaly (anterior to posterior increasing gradient of severity and more prominent in posterior brain regions) | rel=r_associated | relid=0 | w=10
  2506. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lissencephaly (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:lissencephaly (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  2507. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lissencephaly, posterior to anterior gradient
    n1=DYNC2H1 gene | n2=en:lissencephaly, posterior to anterior gradient | rel=r_associated | relid=0 | w=10
  2508. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:little or no speech acquisition
    n1=DYNC2H1 gene | n2=en:little or no speech acquisition | rel=r_associated | relid=0 | w=10
  2509. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:little polarity in remaining neurons
    n1=DYNC2H1 gene | n2=en:little polarity in remaining neurons | rel=r_associated | relid=0 | w=10
  2510. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:little spontaneous limb movement
    n1=DYNC2H1 gene | n2=en:little spontaneous limb movement | rel=r_associated | relid=0 | w=10
  2511. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:little spontaneous movement
    n1=DYNC2H1 gene | n2=en:little spontaneous movement | rel=r_associated | relid=0 | w=10
  2512. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lobar holoprosencephalies
    n1=DYNC2H1 gene | n2=en:lobar holoprosencephalies | rel=r_associated | relid=0 | w=10
  2513. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles
    n1=DYNC2H1 gene | n2=en:lobar hpe shows clear interhemispheric fissure and 2 lateral ventricles | rel=r_associated | relid=0 | w=10
  2514. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:locomotor delay (early-onset form)
    n1=DYNC2H1 gene | n2=en:locomotor delay (early-onset form) | rel=r_associated | relid=0 | w=10
  2515. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:long perforating arteries of the brain are affected
    n1=DYNC2H1 gene | n2=en:long perforating arteries of the brain are affected | rel=r_associated | relid=0 | w=10
  2516. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:long-tract signs
    n1=DYNC2H1 gene | n2=en:long-tract signs | rel=r_associated | relid=0 | w=10
  2517. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:long, thickened cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:long, thickened cerebellar peduncles | rel=r_associated | relid=0 | w=10
  2518. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of ability to walk
    n1=DYNC2H1 gene | n2=en:loss of ability to walk | rel=r_associated | relid=0 | w=10
  2519. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of ability to walk in first decade
    n1=DYNC2H1 gene | n2=en:loss of ability to walk in first decade | rel=r_associated | relid=0 | w=10
  2520. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of ability to walk later
    n1=DYNC2H1 gene | n2=en:loss of ability to walk later | rel=r_associated | relid=0 | w=10
  2521. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of ambulation
    n1=DYNC2H1 gene | n2=en:loss of ambulation | rel=r_associated | relid=0 | w=10
  2522. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of ankle reflexes
    n1=DYNC2H1 gene | n2=en:loss of ankle reflexes | rel=r_associated | relid=0 | w=10
  2523. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of anterior horn cells and gliosis in the spinal cord
    n1=DYNC2H1 gene | n2=en:loss of anterior horn cells and gliosis in the spinal cord | rel=r_associated | relid=0 | w=10
  2524. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of any acquired abilities in early childhood
    n1=DYNC2H1 gene | n2=en:loss of any acquired abilities in early childhood | rel=r_associated | relid=0 | w=10
  2525. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of balance may occur
    n1=DYNC2H1 gene | n2=en:loss of balance may occur | rel=r_associated | relid=0 | w=10
  2526. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of cerebellar granular cells
    n1=DYNC2H1 gene | n2=en:loss of cerebellar granular cells | rel=r_associated | relid=0 | w=10
  2527. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of cerebellar purkinje cells
    n1=DYNC2H1 gene | n2=en:loss of cerebellar purkinje cells | rel=r_associated | relid=0 | w=10
  2528. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of cerebral white matter (in 1 of 3 patients)
    n1=DYNC2H1 gene | n2=en:loss of cerebral white matter (in 1 of 3 patients) | rel=r_associated | relid=0 | w=10
  2529. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of consciousness
    n1=DYNC2H1 gene | n2=en:loss of consciousness | rel=r_associated | relid=0 | w=10
  2530. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of consciousness (1 patient)
    n1=DYNC2H1 gene | n2=en:loss of consciousness (1 patient) | rel=r_associated | relid=0 | w=10
  2531. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of coordination
    n1=DYNC2H1 gene | n2=en:loss of coordination | rel=r_associated | relid=0 | w=10
  2532. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of deep tendon reflexes (later)
    n1=DYNC2H1 gene | n2=en:loss of deep tendon reflexes (later) | rel=r_associated | relid=0 | w=10
  2533. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of developmental milestones
    n1=DYNC2H1 gene | n2=en:loss of developmental milestones | rel=r_associated | relid=0 | w=10
  2534. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of dopaminergic neurons
    n1=DYNC2H1 gene | n2=en:loss of dopaminergic neurons | rel=r_associated | relid=0 | w=10
  2535. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of dopaminergic neurons in the substantia nigra
    n1=DYNC2H1 gene | n2=en:loss of dopaminergic neurons in the substantia nigra | rel=r_associated | relid=0 | w=10
  2536. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of dorsal root ganglion cells
    n1=DYNC2H1 gene | n2=en:loss of dorsal root ganglion cells | rel=r_associated | relid=0 | w=10
  2537. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of executive functions
    n1=DYNC2H1 gene | n2=en:loss of executive functions | rel=r_associated | relid=0 | w=10
  2538. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of fine motor skills
    n1=DYNC2H1 gene | n2=en:loss of fine motor skills | rel=r_associated | relid=0 | w=10
  2539. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of gait (in some)
    n1=DYNC2H1 gene | n2=en:loss of gait (in some) | rel=r_associated | relid=0 | w=10
  2540. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of hypocretin (orexin)-secreting neurons in the hypothalamus
    n1=DYNC2H1 gene | n2=en:loss of hypocretin (orexin)-secreting neurons in the hypothalamus | rel=r_associated | relid=0 | w=10
  2541. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of independent ambulation
    n1=DYNC2H1 gene | n2=en:loss of independent ambulation | rel=r_associated | relid=0 | w=10
  2542. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of independent ambulation (in some patients)
    n1=DYNC2H1 gene | n2=en:loss of independent ambulation (in some patients) | rel=r_associated | relid=0 | w=10
  2543. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of independent ambulation approximately 30 years after onset
    n1=DYNC2H1 gene | n2=en:loss of independent ambulation approximately 30 years after onset | rel=r_associated | relid=0 | w=10
  2544. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of independent ambulation by age 10 years
    n1=DYNC2H1 gene | n2=en:loss of independent ambulation by age 10 years | rel=r_associated | relid=0 | w=10
  2545. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of independent ambulation within a few years
    n1=DYNC2H1 gene | n2=en:loss of independent ambulation within a few years | rel=r_associated | relid=0 | w=10
  2546. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of language ability
    n1=DYNC2H1 gene | n2=en:loss of language ability | rel=r_associated | relid=0 | w=10
  2547. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of lower alpha-motor neurons in the anterior horn of the spinal cord and lower brainstem
    n1=DYNC2H1 gene | 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=10
  2548. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of motor functions
    n1=DYNC2H1 gene | n2=en:loss of motor functions | rel=r_associated | relid=0 | w=10
  2549. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of motor milestones
    n1=DYNC2H1 gene | n2=en:loss of motor milestones | rel=r_associated | relid=0 | w=10
  2550. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of motor neurons in the anterior horn of the spinal cord
    n1=DYNC2H1 gene | n2=en:loss of motor neurons in the anterior horn of the spinal cord | rel=r_associated | relid=0 | w=10
  2551. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of motor neurons in the spinal cord
    n1=DYNC2H1 gene | n2=en:loss of motor neurons in the spinal cord | rel=r_associated | relid=0 | w=10
  2552. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of motor skills
    n1=DYNC2H1 gene | n2=en:loss of motor skills | rel=r_associated | relid=0 | w=10
  2553. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of myelin
    n1=DYNC2H1 gene | n2=en:loss of myelin | rel=r_associated | relid=0 | w=10
  2554. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of myelin and oligodendroglia
    n1=DYNC2H1 gene | n2=en:loss of myelin and oligodendroglia | rel=r_associated | relid=0 | w=10
  2555. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of myelin in the cerebral and cerebellar white matter
    n1=DYNC2H1 gene | n2=en:loss of myelin in the cerebral and cerebellar white matter | rel=r_associated | relid=0 | w=10
  2556. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of myelin in the descending lateral spinal cord tracts
    n1=DYNC2H1 gene | n2=en:loss of myelin in the descending lateral spinal cord tracts | rel=r_associated | relid=0 | w=10
  2557. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of myelin in the pyramidal tracts
    n1=DYNC2H1 gene | n2=en:loss of myelin in the pyramidal tracts | rel=r_associated | relid=0 | w=10
  2558. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of myelinated fibers in spinal cord roots
    n1=DYNC2H1 gene | n2=en:loss of myelinated fibers in spinal cord roots | rel=r_associated | relid=0 | w=10
  2559. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of myelinated fibers with regenerative clusters on biopsy
    n1=DYNC2H1 gene | n2=en:loss of myelinated fibers with regenerative clusters on biopsy | rel=r_associated | relid=0 | w=10
  2560. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of neurons affecting all cortical layers
    n1=DYNC2H1 gene | n2=en:loss of neurons affecting all cortical layers | rel=r_associated | relid=0 | w=10
  2561. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord
    n1=DYNC2H1 gene | n2=en:loss of neurons and gliosis in basal ganglia, cranial nerve nuclei, and spinal cord | rel=r_associated | relid=0 | w=10
  2562. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of pain and temperature in a cape-like distribution
    n1=DYNC2H1 gene | n2=en:loss of pain and temperature in a cape-like distribution | rel=r_associated | relid=0 | w=10
  2563. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of pigmented neurons in the substantia nigra
    n1=DYNC2H1 gene | n2=en:loss of pigmented neurons in the substantia nigra | rel=r_associated | relid=0 | w=10
  2564. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of postural tone
    n1=DYNC2H1 gene | n2=en:loss of postural tone | rel=r_associated | relid=0 | w=10
  2565. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of primary reflexes
    n1=DYNC2H1 gene | n2=en:loss of primary reflexes | rel=r_associated | relid=0 | w=10
  2566. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of purkinje cells
    n1=DYNC2H1 gene | n2=en:loss of purkinje cells | rel=r_associated | relid=0 | w=10
  2567. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of purkinje cells in the cerebellar vermis
    n1=DYNC2H1 gene | n2=en:loss of purkinje cells in the cerebellar vermis | rel=r_associated | relid=0 | w=10
  2568. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of purkinje cells in the cerebellum
    n1=DYNC2H1 gene | n2=en:loss of purkinje cells in the cerebellum | rel=r_associated | relid=0 | w=10
  2569. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of purposeful hand movements
    n1=DYNC2H1 gene | n2=en:loss of purposeful hand movements | rel=r_associated | relid=0 | w=10
  2570. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of reflexes due to myopathy
    n1=DYNC2H1 gene | n2=en:loss of reflexes due to myopathy | rel=r_associated | relid=0 | w=10
  2571. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of speech
    n1=DYNC2H1 gene | n2=en:loss of speech | rel=r_associated | relid=0 | w=10
  2572. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of speech (1 patient)
    n1=DYNC2H1 gene | n2=en:loss of speech (1 patient) | rel=r_associated | relid=0 | w=10
  2573. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of speech development
    n1=DYNC2H1 gene | n2=en:loss of speech development | rel=r_associated | relid=0 | w=10
  2574. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of spontaneous movements
    n1=DYNC2H1 gene | n2=en:loss of spontaneous movements | rel=r_associated | relid=0 | w=10
  2575. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of very early milestones
    n1=DYNC2H1 gene | n2=en:loss of very early milestones | rel=r_associated | relid=0 | w=10
  2576. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:loss of white matter
    n1=DYNC2H1 gene | n2=en:loss of white matter | rel=r_associated | relid=0 | w=10
  2577. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:low apparent diffusion coefficient (adc) values
    n1=DYNC2H1 gene | n2=en:low apparent diffusion coefficient (adc) values | rel=r_associated | relid=0 | w=10
  2578. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:low densities in the basal ganglia similar to leigh syndrome (256000)
    n1=DYNC2H1 gene | n2=en:low densities in the basal ganglia similar to leigh syndrome (256000) | rel=r_associated | relid=0 | w=10
  2579. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:low density white matter on ct scan
    n1=DYNC2H1 gene | n2=en:low density white matter on ct scan | rel=r_associated | relid=0 | w=10
  2580. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:low iq
    n1=DYNC2H1 gene | n2=en:low iq | rel=r_associated | relid=0 | w=10
  2581. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:low-lying cerebellar tonsils
    n1=DYNC2H1 gene | n2=en:low-lying cerebellar tonsils | rel=r_associated | relid=0 | w=10
  2582. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:low-normal intelligence
    n1=DYNC2H1 gene | n2=en:low-normal intelligence | rel=r_associated | relid=0 | w=10
  2583. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:low-normal iq
    n1=DYNC2H1 gene | n2=en:low-normal iq | rel=r_associated | relid=0 | w=10
  2584. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower extremity weakness with febrile episodes (rare)
    n1=DYNC2H1 gene | n2=en:lower extremity weakness with febrile episodes (rare) | rel=r_associated | relid=0 | w=10
  2585. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb atrophy
    n1=DYNC2H1 gene | n2=en:lower limb atrophy | rel=r_associated | relid=0 | w=10
  2586. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb dystonia
    n1=DYNC2H1 gene | n2=en:lower limb dystonia | rel=r_associated | relid=0 | w=10
  2587. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb hyperreflexia
    n1=DYNC2H1 gene | n2=en:lower limb hyperreflexia | rel=r_associated | relid=0 | w=10
  2588. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb hyperreflexia (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:lower limb hyperreflexia (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  2589. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb hypertonia
    n1=DYNC2H1 gene | n2=en:lower limb hypertonia | rel=r_associated | relid=0 | w=10
  2590. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb hypotrophy
    n1=DYNC2H1 gene | n2=en:lower limb hypotrophy | rel=r_associated | relid=0 | w=10
  2591. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb muscle atrophy
    n1=DYNC2H1 gene | n2=en:lower limb muscle atrophy | rel=r_associated | relid=0 | w=10
  2592. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb muscle weakness (occurs later)
    n1=DYNC2H1 gene | n2=en:lower limb muscle weakness (occurs later) | rel=r_associated | relid=0 | w=10
  2593. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb spasticity
    n1=DYNC2H1 gene | n2=en:lower limb spasticity | rel=r_associated | relid=0 | w=10
  2594. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb spasticity, mild
    n1=DYNC2H1 gene | n2=en:lower limb spasticity, mild | rel=r_associated | relid=0 | w=10
  2595. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limb weakness, proximal
    n1=DYNC2H1 gene | n2=en:lower limb weakness, proximal | rel=r_associated | relid=0 | w=10
  2596. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limbs affected before upper limbs
    n1=DYNC2H1 gene | n2=en:lower limbs affected before upper limbs | rel=r_associated | relid=0 | w=10
  2597. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower limbs weakness and atrophy, distal
    n1=DYNC2H1 gene | n2=en:lower limbs weakness and atrophy, distal | rel=r_associated | relid=0 | w=10
  2598. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower motor neuron degeneration
    n1=DYNC2H1 gene | n2=en:lower motor neuron degeneration | rel=r_associated | relid=0 | w=10
  2599. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower motor neuron disease affecting upper and lower limbs
    n1=DYNC2H1 gene | n2=en:lower motor neuron disease affecting upper and lower limbs | rel=r_associated | relid=0 | w=10
  2600. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower motor neuron dysfunction
    n1=DYNC2H1 gene | n2=en:lower motor neuron dysfunction | rel=r_associated | relid=0 | w=10
  2601. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower motor neuron dysfunction involving upper and lower limbs
    n1=DYNC2H1 gene | n2=en:lower motor neuron dysfunction involving upper and lower limbs | rel=r_associated | relid=0 | w=10
  2602. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower motor neuron involvement after long disease duration
    n1=DYNC2H1 gene | n2=en:lower motor neuron involvement after long disease duration | rel=r_associated | relid=0 | w=10
  2603. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower motor neuron involvement, mild, seen on emg (in some patients)
    n1=DYNC2H1 gene | n2=en:lower motor neuron involvement, mild, seen on emg (in some patients) | rel=r_associated | relid=0 | w=10
  2604. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower motor neuron signs, later
    n1=DYNC2H1 gene | n2=en:lower motor neuron signs, later | rel=r_associated | relid=0 | w=10
  2605. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower motor neuron symptoms
    n1=DYNC2H1 gene | n2=en:lower motor neuron symptoms | rel=r_associated | relid=0 | w=10
  2606. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lower motor signs
    n1=DYNC2H1 gene | n2=en:lower motor signs | rel=r_associated | relid=0 | w=10
  2607. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis
    n1=DYNC2H1 gene | n2=en:lumbar paraspinal rigidity causes exaggerated lumbar lordosis | rel=r_associated | relid=0 | w=10
  2608. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lumbosacral meningocele
    n1=DYNC2H1 gene | n2=en:lumbosacral meningocele | rel=r_associated | relid=0 | w=10
  2609. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:lymphocytic infiltration of the brain
    n1=DYNC2H1 gene | n2=en:lymphocytic infiltration of the brain | rel=r_associated | relid=0 | w=10
  2610. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:macrocephaly (due to dandy-walker malformation)
    n1=DYNC2H1 gene | n2=en:macrocephaly (due to dandy-walker malformation) | rel=r_associated | relid=0 | w=10
  2611. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:macroencephaly
    n1=DYNC2H1 gene | n2=en:macroencephaly | rel=r_associated | relid=0 | w=10
  2612. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter
    n1=DYNC2H1 gene | n2=en:magnetic resonance spectroscopy (mrs) shows decreased n-acetylaspartic acid in unaffected white matter | rel=r_associated | relid=0 | w=10
  2613. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:magnetic resonance spectroscopy (mrs) shows increased lactate in the central nervous system
    n1=DYNC2H1 gene | n2=en:magnetic resonance spectroscopy (mrs) shows increased lactate in the central nervous system | rel=r_associated | relid=0 | w=10
  2614. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:magnetic resonance spectroscopy shows increased lactate in white matter
    n1=DYNC2H1 gene | n2=en:magnetic resonance spectroscopy shows increased lactate in white matter | rel=r_associated | relid=0 | w=10
  2615. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:major developmental delay
    n1=DYNC2H1 gene | n2=en:major developmental delay | rel=r_associated | relid=0 | w=10
  2616. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:major developmental milestones are not attained
    n1=DYNC2H1 gene | n2=en:major developmental milestones are not attained | rel=r_associated | relid=0 | w=10
  2617. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:malformation of the insula
    n1=DYNC2H1 gene | n2=en:malformation of the insula | rel=r_associated | relid=0 | w=10
  2618. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:malformation, cerebral arteriovenous
    n1=DYNC2H1 gene | n2=en:malformation, cerebral arteriovenous | rel=r_associated | relid=0 | w=10
  2619. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:malformations of cortical development
    n1=DYNC2H1 gene | n2=en:malformations of cortical development | rel=r_associated | relid=0 | w=10
  2620. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:malformations of cortical development, variable
    n1=DYNC2H1 gene | n2=en:malformations of cortical development, variable | rel=r_associated | relid=0 | w=10
  2621. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:malformations of the mid- and hindbrain
    n1=DYNC2H1 gene | n2=en:malformations of the mid- and hindbrain | rel=r_associated | relid=0 | w=10
  2622. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:malignant neoplasm of peripheral nerves and autonomic nervous system
    n1=DYNC2H1 gene | n2=en:malignant neoplasm of peripheral nerves and autonomic nervous system | rel=r_associated | relid=0 | w=10
  2623. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:markedly delayed nerve conduction velocities
    n1=DYNC2H1 gene | n2=en:markedly delayed nerve conduction velocities | rel=r_associated | relid=0 | w=10
  2624. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mask-like facies
    n1=DYNC2H1 gene | n2=en:mask-like facies | rel=r_associated | relid=0 | w=10
  2625. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mean sleep latency is less than 5 to 8 minutes
    n1=DYNC2H1 gene | n2=en:mean sleep latency is less than 5 to 8 minutes | rel=r_associated | relid=0 | w=10
  2626. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:median nerve paralysis
    n1=DYNC2H1 gene | n2=en:median nerve paralysis | rel=r_associated | relid=0 | w=10
  2627. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:medulloblastoma
    n1=DYNC2H1 gene | n2=en:medulloblastoma | rel=r_associated | relid=0 | w=10
  2628. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mega cisterna magna
    n1=DYNC2H1 gene | n2=en:mega cisterna magna | rel=r_associated | relid=0 | w=10
  2629. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:megacisterna magna (in some patients)
    n1=DYNC2H1 gene | n2=en:megacisterna magna (in some patients) | rel=r_associated | relid=0 | w=10
  2630. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:megacisterna magna (rare)
    n1=DYNC2H1 gene | n2=en:megacisterna magna (rare) | rel=r_associated | relid=0 | w=10
  2631. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:memory defects
    n1=DYNC2H1 gene | n2=en:memory defects | rel=r_associated | relid=0 | w=10
  2632. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:memory impairment
    n1=DYNC2H1 gene | n2=en:memory impairment | rel=r_associated | relid=0 | w=10
  2633. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:memory impairment, progressive
    n1=DYNC2H1 gene | n2=en:memory impairment, progressive | rel=r_associated | relid=0 | w=10
  2634. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:memory loss
    n1=DYNC2H1 gene | n2=en:memory loss | rel=r_associated | relid=0 | w=10
  2635. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:meninges
    n1=DYNC2H1 gene | n2=en:meninges | rel=r_associated | relid=0 | w=10
  2636. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:meningioma
    n1=DYNC2H1 gene | n2=en:meningioma | rel=r_associated | relid=0 | w=10
  2637. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:meningioma (in some patients)
    n1=DYNC2H1 gene | n2=en:meningioma (in some patients) | rel=r_associated | relid=0 | w=10
  2638. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:meningitis
    n1=DYNC2H1 gene | n2=en:meningitis | rel=r_associated | relid=0 | w=10
  2639. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:meningoceles, multiple, lateral
    n1=DYNC2H1 gene | n2=en:meningoceles, multiple, lateral | rel=r_associated | relid=0 | w=10
  2640. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:meningoencephalitis
    n1=DYNC2H1 gene | n2=en:meningoencephalitis | rel=r_associated | relid=0 | w=10
  2641. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:meningoencephalocele (wws)
    n1=DYNC2H1 gene | n2=en:meningoencephalocele (wws) | rel=r_associated | relid=0 | w=10
  2642. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental deficiency
    n1=DYNC2H1 gene | n2=en:mental deficiency | rel=r_associated | relid=0 | w=10
  2643. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental delay or retardation (uncommon)
    n1=DYNC2H1 gene | n2=en:mental delay or retardation (uncommon) | rel=r_associated | relid=0 | w=10
  2644. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental deterioration
    n1=DYNC2H1 gene | n2=en:mental deterioration | rel=r_associated | relid=0 | w=10
  2645. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental deterioration beginning 2 to 5 years after onset of seizures
    n1=DYNC2H1 gene | n2=en:mental deterioration beginning 2 to 5 years after onset of seizures | rel=r_associated | relid=0 | w=10
  2646. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental deterioration in a subset of patients
    n1=DYNC2H1 gene | n2=en:mental deterioration in a subset of patients | rel=r_associated | relid=0 | w=10
  2647. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental deterioration in childhood
    n1=DYNC2H1 gene | n2=en:mental deterioration in childhood | rel=r_associated | relid=0 | w=10
  2648. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental handicap
    n1=DYNC2H1 gene | n2=en:mental handicap | rel=r_associated | relid=0 | w=10
  2649. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental impairment
    n1=DYNC2H1 gene | n2=en:mental impairment | rel=r_associated | relid=0 | w=10
  2650. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental impairment may develop with repeated acute episodes
    n1=DYNC2H1 gene | n2=en:mental impairment may develop with repeated acute episodes | rel=r_associated | relid=0 | w=10
  2651. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental impairment, mild to moderate
    n1=DYNC2H1 gene | n2=en:mental impairment, mild to moderate | rel=r_associated | relid=0 | w=10
  2652. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental lethargy
    n1=DYNC2H1 gene | n2=en:mental lethargy | rel=r_associated | relid=0 | w=10
  2653. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation
    n1=DYNC2H1 gene | n2=en:mental retardation | rel=r_associated | relid=0 | w=10
  2654. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (1 family)
    n1=DYNC2H1 gene | n2=en:mental retardation (1 family) | rel=r_associated | relid=0 | w=10
  2655. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (15%)
    n1=DYNC2H1 gene | n2=en:mental retardation (15%) | rel=r_associated | relid=0 | w=10
  2656. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (18% of patients)
    n1=DYNC2H1 gene | n2=en:mental retardation (18% of patients) | rel=r_associated | relid=0 | w=10
  2657. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (2 patients)
    n1=DYNC2H1 gene | n2=en:mental retardation (2 patients) | rel=r_associated | relid=0 | w=10
  2658. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (2/3 patients)
    n1=DYNC2H1 gene | n2=en:mental retardation (2/3 patients) | rel=r_associated | relid=0 | w=10
  2659. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (20%)
    n1=DYNC2H1 gene | n2=en:mental retardation (20%) | rel=r_associated | relid=0 | w=10
  2660. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (25%)
    n1=DYNC2H1 gene | n2=en:mental retardation (25%) | rel=r_associated | relid=0 | w=10
  2661. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (3 patients)
    n1=DYNC2H1 gene | n2=en:mental retardation (3 patients) | rel=r_associated | relid=0 | w=10
  2662. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (30%)
    n1=DYNC2H1 gene | n2=en:mental retardation (30%) | rel=r_associated | relid=0 | w=10
  2663. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (31%)
    n1=DYNC2H1 gene | n2=en:mental retardation (31%) | rel=r_associated | relid=0 | w=10
  2664. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (38%)
    n1=DYNC2H1 gene | n2=en:mental retardation (38%) | rel=r_associated | relid=0 | w=10
  2665. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (47%)
    n1=DYNC2H1 gene | n2=en:mental retardation (47%) | rel=r_associated | relid=0 | w=10
  2666. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (50% patients)
    n1=DYNC2H1 gene | n2=en:mental retardation (50% patients) | rel=r_associated | relid=0 | w=10
  2667. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (6%)
    n1=DYNC2H1 gene | n2=en:mental retardation (6%) | rel=r_associated | relid=0 | w=10
  2668. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (7%)
    n1=DYNC2H1 gene | n2=en:mental retardation (7%) | rel=r_associated | relid=0 | w=10
  2669. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (70%)
    n1=DYNC2H1 gene | n2=en:mental retardation (70%) | rel=r_associated | relid=0 | w=10
  2670. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (about 40%)
    n1=DYNC2H1 gene | n2=en:mental retardation (about 40%) | rel=r_associated | relid=0 | w=10
  2671. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (average iq 51)
    n1=DYNC2H1 gene | n2=en:mental retardation (average iq 51) | rel=r_associated | relid=0 | w=10
  2672. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (average iq 56)
    n1=DYNC2H1 gene | n2=en:mental retardation (average iq 56) | rel=r_associated | relid=0 | w=10
  2673. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (cvs+)
    n1=DYNC2H1 gene | n2=en:mental retardation (cvs+) | rel=r_associated | relid=0 | w=10
  2674. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (develops later)
    n1=DYNC2H1 gene | n2=en:mental retardation (develops later) | rel=r_associated | relid=0 | w=10
  2675. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (early-onset form)
    n1=DYNC2H1 gene | n2=en:mental retardation (early-onset form) | rel=r_associated | relid=0 | w=10
  2676. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (if left untreated)
    n1=DYNC2H1 gene | n2=en:mental retardation (if left untreated) | rel=r_associated | relid=0 | w=10
  2677. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (if untreated in infancy)
    n1=DYNC2H1 gene | n2=en:mental retardation (if untreated in infancy) | rel=r_associated | relid=0 | w=10
  2678. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (in 2 of 6 patients)
    n1=DYNC2H1 gene | n2=en:mental retardation (in 2 of 6 patients) | rel=r_associated | relid=0 | w=10
  2679. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (in 2 patients) learning disability (in 1 patient)
    n1=DYNC2H1 gene | n2=en:mental retardation (in 2 patients) learning disability (in 1 patient) | rel=r_associated | relid=0 | w=10
  2680. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (in a subset of patients)
    n1=DYNC2H1 gene | n2=en:mental retardation (in a subset of patients) | rel=r_associated | relid=0 | w=10
  2681. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (in most patients)
    n1=DYNC2H1 gene | n2=en:mental retardation (in most patients) | rel=r_associated | relid=0 | w=10
  2682. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (in most)
    n1=DYNC2H1 gene | n2=en:mental retardation (in most) | rel=r_associated | relid=0 | w=10
  2683. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (in some cases)
    n1=DYNC2H1 gene | n2=en:mental retardation (in some cases) | rel=r_associated | relid=0 | w=10
  2684. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (in some patients)
    n1=DYNC2H1 gene | n2=en:mental retardation (in some patients) | rel=r_associated | relid=0 | w=10
  2685. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (in some)
    n1=DYNC2H1 gene | n2=en:mental retardation (in some) | rel=r_associated | relid=0 | w=10
  2686. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (in type iia)
    n1=DYNC2H1 gene | n2=en:mental retardation (in type iia) | rel=r_associated | relid=0 | w=10
  2687. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (iq 20-78)
    n1=DYNC2H1 gene | n2=en:mental retardation (iq 20-78) | rel=r_associated | relid=0 | w=10
  2688. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (iq 24-85) (variable)
    n1=DYNC2H1 gene | n2=en:mental retardation (iq 24-85) (variable) | rel=r_associated | relid=0 | w=10
  2689. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (iq 45-75)
    n1=DYNC2H1 gene | n2=en:mental retardation (iq 45-75) | rel=r_associated | relid=0 | w=10
  2690. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (iq 50-60 combined griffiths and stanford-binet scale)
    n1=DYNC2H1 gene | n2=en:mental retardation (iq 50-60 combined griffiths and stanford-binet scale) | rel=r_associated | relid=0 | w=10
  2691. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (less common)
    n1=DYNC2H1 gene | n2=en:mental retardation (less common) | rel=r_associated | relid=0 | w=10
  2692. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (males)
    n1=DYNC2H1 gene | n2=en:mental retardation (males) | rel=r_associated | relid=0 | w=10
  2693. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (moderate to severe in males)
    n1=DYNC2H1 gene | n2=en:mental retardation (moderate to severe in males) | rel=r_associated | relid=0 | w=10
  2694. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (one patient)
    n1=DYNC2H1 gene | n2=en:mental retardation (one patient) | rel=r_associated | relid=0 | w=10
  2695. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (one-third)
    n1=DYNC2H1 gene | n2=en:mental retardation (one-third) | rel=r_associated | relid=0 | w=10
  2696. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (range mild to severe)
    n1=DYNC2H1 gene | n2=en:mental retardation (range mild to severe) | rel=r_associated | relid=0 | w=10
  2697. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (rare less than 1% of cases)
    n1=DYNC2H1 gene | n2=en:mental retardation (rare less than 1% of cases) | rel=r_associated | relid=0 | w=10
  2698. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (rare)
    n1=DYNC2H1 gene | n2=en:mental retardation (rare) | rel=r_associated | relid=0 | w=10
  2699. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (rarely noted)
    n1=DYNC2H1 gene | n2=en:mental retardation (rarely noted) | rel=r_associated | relid=0 | w=10
  2700. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (reported in 1 family)
    n1=DYNC2H1 gene | n2=en:mental retardation (reported in 1 family) | rel=r_associated | relid=0 | w=10
  2701. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:mental retardation (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  2702. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (secondary to intracranial bleed)
    n1=DYNC2H1 gene | n2=en:mental retardation (secondary to intracranial bleed) | rel=r_associated | relid=0 | w=10
  2703. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (seen in hhs variant)
    n1=DYNC2H1 gene | n2=en:mental retardation (seen in hhs variant) | rel=r_associated | relid=0 | w=10
  2704. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (some)
    n1=DYNC2H1 gene | n2=en:mental retardation (some) | rel=r_associated | relid=0 | w=10
  2705. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (sometimes)
    n1=DYNC2H1 gene | n2=en:mental retardation (sometimes) | rel=r_associated | relid=0 | w=10
  2706. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (type i)
    n1=DYNC2H1 gene | n2=en:mental retardation (type i) | rel=r_associated | relid=0 | w=10
  2707. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (uncommon)
    n1=DYNC2H1 gene | n2=en:mental retardation (uncommon) | rel=r_associated | relid=0 | w=10
  2708. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (untreated hypothyroidism)
    n1=DYNC2H1 gene | n2=en:mental retardation (untreated hypothyroidism) | rel=r_associated | relid=0 | w=10
  2709. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation (variable expression)
    n1=DYNC2H1 gene | n2=en:mental retardation (variable expression) | rel=r_associated | relid=0 | w=10
  2710. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation by age 30 years
    n1=DYNC2H1 gene | n2=en:mental retardation by age 30 years | rel=r_associated | relid=0 | w=10
  2711. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation by the age of 7 years
    n1=DYNC2H1 gene | n2=en:mental retardation by the age of 7 years | rel=r_associated | relid=0 | w=10
  2712. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation can occur in patients with repeated episodes of dehydration
    n1=DYNC2H1 gene | n2=en:mental retardation can occur in patients with repeated episodes of dehydration | rel=r_associated | relid=0 | w=10
  2713. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation due to repeated episodes of hypoglycemia
    n1=DYNC2H1 gene | n2=en:mental retardation due to repeated episodes of hypoglycemia | rel=r_associated | relid=0 | w=10
  2714. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation from rapid mental regression
    n1=DYNC2H1 gene | n2=en:mental retardation from rapid mental regression | rel=r_associated | relid=0 | w=10
  2715. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation has been reported
    n1=DYNC2H1 gene | n2=en:mental retardation has been reported | rel=r_associated | relid=0 | w=10
  2716. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation if untreated
    n1=DYNC2H1 gene | n2=en:mental retardation if untreated | rel=r_associated | relid=0 | w=10
  2717. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation in 5-13%
    n1=DYNC2H1 gene | n2=en:mental retardation in 5-13% | rel=r_associated | relid=0 | w=10
  2718. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation in 75%
    n1=DYNC2H1 gene | n2=en:mental retardation in 75% | rel=r_associated | relid=0 | w=10
  2719. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation in survivors
    n1=DYNC2H1 gene | n2=en:mental retardation in survivors | rel=r_associated | relid=0 | w=10
  2720. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation may occur
    n1=DYNC2H1 gene | n2=en:mental retardation may occur | rel=r_associated | relid=0 | w=10
  2721. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, borderline (1 patient)
    n1=DYNC2H1 gene | n2=en:mental retardation, borderline (1 patient) | rel=r_associated | relid=0 | w=10
  2722. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, borderline to severe
    n1=DYNC2H1 gene | n2=en:mental retardation, borderline to severe | rel=r_associated | relid=0 | w=10
  2723. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, borderline-mild in carrier females
    n1=DYNC2H1 gene | n2=en:mental retardation, borderline-mild in carrier females | rel=r_associated | relid=0 | w=10
  2724. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, in subgroup of patients
    n1=DYNC2H1 gene | n2=en:mental retardation, in subgroup of patients | rel=r_associated | relid=0 | w=10
  2725. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (1 family)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (1 family) | rel=r_associated | relid=0 | w=10
  2726. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (1 patient)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (1 patient) | rel=r_associated | relid=0 | w=10
  2727. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (10%)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (10%) | rel=r_associated | relid=0 | w=10
  2728. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (11%)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (11%) | rel=r_associated | relid=0 | w=10
  2729. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (18%)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (18%) | rel=r_associated | relid=0 | w=10
  2730. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (2 families)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (2 families) | rel=r_associated | relid=0 | w=10
  2731. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (20% have more severe mental retardation)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (20% have more severe mental retardation) | rel=r_associated | relid=0 | w=10
  2732. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (carrier females)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (carrier females) | rel=r_associated | relid=0 | w=10
  2733. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (in some females)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (in some females) | rel=r_associated | relid=0 | w=10
  2734. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (in some patients) | rel=r_associated | relid=0 | w=10
  2735. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (iq range from 50 to 70)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (iq range from 50 to 70) | rel=r_associated | relid=0 | w=10
  2736. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild (rare)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild (rare) | rel=r_associated | relid=0 | w=10
  2737. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild to moderate
    n1=DYNC2H1 gene | n2=en:mental retardation, mild to moderate | rel=r_associated | relid=0 | w=10
  2738. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild to moderate (20% of patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild to moderate (20% of patients) | rel=r_associated | relid=0 | w=10
  2739. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild to moderate (in 12%)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild to moderate (in 12%) | rel=r_associated | relid=0 | w=10
  2740. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild to moderate (in some patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild to moderate (in some patients) | rel=r_associated | relid=0 | w=10
  2741. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild to moderate (iq 30-76)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild to moderate (iq 30-76) | rel=r_associated | relid=0 | w=10
  2742. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild to profound
    n1=DYNC2H1 gene | n2=en:mental retardation, mild to profound | rel=r_associated | relid=0 | w=10
  2743. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild to severe
    n1=DYNC2H1 gene | n2=en:mental retardation, mild to severe | rel=r_associated | relid=0 | w=10
  2744. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild-borderline, nonprogressive
    n1=DYNC2H1 gene | n2=en:mental retardation, mild-borderline, nonprogressive | rel=r_associated | relid=0 | w=10
  2745. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild-moderate (28%, usually in males)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild-moderate (28%, usually in males) | rel=r_associated | relid=0 | w=10
  2746. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild-moderate (some)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild-moderate (some) | rel=r_associated | relid=0 | w=10
  2747. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild, in most carrier females
    n1=DYNC2H1 gene | n2=en:mental retardation, mild, in most carrier females | rel=r_associated | relid=0 | w=10
  2748. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, mild, some patients (iq 70-80)
    n1=DYNC2H1 gene | n2=en:mental retardation, mild, some patients (iq 70-80) | rel=r_associated | relid=0 | w=10
  2749. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate (apparent by age 4 years)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate (apparent by age 4 years) | rel=r_associated | relid=0 | w=10
  2750. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate (in 1 patient)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate (in 1 patient) | rel=r_associated | relid=0 | w=10
  2751. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate (in sister)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate (in sister) | rel=r_associated | relid=0 | w=10
  2752. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate (in some patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate (in some patients) | rel=r_associated | relid=0 | w=10
  2753. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate to profound
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate to profound | rel=r_associated | relid=0 | w=10
  2754. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate to severe
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate to severe | rel=r_associated | relid=0 | w=10
  2755. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate to severe (10-15% of patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate to severe (10-15% of patients) | rel=r_associated | relid=0 | w=10
  2756. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate to severe (in some patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate to severe (in some patients) | rel=r_associated | relid=0 | w=10
  2757. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate to severe (iq 35-50)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate to severe (iq 35-50) | rel=r_associated | relid=0 | w=10
  2758. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate to severe (iq 40 to 60)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate to severe (iq 40 to 60) | rel=r_associated | relid=0 | w=10
  2759. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate to severe (type ii, infantile and juvenile)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate to severe (type ii, infantile and juvenile) | rel=r_associated | relid=0 | w=10
  2760. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, moderate-severe (2p21del)
    n1=DYNC2H1 gene | n2=en:mental retardation, moderate-severe (2p21del) | rel=r_associated | relid=0 | w=10
  2761. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, occasional
    n1=DYNC2H1 gene | n2=en:mental retardation, occasional | rel=r_associated | relid=0 | w=10
  2762. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, profound (wws)
    n1=DYNC2H1 gene | n2=en:mental retardation, profound (wws) | rel=r_associated | relid=0 | w=10
  2763. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, progressive (50% of patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, progressive (50% of patients) | rel=r_associated | relid=0 | w=10
  2764. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, residual mild-to-severe (in some patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, residual mild-to-severe (in some patients) | rel=r_associated | relid=0 | w=10
  2765. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, severe (if untreated)
    n1=DYNC2H1 gene | n2=en:mental retardation, severe (if untreated) | rel=r_associated | relid=0 | w=10
  2766. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, severe (meb)
    n1=DYNC2H1 gene | n2=en:mental retardation, severe (meb) | rel=r_associated | relid=0 | w=10
  2767. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, severe in some patients
    n1=DYNC2H1 gene | n2=en:mental retardation, severe in some patients | rel=r_associated | relid=0 | w=10
  2768. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, severe to profound
    n1=DYNC2H1 gene | n2=en:mental retardation, severe to profound | rel=r_associated | relid=0 | w=10
  2769. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, severe, profound
    n1=DYNC2H1 gene | n2=en:mental retardation, severe, profound | rel=r_associated | relid=0 | w=10
  2770. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, variable (in some patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, variable (in some patients) | rel=r_associated | relid=0 | w=10
  2771. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, variable degree (in some patients)
    n1=DYNC2H1 gene | n2=en:mental retardation, variable degree (in some patients) | rel=r_associated | relid=0 | w=10
  2772. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mental retardation, variable severity
    n1=DYNC2H1 gene | n2=en:mental retardation, variable severity | rel=r_associated | relid=0 | w=10
  2773. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mesial temporal brain malformations
    n1=DYNC2H1 gene | n2=en:mesial temporal brain malformations | rel=r_associated | relid=0 | w=10
  2774. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mesial temporal sclerosis (in 1 patient)
    n1=DYNC2H1 gene | n2=en:mesial temporal sclerosis (in 1 patient) | rel=r_associated | relid=0 | w=10
