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'Refsum (maladie de)'
(id=16811482 ; fe=Refsum (maladie de) ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=9742 creation date=2021-07-24 touchdate=2026-04-24 08:31:55.000)
≈ 309 relations sortantes

  1. Refsum (maladie de) -- r_associated #0: 206 / 1 -> médecine
    n1=Refsum (maladie de) | n2=médecine | rel=r_associated | relid=0 | w=206
  2. Refsum (maladie de) -- r_associated #0: 67 / 0.325 -> maladie
    n1=Refsum (maladie de) | n2=maladie | rel=r_associated | relid=0 | w=67
  3. Refsum (maladie de) -- r_associated #0: 67 / 0.325 -> Refsum
    n1=Refsum (maladie de) | n2=Refsum | rel=r_associated | relid=0 | w=67
  4. Refsum (maladie de) -- r_associated #0: 60 / 0.291 -> acide phytanique
    n1=Refsum (maladie de) | n2=acide phytanique | rel=r_associated | relid=0 | w=60
  5. Refsum (maladie de) -- r_associated #0: 60 / 0.291 -> acide pipécolique
    n1=Refsum (maladie de) | n2=acide pipécolique | rel=r_associated | relid=0 | w=60
  6. Refsum (maladie de) -- r_associated #0: 53 / 0.257 -> maladies
    n1=Refsum (maladie de) | n2=maladies | rel=r_associated | relid=0 | w=53
  7. Refsum (maladie de) -- r_associated #0: 51 / 0.248 -> atrophie musculaire, ataxie, rétinite pigmentaire et diabète sucré
    n1=Refsum (maladie de) | n2=atrophie musculaire, ataxie, rétinite pigmentaire et diabète sucré | rel=r_associated | relid=0 | w=51
  8. Refsum (maladie de) -- r_associated #0: 48 / 0.233 -> en:demyelination
    n1=Refsum (maladie de) | n2=en:demyelination | rel=r_associated | relid=0 | w=48
  9. Refsum (maladie de) -- r_associated #0: 48 / 0.233 -> en:hereditary peripheral neuropathy
    n1=Refsum (maladie de) | n2=en:hereditary peripheral neuropathy | rel=r_associated | relid=0 | w=48
  10. Refsum (maladie de) -- r_associated #0: 48 / 0.233 -> en:wolman disease
    n1=Refsum (maladie de) | n2=en:wolman disease | rel=r_associated | relid=0 | w=48
  11. Refsum (maladie de) -- r_associated #0: 47 / 0.228 -> en:acid cholesteryl ester hydrolase deficiency, type 2
    n1=Refsum (maladie de) | n2=en:acid cholesteryl ester hydrolase deficiency, type 2 | rel=r_associated | relid=0 | w=47
  12. Refsum (maladie de) -- r_associated #0: 47 / 0.228 -> en:neuropathy, hereditary motor and sensory, okinawa type
    n1=Refsum (maladie de) | n2=en:neuropathy, hereditary motor and sensory, okinawa type | rel=r_associated | relid=0 | w=47
  13. Refsum (maladie de) -- r_associated #0: 47 / 0.228 -> en:Refsum's disease
    n1=Refsum (maladie de) | n2=en:Refsum's disease | rel=r_associated | relid=0 | w=47
  14. Refsum (maladie de) -- r_associated #0: 47 / 0.228 -> mal
    n1=Refsum (maladie de) | n2=mal | rel=r_associated | relid=0 | w=47
  15. Refsum (maladie de) -- r_associated #0: 47 / 0.228 -> maladie de l'écaille du poisson
    n1=Refsum (maladie de) | n2=maladie de l'écaille du poisson | rel=r_associated | relid=0 | w=47
  16. Refsum (maladie de) -- r_associated #0: 46 / 0.223 -> en:glycogen storage disease
    n1=Refsum (maladie de) | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=46
  17. Refsum (maladie de) -- r_associated #0: 46 / 0.223 -> en:late onset globoid cell leukodystrophy
    n1=Refsum (maladie de) | n2=en:late onset globoid cell leukodystrophy | rel=r_associated | relid=0 | w=46
  18. Refsum (maladie de) -- r_associated #0: 46 / 0.223 -> en:long-chain fatty acid transport deficiency
    n1=Refsum (maladie de) | n2=en:long-chain fatty acid transport deficiency | rel=r_associated | relid=0 | w=46
  19. Refsum (maladie de) -- r_associated #0: 45 / 0.218 -> déficit en acide phytanique-oxydase
    n1=Refsum (maladie de) | n2=déficit en acide phytanique-oxydase | rel=r_associated | relid=0 | w=45
  20. Refsum (maladie de) -- r_associated #0: 45 / 0.218 -> en:gaucher disease
    n1=Refsum (maladie de) | n2=en:gaucher disease | rel=r_associated | relid=0 | w=45
  21. Refsum (maladie de) -- r_associated #0: 45 / 0.218 -> en:infantile refsum disease
    n1=Refsum (maladie de) | n2=en:infantile refsum disease | rel=r_associated | relid=0 | w=45
  22. Refsum (maladie de) -- r_associated #0: 45 / 0.218 -> en:other peroxisomal disorders
    n1=Refsum (maladie de) | n2=en:other peroxisomal disorders | rel=r_associated | relid=0 | w=45
  23. Refsum (maladie de) -- r_associated #0: 45 / 0.218 -> hérédopathie ataxique polyneuritiforme
    n1=Refsum (maladie de) | n2=hérédopathie ataxique polyneuritiforme | rel=r_associated | relid=0 | w=45
  24. Refsum (maladie de) -- r_associated #0: 44 / 0.214 -> en:carnitine palmitoyltransferase ii deficiency
    n1=Refsum (maladie de) | n2=en:carnitine palmitoyltransferase ii deficiency | rel=r_associated | relid=0 | w=44
  25. Refsum (maladie de) -- r_associated #0: 44 / 0.214 -> en:historical aspects qualifier
    n1=Refsum (maladie de) | n2=en:historical aspects qualifier | rel=r_associated | relid=0 | w=44
  26. Refsum (maladie de) -- r_associated #0: 44 / 0.214 -> en:i-cell disease
    n1=Refsum (maladie de) | n2=en:i-cell disease | rel=r_associated | relid=0 | w=44
  27. Refsum (maladie de) -- r_associated #0: 44 / 0.214 -> en:microbiological
    n1=Refsum (maladie de) | n2=en:microbiological | rel=r_associated | relid=0 | w=44
  28. Refsum (maladie de) -- r_associated #0: 43 / 0.209 -> en:affected infants appear normal
    n1=Refsum (maladie de) | n2=en:affected infants appear normal | rel=r_associated | relid=0 | w=43
  29. Refsum (maladie de) -- r_associated #0: 43 / 0.209 -> en:dysfunctions, single peroxisomal
    n1=Refsum (maladie de) | n2=en:dysfunctions, single peroxisomal | rel=r_associated | relid=0 | w=43
  30. Refsum (maladie de) -- r_associated #0: 43 / 0.209 -> en:mucolipidosis type iv
    n1=Refsum (maladie de) | n2=en:mucolipidosis type iv | rel=r_associated | relid=0 | w=43
  31. Refsum (maladie de) -- r_associated #0: 43 / 0.209 -> ichthyose congénitale
    n1=Refsum (maladie de) | n2=ichthyose congénitale | rel=r_associated | relid=0 | w=43
  32. Refsum (maladie de) -- r_associated #0: 43 / 0.209 -> maladie de surcharge en acide phytanique
    n1=Refsum (maladie de) | n2=maladie de surcharge en acide phytanique | rel=r_associated | relid=0 | w=43
  33. Refsum (maladie de) -- r_associated #0: 42 / 0.204 -> en:autosomal dominant retinitis pigmentosa
    n1=Refsum (maladie de) | n2=en:autosomal dominant retinitis pigmentosa | rel=r_associated | relid=0 | w=42
  34. Refsum (maladie de) -- r_associated #0: 42 / 0.204 -> en:dysmyelinating leukodystrophy
    n1=Refsum (maladie de) | n2=en:dysmyelinating leukodystrophy | rel=r_associated | relid=0 | w=42
  35. Refsum (maladie de) -- r_associated #0: 42 / 0.204 -> en:heredo-ataxia hemeralopica polyneuritiformis
    n1=Refsum (maladie de) | n2=en:heredo-ataxia hemeralopica polyneuritiformis | rel=r_associated | relid=0 | w=42
  36. Refsum (maladie de) -- r_associated #0: 42 / 0.204 -> en:neuraminidase deficiency
    n1=Refsum (maladie de) | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=42
  37. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:2,4-dienoyl-coa reductase deficiency
    n1=Refsum (maladie de) | n2=en:2,4-dienoyl-coa reductase deficiency | rel=r_associated | relid=0 | w=41
  38. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:acyl-coa dehydrogenase, short-chain deficiency
    n1=Refsum (maladie de) | n2=en:acyl-coa dehydrogenase, short-chain deficiency | rel=r_associated | relid=0 | w=41
  39. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:anosmia
    n1=Refsum (maladie de) | n2=en:anosmia | rel=r_associated | relid=0 | w=41
  40. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:autosomal recessive trait
    n1=Refsum (maladie de) | n2=en:autosomal recessive trait | rel=r_associated | relid=0 | w=41
  41. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:cerebral degeneration in generalized lipidoses
    n1=Refsum (maladie de) | n2=en:cerebral degeneration in generalized lipidoses | rel=r_associated | relid=0 | w=41
  42. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:charcot-marie-tooth disease, type 4d
    n1=Refsum (maladie de) | n2=en:charcot-marie-tooth disease, type 4d | rel=r_associated | relid=0 | w=41
  43. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:dejerine-sottas disease (disorder)
    n1=Refsum (maladie de) | n2=en:dejerine-sottas disease (disorder) | rel=r_associated | relid=0 | w=41
  44. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:fabry disease
    n1=Refsum (maladie de) | n2=en:fabry disease | rel=r_associated | relid=0 | w=41
  45. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:homocystinuria
    n1=Refsum (maladie de) | n2=en:homocystinuria | rel=r_associated | relid=0 | w=41
  46. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:maroteaux-lamy syndrome
    n1=Refsum (maladie de) | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=41
  47. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:niemann-pick disease
    n1=Refsum (maladie de) | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=41
  48. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:oculocerebrorenal syndrome
    n1=Refsum (maladie de) | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=41