  2775. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:microbleeds
    n1=DYNC2H1 gene | n2=en:microbleeds | rel=r_associated | relid=0 | w=10
  2776. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:microbleeds (most smaller than 5 mm) occur after age 40 years
    n1=DYNC2H1 gene | n2=en:microbleeds (most smaller than 5 mm) occur after age 40 years | rel=r_associated | relid=0 | w=10
  2777. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:microcephaly
    n1=DYNC2H1 gene | n2=en:microcephaly | rel=r_associated | relid=0 | w=10
  2778. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:microcystic degeneration
    n1=DYNC2H1 gene | n2=en:microcystic degeneration | rel=r_associated | relid=0 | w=10
  2779. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:micrographia
    n1=DYNC2H1 gene | n2=en:micrographia | rel=r_associated | relid=0 | w=10
  2780. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:microgyria
    n1=DYNC2H1 gene | n2=en:microgyria | rel=r_associated | relid=0 | w=10
  2781. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:microlissencephalies
    n1=DYNC2H1 gene | n2=en:microlissencephalies | rel=r_associated | relid=0 | w=10
  2782. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:microvacuolation
    n1=DYNC2H1 gene | n2=en:microvacuolation | rel=r_associated | relid=0 | w=10
  2783. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:microvascular spaces, dilated
    n1=DYNC2H1 gene | n2=en:microvascular spaces, dilated | rel=r_associated | relid=0 | w=10
  2784. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:midbrain atrophy
    n1=DYNC2H1 gene | n2=en:midbrain atrophy | rel=r_associated | relid=0 | w=10
  2785. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:midline brain calcifications
    n1=DYNC2H1 gene | n2=en:midline brain calcifications | rel=r_associated | relid=0 | w=10
  2786. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:midline forebrain defects
    n1=DYNC2H1 gene | n2=en:midline forebrain defects | rel=r_associated | relid=0 | w=10
  2787. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine
    n1=DYNC2H1 gene | n2=en:migraine | rel=r_associated | relid=0 | w=10
  2788. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine (40% of patients)
    n1=DYNC2H1 gene | n2=en:migraine (40% of patients) | rel=r_associated | relid=0 | w=10
  2789. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine (in affected males)
    n1=DYNC2H1 gene | n2=en:migraine (in affected males) | rel=r_associated | relid=0 | w=10
  2790. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine (in some patients)
    n1=DYNC2H1 gene | n2=en:migraine (in some patients) | rel=r_associated | relid=0 | w=10
  2791. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine (uncommon)
    n1=DYNC2H1 gene | n2=en:migraine (uncommon) | rel=r_associated | relid=0 | w=10
  2792. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine headache (less common)
    n1=DYNC2H1 gene | n2=en:migraine headache (less common) | rel=r_associated | relid=0 | w=10
  2793. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine headaches (cvs+)
    n1=DYNC2H1 gene | n2=en:migraine headaches (cvs+) | rel=r_associated | relid=0 | w=10
  2794. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine headaches (ipsilateral to facial hemangioma)
    n1=DYNC2H1 gene | n2=en:migraine headaches (ipsilateral to facial hemangioma) | rel=r_associated | relid=0 | w=10
  2795. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine headaches (onset in adolescence)
    n1=DYNC2H1 gene | n2=en:migraine headaches (onset in adolescence) | rel=r_associated | relid=0 | w=10
  2796. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine with aura
    n1=DYNC2H1 gene | n2=en:migraine with aura | rel=r_associated | relid=0 | w=10
  2797. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine with aura, usually visual (in 50% of patients)
    n1=DYNC2H1 gene | n2=en:migraine with aura, usually visual (in 50% of patients) | rel=r_associated | relid=0 | w=10
  2798. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine without aura
    n1=DYNC2H1 gene | n2=en:migraine without aura | rel=r_associated | relid=0 | w=10
  2799. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraine, with or without aura
    n1=DYNC2H1 gene | n2=en:migraine, with or without aura | rel=r_associated | relid=0 | w=10
  2800. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migraines (less common)
    n1=DYNC2H1 gene | n2=en:migraines (less common) | rel=r_associated | relid=0 | w=10
  2801. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migrating clonic jerks (in some patients)
    n1=DYNC2H1 gene | n2=en:migrating clonic jerks (in some patients) | rel=r_associated | relid=0 | w=10
  2802. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migrating discharges from one cortical region to another seen on eeg (in some patients)
    n1=DYNC2H1 gene | n2=en:migrating discharges from one cortical region to another seen on eeg (in some patients) | rel=r_associated | relid=0 | w=10
  2803. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migrating focal discharges from one cortical region to another seen on eeg
    n1=DYNC2H1 gene | n2=en:migrating focal discharges from one cortical region to another seen on eeg | rel=r_associated | relid=0 | w=10
  2804. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:migrating partial seizures
    n1=DYNC2H1 gene | n2=en:migrating partial seizures | rel=r_associated | relid=0 | w=10
  2805. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild brain anomalies on mri (e.g., dilated ventricles) (in some patients)
    n1=DYNC2H1 gene | n2=en:mild brain anomalies on mri (e.g., dilated ventricles) (in some patients) | rel=r_associated | relid=0 | w=10
  2806. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild cerebellar hypoplasia
    n1=DYNC2H1 gene | n2=en:mild cerebellar hypoplasia | rel=r_associated | relid=0 | w=10
  2807. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild cognitive decline (1 patient)
    n1=DYNC2H1 gene | n2=en:mild cognitive decline (1 patient) | rel=r_associated | relid=0 | w=10
  2808. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild cognitive deterioration in adults
    n1=DYNC2H1 gene | n2=en:mild cognitive deterioration in adults | rel=r_associated | relid=0 | w=10
  2809. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild cognitive disorder
    n1=DYNC2H1 gene | n2=en:mild cognitive disorder | rel=r_associated | relid=0 | w=10
  2810. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild cognitive impairment (in 2 patients)
    n1=DYNC2H1 gene | n2=en:mild cognitive impairment (in 2 patients) | rel=r_associated | relid=0 | w=10
  2811. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild cognitive impairment (in some patients)
    n1=DYNC2H1 gene | n2=en:mild cognitive impairment (in some patients) | rel=r_associated | relid=0 | w=10
  2812. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild cognitive impairment (less common)
    n1=DYNC2H1 gene | n2=en:mild cognitive impairment (less common) | rel=r_associated | relid=0 | w=10
  2813. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild cortical atrophy (in 1 patient)
    n1=DYNC2H1 gene | n2=en:mild cortical atrophy (in 1 patient) | rel=r_associated | relid=0 | w=10
  2814. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild cortical atrophy on ct or mri
    n1=DYNC2H1 gene | n2=en:mild cortical atrophy on ct or mri | rel=r_associated | relid=0 | w=10
  2815. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild distal sensory deficits
    n1=DYNC2H1 gene | n2=en:mild distal sensory deficits | rel=r_associated | relid=0 | w=10
  2816. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild global developmental delay
    n1=DYNC2H1 gene | n2=en:mild global developmental delay | rel=r_associated | relid=0 | w=10
  2817. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild loss of neurons in the cerebellum
    n1=DYNC2H1 gene | n2=en:mild loss of neurons in the cerebellum | rel=r_associated | relid=0 | w=10
  2818. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild memory loss
    n1=DYNC2H1 gene | n2=en:mild memory loss | rel=r_associated | relid=0 | w=10
  2819. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild mental decline
    n1=DYNC2H1 gene | n2=en:mild mental decline | rel=r_associated | relid=0 | w=10
  2820. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild mental deterioration
    n1=DYNC2H1 gene | n2=en:mild mental deterioration | rel=r_associated | relid=0 | w=10
  2821. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild mental retardation
    n1=DYNC2H1 gene | n2=en:mild mental retardation | rel=r_associated | relid=0 | w=10
  2822. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild mental retardation (39%) feeding problems/weak suck (43%)
    n1=DYNC2H1 gene | n2=en:mild mental retardation (39%) feeding problems/weak suck (43%) | rel=r_associated | relid=0 | w=10
  2823. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild mental retardation (in 1/4 patients)
    n1=DYNC2H1 gene | n2=en:mild mental retardation (in 1/4 patients) | rel=r_associated | relid=0 | w=10
  2824. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild mental retardation (some)
    n1=DYNC2H1 gene | n2=en:mild mental retardation (some) | rel=r_associated | relid=0 | w=10
  2825. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild motor development delay
    n1=DYNC2H1 gene | n2=en:mild motor development delay | rel=r_associated | relid=0 | w=10
  2826. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild paraparesis
    n1=DYNC2H1 gene | n2=en:mild paraparesis | rel=r_associated | relid=0 | w=10
  2827. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild psychomotor delay
    n1=DYNC2H1 gene | n2=en:mild psychomotor delay | rel=r_associated | relid=0 | w=10
  2828. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild pyramidal signs (variable expression)
    n1=DYNC2H1 gene | n2=en:mild pyramidal signs (variable expression) | rel=r_associated | relid=0 | w=10
  2829. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild sensorimotor neuropathy
    n1=DYNC2H1 gene | n2=en:mild sensorimotor neuropathy | rel=r_associated | relid=0 | w=10
  2830. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild spasticity
    n1=DYNC2H1 gene | n2=en:mild spasticity | rel=r_associated | relid=0 | w=10
  2831. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild structural abnormalities seen mri (in some patients)
    n1=DYNC2H1 gene | n2=en:mild structural abnormalities seen mri (in some patients) | rel=r_associated | relid=0 | w=10
  2832. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild to moderate learning difficulties
    n1=DYNC2H1 gene | n2=en:mild to moderate learning difficulties | rel=r_associated | relid=0 | w=10
  2833. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild to severe mental retardation (24%)
    n1=DYNC2H1 gene | n2=en:mild to severe mental retardation (24%) | rel=r_associated | relid=0 | w=10
  2834. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild upper limb involvement
    n1=DYNC2H1 gene | n2=en:mild upper limb involvement | rel=r_associated | relid=0 | w=10
  2835. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild-moderate mental retardation (80% affected males)
    n1=DYNC2H1 gene | n2=en:mild-moderate mental retardation (80% affected males) | rel=r_associated | relid=0 | w=10
  2836. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild-moderate ventricular dilatation
    n1=DYNC2H1 gene | n2=en:mild-moderate ventricular dilatation | rel=r_associated | relid=0 | w=10
  2837. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mild-severe mental retardation (20%)
    n1=DYNC2H1 gene | n2=en:mild-severe mental retardation (20%) | rel=r_associated | relid=0 | w=10
  2838. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy
    n1=DYNC2H1 gene | n2=en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy | rel=r_associated | relid=0 | w=10
  2839. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mildly decreased intelligence has been reported
    n1=DYNC2H1 gene | n2=en:mildly decreased intelligence has been reported | rel=r_associated | relid=0 | w=10
  2840. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mildly delayed developmental milestones
    n1=DYNC2H1 gene | n2=en:mildly delayed developmental milestones | rel=r_associated | relid=0 | w=10
  2841. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mildly delayed motor development
    n1=DYNC2H1 gene | n2=en:mildly delayed motor development | rel=r_associated | relid=0 | w=10
  2842. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mildly delayed motor development due to vestibular dysfunction
    n1=DYNC2H1 gene | n2=en:mildly delayed motor development due to vestibular dysfunction | rel=r_associated | relid=0 | w=10
  2843. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mildly enlarged ventricles
    n1=DYNC2H1 gene | n2=en:mildly enlarged ventricles | rel=r_associated | relid=0 | w=10
  2844. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mildly thin corpus callosum
    n1=DYNC2H1 gene | n2=en:mildly thin corpus callosum | rel=r_associated | relid=0 | w=10
  2845. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:minimal gliosis
    n1=DYNC2H1 gene | n2=en:minimal gliosis | rel=r_associated | relid=0 | w=10
  2846. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:minimal or lack of speech
    n1=DYNC2H1 gene | n2=en:minimal or lack of speech | rel=r_associated | relid=0 | w=10
  2847. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:minimal to absent speech
    n1=DYNC2H1 gene | n2=en:minimal to absent speech | rel=r_associated | relid=0 | w=10
  2848. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:minor motor impairment (stage 2)
    n1=DYNC2H1 gene | n2=en:minor motor impairment (stage 2) | rel=r_associated | relid=0 | w=10
  2849. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mirror hand movements (bimanual synkinesis, in some patients)
    n1=DYNC2H1 gene | n2=en:mirror hand movements (bimanual synkinesis, in some patients) | rel=r_associated | relid=0 | w=10
  2850. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mirror movements disorder
    n1=DYNC2H1 gene | n2=en:mirror movements disorder | rel=r_associated | relid=0 | w=10
  2851. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mirror movements, involuntary, affecting the hand and fingers
    n1=DYNC2H1 gene | n2=en:mirror movements, involuntary, affecting the hand and fingers | rel=r_associated | relid=0 | w=10
  2852. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mirror movements, involuntary, usually of the upper limb and hand
    n1=DYNC2H1 gene | n2=en:mirror movements, involuntary, usually of the upper limb and hand | rel=r_associated | relid=0 | w=10
  2853. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:misorientation of pyramidal fibers
    n1=DYNC2H1 gene | n2=en:misorientation of pyramidal fibers | rel=r_associated | relid=0 | w=10
  2854. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:misshapen posterior fossa
    n1=DYNC2H1 gene | n2=en:misshapen posterior fossa | rel=r_associated | relid=0 | w=10
  2855. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mitochondrial dna depletion in brain tissue
    n1=DYNC2H1 gene | n2=en:mitochondrial dna depletion in brain tissue | rel=r_associated | relid=0 | w=10
  2856. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mitochondrial encephalopathy
    n1=DYNC2H1 gene | n2=en:mitochondrial encephalopathy | rel=r_associated | relid=0 | w=10
  2857. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mixed cerebellar/pseudobulbar dysarthria
    n1=DYNC2H1 gene | n2=en:mixed cerebellar/pseudobulbar dysarthria | rel=r_associated | relid=0 | w=10
  2858. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mobility poor
    n1=DYNC2H1 gene | n2=en:mobility poor | rel=r_associated | relid=0 | w=10
  2859. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mobius syndrome
    n1=DYNC2H1 gene | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=10
  2860. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:moderate cortical atrophy (in some patients)
    n1=DYNC2H1 gene | n2=en:moderate cortical atrophy (in some patients) | rel=r_associated | relid=0 | w=10
  2861. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:moderate learning difficulties
    n1=DYNC2H1 gene | n2=en:moderate learning difficulties | rel=r_associated | relid=0 | w=10
  2862. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:moderate mental retardation (i.q. 35-49)
    n1=DYNC2H1 gene | n2=en:moderate mental retardation (i.q. 35-49) | rel=r_associated | relid=0 | w=10
  2863. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:moderate to severe hypotonia
    n1=DYNC2H1 gene | n2=en:moderate to severe hypotonia | rel=r_associated | relid=0 | w=10
  2864. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:moderately thickened cortex
    n1=DYNC2H1 gene | n2=en:moderately thickened cortex | rel=r_associated | relid=0 | w=10
  2865. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:molar tooth sign on brain mri
    n1=DYNC2H1 gene | n2=en:molar tooth sign on brain mri | rel=r_associated | relid=0 | w=10
  2866. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:molar tooth sign on brain mri (subset of patients)
    n1=DYNC2H1 gene | n2=en:molar tooth sign on brain mri (subset of patients) | rel=r_associated | relid=0 | w=10
  2867. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:molar tooth sign on mri
    n1=DYNC2H1 gene | n2=en:molar tooth sign on mri | rel=r_associated | relid=0 | w=10
  2868. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:molar tooth sign seen on mri
    n1=DYNC2H1 gene | n2=en:molar tooth sign seen on mri | rel=r_associated | relid=0 | w=10
  2869. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:monopareses
    n1=DYNC2H1 gene | n2=en:monopareses | rel=r_associated | relid=0 | w=10
  2870. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:monotone speech
    n1=DYNC2H1 gene | n2=en:monotone speech | rel=r_associated | relid=0 | w=10
  2871. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:monotonous speech
    n1=DYNC2H1 gene | n2=en:monotonous speech | rel=r_associated | relid=0 | w=10
  2872. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mood lability
    n1=DYNC2H1 gene | n2=en:mood lability | rel=r_associated | relid=0 | w=10
  2873. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:morning myoclonic jerks
    n1=DYNC2H1 gene | n2=en:morning myoclonic jerks | rel=r_associated | relid=0 | w=10
  2874. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:moro reflex absent
    n1=DYNC2H1 gene | n2=en:moro reflex absent | rel=r_associated | relid=0 | w=10
  2875. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:most never acquire independent ambulation
    n1=DYNC2H1 gene | n2=en:most never acquire independent ambulation | rel=r_associated | relid=0 | w=10
  2876. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:most patients achieve walking with aid
    n1=DYNC2H1 gene | n2=en:most patients achieve walking with aid | rel=r_associated | relid=0 | w=10
  2877. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:most patients are wheelchair-bound
    n1=DYNC2H1 gene | n2=en:most patients are wheelchair-bound | rel=r_associated | relid=0 | w=10
  2878. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:most patients do not achieve independent sitting or walking
    n1=DYNC2H1 gene | n2=en:most patients do not achieve independent sitting or walking | rel=r_associated | relid=0 | w=10
  2879. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:most patients remain stable or improve in years after the abrupt onset of symptoms
    n1=DYNC2H1 gene | n2=en:most patients remain stable or improve in years after the abrupt onset of symptoms | rel=r_associated | relid=0 | w=10
  2880. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mosy patients become wheelchair-bound after 10 years
    n1=DYNC2H1 gene | n2=en:mosy patients become wheelchair-bound after 10 years | rel=r_associated | relid=0 | w=10
  2881. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor abnormalities
    n1=DYNC2H1 gene | n2=en:motor abnormalities | rel=r_associated | relid=0 | w=10
  2882. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor and intellectual disability, severe
    n1=DYNC2H1 gene | n2=en:motor and intellectual disability, severe | rel=r_associated | relid=0 | w=10
  2883. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor and vocal tics
    n1=DYNC2H1 gene | n2=en:motor and vocal tics | rel=r_associated | relid=0 | w=10
  2884. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor automatisms
    n1=DYNC2H1 gene | n2=en:motor automatisms | rel=r_associated | relid=0 | w=10
  2885. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor delay (in one patient)
    n1=DYNC2H1 gene | n2=en:motor delay (in one patient) | rel=r_associated | relid=0 | w=10
  2886. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor deterioration
    n1=DYNC2H1 gene | n2=en:motor deterioration | rel=r_associated | relid=0 | w=10
  2887. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor deterioration in second decade
    n1=DYNC2H1 gene | n2=en:motor deterioration in second decade | rel=r_associated | relid=0 | w=10
  2888. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor development delay (83%)
    n1=DYNC2H1 gene | n2=en:motor development delay (83%) | rel=r_associated | relid=0 | w=10
  2889. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor development delayed (in some patients)
    n1=DYNC2H1 gene | n2=en:motor development delayed (in some patients) | rel=r_associated | relid=0 | w=10
  2890. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor developmental delay
    n1=DYNC2H1 gene | n2=en:motor developmental delay | rel=r_associated | relid=0 | w=10
  2891. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor developmental delay, severe
    n1=DYNC2H1 gene | n2=en:motor developmental delay, severe | rel=r_associated | relid=0 | w=10
  2892. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor disturbances
    n1=DYNC2H1 gene | n2=en:motor disturbances | rel=r_associated | relid=0 | w=10
  2893. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor dysfunction
    n1=DYNC2H1 gene | n2=en:motor dysfunction | rel=r_associated | relid=0 | w=10
  2894. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor dyspraxia
    n1=DYNC2H1 gene | n2=en:motor dyspraxia | rel=r_associated | relid=0 | w=10
  2895. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor incoordination
    n1=DYNC2H1 gene | n2=en:motor incoordination | rel=r_associated | relid=0 | w=10
  2896. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor neuron disease
    n1=DYNC2H1 gene | n2=en:motor neuron disease | rel=r_associated | relid=0 | w=10
  2897. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor neuron disease (less common)
    n1=DYNC2H1 gene | n2=en:motor neuron disease (less common) | rel=r_associated | relid=0 | w=10
  2898. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor neuron disease, lower
    n1=DYNC2H1 gene | n2=en:motor neuron disease, lower | rel=r_associated | relid=0 | w=10
  2899. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor regression
    n1=DYNC2H1 gene | n2=en:motor regression | rel=r_associated | relid=0 | w=10
  2900. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor retardation, mild
    n1=DYNC2H1 gene | n2=en:motor retardation, mild | rel=r_associated | relid=0 | w=10
  2901. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor seizures, nocturnal, usually occur in clusters (up to 8 per night) during dozing or on awakening
    n1=DYNC2H1 gene | 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=10
  2902. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor stereotypy
    n1=DYNC2H1 gene | n2=en:motor stereotypy | rel=r_associated | relid=0 | w=10
  2903. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor symptoms may be present
    n1=DYNC2H1 gene | n2=en:motor symptoms may be present | rel=r_associated | relid=0 | w=10
  2904. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:motor tic
    n1=DYNC2H1 gene | n2=en:motor tic | rel=r_associated | relid=0 | w=10
  2905. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mouth movements
    n1=DYNC2H1 gene | n2=en:mouth movements | rel=r_associated | relid=0 | w=10
  2906. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:movement abnormalities of the extremities
    n1=DYNC2H1 gene | n2=en:movement abnormalities of the extremities | rel=r_associated | relid=0 | w=10
  2907. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:movement disorder
    n1=DYNC2H1 gene | n2=en:movement disorder | rel=r_associated | relid=0 | w=10
  2908. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:movement of visual image - finding
    n1=DYNC2H1 gene | n2=en:movement of visual image - finding | rel=r_associated | relid=0 | w=10
  2909. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:movements ('tremors') characterized by 8 to 10-hz discharges
    n1=DYNC2H1 gene | n2=en:movements ('tremors') characterized by 8 to 10-hz discharges | rel=r_associated | relid=0 | w=10
  2910. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:movements are exacerbated by anxiety
    n1=DYNC2H1 gene | n2=en:movements are exacerbated by anxiety | rel=r_associated | relid=0 | w=10
  2911. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:moyamoya disease
    n1=DYNC2H1 gene | n2=en:moyamoya disease | rel=r_associated | relid=0 | w=10
  2912. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mr spectroscopy shows decreased n-acetyl aspartate
    n1=DYNC2H1 gene | n2=en:mr spectroscopy shows decreased n-acetyl aspartate | rel=r_associated | relid=0 | w=10
  2913. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri - diffuse or focal cerebral and cerebellar white matter disease
    n1=DYNC2H1 gene | n2=en:mri - diffuse or focal cerebral and cerebellar white matter disease | rel=r_associated | relid=0 | w=10
  2914. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri imaging shows cavitation of the basal ganglia
    n1=DYNC2H1 gene | n2=en:mri imaging shows cavitation of the basal ganglia | rel=r_associated | relid=0 | w=10
  2915. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri is best imaging modality to detect lesions
    n1=DYNC2H1 gene | n2=en:mri is best imaging modality to detect lesions | rel=r_associated | relid=0 | w=10
  2916. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri may be normal, especially in type iib
    n1=DYNC2H1 gene | n2=en:mri may be normal, especially in type iib | rel=r_associated | relid=0 | w=10
  2917. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri may show atrophy of the cerebrum
    n1=DYNC2H1 gene | n2=en:mri may show atrophy of the cerebrum | rel=r_associated | relid=0 | w=10
  2918. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri may show lesions in basal ganglia, thalamus, and white matter
    n1=DYNC2H1 gene | n2=en:mri may show lesions in basal ganglia, thalamus, and white matter | rel=r_associated | relid=0 | w=10
  2919. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows absence of the facial nerve
    n1=DYNC2H1 gene | n2=en:mri shows absence of the facial nerve | rel=r_associated | relid=0 | w=10
  2920. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows atretic occipital cephalocele with bony skull defect
    n1=DYNC2H1 gene | n2=en:mri shows atretic occipital cephalocele with bony skull defect | rel=r_associated | relid=0 | w=10
  2921. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows brain asymmetry
    n1=DYNC2H1 gene | n2=en:mri shows brain asymmetry | rel=r_associated | relid=0 | w=10
  2922. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows brainstem hypoplasia
    n1=DYNC2H1 gene | n2=en:mri shows brainstem hypoplasia | rel=r_associated | relid=0 | w=10
  2923. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows cerebellar atrophy
    n1=DYNC2H1 gene | n2=en:mri shows cerebellar atrophy | rel=r_associated | relid=0 | w=10
  2924. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows cerebral atrophy
    n1=DYNC2H1 gene | n2=en:mri shows cerebral atrophy | rel=r_associated | relid=0 | w=10
  2925. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows congenital abnormalities of the posterior fossa
    n1=DYNC2H1 gene | n2=en:mri shows congenital abnormalities of the posterior fossa | rel=r_associated | relid=0 | w=10
  2926. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows decreased signal intensities in the basal ganglia
    n1=DYNC2H1 gene | n2=en:mri shows decreased signal intensities in the basal ganglia | rel=r_associated | relid=0 | w=10
  2927. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows decreased signal intensity in the pallidal nuclei with central hyperintensity ('eye of the tiger' sign)
    n1=DYNC2H1 gene | 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=10
  2928. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows defects of the corpus callosum
    n1=DYNC2H1 gene | n2=en:mri shows defects of the corpus callosum | rel=r_associated | relid=0 | w=10
  2929. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows delayed myelination (1 of 6 patients)
    n1=DYNC2H1 gene | n2=en:mri shows delayed myelination (1 of 6 patients) | rel=r_associated | relid=0 | w=10
  2930. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows diffuse white matter hyperintensities on t2-weighted imaging
    n1=DYNC2H1 gene | n2=en:mri shows diffuse white matter hyperintensities on t2-weighted imaging | rel=r_associated | relid=0 | w=10
  2931. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows dysmyelination
    n1=DYNC2H1 gene | n2=en:mri shows dysmyelination | rel=r_associated | relid=0 | w=10
  2932. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows frontal and temporal cortical atrophy
    n1=DYNC2H1 gene | n2=en:mri shows frontal and temporal cortical atrophy | rel=r_associated | relid=0 | w=10
  2933. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows generalized atrophy
    n1=DYNC2H1 gene | n2=en:mri shows generalized atrophy | rel=r_associated | relid=0 | w=10
  2934. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows global lack of myelination in the cerebral hemispheres
    n1=DYNC2H1 gene | n2=en:mri shows global lack of myelination in the cerebral hemispheres | rel=r_associated | relid=0 | w=10
  2935. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows globus pallidus signal abnormalities
    n1=DYNC2H1 gene | n2=en:mri shows globus pallidus signal abnormalities | rel=r_associated | relid=0 | w=10
  2936. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows high signal intensity of the white matter later
    n1=DYNC2H1 gene | n2=en:mri shows high signal intensity of the white matter later | rel=r_associated | relid=0 | w=10
  2937. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows hypointensity of the thalami early-on
    n1=DYNC2H1 gene | n2=en:mri shows hypointensity of the thalami early-on | rel=r_associated | relid=0 | w=10
  2938. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows increased t2-weighted signals in the globus pallidi
    n1=DYNC2H1 gene | n2=en:mri shows increased t2-weighted signals in the globus pallidi | rel=r_associated | relid=0 | w=10
  2939. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows leukoencephalopathy
    n1=DYNC2H1 gene | n2=en:mri shows leukoencephalopathy | rel=r_associated | relid=0 | w=10
  2940. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows no normal myelination
    n1=DYNC2H1 gene | n2=en:mri shows no normal myelination | rel=r_associated | relid=0 | w=10
  2941. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows short, thick corpus callosum
    n1=DYNC2H1 gene | n2=en:mri shows short, thick corpus callosum | rel=r_associated | relid=0 | w=10
  2942. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows subcortical leukoencephalopathy with cavitation
    n1=DYNC2H1 gene | n2=en:mri shows subcortical leukoencephalopathy with cavitation | rel=r_associated | relid=0 | w=10
  2943. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows symmetric lesions of the basal ganglia (particularly caudate and putamen)
    n1=DYNC2H1 gene | n2=en:mri shows symmetric lesions of the basal ganglia (particularly caudate and putamen) | rel=r_associated | relid=0 | w=10
  2944. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows symmetric, diffuse lesions with csf-like signal intensity
    n1=DYNC2H1 gene | n2=en:mri shows symmetric, diffuse lesions with csf-like signal intensity | rel=r_associated | relid=0 | w=10
  2945. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows t2-weighted signals in the basal ganglia
    n1=DYNC2H1 gene | n2=en:mri shows t2-weighted signals in the basal ganglia | rel=r_associated | relid=0 | w=10
  2946. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mri shows white matter lesions
    n1=DYNC2H1 gene | n2=en:mri shows white matter lesions | rel=r_associated | relid=0 | w=10
  2947. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mrs shows decreased choline in affected white matter
    n1=DYNC2H1 gene | n2=en:mrs shows decreased choline in affected white matter | rel=r_associated | relid=0 | w=10
  2948. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mrs shows decreased creatine in white matter
    n1=DYNC2H1 gene | n2=en:mrs shows decreased creatine in white matter | rel=r_associated | relid=0 | w=10
  2949. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multi-system degeneration
    n1=DYNC2H1 gene | n2=en:multi-system degeneration | rel=r_associated | relid=0 | w=10
  2950. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multi-system degeneration of the autonomic nervous system
    n1=DYNC2H1 gene | n2=en:multi-system degeneration of the autonomic nervous system | rel=r_associated | relid=0 | w=10
  2951. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal areas of laminar dysmorphic neurons (in type iia)
    n1=DYNC2H1 gene | n2=en:multifocal areas of laminar dysmorphic neurons (in type iia) | rel=r_associated | relid=0 | w=10
  2952. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal cerebral white matter abnormalities
    n1=DYNC2H1 gene | n2=en:multifocal cerebral white matter abnormalities | rel=r_associated | relid=0 | w=10
  2953. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal discharges
    n1=DYNC2H1 gene | n2=en:multifocal discharges | rel=r_associated | relid=0 | w=10
  2954. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal discharges associated with contralateral jerky movements
    n1=DYNC2H1 gene | n2=en:multifocal discharges associated with contralateral jerky movements | rel=r_associated | relid=0 | w=10
  2955. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal discharges seen on eeg (in some patients)
    n1=DYNC2H1 gene | n2=en:multifocal discharges seen on eeg (in some patients) | rel=r_associated | relid=0 | w=10
  2956. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal epileptic activity
    n1=DYNC2H1 gene | n2=en:multifocal epileptic activity | rel=r_associated | relid=0 | w=10
  2957. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal epileptiform discharges on diffuse slow background
    n1=DYNC2H1 gene | n2=en:multifocal epileptiform discharges on diffuse slow background | rel=r_associated | relid=0 | w=10
  2958. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal epileptiform spikes seen on eeg
    n1=DYNC2H1 gene | n2=en:multifocal epileptiform spikes seen on eeg | rel=r_associated | relid=0 | w=10
  2959. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal intractable seizures
    n1=DYNC2H1 gene | n2=en:multifocal intractable seizures | rel=r_associated | relid=0 | w=10
  2960. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal seizure
    n1=DYNC2H1 gene | n2=en:multifocal seizure | rel=r_associated | relid=0 | w=10
  2961. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal spike and wave activity
    n1=DYNC2H1 gene | n2=en:multifocal spike and wave activity | rel=r_associated | relid=0 | w=10
  2962. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal spike waves
    n1=DYNC2H1 gene | n2=en:multifocal spike waves | rel=r_associated | relid=0 | w=10
  2963. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal spikes
    n1=DYNC2H1 gene | n2=en:multifocal spikes | rel=r_associated | relid=0 | w=10
  2964. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal spikes and progressive slowing of background activity seen on eeg
    n1=DYNC2H1 gene | n2=en:multifocal spikes and progressive slowing of background activity seen on eeg | rel=r_associated | relid=0 | w=10
  2965. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multifocal white matter lesions
    n1=DYNC2H1 gene | n2=en:multifocal white matter lesions | rel=r_associated | relid=0 | w=10
  2966. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multiple aneurysms
    n1=DYNC2H1 gene | n2=en:multiple aneurysms | rel=r_associated | relid=0 | w=10
  2967. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multiple independent spike foci
    n1=DYNC2H1 gene | n2=en:multiple independent spike foci | rel=r_associated | relid=0 | w=10
  2968. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multiple lesions in the white matter
    n1=DYNC2H1 gene | n2=en:multiple lesions in the white matter | rel=r_associated | relid=0 | w=10
  2969. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multiple sclerosis-like illness (516003.0001)
    n1=DYNC2H1 gene | n2=en:multiple sclerosis-like illness (516003.0001) | rel=r_associated | relid=0 | w=10
  2970. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multiple system atrophy
    n1=DYNC2H1 gene | n2=en:multiple system atrophy | rel=r_associated | relid=0 | w=10
  2971. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:multisystem degeneration of autonomic nervous system
    n1=DYNC2H1 gene | n2=en:multisystem degeneration of autonomic nervous system | rel=r_associated | relid=0 | w=10
  2972. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle atrophy
    n1=DYNC2H1 gene | n2=en:muscle atrophy | rel=r_associated | relid=0 | w=10
  2973. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle biopsy shows neurogenic changes
    n1=DYNC2H1 gene | n2=en:muscle biopsy shows neurogenic changes | rel=r_associated | relid=0 | w=10
  2974. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle cramp
    n1=DYNC2H1 gene | n2=en:muscle cramp | rel=r_associated | relid=0 | w=10
  2975. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle stiffness and rigidity, chronic, fluctuating
    n1=DYNC2H1 gene | n2=en:muscle stiffness and rigidity, chronic, fluctuating | rel=r_associated | relid=0 | w=10
  2976. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle weakness
    n1=DYNC2H1 gene | n2=en:muscle weakness | rel=r_associated | relid=0 | w=10
  2977. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle weakness lower limb
    n1=DYNC2H1 gene | n2=en:muscle weakness lower limb | rel=r_associated | relid=0 | w=10
  2978. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle weakness of limb
    n1=DYNC2H1 gene | n2=en:muscle weakness of limb | rel=r_associated | relid=0 | w=10
  2979. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle weakness, distal (lower limbs more affected than upper limbs), due to motor neuronopathy
    n1=DYNC2H1 gene | n2=en:muscle weakness, distal (lower limbs more affected than upper limbs), due to motor neuronopathy | rel=r_associated | relid=0 | w=10
  2980. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle weakness, distal, upper and lower
    n1=DYNC2H1 gene | n2=en:muscle weakness, distal, upper and lower | rel=r_associated | relid=0 | w=10
  2981. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle weakness, proximal, due to neuronopathy begins in the lower limbs and then progresses to upper limbs
    n1=DYNC2H1 gene | 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=10
  2982. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy
    n1=DYNC2H1 gene | n2=en:muscle weakness, proximal, symmetric (lower limbs more affected than upper limbs) due to motor neuronopathy | rel=r_associated | relid=0 | w=10
  2983. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscle weakness, symmetric, proximal due to motor neuronopathy
    n1=DYNC2H1 gene | n2=en:muscle weakness, symmetric, proximal due to motor neuronopathy | rel=r_associated | relid=0 | w=10
  2984. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscular hypotonia of the trunk
    n1=DYNC2H1 gene | n2=en:muscular hypotonia of the trunk | rel=r_associated | relid=0 | w=10
  2985. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:muscular rigidity
    n1=DYNC2H1 gene | n2=en:muscular rigidity | rel=r_associated | relid=0 | w=10
  2986. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:musician's cramp
    n1=DYNC2H1 gene | n2=en:musician's cramp | rel=r_associated | relid=0 | w=10
  2987. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:mutism
    n1=DYNC2H1 gene | n2=en:mutism | rel=r_associated | relid=0 | w=10
  2988. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myclonus (rare)
    n1=DYNC2H1 gene | n2=en:myclonus (rare) | rel=r_associated | relid=0 | w=10
  2989. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myelin loss in the corticospinal tracts
    n1=DYNC2H1 gene | n2=en:myelin loss in the corticospinal tracts | rel=r_associated | relid=0 | w=10
  2990. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myelin microvacuolation
    n1=DYNC2H1 gene | n2=en:myelin microvacuolation | rel=r_associated | relid=0 | w=10
  2991. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myelin-like lamellar structures in schwann cells
    n1=DYNC2H1 gene | n2=en:myelin-like lamellar structures in schwann cells | rel=r_associated | relid=0 | w=10
  2992. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myelination defect
    n1=DYNC2H1 gene | n2=en:myelination defect | rel=r_associated | relid=0 | w=10
  2993. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myelination defects (type ii)
    n1=DYNC2H1 gene | n2=en:myelination defects (type ii) | rel=r_associated | relid=0 | w=10
  2994. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myelomeningocele
    n1=DYNC2H1 gene | n2=en:myelomeningocele | rel=r_associated | relid=0 | w=10
  2995. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myelomeningocele (less common)
    n1=DYNC2H1 gene | n2=en:myelomeningocele (less common) | rel=r_associated | relid=0 | w=10
  2996. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myelomeningocele (rare)
    n1=DYNC2H1 gene | n2=en:myelomeningocele (rare) | rel=r_associated | relid=0 | w=10
  2997. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myenteric nerve plexus
    n1=DYNC2H1 gene | n2=en:myenteric nerve plexus | rel=r_associated | relid=0 | w=10
  2998. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic epilepsy (1 patient)
    n1=DYNC2H1 gene | n2=en:myoclonic epilepsy (1 patient) | rel=r_associated | relid=0 | w=10
  2999. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic jerk
    n1=DYNC2H1 gene | n2=en:myoclonic jerk | rel=r_associated | relid=0 | w=10
  3000. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic jerks (less common)
    n1=DYNC2H1 gene | n2=en:myoclonic jerks (less common) | rel=r_associated | relid=0 | w=10
  3001. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic jerks (rare)
    n1=DYNC2H1 gene | n2=en:myoclonic jerks (rare) | rel=r_associated | relid=0 | w=10
  3002. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic seizure, refractory
    n1=DYNC2H1 gene | n2=en:myoclonic seizure, refractory | rel=r_associated | relid=0 | w=10
  3003. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic seizures (1 patient)
    n1=DYNC2H1 gene | n2=en:myoclonic seizures (1 patient) | rel=r_associated | relid=0 | w=10
  3004. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic seizures (subtype 3a)
    n1=DYNC2H1 gene | n2=en:myoclonic seizures (subtype 3a) | rel=r_associated | relid=0 | w=10
  3005. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic seizures may occur
    n1=DYNC2H1 gene | n2=en:myoclonic seizures may occur | rel=r_associated | relid=0 | w=10
  3006. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic seizures, frequent, long-lasting (many hours)
    n1=DYNC2H1 gene | n2=en:myoclonic seizures, frequent, long-lasting (many hours) | rel=r_associated | relid=0 | w=10
  3007. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic seizures, progressive
    n1=DYNC2H1 gene | n2=en:myoclonic seizures, progressive | rel=r_associated | relid=0 | w=10
  3008. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic spasms, superimposed episodic, severe, painful (characterized by activation of antagonistic muscle pairs, may involve facial muscles)
    n1=DYNC2H1 gene | 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=10
  3009. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonic-astatic seizures
    n1=DYNC2H1 gene | n2=en:myoclonic-astatic seizures | rel=r_associated | relid=0 | w=10
  3010. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonus (in 1 family)
    n1=DYNC2H1 gene | n2=en:myoclonus (in 1 family) | rel=r_associated | relid=0 | w=10
  3011. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonus (in a subset of patients)
    n1=DYNC2H1 gene | n2=en:myoclonus (in a subset of patients) | rel=r_associated | relid=0 | w=10
  3012. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonus (less common)
    n1=DYNC2H1 gene | n2=en:myoclonus (less common) | rel=r_associated | relid=0 | w=10
  3013. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonus (subtype 3a)
    n1=DYNC2H1 gene | n2=en:myoclonus (subtype 3a) | rel=r_associated | relid=0 | w=10
  3014. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonus (type i and type ii, infantile and juvenile)
    n1=DYNC2H1 gene | n2=en:myoclonus (type i and type ii, infantile and juvenile) | rel=r_associated | relid=0 | w=10
  3015. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonus, axial (predominantly in upper limbs, occurs at rest and increases with activity or changes in posture)
    n1=DYNC2H1 gene | 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=10
  3016. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonus, cortical, multifocal
    n1=DYNC2H1 gene | n2=en:myoclonus, cortical, multifocal | rel=r_associated | relid=0 | w=10
  3017. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myoclonus, paroxysmal
    n1=DYNC2H1 gene | n2=en:myoclonus, paroxysmal | rel=r_associated | relid=0 | w=10
  3018. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myokymia
    n1=DYNC2H1 gene | n2=en:myokymia | rel=r_associated | relid=0 | w=10
  3019. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myokymia (in some patients)
    n1=DYNC2H1 gene | n2=en:myokymia (in some patients) | rel=r_associated | relid=0 | w=10
  3020. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myokymia, especially facial
    n1=DYNC2H1 gene | n2=en:myokymia, especially facial | rel=r_associated | relid=0 | w=10
  3021. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myopathy
    n1=DYNC2H1 gene | n2=en:myopathy | rel=r_associated | relid=0 | w=10
  3022. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myotonia
    n1=DYNC2H1 gene | n2=en:myotonia | rel=r_associated | relid=0 | w=10
  3023. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myotonia (in 1 patient)
    n1=DYNC2H1 gene | n2=en:myotonia (in 1 patient) | rel=r_associated | relid=0 | w=10
  3024. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:myotonic seizures
    n1=DYNC2H1 gene | n2=en:myotonic seizures | rel=r_associated | relid=0 | w=10
  3025. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:narcolepsy
    n1=DYNC2H1 gene | n2=en:narcolepsy | rel=r_associated | relid=0 | w=10
  3026. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neck drop
    n1=DYNC2H1 gene | n2=en:neck drop | rel=r_associated | relid=0 | w=10
  3027. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neck pain
    n1=DYNC2H1 gene | n2=en:neck pain | rel=r_associated | relid=0 | w=10
  3028. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:necrotic process
    n1=DYNC2H1 gene | n2=en:necrotic process | rel=r_associated | relid=0 | w=10
  3029. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:necrotic white matter lesions throughout the brain and brainstem
    n1=DYNC2H1 gene | n2=en:necrotic white matter lesions throughout the brain and brainstem | rel=r_associated | relid=0 | w=10
  3030. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neocortical atrophy
    n1=DYNC2H1 gene | n2=en:neocortical atrophy | rel=r_associated | relid=0 | w=10
  3031. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neocortical dysplasia (27%)
    n1=DYNC2H1 gene | n2=en:neocortical dysplasia (27%) | rel=r_associated | relid=0 | w=10
  3032. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neonatal epileptic encephalopathy (nee)
    n1=DYNC2H1 gene | n2=en:neonatal epileptic encephalopathy (nee) | rel=r_associated | relid=0 | w=10
  3033. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neonatal hypotonia
    n1=DYNC2H1 gene | n2=en:neonatal hypotonia | rel=r_associated | relid=0 | w=10
  3034. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neonatal irresponsiveness
    n1=DYNC2H1 gene | n2=en:neonatal irresponsiveness | rel=r_associated | relid=0 | w=10
  3035. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neonatal irritability
    n1=DYNC2H1 gene | n2=en:neonatal irritability | rel=r_associated | relid=0 | w=10
  3036. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neonatal/early-infantile onset encephalopathy
    n1=DYNC2H1 gene | n2=en:neonatal/early-infantile onset encephalopathy | rel=r_associated | relid=0 | w=10
  3037. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neoplasm of uncertain behavior of peripheral nerves and peripheral autonomic nervous system
    n1=DYNC2H1 gene | n2=en:neoplasm of uncertain behavior of peripheral nerves and peripheral autonomic nervous system | rel=r_associated | relid=0 | w=10
  3038. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern
    n1=DYNC2H1 gene | n2=en:nerve cells show ballooning with membrane-bound vesicles with reticulogranular pattern | rel=r_associated | relid=0 | w=10