  49. Refsum (maladie de) -- r_associated #0: 41 / 0.199 -> en:other disorders of fatty-acid metabolism
    n1=Refsum (maladie de) | n2=en:other disorders of fatty-acid metabolism | rel=r_associated | relid=0 | w=41
  50. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:aicardi syndrome
    n1=Refsum (maladie de) | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=40
  51. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:charcot-marie-tooth disease type 4
    n1=Refsum (maladie de) | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=40
  52. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:charcot-marie-tooth neuropathy x type 1
    n1=Refsum (maladie de) | n2=en:charcot-marie-tooth neuropathy x type 1 | rel=r_associated | relid=0 | w=40
  53. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:congenital
    n1=Refsum (maladie de) | n2=en:congenital | rel=r_associated | relid=0 | w=40
  54. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:disorders of fatty acid oxidation
    n1=Refsum (maladie de) | n2=en:disorders of fatty acid oxidation | rel=r_associated | relid=0 | w=40
  55. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:hereditary motor and sensory neuropathy type i
    n1=Refsum (maladie de) | n2=en:hereditary motor and sensory neuropathy type i | rel=r_associated | relid=0 | w=40
  56. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:hereditary motor and sensory-neuropathy type ii
    n1=Refsum (maladie de) | n2=en:hereditary motor and sensory-neuropathy type ii | rel=r_associated | relid=0 | w=40
  57. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:hmsn type viis
    n1=Refsum (maladie de) | n2=en:hmsn type viis | rel=r_associated | relid=0 | w=40
  58. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:leukodystrophy
    n1=Refsum (maladie de) | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=40
  59. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:malonic aciduria
    n1=Refsum (maladie de) | n2=en:malonic aciduria | rel=r_associated | relid=0 | w=40
  60. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=Refsum (maladie de) | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=40
  61. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:merrf syndrome
    n1=Refsum (maladie de) | n2=en:merrf syndrome | rel=r_associated | relid=0 | w=40
  62. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:metachromatic leukodystrophy
    n1=Refsum (maladie de) | n2=en:metachromatic leukodystrophy | rel=r_associated | relid=0 | w=40
  63. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:multiple acyl-coa dehydrogenase deficiency
    n1=Refsum (maladie de) | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=40
  64. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:myelin sheath alteration
    n1=Refsum (maladie de) | n2=en:myelin sheath alteration | rel=r_associated | relid=0 | w=40
  65. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:peroxisomal disorder
    n1=Refsum (maladie de) | n2=en:peroxisomal disorder | rel=r_associated | relid=0 | w=40
  66. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:pex7 gene
    n1=Refsum (maladie de) | n2=en:pex7 gene | rel=r_associated | relid=0 | w=40
  67. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:physiopathological
    n1=Refsum (maladie de) | n2=en:physiopathological | rel=r_associated | relid=0 | w=40
  68. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:pigmentary retinal deposits
    n1=Refsum (maladie de) | n2=en:pigmentary retinal deposits | rel=r_associated | relid=0 | w=40
  69. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:retinal dystrophy in systemic lipidosis
    n1=Refsum (maladie de) | n2=en:retinal dystrophy in systemic lipidosis | rel=r_associated | relid=0 | w=40
  70. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:sandhoff disease
    n1=Refsum (maladie de) | n2=en:sandhoff disease | rel=r_associated | relid=0 | w=40
  71. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:sanfilippo syndrome
    n1=Refsum (maladie de) | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=40
  72. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:sensory neuropathy, hereditary
    n1=Refsum (maladie de) | n2=en:sensory neuropathy, hereditary | rel=r_associated | relid=0 | w=40
  73. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:sly syndrome
    n1=Refsum (maladie de) | n2=en:sly syndrome | rel=r_associated | relid=0 | w=40
  74. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:sphingolipidosis
    n1=Refsum (maladie de) | n2=en:sphingolipidosis | rel=r_associated | relid=0 | w=40
  75. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:veterinary aspects
    n1=Refsum (maladie de) | n2=en:veterinary aspects | rel=r_associated | relid=0 | w=40
  76. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> en:zellweger syndrome
    n1=Refsum (maladie de) | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=40
  77. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> hérédopathie atactique polynévritiforme
    n1=Refsum (maladie de) | n2=hérédopathie atactique polynévritiforme | rel=r_associated | relid=0 | w=40
  78. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> ichtyose congénitale
    n1=Refsum (maladie de) | n2=ichtyose congénitale | rel=r_associated | relid=0 | w=40
  79. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> maladie de
    n1=Refsum (maladie de) | n2=maladie de | rel=r_associated | relid=0 | w=40
  80. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> maladie de refsum
    n1=Refsum (maladie de) | n2=maladie de refsum | rel=r_associated | relid=0 | w=40
  81. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> peroxysomopathie
    n1=Refsum (maladie de) | n2=peroxysomopathie | rel=r_associated | relid=0 | w=40
  82. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> processus pathologique
    n1=Refsum (maladie de) | n2=processus pathologique | rel=r_associated | relid=0 | w=40
  83. Refsum (maladie de) -- r_associated #0: 40 / 0.194 -> syndrome de Dejerine-Sottas
    n1=Refsum (maladie de) | n2=syndrome de Dejerine-Sottas | rel=r_associated | relid=0 | w=40
  84. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:adrenoleukodystrophy
    n1=Refsum (maladie de) | n2=en:adrenoleukodystrophy | rel=r_associated | relid=0 | w=39
  85. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:adult onset autosomal dominant leukodystrophy
    n1=Refsum (maladie de) | n2=en:adult onset autosomal dominant leukodystrophy | rel=r_associated | relid=0 | w=39
  86. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:alexander disease
    n1=Refsum (maladie de) | n2=en:alexander disease | rel=r_associated | relid=0 | w=39
  87. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:aspects of radionuclide imaging
    n1=Refsum (maladie de) | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=39
  88. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:autosomal recessive retinitis pigmentosa
    n1=Refsum (maladie de) | n2=en:autosomal recessive retinitis pigmentosa | rel=r_associated | relid=0 | w=39
  89. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:cardiac failure (sudden death has been reported)
    n1=Refsum (maladie de) | n2=en:cardiac failure (sudden death has been reported) | rel=r_associated | relid=0 | w=39
  90. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:carnitine deficiency due to inborn error of metabolism
    n1=Refsum (maladie de) | n2=en:carnitine deficiency due to inborn error of metabolism | rel=r_associated | relid=0 | w=39
  91. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:carnitine palmitoyltransferase i deficiency
    n1=Refsum (maladie de) | n2=en:carnitine palmitoyltransferase i deficiency | rel=r_associated | relid=0 | w=39
  92. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:chemically induced
    n1=Refsum (maladie de) | n2=en:chemically induced | rel=r_associated | relid=0 | w=39
  93. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:combined deficiency of long chain 3-hydroxyacyl-coa dehydrogenase and enoyl-coa hydratase
    n1=Refsum (maladie de) | n2=en:combined deficiency of long chain 3-hydroxyacyl-coa dehydrogenase and enoyl-coa hydratase | rel=r_associated | relid=0 | w=39
  94. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:epidemiologic
    n1=Refsum (maladie de) | n2=en:epidemiologic | rel=r_associated | relid=0 | w=39
  95. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:exposure as collected domain
    n1=Refsum (maladie de) | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=39
  96. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:farber lipogranulomatosis
    n1=Refsum (maladie de) | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=39
  97. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:fucosidosis
    n1=Refsum (maladie de) | n2=en:fucosidosis | rel=r_associated | relid=0 | w=39
  98. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:gangliosidoses
    n1=Refsum (maladie de) | n2=en:gangliosidoses | rel=r_associated | relid=0 | w=39
  99. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:gaucher disease, type 2 (disorder)
    n1=Refsum (maladie de) | n2=en:gaucher disease, type 2 (disorder) | rel=r_associated | relid=0 | w=39