  3039. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nerve degeneration
    n1=DYNC2H1 gene | n2=en:nerve degeneration | rel=r_associated | relid=0 | w=10
  3040. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nerve paralysis
    n1=DYNC2H1 gene | n2=en:nerve paralysis | rel=r_associated | relid=0 | w=10
  3041. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nervousness
    n1=DYNC2H1 gene | n2=en:nervousness | rel=r_associated | relid=0 | w=10
  3042. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neural tube defect (in some patients)
    n1=DYNC2H1 gene | n2=en:neural tube defect (in some patients) | rel=r_associated | relid=0 | w=10
  3043. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neural tube defects (4%)
    n1=DYNC2H1 gene | n2=en:neural tube defects (4%) | rel=r_associated | relid=0 | w=10
  3044. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neural tube defects may occur
    n1=DYNC2H1 gene | n2=en:neural tube defects may occur | rel=r_associated | relid=0 | w=10
  3045. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuritis
    n1=DYNC2H1 gene | n2=en:neuritis | rel=r_associated | relid=0 | w=10
  3046. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuroaxonal abnormalities
    n1=DYNC2H1 gene | n2=en:neuroaxonal abnormalities | rel=r_associated | relid=0 | w=10
  3047. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuroaxonal dystrophies
    n1=DYNC2H1 gene | n2=en:neuroaxonal dystrophies | rel=r_associated | relid=0 | w=10
  3048. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuroaxonal spheroids
    n1=DYNC2H1 gene | n2=en:neuroaxonal spheroids | rel=r_associated | relid=0 | w=10
  3049. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurobehavioral changes associated with hyperammonemia
    n1=DYNC2H1 gene | n2=en:neurobehavioral changes associated with hyperammonemia | rel=r_associated | relid=0 | w=10
  3050. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurocirculatory dystonia
    n1=DYNC2H1 gene | n2=en:neurocirculatory dystonia | rel=r_associated | relid=0 | w=10
  3051. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurocognitive impairment, mild (homozygous patient)
    n1=DYNC2H1 gene | n2=en:neurocognitive impairment, mild (homozygous patient) | rel=r_associated | relid=0 | w=10
  3052. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurodegeneration (patient a)
    n1=DYNC2H1 gene | n2=en:neurodegeneration (patient a) | rel=r_associated | relid=0 | w=10
  3053. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurodegeneration in the basal ganglia
    n1=DYNC2H1 gene | n2=en:neurodegeneration in the basal ganglia | rel=r_associated | relid=0 | w=10
  3054. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurodegeneration in the cerebellum
    n1=DYNC2H1 gene | n2=en:neurodegeneration in the cerebellum | rel=r_associated | relid=0 | w=10
  3055. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurodegeneration in the substantia nigra
    n1=DYNC2H1 gene | n2=en:neurodegeneration in the substantia nigra | rel=r_associated | relid=0 | w=10
  3056. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurodegeneration leading to profound mental retardation
    n1=DYNC2H1 gene | n2=en:neurodegeneration leading to profound mental retardation | rel=r_associated | relid=0 | w=10
  3057. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurodegeneration with brain iron accumulation 5
    n1=DYNC2H1 gene | n2=en:neurodegeneration with brain iron accumulation 5 | rel=r_associated | relid=0 | w=10
  3058. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurodevelopmental impairment (early-onset form)
    n1=DYNC2H1 gene | n2=en:neurodevelopmental impairment (early-onset form) | rel=r_associated | relid=0 | w=10
  3059. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurodevelopmental regression
    n1=DYNC2H1 gene | n2=en:neurodevelopmental regression | rel=r_associated | relid=0 | w=10
  3060. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurofibrillary degeneration (morphologic abnormality)
    n1=DYNC2H1 gene | n2=en:neurofibrillary degeneration (morphologic abnormality) | rel=r_associated | relid=0 | w=10
  3061. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurofibrillary mapt (tau)-positive tangles
    n1=DYNC2H1 gene | n2=en:neurofibrillary mapt (tau)-positive tangles | rel=r_associated | relid=0 | w=10
  3062. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurofibrillary tangles composed of disordered microtubules
    n1=DYNC2H1 gene | n2=en:neurofibrillary tangles composed of disordered microtubules | rel=r_associated | relid=0 | w=10
  3063. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurofibrillary tangles may be present
    n1=DYNC2H1 gene | n2=en:neurofibrillary tangles may be present | rel=r_associated | relid=0 | w=10
  3064. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurofibromas can occur at cervical, thoracic, lumbar, and sacral levels
    n1=DYNC2H1 gene | n2=en:neurofibromas can occur at cervical, thoracic, lumbar, and sacral levels | rel=r_associated | relid=0 | w=10
  3065. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurogenic bladder
    n1=DYNC2H1 gene | n2=en:neurogenic bladder | rel=r_associated | relid=0 | w=10
  3066. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurogenic bowel
    n1=DYNC2H1 gene | n2=en:neurogenic bowel | rel=r_associated | relid=0 | w=10
  3067. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurogenic hypertension
    n1=DYNC2H1 gene | n2=en:neurogenic hypertension | rel=r_associated | relid=0 | w=10
  3068. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurogenic muscle atrophy, especially in the lower limbs
    n1=DYNC2H1 gene | n2=en:neurogenic muscle atrophy, especially in the lower limbs | rel=r_associated | relid=0 | w=10
  3069. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuroimaging shows cortical atrophy
    n1=DYNC2H1 gene | n2=en:neuroimaging shows cortical atrophy | rel=r_associated | relid=0 | w=10
  3070. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologia
    n1=DYNC2H1 gene | n2=en:neurologia | rel=r_associated | relid=0 | w=10
  3071. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic abnormalities in about 7%
    n1=DYNC2H1 gene | n2=en:neurologic abnormalities in about 7% | rel=r_associated | relid=0 | w=10
  3072. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic crises with coma (in some patients)
    n1=DYNC2H1 gene | n2=en:neurologic crises with coma (in some patients) | rel=r_associated | relid=0 | w=10
  3073. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic decompensation
    n1=DYNC2H1 gene | n2=en:neurologic decompensation | rel=r_associated | relid=0 | w=10
  3074. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic degeneration
    n1=DYNC2H1 gene | n2=en:neurologic degeneration | rel=r_associated | relid=0 | w=10
  3075. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic deterioration in longterm survivors
    n1=DYNC2H1 gene | n2=en:neurologic deterioration in longterm survivors | rel=r_associated | relid=0 | w=10
  3076. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic dysfunction, progressive
    n1=DYNC2H1 gene | n2=en:neurologic dysfunction, progressive | rel=r_associated | relid=0 | w=10
  3077. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic involvement (in some patients)
    n1=DYNC2H1 gene | n2=en:neurologic involvement (in some patients) | rel=r_associated | relid=0 | w=10
  3078. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic involvement is rare
    n1=DYNC2H1 gene | n2=en:neurologic involvement is rare | rel=r_associated | relid=0 | w=10
  3079. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic regression
    n1=DYNC2H1 gene | n2=en:neurologic regression | rel=r_associated | relid=0 | w=10
  3080. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic regression after age 2 years
    n1=DYNC2H1 gene | n2=en:neurologic regression after age 2 years | rel=r_associated | relid=0 | w=10
  3081. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic regression after prolonged episodes
    n1=DYNC2H1 gene | n2=en:neurologic regression after prolonged episodes | rel=r_associated | relid=0 | w=10
  3082. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic regression around age 3 months
    n1=DYNC2H1 gene | n2=en:neurologic regression around age 3 months | rel=r_associated | relid=0 | w=10
  3083. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic regression following seizure onset
    n1=DYNC2H1 gene | n2=en:neurologic regression following seizure onset | rel=r_associated | relid=0 | w=10
  3084. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic sequelae not always present
    n1=DYNC2H1 gene | n2=en:neurologic sequelae not always present | rel=r_associated | relid=0 | w=10
  3085. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic sequelae of stroke
    n1=DYNC2H1 gene | n2=en:neurologic sequelae of stroke | rel=r_associated | relid=0 | w=10
  3086. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurologic symptoms, if present, usually result from associated syringomyelia
    n1=DYNC2H1 gene | n2=en:neurologic symptoms, if present, usually result from associated syringomyelia | rel=r_associated | relid=0 | w=10
  3087. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuroma
    n1=DYNC2H1 gene | n2=en:neuroma | rel=r_associated | relid=0 | w=10
  3088. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuromuscular disturbances, progressive
    n1=DYNC2H1 gene | n2=en:neuromuscular disturbances, progressive | rel=r_associated | relid=0 | w=10
  3089. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuron apoptotic process
    n1=DYNC2H1 gene | n2=en:neuron apoptotic process | rel=r_associated | relid=0 | w=10
  3090. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuron loss
    n1=DYNC2H1 gene | n2=en:neuron loss | rel=r_associated | relid=0 | w=10
  3091. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal and vascular calcifications
    n1=DYNC2H1 gene | n2=en:neuronal and vascular calcifications | rel=r_associated | relid=0 | w=10
  3092. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal heterotopia
    n1=DYNC2H1 gene | n2=en:neuronal heterotopia | rel=r_associated | relid=0 | w=10
  3093. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal inclusion bodies stain for neuroserpin
    n1=DYNC2H1 gene | n2=en:neuronal inclusion bodies stain for neuroserpin | rel=r_associated | relid=0 | w=10
  3094. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss (patient a)
    n1=DYNC2H1 gene | n2=en:neuronal loss (patient a) | rel=r_associated | relid=0 | w=10
  3095. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss and gliosis in caudate and putamen
    n1=DYNC2H1 gene | n2=en:neuronal loss and gliosis in caudate and putamen | rel=r_associated | relid=0 | w=10
  3096. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss and gliosis in the cerebral cortex
    n1=DYNC2H1 gene | n2=en:neuronal loss and gliosis in the cerebral cortex | rel=r_associated | relid=0 | w=10
  3097. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss and gliosis in the dentate nucleus
    n1=DYNC2H1 gene | n2=en:neuronal loss and gliosis in the dentate nucleus | rel=r_associated | relid=0 | w=10
  3098. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss and gliosis in the inferior olives
    n1=DYNC2H1 gene | n2=en:neuronal loss and gliosis in the inferior olives | rel=r_associated | relid=0 | w=10
  3099. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss and gliosis in the substantia nigra pars compacta
    n1=DYNC2H1 gene | n2=en:neuronal loss and gliosis in the substantia nigra pars compacta | rel=r_associated | relid=0 | w=10
  3100. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in basal ganglia
    n1=DYNC2H1 gene | n2=en:neuronal loss in basal ganglia | rel=r_associated | relid=0 | w=10
  3101. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in central nervous system
    n1=DYNC2H1 gene | n2=en:neuronal loss in central nervous system | rel=r_associated | relid=0 | w=10
  3102. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the brainstem
    n1=DYNC2H1 gene | n2=en:neuronal loss in the brainstem | rel=r_associated | relid=0 | w=10
  3103. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the cerebral cortex
    n1=DYNC2H1 gene | n2=en:neuronal loss in the cerebral cortex | rel=r_associated | relid=0 | w=10
  3104. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the cerebrum and cerebellum
    n1=DYNC2H1 gene | n2=en:neuronal loss in the cerebrum and cerebellum | rel=r_associated | relid=0 | w=10
  3105. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the dentate nuclei
    n1=DYNC2H1 gene | n2=en:neuronal loss in the dentate nuclei | rel=r_associated | relid=0 | w=10
  3106. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the hippocampus
    n1=DYNC2H1 gene | n2=en:neuronal loss in the hippocampus | rel=r_associated | relid=0 | w=10
  3107. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the inferior olives
    n1=DYNC2H1 gene | n2=en:neuronal loss in the inferior olives | rel=r_associated | relid=0 | w=10
  3108. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the locus ceruleus
    n1=DYNC2H1 gene | n2=en:neuronal loss in the locus ceruleus | rel=r_associated | relid=0 | w=10
  3109. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the purkinje cell layer of the cerebellar vermis
    n1=DYNC2H1 gene | n2=en:neuronal loss in the purkinje cell layer of the cerebellar vermis | rel=r_associated | relid=0 | w=10
  3110. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients)
    n1=DYNC2H1 gene | n2=en:neuronal loss in the striatum, cerebral cortex, and cerebellum (in some patients) | rel=r_associated | relid=0 | w=10
  3111. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives
    n1=DYNC2H1 gene | n2=en:neuronal loss in the striatum, medial thalamic nuclei, and inferior olives | rel=r_associated | relid=0 | w=10
  3112. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss in the substantia nigra
    n1=DYNC2H1 gene | n2=en:neuronal loss in the substantia nigra | rel=r_associated | relid=0 | w=10
  3113. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss, diffuse
    n1=DYNC2H1 gene | n2=en:neuronal loss, diffuse | rel=r_associated | relid=0 | w=10
  3114. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal loss, particularly of cerebellar purkinje cells
    n1=DYNC2H1 gene | n2=en:neuronal loss, particularly of cerebellar purkinje cells | rel=r_associated | relid=0 | w=10
  3115. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal migration defect
    n1=DYNC2H1 gene | n2=en:neuronal migration defect | rel=r_associated | relid=0 | w=10
  3116. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuronal migration disorder
    n1=DYNC2H1 gene | n2=en:neuronal migration disorder | rel=r_associated | relid=0 | w=10
  3117. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathologic examination shows calcification of the small brain vessels
    n1=DYNC2H1 gene | n2=en:neuropathologic examination shows calcification of the small brain vessels | rel=r_associated | relid=0 | w=10
  3118. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathologic examination shows extensive spongiosis and gliosis
    n1=DYNC2H1 gene | n2=en:neuropathologic examination shows extensive spongiosis and gliosis | rel=r_associated | relid=0 | w=10
  3119. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathologic examination shows severe demyelination
    n1=DYNC2H1 gene | n2=en:neuropathologic examination shows severe demyelination | rel=r_associated | relid=0 | w=10
  3120. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially)
    n1=DYNC2H1 gene | n2=en:neuropathologic findings include leukoencephalopathy, predominantly in the upper corticospinal tract and cerebellar peduncles (initially) | rel=r_associated | relid=0 | w=10
  3121. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells
    n1=DYNC2H1 gene | n2=en:neuropathology shows alpha-synuclein-containing cytoplasmic inclusions in glial cells | rel=r_associated | relid=0 | w=10
  3122. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathology shows diffuse demyelination of the cerebral white matter
    n1=DYNC2H1 gene | n2=en:neuropathology shows diffuse demyelination of the cerebral white matter | rel=r_associated | relid=0 | w=10
  3123. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathology shows fmr1 mrna-positive inclusions in neurons and astrocytes
    n1=DYNC2H1 gene | n2=en:neuropathology shows fmr1 mrna-positive inclusions in neurons and astrocytes | rel=r_associated | relid=0 | w=10
  3124. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathology shows neuronal degeneration
    n1=DYNC2H1 gene | n2=en:neuropathology shows neuronal degeneration | rel=r_associated | relid=0 | w=10
  3125. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathology shows neuronal loss in basal ganglia, brainstem, and cerebellum
    n1=DYNC2H1 gene | n2=en:neuropathology shows neuronal loss in basal ganglia, brainstem, and cerebellum | rel=r_associated | relid=0 | w=10
  3126. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum
    n1=DYNC2H1 gene | n2=en:neuropathology shows severe neuronal loss in the inner granular layer of the cerebellum | rel=r_associated | relid=0 | w=10
  3127. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurophysiologic abnormalities (eeg, sep, vep)
    n1=DYNC2H1 gene | n2=en:neurophysiologic abnormalities (eeg, sep, vep) | rel=r_associated | relid=0 | w=10
  3128. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurophysiologic abnormalities (eeg, vep, sep)
    n1=DYNC2H1 gene | n2=en:neurophysiologic abnormalities (eeg, vep, sep) | rel=r_associated | relid=0 | w=10
  3129. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurophysiologic studies show evidence of denervation and renervation
    n1=DYNC2H1 gene | n2=en:neurophysiologic studies show evidence of denervation and renervation | rel=r_associated | relid=0 | w=10
  3130. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropil
    n1=DYNC2H1 gene | n2=en:neuropil | rel=r_associated | relid=0 | w=10
  3131. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropsychologic cognitive abnormalities
    n1=DYNC2H1 gene | n2=en:neuropsychologic cognitive abnormalities | rel=r_associated | relid=0 | w=10
  3132. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neuropsychologic impairment
    n1=DYNC2H1 gene | n2=en:neuropsychologic impairment | rel=r_associated | relid=0 | w=10
  3133. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurosarcoidosis (5-16% of patients)
    n1=DYNC2H1 gene | n2=en:neurosarcoidosis (5-16% of patients) | rel=r_associated | relid=0 | w=10
  3134. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:neurovegetative neurosis
    n1=DYNC2H1 gene | n2=en:neurovegetative neurosis | rel=r_associated | relid=0 | w=10
  3135. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:never able to walk
    n1=DYNC2H1 gene | n2=en:never able to walk | rel=r_associated | relid=0 | w=10
  3136. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:never learn to walk (some patients)
    n1=DYNC2H1 gene | n2=en:never learn to walk (some patients) | rel=r_associated | relid=0 | w=10
  3137. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nigrostriatal degeneration
    n1=DYNC2H1 gene | n2=en:nigrostriatal degeneration | rel=r_associated | relid=0 | w=10
  3138. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no amyloid plaques
    n1=DYNC2H1 gene | n2=en:no amyloid plaques | rel=r_associated | relid=0 | w=10
  3139. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no autistic features
    n1=DYNC2H1 gene | n2=en:no autistic features | rel=r_associated | relid=0 | w=10
  3140. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no bulbar involvement
    n1=DYNC2H1 gene | n2=en:no bulbar involvement | rel=r_associated | relid=0 | w=10
  3141. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no central nervous system abnormalities
    n1=DYNC2H1 gene | n2=en:no central nervous system abnormalities | rel=r_associated | relid=0 | w=10
  3142. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no cerebellar signs
    n1=DYNC2H1 gene | n2=en:no cerebellar signs | rel=r_associated | relid=0 | w=10
  3143. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no cerebellar vermis aplasia/hypoplasia
    n1=DYNC2H1 gene | n2=en:no cerebellar vermis aplasia/hypoplasia | rel=r_associated | relid=0 | w=10
  3144. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no cognitive decline
    n1=DYNC2H1 gene | n2=en:no cognitive decline | rel=r_associated | relid=0 | w=10
  3145. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no dementia
    n1=DYNC2H1 gene | n2=en:no dementia | rel=r_associated | relid=0 | w=10
  3146. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no development
    n1=DYNC2H1 gene | n2=en:no development | rel=r_associated | relid=0 | w=10
  3147. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no developmental progress
    n1=DYNC2H1 gene | n2=en:no developmental progress | rel=r_associated | relid=0 | w=10
  3148. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no gaze contact
    n1=DYNC2H1 gene | n2=en:no gaze contact | rel=r_associated | relid=0 | w=10
  3149. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no head control
    n1=DYNC2H1 gene | n2=en:no head control | rel=r_associated | relid=0 | w=10
  3150. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no hippocampal sclerosis
    n1=DYNC2H1 gene | n2=en:no hippocampal sclerosis | rel=r_associated | relid=0 | w=10
  3151. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no hydrocephalus
    n1=DYNC2H1 gene | n2=en:no hydrocephalus | rel=r_associated | relid=0 | w=10
  3152. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no language
    n1=DYNC2H1 gene | n2=en:no language | rel=r_associated | relid=0 | w=10
  3153. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no language development
    n1=DYNC2H1 gene | n2=en:no language development | rel=r_associated | relid=0 | w=10
  3154. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no lewy bodies
    n1=DYNC2H1 gene | n2=en:no lewy bodies | rel=r_associated | relid=0 | w=10
  3155. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no mental retardation
    n1=DYNC2H1 gene | n2=en:no mental retardation | rel=r_associated | relid=0 | w=10
  3156. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no motor skills acquired (in some)
    n1=DYNC2H1 gene | n2=en:no motor skills acquired (in some) | rel=r_associated | relid=0 | w=10
  3157. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no myoclonus
    n1=DYNC2H1 gene | n2=en:no myoclonus | rel=r_associated | relid=0 | w=10
  3158. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no neurofibrillary tangles
    n1=DYNC2H1 gene | n2=en:no neurofibrillary tangles | rel=r_associated | relid=0 | w=10
  3159. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no neurofibromas
    n1=DYNC2H1 gene | n2=en:no neurofibromas | rel=r_associated | relid=0 | w=10
  3160. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no other neurologic deficits
    n1=DYNC2H1 gene | n2=en:no other neurologic deficits | rel=r_associated | relid=0 | w=10
  3161. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no other neurologic disorder
    n1=DYNC2H1 gene | n2=en:no other neurologic disorder | rel=r_associated | relid=0 | w=10
  3162. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no overt seizures
    n1=DYNC2H1 gene | n2=en:no overt seizures | rel=r_associated | relid=0 | w=10
  3163. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no pick bodies or lewy bodies
    n1=DYNC2H1 gene | n2=en:no pick bodies or lewy bodies | rel=r_associated | relid=0 | w=10
  3164. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no response to l-dopa treatment
    n1=DYNC2H1 gene | n2=en:no response to l-dopa treatment | rel=r_associated | relid=0 | w=10
  3165. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no seizures
    n1=DYNC2H1 gene | n2=en:no seizures | rel=r_associated | relid=0 | w=10
  3166. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no seizures (hcs)
    n1=DYNC2H1 gene | n2=en:no seizures (hcs) | rel=r_associated | relid=0 | w=10
  3167. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no sensory deficit
    n1=DYNC2H1 gene | n2=en:no sensory deficit | rel=r_associated | relid=0 | w=10
  3168. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no sensory symptoms
    n1=DYNC2H1 gene | n2=en:no sensory symptoms | rel=r_associated | relid=0 | w=10
  3169. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no speech acquisition
    n1=DYNC2H1 gene | n2=en:no speech acquisition | rel=r_associated | relid=0 | w=10
  3170. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no speech development (in most patients)
    n1=DYNC2H1 gene | n2=en:no speech development (in most patients) | rel=r_associated | relid=0 | w=10
  3171. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no speech problem
    n1=DYNC2H1 gene | n2=en:no speech problem | rel=r_associated | relid=0 | w=10
  3172. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no spontaneous movements
    n1=DYNC2H1 gene | n2=en:no spontaneous movements | rel=r_associated | relid=0 | w=10
  3173. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no structural brain abnormalities seen on mri
    n1=DYNC2H1 gene | n2=en:no structural brain abnormalities seen on mri | rel=r_associated | relid=0 | w=10
  3174. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no structural brain anomalies
    n1=DYNC2H1 gene | n2=en:no structural brain anomalies | rel=r_associated | relid=0 | w=10
  3175. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no tau pathology
    n1=DYNC2H1 gene | n2=en:no tau pathology | rel=r_associated | relid=0 | w=10
  3176. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no tremor
    n1=DYNC2H1 gene | n2=en:no tremor | rel=r_associated | relid=0 | w=10
  3177. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no visual fixation
    n1=DYNC2H1 gene | n2=en:no visual fixation | rel=r_associated | relid=0 | w=10
  3178. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:no voluntary movement
    n1=DYNC2H1 gene | n2=en:no voluntary movement | rel=r_associated | relid=0 | w=10
  3179. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nocturnal occurrence
    n1=DYNC2H1 gene | n2=en:nocturnal occurrence | rel=r_associated | relid=0 | w=10
  3180. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nocturnal occurrence, usually during light sleep
    n1=DYNC2H1 gene | n2=en:nocturnal occurrence, usually during light sleep | rel=r_associated | relid=0 | w=10
  3181. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nocturnal seizures
    n1=DYNC2H1 gene | n2=en:nocturnal seizures | rel=r_associated | relid=0 | w=10
  3182. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nocturnal seizures (in some patients)
    n1=DYNC2H1 gene | n2=en:nocturnal seizures (in some patients) | rel=r_associated | relid=0 | w=10
  3183. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nocturnal sleep disruption
    n1=DYNC2H1 gene | n2=en:nocturnal sleep disruption | rel=r_associated | relid=0 | w=10
  3184. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nodding of head
    n1=DYNC2H1 gene | n2=en:nodding of head | rel=r_associated | relid=0 | w=10
  3185. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nodular heterotopia
    n1=DYNC2H1 gene | n2=en:nodular heterotopia | rel=r_associated | relid=0 | w=10
  3186. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nodular heterotopia (in some patients)
    n1=DYNC2H1 gene | n2=en:nodular heterotopia (in some patients) | rel=r_associated | relid=0 | w=10
  3187. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nodular heterotopia (less common)
    n1=DYNC2H1 gene | n2=en:nodular heterotopia (less common) | rel=r_associated | relid=0 | w=10
  3188. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nodular heterotopia (rare)
    n1=DYNC2H1 gene | n2=en:nodular heterotopia (rare) | rel=r_associated | relid=0 | w=10
  3189. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nodular heterotopia of the grey matter
    n1=DYNC2H1 gene | n2=en:nodular heterotopia of the grey matter | rel=r_associated | relid=0 | w=10
  3190. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:non-febrile seizures later
    n1=DYNC2H1 gene | n2=en:non-febrile seizures later | rel=r_associated | relid=0 | w=10
  3191. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:non-purposeful arm movements, choreoathetoid-like
    n1=DYNC2H1 gene | n2=en:non-purposeful arm movements, choreoathetoid-like | rel=r_associated | relid=0 | w=10
  3192. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nonprogressive cerebellar ataxia
    n1=DYNC2H1 gene | n2=en:nonprogressive cerebellar ataxia | rel=r_associated | relid=0 | w=10
  3193. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nonspecific leukoencephalopathy (52%)
    n1=DYNC2H1 gene | n2=en:nonspecific leukoencephalopathy (52%) | rel=r_associated | relid=0 | w=10
  3194. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nonspecific spongiform degeneration
    n1=DYNC2H1 gene | n2=en:nonspecific spongiform degeneration | rel=r_associated | relid=0 | w=10
  3195. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nonverbal (in some patients)
    n1=DYNC2H1 gene | n2=en:nonverbal (in some patients) | rel=r_associated | relid=0 | w=10
  3196. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal brain mri or ct scan
    n1=DYNC2H1 gene | n2=en:normal brain mri or ct scan | rel=r_associated | relid=0 | w=10
  3197. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal cognition (1 patient)
    n1=DYNC2H1 gene | n2=en:normal cognition (1 patient) | rel=r_associated | relid=0 | w=10
  3198. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal cognition (in some patients)
    n1=DYNC2H1 gene | n2=en:normal cognition (in some patients) | rel=r_associated | relid=0 | w=10
  3199. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal cognition (reported in 1 patient who survived to age 20 years)
    n1=DYNC2H1 gene | n2=en:normal cognition (reported in 1 patient who survived to age 20 years) | rel=r_associated | relid=0 | w=10
  3200. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal cognition (reported in some patients)
    n1=DYNC2H1 gene | n2=en:normal cognition (reported in some patients) | rel=r_associated | relid=0 | w=10
  3201. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal cognition and intellectual function
    n1=DYNC2H1 gene | n2=en:normal cognition and intellectual function | rel=r_associated | relid=0 | w=10
  3202. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal development
    n1=DYNC2H1 gene | n2=en:normal development | rel=r_associated | relid=0 | w=10
  3203. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal development (in 2 of 6 patients)
    n1=DYNC2H1 gene | n2=en:normal development (in 2 of 6 patients) | rel=r_associated | relid=0 | w=10
  3204. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal development in some patients
    n1=DYNC2H1 gene | n2=en:normal development in some patients | rel=r_associated | relid=0 | w=10
  3205. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal development until 6-18 months
    n1=DYNC2H1 gene | n2=en:normal development until 6-18 months | rel=r_associated | relid=0 | w=10
  3206. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal early development
    n1=DYNC2H1 gene | n2=en:normal early development | rel=r_associated | relid=0 | w=10
  3207. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal early development, up to 8 to 15 months of age
    n1=DYNC2H1 gene | n2=en:normal early development, up to 8 to 15 months of age | rel=r_associated | relid=0 | w=10
  3208. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal early developmental milestones
    n1=DYNC2H1 gene | n2=en:normal early developmental milestones | rel=r_associated | relid=0 | w=10
  3209. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal early psychomotor development
    n1=DYNC2H1 gene | n2=en:normal early psychomotor development | rel=r_associated | relid=0 | w=10
  3210. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal fine motor activity
    n1=DYNC2H1 gene | n2=en:normal fine motor activity | rel=r_associated | relid=0 | w=10
  3211. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal initial psychomotor development
    n1=DYNC2H1 gene | n2=en:normal initial psychomotor development | rel=r_associated | relid=0 | w=10
  3212. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal intellectual development
    n1=DYNC2H1 gene | n2=en:normal intellectual development | rel=r_associated | relid=0 | w=10
  3213. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal intellectual function
    n1=DYNC2H1 gene | n2=en:normal intellectual function | rel=r_associated | relid=0 | w=10
  3214. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal intelligence (in some patients)
    n1=DYNC2H1 gene | n2=en:normal intelligence (in some patients) | rel=r_associated | relid=0 | w=10
  3215. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal intelligence (majority)
    n1=DYNC2H1 gene | n2=en:normal intelligence (majority) | rel=r_associated | relid=0 | w=10
  3216. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal intelligence in carrier females
    n1=DYNC2H1 gene | n2=en:normal intelligence in carrier females | rel=r_associated | relid=0 | w=10
  3217. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal intelligence in iib
    n1=DYNC2H1 gene | n2=en:normal intelligence in iib | rel=r_associated | relid=0 | w=10
  3218. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal intelligence in majority
    n1=DYNC2H1 gene | n2=en:normal intelligence in majority | rel=r_associated | relid=0 | w=10
  3219. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal intelligence in most cases
    n1=DYNC2H1 gene | n2=en:normal intelligence in most cases | rel=r_associated | relid=0 | w=10
  3220. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal intelligence to mild or moderate mental retardation
    n1=DYNC2H1 gene | n2=en:normal intelligence to mild or moderate mental retardation | rel=r_associated | relid=0 | w=10
  3221. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal interictal eeg
    n1=DYNC2H1 gene | n2=en:normal interictal eeg | rel=r_associated | relid=0 | w=10
  3222. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal interictal neurologic examination
    n1=DYNC2H1 gene | n2=en:normal interictal neurologic examination | rel=r_associated | relid=0 | w=10
  3223. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal iq in infancy, then iq drops with age
    n1=DYNC2H1 gene | n2=en:normal iq in infancy, then iq drops with age | rel=r_associated | relid=0 | w=10
  3224. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal mental development
    n1=DYNC2H1 gene | n2=en:normal mental development | rel=r_associated | relid=0 | w=10
  3225. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal motor conduction studies (initially)
    n1=DYNC2H1 gene | n2=en:normal motor conduction studies (initially) | rel=r_associated | relid=0 | w=10
  3226. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal motor development
    n1=DYNC2H1 gene | n2=en:normal motor development | rel=r_associated | relid=0 | w=10
  3227. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal muscle strength
    n1=DYNC2H1 gene | n2=en:normal muscle strength | rel=r_associated | relid=0 | w=10
  3228. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal neurologic development in most cases
    n1=DYNC2H1 gene | n2=en:normal neurologic development in most cases | rel=r_associated | relid=0 | w=10
  3229. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal neurological development is possible
    n1=DYNC2H1 gene | n2=en:normal neurological development is possible | rel=r_associated | relid=0 | w=10
  3230. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal neuromuscular studies
    n1=DYNC2H1 gene | n2=en:normal neuromuscular studies | rel=r_associated | relid=0 | w=10
  3231. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal psychomotor development
    n1=DYNC2H1 gene | n2=en:normal psychomotor development | rel=r_associated | relid=0 | w=10
  3232. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal psychomotor development in most
    n1=DYNC2H1 gene | n2=en:normal psychomotor development in most | rel=r_associated | relid=0 | w=10
  3233. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal psychomotor development until age 2 to 3 years
    n1=DYNC2H1 gene | n2=en:normal psychomotor development until age 2 to 3 years | rel=r_associated | relid=0 | w=10
  3234. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal sleep-onset time (normal time of falling asleep)
    n1=DYNC2H1 gene | n2=en:normal sleep-onset time (normal time of falling asleep) | rel=r_associated | relid=0 | w=10
  3235. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal to mild mental retardation
    n1=DYNC2H1 gene | n2=en:normal to mild mental retardation | rel=r_associated | relid=0 | w=10
  3236. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal to mildly delayed development
    n1=DYNC2H1 gene | n2=en:normal to mildly delayed development | rel=r_associated | relid=0 | w=10
  3237. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:normal, timely language development
    n1=DYNC2H1 gene | n2=en:normal, timely language development | rel=r_associated | relid=0 | w=10
  3238. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nuclear magnetic resonance imaging brain normal
    n1=DYNC2H1 gene | n2=en:nuclear magnetic resonance imaging brain normal | rel=r_associated | relid=0 | w=10
  3239. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:numbness
    n1=DYNC2H1 gene | n2=en:numbness | rel=r_associated | relid=0 | w=10
  3240. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nystagmus
    n1=DYNC2H1 gene | n2=en:nystagmus | rel=r_associated | relid=0 | w=10
  3241. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nystagmus decreases on convergence
    n1=DYNC2H1 gene | n2=en:nystagmus decreases on convergence | rel=r_associated | relid=0 | w=10
  3242. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit
    n1=DYNC2H1 gene | n2=en:nystagmus is accentuated by fixation, lateral gaze, smooth pursuit | rel=r_associated | relid=0 | w=10
  3243. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nystagmus, horizontal
    n1=DYNC2H1 gene | n2=en:nystagmus, horizontal | rel=r_associated | relid=0 | w=10
  3244. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nystagmus, jerky, horizontal, congenital
    n1=DYNC2H1 gene | n2=en:nystagmus, jerky, horizontal, congenital | rel=r_associated | relid=0 | w=10
  3245. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:nystagmus, mild
    n1=DYNC2H1 gene | n2=en:nystagmus, mild | rel=r_associated | relid=0 | w=10
  3246. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:obsessive compulsive behavior
    n1=DYNC2H1 gene | n2=en:obsessive compulsive behavior | rel=r_associated | relid=0 | w=10
  3247. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:obstruction of the foramen of monro (variable)
    n1=DYNC2H1 gene | n2=en:obstruction of the foramen of monro (variable) | rel=r_associated | relid=0 | w=10
  3248. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occasional degeneration of the globus pallidus
    n1=DYNC2H1 gene | n2=en:occasional degeneration of the globus pallidus | rel=r_associated | relid=0 | w=10
  3249. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital dermal sinus tract
    n1=DYNC2H1 gene | n2=en:occipital dermal sinus tract | rel=r_associated | relid=0 | w=10
  3250. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital encephalocele (in some patients)
    n1=DYNC2H1 gene | n2=en:occipital encephalocele (in some patients) | rel=r_associated | relid=0 | w=10
  3251. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital encephalocele (wws)
    n1=DYNC2H1 gene | n2=en:occipital encephalocele (wws) | rel=r_associated | relid=0 | w=10
  3252. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital encephaloceles
    n1=DYNC2H1 gene | n2=en:occipital encephaloceles | rel=r_associated | relid=0 | w=10
  3253. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital headache
    n1=DYNC2H1 gene | n2=en:occipital headache | rel=r_associated | relid=0 | w=10
  3254. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital lobe atrophy
    n1=DYNC2H1 gene | n2=en:occipital lobe atrophy | rel=r_associated | relid=0 | w=10
  3255. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital lobe infarct (rare)
    n1=DYNC2H1 gene | n2=en:occipital lobe infarct (rare) | rel=r_associated | relid=0 | w=10
  3256. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital meningocele
    n1=DYNC2H1 gene | n2=en:occipital meningocele | rel=r_associated | relid=0 | w=10
  3257. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital meningocele (less common)
    n1=DYNC2H1 gene | n2=en:occipital meningocele (less common) | rel=r_associated | relid=0 | w=10
  3258. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital myelomeningocele (less common)
    n1=DYNC2H1 gene | n2=en:occipital myelomeningocele (less common) | rel=r_associated | relid=0 | w=10
  3259. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occipital neural tube defects
    n1=DYNC2H1 gene | n2=en:occipital neural tube defects | rel=r_associated | relid=0 | w=10
  3260. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occlusive hydrocephalus, congenital
    n1=DYNC2H1 gene | n2=en:occlusive hydrocephalus, congenital | rel=r_associated | relid=0 | w=10
  3261. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:occurs most often during the night or early morning
    n1=DYNC2H1 gene | n2=en:occurs most often during the night or early morning | rel=r_associated | relid=0 | w=10
  3262. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ocular motility spared
    n1=DYNC2H1 gene | n2=en:ocular motility spared | rel=r_associated | relid=0 | w=10
  3263. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ocular muscle abnormalities
    n1=DYNC2H1 gene | n2=en:ocular muscle abnormalities | rel=r_associated | relid=0 | w=10
  3264. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ocular palsies
    n1=DYNC2H1 gene | n2=en:ocular palsies | rel=r_associated | relid=0 | w=10
  3265. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:oculomotor apraxia
    n1=DYNC2H1 gene | n2=en:oculomotor apraxia | rel=r_associated | relid=0 | w=10
  3266. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:olfactory lobe agenesis
    n1=DYNC2H1 gene | n2=en:olfactory lobe agenesis | rel=r_associated | relid=0 | w=10
  3267. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:olfactory or auditory hallucinations
    n1=DYNC2H1 gene | n2=en:olfactory or auditory hallucinations | rel=r_associated | relid=0 | w=10
  3268. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:oligodendrocytes with foamy cytoplasm
    n1=DYNC2H1 gene | n2=en:oligodendrocytes with foamy cytoplasm | rel=r_associated | relid=0 | w=10
  3269. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:olivopontocerebellar atrophy
    n1=DYNC2H1 gene | n2=en:olivopontocerebellar atrophy | rel=r_associated | relid=0 | w=10
  3270. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:olivopontocerebellar hypoplasia, fetal-onset
    n1=DYNC2H1 gene | n2=en:olivopontocerebellar hypoplasia, fetal-onset | rel=r_associated | relid=0 | w=10
  3271. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:olivopontocerebellar hypoplasia, severe
    n1=DYNC2H1 gene | n2=en:olivopontocerebellar hypoplasia, severe | rel=r_associated | relid=0 | w=10
  3272. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:only some achieve rolling or sitting
    n1=DYNC2H1 gene | n2=en:only some achieve rolling or sitting | rel=r_associated | relid=0 | w=10
  3273. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:only walking achieved
    n1=DYNC2H1 gene | n2=en:only walking achieved | rel=r_associated | relid=0 | w=10
  3274. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:onset may be triggered by emotional stress, fever, exercise, exposure to heat
    n1=DYNC2H1 gene | n2=en:onset may be triggered by emotional stress, fever, exercise, exposure to heat | rel=r_associated | relid=0 | w=10
  3275. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:open operculum
    n1=DYNC2H1 gene | n2=en:open operculum | rel=r_associated | relid=0 | w=10
  3276. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:open spina bifida (myelomeningocele, 182940)
    n1=DYNC2H1 gene | n2=en:open spina bifida (myelomeningocele, 182940) | rel=r_associated | relid=0 | w=10
  3277. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:open sylvian fissures
    n1=DYNC2H1 gene | n2=en:open sylvian fissures | rel=r_associated | relid=0 | w=10
  3278. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:opisthotonic posturing
    n1=DYNC2H1 gene | n2=en:opisthotonic posturing | rel=r_associated | relid=0 | w=10
  3279. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:opisthotonos (type ii)
    n1=DYNC2H1 gene | n2=en:opisthotonos (type ii) | rel=r_associated | relid=0 | w=10
  3280. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:opisthotonus
    n1=DYNC2H1 gene | n2=en:opisthotonus | rel=r_associated | relid=0 | w=10
  3281. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:opsoclonus
    n1=DYNC2H1 gene | n2=en:opsoclonus | rel=r_associated | relid=0 | w=10
  3282. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:optic ataxia (in a subset of patients)
    n1=DYNC2H1 gene | n2=en:optic ataxia (in a subset of patients) | rel=r_associated | relid=0 | w=10
  3283. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:optic nerve hypoplasia
    n1=DYNC2H1 gene | n2=en:optic nerve hypoplasia | rel=r_associated | relid=0 | w=10
  3284. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:optic tract agenesis
    n1=DYNC2H1 gene | n2=en:optic tract agenesis | rel=r_associated | relid=0 | w=10
  3285. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:optic tract and chiasm hypoplasia
    n1=DYNC2H1 gene | n2=en:optic tract and chiasm hypoplasia | rel=r_associated | relid=0 | w=10
  3286. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:organic writer's cramp
    n1=DYNC2H1 gene | n2=en:organic writer's cramp | rel=r_associated | relid=0 | w=10
  3287. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:orofacial dyspraxia, linguistic and nonlinguistic
    n1=DYNC2H1 gene | n2=en:orofacial dyspraxia, linguistic and nonlinguistic | rel=r_associated | relid=0 | w=10
  3288. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:orofacial dystonia
    n1=DYNC2H1 gene | n2=en:orofacial dystonia | rel=r_associated | relid=0 | w=10
  3289. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:oromandibular dystonia
    n1=DYNC2H1 gene | n2=en:oromandibular dystonia | rel=r_associated | relid=0 | w=10
  3290. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:orthostatic hypertension
    n1=DYNC2H1 gene | n2=en:orthostatic hypertension | rel=r_associated | relid=0 | w=10
  3291. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:orthostatic hypotension
    n1=DYNC2H1 gene | n2=en:orthostatic hypotension | rel=r_associated | relid=0 | w=10
  3292. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:orthostatic intolerance
    n1=DYNC2H1 gene | n2=en:orthostatic intolerance | rel=r_associated | relid=0 | w=10
  3293. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:orthostatic tachycardia
    n1=DYNC2H1 gene | n2=en:orthostatic tachycardia | rel=r_associated | relid=0 | w=10
  3294. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ossification of the faux cerebri (less common)
    n1=DYNC2H1 gene | n2=en:ossification of the faux cerebri (less common) | rel=r_associated | relid=0 | w=10
  3295. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:other auras may occur
    n1=DYNC2H1 gene | n2=en:other auras may occur | rel=r_associated | relid=0 | w=10
  3296. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:other cranial nerves may be involved
    n1=DYNC2H1 gene | n2=en:other cranial nerves may be involved | rel=r_associated | relid=0 | w=10
  3297. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:other disorders of autonomic nervous system
    n1=DYNC2H1 gene | n2=en:other disorders of autonomic nervous system | rel=r_associated | relid=0 | w=10
  3298. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:other seizure types (in some patients)
    n1=DYNC2H1 gene | n2=en:other seizure types (in some patients) | rel=r_associated | relid=0 | w=10
  3299. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:over time, white matter vanishes and is replaced by csf
    n1=DYNC2H1 gene | n2=en:over time, white matter vanishes and is replaced by csf | rel=r_associated | relid=0 | w=10
  3300. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:overlapping malignant neoplasm of peripheral nerves and autonomic nervous system
    n1=DYNC2H1 gene | n2=en:overlapping malignant neoplasm of peripheral nerves and autonomic nervous system | rel=r_associated | relid=0 | w=10
  3301. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria (1 patient)
    n1=DYNC2H1 gene | n2=en:pachygyria (1 patient) | rel=r_associated | relid=0 | w=10
  3302. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria (less common)
    n1=DYNC2H1 gene | n2=en:pachygyria (less common) | rel=r_associated | relid=0 | w=10
  3303. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria (posterior-to-anterior gradient)
    n1=DYNC2H1 gene | n2=en:pachygyria (posterior-to-anterior gradient) | rel=r_associated | relid=0 | w=10
  3304. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria (rare)
    n1=DYNC2H1 gene | n2=en:pachygyria (rare) | rel=r_associated | relid=0 | w=10
  3305. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria with preferential frontoparietal involvement (meb)
    n1=DYNC2H1 gene | n2=en:pachygyria with preferential frontoparietal involvement (meb) | rel=r_associated | relid=0 | w=10
  3306. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria, bilateral frontotemporal
    n1=DYNC2H1 gene | n2=en:pachygyria, bilateral frontotemporal | rel=r_associated | relid=0 | w=10
  3307. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria, frontoparietal