  100. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:gaucher disease, type 3 (disorder)
    n1=Refsum (maladie de) | n2=en:gaucher disease, type 3 (disorder) | rel=r_associated | relid=0 | w=39
  101. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:genetic aspects
    n1=Refsum (maladie de) | n2=en:genetic aspects | rel=r_associated | relid=0 | w=39
  102. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:glycine encephalopathy
    n1=Refsum (maladie de) | n2=en:glycine encephalopathy | rel=r_associated | relid=0 | w=39
  103. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:gm1 gangliosidosis
    n1=Refsum (maladie de) | n2=en:gm1 gangliosidosis | rel=r_associated | relid=0 | w=39
  104. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:hermansky-pudlak syndrome
    n1=Refsum (maladie de) | n2=en:hermansky-pudlak syndrome | rel=r_associated | relid=0 | w=39
  105. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:hyperlysinemia
    n1=Refsum (maladie de) | n2=en:hyperlysinemia | rel=r_associated | relid=0 | w=39
  106. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:ichthyosis
    n1=Refsum (maladie de) | n2=en:ichthyosis | rel=r_associated | relid=0 | w=39
  107. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:lesch-nyhan syndrome
    n1=Refsum (maladie de) | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=39
  108. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:lysosomal storage disease
    n1=Refsum (maladie de) | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=39
  109. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:lysosomal storage diseases, nervous system
    n1=Refsum (maladie de) | n2=en:lysosomal storage diseases, nervous system | rel=r_associated | relid=0 | w=39
  110. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:other group 2 peroxisomal disorders
    n1=Refsum (maladie de) | n2=en:other group 2 peroxisomal disorders | rel=r_associated | relid=0 | w=39
  111. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:pancreatic triacylglycerol lipase deficiency
    n1=Refsum (maladie de) | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=39
  112. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:parasitology
    n1=Refsum (maladie de) | n2=en:parasitology | rel=r_associated | relid=0 | w=39
  113. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:pelizaeus merzbacher like disease
    n1=Refsum (maladie de) | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=39
  114. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:radiotherapeutic
    n1=Refsum (maladie de) | n2=en:radiotherapeutic | rel=r_associated | relid=0 | w=39
  115. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:refsum disease, phytanoyl coa hydroxylase deficiency
    n1=Refsum (maladie de) | n2=en:refsum disease, phytanoyl coa hydroxylase deficiency | rel=r_associated | relid=0 | w=39
  116. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:rhizomelic chondrodysplasia punctata
    n1=Refsum (maladie de) | n2=en:rhizomelic chondrodysplasia punctata | rel=r_associated | relid=0 | w=39
  117. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:scheie syndrome
    n1=Refsum (maladie de) | n2=en:scheie syndrome | rel=r_associated | relid=0 | w=39
  118. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:sialic acid storage disease, finnish type (disorder)
    n1=Refsum (maladie de) | n2=en:sialic acid storage disease, finnish type (disorder) | rel=r_associated | relid=0 | w=39
  119. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:therapeutic aspects
    n1=Refsum (maladie de) | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=39
  120. Refsum (maladie de) -- r_associated #0: 39 / 0.189 -> en:use of ultrasonography
    n1=Refsum (maladie de) | n2=en:use of ultrasonography | rel=r_associated | relid=0 | w=39
  121. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:canavan disease
    n1=Refsum (maladie de) | n2=en:canavan disease | rel=r_associated | relid=0 | w=37
  122. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:cerebrotendinous xanthomatosis
    n1=Refsum (maladie de) | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=37
  123. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:charcot-marie-tooth disease
    n1=Refsum (maladie de) | n2=en:charcot-marie-tooth disease | rel=r_associated | relid=0 | w=37
  124. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:congenital ichthyosis
    n1=Refsum (maladie de) | n2=en:congenital ichthyosis | rel=r_associated | relid=0 | w=37
  125. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:ethnologic
    n1=Refsum (maladie de) | n2=en:ethnologic | rel=r_associated | relid=0 | w=37
  126. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:etiology aspects
    n1=Refsum (maladie de) | n2=en:etiology aspects | rel=r_associated | relid=0 | w=37
  127. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:general peroxisomal dysfunctions
    n1=Refsum (maladie de) | n2=en:general peroxisomal dysfunctions | rel=r_associated | relid=0 | w=37
  128. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:hereditary motor and sensory neuropathy with optic atrophy (disorder)
    n1=Refsum (maladie de) | n2=en:hereditary motor and sensory neuropathy with optic atrophy (disorder) | rel=r_associated | relid=0 | w=37
  129. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:hypoesthesia
    n1=Refsum (maladie de) | n2=en:hypoesthesia | rel=r_associated | relid=0 | w=37
  130. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:in urine
    n1=Refsum (maladie de) | n2=en:in urine | rel=r_associated | relid=0 | w=37
  131. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:kearns-sayre syndrome
    n1=Refsum (maladie de) | n2=en:kearns-sayre syndrome | rel=r_associated | relid=0 | w=37
  132. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:mucopolysaccharidosis
    n1=Refsum (maladie de) | n2=en:mucopolysaccharidosis | rel=r_associated | relid=0 | w=37
  133. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:mucopolysaccharidosis type i
    n1=Refsum (maladie de) | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=37
  134. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:muscle weakness of limb
    n1=Refsum (maladie de) | n2=en:muscle weakness of limb | rel=r_associated | relid=0 | w=37
  135. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:nursing therapy
    n1=Refsum (maladie de) | n2=en:nursing therapy | rel=r_associated | relid=0 | w=37
  136. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:phenylketonuria
    n1=Refsum (maladie de) | n2=en:phenylketonuria | rel=r_associated | relid=0 | w=37
  137. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:rarefaction of retinal pigmentation
    n1=Refsum (maladie de) | n2=en:rarefaction of retinal pigmentation | rel=r_associated | relid=0 | w=37
  138. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:ravine syndrome
    n1=Refsum (maladie de) | n2=en:ravine syndrome | rel=r_associated | relid=0 | w=37
  139. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:retinitis pigmentosa inversa
    n1=Refsum (maladie de) | n2=en:retinitis pigmentosa inversa | rel=r_associated | relid=0 | w=37
  140. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:rna polymerase iii-related leukodystrophy
    n1=Refsum (maladie de) | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=37
  141. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:roentgenographic
    n1=Refsum (maladie de) | n2=en:roentgenographic | rel=r_associated | relid=0 | w=37
  142. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:short metacarpal
    n1=Refsum (maladie de) | n2=en:short metacarpal | rel=r_associated | relid=0 | w=37
  143. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:symptoms show insidious onset in the late first through third decades
    n1=Refsum (maladie de) | n2=en:symptoms show insidious onset in the late first through third decades | rel=r_associated | relid=0 | w=37
  144. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:tyrosinemia
    n1=Refsum (maladie de) | n2=en:tyrosinemia | rel=r_associated | relid=0 | w=37
  145. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> en:very long-chain acyl-coa dehydrogenase deficiency
    n1=Refsum (maladie de) | n2=en:very long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=37
  146. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> ichtyose
    n1=Refsum (maladie de) | n2=ichtyose | rel=r_associated | relid=0 | w=37
  147. Refsum (maladie de) -- r_associated #0: 37 / 0.18 -> maladie infantile de stockage de l'acide phytanique
    n1=Refsum (maladie de) | n2=maladie infantile de stockage de l'acide phytanique | rel=r_associated | relid=0 | w=37
  148. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> accumulation d'acide phytanique dans les tissus
    n1=Refsum (maladie de) | n2=accumulation d'acide phytanique dans les tissus | rel=r_associated | relid=0 | w=36
  149. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:18q partial monosomy syndrome
    n1=Refsum (maladie de) | n2=en:18q partial monosomy syndrome | rel=r_associated | relid=0 | w=36
  150. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:acid phosphatase deficiency