    n1=DYNC2H1 gene | n2=en:pachygyria, frontoparietal | rel=r_associated | relid=0 | w=10
  3308. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria, most prominent in the frontal lobes
    n1=DYNC2H1 gene | n2=en:pachygyria, most prominent in the frontal lobes | rel=r_associated | relid=0 | w=10
  3309. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria, occipital
    n1=DYNC2H1 gene | n2=en:pachygyria, occipital | rel=r_associated | relid=0 | w=10
  3310. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyria, usually posterior
    n1=DYNC2H1 gene | n2=en:pachygyria, usually posterior | rel=r_associated | relid=0 | w=10
  3311. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachygyrias
    n1=DYNC2H1 gene | n2=en:pachygyrias | rel=r_associated | relid=0 | w=10
  3312. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachymacrogyria
    n1=DYNC2H1 gene | n2=en:pachymacrogyria | rel=r_associated | relid=0 | w=10
  3313. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pachymeningitis cervicalis (cervical cord compression due to thickened dura)
    n1=DYNC2H1 gene | n2=en:pachymeningitis cervicalis (cervical cord compression due to thickened dura) | rel=r_associated | relid=0 | w=10
  3314. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pain
    n1=DYNC2H1 gene | n2=en:pain | rel=r_associated | relid=0 | w=10
  3315. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pain (sharp, boring, drilling, piercing)
    n1=DYNC2H1 gene | n2=en:pain (sharp, boring, drilling, piercing) | rel=r_associated | relid=0 | w=10
  3316. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pain affects upper body
    n1=DYNC2H1 gene | n2=en:pain affects upper body | rel=r_associated | relid=0 | w=10
  3317. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pain, episodic
    n1=DYNC2H1 gene | n2=en:pain, episodic | rel=r_associated | relid=0 | w=10
  3318. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:palatal myoclonus
    n1=DYNC2H1 gene | n2=en:palatal myoclonus | rel=r_associated | relid=0 | w=10
  3319. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pallidal degeneration
    n1=DYNC2H1 gene | n2=en:pallidal degeneration | rel=r_associated | relid=0 | w=10
  3320. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pallor of dorsal columns of the spinal cord
    n1=DYNC2H1 gene | n2=en:pallor of dorsal columns of the spinal cord | rel=r_associated | relid=0 | w=10
  3321. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paracusis
    n1=DYNC2H1 gene | n2=en:paracusis | rel=r_associated | relid=0 | w=10
  3322. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paradoxical cerebral emboli
    n1=DYNC2H1 gene | n2=en:paradoxical cerebral emboli | rel=r_associated | relid=0 | w=10
  3323. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paralysis
    n1=DYNC2H1 gene | n2=en:paralysis | rel=r_associated | relid=0 | w=10
  3324. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paralysis, episodic, after strenuous exercise
    n1=DYNC2H1 gene | n2=en:paralysis, episodic, after strenuous exercise | rel=r_associated | relid=0 | w=10
  3325. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paraneoplastic autonomic dysfunctions
    n1=DYNC2H1 gene | n2=en:paraneoplastic autonomic dysfunctions | rel=r_associated | relid=0 | w=10
  3326. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paraneoplastic syndrome
    n1=DYNC2H1 gene | n2=en:paraneoplastic syndrome | rel=r_associated | relid=0 | w=10
  3327. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paraparesis
    n1=DYNC2H1 gene | n2=en:paraparesis | rel=r_associated | relid=0 | w=10
  3328. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paraparesis, spastic
    n1=DYNC2H1 gene | n2=en:paraparesis, spastic | rel=r_associated | relid=0 | w=10
  3329. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paraplegia
    n1=DYNC2H1 gene | n2=en:paraplegia | rel=r_associated | relid=0 | w=10
  3330. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paraplegia secondary to spinal cord compression due to severe kyphosis
    n1=DYNC2H1 gene | n2=en:paraplegia secondary to spinal cord compression due to severe kyphosis | rel=r_associated | relid=0 | w=10
  3331. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paraspinal masses
    n1=DYNC2H1 gene | n2=en:paraspinal masses | rel=r_associated | relid=0 | w=10
  3332. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parasympathetic nerve injury
    n1=DYNC2H1 gene | n2=en:parasympathetic nerve injury | rel=r_associated | relid=0 | w=10
  3333. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parasympathetic nervous system
    n1=DYNC2H1 gene | n2=en:parasympathetic nervous system | rel=r_associated | relid=0 | w=10
  3334. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parasympatholytics
    n1=DYNC2H1 gene | n2=en:parasympatholytics | rel=r_associated | relid=0 | w=10
  3335. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parasympathomimetic disorders
    n1=DYNC2H1 gene | n2=en:parasympathomimetic disorders | rel=r_associated | relid=0 | w=10
  3336. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paraventricular cysts
    n1=DYNC2H1 gene | n2=en:paraventricular cysts | rel=r_associated | relid=0 | w=10
  3337. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parenchymal neuromelanosis
    n1=DYNC2H1 gene | n2=en:parenchymal neuromelanosis | rel=r_associated | relid=0 | w=10
  3338. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paresis (hcp)
    n1=DYNC2H1 gene | n2=en:paresis (hcp) | rel=r_associated | relid=0 | w=10
  3339. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paresis of extensor muscles of the big toe is presenting symptom
    n1=DYNC2H1 gene | n2=en:paresis of extensor muscles of the big toe is presenting symptom | rel=r_associated | relid=0 | w=10
  3340. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paresthesia
    n1=DYNC2H1 gene | n2=en:paresthesia | rel=r_associated | relid=0 | w=10
  3341. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parietal lobe epilepsy
    n1=DYNC2H1 gene | n2=en:parietal lobe epilepsy | rel=r_associated | relid=0 | w=10
  3342. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism
    n1=DYNC2H1 gene | n2=en:parkinsonism | rel=r_associated | relid=0 | w=10
  3343. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism (in some patients)
    n1=DYNC2H1 gene | n2=en:parkinsonism (in some patients) | rel=r_associated | relid=0 | w=10
  3344. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism (in some)
    n1=DYNC2H1 gene | n2=en:parkinsonism (in some) | rel=r_associated | relid=0 | w=10
  3345. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism (later onset)
    n1=DYNC2H1 gene | n2=en:parkinsonism (later onset) | rel=r_associated | relid=0 | w=10
  3346. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism (later)
    n1=DYNC2H1 gene | n2=en:parkinsonism (later) | rel=r_associated | relid=0 | w=10
  3347. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism (less common)
    n1=DYNC2H1 gene | n2=en:parkinsonism (less common) | rel=r_associated | relid=0 | w=10
  3348. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism has been described in 1 family
    n1=DYNC2H1 gene | n2=en:parkinsonism has been described in 1 family | rel=r_associated | relid=0 | w=10
  3349. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism may occur
    n1=DYNC2H1 gene | n2=en:parkinsonism may occur | rel=r_associated | relid=0 | w=10
  3350. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism, early-onset
    n1=DYNC2H1 gene | n2=en:parkinsonism, early-onset | rel=r_associated | relid=0 | w=10
  3351. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism, l-dopa responsive
    n1=DYNC2H1 gene | n2=en:parkinsonism, l-dopa responsive | rel=r_associated | relid=0 | w=10
  3352. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms)
    n1=DYNC2H1 gene | n2=en:parkinsonism, levodopa-responsive (occurs at later stages, may replace dystonia symptoms) | rel=r_associated | relid=0 | w=10
  3353. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paroxysmal choreoathetosis
    n1=DYNC2H1 gene | n2=en:paroxysmal choreoathetosis | rel=r_associated | relid=0 | w=10
  3354. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paroxysmal dystonia
    n1=DYNC2H1 gene | n2=en:paroxysmal dystonia | rel=r_associated | relid=0 | w=10
  3355. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paroxysmal lethargy
    n1=DYNC2H1 gene | n2=en:paroxysmal lethargy | rel=r_associated | relid=0 | w=10
  3356. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paroxysmal nonkinesigenic dyskinesia
    n1=DYNC2H1 gene | n2=en:paroxysmal nonkinesigenic dyskinesia | rel=r_associated | relid=0 | w=10
  3357. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paroxysmal oculogyric crises
    n1=DYNC2H1 gene | n2=en:paroxysmal oculogyric crises | rel=r_associated | relid=0 | w=10
  3358. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paroxysmal sympathetic hyperactivity
    n1=DYNC2H1 gene | n2=en:paroxysmal sympathetic hyperactivity | rel=r_associated | relid=0 | w=10
  3359. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial absence of the corpus callosum (in one patient)
    n1=DYNC2H1 gene | n2=en:partial absence of the corpus callosum (in one patient) | rel=r_associated | relid=0 | w=10
  3360. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial agenesis of corpus callosum
    n1=DYNC2H1 gene | n2=en:partial agenesis of corpus callosum | rel=r_associated | relid=0 | w=10
  3361. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial agenesis of corpus callosum (rare, in males)
    n1=DYNC2H1 gene | n2=en:partial agenesis of corpus callosum (rare, in males) | rel=r_associated | relid=0 | w=10
  3362. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial agenesis of the corpus callosum (in 1 of 2 sibs)
    n1=DYNC2H1 gene | n2=en:partial agenesis of the corpus callosum (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=10
  3363. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial agenesis of the corpus callosum (rare)
    n1=DYNC2H1 gene | n2=en:partial agenesis of the corpus callosum (rare) | rel=r_associated | relid=0 | w=10
  3364. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial empty sella turcica
    n1=DYNC2H1 gene | n2=en:partial empty sella turcica | rel=r_associated | relid=0 | w=10
  3365. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial epilepsy
    n1=DYNC2H1 gene | n2=en:partial epilepsy | rel=r_associated | relid=0 | w=10
  3366. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial migrating seizures seen on eeg (in some patients)
    n1=DYNC2H1 gene | n2=en:partial migrating seizures seen on eeg (in some patients) | rel=r_associated | relid=0 | w=10
  3367. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial or complete absence of the cerebellar vermis consistent with dandy walker malformation
    n1=DYNC2H1 gene | n2=en:partial or complete absence of the cerebellar vermis consistent with dandy walker malformation | rel=r_associated | relid=0 | w=10
  3368. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial or complete agenesis of corpus callosum
    n1=DYNC2H1 gene | n2=en:partial or complete agenesis of corpus callosum | rel=r_associated | relid=0 | w=10
  3369. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial or total agenesis of the corpus callosum (33%)
    n1=DYNC2H1 gene | n2=en:partial or total agenesis of the corpus callosum (33%) | rel=r_associated | relid=0 | w=10
  3370. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial pachygyria
    n1=DYNC2H1 gene | n2=en:partial pachygyria | rel=r_associated | relid=0 | w=10
  3371. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial response to pyridoxine
    n1=DYNC2H1 gene | n2=en:partial response to pyridoxine | rel=r_associated | relid=0 | w=10
  3372. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial seizure
    n1=DYNC2H1 gene | n2=en:partial seizure | rel=r_associated | relid=0 | w=10
  3373. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:partial seizures, simple and complex
    n1=DYNC2H1 gene | n2=en:partial seizures, simple and complex | rel=r_associated | relid=0 | w=10
  3374. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patchy demyelination of subcortical white matter
    n1=DYNC2H1 gene | n2=en:patchy demyelination of subcortical white matter | rel=r_associated | relid=0 | w=10
  3375. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patchy diffuse hyperintensities on t2-weighted mri
    n1=DYNC2H1 gene | n2=en:patchy diffuse hyperintensities on t2-weighted mri | rel=r_associated | relid=0 | w=10
  3376. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patellar and ankle clonus
    n1=DYNC2H1 gene | n2=en:patellar and ankle clonus | rel=r_associated | relid=0 | w=10
  3377. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patellar tendon reflexes hyperactive
    n1=DYNC2H1 gene | n2=en:patellar tendon reflexes hyperactive | rel=r_associated | relid=0 | w=10
  3378. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pathologic calcification, calcified structure
    n1=DYNC2H1 gene | n2=en:pathologic calcification, calcified structure | rel=r_associated | relid=0 | w=10
  3379. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pathologic changes in anterior horn cells and lateral corticospinal tracts
    n1=DYNC2H1 gene | n2=en:pathologic changes in anterior horn cells and lateral corticospinal tracts | rel=r_associated | relid=0 | w=10
  3380. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pathology includes spongiform changes, diffuse nerve cell degeneration and glial proliferation
    n1=DYNC2H1 gene | n2=en:pathology includes spongiform changes, diffuse nerve cell degeneration and glial proliferation | rel=r_associated | relid=0 | w=10
  3381. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patients 20-30 years old have hyperintense lesions on t2-weighted mri in the frontal and anterior temporal lobes
    n1=DYNC2H1 gene | 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=10
  3382. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patients 30-40 years old have hyperintense lesions in periventricular areas, the external capsule, basal ganglia, thalamus, and brainstem
    n1=DYNC2H1 gene | 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=10
  3383. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patients achieve ambulation
    n1=DYNC2H1 gene | n2=en:patients achieve ambulation | rel=r_associated | relid=0 | w=10
  3384. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patients may develop a seizure disorder later in life
    n1=DYNC2H1 gene | n2=en:patients may develop a seizure disorder later in life | rel=r_associated | relid=0 | w=10
  3385. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patients may have no structural abnormalities in the central nervous system
    n1=DYNC2H1 gene | n2=en:patients may have no structural abnormalities in the central nervous system | rel=r_associated | relid=0 | w=10
  3386. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patients may only achieve sitting or walking
    n1=DYNC2H1 gene | n2=en:patients may only achieve sitting or walking | rel=r_associated | relid=0 | w=10
  3387. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds
    n1=DYNC2H1 gene | n2=en:patients older than 50 years have hyperintensities, lacunar infarcts, and microbleeds | rel=r_associated | relid=0 | w=10
  3388. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:patients show normal psychomotor development
    n1=DYNC2H1 gene | n2=en:patients show normal psychomotor development | rel=r_associated | relid=0 | w=10
  3389. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:paucity of anterior horn motor neurons
    n1=DYNC2H1 gene | n2=en:paucity of anterior horn motor neurons | rel=r_associated | relid=0 | w=10
  3390. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peak frequency of vomiting every 10 to 15 minutes
    n1=DYNC2H1 gene | n2=en:peak frequency of vomiting every 10 to 15 minutes | rel=r_associated | relid=0 | w=10
  3391. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peculiar gait (if left untreated)
    n1=DYNC2H1 gene | n2=en:peculiar gait (if left untreated) | rel=r_associated | relid=0 | w=10
  3392. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peculiar stance and sitting posture (if left untreated)
    n1=DYNC2H1 gene | n2=en:peculiar stance and sitting posture (if left untreated) | rel=r_associated | relid=0 | w=10
  3393. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pericystic abnormal myelination
    n1=DYNC2H1 gene | n2=en:pericystic abnormal myelination | rel=r_associated | relid=0 | w=10
  3394. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periodic paralysis (finding)
    n1=DYNC2H1 gene | n2=en:periodic paralysis (finding) | rel=r_associated | relid=0 | w=10
  3395. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periodic paralysis, usually hypokalemic
    n1=DYNC2H1 gene | n2=en:periodic paralysis, usually hypokalemic | rel=r_associated | relid=0 | w=10
  3396. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periodic stiffness
    n1=DYNC2H1 gene | n2=en:periodic stiffness | rel=r_associated | relid=0 | w=10
  3397. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peripheral autonomic neuropathy in disorders classified elsewhere
    n1=DYNC2H1 gene | n2=en:peripheral autonomic neuropathy in disorders classified elsewhere | rel=r_associated | relid=0 | w=10
  3398. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peripheral hypertonia
    n1=DYNC2H1 gene | n2=en:peripheral hypertonia | rel=r_associated | relid=0 | w=10
  3399. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peripheral motor neuropathy
    n1=DYNC2H1 gene | n2=en:peripheral motor neuropathy | rel=r_associated | relid=0 | w=10
  3400. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peripheral nerve
    n1=DYNC2H1 gene | n2=en:peripheral nerve | rel=r_associated | relid=0 | w=10
  3401. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peripheral nervous system disorder
    n1=DYNC2H1 gene | n2=en:peripheral nervous system disorder | rel=r_associated | relid=0 | w=10
  3402. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peripheral nervous system infectious disorder
    n1=DYNC2H1 gene | n2=en:peripheral nervous system infectious disorder | rel=r_associated | relid=0 | w=10
  3403. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peripheral sensory neuropathy
    n1=DYNC2H1 gene | n2=en:peripheral sensory neuropathy | rel=r_associated | relid=0 | w=10
  3404. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:perisylvian polymicrogyria
    n1=DYNC2H1 gene | n2=en:perisylvian polymicrogyria | rel=r_associated | relid=0 | w=10
  3405. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:perivascular spaces
    n1=DYNC2H1 gene | n2=en:perivascular spaces | rel=r_associated | relid=0 | w=10
  3406. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular and subcortical white matter abnormalities
    n1=DYNC2H1 gene | n2=en:periventricular and subcortical white matter abnormalities | rel=r_associated | relid=0 | w=10
  3407. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular calcifications
    n1=DYNC2H1 gene | n2=en:periventricular calcifications | rel=r_associated | relid=0 | w=10
  3408. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular cysts
    n1=DYNC2H1 gene | n2=en:periventricular cysts | rel=r_associated | relid=0 | w=10
  3409. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular gray matter heterotopia
    n1=DYNC2H1 gene | n2=en:periventricular gray matter heterotopia | rel=r_associated | relid=0 | w=10
  3410. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular hemorrhagic infarction
    n1=DYNC2H1 gene | n2=en:periventricular hemorrhagic infarction | rel=r_associated | relid=0 | w=10
  3411. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular leukomalacia
    n1=DYNC2H1 gene | n2=en:periventricular leukomalacia | rel=r_associated | relid=0 | w=10
  3412. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular leukomalacia (reported in 2 patients)
    n1=DYNC2H1 gene | n2=en:periventricular leukomalacia (reported in 2 patients) | rel=r_associated | relid=0 | w=10
  3413. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular nodular heterotopia
    n1=DYNC2H1 gene | n2=en:periventricular nodular heterotopia | rel=r_associated | relid=0 | w=10
  3414. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular nodular heterotopia seen on mri
    n1=DYNC2H1 gene | n2=en:periventricular nodular heterotopia seen on mri | rel=r_associated | relid=0 | w=10
  3415. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular white matter abnormalities
    n1=DYNC2H1 gene | n2=en:periventricular white matter abnormalities | rel=r_associated | relid=0 | w=10
  3416. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular white matter abnormalities (in some patients)
    n1=DYNC2H1 gene | n2=en:periventricular white matter abnormalities (in some patients) | rel=r_associated | relid=0 | w=10
  3417. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular white matter changes
    n1=DYNC2H1 gene | n2=en:periventricular white matter changes | rel=r_associated | relid=0 | w=10
  3418. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular white matter changes (meb)
    n1=DYNC2H1 gene | n2=en:periventricular white matter changes (meb) | rel=r_associated | relid=0 | w=10
  3419. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular white matter gliosis (in some patients)
    n1=DYNC2H1 gene | n2=en:periventricular white matter gliosis (in some patients) | rel=r_associated | relid=0 | w=10
  3420. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular white matter hyperintensities, bilateral
    n1=DYNC2H1 gene | n2=en:periventricular white matter hyperintensities, bilateral | rel=r_associated | relid=0 | w=10
  3421. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:periventricular white matter lesions
    n1=DYNC2H1 gene | n2=en:periventricular white matter lesions | rel=r_associated | relid=0 | w=10
  3422. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:peroneal nerve paralysis
    n1=DYNC2H1 gene | n2=en:peroneal nerve paralysis | rel=r_associated | relid=0 | w=10
  3423. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:perseveration
    n1=DYNC2H1 gene | n2=en:perseveration | rel=r_associated | relid=0 | w=10
  3424. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:persistent cavum septum pellucidum
    n1=DYNC2H1 gene | n2=en:persistent cavum septum pellucidum | rel=r_associated | relid=0 | w=10
  3425. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:persistent cavus septum pellucidum
    n1=DYNC2H1 gene | n2=en:persistent cavus septum pellucidum | rel=r_associated | relid=0 | w=10
  3426. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:persistent falcine venous sinus
    n1=DYNC2H1 gene | n2=en:persistent falcine venous sinus | rel=r_associated | relid=0 | w=10
  3427. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:personality change
    n1=DYNC2H1 gene | n2=en:personality change | rel=r_associated | relid=0 | w=10
  3428. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:petit mal epilepsy
    n1=DYNC2H1 gene | n2=en:petit mal epilepsy | rel=r_associated | relid=0 | w=10
  3429. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pharyngeal gag reflex negative
    n1=DYNC2H1 gene | n2=en:pharyngeal gag reflex negative | rel=r_associated | relid=0 | w=10
  3430. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:phonology deficits
    n1=DYNC2H1 gene | n2=en:phonology deficits | rel=r_associated | relid=0 | w=10
  3431. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:phonophobia
    n1=DYNC2H1 gene | n2=en:phonophobia | rel=r_associated | relid=0 | w=10
  3432. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:photoparoxysmal and photomyoclonic responses
    n1=DYNC2H1 gene | n2=en:photoparoxysmal and photomyoclonic responses | rel=r_associated | relid=0 | w=10
  3433. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:photoparoxysmal response (in some)
    n1=DYNC2H1 gene | n2=en:photoparoxysmal response (in some) | rel=r_associated | relid=0 | w=10
  3434. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:photophobia
    n1=DYNC2H1 gene | n2=en:photophobia | rel=r_associated | relid=0 | w=10
  3435. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:photosensitive tonic-clonic seizures
    n1=DYNC2H1 gene | n2=en:photosensitive tonic-clonic seizures | rel=r_associated | relid=0 | w=10
  3436. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:photosensitivity in one-third of patients
    n1=DYNC2H1 gene | n2=en:photosensitivity in one-third of patients | rel=r_associated | relid=0 | w=10
  3437. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus
    n1=DYNC2H1 gene | n2=en:pick bodies found in neocortical layers, granule cells of the dentate gyrus, and throughout the hippocampus | rel=r_associated | relid=0 | w=10
  3438. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pigmentary loss in the substantia nigra
    n1=DYNC2H1 gene | n2=en:pigmentary loss in the substantia nigra | rel=r_associated | relid=0 | w=10
  3439. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pineal gland
    n1=DYNC2H1 gene | n2=en:pineal gland | rel=r_associated | relid=0 | w=10
  3440. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pineal hypertrophy
    n1=DYNC2H1 gene | n2=en:pineal hypertrophy | rel=r_associated | relid=0 | w=10
  3441. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pituitary agenesis
    n1=DYNC2H1 gene | n2=en:pituitary agenesis | rel=r_associated | relid=0 | w=10
  3442. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pituitary agenesis (rare)
    n1=DYNC2H1 gene | n2=en:pituitary agenesis (rare) | rel=r_associated | relid=0 | w=10
  3443. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pituitary aplasia or dysplasia
    n1=DYNC2H1 gene | n2=en:pituitary aplasia or dysplasia | rel=r_associated | relid=0 | w=10
  3444. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pituitary gland adenoma
    n1=DYNC2H1 gene | n2=en:pituitary gland adenoma | rel=r_associated | relid=0 | w=10
  3445. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pituitary gland hypoplasia
    n1=DYNC2H1 gene | n2=en:pituitary gland hypoplasia | rel=r_associated | relid=0 | w=10
  3446. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pituitary hypoplasia (in some patients)
    n1=DYNC2H1 gene | n2=en:pituitary hypoplasia (in some patients) | rel=r_associated | relid=0 | w=10
  3447. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:plaque, amyloid
    n1=DYNC2H1 gene | n2=en:plaque, amyloid | rel=r_associated | relid=0 | w=10
  3448. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:platybasia
    n1=DYNC2H1 gene | n2=en:platybasia | rel=r_associated | relid=0 | w=10
  3449. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poisoning by antiadrenergic drug
    n1=DYNC2H1 gene | n2=en:poisoning by antiadrenergic drug | rel=r_associated | relid=0 | w=10
  3450. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poisoning by parasympathomimetic drug
    n1=DYNC2H1 gene | n2=en:poisoning by parasympathomimetic drug | rel=r_associated | relid=0 | w=10
  3451. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poisoning by sympathomimetic drug
    n1=DYNC2H1 gene | n2=en:poisoning by sympathomimetic drug | rel=r_associated | relid=0 | w=10
  3452. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polyglucosan bodies (round intracellular inclusions) found in neuronal and astrocytic processes
    n1=DYNC2H1 gene | n2=en:polyglucosan bodies (round intracellular inclusions) found in neuronal and astrocytic processes | rel=r_associated | relid=0 | w=10
  3453. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polygyria
    n1=DYNC2H1 gene | n2=en:polygyria | rel=r_associated | relid=0 | w=10
  3454. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria
    n1=DYNC2H1 gene | n2=en:polymicrogyria | rel=r_associated | relid=0 | w=10
  3455. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria (64%)
    n1=DYNC2H1 gene | n2=en:polymicrogyria (64%) | rel=r_associated | relid=0 | w=10
  3456. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria (meb)
    n1=DYNC2H1 gene | n2=en:polymicrogyria (meb) | rel=r_associated | relid=0 | w=10
  3457. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria (rare)
    n1=DYNC2H1 gene | n2=en:polymicrogyria (rare) | rel=r_associated | relid=0 | w=10
  3458. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:polymicrogyria (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  3459. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, anterior to posterior gradient
    n1=DYNC2H1 gene | n2=en:polymicrogyria, anterior to posterior gradient | rel=r_associated | relid=0 | w=10
  3460. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, asymmetric or symmetric
    n1=DYNC2H1 gene | n2=en:polymicrogyria, asymmetric or symmetric | rel=r_associated | relid=0 | w=10
  3461. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, bilateral frontoparietal
    n1=DYNC2H1 gene | n2=en:polymicrogyria, bilateral frontoparietal | rel=r_associated | relid=0 | w=10
  3462. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, diffuse, asymmetric
    n1=DYNC2H1 gene | n2=en:polymicrogyria, diffuse, asymmetric | rel=r_associated | relid=0 | w=10
  3463. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, frontal
    n1=DYNC2H1 gene | n2=en:polymicrogyria, frontal | rel=r_associated | relid=0 | w=10
  3464. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, most severe in the frontoparietal regions
    n1=DYNC2H1 gene | n2=en:polymicrogyria, most severe in the frontoparietal regions | rel=r_associated | relid=0 | w=10
  3465. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, occipital
    n1=DYNC2H1 gene | n2=en:polymicrogyria, occipital | rel=r_associated | relid=0 | w=10
  3466. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, predominantly frontal and perisylvian
    n1=DYNC2H1 gene | n2=en:polymicrogyria, predominantly frontal and perisylvian | rel=r_associated | relid=0 | w=10
  3467. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, temporo-occipital
    n1=DYNC2H1 gene | n2=en:polymicrogyria, temporo-occipital | rel=r_associated | relid=0 | w=10
  3468. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polymicrogyria, usually frontal (in some patients)
    n1=DYNC2H1 gene | n2=en:polymicrogyria, usually frontal (in some patients) | rel=r_associated | relid=0 | w=10
  3469. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polyneuropathies, motor
    n1=DYNC2H1 gene | n2=en:polyneuropathies, motor | rel=r_associated | relid=0 | w=10
  3470. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:polyneuropathy
    n1=DYNC2H1 gene | n2=en:polyneuropathy | rel=r_associated | relid=0 | w=10
  3471. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pons damage
    n1=DYNC2H1 gene | n2=en:pons damage | rel=r_associated | relid=0 | w=10
  3472. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pontine atrophy
    n1=DYNC2H1 gene | n2=en:pontine atrophy | rel=r_associated | relid=0 | w=10
  3473. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pontine dysraphia
    n1=DYNC2H1 gene | n2=en:pontine dysraphia | rel=r_associated | relid=0 | w=10
  3474. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pontine hypoplasia (1 family)
    n1=DYNC2H1 gene | n2=en:pontine hypoplasia (1 family) | rel=r_associated | relid=0 | w=10
  3475. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pontine hypoplasia, mild
    n1=DYNC2H1 gene | n2=en:pontine hypoplasia, mild | rel=r_associated | relid=0 | w=10
  3476. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pontocerebellar arachnoid cyst (reported in 2 patients)
    n1=DYNC2H1 gene | n2=en:pontocerebellar arachnoid cyst (reported in 2 patients) | rel=r_associated | relid=0 | w=10
  3477. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pontocerebellar atrophy
    n1=DYNC2H1 gene | n2=en:pontocerebellar atrophy | rel=r_associated | relid=0 | w=10
  3478. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pontoneocerebellar hypoplasia
    n1=DYNC2H1 gene | n2=en:pontoneocerebellar hypoplasia | rel=r_associated | relid=0 | w=10
  3479. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor adaptive skills
    n1=DYNC2H1 gene | n2=en:poor adaptive skills | rel=r_associated | relid=0 | w=10
  3480. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor balance (finding)
    n1=DYNC2H1 gene | n2=en:poor balance (finding) | rel=r_associated | relid=0 | w=10
  3481. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor cognition
    n1=DYNC2H1 gene | n2=en:poor cognition | rel=r_associated | relid=0 | w=10
  3482. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor communication
    n1=DYNC2H1 gene | n2=en:poor communication | rel=r_associated | relid=0 | w=10
  3483. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor concentration
    n1=DYNC2H1 gene | n2=en:poor concentration | rel=r_associated | relid=0 | w=10
  3484. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor coordination
    n1=DYNC2H1 gene | n2=en:poor coordination | rel=r_associated | relid=0 | w=10
  3485. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor coordination (83%)
    n1=DYNC2H1 gene | n2=en:poor coordination (83%) | rel=r_associated | relid=0 | w=10
  3486. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor delineation of cerebral cortical regions
    n1=DYNC2H1 gene | n2=en:poor delineation of cerebral cortical regions | rel=r_associated | relid=0 | w=10
  3487. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor dendritic maturation
    n1=DYNC2H1 gene | n2=en:poor dendritic maturation | rel=r_associated | relid=0 | w=10
  3488. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor differentiation of gray and white matter on t2-weighted mri
    n1=DYNC2H1 gene | n2=en:poor differentiation of gray and white matter on t2-weighted mri | rel=r_associated | relid=0 | w=10
  3489. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor eye contact
    n1=DYNC2H1 gene | n2=en:poor eye contact | rel=r_associated | relid=0 | w=10
  3490. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor feeding (congenital form form)
    n1=DYNC2H1 gene | n2=en:poor feeding (congenital form form) | rel=r_associated | relid=0 | w=10
  3491. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor fine and gross motor coordination
    n1=DYNC2H1 gene | n2=en:poor fine and gross motor coordination | rel=r_associated | relid=0 | w=10
  3492. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor fine motor coordination
    n1=DYNC2H1 gene | n2=en:poor fine motor coordination | rel=r_associated | relid=0 | w=10
  3493. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor fine motor skills
    n1=DYNC2H1 gene | n2=en:poor fine motor skills | rel=r_associated | relid=0 | w=10
  3494. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor gross motor coordination
    n1=DYNC2H1 gene | n2=en:poor gross motor coordination | rel=r_associated | relid=0 | w=10
  3495. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor hand-eye coordination
    n1=DYNC2H1 gene | n2=en:poor hand-eye coordination | rel=r_associated | relid=0 | w=10
  3496. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor head and trunk control in infancy
    n1=DYNC2H1 gene | n2=en:poor head and trunk control in infancy | rel=r_associated | relid=0 | w=10
  3497. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor head control
    n1=DYNC2H1 gene | n2=en:poor head control | rel=r_associated | relid=0 | w=10
  3498. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor language
    n1=DYNC2H1 gene | n2=en:poor language | rel=r_associated | relid=0 | w=10
  3499. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor language and speech development
    n1=DYNC2H1 gene | n2=en:poor language and speech development | rel=r_associated | relid=0 | w=10
  3500. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor motor coordination
    n1=DYNC2H1 gene | n2=en:poor motor coordination | rel=r_associated | relid=0 | w=10
  3501. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor motor development
    n1=DYNC2H1 gene | n2=en:poor motor development | rel=r_associated | relid=0 | w=10
  3502. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor myelination
    n1=DYNC2H1 gene | n2=en:poor myelination | rel=r_associated | relid=0 | w=10
  3503. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor neonatal suck and swallow reflexes
    n1=DYNC2H1 gene | n2=en:poor neonatal suck and swallow reflexes | rel=r_associated | relid=0 | w=10
  3504. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor or absent independent walking
    n1=DYNC2H1 gene | n2=en:poor or absent independent walking | rel=r_associated | relid=0 | w=10
  3505. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor or absent smooth pursuit
    n1=DYNC2H1 gene | n2=en:poor or absent smooth pursuit | rel=r_associated | relid=0 | w=10
  3506. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor or absent speech
    n1=DYNC2H1 gene | n2=en:poor or absent speech | rel=r_associated | relid=0 | w=10
  3507. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor or absent speech acquisition
    n1=DYNC2H1 gene | n2=en:poor or absent speech acquisition | rel=r_associated | relid=0 | w=10
  3508. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor or absent speech development
    n1=DYNC2H1 gene | n2=en:poor or absent speech development | rel=r_associated | relid=0 | w=10
  3509. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor responsiveness
    n1=DYNC2H1 gene | n2=en:poor responsiveness | rel=r_associated | relid=0 | w=10
  3510. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor school performance
    n1=DYNC2H1 gene | n2=en:poor school performance | rel=r_associated | relid=0 | w=10
  3511. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor speech
    n1=DYNC2H1 gene | n2=en:poor speech | rel=r_associated | relid=0 | w=10
  3512. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor speech or lack of speech development
    n1=DYNC2H1 gene | n2=en:poor speech or lack of speech development | rel=r_associated | relid=0 | w=10
  3513. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor speech or no speech
    n1=DYNC2H1 gene | n2=en:poor speech or no speech | rel=r_associated | relid=0 | w=10
  3514. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor spontaneous movements
    n1=DYNC2H1 gene | n2=en:poor spontaneous movements | rel=r_associated | relid=0 | w=10
  3515. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor vestibuloocular reflex
    n1=DYNC2H1 gene | n2=en:poor vestibuloocular reflex | rel=r_associated | relid=0 | w=10
  3516. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor visual-motor integration (range 41-80)
    n1=DYNC2H1 gene | n2=en:poor visual-motor integration (range 41-80) | rel=r_associated | relid=0 | w=10
  3517. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor visual-spatial construction
    n1=DYNC2H1 gene | n2=en:poor visual-spatial construction | rel=r_associated | relid=0 | w=10
  3518. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poor-absent neurologic development
    n1=DYNC2H1 gene | n2=en:poor-absent neurologic development | rel=r_associated | relid=0 | w=10
  3519. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:porencephalic changes
    n1=DYNC2H1 gene | n2=en:porencephalic changes | rel=r_associated | relid=0 | w=10
  3520. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:porencephalic cyst
    n1=DYNC2H1 gene | n2=en:porencephalic cyst | rel=r_associated | relid=0 | w=10
  3521. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:porencephaly (in some patients)
    n1=DYNC2H1 gene | n2=en:porencephaly (in some patients) | rel=r_associated | relid=0 | w=10
  3522. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:poruchy sluchu nec in mdrcze18_1
    n1=DYNC2H1 gene | n2=en:poruchy sluchu nec in mdrcze18_1 | rel=r_associated | relid=0 | w=10
  3523. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior column degeneration
    n1=DYNC2H1 gene | n2=en:posterior column degeneration | rel=r_associated | relid=0 | w=10
  3524. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior column sensory loss
    n1=DYNC2H1 gene | n2=en:posterior column sensory loss | rel=r_associated | relid=0 | w=10
  3525. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior fossa abnormalities (rare)
    n1=DYNC2H1 gene | n2=en:posterior fossa abnormalities (rare) | rel=r_associated | relid=0 | w=10
  3526. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior fossa arachnoid cyst
    n1=DYNC2H1 gene | n2=en:posterior fossa arachnoid cyst | rel=r_associated | relid=0 | w=10
  3527. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior fossa compression syndrome
    n1=DYNC2H1 gene | n2=en:posterior fossa compression syndrome | rel=r_associated | relid=0 | w=10
  3528. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior fossa crowding, progressive
    n1=DYNC2H1 gene | n2=en:posterior fossa crowding, progressive | rel=r_associated | relid=0 | w=10
  3529. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior fossa cyst
    n1=DYNC2H1 gene | n2=en:posterior fossa cyst | rel=r_associated | relid=0 | w=10
  3530. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior fossa cyst (in 1 of 2 patients)
    n1=DYNC2H1 gene | n2=en:posterior fossa cyst (in 1 of 2 patients) | rel=r_associated | relid=0 | w=10
  3531. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior fossa cyst continuous with the fourth ventricle
    n1=DYNC2H1 gene | n2=en:posterior fossa cyst continuous with the fourth ventricle | rel=r_associated | relid=0 | w=10
  3532. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior fossa cysts (wws)
    n1=DYNC2H1 gene | n2=en:posterior fossa cysts (wws) | rel=r_associated | relid=0 | w=10
  3533. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior fossa malformations
    n1=DYNC2H1 gene | n2=en:posterior fossa malformations | rel=r_associated | relid=0 | w=10
  3534. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior pachygyria
    n1=DYNC2H1 gene | n2=en:posterior pachygyria | rel=r_associated | relid=0 | w=10
  3535. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posterior slow-wave activity on eeg
    n1=DYNC2H1 gene | n2=en:posterior slow-wave activity on eeg | rel=r_associated | relid=0 | w=10
  3536. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:postganglionic autonomic fiber
    n1=DYNC2H1 gene | n2=en:postganglionic autonomic fiber | rel=r_associated | relid=0 | w=10
  3537. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:postnatal development of hypertonic extremities
    n1=DYNC2H1 gene | n2=en:postnatal development of hypertonic extremities | rel=r_associated | relid=0 | w=10
  3538. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:postural dystonia (onset is restricted to 1 extremity, usually lower, with foot dystonia)
    n1=DYNC2H1 gene | n2=en:postural dystonia (onset is restricted to 1 extremity, usually lower, with foot dystonia) | rel=r_associated | relid=0 | w=10
  3539. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:postural hand tremor
    n1=DYNC2H1 gene | n2=en:postural hand tremor | rel=r_associated | relid=0 | w=10
  3540. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:postural instability
    n1=DYNC2H1 gene | n2=en:postural instability | rel=r_associated | relid=0 | w=10
  3541. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:postural instability (63%)
    n1=DYNC2H1 gene | n2=en:postural instability (63%) | rel=r_associated | relid=0 | w=10
  3542. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:postural orthostatic tachycardia syndrome
    n1=DYNC2H1 gene | n2=en:postural orthostatic tachycardia syndrome | rel=r_associated | relid=0 | w=10
  3543. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:postural tremor (later onset, spreads to all limbs and neck)
    n1=DYNC2H1 gene | n2=en:postural tremor (later onset, spreads to all limbs and neck) | rel=r_associated | relid=0 | w=10
  3544. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:postural tremor, slow, irregular (in some patients)
    n1=DYNC2H1 gene | n2=en:postural tremor, slow, irregular (in some patients) | rel=r_associated | relid=0 | w=10
  3545. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:posturing
    n1=DYNC2H1 gene | n2=en:posturing | rel=r_associated | relid=0 | w=10
  3546. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:praxis
    n1=DYNC2H1 gene | n2=en:praxis | rel=r_associated | relid=0 | w=10
  3547. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pre-senile dementia
    n1=DYNC2H1 gene | n2=en:pre-senile dementia | rel=r_associated | relid=0 | w=10
  3548. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:preganglionic autonomic fiber
    n1=DYNC2H1 gene | n2=en:preganglionic autonomic fiber | rel=r_associated | relid=0 | w=10
  3549. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:premature stroke
    n1=DYNC2H1 gene | n2=en:premature stroke | rel=r_associated | relid=0 | w=10
  3550. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments)
    n1=DYNC2H1 gene | n2=en:presence of rosenthal fibers (eosinophilic bodies near astrocyte filaments) | rel=r_associated | relid=0 | w=10
  3551. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:presenile and senile dementia
    n1=DYNC2H1 gene | n2=en:presenile and senile dementia | rel=r_associated | relid=0 | w=10
  3552. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:preservation of u fibers
    n1=DYNC2H1 gene | n2=en:preservation of u fibers | rel=r_associated | relid=0 | w=10
  3553. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:priapism
    n1=DYNC2H1 gene | n2=en:priapism | rel=r_associated | relid=0 | w=10
  3554. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:primarily affects distal lower limbs
    n1=DYNC2H1 gene | n2=en:primarily affects distal lower limbs | rel=r_associated | relid=0 | w=10
  3555. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:primary dysautonomias
    n1=DYNC2H1 gene | n2=en:primary dysautonomias | rel=r_associated | relid=0 | w=10
  3556. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:primary malignant neoplasm of peripheral nerves and peripheral autonomic nervous system
    n1=DYNC2H1 gene | n2=en:primary malignant neoplasm of peripheral nerves and peripheral autonomic nervous system | rel=r_associated | relid=0 | w=10
  3557. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:primitive reflex
    n1=DYNC2H1 gene | n2=en:primitive reflex | rel=r_associated | relid=0 | w=10
  3558. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:primitive reflexes (in some patients)
    n1=DYNC2H1 gene | n2=en:primitive reflexes (in some patients) | rel=r_associated | relid=0 | w=10
  3559. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:primitive reflexes (palmomental, snout, glabellar)
    n1=DYNC2H1 gene | n2=en:primitive reflexes (palmomental, snout, glabellar) | rel=r_associated | relid=0 | w=10
  3560. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:primitive sylvian fissures
    n1=DYNC2H1 gene | n2=en:primitive sylvian fissures | rel=r_associated | relid=0 | w=10
  3561. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prion protein-positive senile plaques
    n1=DYNC2H1 gene | n2=en:prion protein-positive senile plaques | rel=r_associated | relid=0 | w=10
  3562. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients)
    n1=DYNC2H1 gene | n2=en:prnp-immunoreactive cerebral amyloid angiopathy (in some patients) | rel=r_associated | relid=0 | w=10
  3563. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:profound global developmental delay
    n1=DYNC2H1 gene | n2=en:profound global developmental delay | rel=r_associated | relid=0 | w=10
  3564. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:profound intellectual disabilities
    n1=DYNC2H1 gene | n2=en:profound intellectual disabilities | rel=r_associated | relid=0 | w=10
  3565. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:profound mental retardation and hypotonia in survivors
    n1=DYNC2H1 gene | n2=en:profound mental retardation and hypotonia in survivors | rel=r_associated | relid=0 | w=10
  3566. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progression to paralysis and atrophy of distal lower limb muscles
    n1=DYNC2H1 gene | n2=en:progression to paralysis and atrophy of distal lower limb muscles | rel=r_associated | relid=0 | w=10
  3567. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progression to tetraplegia and decerebrate state
    n1=DYNC2H1 gene | n2=en:progression to tetraplegia and decerebrate state | rel=r_associated | relid=0 | w=10
  3568. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive ataxia (onset second year of life)
    n1=DYNC2H1 gene | n2=en:progressive ataxia (onset second year of life) | rel=r_associated | relid=0 | w=10
  3569. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive bulbar palsy
    n1=DYNC2H1 gene | n2=en:progressive bulbar palsy | rel=r_associated | relid=0 | w=10
  3570. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive cerebellar ataxia
    n1=DYNC2H1 gene | n2=en:progressive cerebellar ataxia | rel=r_associated | relid=0 | w=10
  3571. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive cerebellar degeneration
    n1=DYNC2H1 gene | n2=en:progressive cerebellar degeneration | rel=r_associated | relid=0 | w=10
  3572. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive cerebral atrophy seen on mri
    n1=DYNC2H1 gene | n2=en:progressive cerebral atrophy seen on mri | rel=r_associated | relid=0 | w=10
  3573. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive choreoathetosis
    n1=DYNC2H1 gene | n2=en:progressive choreoathetosis | rel=r_associated | relid=0 | w=10
  3574. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive cns degeneration
    n1=DYNC2H1 gene | n2=en:progressive cns degeneration | rel=r_associated | relid=0 | w=10
  3575. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive cognitive decline following normal development in childhood (in some patients)
    n1=DYNC2H1 gene | n2=en:progressive cognitive decline following normal development in childhood (in some patients) | rel=r_associated | relid=0 | w=10