    n1=Refsum (maladie de) | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=36
  151. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:alstrom syndrome
    n1=Refsum (maladie de) | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=36
  152. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:arylsulfatase a deficiency
    n1=Refsum (maladie de) | n2=en:arylsulfatase a deficiency | rel=r_associated | relid=0 | w=36
  153. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:brain diseases, metabolic, inborn
    n1=Refsum (maladie de) | n2=en:brain diseases, metabolic, inborn | rel=r_associated | relid=0 | w=36
  154. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:carnitine-acylcarnitine translocase deficiency
    n1=Refsum (maladie de) | n2=en:carnitine-acylcarnitine translocase deficiency | rel=r_associated | relid=0 | w=36
  155. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:cerebral lipidosis
    n1=Refsum (maladie de) | n2=en:cerebral lipidosis | rel=r_associated | relid=0 | w=36
  156. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:ctrp disease terminology
    n1=Refsum (maladie de) | n2=en:ctrp disease terminology | rel=r_associated | relid=0 | w=36
  157. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:decreased phytanic acid oxidase activity
    n1=Refsum (maladie de) | n2=en:decreased phytanic acid oxidase activity | rel=r_associated | relid=0 | w=36
  158. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:diagnosis aspect
    n1=Refsum (maladie de) | n2=en:diagnosis aspect | rel=r_associated | relid=0 | w=36
  159. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:dysfunctions, multiple peroxisomal
    n1=Refsum (maladie de) | n2=en:dysfunctions, multiple peroxisomal | rel=r_associated | relid=0 | w=36
  160. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:glycoprotein storage disorder
    n1=Refsum (maladie de) | n2=en:glycoprotein storage disorder | rel=r_associated | relid=0 | w=36
  161. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:hepatolenticular degeneration
    n1=Refsum (maladie de) | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=36
  162. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:hereditary motor and sensory neuropathies
    n1=Refsum (maladie de) | n2=en:hereditary motor and sensory neuropathies | rel=r_associated | relid=0 | w=36
  163. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:hyporeflexia
    n1=Refsum (maladie de) | n2=en:hyporeflexia | rel=r_associated | relid=0 | w=36
  164. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:immunology aspects
    n1=Refsum (maladie de) | n2=en:immunology aspects | rel=r_associated | relid=0 | w=36
  165. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:in blood
    n1=Refsum (maladie de) | n2=en:in blood | rel=r_associated | relid=0 | w=36
  166. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:leucodystrophy without a known biochemical basis
    n1=Refsum (maladie de) | n2=en:leucodystrophy without a known biochemical basis | rel=r_associated | relid=0 | w=36
  167. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:lipoidosis
    n1=Refsum (maladie de) | n2=en:lipoidosis | rel=r_associated | relid=0 | w=36
  168. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:mannosidosis
    n1=Refsum (maladie de) | n2=en:mannosidosis | rel=r_associated | relid=0 | w=36
  169. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:melas syndrome
    n1=Refsum (maladie de) | n2=en:melas syndrome | rel=r_associated | relid=0 | w=36
  170. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:menkes disease
    n1=Refsum (maladie de) | n2=en:menkes disease | rel=r_associated | relid=0 | w=36
  171. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:morquio syndrome
    n1=Refsum (maladie de) | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=36
  172. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:mucolipidosis
    n1=Refsum (maladie de) | n2=en:mucolipidosis | rel=r_associated | relid=0 | w=36
  173. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:neuraxonal leucodystrophy
    n1=Refsum (maladie de) | n2=en:neuraxonal leucodystrophy | rel=r_associated | relid=0 | w=36
  174. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:neuronal ceroid lipofuscinosis
    n1=Refsum (maladie de) | n2=en:neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=36
  175. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:other hereditary and idiopathic neuropathies
    n1=Refsum (maladie de) | n2=en:other hereditary and idiopathic neuropathies | rel=r_associated | relid=0 | w=36
  176. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:other specified idiopathic peripheral neuropathy
    n1=Refsum (maladie de) | n2=en:other specified idiopathic peripheral neuropathy | rel=r_associated | relid=0 | w=36
  177. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:pelizaeus-merzbacher disease
    n1=Refsum (maladie de) | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=36
  178. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:pharmacotherapeutic
    n1=Refsum (maladie de) | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=36
  179. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:refsum disease with increased pipecolic acidemia
    n1=Refsum (maladie de) | n2=en:refsum disease with increased pipecolic acidemia | rel=r_associated | relid=0 | w=36
  180. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:short metatarsal bones
    n1=Refsum (maladie de) | n2=en:short metatarsal bones | rel=r_associated | relid=0 | w=36
  181. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:tapetoretinal dystrophy
    n1=Refsum (maladie de) | n2=en:tapetoretinal dystrophy | rel=r_associated | relid=0 | w=36
  182. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:tay-sachs disease
    n1=Refsum (maladie de) | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=36
  183. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> en:unspecified hereditary and idiopathic peripheral neuropathy
    n1=Refsum (maladie de) | n2=en:unspecified hereditary and idiopathic peripheral neuropathy | rel=r_associated | relid=0 | w=36
  184. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> hérédopathie ataxique héméralopique polynévritiforme
    n1=Refsum (maladie de) | n2=hérédopathie ataxique héméralopique polynévritiforme | rel=r_associated | relid=0 | w=36
  185. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> maladie
    (médecine)
    n1=Refsum (maladie de) | n2=maladie
    (médecine)
    | rel=r_associated | relid=0 | w=36
  186. Refsum (maladie de) -- r_associated #0: 36 / 0.175 -> syndrome de Refsum
    n1=Refsum (maladie de) | n2=syndrome de Refsum | rel=r_associated | relid=0 | w=36
  187. Refsum (maladie de) -- r_associated #0: 35 / 0.17 -> en:refsum disease
    n1=Refsum (maladie de) | n2=en:refsum disease | rel=r_associated | relid=0 | w=35
  188. Refsum (maladie de) -- r_associated #0: 35 / 0.17 -> peroxysome
    n1=Refsum (maladie de) | n2=peroxysome | rel=r_associated | relid=0 | w=35
  189. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:aspartylglycosaminuria
    n1=Refsum (maladie de) | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=34
  190. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:carnitine acetyltransferase deficiency
    n1=Refsum (maladie de) | n2=en:carnitine acetyltransferase deficiency | rel=r_associated | relid=0 | w=34
  191. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:caused by mutation in the peroxisome biogenesis factor 7 gene (pex7, 601757.0007)
    n1=Refsum (maladie de) | n2=en:caused by mutation in the peroxisome biogenesis factor 7 gene (pex7, 601757.0007) | rel=r_associated | relid=0 | w=34
  192. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:corpus callosum agenesis neuronopathy
    n1=Refsum (maladie de) | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=34
  193. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:genetic disorder of lipid storage
    n1=Refsum (maladie de) | n2=en:genetic disorder of lipid storage | rel=r_associated | relid=0 | w=34
  194. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:giant axonal neuropathy
    n1=Refsum (maladie de) | n2=en:giant axonal neuropathy | rel=r_associated | relid=0 | w=34
  195. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:hereditary and idiopathic peripheral neuropathy
    n1=Refsum (maladie de) | n2=en:hereditary and idiopathic peripheral neuropathy | rel=r_associated | relid=0 | w=34
  196. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:idiopathic progressive polyneuropathy
    n1=Refsum (maladie de) | n2=en:idiopathic progressive polyneuropathy | rel=r_associated | relid=0 | w=34
  197. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:increased phytanic acid in body tissues and fluids
    n1=Refsum (maladie de) | n2=en:increased phytanic acid in body tissues and fluids | rel=r_associated | relid=0 | w=34
  198. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:krabbe disease
    n1=Refsum (maladie de) | n2=en:krabbe disease | rel=r_associated | relid=0 | w=34
  199. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:maple syrup urine disease