  3576. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive encephalopathy
    n1=DYNC2H1 gene | n2=en:progressive encephalopathy | rel=r_associated | relid=0 | w=10
  3577. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive extrapyramidal movement disorder
    n1=DYNC2H1 gene | n2=en:progressive extrapyramidal movement disorder | rel=r_associated | relid=0 | w=10
  3578. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive forgetfulness
    n1=DYNC2H1 gene | n2=en:progressive forgetfulness | rel=r_associated | relid=0 | w=10
  3579. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive gait ataxia
    n1=DYNC2H1 gene | n2=en:progressive gait ataxia | rel=r_associated | relid=0 | w=10
  3580. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive impairment of gait
    n1=DYNC2H1 gene | n2=en:progressive impairment of gait | rel=r_associated | relid=0 | w=10
  3581. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive inability to walk
    n1=DYNC2H1 gene | n2=en:progressive inability to walk | rel=r_associated | relid=0 | w=10
  3582. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive intellectual decline
    n1=DYNC2H1 gene | n2=en:progressive intellectual decline | rel=r_associated | relid=0 | w=10
  3583. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive language deterioration
    n1=DYNC2H1 gene | n2=en:progressive language deterioration | rel=r_associated | relid=0 | w=10
  3584. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive leukoencephalopathy
    n1=DYNC2H1 gene | n2=en:progressive leukoencephalopathy | rel=r_associated | relid=0 | w=10
  3585. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive loss of movement control
    n1=DYNC2H1 gene | n2=en:progressive loss of movement control | rel=r_associated | relid=0 | w=10
  3586. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive myoclonus epilepsy
    n1=DYNC2H1 gene | n2=en:progressive myoclonus epilepsy | rel=r_associated | relid=0 | w=10
  3587. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive neurologic deterioration
    n1=DYNC2H1 gene | n2=en:progressive neurologic deterioration | rel=r_associated | relid=0 | w=10
  3588. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive psychomotor deterioration
    n1=DYNC2H1 gene | n2=en:progressive psychomotor deterioration | rel=r_associated | relid=0 | w=10
  3589. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive pyramidal and cerebellar signs
    n1=DYNC2H1 gene | n2=en:progressive pyramidal and cerebellar signs | rel=r_associated | relid=0 | w=10
  3590. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive spastic diplegia to quadriplegia
    n1=DYNC2H1 gene | n2=en:progressive spastic diplegia to quadriplegia | rel=r_associated | relid=0 | w=10
  3591. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive spastic paraplegia
    n1=DYNC2H1 gene | n2=en:progressive spastic paraplegia | rel=r_associated | relid=0 | w=10
  3592. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive spastic quadriplegia
    n1=DYNC2H1 gene | n2=en:progressive spastic quadriplegia | rel=r_associated | relid=0 | w=10
  3593. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive spasticity
    n1=DYNC2H1 gene | n2=en:progressive spasticity | rel=r_associated | relid=0 | w=10
  3594. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive truncal ataxia
    n1=DYNC2H1 gene | n2=en:progressive truncal ataxia | rel=r_associated | relid=0 | w=10
  3595. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive ventriculomegaly
    n1=DYNC2H1 gene | n2=en:progressive ventriculomegaly | rel=r_associated | relid=0 | w=10
  3596. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive white matter lesions in the brain
    n1=DYNC2H1 gene | n2=en:progressive white matter lesions in the brain | rel=r_associated | relid=0 | w=10
  3597. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:progressive, symmetric degeneration of the caudate and putamen
    n1=DYNC2H1 gene | n2=en:progressive, symmetric degeneration of the caudate and putamen | rel=r_associated | relid=0 | w=10
  3598. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prolonged seizure
    n1=DYNC2H1 gene | n2=en:prolonged seizure | rel=r_associated | relid=0 | w=10
  3599. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prolonged somatosensory evoked potentials (seps)
    n1=DYNC2H1 gene | n2=en:prolonged somatosensory evoked potentials (seps) | rel=r_associated | relid=0 | w=10
  3600. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prominent cortical sulci
    n1=DYNC2H1 gene | n2=en:prominent cortical sulci | rel=r_associated | relid=0 | w=10
  3601. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prominent csf spaces (in some patients)
    n1=DYNC2H1 gene | n2=en:prominent csf spaces (in some patients) | rel=r_associated | relid=0 | w=10
  3602. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prominent perivascular spaces
    n1=DYNC2H1 gene | n2=en:prominent perivascular spaces | rel=r_associated | relid=0 | w=10
  3603. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prominent perivascular spaces with surrounding gliosis in periatrial white matter
    n1=DYNC2H1 gene | n2=en:prominent perivascular spaces with surrounding gliosis in periatrial white matter | rel=r_associated | relid=0 | w=10
  3604. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prominent sulci
    n1=DYNC2H1 gene | n2=en:prominent sulci | rel=r_associated | relid=0 | w=10
  3605. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prominent trigone and occipital horns
    n1=DYNC2H1 gene | n2=en:prominent trigone and occipital horns | rel=r_associated | relid=0 | w=10
  3606. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prominent ventricles (in some patients)
    n1=DYNC2H1 gene | n2=en:prominent ventricles (in some patients) | rel=r_associated | relid=0 | w=10
  3607. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:proximal amyotrophy
    n1=DYNC2H1 gene | n2=en:proximal amyotrophy | rel=r_associated | relid=0 | w=10
  3608. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:proximal limb muscle stiffness
    n1=DYNC2H1 gene | n2=en:proximal limb muscle stiffness | rel=r_associated | relid=0 | w=10
  3609. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:proximal muscle weakness
    n1=DYNC2H1 gene | n2=en:proximal muscle weakness | rel=r_associated | relid=0 | w=10
  3610. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:proximal muscle weakness in lower limbs
    n1=DYNC2H1 gene | n2=en:proximal muscle weakness in lower limbs | rel=r_associated | relid=0 | w=10
  3611. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:proximal weakness occurs first
    n1=DYNC2H1 gene | n2=en:proximal weakness occurs first | rel=r_associated | relid=0 | w=10
  3612. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:proximal weakness occurs later
    n1=DYNC2H1 gene | n2=en:proximal weakness occurs later | rel=r_associated | relid=0 | w=10
  3613. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:proximal weakness of the lower extremities
    n1=DYNC2H1 gene | n2=en:proximal weakness of the lower extremities | rel=r_associated | relid=0 | w=10
  3614. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:prp immunoreactivity limited to cerebellum and putamen
    n1=DYNC2H1 gene | n2=en:prp immunoreactivity limited to cerebellum and putamen | rel=r_associated | relid=0 | w=10
  3615. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pseudobulbar palsy
    n1=DYNC2H1 gene | n2=en:pseudobulbar palsy | rel=r_associated | relid=0 | w=10
  3616. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pseudobulbar palsy (e.g. involuntary weeping or laughter)
    n1=DYNC2H1 gene | n2=en:pseudobulbar palsy (e.g. involuntary weeping or laughter) | rel=r_associated | relid=0 | w=10
  3617. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pseudobulbar signs
    n1=DYNC2H1 gene | n2=en:pseudobulbar signs | rel=r_associated | relid=0 | w=10
  3618. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pseudobulbar symptoms (uncontrolled laughter, weeping)
    n1=DYNC2H1 gene | n2=en:pseudobulbar symptoms (uncontrolled laughter, weeping) | rel=r_associated | relid=0 | w=10
  3619. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pseudolaminar spongiform changes
    n1=DYNC2H1 gene | n2=en:pseudolaminar spongiform changes | rel=r_associated | relid=0 | w=10
  3620. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pseudotumor
    n1=DYNC2H1 gene | n2=en:pseudotumor | rel=r_associated | relid=0 | w=10
  3621. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pseudotumor cerebri
    n1=DYNC2H1 gene | n2=en:pseudotumor cerebri | rel=r_associated | relid=0 | w=10
  3622. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychiatric disorder
    n1=DYNC2H1 gene | n2=en:psychiatric disorder | rel=r_associated | relid=0 | w=10
  3623. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychiatric symptoms (delusions, hallucinations)
    n1=DYNC2H1 gene | n2=en:psychiatric symptoms (delusions, hallucinations) | rel=r_associated | relid=0 | w=10
  3624. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor agitation
    n1=DYNC2H1 gene | n2=en:psychomotor agitation | rel=r_associated | relid=0 | w=10
  3625. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor arrest and regression
    n1=DYNC2H1 gene | n2=en:psychomotor arrest and regression | rel=r_associated | relid=0 | w=10
  3626. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor delay (evident at 3 months)
    n1=DYNC2H1 gene | n2=en:psychomotor delay (evident at 3 months) | rel=r_associated | relid=0 | w=10
  3627. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor delay (in one family)
    n1=DYNC2H1 gene | n2=en:psychomotor delay (in one family) | rel=r_associated | relid=0 | w=10
  3628. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor delay (rare)
    n1=DYNC2H1 gene | n2=en:psychomotor delay (rare) | rel=r_associated | relid=0 | w=10
  3629. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor delay after second year
    n1=DYNC2H1 gene | n2=en:psychomotor delay after second year | rel=r_associated | relid=0 | w=10
  3630. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor delay, mild to moderate
    n1=DYNC2H1 gene | n2=en:psychomotor delay, mild to moderate | rel=r_associated | relid=0 | w=10
  3631. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor delay, severe
    n1=DYNC2H1 gene | n2=en:psychomotor delay, severe | rel=r_associated | relid=0 | w=10
  3632. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor deterioration
    n1=DYNC2H1 gene | n2=en:psychomotor deterioration | rel=r_associated | relid=0 | w=10
  3633. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor deterioration (classical form)
    n1=DYNC2H1 gene | n2=en:psychomotor deterioration (classical form) | rel=r_associated | relid=0 | w=10
  3634. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor impairments
    n1=DYNC2H1 gene | n2=en:psychomotor impairments | rel=r_associated | relid=0 | w=10
  3635. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression
    n1=DYNC2H1 gene | n2=en:psychomotor regression | rel=r_associated | relid=0 | w=10
  3636. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression (in milder cases)
    n1=DYNC2H1 gene | n2=en:psychomotor regression (in milder cases) | rel=r_associated | relid=0 | w=10
  3637. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression (in some patients)
    n1=DYNC2H1 gene | n2=en:psychomotor regression (in some patients) | rel=r_associated | relid=0 | w=10
  3638. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression (in some)
    n1=DYNC2H1 gene | n2=en:psychomotor regression (in some) | rel=r_associated | relid=0 | w=10
  3639. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression (onset within first year of life)
    n1=DYNC2H1 gene | n2=en:psychomotor regression (onset within first year of life) | rel=r_associated | relid=0 | w=10
  3640. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression beginning in infancy
    n1=DYNC2H1 gene | n2=en:psychomotor regression beginning in infancy | rel=r_associated | relid=0 | w=10
  3641. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression in infants
    n1=DYNC2H1 gene | n2=en:psychomotor regression in infants | rel=r_associated | relid=0 | w=10
  3642. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression may occur
    n1=DYNC2H1 gene | n2=en:psychomotor regression may occur | rel=r_associated | relid=0 | w=10
  3643. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression, episodic, often associated with common childhood infections
    n1=DYNC2H1 gene | n2=en:psychomotor regression, episodic, often associated with common childhood infections | rel=r_associated | relid=0 | w=10
  3644. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression, progressive
    n1=DYNC2H1 gene | n2=en:psychomotor regression, progressive | rel=r_associated | relid=0 | w=10
  3645. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor regression, severe
    n1=DYNC2H1 gene | n2=en:psychomotor regression, severe | rel=r_associated | relid=0 | w=10
  3646. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation
    n1=DYNC2H1 gene | n2=en:psychomotor retardation | rel=r_associated | relid=0 | w=10
  3647. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation (2/4 patients)
    n1=DYNC2H1 gene | n2=en:psychomotor retardation (2/4 patients) | rel=r_associated | relid=0 | w=10
  3648. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation (in 1 patient)
    n1=DYNC2H1 gene | n2=en:psychomotor retardation (in 1 patient) | rel=r_associated | relid=0 | w=10
  3649. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation (in some patients)
    n1=DYNC2H1 gene | n2=en:psychomotor retardation (in some patients) | rel=r_associated | relid=0 | w=10
  3650. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation in those that survive
    n1=DYNC2H1 gene | n2=en:psychomotor retardation in those that survive | rel=r_associated | relid=0 | w=10
  3651. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation, mild
    n1=DYNC2H1 gene | n2=en:psychomotor retardation, mild | rel=r_associated | relid=0 | w=10
  3652. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation, mild to moderate
    n1=DYNC2H1 gene | n2=en:psychomotor retardation, mild to moderate | rel=r_associated | relid=0 | w=10
  3653. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation, moderate
    n1=DYNC2H1 gene | n2=en:psychomotor retardation, moderate | rel=r_associated | relid=0 | w=10
  3654. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation, profound
    n1=DYNC2H1 gene | n2=en:psychomotor retardation, profound | rel=r_associated | relid=0 | w=10
  3655. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation, profound, in those who survive
    n1=DYNC2H1 gene | n2=en:psychomotor retardation, profound, in those who survive | rel=r_associated | relid=0 | w=10
  3656. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation, severe to profound
    n1=DYNC2H1 gene | n2=en:psychomotor retardation, severe to profound | rel=r_associated | relid=0 | w=10
  3657. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychomotor retardation, variable
    n1=DYNC2H1 gene | n2=en:psychomotor retardation, variable | rel=r_associated | relid=0 | w=10
  3658. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychosis
    n1=DYNC2H1 gene | n2=en:psychosis | rel=r_associated | relid=0 | w=10
  3659. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychosis (rare)
    n1=DYNC2H1 gene | n2=en:psychosis (rare) | rel=r_associated | relid=0 | w=10
  3660. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychotic episodes
    n1=DYNC2H1 gene | n2=en:psychotic episodes | rel=r_associated | relid=0 | w=10
  3661. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:psychovegetative syndrome
    n1=DYNC2H1 gene | n2=en:psychovegetative syndrome | rel=r_associated | relid=0 | w=10
  3662. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pulsating quality
    n1=DYNC2H1 gene | n2=en:pulsating quality | rel=r_associated | relid=0 | w=10
  3663. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pure autonomic failure
    n1=DYNC2H1 gene | n2=en:pure autonomic failure | rel=r_associated | relid=0 | w=10
  3664. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:purposeless movements (if left untreated)
    n1=DYNC2H1 gene | n2=en:purposeless movements (if left untreated) | rel=r_associated | relid=0 | w=10
  3665. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:putamen atrophy
    n1=DYNC2H1 gene | n2=en:putamen atrophy | rel=r_associated | relid=0 | w=10
  3666. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal features (rare)
    n1=DYNC2H1 gene | n2=en:pyramidal features (rare) | rel=r_associated | relid=0 | w=10
  3667. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal hypertonia
    n1=DYNC2H1 gene | n2=en:pyramidal hypertonia | rel=r_associated | relid=0 | w=10
  3668. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal sign
    n1=DYNC2H1 gene | n2=en:pyramidal sign | rel=r_associated | relid=0 | w=10
  3669. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal signs (1 family)
    n1=DYNC2H1 gene | n2=en:pyramidal signs (1 family) | rel=r_associated | relid=0 | w=10
  3670. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal signs (1 patient)
    n1=DYNC2H1 gene | n2=en:pyramidal signs (1 patient) | rel=r_associated | relid=0 | w=10
  3671. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal signs (21% of patients)
    n1=DYNC2H1 gene | n2=en:pyramidal signs (21% of patients) | rel=r_associated | relid=0 | w=10
  3672. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal signs (in some patients)
    n1=DYNC2H1 gene | n2=en:pyramidal signs (in some patients) | rel=r_associated | relid=0 | w=10
  3673. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal signs (in some)
    n1=DYNC2H1 gene | n2=en:pyramidal signs (in some) | rel=r_associated | relid=0 | w=10
  3674. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal signs (less common)
    n1=DYNC2H1 gene | n2=en:pyramidal signs (less common) | rel=r_associated | relid=0 | w=10
  3675. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal signs, mild
    n1=DYNC2H1 gene | n2=en:pyramidal signs, mild | rel=r_associated | relid=0 | w=10
  3676. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal signs, mild (uncommon)
    n1=DYNC2H1 gene | n2=en:pyramidal signs, mild (uncommon) | rel=r_associated | relid=0 | w=10
  3677. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal symptoms
    n1=DYNC2H1 gene | n2=en:pyramidal symptoms | rel=r_associated | relid=0 | w=10
  3678. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal syndrome
    n1=DYNC2H1 gene | n2=en:pyramidal syndrome | rel=r_associated | relid=0 | w=10
  3679. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal syndrome of the lower limbs
    n1=DYNC2H1 gene | n2=en:pyramidal syndrome of the lower limbs | rel=r_associated | relid=0 | w=10
  3680. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal system
    n1=DYNC2H1 gene | n2=en:pyramidal system | rel=r_associated | relid=0 | w=10
  3681. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal tetraparesis
    n1=DYNC2H1 gene | n2=en:pyramidal tetraparesis | rel=r_associated | relid=0 | w=10
  3682. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal tract dysfunction (juvenile-onset, less common)
    n1=DYNC2H1 gene | n2=en:pyramidal tract dysfunction (juvenile-onset, less common) | rel=r_associated | relid=0 | w=10
  3683. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal tract involvement
    n1=DYNC2H1 gene | n2=en:pyramidal tract involvement | rel=r_associated | relid=0 | w=10
  3684. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:pyramidal tract signs (in some patients)
    n1=DYNC2H1 gene | n2=en:pyramidal tract signs (in some patients) | rel=r_associated | relid=0 | w=10
  3685. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:quadriparesis
    n1=DYNC2H1 gene | n2=en:quadriparesis | rel=r_associated | relid=0 | w=10
  3686. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:quadriplegia
    n1=DYNC2H1 gene | n2=en:quadriplegia | rel=r_associated | relid=0 | w=10
  3687. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:quadriplegia, episodic
    n1=DYNC2H1 gene | n2=en:quadriplegia, episodic | rel=r_associated | relid=0 | w=10
  3688. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:quadriplegia, flaccid
    n1=DYNC2H1 gene | n2=en:quadriplegia, flaccid | rel=r_associated | relid=0 | w=10
  3689. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:quadriplegic dyskinesia
    n1=DYNC2H1 gene | n2=en:quadriplegic dyskinesia | rel=r_associated | relid=0 | w=10
  3690. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:quadrupedal gait
    n1=DYNC2H1 gene | n2=en:quadrupedal gait | rel=r_associated | relid=0 | w=10
  3691. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:quadrupedal gait (in some)
    n1=DYNC2H1 gene | n2=en:quadrupedal gait (in some) | rel=r_associated | relid=0 | w=10
  3692. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:quadrupedal gait (palm of hands, legs straight) with diagonal walking
    n1=DYNC2H1 gene | n2=en:quadrupedal gait (palm of hands, legs straight) with diagonal walking | rel=r_associated | relid=0 | w=10
  3693. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:quadrupedal locomotion (in some patients)
    n1=DYNC2H1 gene | n2=en:quadrupedal locomotion (in some patients) | rel=r_associated | relid=0 | w=10
  3694. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:radiculitis
    n1=DYNC2H1 gene | n2=en:radiculitis | rel=r_associated | relid=0 | w=10
  3695. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rapid complete resolution of symptoms
    n1=DYNC2H1 gene | n2=en:rapid complete resolution of symptoms | rel=r_associated | relid=0 | w=10
  3696. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rapid initial onset of symptoms (hours to weeks)
    n1=DYNC2H1 gene | n2=en:rapid initial onset of symptoms (hours to weeks) | rel=r_associated | relid=0 | w=10
  3697. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rapid onset
    n1=DYNC2H1 gene | n2=en:rapid onset | rel=r_associated | relid=0 | w=10
  3698. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rapid regression
    n1=DYNC2H1 gene | n2=en:rapid regression | rel=r_associated | relid=0 | w=10
  3699. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rapid, instantaneous neurologic decline may occur after fright
    n1=DYNC2H1 gene | n2=en:rapid, instantaneous neurologic decline may occur after fright | rel=r_associated | relid=0 | w=10
  3700. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rapid, jerky movements
    n1=DYNC2H1 gene | n2=en:rapid, jerky movements | rel=r_associated | relid=0 | w=10
  3701. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rapidly progressive brainstem degeneration
    n1=DYNC2H1 gene | n2=en:rapidly progressive brainstem degeneration | rel=r_associated | relid=0 | w=10
  3702. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rare dementia
    n1=DYNC2H1 gene | n2=en:rare dementia | rel=r_associated | relid=0 | w=10
  3703. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rare secondary generalization
    n1=DYNC2H1 gene | n2=en:rare secondary generalization | rel=r_associated | relid=0 | w=10
  3704. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reactive gliosis
    n1=DYNC2H1 gene | n2=en:reactive gliosis | rel=r_associated | relid=0 | w=10
  3705. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:recurrent bacterial meningitis
    n1=DYNC2H1 gene | n2=en:recurrent bacterial meningitis | rel=r_associated | relid=0 | w=10
  3706. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:recurrent encephalopathy
    n1=DYNC2H1 gene | n2=en:recurrent encephalopathy | rel=r_associated | relid=0 | w=10
  3707. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:recurrent meningitis
    n1=DYNC2H1 gene | n2=en:recurrent meningitis | rel=r_associated | relid=0 | w=10
  3708. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:recurrent muscle twitches (symptom)
    n1=DYNC2H1 gene | n2=en:recurrent muscle twitches (symptom) | rel=r_associated | relid=0 | w=10
  3709. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:recurrent seizures nos
    n1=DYNC2H1 gene | n2=en:recurrent seizures nos | rel=r_associated | relid=0 | w=10
  3710. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:recurrent subcortical infarcts (strokes)
    n1=DYNC2H1 gene | n2=en:recurrent subcortical infarcts (strokes) | rel=r_associated | relid=0 | w=10
  3711. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced brain gyri
    n1=DYNC2H1 gene | n2=en:reduced brain gyri | rel=r_associated | relid=0 | w=10
  3712. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced brain size
    n1=DYNC2H1 gene | n2=en:reduced brain size | rel=r_associated | relid=0 | w=10
  3713. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced cerebral white matter
    n1=DYNC2H1 gene | n2=en:reduced cerebral white matter | rel=r_associated | relid=0 | w=10
  3714. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced concentration span
    n1=DYNC2H1 gene | n2=en:reduced concentration span | rel=r_associated | relid=0 | w=10
  3715. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced consciousness
    n1=DYNC2H1 gene | n2=en:reduced consciousness | rel=r_associated | relid=0 | w=10
  3716. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced consciousness, hypoglycemia-related
    n1=DYNC2H1 gene | n2=en:reduced consciousness, hypoglycemia-related | rel=r_associated | relid=0 | w=10
  3717. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced numbers of neurons
    n1=DYNC2H1 gene | n2=en:reduced numbers of neurons | rel=r_associated | relid=0 | w=10
  3718. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced posterior white matter volume (in some patients)
    n1=DYNC2H1 gene | n2=en:reduced posterior white matter volume (in some patients) | rel=r_associated | relid=0 | w=10
  3719. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced size of the pituitary gland
    n1=DYNC2H1 gene | n2=en:reduced size of the pituitary gland | rel=r_associated | relid=0 | w=10
  3720. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced sleep latency
    n1=DYNC2H1 gene | n2=en:reduced sleep latency | rel=r_associated | relid=0 | w=10
  3721. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced tendon reflexes
    n1=DYNC2H1 gene | n2=en:reduced tendon reflexes | rel=r_associated | relid=0 | w=10
  3722. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced white matter
    n1=DYNC2H1 gene | n2=en:reduced white matter | rel=r_associated | relid=0 | w=10
  3723. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduced white matter volume
    n1=DYNC2H1 gene | n2=en:reduced white matter volume | rel=r_associated | relid=0 | w=10
  3724. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduction of white matter, generalized
    n1=DYNC2H1 gene | n2=en:reduction of white matter, generalized | rel=r_associated | relid=0 | w=10
  3725. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reduction or loss of acquired skills (e.g., purposeful hand use, speech)
    n1=DYNC2H1 gene | n2=en:reduction or loss of acquired skills (e.g., purposeful hand use, speech) | rel=r_associated | relid=0 | w=10
  3726. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reflex epilepsy, photosensitive
    n1=DYNC2H1 gene | n2=en:reflex epilepsy, photosensitive | rel=r_associated | relid=0 | w=10
  3727. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reflex, deep tendon, absent
    n1=DYNC2H1 gene | n2=en:reflex, deep tendon, absent | rel=r_associated | relid=0 | w=10
  3728. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:regression of development
    n1=DYNC2H1 gene | n2=en:regression of development | rel=r_associated | relid=0 | w=10
  3729. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:regression of early motor skills
    n1=DYNC2H1 gene | n2=en:regression of early motor skills | rel=r_associated | relid=0 | w=10
  3730. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:regression of motor development
    n1=DYNC2H1 gene | n2=en:regression of motor development | rel=r_associated | relid=0 | w=10
  3731. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:relative preservation of purkinje cells, but they are deformed and disaligned
    n1=DYNC2H1 gene | n2=en:relative preservation of purkinje cells, but they are deformed and disaligned | rel=r_associated | relid=0 | w=10
  3732. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:relative preservation of the cerebellar folia
    n1=DYNC2H1 gene | n2=en:relative preservation of the cerebellar folia | rel=r_associated | relid=0 | w=10
  3733. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:relative preservation of the cerebellum
    n1=DYNC2H1 gene | n2=en:relative preservation of the cerebellum | rel=r_associated | relid=0 | w=10
  3734. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:relative sparing of language
    n1=DYNC2H1 gene | n2=en:relative sparing of language | rel=r_associated | relid=0 | w=10
  3735. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:relief with motor activation
    n1=DYNC2H1 gene | n2=en:relief with motor activation | rel=r_associated | relid=0 | w=10
  3736. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rem sleep behavior disorder
    n1=DYNC2H1 gene | n2=en:rem sleep behavior disorder | rel=r_associated | relid=0 | w=10
  3737. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:residual ataxia
    n1=DYNC2H1 gene | n2=en:residual ataxia | rel=r_associated | relid=0 | w=10
  3738. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:response to pyridoxal phosphate
    n1=DYNC2H1 gene | n2=en:response to pyridoxal phosphate | rel=r_associated | relid=0 | w=10
  3739. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:resting myoclonus
    n1=DYNC2H1 gene | n2=en:resting myoclonus | rel=r_associated | relid=0 | w=10
  3740. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:resting tremor (in some patients)
    n1=DYNC2H1 gene | n2=en:resting tremor (in some patients) | rel=r_associated | relid=0 | w=10
  3741. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:resting tremors
    n1=DYNC2H1 gene | n2=en:resting tremors | rel=r_associated | relid=0 | w=10
  3742. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:restlessness at birth
    n1=DYNC2H1 gene | n2=en:restlessness at birth | rel=r_associated | relid=0 | w=10
  3743. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:restrictive behavior, interests, and activities
    n1=DYNC2H1 gene | n2=en:restrictive behavior, interests, and activities | rel=r_associated | relid=0 | w=10
  3744. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:results in nocturnal insomnia and chronic sleep deprivation
    n1=DYNC2H1 gene | n2=en:results in nocturnal insomnia and chronic sleep deprivation | rel=r_associated | relid=0 | w=10
  3745. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:retrocerebellar cyst
    n1=DYNC2H1 gene | n2=en:retrocerebellar cyst | rel=r_associated | relid=0 | w=10
  3746. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:retrocerebellar cyst (in some patients)
    n1=DYNC2H1 gene | n2=en:retrocerebellar cyst (in some patients) | rel=r_associated | relid=0 | w=10
  3747. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:retrocerebellar cyst (rare)
    n1=DYNC2H1 gene | n2=en:retrocerebellar cyst (rare) | rel=r_associated | relid=0 | w=10
  3748. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:retrocollis
    n1=DYNC2H1 gene | n2=en:retrocollis | rel=r_associated | relid=0 | w=10
  3749. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:retroflexion of the neck
    n1=DYNC2H1 gene | n2=en:retroflexion of the neck | rel=r_associated | relid=0 | w=10
  3750. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:reye syndrome
    n1=DYNC2H1 gene | n2=en:reye syndrome | rel=r_associated | relid=0 | w=10
  3751. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rhombencephalosynapsis
    n1=DYNC2H1 gene | n2=en:rhombencephalosynapsis | rel=r_associated | relid=0 | w=10
  3752. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rigidity (juvenile form)
    n1=DYNC2H1 gene | n2=en:rigidity (juvenile form) | rel=r_associated | relid=0 | w=10
  3753. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rigidity (later)
    n1=DYNC2H1 gene | n2=en:rigidity (later) | rel=r_associated | relid=0 | w=10
  3754. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rigidity and multifocal seizure syndrome, lethal neonatal
    n1=DYNC2H1 gene | n2=en:rigidity and multifocal seizure syndrome, lethal neonatal | rel=r_associated | relid=0 | w=10
  3755. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rigidity during seizures
    n1=DYNC2H1 gene | n2=en:rigidity during seizures | rel=r_associated | relid=0 | w=10
  3756. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rigidity of limbs
    n1=DYNC2H1 gene | n2=en:rigidity of limbs | rel=r_associated | relid=0 | w=10
  3757. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rigidity, axial and limb
    n1=DYNC2H1 gene | n2=en:rigidity, axial and limb | rel=r_associated | relid=0 | w=10
  3758. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:romberg's sign positive
    n1=DYNC2H1 gene | n2=en:romberg's sign positive | rel=r_associated | relid=0 | w=10
  3759. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ross syndrome
    n1=DYNC2H1 gene | n2=en:ross syndrome | rel=r_associated | relid=0 | w=10
  3760. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rotary head movements ('rolling,' 'tremor')
    n1=DYNC2H1 gene | n2=en:rotary head movements ('rolling,' 'tremor') | rel=r_associated | relid=0 | w=10
  3761. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:roving eye movements (infancy)
    n1=DYNC2H1 gene | n2=en:roving eye movements (infancy) | rel=r_associated | relid=0 | w=10
  3762. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:rudimentary white matter
    n1=DYNC2H1 gene | n2=en:rudimentary white matter | rel=r_associated | relid=0 | w=10
  3763. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sagittal sinus thrombosis
    n1=DYNC2H1 gene | n2=en:sagittal sinus thrombosis | rel=r_associated | relid=0 | w=10
  3764. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:salaam seizures
    n1=DYNC2H1 gene | n2=en:salaam seizures | rel=r_associated | relid=0 | w=10
  3765. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:scanning speech
    n1=DYNC2H1 gene | n2=en:scanning speech | rel=r_associated | relid=0 | w=10
  3766. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:scant iron deposition in the brain (1 family)
    n1=DYNC2H1 gene | n2=en:scant iron deposition in the brain (1 family) | rel=r_associated | relid=0 | w=10
  3767. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:scattered cns demyelination
    n1=DYNC2H1 gene | n2=en:scattered cns demyelination | rel=r_associated | relid=0 | w=10
  3768. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:schizencephaly
    n1=DYNC2H1 gene | n2=en:schizencephaly | rel=r_associated | relid=0 | w=10
  3769. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:schizophrenia
    n1=DYNC2H1 gene | n2=en:schizophrenia | rel=r_associated | relid=0 | w=10
  3770. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:school problem (finding)
    n1=DYNC2H1 gene | n2=en:school problem (finding) | rel=r_associated | relid=0 | w=10
  3771. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:scissoring
    n1=DYNC2H1 gene | n2=en:scissoring | rel=r_associated | relid=0 | w=10
  3772. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:scissors gait
    n1=DYNC2H1 gene | n2=en:scissors gait | rel=r_associated | relid=0 | w=10
  3773. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary generalization
    n1=DYNC2H1 gene | n2=en:secondary generalization | rel=r_associated | relid=0 | w=10
  3774. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary generalization may occur
    n1=DYNC2H1 gene | n2=en:secondary generalization may occur | rel=r_associated | relid=0 | w=10
  3775. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary generalization occurs in about 33% of patients
    n1=DYNC2H1 gene | n2=en:secondary generalization occurs in about 33% of patients | rel=r_associated | relid=0 | w=10
  3776. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary generalized tonic-clonic seizures may occur
    n1=DYNC2H1 gene | n2=en:secondary generalized tonic-clonic seizures may occur | rel=r_associated | relid=0 | w=10
  3777. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles
    n1=DYNC2H1 gene | n2=en:secondary hand muscle weakness predominating at the wrist and finger extensor muscles | rel=r_associated | relid=0 | w=10
  3778. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary hypertonia
    n1=DYNC2H1 gene | n2=en:secondary hypertonia | rel=r_associated | relid=0 | w=10
  3779. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary involvement of proximal and trunk muscles
    n1=DYNC2H1 gene | n2=en:secondary involvement of proximal and trunk muscles | rel=r_associated | relid=0 | w=10
  3780. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary motor complications develop in 50% of those on levodopa therapy
    n1=DYNC2H1 gene | n2=en:secondary motor complications develop in 50% of those on levodopa therapy | rel=r_associated | relid=0 | w=10
  3781. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary seizures (in some patients)
    n1=DYNC2H1 gene | n2=en:secondary seizures (in some patients) | rel=r_associated | relid=0 | w=10
  3782. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:secondary spinal cord compression may occur
    n1=DYNC2H1 gene | n2=en:secondary spinal cord compression may occur | rel=r_associated | relid=0 | w=10
  3783. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:see juvenile myoclonic epilepsy (606904)
    n1=DYNC2H1 gene | n2=en:see juvenile myoclonic epilepsy (606904) | rel=r_associated | relid=0 | w=10
  3784. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:see spg5a (270800)
    n1=DYNC2H1 gene | n2=en:see spg5a (270800) | rel=r_associated | relid=0 | w=10
  3785. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:segmental callosal hypoplasia, mild
    n1=DYNC2H1 gene | n2=en:segmental callosal hypoplasia, mild | rel=r_associated | relid=0 | w=10
  3786. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:segmental sensory loss, especially of pain and temperature
    n1=DYNC2H1 gene | n2=en:segmental sensory loss, especially of pain and temperature | rel=r_associated | relid=0 | w=10
  3787. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizure
    n1=DYNC2H1 gene | n2=en:seizure | rel=r_associated | relid=0 | w=10
  3788. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizure (in a subset of patients in infancy)
    n1=DYNC2H1 gene | n2=en:seizure (in a subset of patients in infancy) | rel=r_associated | relid=0 | w=10
  3789. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizure disorder
    n1=DYNC2H1 gene | n2=en:seizure disorder | rel=r_associated | relid=0 | w=10
  3790. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizure disorder (homozygote)
    n1=DYNC2H1 gene | n2=en:seizure disorder (homozygote) | rel=r_associated | relid=0 | w=10
  3791. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizure including seizure-like activity in utero starting around 18 weeks gestation
    n1=DYNC2H1 gene | n2=en:seizure including seizure-like activity in utero starting around 18 weeks gestation | rel=r_associated | relid=0 | w=10
  3792. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizure, febrile (2/3 children)
    n1=DYNC2H1 gene | n2=en:seizure, febrile (2/3 children) | rel=r_associated | relid=0 | w=10
  3793. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizure, focal or multifocal onset
    n1=DYNC2H1 gene | n2=en:seizure, focal or multifocal onset | rel=r_associated | relid=0 | w=10
  3794. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (> 90%)
    n1=DYNC2H1 gene | n2=en:seizures (> 90%) | rel=r_associated | relid=0 | w=10
  3795. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (1 family)
    n1=DYNC2H1 gene | n2=en:seizures (1 family) | rel=r_associated | relid=0 | w=10
  3796. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (1 patient)
    n1=DYNC2H1 gene | n2=en:seizures (1 patient) | rel=r_associated | relid=0 | w=10
  3797. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (2-10% of patients)
    n1=DYNC2H1 gene | n2=en:seizures (2-10% of patients) | rel=r_associated | relid=0 | w=10
  3798. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (3 patients)
    n1=DYNC2H1 gene | n2=en:seizures (3 patients) | rel=r_associated | relid=0 | w=10
  3799. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (40%)
    n1=DYNC2H1 gene | n2=en:seizures (40%) | rel=r_associated | relid=0 | w=10
  3800. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (50% of patients)
    n1=DYNC2H1 gene | n2=en:seizures (50% of patients) | rel=r_associated | relid=0 | w=10
  3801. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (50%)
    n1=DYNC2H1 gene | n2=en:seizures (50%) | rel=r_associated | relid=0 | w=10
  3802. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (about 50% of patients)
    n1=DYNC2H1 gene | n2=en:seizures (about 50% of patients) | rel=r_associated | relid=0 | w=10
  3803. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (adult)
    n1=DYNC2H1 gene | n2=en:seizures (adult) | rel=r_associated | relid=0 | w=10
  3804. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (cvs+)
    n1=DYNC2H1 gene | n2=en:seizures (cvs+) | rel=r_associated | relid=0 | w=10
  3805. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (eclampsia)
    n1=DYNC2H1 gene | n2=en:seizures (eclampsia) | rel=r_associated | relid=0 | w=10
  3806. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (if left untreated)
    n1=DYNC2H1 gene | n2=en:seizures (if left untreated) | rel=r_associated | relid=0 | w=10
  3807. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (in 1 of 2 sibs)
    n1=DYNC2H1 gene | n2=en:seizures (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=10
  3808. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (in 1 of 3 patients)
    n1=DYNC2H1 gene | n2=en:seizures (in 1 of 3 patients) | rel=r_associated | relid=0 | w=10
  3809. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (in 2 of 6 patients)
    n1=DYNC2H1 gene | n2=en:seizures (in 2 of 6 patients) | rel=r_associated | relid=0 | w=10
  3810. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (in 2 of 9 patients)
    n1=DYNC2H1 gene | n2=en:seizures (in 2 of 9 patients) | rel=r_associated | relid=0 | w=10
  3811. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (in 35%)
    n1=DYNC2H1 gene | n2=en:seizures (in 35%) | rel=r_associated | relid=0 | w=10
  3812. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (in one patient)
    n1=DYNC2H1 gene | n2=en:seizures (in one patient) | rel=r_associated | relid=0 | w=10
  3813. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (in some patients)
    n1=DYNC2H1 gene | n2=en:seizures (in some patients) | rel=r_associated | relid=0 | w=10
  3814. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (in some)
    n1=DYNC2H1 gene | n2=en:seizures (in some) | rel=r_associated | relid=0 | w=10
  3815. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (juvenile form)
    n1=DYNC2H1 gene | n2=en:seizures (juvenile form) | rel=r_associated | relid=0 | w=10
  3816. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (less common)
    n1=DYNC2H1 gene | n2=en:seizures (less common) | rel=r_associated | relid=0 | w=10
  3817. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (may be difficult to control)
    n1=DYNC2H1 gene | n2=en:seizures (may be difficult to control) | rel=r_associated | relid=0 | w=10
  3818. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (mean onset 4-5 months)
    n1=DYNC2H1 gene | n2=en:seizures (mean onset 4-5 months) | rel=r_associated | relid=0 | w=10
  3819. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (meb)
    n1=DYNC2H1 gene | n2=en:seizures (meb) | rel=r_associated | relid=0 | w=10
  3820. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (onset <2 years)
    n1=DYNC2H1 gene | n2=en:seizures (onset <2 years) | rel=r_associated | relid=0 | w=10
  3821. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (rare, in males)
    n1=DYNC2H1 gene | n2=en:seizures (rare, in males) | rel=r_associated | relid=0 | w=10
  3822. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (rare)
    n1=DYNC2H1 gene | n2=en:seizures (rare) | rel=r_associated | relid=0 | w=10
  3823. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (reported in 1 family)
    n1=DYNC2H1 gene | n2=en:seizures (reported in 1 family) | rel=r_associated | relid=0 | w=10
  3824. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (reported in 2 patients)
    n1=DYNC2H1 gene | n2=en:seizures (reported in 2 patients) | rel=r_associated | relid=0 | w=10
  3825. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (tetany)
    n1=DYNC2H1 gene | n2=en:seizures (tetany) | rel=r_associated | relid=0 | w=10
  3826. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (type i and type ii, juvenile)
    n1=DYNC2H1 gene | n2=en:seizures (type i and type ii, juvenile) | rel=r_associated | relid=0 | w=10
  3827. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (uncommon)
    n1=DYNC2H1 gene | n2=en:seizures (uncommon) | rel=r_associated | relid=0 | w=10
  3828. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures (variable)
    n1=DYNC2H1 gene | n2=en:seizures (variable) | rel=r_associated | relid=0 | w=10
  3829. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures affect the vocal cords, lips, mouth, and face
    n1=DYNC2H1 gene | n2=en:seizures affect the vocal cords, lips, mouth, and face | rel=r_associated | relid=0 | w=10
  3830. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures are poorly controlled
    n1=DYNC2H1 gene | n2=en:seizures are poorly controlled | rel=r_associated | relid=0 | w=10
  3831. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures in 15-30%
    n1=DYNC2H1 gene | n2=en:seizures in 15-30% | rel=r_associated | relid=0 | w=10
  3832. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures in the newborn, refractory
    n1=DYNC2H1 gene | n2=en:seizures in the newborn, refractory | rel=r_associated | relid=0 | w=10
  3833. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures may occur during hypotensive episodes
    n1=DYNC2H1 gene | n2=en:seizures may occur during hypotensive episodes | rel=r_associated | relid=0 | w=10
  3834. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause
    n1=DYNC2H1 gene | n2=en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause | rel=r_associated | relid=0 | w=10
  3835. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures occur in clusters
    n1=DYNC2H1 gene | n2=en:seizures occur in clusters | rel=r_associated | relid=0 | w=10
  3836. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures occur in clusters over 1 or several days
    n1=DYNC2H1 gene | n2=en:seizures occur in clusters over 1 or several days | rel=r_associated | relid=0 | w=10
  3837. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures occur multiple times per day
    n1=DYNC2H1 gene | n2=en:seizures occur multiple times per day | rel=r_associated | relid=0 | w=10
  3838. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures often associated with infections
    n1=DYNC2H1 gene | n2=en:seizures often associated with infections | rel=r_associated | relid=0 | w=10
  3839. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures often begin focally with head and eye deviation
    n1=DYNC2H1 gene | n2=en:seizures often begin focally with head and eye deviation | rel=r_associated | relid=0 | w=10
  3840. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures often begin with head and eye deviation
    n1=DYNC2H1 gene | n2=en:seizures often begin with head and eye deviation | rel=r_associated | relid=0 | w=10
  3841. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures provoked by tactile stimulation or extreme emotion
    n1=DYNC2H1 gene | n2=en:seizures provoked by tactile stimulation or extreme emotion | rel=r_associated | relid=0 | w=10
  3842. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures recur in 33% of patients
    n1=DYNC2H1 gene | n2=en:seizures recur in 33% of patients | rel=r_associated | relid=0 | w=10
  3843. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures usually last 1 to 5 minutes (less commonly up to 10 minutes)
    n1=DYNC2H1 gene | n2=en:seizures usually last 1 to 5 minutes (less commonly up to 10 minutes) | rel=r_associated | relid=0 | w=10
  3844. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures usually last less than 15 minutes
    n1=DYNC2H1 gene | n2=en:seizures usually last less than 15 minutes | rel=r_associated | relid=0 | w=10
  3845. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures usually occur less than 3 times
    n1=DYNC2H1 gene | n2=en:seizures usually occur less than 3 times | rel=r_associated | relid=0 | w=10
  3846. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, complex partial, episodic
    n1=DYNC2H1 gene | n2=en:seizures, complex partial, episodic | rel=r_associated | relid=0 | w=10
  3847. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, complex, myoclonic
    n1=DYNC2H1 gene | n2=en:seizures, complex, myoclonic | rel=r_associated | relid=0 | w=10
  3848. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, continuous, refractory
    n1=DYNC2H1 gene | n2=en:seizures, continuous, refractory | rel=r_associated | relid=0 | w=10
  3849. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, diurnal partial, rare (in some patients)
    n1=DYNC2H1 gene | n2=en:seizures, diurnal partial, rare (in some patients) | rel=r_associated | relid=0 | w=10
  3850. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, early onset
    n1=DYNC2H1 gene | n2=en:seizures, early onset | rel=r_associated | relid=0 | w=10
  3851. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, early-onset (1 family)
    n1=DYNC2H1 gene | n2=en:seizures, early-onset (1 family) | rel=r_associated | relid=0 | w=10
  3852. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, febrile (1 family)