    n1=Refsum (maladie de) | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=34
  200. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:metachromatic leukodystrophy variant
    n1=Refsum (maladie de) | n2=en:metachromatic leukodystrophy variant | rel=r_associated | relid=0 | w=34
  201. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:mitochondrial trifunctional protein deficiency
    n1=Refsum (maladie de) | n2=en:mitochondrial trifunctional protein deficiency | rel=r_associated | relid=0 | w=34
  202. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:multiple sulfatase deficiency disease
    n1=Refsum (maladie de) | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=34
  203. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:nerve hypertrophy
    n1=Refsum (maladie de) | n2=en:nerve hypertrophy | rel=r_associated | relid=0 | w=34
  204. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:phyh gene
    n1=Refsum (maladie de) | n2=en:phyh gene | rel=r_associated | relid=0 | w=34
  205. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:pigmentary retinal degeneration
    n1=Refsum (maladie de) | n2=en:pigmentary retinal degeneration | rel=r_associated | relid=0 | w=34
  206. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:pseudo-hurler polydystrophy
    n1=Refsum (maladie de) | n2=en:pseudo-hurler polydystrophy | rel=r_associated | relid=0 | w=34
  207. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:pycnodysostosis
    n1=Refsum (maladie de) | n2=en:pycnodysostosis | rel=r_associated | relid=0 | w=34
  208. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:retinal dystrophy in cerebroretinal lipidosis
    n1=Refsum (maladie de) | n2=en:retinal dystrophy in cerebroretinal lipidosis | rel=r_associated | relid=0 | w=34
  209. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> en:succinyl-coa:3-oxoacid coa transferase deficiency
    n1=Refsum (maladie de) | n2=en:succinyl-coa:3-oxoacid coa transferase deficiency | rel=r_associated | relid=0 | w=34
  210. Refsum (maladie de) -- r_associated #0: 34 / 0.165 -> neuropathie motrice et sensitive héréditaire de type 4
    n1=Refsum (maladie de) | n2=neuropathie motrice et sensitive héréditaire de type 4 | rel=r_associated | relid=0 | w=34
  211. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:acyl-coa dehydrogenase deficiency
    n1=Refsum (maladie de) | n2=en:acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=33
  212. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:arylsulfatase deficiency without mld
    n1=Refsum (maladie de) | n2=en:arylsulfatase deficiency without mld | rel=r_associated | relid=0 | w=33
  213. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:cardiomegaly
    n1=Refsum (maladie de) | n2=en:cardiomegaly | rel=r_associated | relid=0 | w=33
  214. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:caused by mutation in the phytanoyl-coa hydroxylase gene (phyh, 602026.0001)
    n1=Refsum (maladie de) | n2=en:caused by mutation in the phytanoyl-coa hydroxylase gene (phyh, 602026.0001) | rel=r_associated | relid=0 | w=33
  215. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:chemically-induced lipidosis
    n1=Refsum (maladie de) | n2=en:chemically-induced lipidosis | rel=r_associated | relid=0 | w=33
  216. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:complication aspects
    n1=Refsum (maladie de) | n2=en:complication aspects | rel=r_associated | relid=0 | w=33
  217. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:dystrophy
    n1=Refsum (maladie de) | n2=en:dystrophy | rel=r_associated | relid=0 | w=33
  218. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:embryologic
    n1=Refsum (maladie de) | n2=en:embryologic | rel=r_associated | relid=0 | w=33
  219. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:familial disease with storage of sterols (other than cholesterol)
    n1=Refsum (maladie de) | n2=en:familial disease with storage of sterols (other than cholesterol) | rel=r_associated | relid=0 | w=33
  220. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:galactosemia
    n1=Refsum (maladie de) | n2=en:galactosemia | rel=r_associated | relid=0 | w=33
  221. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:gaucher disease, type 1
    n1=Refsum (maladie de) | n2=en:gaucher disease, type 1 | rel=r_associated | relid=0 | w=33
  222. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:hartnup disease
    n1=Refsum (maladie de) | n2=en:hartnup disease | rel=r_associated | relid=0 | w=33
  223. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:leigh disease
    n1=Refsum (maladie de) | n2=en:leigh disease | rel=r_associated | relid=0 | w=33
  224. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:long-chain acyl-coa dehydrogenase deficiency
    n1=Refsum (maladie de) | n2=en:long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=33
  225. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:metabolic aspects
    n1=Refsum (maladie de) | n2=en:metabolic aspects | rel=r_associated | relid=0 | w=33
  226. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:multiple epiphyseal dysplasia
    n1=Refsum (maladie de) | n2=en:multiple epiphyseal dysplasia | rel=r_associated | relid=0 | w=33
  227. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:pulmonary lipid storage disease
    n1=Refsum (maladie de) | n2=en:pulmonary lipid storage disease | rel=r_associated | relid=0 | w=33
  228. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:spastic paraplegia, hereditary
    n1=Refsum (maladie de) | n2=en:spastic paraplegia, hereditary | rel=r_associated | relid=0 | w=33
  229. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> en:x-linked retinitis pigmentosa heterozygote
    n1=Refsum (maladie de) | n2=en:x-linked retinitis pigmentosa heterozygote | rel=r_associated | relid=0 | w=33
  230. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> maladie de refsum-thiébaut
    n1=Refsum (maladie de) | n2=maladie de refsum-thiébaut | rel=r_associated | relid=0 | w=33
  231. Refsum (maladie de) -- r_associated #0: 33 / 0.16 -> neuropathie héréditaire motrice et sensitive de type 4
    n1=Refsum (maladie de) | n2=neuropathie héréditaire motrice et sensitive de type 4 | rel=r_associated | relid=0 | w=33
  232. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:acatalasemia
    n1=Refsum (maladie de) | n2=en:acatalasemia | rel=r_associated | relid=0 | w=32
  233. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:aspects of mortality statistics
    n1=Refsum (maladie de) | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=32
  234. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:autosomal recessive inheritance
    n1=Refsum (maladie de) | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=32
  235. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:cadasil syndrome
    n1=Refsum (maladie de) | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=32
  236. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:carnitine palmitoyltransferase deficiency
    n1=Refsum (maladie de) | n2=en:carnitine palmitoyltransferase deficiency | rel=r_associated | relid=0 | w=32
  237. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:cholesterol ester storage disease
    n1=Refsum (maladie de) | n2=en:cholesterol ester storage disease | rel=r_associated | relid=0 | w=32
  238. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:dysostosis multiplex group
    n1=Refsum (maladie de) | n2=en:dysostosis multiplex group | rel=r_associated | relid=0 | w=32
  239. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:hereditary central nervous system demyelinating diseases
    n1=Refsum (maladie de) | n2=en:hereditary central nervous system demyelinating diseases | rel=r_associated | relid=0 | w=32
  240. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:hereditary cerebral amyloid angiopathy, icelandic type
    n1=Refsum (maladie de) | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=32
  241. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:increased csf protein with normal cell count
    n1=Refsum (maladie de) | n2=en:increased csf protein with normal cell count | rel=r_associated | relid=0 | w=32
  242. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:lipofuscinosis
    n1=Refsum (maladie de) | n2=en:lipofuscinosis | rel=r_associated | relid=0 | w=32
  243. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:myopathy with abnormal lipid metabolism
    n1=Refsum (maladie de) | n2=en:myopathy with abnormal lipid metabolism | rel=r_associated | relid=0 | w=32
  244. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:neuropathy, hereditary thermosensitive
    n1=Refsum (maladie de) | n2=en:neuropathy, hereditary thermosensitive | rel=r_associated | relid=0 | w=32
  245. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:nutritional management
    n1=Refsum (maladie de) | n2=en:nutritional management | rel=r_associated | relid=0 | w=32
  246. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:pathological aspects
    n1=Refsum (maladie de) | n2=en:pathological aspects | rel=r_associated | relid=0 | w=32
  247. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:peroxisome biogenesis disorders
    n1=Refsum (maladie de) | n2=en:peroxisome biogenesis disorders | rel=r_associated | relid=0 | w=32
  248. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:primary carnitine deficiency
    n1=Refsum (maladie de) | n2=en:primary carnitine deficiency | rel=r_associated | relid=0 | w=32
  249. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:refsum disease, adult, 1
    n1=Refsum (maladie de) | n2=en:refsum disease, adult, 1 | rel=r_associated | relid=0 | w=32
  250. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:rehabilitation aspects
    n1=Refsum (maladie de) | n2=en:rehabilitation aspects | rel=r_associated | relid=0 | w=32
  251. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:sensorimotor neuropathy
    n1=Refsum (maladie de) | n2=en:sensorimotor neuropathy | rel=r_associated | relid=0 | w=32
  252. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:talipes cavus
    n1=Refsum (maladie de) | n2=en:talipes cavus | rel=r_associated | relid=0 | w=32
  253. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> en:usher syndrome
    n1=Refsum (maladie de) | n2=en:usher syndrome | rel=r_associated | relid=0 | w=32
  254. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> ichthyose
    n1=Refsum (maladie de) | n2=ichthyose | rel=r_associated | relid=0 | w=32
  255. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> ichtyose congénitale de la peau
    n1=Refsum (maladie de) | n2=ichtyose congénitale de la peau | rel=r_associated | relid=0 | w=32
  256. Refsum (maladie de) -- r_associated #0: 32 / 0.155 -> neuropathie héréditaire motrice et sensorielle de type 4
    n1=Refsum (maladie de) | n2=neuropathie héréditaire motrice et sensorielle de type 4 | rel=r_associated | relid=0 | w=32
  257. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:angiokeratoma corporis diffusum
    n1=Refsum (maladie de) | n2=en:angiokeratoma corporis diffusum | rel=r_associated | relid=0 | w=31
  258. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:cardiomyopathy
    n1=Refsum (maladie de) | n2=en:cardiomyopathy | rel=r_associated | relid=0 | w=31
  259. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:complete mevalonate kinase deficiency
    n1=Refsum (maladie de) | n2=en:complete mevalonate kinase deficiency | rel=r_associated | relid=0 | w=31
  260. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:cystinosis
    n1=Refsum (maladie de) | n2=en:cystinosis | rel=r_associated | relid=0 | w=31
  261. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:dilated cardiomyopathy secondary to phytanic acid storage disease
    n1=Refsum (maladie de) | n2=en:dilated cardiomyopathy secondary to phytanic acid storage disease | rel=r_associated | relid=0 | w=31
  262. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:disorder of ketone metabolism
    n1=Refsum (maladie de) | n2=en:disorder of ketone metabolism | rel=r_associated | relid=0 | w=31
  263. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:electrocardiogram abnormal
    n1=Refsum (maladie de) | n2=en:electrocardiogram abnormal | rel=r_associated | relid=0 | w=31
  264. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:enzymology
    n1=Refsum (maladie de) | n2=en:enzymology | rel=r_associated | relid=0 | w=31
  265. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:hunter syndrome
    n1=Refsum (maladie de) | n2=en:hunter syndrome | rel=r_associated | relid=0 | w=31
  266. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:idiopathic progressive neuropathy
    n1=Refsum (maladie de) | n2=en:idiopathic progressive neuropathy | rel=r_associated | relid=0 | w=31
  267. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:in cerebrospinal fluid
    n1=Refsum (maladie de) | n2=en:in cerebrospinal fluid | rel=r_associated | relid=0 | w=31
  268. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:limb atrophy
    n1=Refsum (maladie de) | n2=en:limb atrophy | rel=r_associated | relid=0 | w=31
  269. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:neuropathy in association with hereditary ataxia
    n1=Refsum (maladie de) | n2=en:neuropathy in association with hereditary ataxia | rel=r_associated | relid=0 | w=31
  270. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:psychology qualifier
    n1=Refsum (maladie de) | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=31
  271. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:pyruvate carboxylase deficiency
    n1=Refsum (maladie de) | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=31
  272. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:pyruvate dehydrogenase deficiency
    n1=Refsum (maladie de) | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  273. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:refsum disease, adult, 2
    n1=Refsum (maladie de) | n2=en:refsum disease, adult, 2 | rel=r_associated | relid=0 | w=31
  274. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:retinopathy, pericentral pigmentary, autosomal recessive
    n1=Refsum (maladie de) | n2=en:retinopathy, pericentral pigmentary, autosomal recessive | rel=r_associated | relid=0 | w=31
  275. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:sensorineural deafness, progressive
    n1=Refsum (maladie de) | n2=en:sensorineural deafness, progressive | rel=r_associated | relid=0 | w=31
  276. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:sialic acid storage disease
    n1=Refsum (maladie de) | n2=en:sialic acid storage disease | rel=r_associated | relid=0 | w=31
  277. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:sjogren-larsson syndrome
    n1=Refsum (maladie de) | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=31
  278. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:surgical aspects
    n1=Refsum (maladie de) | n2=en:surgical aspects | rel=r_associated | relid=0 | w=31
  279. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:taxonomic
    n1=Refsum (maladie de) | n2=en:taxonomic | rel=r_associated | relid=0 | w=31
  280. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:triglyceride storage disease with ichthyosis
    n1=Refsum (maladie de) | n2=en:triglyceride storage disease with ichthyosis | rel=r_associated | relid=0 | w=31
  281. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:urea cycle metabolism disorder
    n1=Refsum (maladie de) | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=31
  282. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:viruses
    n1=Refsum (maladie de) | n2=en:viruses | rel=r_associated | relid=0 | w=31
  283. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> en:x-linked retinitis pigmentosa
    n1=Refsum (maladie de) | n2=en:x-linked retinitis pigmentosa | rel=r_associated | relid=0 | w=31
  284. Refsum (maladie de) -- r_associated #0: 31 / 0.15 -> hérédopathie ataxique polynévritique
    n1=Refsum (maladie de) | n2=hérédopathie ataxique polynévritique | rel=r_associated | relid=0 | w=31
  285. Refsum (maladie de) -- r_associated #0: 28 / 0.136 -> maladie de Refsum
    n1=Refsum (maladie de) | n2=maladie de Refsum | rel=r_associated | relid=0 | w=28
  286. Refsum (maladie de) -- r_associated #0: 25 / 0.121 -> en:medicine
    n1=Refsum (maladie de) | n2=en:medicine | rel=r_associated | relid=0 | w=25
  287. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> acide phocénique
    n1=Refsum (maladie de) | n2=acide phocénique | rel=r_associated | relid=0 | w=20
  288. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> acide phospho-2-glycérique
    n1=Refsum (maladie de) | n2=acide phospho-2-glycérique | rel=r_associated | relid=0 | w=20
  289. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> acide phosphoénolpyruvique
    n1=Refsum (maladie de) | n2=acide phosphoénolpyruvique | rel=r_associated | relid=0 | w=20
  290. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> acide phosphomévalonique
    n1=Refsum (maladie de) | n2=acide phosphomévalonique | rel=r_associated | relid=0 | w=20
  291. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> acide phosphonique
    n1=Refsum (maladie de) | n2=acide phosphonique | rel=r_associated | relid=0 | w=20
  292. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> acide physétérique
    n1=Refsum (maladie de) | n2=acide physétérique | rel=r_associated | relid=0 | w=20
  293. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> Acide phytanique
    n1=Refsum (maladie de) | n2=Acide phytanique | rel=r_associated | relid=0 | w=20
  294. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> en:(7R,11R)-3,7,11,15-tetramethylhexadecanoic acid
    n1=Refsum (maladie de) | n2=en:(7R,11R)-3,7,11,15-tetramethylhexadecanoic acid | rel=r_associated | relid=0 | w=20
  295. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> en:ataxia
    n1=Refsum (maladie de) | n2=en:ataxia | rel=r_associated | relid=0 | w=20
  296. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> en:Dejerine-Sottas's disease
    n1=Refsum (maladie de) | n2=en:Dejerine-Sottas's disease | rel=r_associated | relid=0 | w=20
  297. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> en:peroxisome
    n1=Refsum (maladie de) | n2=en:peroxisome | rel=r_associated | relid=0 | w=20