    n1=DYNC2H1 gene | n2=en:seizures, febrile (1 family) | rel=r_associated | relid=0 | w=10
  3853. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, focal, partial, motor
    n1=DYNC2H1 gene | n2=en:seizures, focal, partial, motor | rel=r_associated | relid=0 | w=10
  3854. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> 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=DYNC2H1 gene | 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=10
  3855. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, generalized, afebrile
    n1=DYNC2H1 gene | n2=en:seizures, generalized, afebrile | rel=r_associated | relid=0 | w=10
  3856. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, generalized, may occur
    n1=DYNC2H1 gene | n2=en:seizures, generalized, may occur | rel=r_associated | relid=0 | w=10
  3857. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, hypoglycemic (in some patients)
    n1=DYNC2H1 gene | n2=en:seizures, hypoglycemic (in some patients) | rel=r_associated | relid=0 | w=10
  3858. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, infantile-onset
    n1=DYNC2H1 gene | n2=en:seizures, infantile-onset | rel=r_associated | relid=0 | w=10
  3859. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, intractable
    n1=DYNC2H1 gene | n2=en:seizures, intractable | rel=r_associated | relid=0 | w=10
  3860. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, intractable (in 1 family)
    n1=DYNC2H1 gene | n2=en:seizures, intractable (in 1 family) | rel=r_associated | relid=0 | w=10
  3861. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, juvenile myoclonic
    n1=DYNC2H1 gene | n2=en:seizures, juvenile myoclonic | rel=r_associated | relid=0 | w=10
  3862. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, mild
    n1=DYNC2H1 gene | n2=en:seizures, mild | rel=r_associated | relid=0 | w=10
  3863. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, multiple types
    n1=DYNC2H1 gene | n2=en:seizures, multiple types | rel=r_associated | relid=0 | w=10
  3864. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, neonatal (2p21del)
    n1=DYNC2H1 gene | n2=en:seizures, neonatal (2p21del) | rel=r_associated | relid=0 | w=10
  3865. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, nocturnal, usually occur in daily clusters
    n1=DYNC2H1 gene | n2=en:seizures, nocturnal, usually occur in daily clusters | rel=r_associated | relid=0 | w=10
  3866. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, onset age 5 to 10 years
    n1=DYNC2H1 gene | n2=en:seizures, onset age 5 to 10 years | rel=r_associated | relid=0 | w=10
  3867. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, partial complex (rare)
    n1=DYNC2H1 gene | n2=en:seizures, partial complex (rare) | rel=r_associated | relid=0 | w=10
  3868. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, partial with secondary generalization, focal at onset, usually motor
    n1=DYNC2H1 gene | n2=en:seizures, partial with secondary generalization, focal at onset, usually motor | rel=r_associated | relid=0 | w=10
  3869. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, partial, often hemifacial
    n1=DYNC2H1 gene | n2=en:seizures, partial, often hemifacial | rel=r_associated | relid=0 | w=10
  3870. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, partial, unilateral
    n1=DYNC2H1 gene | n2=en:seizures, partial, unilateral | rel=r_associated | relid=0 | w=10
  3871. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, particularly absence (in some patients)
    n1=DYNC2H1 gene | n2=en:seizures, particularly absence (in some patients) | rel=r_associated | relid=0 | w=10
  3872. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, poorly controlled
    n1=DYNC2H1 gene | n2=en:seizures, poorly controlled | rel=r_associated | relid=0 | w=10
  3873. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, recurrent, refractory
    n1=DYNC2H1 gene | n2=en:seizures, recurrent, refractory | rel=r_associated | relid=0 | w=10
  3874. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, refractory
    n1=DYNC2H1 gene | n2=en:seizures, refractory | rel=r_associated | relid=0 | w=10
  3875. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, refractory to treatment
    n1=DYNC2H1 gene | n2=en:seizures, refractory to treatment | rel=r_associated | relid=0 | w=10
  3876. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, refractory, infantile-onset
    n1=DYNC2H1 gene | n2=en:seizures, refractory, infantile-onset | rel=r_associated | relid=0 | w=10
  3877. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, severe, drug-resistant, intractable
    n1=DYNC2H1 gene | n2=en:seizures, severe, drug-resistant, intractable | rel=r_associated | relid=0 | w=10
  3878. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, severe, intractable
    n1=DYNC2H1 gene | n2=en:seizures, severe, intractable | rel=r_associated | relid=0 | w=10
  3879. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, sudden-onset, drug-resistant
    n1=DYNC2H1 gene | n2=en:seizures, sudden-onset, drug-resistant | rel=r_associated | relid=0 | w=10
  3880. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, tonic-clonic (1 patient)
    n1=DYNC2H1 gene | n2=en:seizures, tonic-clonic (1 patient) | rel=r_associated | relid=0 | w=10
  3881. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, tonic-clonic (rare)
    n1=DYNC2H1 gene | n2=en:seizures, tonic-clonic (rare) | rel=r_associated | relid=0 | w=10
  3882. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, tonic-clonic or absence (in some patients)
    n1=DYNC2H1 gene | n2=en:seizures, tonic-clonic or absence (in some patients) | rel=r_associated | relid=0 | w=10
  3883. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, tonic, clonic, focal
    n1=DYNC2H1 gene | n2=en:seizures, tonic, clonic, focal | rel=r_associated | relid=0 | w=10
  3884. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:seizures, tonic, hyperekplectic
    n1=DYNC2H1 gene | n2=en:seizures, tonic, hyperekplectic | rel=r_associated | relid=0 | w=10
  3885. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:selective loss of cerebellar purkinje cells
    n1=DYNC2H1 gene | n2=en:selective loss of cerebellar purkinje cells | rel=r_associated | relid=0 | w=10
  3886. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:self mutilation
    n1=DYNC2H1 gene | n2=en:self mutilation | rel=r_associated | relid=0 | w=10
  3887. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:self-injurious behavior, median onset age 2 years
    n1=DYNC2H1 gene | n2=en:self-injurious behavior, median onset age 2 years | rel=r_associated | relid=0 | w=10
  3888. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:semilobar holoprosencephalies
    n1=DYNC2H1 gene | n2=en:semilobar holoprosencephalies | rel=r_associated | relid=0 | w=10
  3889. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle
    n1=DYNC2H1 gene | n2=en:semilobar hpe shows posterior interhemispheric fissure with rudimentary cerebral hemispheres and single ventricle | rel=r_associated | relid=0 | w=10
  3890. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sensitivity to neuroleptic medication
    n1=DYNC2H1 gene | n2=en:sensitivity to neuroleptic medication | rel=r_associated | relid=0 | w=10
  3891. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sensorineural hearing loss
    n1=DYNC2H1 gene | n2=en:sensorineural hearing loss | rel=r_associated | relid=0 | w=10
  3892. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sensory ataxia (less common)
    n1=DYNC2H1 gene | n2=en:sensory ataxia (less common) | rel=r_associated | relid=0 | w=10
  3893. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sensory aura may occur
    n1=DYNC2H1 gene | n2=en:sensory aura may occur | rel=r_associated | relid=0 | w=10
  3894. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:septum pellucidum deficient or cavum
    n1=DYNC2H1 gene | n2=en:septum pellucidum deficient or cavum | rel=r_associated | relid=0 | w=10
  3895. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe behavioral problems at age 3-4
    n1=DYNC2H1 gene | n2=en:severe behavioral problems at age 3-4 | rel=r_associated | relid=0 | w=10
  3896. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe brain damage
    n1=DYNC2H1 gene | n2=en:severe brain damage | rel=r_associated | relid=0 | w=10
  3897. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe cognitive deficits (develop later)
    n1=DYNC2H1 gene | n2=en:severe cognitive deficits (develop later) | rel=r_associated | relid=0 | w=10
  3898. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe cognitive impairment
    n1=DYNC2H1 gene | n2=en:severe cognitive impairment | rel=r_associated | relid=0 | w=10
  3899. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe delay in myelination
    n1=DYNC2H1 gene | n2=en:severe delay in myelination | rel=r_associated | relid=0 | w=10
  3900. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe demyelination of the white matter
    n1=DYNC2H1 gene | n2=en:severe demyelination of the white matter | rel=r_associated | relid=0 | w=10
  3901. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe developmental delay in survivors
    n1=DYNC2H1 gene | n2=en:severe developmental delay in survivors | rel=r_associated | relid=0 | w=10
  3902. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe expressive language delay
    n1=DYNC2H1 gene | n2=en:severe expressive language delay | rel=r_associated | relid=0 | w=10
  3903. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe expressive speech delay
    n1=DYNC2H1 gene | n2=en:severe expressive speech delay | rel=r_associated | relid=0 | w=10
  3904. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe form may never achieve sitting or walking
    n1=DYNC2H1 gene | n2=en:severe form may never achieve sitting or walking | rel=r_associated | relid=0 | w=10
  3905. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe global developmental delay
    n1=DYNC2H1 gene | n2=en:severe global developmental delay | rel=r_associated | relid=0 | w=10
  3906. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe hydrocephalus
    n1=DYNC2H1 gene | n2=en:severe hydrocephalus | rel=r_associated | relid=0 | w=10
  3907. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe involvement of globus pallidus
    n1=DYNC2H1 gene | n2=en:severe involvement of globus pallidus | rel=r_associated | relid=0 | w=10
  3908. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe mental retardation (congenital form)
    n1=DYNC2H1 gene | n2=en:severe mental retardation (congenital form) | rel=r_associated | relid=0 | w=10
  3909. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe mental retardation (i.q. 20-34)
    n1=DYNC2H1 gene | n2=en:severe mental retardation (i.q. 20-34) | rel=r_associated | relid=0 | w=10
  3910. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe mental retardation (iq 10-40)
    n1=DYNC2H1 gene | n2=en:severe mental retardation (iq 10-40) | rel=r_associated | relid=0 | w=10
  3911. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe muscular hypotonia
    n1=DYNC2H1 gene | n2=en:severe muscular hypotonia | rel=r_associated | relid=0 | w=10
  3912. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe neonatal hypotonia improving with age
    n1=DYNC2H1 gene | n2=en:severe neonatal hypotonia improving with age | rel=r_associated | relid=0 | w=10
  3913. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe prenatal onset hydrocephalus
    n1=DYNC2H1 gene | n2=en:severe prenatal onset hydrocephalus | rel=r_associated | relid=0 | w=10
  3914. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe psychomotor retardation
    n1=DYNC2H1 gene | n2=en:severe psychomotor retardation | rel=r_associated | relid=0 | w=10
  3915. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe psychomotor retardation (iq 35-65)
    n1=DYNC2H1 gene | n2=en:severe psychomotor retardation (iq 35-65) | rel=r_associated | relid=0 | w=10
  3916. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe psychomotor retardation from birth
    n1=DYNC2H1 gene | n2=en:severe psychomotor retardation from birth | rel=r_associated | relid=0 | w=10
  3917. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe speech delay
    n1=DYNC2H1 gene | n2=en:severe speech delay | rel=r_associated | relid=0 | w=10
  3918. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severe speech impairment
    n1=DYNC2H1 gene | n2=en:severe speech impairment | rel=r_associated | relid=0 | w=10
  3919. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severely delayed psychomotor development
    n1=DYNC2H1 gene | n2=en:severely delayed psychomotor development | rel=r_associated | relid=0 | w=10
  3920. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severely impaired or absent speech
    n1=DYNC2H1 gene | n2=en:severely impaired or absent speech | rel=r_associated | relid=0 | w=10
  3921. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:severity of symptoms peak in the second decade and do not progress
    n1=DYNC2H1 gene | n2=en:severity of symptoms peak in the second decade and do not progress | rel=r_associated | relid=0 | w=10
  3922. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:shivering sensation
    n1=DYNC2H1 gene | n2=en:shivering sensation | rel=r_associated | relid=0 | w=10
  3923. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:short pons
    n1=DYNC2H1 gene | n2=en:short pons | rel=r_associated | relid=0 | w=10
  3924. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:shorter daily total sleep times compared to age-matched controls
    n1=DYNC2H1 gene | n2=en:shorter daily total sleep times compared to age-matched controls | rel=r_associated | relid=0 | w=10
  3925. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:shrunken inferior olivary nuclei
    n1=DYNC2H1 gene | n2=en:shrunken inferior olivary nuclei | rel=r_associated | relid=0 | w=10
  3926. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:shuffling gaits
    n1=DYNC2H1 gene | n2=en:shuffling gaits | rel=r_associated | relid=0 | w=10
  3927. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sign or symptom
    n1=DYNC2H1 gene | n2=en:sign or symptom | rel=r_associated | relid=0 | w=10
  3928. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> 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=DYNC2H1 gene | 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=10
  3929. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:signal changes in the caudate and putamen
    n1=DYNC2H1 gene | n2=en:signal changes in the caudate and putamen | rel=r_associated | relid=0 | w=10
  3930. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simple partial seizures
    n1=DYNC2H1 gene | n2=en:simple partial seizures | rel=r_associated | relid=0 | w=10
  3931. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simple partial seizures with secondary generalization
    n1=DYNC2H1 gene | n2=en:simple partial seizures with secondary generalization | rel=r_associated | relid=0 | w=10
  3932. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simplified cortical gyral pattern
    n1=DYNC2H1 gene | n2=en:simplified cortical gyral pattern | rel=r_associated | relid=0 | w=10
  3933. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simplified cortical gyration pattern
    n1=DYNC2H1 gene | n2=en:simplified cortical gyration pattern | rel=r_associated | relid=0 | w=10
  3934. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simplified gyral pattern (1 patient)
    n1=DYNC2H1 gene | n2=en:simplified gyral pattern (1 patient) | rel=r_associated | relid=0 | w=10
  3935. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simplified gyral pattern (in 1 of 2 sibs)
    n1=DYNC2H1 gene | n2=en:simplified gyral pattern (in 1 of 2 sibs) | rel=r_associated | relid=0 | w=10
  3936. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simplified gyral pattern (in one patient)
    n1=DYNC2H1 gene | n2=en:simplified gyral pattern (in one patient) | rel=r_associated | relid=0 | w=10
  3937. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simplified gyral pattern (in some patients)
    n1=DYNC2H1 gene | n2=en:simplified gyral pattern (in some patients) | rel=r_associated | relid=0 | w=10
  3938. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simplified gyration in the frontal cortex (less common)
    n1=DYNC2H1 gene | n2=en:simplified gyration in the frontal cortex (less common) | rel=r_associated | relid=0 | w=10
  3939. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:simplified gyration pattern
    n1=DYNC2H1 gene | n2=en:simplified gyration pattern | rel=r_associated | relid=0 | w=10
  3940. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sinus pericranii (rare)
    n1=DYNC2H1 gene | n2=en:sinus pericranii (rare) | rel=r_associated | relid=0 | w=10
  3941. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:skin photosensitivity
    n1=DYNC2H1 gene | n2=en:skin photosensitivity | rel=r_associated | relid=0 | w=10
  3942. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep abnormalities
    n1=DYNC2H1 gene | n2=en:sleep abnormalities | rel=r_associated | relid=0 | w=10
  3943. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep apnea
    n1=DYNC2H1 gene | n2=en:sleep apnea | rel=r_associated | relid=0 | w=10
  3944. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep apnea (in 1/4 patients)
    n1=DYNC2H1 gene | n2=en:sleep apnea (in 1/4 patients) | rel=r_associated | relid=0 | w=10
  3945. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep benefit (31%)
    n1=DYNC2H1 gene | n2=en:sleep benefit (31%) | rel=r_associated | relid=0 | w=10
  3946. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep disorder
    n1=DYNC2H1 gene | n2=en:sleep disorder | rel=r_associated | relid=0 | w=10
  3947. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep disorder (rare)
    n1=DYNC2H1 gene | n2=en:sleep disorder (rare) | rel=r_associated | relid=0 | w=10
  3948. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep disorder with severe insomnia (in adulthood)
    n1=DYNC2H1 gene | n2=en:sleep disorder with severe insomnia (in adulthood) | rel=r_associated | relid=0 | w=10
  3949. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep disturbances
    n1=DYNC2H1 gene | n2=en:sleep disturbances | rel=r_associated | relid=0 | w=10
  3950. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep disturbances (in some patients)
    n1=DYNC2H1 gene | n2=en:sleep disturbances (in some patients) | rel=r_associated | relid=0 | w=10
  3951. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep disturbances common
    n1=DYNC2H1 gene | n2=en:sleep disturbances common | rel=r_associated | relid=0 | w=10
  3952. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep impairment, progressive
    n1=DYNC2H1 gene | n2=en:sleep impairment, progressive | rel=r_associated | relid=0 | w=10
  3953. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep paralysis at beginning or end of sleep period (in 60% of patients)
    n1=DYNC2H1 gene | n2=en:sleep paralysis at beginning or end of sleep period (in 60% of patients) | rel=r_associated | relid=0 | w=10
  3954. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep pattern disturbance
    n1=DYNC2H1 gene | n2=en:sleep pattern disturbance | rel=r_associated | relid=0 | w=10
  3955. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep talking
    n1=DYNC2H1 gene | n2=en:sleep talking | rel=r_associated | relid=0 | w=10
  3956. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep-onset rem
    n1=DYNC2H1 gene | n2=en:sleep-onset rem | rel=r_associated | relid=0 | w=10
  3957. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleep-wake cycle disturbance
    n1=DYNC2H1 gene | n2=en:sleep-wake cycle disturbance | rel=r_associated | relid=0 | w=10
  3958. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sleepiness
    n1=DYNC2H1 gene | n2=en:sleepiness | rel=r_associated | relid=0 | w=10
  3959. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slow gait
    n1=DYNC2H1 gene | n2=en:slow gait | rel=r_associated | relid=0 | w=10
  3960. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slow gross motor activity
    n1=DYNC2H1 gene | n2=en:slow gross motor activity | rel=r_associated | relid=0 | w=10
  3961. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slow paraparetic gait
    n1=DYNC2H1 gene | n2=en:slow paraparetic gait | rel=r_associated | relid=0 | w=10
  3962. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slow reactions
    n1=DYNC2H1 gene | n2=en:slow reactions | rel=r_associated | relid=0 | w=10
  3963. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slow speech
    n1=DYNC2H1 gene | n2=en:slow speech | rel=r_associated | relid=0 | w=10
  3964. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slow spike-wave discharges
    n1=DYNC2H1 gene | n2=en:slow spike-wave discharges | rel=r_associated | relid=0 | w=10
  3965. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slow, broad-based gait
    n1=DYNC2H1 gene | n2=en:slow, broad-based gait | rel=r_associated | relid=0 | w=10
  3966. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slowed background activity
    n1=DYNC2H1 gene | n2=en:slowed background activity | rel=r_associated | relid=0 | w=10
  3967. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slowing mental development by 1.5 to 3 years
    n1=DYNC2H1 gene | n2=en:slowing mental development by 1.5 to 3 years | rel=r_associated | relid=0 | w=10
  3968. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slowing mental development by 1.5 to 3 years of age
    n1=DYNC2H1 gene | n2=en:slowing mental development by 1.5 to 3 years of age | rel=r_associated | relid=0 | w=10
  3969. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slowly progressive neurologic deterioration
    n1=DYNC2H1 gene | n2=en:slowly progressive neurologic deterioration | rel=r_associated | relid=0 | w=10
  3970. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slurred speech, episodic
    n1=DYNC2H1 gene | n2=en:slurred speech, episodic | rel=r_associated | relid=0 | w=10
  3971. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:slurring of speech
    n1=DYNC2H1 gene | n2=en:slurring of speech | rel=r_associated | relid=0 | w=10
  3972. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration
    n1=DYNC2H1 gene | n2=en:small and medium-sized leptomeningeal arteries show luminal narrowing or obliteration | rel=r_associated | relid=0 | w=10
  3973. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small anterior commissure
    n1=DYNC2H1 gene | n2=en:small anterior commissure | rel=r_associated | relid=0 | w=10
  3974. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small brain
    n1=DYNC2H1 gene | n2=en:small brain | rel=r_associated | relid=0 | w=10
  3975. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small brain size (some patients)
    n1=DYNC2H1 gene | n2=en:small brain size (some patients) | rel=r_associated | relid=0 | w=10
  3976. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small brain with no other malformation see on mri
    n1=DYNC2H1 gene | n2=en:small brain with no other malformation see on mri | rel=r_associated | relid=0 | w=10
  3977. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small but structurally normal cerebral cortex
    n1=DYNC2H1 gene | n2=en:small but structurally normal cerebral cortex | rel=r_associated | relid=0 | w=10
  3978. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small caudate
    n1=DYNC2H1 gene | n2=en:small caudate | rel=r_associated | relid=0 | w=10
  3979. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small cavum septum
    n1=DYNC2H1 gene | n2=en:small cavum septum | rel=r_associated | relid=0 | w=10
  3980. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small cerebellum
    n1=DYNC2H1 gene | n2=en:small cerebellum | rel=r_associated | relid=0 | w=10
  3981. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small cerebellum (especially vermis)
    n1=DYNC2H1 gene | n2=en:small cerebellum (especially vermis) | rel=r_associated | relid=0 | w=10
  3982. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small cerebral cortex
    n1=DYNC2H1 gene | n2=en:small cerebral cortex | rel=r_associated | relid=0 | w=10
  3983. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small frontal lobes (in one patient)
    n1=DYNC2H1 gene | n2=en:small frontal lobes (in one patient) | rel=r_associated | relid=0 | w=10
  3984. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small hippocampi (1 patient)
    n1=DYNC2H1 gene | n2=en:small hippocampi (1 patient) | rel=r_associated | relid=0 | w=10
  3985. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small midbrain
    n1=DYNC2H1 gene | n2=en:small midbrain | rel=r_associated | relid=0 | w=10
  3986. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small pituitary gland (in some patients)
    n1=DYNC2H1 gene | n2=en:small pituitary gland (in some patients) | rel=r_associated | relid=0 | w=10
  3987. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small rotary component may be present
    n1=DYNC2H1 gene | n2=en:small rotary component may be present | rel=r_associated | relid=0 | w=10
  3988. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small sella
    n1=DYNC2H1 gene | n2=en:small sella | rel=r_associated | relid=0 | w=10
  3989. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small shrunken brain
    n1=DYNC2H1 gene | n2=en:small shrunken brain | rel=r_associated | relid=0 | w=10
  3990. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small size of the left hippocampus gyri
    n1=DYNC2H1 gene | n2=en:small size of the left hippocampus gyri | rel=r_associated | relid=0 | w=10
  3991. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small thalami
    n1=DYNC2H1 gene | n2=en:small thalami | rel=r_associated | relid=0 | w=10
  3992. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small, smooth cerebellum
    n1=DYNC2H1 gene | n2=en:small, smooth cerebellum | rel=r_associated | relid=0 | w=10
  3993. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:small, thin cerebellum
    n1=DYNC2H1 gene | n2=en:small, thin cerebellum | rel=r_associated | relid=0 | w=10
  3994. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:smooth brain surface
    n1=DYNC2H1 gene | n2=en:smooth brain surface | rel=r_associated | relid=0 | w=10
  3995. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:smooth, thin cortical mantle (wws)
    n1=DYNC2H1 gene | n2=en:smooth, thin cortical mantle (wws) | rel=r_associated | relid=0 | w=10
  3996. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:social and occupational deterioration
    n1=DYNC2H1 gene | n2=en:social and occupational deterioration | rel=r_associated | relid=0 | w=10
  3997. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:social communication disorder
    n1=DYNC2H1 gene | n2=en:social communication disorder | rel=r_associated | relid=0 | w=10
  3998. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:somatoform autonomic dysfunction
    n1=DYNC2H1 gene | n2=en:somatoform autonomic dysfunction | rel=r_associated | relid=0 | w=10
  3999. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:somatosensory evoked potentials show prolonged latency
    n1=DYNC2H1 gene | n2=en:somatosensory evoked potentials show prolonged latency | rel=r_associated | relid=0 | w=10
  4000. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:some may not achieve ambulation
    n1=DYNC2H1 gene | n2=en:some may not achieve ambulation | rel=r_associated | relid=0 | w=10
  4001. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:some patients do not achieve ability to walk
    n1=DYNC2H1 gene | n2=en:some patients do not achieve ability to walk | rel=r_associated | relid=0 | w=10
  4002. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:some patients have neurologic involvement
    n1=DYNC2H1 gene | n2=en:some patients have neurologic involvement | rel=r_associated | relid=0 | w=10
  4003. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:some patients have no structural brain abnormalities
    n1=DYNC2H1 gene | n2=en:some patients have no structural brain abnormalities | rel=r_associated | relid=0 | w=10
  4004. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:some patients have periodic wave complexes on eeg
    n1=DYNC2H1 gene | n2=en:some patients have periodic wave complexes on eeg | rel=r_associated | relid=0 | w=10
  4005. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:some patients may develop afebrile seizures later in life
    n1=DYNC2H1 gene | n2=en:some patients may develop afebrile seizures later in life | rel=r_associated | relid=0 | w=10
  4006. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:some patients may show normal early development
    n1=DYNC2H1 gene | n2=en:some patients may show normal early development | rel=r_associated | relid=0 | w=10
  4007. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:some patients never achieve independent ambulation
    n1=DYNC2H1 gene | n2=en:some patients never achieve independent ambulation | rel=r_associated | relid=0 | w=10
  4008. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:some patients only achieve sitting
    n1=DYNC2H1 gene | n2=en:some patients only achieve sitting | rel=r_associated | relid=0 | w=10
  4009. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:somnolence
    n1=DYNC2H1 gene | n2=en:somnolence | rel=r_associated | relid=0 | w=10
  4010. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sparing of central white matter structures
    n1=DYNC2H1 gene | n2=en:sparing of central white matter structures | rel=r_associated | relid=0 | w=10
  4011. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sparing of optic tracts
    n1=DYNC2H1 gene | n2=en:sparing of optic tracts | rel=r_associated | relid=0 | w=10
  4012. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sparing of the inferior olives
    n1=DYNC2H1 gene | n2=en:sparing of the inferior olives | rel=r_associated | relid=0 | w=10
  4013. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasmodic dysphonia
    n1=DYNC2H1 gene | n2=en:spasmodic dysphonia | rel=r_associated | relid=0 | w=10
  4014. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasmodic torticollis
    n1=DYNC2H1 gene | n2=en:spasmodic torticollis | rel=r_associated | relid=0 | w=10
  4015. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic ataxia
    n1=DYNC2H1 gene | n2=en:spastic ataxia | rel=r_associated | relid=0 | w=10
  4016. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic cerebral palsy
    n1=DYNC2H1 gene | n2=en:spastic cerebral palsy | rel=r_associated | relid=0 | w=10
  4017. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic diplegia
    n1=DYNC2H1 gene | n2=en:spastic diplegia | rel=r_associated | relid=0 | w=10
  4018. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic diplegia (1 patient)
    n1=DYNC2H1 gene | n2=en:spastic diplegia (1 patient) | rel=r_associated | relid=0 | w=10
  4019. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic diplegia (in some patients)
    n1=DYNC2H1 gene | n2=en:spastic diplegia (in some patients) | rel=r_associated | relid=0 | w=10
  4020. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic diplegia, progressive
    n1=DYNC2H1 gene | n2=en:spastic diplegia, progressive | rel=r_associated | relid=0 | w=10
  4021. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic diplegia, symmetric
    n1=DYNC2H1 gene | n2=en:spastic diplegia, symmetric | rel=r_associated | relid=0 | w=10
  4022. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic dystonia
    n1=DYNC2H1 gene | n2=en:spastic dystonia | rel=r_associated | relid=0 | w=10
  4023. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic gait
    n1=DYNC2H1 gene | n2=en:spastic gait | rel=r_associated | relid=0 | w=10
  4024. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic paralysis
    n1=DYNC2H1 gene | n2=en:spastic paralysis | rel=r_associated | relid=0 | w=10
  4025. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic paraparesis (1 patient)
    n1=DYNC2H1 gene | n2=en:spastic paraparesis (1 patient) | rel=r_associated | relid=0 | w=10
  4026. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic paraparesis (rare)
    n1=DYNC2H1 gene | n2=en:spastic paraparesis (rare) | rel=r_associated | relid=0 | w=10
  4027. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic paraplegia
    n1=DYNC2H1 gene | n2=en:spastic paraplegia | rel=r_associated | relid=0 | w=10
  4028. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic paraplegia (in some patients)
    n1=DYNC2H1 gene | n2=en:spastic paraplegia (in some patients) | rel=r_associated | relid=0 | w=10
  4029. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic paraplegia, later onset (in one patient)
    n1=DYNC2H1 gene | n2=en:spastic paraplegia, later onset (in one patient) | rel=r_associated | relid=0 | w=10
  4030. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic paraplegia, pure
    n1=DYNC2H1 gene | n2=en:spastic paraplegia, pure | rel=r_associated | relid=0 | w=10
  4031. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic paraplegia, severe
    n1=DYNC2H1 gene | n2=en:spastic paraplegia, severe | rel=r_associated | relid=0 | w=10
  4032. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic paraplegia, slowly progressive
    n1=DYNC2H1 gene | n2=en:spastic paraplegia, slowly progressive | rel=r_associated | relid=0 | w=10
  4033. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic quadriplegia
    n1=DYNC2H1 gene | n2=en:spastic quadriplegia | rel=r_associated | relid=0 | w=10
  4034. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic quadriplegia (in one patient)
    n1=DYNC2H1 gene | n2=en:spastic quadriplegia (in one patient) | rel=r_associated | relid=0 | w=10
  4035. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic quadriplegia, residual mild-to-severe (in some patients)
    n1=DYNC2H1 gene | n2=en:spastic quadriplegia, residual mild-to-severe (in some patients) | rel=r_associated | relid=0 | w=10
  4036. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic quadriplegia, severe
    n1=DYNC2H1 gene | n2=en:spastic quadriplegia, severe | rel=r_associated | relid=0 | w=10
  4037. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic tetraparesis
    n1=DYNC2H1 gene | n2=en:spastic tetraparesis | rel=r_associated | relid=0 | w=10
  4038. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic tetraparesis (in severe cases)
    n1=DYNC2H1 gene | n2=en:spastic tetraparesis (in severe cases) | rel=r_associated | relid=0 | w=10
  4039. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic tetraplegia (in some patients)
    n1=DYNC2H1 gene | n2=en:spastic tetraplegia (in some patients) | rel=r_associated | relid=0 | w=10
  4040. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic tetraplegia (onset in the second decade)
    n1=DYNC2H1 gene | n2=en:spastic tetraplegia (onset in the second decade) | rel=r_associated | relid=0 | w=10
  4041. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic-ataxic gait
    n1=DYNC2H1 gene | n2=en:spastic-ataxic gait | rel=r_associated | relid=0 | w=10
  4042. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spastic-ataxic tetraparesis
    n1=DYNC2H1 gene | n2=en:spastic-ataxic tetraparesis | rel=r_associated | relid=0 | w=10
  4043. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity
    n1=DYNC2H1 gene | n2=en:spasticity | rel=r_associated | relid=0 | w=10
  4044. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (1 family)
    n1=DYNC2H1 gene | n2=en:spasticity (1 family) | rel=r_associated | relid=0 | w=10
  4045. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (1 of 4 patients)
    n1=DYNC2H1 gene | n2=en:spasticity (1 of 4 patients) | rel=r_associated | relid=0 | w=10
  4046. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (in some patients)
    n1=DYNC2H1 gene | n2=en:spasticity (in some patients) | rel=r_associated | relid=0 | w=10
  4047. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (in some)
    n1=DYNC2H1 gene | n2=en:spasticity (in some) | rel=r_associated | relid=0 | w=10
  4048. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (later onset)
    n1=DYNC2H1 gene | n2=en:spasticity (later onset) | rel=r_associated | relid=0 | w=10
  4049. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (later)
    n1=DYNC2H1 gene | n2=en:spasticity (later) | rel=r_associated | relid=0 | w=10
  4050. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (less common)
    n1=DYNC2H1 gene | n2=en:spasticity (less common) | rel=r_associated | relid=0 | w=10
  4051. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (patient a)
    n1=DYNC2H1 gene | n2=en:spasticity (patient a) | rel=r_associated | relid=0 | w=10
  4052. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (rare)
    n1=DYNC2H1 gene | n2=en:spasticity (rare) | rel=r_associated | relid=0 | w=10
  4053. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (reported in 1 patient)
    n1=DYNC2H1 gene | n2=en:spasticity (reported in 1 patient) | rel=r_associated | relid=0 | w=10
  4054. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity (type ii)
    n1=DYNC2H1 gene | n2=en:spasticity (type ii) | rel=r_associated | relid=0 | w=10
  4055. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity in infancy (1 patient)
    n1=DYNC2H1 gene | n2=en:spasticity in infancy (1 patient) | rel=r_associated | relid=0 | w=10
  4056. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity may be present
    n1=DYNC2H1 gene | n2=en:spasticity may be present | rel=r_associated | relid=0 | w=10
  4057. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity may occur
    n1=DYNC2H1 gene | n2=en:spasticity may occur | rel=r_associated | relid=0 | w=10
  4058. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity of facial muscles
    n1=DYNC2H1 gene | n2=en:spasticity of facial muscles | rel=r_associated | relid=0 | w=10
  4059. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity of lower and upper limbs
    n1=DYNC2H1 gene | n2=en:spasticity of lower and upper limbs | rel=r_associated | relid=0 | w=10
  4060. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity of pharyngeal muscles
    n1=DYNC2H1 gene | n2=en:spasticity of pharyngeal muscles | rel=r_associated | relid=0 | w=10
  4061. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, distal
    n1=DYNC2H1 gene | n2=en:spasticity, distal | rel=r_associated | relid=0 | w=10
  4062. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, hyperreflexia
    n1=DYNC2H1 gene | n2=en:spasticity, hyperreflexia | rel=r_associated | relid=0 | w=10
  4063. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, lower limbs greater than upper limbs
    n1=DYNC2H1 gene | n2=en:spasticity, lower limbs greater than upper limbs | rel=r_associated | relid=0 | w=10
  4064. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, mainly in the lower limbs
    n1=DYNC2H1 gene | n2=en:spasticity, mainly in the lower limbs | rel=r_associated | relid=0 | w=10
  4065. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, mild (in some patients)
    n1=DYNC2H1 gene | n2=en:spasticity, mild (in some patients) | rel=r_associated | relid=0 | w=10
  4066. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, more apparent in the lower limbs
    n1=DYNC2H1 gene | n2=en:spasticity, more apparent in the lower limbs | rel=r_associated | relid=0 | w=10
  4067. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, primarily lower limbs, but upper limbs may be involved
    n1=DYNC2H1 gene | n2=en:spasticity, primarily lower limbs, but upper limbs may be involved | rel=r_associated | relid=0 | w=10
  4068. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, progressive, develops in childhood
    n1=DYNC2H1 gene | n2=en:spasticity, progressive, develops in childhood | rel=r_associated | relid=0 | w=10
  4069. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, severe
    n1=DYNC2H1 gene | n2=en:spasticity, severe | rel=r_associated | relid=0 | w=10
  4070. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, severe, affecting lower limbs
    n1=DYNC2H1 gene | n2=en:spasticity, severe, affecting lower limbs | rel=r_associated | relid=0 | w=10
  4071. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity, usually of the lower limbs
    n1=DYNC2H1 gene | n2=en:spasticity, usually of the lower limbs | rel=r_associated | relid=0 | w=10
  4072. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spasticity/paresis (rare)
    n1=DYNC2H1 gene | n2=en:spasticity/paresis (rare) | rel=r_associated | relid=0 | w=10
  4073. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:specific visual spatial processing defect
    n1=DYNC2H1 gene | n2=en:specific visual spatial processing defect | rel=r_associated | relid=0 | w=10
  4074. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spect scan may show hypermetabolism of the temporal lobe
    n1=DYNC2H1 gene | n2=en:spect scan may show hypermetabolism of the temporal lobe | rel=r_associated | relid=0 | w=10
  4075. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech abnormalities (palilalia)
    n1=DYNC2H1 gene | n2=en:speech abnormalities (palilalia) | rel=r_associated | relid=0 | w=10
  4076. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech absent or delayed
    n1=DYNC2H1 gene | n2=en:speech absent or delayed | rel=r_associated | relid=0 | w=10
  4077. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech and language delay (rare)
    n1=DYNC2H1 gene | n2=en:speech and language delay (rare) | rel=r_associated | relid=0 | w=10
  4078. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech and language delay, severe
    n1=DYNC2H1 gene | n2=en:speech and language delay, severe | rel=r_associated | relid=0 | w=10
  4079. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech and language disorder
    n1=DYNC2H1 gene | n2=en:speech and language disorder | rel=r_associated | relid=0 | w=10
  4080. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech and language regression
    n1=DYNC2H1 gene | n2=en:speech and language regression | rel=r_associated | relid=0 | w=10
  4081. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech articulation defects
    n1=DYNC2H1 gene | n2=en:speech articulation defects | rel=r_associated | relid=0 | w=10
  4082. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech articulation problems
    n1=DYNC2H1 gene | n2=en:speech articulation problems | rel=r_associated | relid=0 | w=10
  4083. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech deficits
    n1=DYNC2H1 gene | n2=en:speech deficits | rel=r_associated | relid=0 | w=10
  4084. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech delay
    n1=DYNC2H1 gene | n2=en:speech delay | rel=r_associated | relid=0 | w=10
  4085. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech delay (1 patient)
    n1=DYNC2H1 gene | n2=en:speech delay (1 patient) | rel=r_associated | relid=0 | w=10
  4086. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech delay (10%)
    n1=DYNC2H1 gene | n2=en:speech delay (10%) | rel=r_associated | relid=0 | w=10
  4087. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech delay (59%)
    n1=DYNC2H1 gene | n2=en:speech delay (59%) | rel=r_associated | relid=0 | w=10
  4088. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech delay (in all patients)
    n1=DYNC2H1 gene | n2=en:speech delay (in all patients) | rel=r_associated | relid=0 | w=10
  4089. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech delay (in some patients)
    n1=DYNC2H1 gene | n2=en:speech delay (in some patients) | rel=r_associated | relid=0 | w=10
  4090. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech deterioration
    n1=DYNC2H1 gene | n2=en:speech deterioration | rel=r_associated | relid=0 | w=10
  4091. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech development delayed (in some patients)
    n1=DYNC2H1 gene | n2=en:speech development delayed (in some patients) | rel=r_associated | relid=0 | w=10
  4092. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech difficulties (48%)
    n1=DYNC2H1 gene | n2=en:speech difficulties (48%) | rel=r_associated | relid=0 | w=10
  4093. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech difficulties due to hypoglossia
    n1=DYNC2H1 gene | n2=en:speech difficulties due to hypoglossia | rel=r_associated | relid=0 | w=10
  4094. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech disability
    n1=DYNC2H1 gene | n2=en:speech disability | rel=r_associated | relid=0 | w=10
  4095. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech disorder
    n1=DYNC2H1 gene | n2=en:speech disorder | rel=r_associated | relid=0 | w=10
  4096. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech disorder (in 1 of 6 patients)
    n1=DYNC2H1 gene | n2=en:speech disorder (in 1 of 6 patients) | rel=r_associated | relid=0 | w=10
  4097. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech disorders (rare)
    n1=DYNC2H1 gene | n2=en:speech disorders (rare) | rel=r_associated | relid=0 | w=10
  4098. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech hesitancy
    n1=DYNC2H1 gene | n2=en:speech hesitancy | rel=r_associated | relid=0 | w=10
  4099. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech impairment
    n1=DYNC2H1 gene | n2=en:speech impairment | rel=r_associated | relid=0 | w=10
  4100. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech limited
    n1=DYNC2H1 gene | n2=en:speech limited | rel=r_associated | relid=0 | w=10
  4101. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech limited to single word or no words
    n1=DYNC2H1 gene | n2=en:speech limited to single word or no words | rel=r_associated | relid=0 | w=10
  4102. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech never acquired
    n1=DYNC2H1 gene | n2=en:speech never acquired | rel=r_associated | relid=0 | w=10
  4103. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech severely limited or absent
    n1=DYNC2H1 gene | n2=en:speech severely limited or absent | rel=r_associated | relid=0 | w=10
  4104. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:speech, limited or nonverbal
    n1=DYNC2H1 gene | n2=en:speech, limited or nonverbal | rel=r_associated | relid=0 | w=10
  4105. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spheroids contain neurofilaments
    n1=DYNC2H1 gene | n2=en:spheroids contain neurofilaments | rel=r_associated | relid=0 | w=10
  4106. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spina bifida
    n1=DYNC2H1 gene | n2=en:spina bifida | rel=r_associated | relid=0 | w=10
  4107. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spina bifida (less common)
    n1=DYNC2H1 gene | n2=en:spina bifida (less common) | rel=r_associated | relid=0 | w=10
  4108. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spina bifida occulta
    n1=DYNC2H1 gene | n2=en:spina bifida occulta | rel=r_associated | relid=0 | w=10
  4109. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal arteriovenous malformation
    n1=DYNC2H1 gene | n2=en:spinal arteriovenous malformation | rel=r_associated | relid=0 | w=10
  4110. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal cord atrophy (1 family)
    n1=DYNC2H1 gene | n2=en:spinal cord atrophy (1 family) | rel=r_associated | relid=0 | w=10
  4111. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal cord atrophy (rare)
    n1=DYNC2H1 gene | n2=en:spinal cord atrophy (rare) | rel=r_associated | relid=0 | w=10
  4112. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal cord compression
    n1=DYNC2H1 gene | n2=en:spinal cord compression | rel=r_associated | relid=0 | w=10
  4113. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal cord compression by tumor infiltration
    n1=DYNC2H1 gene | n2=en:spinal cord compression by tumor infiltration | rel=r_associated | relid=0 | w=10
  4114. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal cord disorder
    n1=DYNC2H1 gene | n2=en:spinal cord disorder | rel=r_associated | relid=0 | w=10
  4115. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal cord glial hyperplasia
    n1=DYNC2H1 gene | n2=en:spinal cord glial hyperplasia | rel=r_associated | relid=0 | w=10
  4116. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal cord paresis
    n1=DYNC2H1 gene | n2=en:spinal cord paresis | rel=r_associated | relid=0 | w=10
  4117. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal cord syrinx (in 2 patients)
    n1=DYNC2H1 gene | n2=en:spinal cord syrinx (in 2 patients) | rel=r_associated | relid=0 | w=10
  4118. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal cysts (in some patients)
    n1=DYNC2H1 gene | n2=en:spinal cysts (in some patients) | rel=r_associated | relid=0 | w=10
  4119. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal muscular atrophy
    n1=DYNC2H1 gene | n2=en:spinal muscular atrophy | rel=r_associated | relid=0 | w=10
  4120. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal neurofibromas (64%)
    n1=DYNC2H1 gene | n2=en:spinal neurofibromas (64%) | rel=r_associated | relid=0 | w=10
  4121. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal neuropathy
    n1=DYNC2H1 gene | n2=en:spinal neuropathy | rel=r_associated | relid=0 | w=10
  4122. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal stenosis
    n1=DYNC2H1 gene | n2=en:spinal stenosis | rel=r_associated | relid=0 | w=10
  4123. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinal tract degeneration
    n1=DYNC2H1 gene | n2=en:spinal tract degeneration | rel=r_associated | relid=0 | w=10
  4124. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinocerebellar ataxia
    n1=DYNC2H1 gene | n2=en:spinocerebellar ataxia | rel=r_associated | relid=0 | w=10
  4125. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinocerebellar ataxia (in some patients)
    n1=DYNC2H1 gene | n2=en:spinocerebellar ataxia (in some patients) | rel=r_associated | relid=0 | w=10
  4126. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinocerebellar ataxia (upper and lower limb involvement)
    n1=DYNC2H1 gene | n2=en:spinocerebellar ataxia (upper and lower limb involvement) | rel=r_associated | relid=0 | w=10
  4127. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinocerebellar degeneration
    n1=DYNC2H1 gene | n2=en:spinocerebellar degeneration | rel=r_associated | relid=0 | w=10
  4128. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinocerebellar tract degeneration
    n1=DYNC2H1 gene | n2=en:spinocerebellar tract degeneration | rel=r_associated | relid=0 | w=10
  4129. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spinocerebellar tract disease in lower limbs (in adulthood)