  298. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> en:phytanic acid
    n1=Refsum (maladie de) | n2=en:phytanic acid | rel=r_associated | relid=0 | w=20
  299. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> en:phytanic acid oxidase deficiency
    n1=Refsum (maladie de) | n2=en:phytanic acid oxidase deficiency | rel=r_associated | relid=0 | w=20
  300. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> en:phytanoic acid
    n1=Refsum (maladie de) | n2=en:phytanoic acid | rel=r_associated | relid=0 | w=20
  301. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> en:pipecolic acid
    n1=Refsum (maladie de) | n2=en:pipecolic acid | rel=r_associated | relid=0 | w=20
  302. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> Maladie de Refsum
    n1=Refsum (maladie de) | n2=Maladie de Refsum | rel=r_associated | relid=0 | w=20
  303. Refsum (maladie de) -- r_associated #0: 20 / 0.097 -> s. PAB
    n1=Refsum (maladie de) | n2=s. PAB | rel=r_associated | relid=0 | w=20
  304. Refsum (maladie de) -- r_associated #0: 10 / 0.049 -> en:heredopathia atactica polyneuritiformis
    n1=Refsum (maladie de) | n2=en:heredopathia atactica polyneuritiformis | rel=r_associated | relid=0 | w=10
  305. Refsum (maladie de) -- r_associated #0: 10 / 0.049 -> en:Refsum's syndrome
    n1=Refsum (maladie de) | n2=en:Refsum's syndrome | rel=r_associated | relid=0 | w=10
  306. Refsum (maladie de) -- r_associated #0: 10 / 0.049 -> Refsum (syndrome de)
    n1=Refsum (maladie de) | n2=Refsum (syndrome de) | rel=r_associated | relid=0 | w=10
  307. Refsum (maladie de) -- r_associated #0: 5 / 0.024 -> Médecine
    n1=Refsum (maladie de) | n2=Médecine | rel=r_associated | relid=0 | w=5
  308. Refsum (maladie de) -- r_associated #0: 1 / 0.005 -> pathologie
    n1=Refsum (maladie de) | n2=pathologie | rel=r_associated | relid=0 | w=1
  309. Refsum (maladie de) -- r_associated #0: 1 / 0.005 -> processus
    n1=Refsum (maladie de) | n2=processus | rel=r_associated | relid=0 | w=1
≈ 407 relations entrantes

  1. médecine --- r_associated #0: 179 --> Refsum (maladie de)
    n1=médecine | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=179
  2. acide phytanique --- r_associated #0: 60 --> Refsum (maladie de)
    n1=acide phytanique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=60
  3. acide pipécolique --- r_associated #0: 60 --> Refsum (maladie de)
    n1=acide pipécolique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=60
  4. atrophie musculaire, ataxie, rétinite pigmentaire et diabète sucré --- r_associated #0: 58 --> Refsum (maladie de)
    n1=atrophie musculaire, ataxie, rétinite pigmentaire et diabète sucré | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=58
  5. Maladie de Refsum --- r_associated #0: 54 --> Refsum (maladie de)
    n1=Maladie de Refsum | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=54
  6. maladie de Refsum --- r_associated #0: 51 --> Refsum (maladie de)
    n1=maladie de Refsum | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=51
  7. en:Refsum's disease --- r_associated #0: 46 --> Refsum (maladie de)
    n1=en:Refsum's disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=46
  8. en:refsum disease --- r_associated #0: 46 --> Refsum (maladie de)
    n1=en:refsum disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=46
  9. maladie de refsum --- r_associated #0: 46 --> Refsum (maladie de)
    n1=maladie de refsum | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=46
  10. Acide phytanique --- r_associated #0: 44 --> Refsum (maladie de)
    n1=Acide phytanique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=44
  11. s. PAB --- r_associated #0: 44 --> Refsum (maladie de)
    n1=s. PAB | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=44
  12. déficit en acide phytanique-oxydase --- r_associated #0: 40 --> Refsum (maladie de)
    n1=déficit en acide phytanique-oxydase | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=40
  13. en:phytanoic acid --- r_associated #0: 40 --> Refsum (maladie de)
    n1=en:phytanoic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=40
  14. hérédopathie atactique polynévritiforme --- r_associated #0: 40 --> Refsum (maladie de)
    n1=hérédopathie atactique polynévritiforme | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=40
  15. hérédopathie ataxique polyneuritiforme --- r_associated #0: 40 --> Refsum (maladie de)
    n1=hérédopathie ataxique polyneuritiforme | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=40
  16. hérédopathie ataxique polynévritique --- r_associated #0: 40 --> Refsum (maladie de)
    n1=hérédopathie ataxique polynévritique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=40
  17. peroxysome --- r_associated #0: 40 --> Refsum (maladie de)
    n1=peroxysome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=40
  18. syndrome de Dejerine-Sottas --- r_associated #0: 40 --> Refsum (maladie de)
    n1=syndrome de Dejerine-Sottas | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=40
  19. en:(7R,11R)-3,7,11,15-tetramethylhexadecanoic acid --- r_associated #0: 39 --> Refsum (maladie de)
    n1=en:(7R,11R)-3,7,11,15-tetramethylhexadecanoic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=39
  20. en:peroxisome --- r_associated #0: 36 --> Refsum (maladie de)
    n1=en:peroxisome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=36
  21. peroxysomopathie --- r_associated #0: 35 --> Refsum (maladie de)
    n1=peroxysomopathie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=35
  22. acide phosphomévalonique --- r_associated #0: 30 --> Refsum (maladie de)
    n1=acide phosphomévalonique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=30
  23. acide physétérique --- r_associated #0: 30 --> Refsum (maladie de)
    n1=acide physétérique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=30
  24. acide phospho-2-glycérique --- r_associated #0: 29 --> Refsum (maladie de)
    n1=acide phospho-2-glycérique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=29
  25. acide phosphoénolpyruvique --- r_associated #0: 29 --> Refsum (maladie de)
    n1=acide phosphoénolpyruvique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=29
  26. en:phytanic acid --- r_associated #0: 29 --> Refsum (maladie de)
    n1=en:phytanic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=29
  27. acide phosphonique --- r_associated #0: 28 --> Refsum (maladie de)
    n1=acide phosphonique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=28
  28. en:Dejerine-Sottas's disease --- r_associated #0: 28 --> Refsum (maladie de)
    n1=en:Dejerine-Sottas's disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=28
  29. en:heredo-ataxia hemeralopica polyneuritiformis --- r_associated #0: 28 --> Refsum (maladie de)
    n1=en:heredo-ataxia hemeralopica polyneuritiformis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=28
  30. en:phytanic acid oxidase deficiency --- r_associated #0: 28 --> Refsum (maladie de)
    n1=en:phytanic acid oxidase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=28
  31. acide phocénique --- r_associated #0: 27 --> Refsum (maladie de)
    n1=acide phocénique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=27
  32. en:ataxia --- r_associated #0: 26 --> Refsum (maladie de)
    n1=en:ataxia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=26
  33. en:pipecolic acid --- r_associated #0: 26 --> Refsum (maladie de)
    n1=en:pipecolic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=26
  34. acide phosphatidique --- r_associated #0: 25 --> Refsum (maladie de)
    n1=acide phosphatidique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=25
  35. acide phosphogluconique --- r_associated #0: 25 --> Refsum (maladie de)
    n1=acide phosphogluconique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=25
  36. acide phosphorique --- r_associated #0: 25 --> Refsum (maladie de)
    n1=acide phosphorique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=25
  37. leucinose --- r_associated #0: 25 --> Refsum (maladie de)
    n1=leucinose | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=25
  38. acide para-aminobenzoïque --- r_associated #0: 24 --> Refsum (maladie de)
    n1=acide para-aminobenzoïque | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=24
  39. en:retinitis pigmentosa --- r_associated #0: 23 --> Refsum (maladie de)
    n1=en:retinitis pigmentosa | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=23
  40. acide phospho-3-glycérique --- r_associated #0: 22 --> Refsum (maladie de)
    n1=acide phospho-3-glycérique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=22
  41. peroxydases (réaction des) --- r_associated #0: 22 --> Refsum (maladie de)
    n1=peroxydases (réaction des) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=22
  42. en:and diabetes mellitus --- r_associated #0: 21 --> Refsum (maladie de)
    n1=en:and diabetes mellitus | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=21
  43. en:muscular atrophy --- r_associated #0: 21 --> Refsum (maladie de)
    n1=en:muscular atrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=21
  44. en:phosphatidic acid --- r_associated #0: 21 --> Refsum (maladie de)
    n1=en:phosphatidic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=21