    n1=DYNC2H1 gene | n2=en:spinocerebellar tract disease in lower limbs (in adulthood) | rel=r_associated | relid=0 | w=10
  4130. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spongiform changes are mild or may not be present
    n1=DYNC2H1 gene | n2=en:spongiform changes are mild or may not be present | rel=r_associated | relid=0 | w=10
  4131. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spongiform degeneration
    n1=DYNC2H1 gene | n2=en:spongiform degeneration | rel=r_associated | relid=0 | w=10
  4132. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spongiform encephalomyelopathy
    n1=DYNC2H1 gene | n2=en:spongiform encephalomyelopathy | rel=r_associated | relid=0 | w=10
  4133. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spongiosis, mild
    n1=DYNC2H1 gene | n2=en:spongiosis, mild | rel=r_associated | relid=0 | w=10
  4134. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spongy degeneration
    n1=DYNC2H1 gene | n2=en:spongy degeneration | rel=r_associated | relid=0 | w=10
  4135. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:spongy gliosis
    n1=DYNC2H1 gene | n2=en:spongy gliosis | rel=r_associated | relid=0 | w=10
  4136. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stance ataxia
    n1=DYNC2H1 gene | n2=en:stance ataxia | rel=r_associated | relid=0 | w=10
  4137. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:staring
    n1=DYNC2H1 gene | n2=en:staring | rel=r_associated | relid=0 | w=10
  4138. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:staring episodes during seizures
    n1=DYNC2H1 gene | n2=en:staring episodes during seizures | rel=r_associated | relid=0 | w=10
  4139. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:staring spells
    n1=DYNC2H1 gene | n2=en:staring spells | rel=r_associated | relid=0 | w=10
  4140. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:start with tonic posturing
    n1=DYNC2H1 gene | n2=en:start with tonic posturing | rel=r_associated | relid=0 | w=10
  4141. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:startle myoclonus
    n1=DYNC2H1 gene | n2=en:startle myoclonus | rel=r_associated | relid=0 | w=10
  4142. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:status dystonicus
    n1=DYNC2H1 gene | n2=en:status dystonicus | rel=r_associated | relid=0 | w=10
  4143. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:status epilepticus
    n1=DYNC2H1 gene | n2=en:status epilepticus | rel=r_associated | relid=0 | w=10
  4144. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:status epilepticus (in 1 of 6 patients)
    n1=DYNC2H1 gene | n2=en:status epilepticus (in 1 of 6 patients) | rel=r_associated | relid=0 | w=10
  4145. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:status epilepticus (in some patients)
    n1=DYNC2H1 gene | n2=en:status epilepticus (in some patients) | rel=r_associated | relid=0 | w=10
  4146. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:status epilepticus (in some)
    n1=DYNC2H1 gene | n2=en:status epilepticus (in some) | rel=r_associated | relid=0 | w=10
  4147. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:status epilepticus may occur
    n1=DYNC2H1 gene | n2=en:status epilepticus may occur | rel=r_associated | relid=0 | w=10
  4148. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:status epilepticus rarely occurs
    n1=DYNC2H1 gene | n2=en:status epilepticus rarely occurs | rel=r_associated | relid=0 | w=10
  4149. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stenosis of the aqueduct of sylvius (rare)
    n1=DYNC2H1 gene | n2=en:stenosis of the aqueduct of sylvius (rare) | rel=r_associated | relid=0 | w=10
  4150. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stenosis of the jugular foramen
    n1=DYNC2H1 gene | n2=en:stenosis of the jugular foramen | rel=r_associated | relid=0 | w=10
  4151. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stereotypic movements
    n1=DYNC2H1 gene | n2=en:stereotypic movements | rel=r_associated | relid=0 | w=10
  4152. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stiff gait
    n1=DYNC2H1 gene | n2=en:stiff gait | rel=r_associated | relid=0 | w=10
  4153. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stiff limbs
    n1=DYNC2H1 gene | n2=en:stiff limbs | rel=r_associated | relid=0 | w=10
  4154. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stiffness
    n1=DYNC2H1 gene | n2=en:stiffness | rel=r_associated | relid=0 | w=10
  4155. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stiffness of the lower limbs
    n1=DYNC2H1 gene | n2=en:stiffness of the lower limbs | rel=r_associated | relid=0 | w=10
  4156. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stiffness while walking
    n1=DYNC2H1 gene | n2=en:stiffness while walking | rel=r_associated | relid=0 | w=10
  4157. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stimulation sensitive generalized myoclonus (stage 3)
    n1=DYNC2H1 gene | n2=en:stimulation sensitive generalized myoclonus (stage 3) | rel=r_associated | relid=0 | w=10
  4158. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stimulation sensitive segmental myoclonus (stage 2)
    n1=DYNC2H1 gene | n2=en:stimulation sensitive segmental myoclonus (stage 2) | rel=r_associated | relid=0 | w=10
  4159. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stoke-like lesions
    n1=DYNC2H1 gene | n2=en:stoke-like lesions | rel=r_associated | relid=0 | w=10
  4160. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stretched cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:stretched cerebellar peduncles | rel=r_associated | relid=0 | w=10
  4161. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:striatal atrophy
    n1=DYNC2H1 gene | n2=en:striatal atrophy | rel=r_associated | relid=0 | w=10
  4162. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:striatal lesions
    n1=DYNC2H1 gene | n2=en:striatal lesions | rel=r_associated | relid=0 | w=10
  4163. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:striatal necrosis
    n1=DYNC2H1 gene | n2=en:striatal necrosis | rel=r_associated | relid=0 | w=10
  4164. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stroke (in some patients)
    n1=DYNC2H1 gene | n2=en:stroke (in some patients) | rel=r_associated | relid=0 | w=10
  4165. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stroke (rare)
    n1=DYNC2H1 gene | n2=en:stroke (rare) | rel=r_associated | relid=0 | w=10
  4166. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stroke (uncommon)
    n1=DYNC2H1 gene | n2=en:stroke (uncommon) | rel=r_associated | relid=0 | w=10
  4167. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stroke-like episodes
    n1=DYNC2H1 gene | n2=en:stroke-like episodes | rel=r_associated | relid=0 | w=10
  4168. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stroke-like episodes (in some patients)
    n1=DYNC2H1 gene | n2=en:stroke-like episodes (in some patients) | rel=r_associated | relid=0 | w=10
  4169. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stroke-like symptoms
    n1=DYNC2H1 gene | n2=en:stroke-like symptoms | rel=r_associated | relid=0 | w=10
  4170. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:strokes due to coagulopathy
    n1=DYNC2H1 gene | n2=en:strokes due to coagulopathy | rel=r_associated | relid=0 | w=10
  4171. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structural abnormalities in the basal ganglia (especially caudate)
    n1=DYNC2H1 gene | n2=en:structural abnormalities in the basal ganglia (especially caudate) | rel=r_associated | relid=0 | w=10
  4172. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structural abnormalities of cerebellum
    n1=DYNC2H1 gene | n2=en:structural abnormalities of cerebellum | rel=r_associated | relid=0 | w=10
  4173. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structural brain abnormalities
    n1=DYNC2H1 gene | n2=en:structural brain abnormalities | rel=r_associated | relid=0 | w=10
  4174. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structural brain anomalies
    n1=DYNC2H1 gene | n2=en:structural brain anomalies | rel=r_associated | relid=0 | w=10
  4175. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structural changes in the temporal lobe
    n1=DYNC2H1 gene | n2=en:structural changes in the temporal lobe | rel=r_associated | relid=0 | w=10
  4176. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structure of central auditory system
    n1=DYNC2H1 gene | n2=en:structure of central auditory system | rel=r_associated | relid=0 | w=10
  4177. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structure of central sensory visual system
    n1=DYNC2H1 gene | n2=en:structure of central sensory visual system | rel=r_associated | relid=0 | w=10
  4178. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structure of decussation of superior cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:structure of decussation of superior cerebellar peduncles | rel=r_associated | relid=0 | w=10
  4179. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structure of peripheral part of autonomic nervous system
    n1=DYNC2H1 gene | n2=en:structure of peripheral part of autonomic nervous system | rel=r_associated | relid=0 | w=10
  4180. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:structure of rami communicantes of spinal nerve of cauda equina
    n1=DYNC2H1 gene | n2=en:structure of rami communicantes of spinal nerve of cauda equina | rel=r_associated | relid=0 | w=10
  4181. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sturge-weber syndrome
    n1=DYNC2H1 gene | n2=en:sturge-weber syndrome | rel=r_associated | relid=0 | w=10
  4182. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:stuve-wiedemann syndrome
    n1=DYNC2H1 gene | n2=en:stuve-wiedemann syndrome | rel=r_associated | relid=0 | w=10
  4183. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subacute neurologic deterioration
    n1=DYNC2H1 gene | n2=en:subacute neurologic deterioration | rel=r_associated | relid=0 | w=10
  4184. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subarachnoid cyst
    n1=DYNC2H1 gene | n2=en:subarachnoid cyst | rel=r_associated | relid=0 | w=10
  4185. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subarachnoid hemorrhage
    n1=DYNC2H1 gene | n2=en:subarachnoid hemorrhage | rel=r_associated | relid=0 | w=10
  4186. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subarachnoid hemorrhage (rare)
    n1=DYNC2H1 gene | n2=en:subarachnoid hemorrhage (rare) | rel=r_associated | relid=0 | w=10
  4187. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subclinical absence seizures
    n1=DYNC2H1 gene | n2=en:subclinical absence seizures | rel=r_associated | relid=0 | w=10
  4188. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical and periventricular white matter abnormalities seen on mri (in some patients)
    n1=DYNC2H1 gene | n2=en:subcortical and periventricular white matter abnormalities seen on mri (in some patients) | rel=r_associated | relid=0 | w=10
  4189. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical atrophy (in some patients)
    n1=DYNC2H1 gene | n2=en:subcortical atrophy (in some patients) | rel=r_associated | relid=0 | w=10
  4190. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical band or laminar heterotopia (in female carriers)
    n1=DYNC2H1 gene | n2=en:subcortical band or laminar heterotopia (in female carriers) | rel=r_associated | relid=0 | w=10
  4191. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical cysts in frontal and temporal lobes
    n1=DYNC2H1 gene | n2=en:subcortical cysts in frontal and temporal lobes | rel=r_associated | relid=0 | w=10
  4192. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical cysts may occur elsewhere
    n1=DYNC2H1 gene | n2=en:subcortical cysts may occur elsewhere | rel=r_associated | relid=0 | w=10
  4193. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical cysts temporal lobe
    n1=DYNC2H1 gene | n2=en:subcortical cysts temporal lobe | rel=r_associated | relid=0 | w=10
  4194. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical dementia, progressive (6% of patients)
    n1=DYNC2H1 gene | n2=en:subcortical dementia, progressive (6% of patients) | rel=r_associated | relid=0 | w=10
  4195. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical focal lacunae
    n1=DYNC2H1 gene | n2=en:subcortical focal lacunae | rel=r_associated | relid=0 | w=10
  4196. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical gliosis
    n1=DYNC2H1 gene | n2=en:subcortical gliosis | rel=r_associated | relid=0 | w=10
  4197. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical heterotopia
    n1=DYNC2H1 gene | n2=en:subcortical heterotopia | rel=r_associated | relid=0 | w=10
  4198. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical hypomyelination
    n1=DYNC2H1 gene | n2=en:subcortical hypomyelination | rel=r_associated | relid=0 | w=10
  4199. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical lacunar lesions seen early in disease
    n1=DYNC2H1 gene | n2=en:subcortical lacunar lesions seen early in disease | rel=r_associated | relid=0 | w=10
  4200. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical lesions
    n1=DYNC2H1 gene | n2=en:subcortical lesions | rel=r_associated | relid=0 | w=10
  4201. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical lesions with edema
    n1=DYNC2H1 gene | n2=en:subcortical lesions with edema | rel=r_associated | relid=0 | w=10
  4202. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical leukodystrophy
    n1=DYNC2H1 gene | n2=en:subcortical leukodystrophy | rel=r_associated | relid=0 | w=10
  4203. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical nodular grey matter heterotopia
    n1=DYNC2H1 gene | n2=en:subcortical nodular grey matter heterotopia | rel=r_associated | relid=0 | w=10
  4204. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical nodular lesions in perivascular white matter
    n1=DYNC2H1 gene | n2=en:subcortical nodular lesions in perivascular white matter | rel=r_associated | relid=0 | w=10
  4205. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical origin of the myoclonus based on neurophysiologic studies
    n1=DYNC2H1 gene | n2=en:subcortical origin of the myoclonus based on neurophysiologic studies | rel=r_associated | relid=0 | w=10
  4206. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical temporal white matter disease, moderate
    n1=DYNC2H1 gene | n2=en:subcortical temporal white matter disease, moderate | rel=r_associated | relid=0 | w=10
  4207. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical white matter abnormalities (rare)
    n1=DYNC2H1 gene | n2=en:subcortical white matter abnormalities (rare) | rel=r_associated | relid=0 | w=10
  4208. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical white matter abnormalities seen on mri
    n1=DYNC2H1 gene | n2=en:subcortical white matter abnormalities seen on mri | rel=r_associated | relid=0 | w=10
  4209. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical white matter calcifications
    n1=DYNC2H1 gene | n2=en:subcortical white matter calcifications | rel=r_associated | relid=0 | w=10
  4210. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subcortical white matter lesions in the temporal lobes seen on brain mri
    n1=DYNC2H1 gene | n2=en:subcortical white matter lesions in the temporal lobes seen on brain mri | rel=r_associated | relid=0 | w=10
  4211. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subdivision of parasympathetic nervous system
    n1=DYNC2H1 gene | n2=en:subdivision of parasympathetic nervous system | rel=r_associated | relid=0 | w=10
  4212. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subdivision of sympathetic nervous system
    n1=DYNC2H1 gene | n2=en:subdivision of sympathetic nervous system | rel=r_associated | relid=0 | w=10
  4213. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subependymal calcifications
    n1=DYNC2H1 gene | n2=en:subependymal calcifications | rel=r_associated | relid=0 | w=10
  4214. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subependymal hemorrhage
    n1=DYNC2H1 gene | n2=en:subependymal hemorrhage | rel=r_associated | relid=0 | w=10
  4215. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subependymal heterotopias
    n1=DYNC2H1 gene | n2=en:subependymal heterotopias | rel=r_associated | relid=0 | w=10
  4216. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subependymal heterotopic nodules
    n1=DYNC2H1 gene | n2=en:subependymal heterotopic nodules | rel=r_associated | relid=0 | w=10
  4217. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subependymal nodules
    n1=DYNC2H1 gene | n2=en:subependymal nodules | rel=r_associated | relid=0 | w=10
  4218. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subependymal pseudocyst
    n1=DYNC2H1 gene | n2=en:subependymal pseudocyst | rel=r_associated | relid=0 | w=10
  4219. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subnormal cognition
    n1=DYNC2H1 gene | n2=en:subnormal cognition | rel=r_associated | relid=0 | w=10
  4220. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:subnormal intelligence (62%)
    n1=DYNC2H1 gene | n2=en:subnormal intelligence (62%) | rel=r_associated | relid=0 | w=10
  4221. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:substantia nigra gliosis
    n1=DYNC2H1 gene | n2=en:substantia nigra gliosis | rel=r_associated | relid=0 | w=10
  4222. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sudden arousal from slow-wave sleep with screaming, autonomic, and behavioral manifestations of intense fear (sleep terrors)
    n1=DYNC2H1 gene | 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=10
  4223. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sudden awakening
    n1=DYNC2H1 gene | n2=en:sudden awakening | rel=r_associated | relid=0 | w=10
  4224. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sudden onset of neuropsychiatric symptoms
    n1=DYNC2H1 gene | n2=en:sudden onset of neuropsychiatric symptoms | rel=r_associated | relid=0 | w=10
  4225. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:superficial laminar spongiosis
    n1=DYNC2H1 gene | n2=en:superficial laminar spongiosis | rel=r_associated | relid=0 | w=10
  4226. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:suppression-burst pattern
    n1=DYNC2H1 gene | n2=en:suppression-burst pattern | rel=r_associated | relid=0 | w=10
  4227. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:suppression-burst pattern see on eeg
    n1=DYNC2H1 gene | n2=en:suppression-burst pattern see on eeg | rel=r_associated | relid=0 | w=10
  4228. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:supranuclear gaze palsy
    n1=DYNC2H1 gene | n2=en:supranuclear gaze palsy | rel=r_associated | relid=0 | w=10
  4229. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:supratentorial structures unformed or regressed
    n1=DYNC2H1 gene | n2=en:supratentorial structures unformed or regressed | rel=r_associated | relid=0 | w=10
  4230. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sweating problem
    n1=DYNC2H1 gene | n2=en:sweating problem | rel=r_associated | relid=0 | w=10
  4231. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sweating, gustatory
    n1=DYNC2H1 gene | n2=en:sweating, gustatory | rel=r_associated | relid=0 | w=10
  4232. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:swelling of the cerebral white matter
    n1=DYNC2H1 gene | n2=en:swelling of the cerebral white matter | rel=r_associated | relid=0 | w=10
  4233. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:swelling of the deep white matter seen on mri
    n1=DYNC2H1 gene | n2=en:swelling of the deep white matter seen on mri | rel=r_associated | relid=0 | w=10
  4234. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:swollen achromatic cells (pick cells)
    n1=DYNC2H1 gene | n2=en:swollen achromatic cells (pick cells) | rel=r_associated | relid=0 | w=10
  4235. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients
    n1=DYNC2H1 gene | n2=en:symmetric lesions in the basal ganglia consistent with leigh syndrome (256000), in a subset of patients | rel=r_associated | relid=0 | w=10
  4236. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:symmetric spinal nerve root neurofibromas
    n1=DYNC2H1 gene | n2=en:symmetric spinal nerve root neurofibromas | rel=r_associated | relid=0 | w=10
  4237. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:symmetric ventriculomegaly
    n1=DYNC2H1 gene | n2=en:symmetric ventriculomegaly | rel=r_associated | relid=0 | w=10
  4238. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:symmetrical progressive demyelination
    n1=DYNC2H1 gene | n2=en:symmetrical progressive demyelination | rel=r_associated | relid=0 | w=10
  4239. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sympathetic nervous system
    n1=DYNC2H1 gene | n2=en:sympathetic nervous system | rel=r_associated | relid=0 | w=10
  4240. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sympathicotonia
    n1=DYNC2H1 gene | n2=en:sympathicotonia | rel=r_associated | relid=0 | w=10
  4241. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sympatholytics
    n1=DYNC2H1 gene | n2=en:sympatholytics | rel=r_associated | relid=0 | w=10
  4242. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sympathomimetic disorder
    n1=DYNC2H1 gene | n2=en:sympathomimetic disorder | rel=r_associated | relid=0 | w=10
  4243. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:sympathotonic orthostatic hypotension
    n1=DYNC2H1 gene | n2=en:sympathotonic orthostatic hypotension | rel=r_associated | relid=0 | w=10
  4244. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:symptoms are exacerbated during pregnancy
    n1=DYNC2H1 gene | n2=en:symptoms are exacerbated during pregnancy | rel=r_associated | relid=0 | w=10
  4245. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:symptoms occur at rest
    n1=DYNC2H1 gene | n2=en:symptoms occur at rest | rel=r_associated | relid=0 | w=10
  4246. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:symptoms of hypothalamic disturbances (in some patients)
    n1=DYNC2H1 gene | n2=en:symptoms of hypothalamic disturbances (in some patients) | rel=r_associated | relid=0 | w=10
  4247. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:symptoms stabilize within 4 weeks
    n1=DYNC2H1 gene | n2=en:symptoms stabilize within 4 weeks | rel=r_associated | relid=0 | w=10
  4248. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:syncope
    n1=DYNC2H1 gene | n2=en:syncope | rel=r_associated | relid=0 | w=10
  4249. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:syndrome screaming
    n1=DYNC2H1 gene | n2=en:syndrome screaming | rel=r_associated | relid=0 | w=10
  4250. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:synkinesia (rare)
    n1=DYNC2H1 gene | n2=en:synkinesia (rare) | rel=r_associated | relid=0 | w=10
  4251. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:synkinesis
    n1=DYNC2H1 gene | n2=en:synkinesis | rel=r_associated | relid=0 | w=10
  4252. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:syringomyelia
    n1=DYNC2H1 gene | n2=en:syringomyelia | rel=r_associated | relid=0 | w=10
  4253. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:syringomyelia (in some patients)
    n1=DYNC2H1 gene | n2=en:syringomyelia (in some patients) | rel=r_associated | relid=0 | w=10
  4254. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:syringomyelia, noncommunicating (80% of cases)
    n1=DYNC2H1 gene | n2=en:syringomyelia, noncommunicating (80% of cases) | rel=r_associated | relid=0 | w=10
  4255. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:systema nervosum
    n1=DYNC2H1 gene | n2=en:systema nervosum | rel=r_associated | relid=0 | w=10
  4256. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra
    n1=DYNC2H1 gene | n2=en:t1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra | rel=r_associated | relid=0 | w=10
  4257. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem
    n1=DYNC2H1 gene | n2=en:t2-weighted hyperintense lesions in the thalamus, basal ganglia, and brainstem | rel=r_associated | relid=0 | w=10
  4258. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintensities in deep brain regions
    n1=DYNC2H1 gene | n2=en:t2-weighted hyperintensities in deep brain regions | rel=r_associated | relid=0 | w=10
  4259. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintensities in deep cerebral white matter, brainstem, and cerebellar white matter with sparing of the periventricular rim
    n1=DYNC2H1 gene | 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=10
  4260. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintensities in subcortical brain regions seen on mri
    n1=DYNC2H1 gene | n2=en:t2-weighted hyperintensities in subcortical brain regions seen on mri | rel=r_associated | relid=0 | w=10
  4261. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintensities in the basal ganglia
    n1=DYNC2H1 gene | n2=en:t2-weighted hyperintensities in the basal ganglia | rel=r_associated | relid=0 | w=10
  4262. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri
    n1=DYNC2H1 gene | n2=en:t2-weighted hyperintensities in the basal ganglia, corpus callosum, and brainstem seen on mri | rel=r_associated | relid=0 | w=10
  4263. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintensities in the corticospinal tracts and posterior arms of the internal capsule in older patients seen on mri
    n1=DYNC2H1 gene | 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=10
  4264. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter
    n1=DYNC2H1 gene | n2=en:t2-weighted hyperintensities in the periventricular and deep subcortical white matter | rel=r_associated | relid=0 | w=10
  4265. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintensities in the putamen and caudate nuclei
    n1=DYNC2H1 gene | n2=en:t2-weighted hyperintensities in the putamen and caudate nuclei | rel=r_associated | relid=0 | w=10
  4266. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hyperintensities in the supratentorial white matter seen on brain mri
    n1=DYNC2H1 gene | n2=en:t2-weighted hyperintensities in the supratentorial white matter seen on brain mri | rel=r_associated | relid=0 | w=10
  4267. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted hypodensities in the basal ganglia
    n1=DYNC2H1 gene | n2=en:t2-weighted hypodensities in the basal ganglia | rel=r_associated | relid=0 | w=10
  4268. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted mri shows hyperintensities in the thalamus, basal ganglia, and brainstem during acute illness (may later resolve)
    n1=DYNC2H1 gene | 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=10
  4269. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:t2-weighted signal abnormalities in the deep white matter
    n1=DYNC2H1 gene | n2=en:t2-weighted signal abnormalities in the deep white matter | rel=r_associated | relid=0 | w=10
  4270. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tau immunreactivity
    n1=DYNC2H1 gene | n2=en:tau immunreactivity | rel=r_associated | relid=0 | w=10
  4271. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tau inclusions are 'flame-shaped' or 'tuft-like'
    n1=DYNC2H1 gene | n2=en:tau inclusions are 'flame-shaped' or 'tuft-like' | rel=r_associated | relid=0 | w=10
  4272. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tau-containing inclusions
    n1=DYNC2H1 gene | n2=en:tau-containing inclusions | rel=r_associated | relid=0 | w=10
  4273. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tau-immunoreactive inclusions in neurons and astrocytes
    n1=DYNC2H1 gene | n2=en:tau-immunoreactive inclusions in neurons and astrocytes | rel=r_associated | relid=0 | w=10
  4274. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tau-positive inclusions may be found
    n1=DYNC2H1 gene | n2=en:tau-positive inclusions may be found | rel=r_associated | relid=0 | w=10
  4275. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tbp- and 1c2-immunoreactive neuronal inclusions
    n1=DYNC2H1 gene | n2=en:tbp- and 1c2-immunoreactive neuronal inclusions | rel=r_associated | relid=0 | w=10
  4276. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tdp43-positive inclusions
    n1=DYNC2H1 gene | n2=en:tdp43-positive inclusions | rel=r_associated | relid=0 | w=10
  4277. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tdp43-positive neuronal and glial cytoplasmic inclusions
    n1=DYNC2H1 gene | n2=en:tdp43-positive neuronal and glial cytoplasmic inclusions | rel=r_associated | relid=0 | w=10
  4278. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tdp43-positive neuronal inclusions
    n1=DYNC2H1 gene | n2=en:tdp43-positive neuronal inclusions | rel=r_associated | relid=0 | w=10
  4279. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tectal enlargement
    n1=DYNC2H1 gene | n2=en:tectal enlargement | rel=r_associated | relid=0 | w=10
  4280. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:temporal epileptiform discharges seen on eeg
    n1=DYNC2H1 gene | n2=en:temporal epileptiform discharges seen on eeg | rel=r_associated | relid=0 | w=10
  4281. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:temporal lobe epilepsy (1 patient)
    n1=DYNC2H1 gene | n2=en:temporal lobe epilepsy (1 patient) | rel=r_associated | relid=0 | w=10
  4282. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:temporal lobe heterotopias
    n1=DYNC2H1 gene | n2=en:temporal lobe heterotopias | rel=r_associated | relid=0 | w=10
  4283. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:temporal lobe infarct (rare)
    n1=DYNC2H1 gene | n2=en:temporal lobe infarct (rare) | rel=r_associated | relid=0 | w=10
  4284. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:temporal lobe seizures (in 1 patient)
    n1=DYNC2H1 gene | n2=en:temporal lobe seizures (in 1 patient) | rel=r_associated | relid=0 | w=10
  4285. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tendency to walk on toes
    n1=DYNC2H1 gene | n2=en:tendency to walk on toes | rel=r_associated | relid=0 | w=10
  4286. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tetany
    n1=DYNC2H1 gene | n2=en:tetany | rel=r_associated | relid=0 | w=10
  4287. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tetany, hypocalcemic (in some patients)
    n1=DYNC2H1 gene | n2=en:tetany, hypocalcemic (in some patients) | rel=r_associated | relid=0 | w=10
  4288. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tetany, hypocalcemic, episodic
    n1=DYNC2H1 gene | n2=en:tetany, hypocalcemic, episodic | rel=r_associated | relid=0 | w=10
  4289. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tethered cord (rare)
    n1=DYNC2H1 gene | n2=en:tethered cord (rare) | rel=r_associated | relid=0 | w=10
  4290. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tethered cord (uncommon)
    n1=DYNC2H1 gene | n2=en:tethered cord (uncommon) | rel=r_associated | relid=0 | w=10
  4291. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tethered spinal cord
    n1=DYNC2H1 gene | n2=en:tethered spinal cord | rel=r_associated | relid=0 | w=10
  4292. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tethered spinal cord syndrome
    n1=DYNC2H1 gene | n2=en:tethered spinal cord syndrome | rel=r_associated | relid=0 | w=10
  4293. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tetraplegic spasticity
    n1=DYNC2H1 gene | n2=en:tetraplegic spasticity | rel=r_associated | relid=0 | w=10
  4294. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tfg- and tdp43-positive intraneuronal inclusions in some sensory and motor spinal cord neurons
    n1=DYNC2H1 gene | n2=en:tfg- and tdp43-positive intraneuronal inclusions in some sensory and motor spinal cord neurons | rel=r_associated | relid=0 | w=10
  4295. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thalamic hypoplasia
    n1=DYNC2H1 gene | n2=en:thalamic hypoplasia | rel=r_associated | relid=0 | w=10
  4296. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thalamic lesions
    n1=DYNC2H1 gene | n2=en:thalamic lesions | rel=r_associated | relid=0 | w=10
  4297. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thalamic neuronal loss, especially in the medial dorsal nucleus
    n1=DYNC2H1 gene | n2=en:thalamic neuronal loss, especially in the medial dorsal nucleus | rel=r_associated | relid=0 | w=10
  4298. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thenar muscle atrophy
    n1=DYNC2H1 gene | n2=en:thenar muscle atrophy | rel=r_associated | relid=0 | w=10
  4299. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thenar muscle weakness
    n1=DYNC2H1 gene | n2=en:thenar muscle weakness | rel=r_associated | relid=0 | w=10
  4300. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thick and elongated superior cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:thick and elongated superior cerebellar peduncles | rel=r_associated | relid=0 | w=10
  4301. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thick corpus callosum
    n1=DYNC2H1 gene | n2=en:thick corpus callosum | rel=r_associated | relid=0 | w=10
  4302. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thick cortex
    n1=DYNC2H1 gene | n2=en:thick cortex | rel=r_associated | relid=0 | w=10
  4303. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thick, maloriented superior cerebellar peduncles
    n1=DYNC2H1 gene | n2=en:thick, maloriented superior cerebellar peduncles | rel=r_associated | relid=0 | w=10
  4304. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thick, short corpus callosum
    n1=DYNC2H1 gene | n2=en:thick, short corpus callosum | rel=r_associated | relid=0 | w=10
  4305. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thickened cortices
    n1=DYNC2H1 gene | n2=en:thickened cortices | rel=r_associated | relid=0 | w=10
  4306. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thickened frontal cortex
    n1=DYNC2H1 gene | n2=en:thickened frontal cortex | rel=r_associated | relid=0 | w=10
  4307. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thickened optic nerve sheath
    n1=DYNC2H1 gene | n2=en:thickened optic nerve sheath | rel=r_associated | relid=0 | w=10
  4308. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thickening of the skull (less common)
    n1=DYNC2H1 gene | n2=en:thickening of the skull (less common) | rel=r_associated | relid=0 | w=10
  4309. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin bony cortex
    n1=DYNC2H1 gene | n2=en:thin bony cortex | rel=r_associated | relid=0 | w=10
  4310. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin brainstem
    n1=DYNC2H1 gene | n2=en:thin brainstem | rel=r_associated | relid=0 | w=10
  4311. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin cerebral cortex
    n1=DYNC2H1 gene | n2=en:thin cerebral cortex | rel=r_associated | relid=0 | w=10
  4312. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin corpus callosum (1 family)
    n1=DYNC2H1 gene | n2=en:thin corpus callosum (1 family) | rel=r_associated | relid=0 | w=10
  4313. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin corpus callosum (1 patient)
    n1=DYNC2H1 gene | n2=en:thin corpus callosum (1 patient) | rel=r_associated | relid=0 | w=10
  4314. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin corpus callosum (1/4 patients)
    n1=DYNC2H1 gene | n2=en:thin corpus callosum (1/4 patients) | rel=r_associated | relid=0 | w=10
  4315. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin corpus callosum (in some patients)
    n1=DYNC2H1 gene | n2=en:thin corpus callosum (in some patients) | rel=r_associated | relid=0 | w=10
  4316. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin corpus callosum enlarged ventricles
    n1=DYNC2H1 gene | n2=en:thin corpus callosum enlarged ventricles | rel=r_associated | relid=0 | w=10
  4317. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin cortical mantle (wws)
    n1=DYNC2H1 gene | n2=en:thin cortical mantle (wws) | rel=r_associated | relid=0 | w=10
  4318. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin optic chiasm
    n1=DYNC2H1 gene | n2=en:thin optic chiasm | rel=r_associated | relid=0 | w=10
  4319. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thin pituitary stalk
    n1=DYNC2H1 gene | n2=en:thin pituitary stalk | rel=r_associated | relid=0 | w=10
  4320. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thinning of the cerebellopontine tracts
    n1=DYNC2H1 gene | n2=en:thinning of the cerebellopontine tracts | rel=r_associated | relid=0 | w=10
  4321. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:third ventricle subependymal focal gliosis
    n1=DYNC2H1 gene | n2=en:third ventricle subependymal focal gliosis | rel=r_associated | relid=0 | w=10
  4322. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:thrombosis of cerebral veins
    n1=DYNC2H1 gene | n2=en:thrombosis of cerebral veins | rel=r_associated | relid=0 | w=10
  4323. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tip-toe gait
    n1=DYNC2H1 gene | n2=en:tip-toe gait | rel=r_associated | relid=0 | w=10
  4324. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:toe-walking gait
    n1=DYNC2H1 gene | n2=en:toe-walking gait | rel=r_associated | relid=0 | w=10
  4325. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:toe-walking in early childhood
    n1=DYNC2H1 gene | n2=en:toe-walking in early childhood | rel=r_associated | relid=0 | w=10
  4326. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tongue movements, protrusions
    n1=DYNC2H1 gene | n2=en:tongue movements, protrusions | rel=r_associated | relid=0 | w=10
  4327. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tonic clonic seizures, infrequent (in one patient)
    n1=DYNC2H1 gene | n2=en:tonic clonic seizures, infrequent (in one patient) | rel=r_associated | relid=0 | w=10
  4328. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tonic convulsion
    n1=DYNC2H1 gene | n2=en:tonic convulsion | rel=r_associated | relid=0 | w=10
  4329. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tonic head extension
    n1=DYNC2H1 gene | n2=en:tonic head extension | rel=r_associated | relid=0 | w=10
  4330. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tonic posturing
    n1=DYNC2H1 gene | n2=en:tonic posturing | rel=r_associated | relid=0 | w=10
  4331. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tonic pupil
    n1=DYNC2H1 gene | n2=en:tonic pupil | rel=r_associated | relid=0 | w=10
  4332. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tonic seizures, refractory
    n1=DYNC2H1 gene | n2=en:tonic seizures, refractory | rel=r_associated | relid=0 | w=10
  4333. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tonic spasms
    n1=DYNC2H1 gene | n2=en:tonic spasms | rel=r_associated | relid=0 | w=10
  4334. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tonic-clonic seizures (less common)
    n1=DYNC2H1 gene | n2=en:tonic-clonic seizures (less common) | rel=r_associated | relid=0 | w=10
  4335. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tonus dysregulation
    n1=DYNC2H1 gene | n2=en:tonus dysregulation | rel=r_associated | relid=0 | w=10
  4336. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing)
    n1=DYNC2H1 gene | n2=en:torsion dystonia (involuntary sustained muscle contractions, twisting and repetitive movements, abnormal posturing) | rel=r_associated | relid=0 | w=10
  4337. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:torticollis
    n1=DYNC2H1 gene | n2=en:torticollis | rel=r_associated | relid=0 | w=10
  4338. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:total body paralysis, paroxysmal
    n1=DYNC2H1 gene | n2=en:total body paralysis, paroxysmal | rel=r_associated | relid=0 | w=10
  4339. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:touch, vibration, and limb position may or may not be affected
    n1=DYNC2H1 gene | n2=en:touch, vibration, and limb position may or may not be affected | rel=r_associated | relid=0 | w=10
  4340. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tow-walking
    n1=DYNC2H1 gene | n2=en:tow-walking | rel=r_associated | relid=0 | w=10
  4341. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:transient ataxia
    n1=DYNC2H1 gene | n2=en:transient ataxia | rel=r_associated | relid=0 | w=10
  4342. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:transient ischemic attack
    n1=DYNC2H1 gene | n2=en:transient ischemic attack | rel=r_associated | relid=0 | w=10
  4343. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:transient mild dystonia may precede abrupt onset of disorder by several years
    n1=DYNC2H1 gene | n2=en:transient mild dystonia may precede abrupt onset of disorder by several years | rel=r_associated | relid=0 | w=10
  4344. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:transient, reversible neurologic deficits
    n1=DYNC2H1 gene | n2=en:transient, reversible neurologic deficits | rel=r_associated | relid=0 | w=10
  4345. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:transitional facial palsy (15%)
    n1=DYNC2H1 gene | n2=en:transitional facial palsy (15%) | rel=r_associated | relid=0 | w=10
  4346. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor
    n1=DYNC2H1 gene | n2=en:tremor | rel=r_associated | relid=0 | w=10
  4347. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor (1 patient)
    n1=DYNC2H1 gene | n2=en:tremor (1 patient) | rel=r_associated | relid=0 | w=10
  4348. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor (3 patients)
    n1=DYNC2H1 gene | n2=en:tremor (3 patients) | rel=r_associated | relid=0 | w=10
  4349. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor (30%)
    n1=DYNC2H1 gene | n2=en:tremor (30%) | rel=r_associated | relid=0 | w=10
  4350. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor (57% of patients)
    n1=DYNC2H1 gene | n2=en:tremor (57% of patients) | rel=r_associated | relid=0 | w=10
  4351. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor (in some patients)
    n1=DYNC2H1 gene | n2=en:tremor (in some patients) | rel=r_associated | relid=0 | w=10
  4352. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor (later-onset)
    n1=DYNC2H1 gene | n2=en:tremor (later-onset) | rel=r_associated | relid=0 | w=10
  4353. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor (less common)
    n1=DYNC2H1 gene | n2=en:tremor (less common) | rel=r_associated | relid=0 | w=10
  4354. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor (rare)
    n1=DYNC2H1 gene | n2=en:tremor (rare) | rel=r_associated | relid=0 | w=10
  4355. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor due to hyperthyroidism
    n1=DYNC2H1 gene | n2=en:tremor due to hyperthyroidism | rel=r_associated | relid=0 | w=10
  4356. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor is exacerbated by stress and exercise
    n1=DYNC2H1 gene | n2=en:tremor is exacerbated by stress and exercise | rel=r_associated | relid=0 | w=10
  4357. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor of hands
    n1=DYNC2H1 gene | n2=en:tremor of hands | rel=r_associated | relid=0 | w=10
  4358. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor of palate
    n1=DYNC2H1 gene | n2=en:tremor of palate | rel=r_associated | relid=0 | w=10
  4359. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor of the upper limb
    n1=DYNC2H1 gene | n2=en:tremor of the upper limb | rel=r_associated | relid=0 | w=10
  4360. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor with febrile episodes (rare)
    n1=DYNC2H1 gene | n2=en:tremor with febrile episodes (rare) | rel=r_associated | relid=0 | w=10
  4361. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor, action (arms, tongue, head, legs and trunk)
    n1=DYNC2H1 gene | n2=en:tremor, action (arms, tongue, head, legs and trunk) | rel=r_associated | relid=0 | w=10
  4362. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor, action, progressive
    n1=DYNC2H1 gene | n2=en:tremor, action, progressive | rel=r_associated | relid=0 | w=10
  4363. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor, mild
    n1=DYNC2H1 gene | n2=en:tremor, mild | rel=r_associated | relid=0 | w=10
  4364. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor, postural (arms, tongue, head, legs and trunk)
    n1=DYNC2H1 gene | n2=en:tremor, postural (arms, tongue, head, legs and trunk) | rel=r_associated | relid=0 | w=10
  4365. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family)
    n1=DYNC2H1 gene | n2=en:tremor, postural, upper limb, onset in fourth decade (reported in 1 family) | rel=r_associated | relid=0 | w=10
  4366. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor, small-amplitude, high-frequency, restricted to the hands
    n1=DYNC2H1 gene | n2=en:tremor, small-amplitude, high-frequency, restricted to the hands | rel=r_associated | relid=0 | w=10
  4367. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor, static
    n1=DYNC2H1 gene | n2=en:tremor, static | rel=r_associated | relid=0 | w=10
  4368. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremor, variable
    n1=DYNC2H1 gene | n2=en:tremor, variable | rel=r_associated | relid=0 | w=10
  4369. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremors, action
    n1=DYNC2H1 gene | n2=en:tremors, action | rel=r_associated | relid=0 | w=10
  4370. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tremors, limb
    n1=DYNC2H1 gene | n2=en:tremors, limb | rel=r_associated | relid=0 | w=10
  4371. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:trigeminal anesthesia
    n1=DYNC2H1 gene | n2=en:trigeminal anesthesia | rel=r_associated | relid=0 | w=10
  4372. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:trigeminal neuralgia
    n1=DYNC2H1 gene | n2=en:trigeminal neuralgia | rel=r_associated | relid=0 | w=10
  4373. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:trismus (rare)
    n1=DYNC2H1 gene | n2=en:trismus (rare) | rel=r_associated | relid=0 | w=10
  4374. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:truncal arching
    n1=DYNC2H1 gene | n2=en:truncal arching | rel=r_associated | relid=0 | w=10
  4375. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:truncal ataxia, mild
    n1=DYNC2H1 gene | n2=en:truncal ataxia, mild | rel=r_associated | relid=0 | w=10
  4376. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:truncal ataxia, severe
    n1=DYNC2H1 gene | n2=en:truncal ataxia, severe | rel=r_associated | relid=0 | w=10
  4377. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:truncal instability
    n1=DYNC2H1 gene | n2=en:truncal instability | rel=r_associated | relid=0 | w=10
  4378. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:truncal titubation
    n1=DYNC2H1 gene | n2=en:truncal titubation | rel=r_associated | relid=0 | w=10
  4379. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tussive syncopes
    n1=DYNC2H1 gene | n2=en:tussive syncopes | rel=r_associated | relid=0 | w=10
  4380. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:twitching of the fingers and toes
    n1=DYNC2H1 gene | n2=en:twitching of the fingers and toes | rel=r_associated | relid=0 | w=10
  4381. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:tympanic membrane disorder
    n1=DYNC2H1 gene | n2=en:tympanic membrane disorder | rel=r_associated | relid=0 | w=10
  4382. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:type i arnold chiari malformation
    n1=DYNC2H1 gene | n2=en:type i arnold chiari malformation | rel=r_associated | relid=0 | w=10
  4383. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:type i eeg response is occipital spikes
    n1=DYNC2H1 gene | n2=en:type i eeg response is occipital spikes | rel=r_associated | relid=0 | w=10
  4384. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves
    n1=DYNC2H1 gene | n2=en:type ii eeg response is parietooccipital spikes followed by biphasic slow waves | rel=r_associated | relid=0 | w=10
  4385. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:type iii eeg response is parietooccipital spikes followed by biphasic slow waves and spreading to the frontal region
    n1=DYNC2H1 gene | 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=10
  4386. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:type iv eeg response is generalized spike-wave discharges
    n1=DYNC2H1 gene | n2=en:type iv eeg response is generalized spike-wave discharges | rel=r_associated | relid=0 | w=10
  4387. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions
    n1=DYNC2H1 gene | n2=en:ubiquitin-positive cytoplasmic and intranuclear neuronal inclusions | rel=r_associated | relid=0 | w=10
  4388. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ubiquitin-positive inclusions
    n1=DYNC2H1 gene | n2=en:ubiquitin-positive inclusions | rel=r_associated | relid=0 | w=10
  4389. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ubiquitin-positive intranuclear neuronal inclusions
    n1=DYNC2H1 gene | n2=en:ubiquitin-positive intranuclear neuronal inclusions | rel=r_associated | relid=0 | w=10
  4390. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ubqln2- and tdp43-immunopositive inclusions in spinal motor, brainstem, and hippocampal neurons
    n1=DYNC2H1 gene | n2=en:ubqln2- and tdp43-immunopositive inclusions in spinal motor, brainstem, and hippocampal neurons | rel=r_associated | relid=0 | w=10
  4391. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unable to grasp objects
    n1=DYNC2H1 gene | n2=en:unable to grasp objects | rel=r_associated | relid=0 | w=10
  4392. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unable to sit unsupported
    n1=DYNC2H1 gene | n2=en:unable to sit unsupported | rel=r_associated | relid=0 | w=10
  4393. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unable to stand
    n1=DYNC2H1 gene | n2=en:unable to stand | rel=r_associated | relid=0 | w=10
  4394. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unable to talk
    n1=DYNC2H1 gene | n2=en:unable to talk | rel=r_associated | relid=0 | w=10
  4395. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unable to walk
    n1=DYNC2H1 gene | n2=en:unable to walk | rel=r_associated | relid=0 | w=10
  4396. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:uncoordinated movements
    n1=DYNC2H1 gene | n2=en:uncoordinated movements | rel=r_associated | relid=0 | w=10
  4397. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:underdeveloped corpus callosum (3 patients)
    n1=DYNC2H1 gene | n2=en:underdeveloped corpus callosum (3 patients) | rel=r_associated | relid=0 | w=10
  4398. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:undersulcation of the frontal lobes
    n1=DYNC2H1 gene | n2=en:undersulcation of the frontal lobes | rel=r_associated | relid=0 | w=10
  4399. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unidentified bright objects on brain mri
    n1=DYNC2H1 gene | n2=en:unidentified bright objects on brain mri | rel=r_associated | relid=0 | w=10
  4400. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unilateral cerebellar hypoplasia
    n1=DYNC2H1 gene | n2=en:unilateral cerebellar hypoplasia | rel=r_associated | relid=0 | w=10
  4401. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unilateral headache location
    n1=DYNC2H1 gene | n2=en:unilateral headache location | rel=r_associated | relid=0 | w=10
  4402. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unintelligible speech, vocalizations, grunting
    n1=DYNC2H1 gene | n2=en:unintelligible speech, vocalizations, grunting | rel=r_associated | relid=0 | w=10
  4403. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unresponsive to stimuli
    n1=DYNC2H1 gene | n2=en:unresponsive to stimuli | rel=r_associated | relid=0 | w=10
  4404. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unresponsiveness
    n1=DYNC2H1 gene | n2=en:unresponsiveness | rel=r_associated | relid=0 | w=10
  4405. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unstable, ataxic gait
    n1=DYNC2H1 gene | n2=en:unstable, ataxic gait | rel=r_associated | relid=0 | w=10
  4406. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unsteadiness, episodic
    n1=DYNC2H1 gene | n2=en:unsteadiness, episodic | rel=r_associated | relid=0 | w=10
  4407. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unsteady gait due to muscle weakness
    n1=DYNC2H1 gene | n2=en:unsteady gait due to muscle weakness | rel=r_associated | relid=0 | w=10
  4408. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unsteady standing
    n1=DYNC2H1 gene | n2=en:unsteady standing | rel=r_associated | relid=0 | w=10
  4409. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:unusual aura symptoms include alien limb phenomenon, diplopia, apraxia, dysarthria, impaired hearing, vertigo
    n1=DYNC2H1 gene | n2=en:unusual aura symptoms include alien limb phenomenon, diplopia, apraxia, dysarthria, impaired hearing, vertigo | rel=r_associated | relid=0 | w=10
  4410. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upbeat central vestibular nystagmus
    n1=DYNC2H1 gene | n2=en:upbeat central vestibular nystagmus | rel=r_associated | relid=0 | w=10
  4411. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper and lower motor neuron degeneration
    n1=DYNC2H1 gene | n2=en:upper and lower motor neuron degeneration | rel=r_associated | relid=0 | w=10
  4412. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper and lower motor neuron disease
    n1=DYNC2H1 gene | n2=en:upper and lower motor neuron disease | rel=r_associated | relid=0 | w=10
  4413. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper and lower neuron manifestations
    n1=DYNC2H1 gene | n2=en:upper and lower neuron manifestations | rel=r_associated | relid=0 | w=10
  4414. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper body involvement
    n1=DYNC2H1 gene | n2=en:upper body involvement | rel=r_associated | relid=0 | w=10
  4415. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper extremities may be involved
    n1=DYNC2H1 gene | n2=en:upper extremities may be involved | rel=r_associated | relid=0 | w=10
  4416. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper extremity action tremor
    n1=DYNC2H1 gene | n2=en:upper extremity action tremor | rel=r_associated | relid=0 | w=10
  4417. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb ataxia
    n1=DYNC2H1 gene | n2=en:upper limb ataxia | rel=r_associated | relid=0 | w=10
  4418. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb dysmetria
    n1=DYNC2H1 gene | n2=en:upper limb dysmetria | rel=r_associated | relid=0 | w=10
  4419. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb dystonia
    n1=DYNC2H1 gene | n2=en:upper limb dystonia | rel=r_associated | relid=0 | w=10
  4420. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb hyperreflexia (in some patients)
    n1=DYNC2H1 gene | n2=en:upper limb hyperreflexia (in some patients) | rel=r_associated | relid=0 | w=10
  4421. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb hyperreflexia (some)
    n1=DYNC2H1 gene | n2=en:upper limb hyperreflexia (some) | rel=r_associated | relid=0 | w=10
  4422. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb involvement
    n1=DYNC2H1 gene | n2=en:upper limb involvement | rel=r_associated | relid=0 | w=10
  4423. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb involvement (in some patients)
    n1=DYNC2H1 gene | n2=en:upper limb involvement (in some patients) | rel=r_associated | relid=0 | w=10
  4424. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb involvement (onset in the first decade)
    n1=DYNC2H1 gene | n2=en:upper limb involvement (onset in the first decade) | rel=r_associated | relid=0 | w=10
  4425. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb involvement may occur
    n1=DYNC2H1 gene | n2=en:upper limb involvement may occur | rel=r_associated | relid=0 | w=10
  4426. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb spasticity
    n1=DYNC2H1 gene | n2=en:upper limb spasticity | rel=r_associated | relid=0 | w=10
  4427. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb spasticity (in some patients)
    n1=DYNC2H1 gene | n2=en:upper limb spasticity (in some patients) | rel=r_associated | relid=0 | w=10
  4428. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb spasticity (some)
    n1=DYNC2H1 gene | n2=en:upper limb spasticity (some) | rel=r_associated | relid=0 | w=10
  4429. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb spasticity, mild
    n1=DYNC2H1 gene | n2=en:upper limb spasticity, mild | rel=r_associated | relid=0 | w=10
  4430. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb weakness
    n1=DYNC2H1 gene | n2=en:upper limb weakness | rel=r_associated | relid=0 | w=10
  4431. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limb weakness may occur later
    n1=DYNC2H1 gene | n2=en:upper limb weakness may occur later | rel=r_associated | relid=0 | w=10
  4432. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limbs affected
    n1=DYNC2H1 gene | n2=en:upper limbs affected | rel=r_associated | relid=0 | w=10
  4433. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limbs may be affected
    n1=DYNC2H1 gene | n2=en:upper limbs may be affected | rel=r_associated | relid=0 | w=10
  4434. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limbs may show hyperreflexia
    n1=DYNC2H1 gene | n2=en:upper limbs may show hyperreflexia | rel=r_associated | relid=0 | w=10
  4435. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limbs may show mild involvement
    n1=DYNC2H1 gene | n2=en:upper limbs may show mild involvement | rel=r_associated | relid=0 | w=10
  4436. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper limbs more often affected than lower limbs
    n1=DYNC2H1 gene | n2=en:upper limbs more often affected than lower limbs | rel=r_associated | relid=0 | w=10
  4437. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper motor involvement (some patient)
    n1=DYNC2H1 gene | n2=en:upper motor involvement (some patient) | rel=r_associated | relid=0 | w=10
  4438. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper motor neuron degeneration
    n1=DYNC2H1 gene | n2=en:upper motor neuron degeneration | rel=r_associated | relid=0 | w=10
  4439. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper motor neuron dysfunction
    n1=DYNC2H1 gene | n2=en:upper motor neuron dysfunction | rel=r_associated | relid=0 | w=10
  4440. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper motor neuron signs
    n1=DYNC2H1 gene | n2=en:upper motor neuron signs | rel=r_associated | relid=0 | w=10
  4441. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper motor neuron signs (in some patients)
    n1=DYNC2H1 gene | n2=en:upper motor neuron signs (in some patients) | rel=r_associated | relid=0 | w=10
  4442. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper motor neuron signs, early
    n1=DYNC2H1 gene | n2=en:upper motor neuron signs, early | rel=r_associated | relid=0 | w=10
  4443. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper motor signs
    n1=DYNC2H1 gene | n2=en:upper motor signs | rel=r_associated | relid=0 | w=10
  4444. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:upper motor signs (in some patients)
    n1=DYNC2H1 gene | n2=en:upper motor signs (in some patients) | rel=r_associated | relid=0 | w=10
  4445. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:urinary incontinence
    n1=DYNC2H1 gene | n2=en:urinary incontinence | rel=r_associated | relid=0 | w=10
  4446. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:usually occurs at night
    n1=DYNC2H1 gene | n2=en:usually occurs at night | rel=r_associated | relid=0 | w=10
  4447. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vacuolated neurons
    n1=DYNC2H1 gene | n2=en:vacuolated neurons | rel=r_associated | relid=0 | w=10
  4448. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vacuolization (patient a)
    n1=DYNC2H1 gene | n2=en:vacuolization (patient a) | rel=r_associated | relid=0 | w=10
  4449. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vacuolizing myelinopathy
    n1=DYNC2H1 gene | n2=en:vacuolizing myelinopathy | rel=r_associated | relid=0 | w=10
  4450. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:variable delay (iq range 52-104)
    n1=DYNC2H1 gene | n2=en:variable delay (iq range 52-104) | rel=r_associated | relid=0 | w=10
  4451. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:variable intracranial abnormalities
    n1=DYNC2H1 gene | n2=en:variable intracranial abnormalities | rel=r_associated | relid=0 | w=10
  4452. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:variable mental retardation
    n1=DYNC2H1 gene | n2=en:variable mental retardation | rel=r_associated | relid=0 | w=10
  4453. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:variable mental retardation (40%)
    n1=DYNC2H1 gene | n2=en:variable mental retardation (40%) | rel=r_associated | relid=0 | w=10
  4454. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation
    n1=DYNC2H1 gene | n2=en:variable mental retardation ranging from severe neurodegeneration to mild mental retardation | rel=r_associated | relid=0 | w=10
  4455. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:variable neurologic deterioration (likely result of hemophagocytic syndrome)
    n1=DYNC2H1 gene | n2=en:variable neurologic deterioration (likely result of hemophagocytic syndrome) | rel=r_associated | relid=0 | w=10
  4456. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:variable outcome after acute illness
    n1=DYNC2H1 gene | n2=en:variable outcome after acute illness | rel=r_associated | relid=0 | w=10
  4457. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:varying degree of mental retardation
    n1=DYNC2H1 gene | n2=en:varying degree of mental retardation | rel=r_associated | relid=0 | w=10
  4458. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vasculopathy of the small arteries penetrating the white matter
    n1=DYNC2H1 gene | n2=en:vasculopathy of the small arteries penetrating the white matter | rel=r_associated | relid=0 | w=10
  4459. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vasoneurosis
    n1=DYNC2H1 gene | n2=en:vasoneurosis | rel=r_associated | relid=0 | w=10
  4460. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vasovagal syncope
    n1=DYNC2H1 gene | n2=en:vasovagal syncope | rel=r_associated | relid=0 | w=10
  4461. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vcp-positive inclusions
    n1=DYNC2H1 gene | n2=en:vcp-positive inclusions | rel=r_associated | relid=0 | w=10
  4462. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vegetative dystonia
    n1=DYNC2H1 gene | n2=en:vegetative dystonia | rel=r_associated | relid=0 | w=10
  4463. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vegetative nerve functional disturbance
    n1=DYNC2H1 gene | n2=en:vegetative nerve functional disturbance | rel=r_associated | relid=0 | w=10
  4464. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vegetative neurosis
    n1=DYNC2H1 gene | n2=en:vegetative neurosis | rel=r_associated | relid=0 | w=10
  4465. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vegetovascular dystonia
    n1=DYNC2H1 gene | n2=en:vegetovascular dystonia | rel=r_associated | relid=0 | w=10
  4466. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventricles slightly enlarged
    n1=DYNC2H1 gene | n2=en:ventricles slightly enlarged | rel=r_associated | relid=0 | w=10
  4467. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventricular anomalies
    n1=DYNC2H1 gene | n2=en:ventricular anomalies | rel=r_associated | relid=0 | w=10
  4468. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventricular asymmetry
    n1=DYNC2H1 gene | n2=en:ventricular asymmetry | rel=r_associated | relid=0 | w=10
  4469. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventricular dilatation (29%)
    n1=DYNC2H1 gene | n2=en:ventricular dilatation (29%) | rel=r_associated | relid=0 | w=10
  4470. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventricular dilatation (in some patients)
    n1=DYNC2H1 gene | n2=en:ventricular dilatation (in some patients) | rel=r_associated | relid=0 | w=10
  4471. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventricular dilatation (rare)
    n1=DYNC2H1 gene | n2=en:ventricular dilatation (rare) | rel=r_associated | relid=0 | w=10
  4472. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventricular enlargement
    n1=DYNC2H1 gene | n2=en:ventricular enlargement | rel=r_associated | relid=0 | w=10
  4473. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventricular enlargement, mild
    n1=DYNC2H1 gene | n2=en:ventricular enlargement, mild | rel=r_associated | relid=0 | w=10
  4474. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventriculomegaly (38%)
    n1=DYNC2H1 gene | n2=en:ventriculomegaly (38%) | rel=r_associated | relid=0 | w=10
  4475. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventriculomegaly (in some patients)
    n1=DYNC2H1 gene | n2=en:ventriculomegaly (in some patients) | rel=r_associated | relid=0 | w=10
  4476. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventriculomegaly (variable)
    n1=DYNC2H1 gene | n2=en:ventriculomegaly (variable) | rel=r_associated | relid=0 | w=10
  4477. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventriculomegaly, mild (rare)
    n1=DYNC2H1 gene | n2=en:ventriculomegaly, mild (rare) | rel=r_associated | relid=0 | w=10
  4478. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:ventriculomeglia
    n1=DYNC2H1 gene | n2=en:ventriculomeglia | rel=r_associated | relid=0 | w=10
  4479. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:verbal delay (in some patients)
    n1=DYNC2H1 gene | n2=en:verbal delay (in some patients) | rel=r_associated | relid=0 | w=10
  4480. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vermian hypoplasia
    n1=DYNC2H1 gene | n2=en:vermian hypoplasia | rel=r_associated | relid=0 | w=10
  4481. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vertical orientation of hippocampus
    n1=DYNC2H1 gene | n2=en:vertical orientation of hippocampus | rel=r_associated | relid=0 | w=10
  4482. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vertigo
    n1=DYNC2H1 gene | n2=en:vertigo | rel=r_associated | relid=0 | w=10
  4483. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vertigo, episodic (onset in second or third decade)
    n1=DYNC2H1 gene | n2=en:vertigo, episodic (onset in second or third decade) | rel=r_associated | relid=0 | w=10
  4484. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vertigo, mild
    n1=DYNC2H1 gene | n2=en:vertigo, mild | rel=r_associated | relid=0 | w=10
  4485. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:very poor expressive speech
    n1=DYNC2H1 gene | n2=en:very poor expressive speech | rel=r_associated | relid=0 | w=10
  4486. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vestibular anomalies (less common)
    n1=DYNC2H1 gene | n2=en:vestibular anomalies (less common) | rel=r_associated | relid=0 | w=10
  4487. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vestibular dysfunction
    n1=DYNC2H1 gene | n2=en:vestibular dysfunction | rel=r_associated | relid=0 | w=10
  4488. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vestibular dysfunction, mild
    n1=DYNC2H1 gene | n2=en:vestibular dysfunction, mild | rel=r_associated | relid=0 | w=10
  4489. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade)
    n1=DYNC2H1 gene | n2=en:vestibulopathy, bilateral, progressive (onset in fourth or fifth decade) | rel=r_associated | relid=0 | w=10
  4490. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:virtual absence of pyramidal tracts (wws)
    n1=DYNC2H1 gene | n2=en:virtual absence of pyramidal tracts (wws) | rel=r_associated | relid=0 | w=10
  4491. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visceroautonomic dysfunction
    n1=DYNC2H1 gene | n2=en:visceroautonomic dysfunction | rel=r_associated | relid=0 | w=10
  4492. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visual acuity is normal
    n1=DYNC2H1 gene | n2=en:visual acuity is normal | rel=r_associated | relid=0 | w=10
  4493. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visual auras
    n1=DYNC2H1 gene | n2=en:visual auras | rel=r_associated | relid=0 | w=10
  4494. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visual blackouts (stage 1)
    n1=DYNC2H1 gene | n2=en:visual blackouts (stage 1) | rel=r_associated | relid=0 | w=10
  4495. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visual changes
    n1=DYNC2H1 gene | n2=en:visual changes | rel=r_associated | relid=0 | w=10
  4496. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visual hallucination
    n1=DYNC2H1 gene | n2=en:visual hallucination | rel=r_associated | relid=0 | w=10
  4497. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visual hallucinations may occur
    n1=DYNC2H1 gene | n2=en:visual hallucinations may occur | rel=r_associated | relid=0 | w=10
  4498. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visual impairment
    n1=DYNC2H1 gene | n2=en:visual impairment | rel=r_associated | relid=0 | w=10
  4499. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visual inattention
    n1=DYNC2H1 gene | n2=en:visual inattention | rel=r_associated | relid=0 | w=10
  4500. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visual symptoms (in 60% of patients)
    n1=DYNC2H1 gene | n2=en:visual symptoms (in 60% of patients) | rel=r_associated | relid=0 | w=10
  4501. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:visuospatial agnosia (in a subset of patients)
    n1=DYNC2H1 gene | n2=en:visuospatial agnosia (in a subset of patients) | rel=r_associated | relid=0 | w=10
  4502. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:vocalization (finding)
    n1=DYNC2H1 gene | n2=en:vocalization (finding) | rel=r_associated | relid=0 | w=10
  4503. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:waddling gait
    n1=DYNC2H1 gene | n2=en:waddling gait | rel=r_associated | relid=0 | w=10
  4504. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:walking delay
    n1=DYNC2H1 gene | n2=en:walking delay | rel=r_associated | relid=0 | w=10
  4505. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:walking during slow-wave sleep (sleepwalking)
    n1=DYNC2H1 gene | n2=en:walking during slow-wave sleep (sleepwalking) | rel=r_associated | relid=0 | w=10
  4506. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:walking impairment due to myoclonus late in disease
    n1=DYNC2H1 gene | n2=en:walking impairment due to myoclonus late in disease | rel=r_associated | relid=0 | w=10
  4507. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:walking independently at 2.5 years to 4 years of age
    n1=DYNC2H1 gene | n2=en:walking independently at 2.5 years to 4 years of age | rel=r_associated | relid=0 | w=10
  4508. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:weak or absent tendon reflexes of knees and ankles (in some patients)
    n1=DYNC2H1 gene | n2=en:weak or absent tendon reflexes of knees and ankles (in some patients) | rel=r_associated | relid=0 | w=10
  4509. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:weakness
    n1=DYNC2H1 gene | n2=en:weakness | rel=r_associated | relid=0 | w=10
  4510. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:weakness of hip and ankle flexion
    n1=DYNC2H1 gene | n2=en:weakness of hip and ankle flexion | rel=r_associated | relid=0 | w=10
  4511. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:west syndrome
    n1=DYNC2H1 gene | n2=en:west syndrome | rel=r_associated | relid=0 | w=10
  4512. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white mater abnormalities in the posterior periventricular region
    n1=DYNC2H1 gene | n2=en:white mater abnormalities in the posterior periventricular region | rel=r_associated | relid=0 | w=10
  4513. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter
    n1=DYNC2H1 gene | n2=en:white matter | rel=r_associated | relid=0 | w=10
  4514. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter abnormalities (1 patient)
    n1=DYNC2H1 gene | n2=en:white matter abnormalities (1 patient) | rel=r_associated | relid=0 | w=10
  4515. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter abnormalities (in some)
    n1=DYNC2H1 gene | n2=en:white matter abnormalities (in some) | rel=r_associated | relid=0 | w=10
  4516. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter abnormalities (rare)
    n1=DYNC2H1 gene | n2=en:white matter abnormalities (rare) | rel=r_associated | relid=0 | w=10
  4517. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter abnormalities (uncommon)
    n1=DYNC2H1 gene | n2=en:white matter abnormalities (uncommon) | rel=r_associated | relid=0 | w=10
  4518. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter abnormalities in the periventricular regions (1 patient)
    n1=DYNC2H1 gene | n2=en:white matter abnormalities in the periventricular regions (1 patient) | rel=r_associated | relid=0 | w=10
  4519. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter abnormalities on mri
    n1=DYNC2H1 gene | n2=en:white matter abnormalities on mri | rel=r_associated | relid=0 | w=10
  4520. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter abnormalities seen on mri
    n1=DYNC2H1 gene | n2=en:white matter abnormalities seen on mri | rel=r_associated | relid=0 | w=10
  4521. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter abnormalities seen on mri which resolve over time
    n1=DYNC2H1 gene | n2=en:white matter abnormalities seen on mri which resolve over time | rel=r_associated | relid=0 | w=10
  4522. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter alterations (in one family)
    n1=DYNC2H1 gene | n2=en:white matter alterations (in one family) | rel=r_associated | relid=0 | w=10
  4523. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter changes
    n1=DYNC2H1 gene | n2=en:white matter changes | rel=r_associated | relid=0 | w=10
  4524. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter changes may occur (in adulthood)
    n1=DYNC2H1 gene | n2=en:white matter changes may occur (in adulthood) | rel=r_associated | relid=0 | w=10
  4525. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter changes on brain imaging (less common)
    n1=DYNC2H1 gene | n2=en:white matter changes on brain imaging (less common) | rel=r_associated | relid=0 | w=10
  4526. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter degeneration
    n1=DYNC2H1 gene | n2=en:white matter degeneration | rel=r_associated | relid=0 | w=10
  4527. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter dysmyelination/demyelination (71%)
    n1=DYNC2H1 gene | n2=en:white matter dysmyelination/demyelination (71%) | rel=r_associated | relid=0 | w=10
  4528. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter hyperintensities
    n1=DYNC2H1 gene | n2=en:white matter hyperintensities | rel=r_associated | relid=0 | w=10
  4529. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts
    n1=DYNC2H1 gene | n2=en:white matter hyperintensities (mri, t2 images) suggestive of old infarcts | rel=r_associated | relid=0 | w=10
  4530. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter hyperintensities in t2 imaging
    n1=DYNC2H1 gene | n2=en:white matter hyperintensities in t2 imaging | rel=r_associated | relid=0 | w=10
  4531. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter hyperintensities in various brain regions
    n1=DYNC2H1 gene | n2=en:white matter hyperintensities in various brain regions | rel=r_associated | relid=0 | w=10
  4532. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter hypodensities on brain imaging
    n1=DYNC2H1 gene | n2=en:white matter hypodensities on brain imaging | rel=r_associated | relid=0 | w=10
  4533. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter hypodensities seen on mri
    n1=DYNC2H1 gene | n2=en:white matter hypodensities seen on mri | rel=r_associated | relid=0 | w=10
  4534. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter immaturity
    n1=DYNC2H1 gene | n2=en:white matter immaturity | rel=r_associated | relid=0 | w=10
  4535. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter lacks axons and myelin
    n1=DYNC2H1 gene | n2=en:white matter lacks axons and myelin | rel=r_associated | relid=0 | w=10
  4536. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter lesion
    n1=DYNC2H1 gene | n2=en:white matter lesion | rel=r_associated | relid=0 | w=10
  4537. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter lesions (1 patient)
    n1=DYNC2H1 gene | n2=en:white matter lesions (1 patient) | rel=r_associated | relid=0 | w=10
  4538. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter lesions in the basal ganglia
    n1=DYNC2H1 gene | n2=en:white matter lesions in the basal ganglia | rel=r_associated | relid=0 | w=10
  4539. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter lesions in the brainstem may occur
    n1=DYNC2H1 gene | n2=en:white matter lesions in the brainstem may occur | rel=r_associated | relid=0 | w=10
  4540. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter lesions in the supratentorial white matter, brainstem, cerebellum, and spinal cord
    n1=DYNC2H1 gene | n2=en:white matter lesions in the supratentorial white matter, brainstem, cerebellum, and spinal cord | rel=r_associated | relid=0 | w=10
  4541. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter lesions may occur in the thalami, basal ganglia, and periventricular white matter (see leigh syndrome, 256000)
    n1=DYNC2H1 gene | 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=10
  4542. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter lesions seen on brain imaging
    n1=DYNC2H1 gene | n2=en:white matter lesions seen on brain imaging | rel=r_associated | relid=0 | w=10
  4543. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter neuronal heterotopia
    n1=DYNC2H1 gene | n2=en:white matter neuronal heterotopia | rel=r_associated | relid=0 | w=10
  4544. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter rarefaction and cystic degeneration
    n1=DYNC2H1 gene | n2=en:white matter rarefaction and cystic degeneration | rel=r_associated | relid=0 | w=10
  4545. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter signal abnormalities in the deep white matter and periventricular regions
    n1=DYNC2H1 gene | n2=en:white matter signal abnormalities in the deep white matter and periventricular regions | rel=r_associated | relid=0 | w=10
  4546. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter signal abnormalities in various brain regions
    n1=DYNC2H1 gene | n2=en:white matter signal abnormalities in various brain regions | rel=r_associated | relid=0 | w=10
  4547. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter streaks
    n1=DYNC2H1 gene | n2=en:white matter streaks | rel=r_associated | relid=0 | w=10
  4548. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:white matter vacuolization
    n1=DYNC2H1 gene | n2=en:white matter vacuolization | rel=r_associated | relid=0 | w=10
  4549. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:wide subarachnoid spaces
    n1=DYNC2H1 gene | n2=en:wide subarachnoid spaces | rel=r_associated | relid=0 | w=10
  4550. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:wide sylvian fissures
    n1=DYNC2H1 gene | n2=en:wide sylvian fissures | rel=r_associated | relid=0 | w=10
  4551. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:wide sylvian fissures with incomplete opercularization
    n1=DYNC2H1 gene | n2=en:wide sylvian fissures with incomplete opercularization | rel=r_associated | relid=0 | w=10
  4552. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widened lateral ventricles
    n1=DYNC2H1 gene | n2=en:widened lateral ventricles | rel=r_associated | relid=0 | w=10
  4553. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widened subarachnoid spaces
    n1=DYNC2H1 gene | n2=en:widened subarachnoid spaces | rel=r_associated | relid=0 | w=10
  4554. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widening of cortical sulci
    n1=DYNC2H1 gene | n2=en:widening of cortical sulci | rel=r_associated | relid=0 | w=10
  4555. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widening of the operculum
    n1=DYNC2H1 gene | n2=en:widening of the operculum | rel=r_associated | relid=0 | w=10
  4556. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widening of the spinal canal
    n1=DYNC2H1 gene | n2=en:widening of the spinal canal | rel=r_associated | relid=0 | w=10
  4557. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widening of the ventricles
    n1=DYNC2H1 gene | n2=en:widening of the ventricles | rel=r_associated | relid=0 | w=10
  4558. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widespread brain atrophy
    n1=DYNC2H1 gene | n2=en:widespread brain atrophy | rel=r_associated | relid=0 | w=10
  4559. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widespread brain calcifications
    n1=DYNC2H1 gene | n2=en:widespread brain calcifications | rel=r_associated | relid=0 | w=10
  4560. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widespread neuronal loss
    n1=DYNC2H1 gene | n2=en:widespread neuronal loss | rel=r_associated | relid=0 | w=10
  4561. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:widespread tau (mapt)-positive glial and neuronal inclusions
    n1=DYNC2H1 gene | n2=en:widespread tau (mapt)-positive glial and neuronal inclusions | rel=r_associated | relid=0 | w=10
  4562. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:word finding difficulty (disorder)
    n1=DYNC2H1 gene | n2=en:word finding difficulty (disorder) | rel=r_associated | relid=0 | w=10
  4563. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> en:writing fatigability
    n1=DYNC2H1 gene | n2=en:writing fatigability | rel=r_associated | relid=0 | w=10
  4564. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> enfant
    n1=DYNC2H1 gene | n2=enfant | rel=r_associated | relid=0 | w=10
  4565. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> entendre
    n1=DYNC2H1 gene | n2=entendre | rel=r_associated | relid=0 | w=10
  4566. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> fatigue
    n1=DYNC2H1 gene | n2=fatigue | rel=r_associated | relid=0 | w=10
  4567. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> fatigue
    (physiologie, faiblesse physique)
    n1=DYNC2H1 gene | n2=fatigue
    (physiologie, faiblesse physique)
    | rel=r_associated | relid=0 | w=10
  4568. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> frustration
    n1=DYNC2H1 gene | n2=frustration | rel=r_associated | relid=0 | w=10
  4569. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> gras
    n1=DYNC2H1 gene | n2=gras | rel=r_associated | relid=0 | w=10
  4570. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> handicap
    n1=DYNC2H1 gene | n2=handicap | rel=r_associated | relid=0 | w=10
  4571. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> hyperacousie
    n1=DYNC2H1 gene | n2=hyperacousie | rel=r_associated | relid=0 | w=10
  4572. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> hyperesthésie auditive
    n1=DYNC2H1 gene | n2=hyperesthésie auditive | rel=r_associated | relid=0 | w=10
  4573. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> hypotension orthostatique idiopathique et neurologie
    n1=DYNC2H1 gene | n2=hypotension orthostatique idiopathique et neurologie | rel=r_associated | relid=0 | w=10
  4574. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> insomnie familiale fatale
    n1=DYNC2H1 gene | n2=insomnie familiale fatale | rel=r_associated | relid=0 | w=10
  4575. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> isolement
    n1=DYNC2H1 gene | n2=isolement | rel=r_associated | relid=0 | w=10
  4576. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> Kennedy (atrophie spinobulbaire de)
    n1=DYNC2H1 gene | n2=Kennedy (atrophie spinobulbaire de) | rel=r_associated | relid=0 | w=10
  4577. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> langage
    n1=DYNC2H1 gene | n2=langage | rel=r_associated | relid=0 | w=10
  4578. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> langage empâté
    n1=DYNC2H1 gene | n2=langage empâté | rel=r_associated | relid=0 | w=10
  4579. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> langage incohérent
    n1=DYNC2H1 gene | n2=langage incohérent | rel=r_associated | relid=0 | w=10
  4580. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> lésion
    n1=DYNC2H1 gene | n2=lésion | rel=r_associated | relid=0 | w=10
  4581. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> lésion
    (médecine)
    n1=DYNC2H1 gene | n2=lésion
    (médecine)
    | rel=r_associated | relid=0 | w=10
  4582. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> maladie de Parkinson
    n1=DYNC2H1 gene | n2=maladie de Parkinson | rel=r_associated | relid=0 | w=10
  4583. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> maladie
    (médecine)
    n1=DYNC2H1 gene | n2=maladie
    (médecine)
    | rel=r_associated | relid=0 | w=10
  4584. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> maladies
    n1=DYNC2H1 gene | n2=maladies | rel=r_associated | relid=0 | w=10
  4585. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> maladies du système nerveux autonome
    n1=DYNC2H1 gene | n2=maladies du système nerveux autonome | rel=r_associated | relid=0 | w=10
  4586. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> maladies du système nerveux périphérique autonome
    n1=DYNC2H1 gene | n2=maladies du système nerveux périphérique autonome | rel=r_associated | relid=0 | w=10
  4587. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> maladies du système nerveux végétatif
    n1=DYNC2H1 gene | n2=maladies du système nerveux végétatif | rel=r_associated | relid=0 | w=10
  4588. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> mogiarthie (désuet)
    n1=DYNC2H1 gene | n2=mogiarthie (désuet) | rel=r_associated | relid=0 | w=10
  4589. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> mucopolysaccharidose de type VII
    n1=DYNC2H1 gene | n2=mucopolysaccharidose de type VII | rel=r_associated | relid=0 | w=10
  4590. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> musiciens
    n1=DYNC2H1 gene | n2=musiciens | rel=r_associated | relid=0 | w=10
  4591. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> nausées
    n1=DYNC2H1 gene | n2=nausées | rel=r_associated | relid=0 | w=10
  4592. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> neurologie
    n1=DYNC2H1 gene | n2=neurologie | rel=r_associated | relid=0 | w=10
  4593. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> neuropathie héréditaire sensitive
    n1=DYNC2H1 gene | n2=neuropathie héréditaire sensitive | rel=r_associated | relid=0 | w=10
  4594. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> neuropathie végétative
    n1=DYNC2H1 gene | n2=neuropathie végétative | rel=r_associated | relid=0 | w=10
  4595. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> obèse
    n1=DYNC2H1 gene | n2=obèse | rel=r_associated | relid=0 | w=10
  4596. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> odynacousie
    n1=DYNC2H1 gene | n2=odynacousie | rel=r_associated | relid=0 | w=10
  4597. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> oreille
    n1=DYNC2H1 gene | n2=oreille | rel=r_associated | relid=0 | w=10
  4598. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> oreille
    (organe)
    n1=DYNC2H1 gene | n2=oreille
    (organe)
    | rel=r_associated | relid=0 | w=10
  4599. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> oreille
    (ouïe)
    n1=DYNC2H1 gene | n2=oreille
    (ouïe)
    | rel=r_associated | relid=0 | w=10
  4600. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> oreilles
    n1=DYNC2H1 gene | n2=oreilles | rel=r_associated | relid=0 | w=10
  4601. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> ORL
    (oto-rhino-laryngologiste)
    n1=DYNC2H1 gene | n2=ORL
    (oto-rhino-laryngologiste)
    | rel=r_associated | relid=0 | w=10
  4602. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> otalgie
    n1=DYNC2H1 gene | n2=otalgie | rel=r_associated | relid=0 | w=10
  4603. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> oto-rhino-laryngologiste
    n1=DYNC2H1 gene | n2=oto-rhino-laryngologiste | rel=r_associated | relid=0 | w=10
  4604. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> ouïe
    n1=DYNC2H1 gene | n2=ouïe | rel=r_associated | relid=0 | w=10
  4605. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> ouïe
    (sens)
    n1=DYNC2H1 gene | n2=ouïe
    (sens)
    | rel=r_associated | relid=0 | w=10
  4606. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> ouïr
    n1=DYNC2H1 gene | n2=ouïr | rel=r_associated | relid=0 | w=10
  4607. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> palilalie
    n1=DYNC2H1 gene | n2=palilalie | rel=r_associated | relid=0 | w=10
  4608. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> pandysautonomie aigüe
    n1=DYNC2H1 gene | n2=pandysautonomie aigüe | rel=r_associated | relid=0 | w=10
  4609. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> pandysautonomie aigüe réversible
    n1=DYNC2H1 gene | n2=pandysautonomie aigüe réversible | rel=r_associated | relid=0 | w=10
  4610. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> paranéoplasiques (syndromes neurologiques et auto-immunité)
    n1=DYNC2H1 gene | n2=paranéoplasiques (syndromes neurologiques et auto-immunité) | rel=r_associated | relid=0 | w=10
  4611. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> parler
    n1=DYNC2H1 gene | n2=parler | rel=r_associated | relid=0 | w=10
  4612. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> parler
    (dialoguer)
    n1=DYNC2H1 gene | n2=parler
    (dialoguer)
    | rel=r_associated | relid=0 | w=10
  4613. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> parole
    n1=DYNC2H1 gene | n2=parole | rel=r_associated | relid=0 | w=10
  4614. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> parole embarrassée
    n1=DYNC2H1 gene | n2=parole embarrassée | rel=r_associated | relid=0 | w=10
  4615. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> parole
    (éloquence)
    n1=DYNC2H1 gene | n2=parole
    (éloquence)
    | rel=r_associated | relid=0 | w=10
  4616. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> pathologie
    (maladie)
    n1=DYNC2H1 gene | n2=pathologie
    (maladie)
    | rel=r_associated | relid=0 | w=10
  4617. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> phobie
    n1=DYNC2H1 gene | n2=phobie | rel=r_associated | relid=0 | w=10
  4618. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> phonophobie
    n1=DYNC2H1 gene | n2=phonophobie | rel=r_associated | relid=0 | w=10
  4619. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> polyradiculonévrite chronique
    n1=DYNC2H1 gene | n2=polyradiculonévrite chronique | rel=r_associated | relid=0 | w=10
  4620. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> renflé
    n1=DYNC2H1 gene | n2=renflé | rel=r_associated | relid=0 | w=10
  4621. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> Riley-Day (syndrome de)
    n1=DYNC2H1 gene | n2=Riley-Day (syndrome de) | rel=r_associated | relid=0 | w=10
  4622. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> rythme saccadé
    n1=DYNC2H1 gene | n2=rythme saccadé | rel=r_associated | relid=0 | w=10
  4623. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> sclérose en plaques
    n1=DYNC2H1 gene | n2=sclérose en plaques | rel=r_associated | relid=0 | w=10
  4624. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> signe clinique
    n1=DYNC2H1 gene | n2=signe clinique | rel=r_associated | relid=0 | w=10
  4625. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> solitude
    n1=DYNC2H1 gene | n2=solitude | rel=r_associated | relid=0 | w=10
  4626. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> son
    n1=DYNC2H1 gene | n2=son | rel=r_associated | relid=0 | w=10
  4627. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> son
    (bruit)
    n1=DYNC2H1 gene | n2=son
    (bruit)
    | rel=r_associated | relid=0 | w=10
  4628. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> sons
    n1=DYNC2H1 gene | n2=sons | rel=r_associated | relid=0 | w=10
  4629. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> stress
    n1=DYNC2H1 gene | n2=stress | rel=r_associated | relid=0 | w=10
  4630. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> surdité
    n1=DYNC2H1 gene | n2=surdité | rel=r_associated | relid=0 | w=10
  4631. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> sympathique
    n1=DYNC2H1 gene | n2=sympathique | rel=r_associated | relid=0 | w=10
  4632. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> symptôme
    n1=DYNC2H1 gene | n2=symptôme | rel=r_associated | relid=0 | w=10
  4633. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> syndrome
    n1=DYNC2H1 gene | n2=syndrome | rel=r_associated | relid=0 | w=10
  4634. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> syndrome de
    n1=DYNC2H1 gene | n2=syndrome de | rel=r_associated | relid=0 | w=10
  4635. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> syndrome de Allgrove
    n1=DYNC2H1 gene | n2=syndrome de Allgrove | rel=r_associated | relid=0 | w=10
  4636. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> syndrome de Marinesco-Sjögren
    n1=DYNC2H1 gene | n2=syndrome de Marinesco-Sjögren | rel=r_associated | relid=0 | w=10
  4637. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> syndrome de Wadia-Swami
    n1=DYNC2H1 gene | n2=syndrome de Wadia-Swami | rel=r_associated | relid=0 | w=10
  4638. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> système nerveux
    n1=DYNC2H1 gene | n2=système nerveux | rel=r_associated | relid=0 | w=10
  4639. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> système nerveux central
    n1=DYNC2H1 gene | n2=système nerveux central | rel=r_associated | relid=0 | w=10
  4640. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> trouble auditif
    n1=DYNC2H1 gene | n2=trouble auditif | rel=r_associated | relid=0 | w=10
  4641. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> trouble audition
    n1=DYNC2H1 gene | n2=trouble audition | rel=r_associated | relid=0 | w=10
  4642. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> trouble de l'audition
    n1=DYNC2H1 gene | n2=trouble de l'audition | rel=r_associated | relid=0 | w=10
  4643. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> trouble de la parole
    n1=DYNC2H1 gene | n2=trouble de la parole | rel=r_associated | relid=0 | w=10
  4644. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> trouble du développement de l'articulation
    n1=DYNC2H1 gene | n2=trouble du développement de l'articulation | rel=r_associated | relid=0 | w=10
  4645. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> trouble du langage
    n1=DYNC2H1 gene | n2=trouble du langage | rel=r_associated | relid=0 | w=10
  4646. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> troubles auditifs
    n1=DYNC2H1 gene | n2=troubles auditifs | rel=r_associated | relid=0 | w=10
  4647. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> troubles audition
    n1=DYNC2H1 gene | n2=troubles audition | rel=r_associated | relid=0 | w=10
  4648. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> troubles de audition
    n1=DYNC2H1 gene | n2=troubles de audition | rel=r_associated | relid=0 | w=10
  4649. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> troubles de l'acquisition de l'articulation
    n1=DYNC2H1 gene | n2=troubles de l'acquisition de l'articulation | rel=r_associated | relid=0 | w=10
  4650. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> troubles de l'audition
    n1=DYNC2H1 gene | n2=troubles de l'audition | rel=r_associated | relid=0 | w=10
  4651. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> troubles de la parole
    n1=DYNC2H1 gene | n2=troubles de la parole | rel=r_associated | relid=0 | w=10
  4652. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> VIH (neuropathies du)
    n1=DYNC2H1 gene | n2=VIH (neuropathies du) | rel=r_associated | relid=0 | w=10
  4653. DYNC2H1 gene -- r_associated #0: 10 / 0.139 -> Young et Adams (pandysautonomie aigüe de)
    n1=DYNC2H1 gene | n2=Young et Adams (pandysautonomie aigüe de) | rel=r_associated | relid=0 | w=10
  4654. DYNC2H1 gene -- r_associated #0: 5 / 0.069 -> sarcopénie
    n1=DYNC2H1 gene | n2=sarcopénie | rel=r_associated | relid=0 | w=5
≈ 35 relations entrantes

  1. médecine --- r_associated #0: 61 --> DYNC2H1 gene
    n1=médecine | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=61
  2. dysplasie thoracique asphyxiante --- r_associated #0: 40 --> DYNC2H1 gene
    n1=dysplasie thoracique asphyxiante | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=40
  3. fr. DEXA --- r_associated #0: 30 --> DYNC2H1 gene
    n1=fr. DEXA | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=30
  4. dynapénia --- r_associated #0: 26 --> DYNC2H1 gene
    n1=dynapénia | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=26
  5. DYNC2H1 --- r_associated #0: 20 --> DYNC2H1 gene
    n1=DYNC2H1 | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=20
  6. gene --- r_associated #0: 20 --> DYNC2H1 gene
    n1=gene | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=20
  7. dynamique (point de vue) --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dynamique (point de vue) | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  8. dynamométre --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dynamométre | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  9. dynamométrie --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dynamométrie | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  10. dynode --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dynode | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  11. dynorphine --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dynorphine | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  12. dynéine --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dynéine | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  13. dysacousie --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dysacousie | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  14. dysarthrie --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dysarthrie | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  15. dysarthrie de l'enfant --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dysarthrie de l'enfant | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  16. dysautonomie --- r_associated #0: 15 --> DYNC2H1 gene
    n1=dysautonomie | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  17. en:dynamic point of view --- r_associated #0: 15 --> DYNC2H1 gene
    n1=en:dynamic point of view | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=15
  18. Dynamométrie --- r_associated #0: 10 --> DYNC2H1 gene
    n1=Dynamométrie | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  19. Dysarthrie --- r_associated #0: 10 --> DYNC2H1 gene
    n1=Dysarthrie | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  20. Dysautonomie --- r_associated #0: 10 --> DYNC2H1 gene
    n1=Dysautonomie | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  21. en:child dysarthria --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:child dysarthria | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  22. en:dynamometer --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dynamometer | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  23. en:dynamometry --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dynamometry | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  24. en:dynein --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dynein | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  25. en:dynod --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dynod | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  26. en:dynorphin --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dynorphin | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  27. en:dysacousia --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dysacousia | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  28. en:dysacousma --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dysacousma | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  29. en:dysacusis --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dysacusis | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  30. en:dysarthria --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dysarthria | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  31. en:dysautonomia --- r_associated #0: 10 --> DYNC2H1 gene
    n1=en:dysautonomia | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=10
  32. dydrogestone --- r_associated #0: 5 --> DYNC2H1 gene
    n1=dydrogestone | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=5
  33. dye-test --- r_associated #0: 5 --> DYNC2H1 gene
    n1=dye-test | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=5
  34. dynamine --- r_associated #0: 5 --> DYNC2H1 gene
    n1=dynamine | n2=DYNC2H1 gene | rel=r_associated | relid=0 | w=5
  35. dysautonomie dégénérative --- r_associated #0: 5 --> DYNC2H1 gene
    n1=dysautonomie dégénérative | n2=DYNC2H1 gene | 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