  45. Refsum --- r_associated #0: 20 --> Refsum (maladie de)
    n1=Refsum | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  46. accumulation d'acide phytanique dans les tissus --- r_associated #0: 20 --> Refsum (maladie de)
    n1=accumulation d'acide phytanique dans les tissus | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  47. adréno-leucodystrophie --- r_associated #0: 20 --> Refsum (maladie de)
    n1=adréno-leucodystrophie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  48. congenital --- r_associated #0: 20 --> Refsum (maladie de)
    n1=congenital | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  49. dystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=dystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  50. déficit en pyruvate carboxylase --- r_associated #0: 20 --> Refsum (maladie de)
    n1=déficit en pyruvate carboxylase | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  51. en:18q partial monosomy syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:18q partial monosomy syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  52. en:2,4-dienoyl-coa reductase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:2,4-dienoyl-coa reductase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  53. en:acatalasemia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:acatalasemia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  54. en:acid cholesteryl ester hydrolase deficiency, type 2 --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:acid cholesteryl ester hydrolase deficiency, type 2 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  55. en:acid phosphatase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:acid phosphatase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  56. en:acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:acyl-coa dehydrogenase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  57. en:acyl-coa dehydrogenase, short-chain deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:acyl-coa dehydrogenase, short-chain deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  58. en:adrenoleukodystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:adrenoleukodystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  59. en:adult onset autosomal dominant leukodystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:adult onset autosomal dominant leukodystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  60. en:affected infants appear normal --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:affected infants appear normal | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  61. en:aicardi syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:aicardi syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  62. en:alexander disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:alexander disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  63. en:alstrom syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:alstrom syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  64. en:angiokeratoma corporis diffusum --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:angiokeratoma corporis diffusum | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  65. en:anosmia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:anosmia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  66. en:arylsulfatase a deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:arylsulfatase a deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  67. en:arylsulfatase deficiency without mld --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:arylsulfatase deficiency without mld | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  68. en:aspartylglycosaminuria --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:aspartylglycosaminuria | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  69. en:aspects of mortality statistics --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:aspects of mortality statistics | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  70. en:aspects of radionuclide imaging --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:aspects of radionuclide imaging | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  71. en:autosomal dominant retinitis pigmentosa --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:autosomal dominant retinitis pigmentosa | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  72. en:autosomal recessive inheritance --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:autosomal recessive inheritance | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  73. en:autosomal recessive retinitis pigmentosa --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:autosomal recessive retinitis pigmentosa | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  74. en:autosomal recessive trait --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:autosomal recessive trait | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  75. en:brain diseases, metabolic, inborn --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:brain diseases, metabolic, inborn | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  76. en:cadasil syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:cadasil syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  77. en:canavan disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:canavan disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  78. en:cardiac failure (sudden death has been reported) --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:cardiac failure (sudden death has been reported) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  79. en:cardiomegaly --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:cardiomegaly | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  80. en:cardiomyopathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:cardiomyopathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  81. en:carnitine acetyltransferase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:carnitine acetyltransferase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  82. en:carnitine deficiency due to inborn error of metabolism --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:carnitine deficiency due to inborn error of metabolism | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  83. en:carnitine palmitoyltransferase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:carnitine palmitoyltransferase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  84. en:carnitine palmitoyltransferase i deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:carnitine palmitoyltransferase i deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  85. en:carnitine palmitoyltransferase ii deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:carnitine palmitoyltransferase ii deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  86. en:carnitine-acylcarnitine translocase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:carnitine-acylcarnitine translocase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  87. en:caused by mutation in the peroxisome biogenesis factor 7 gene (pex7, 601757.0007) --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:caused by mutation in the peroxisome biogenesis factor 7 gene (pex7, 601757.0007) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  88. en:caused by mutation in the phytanoyl-coa hydroxylase gene (phyh, 602026.0001) --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:caused by mutation in the phytanoyl-coa hydroxylase gene (phyh, 602026.0001) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  89. en:cerebral degeneration in generalized lipidoses --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:cerebral degeneration in generalized lipidoses | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  90. en:cerebral lipidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:cerebral lipidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  91. en:cerebrotendinous xanthomatosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:cerebrotendinous xanthomatosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  92. en:charcot-marie-tooth disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:charcot-marie-tooth disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  93. en:charcot-marie-tooth disease type 4 --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:charcot-marie-tooth disease type 4 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  94. en:charcot-marie-tooth disease, type 4d --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:charcot-marie-tooth disease, type 4d | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  95. en:charcot-marie-tooth neuropathy x type 1 --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:charcot-marie-tooth neuropathy x type 1 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  96. en:chemically induced --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:chemically induced | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  97. en:chemically-induced lipidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:chemically-induced lipidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  98. en:cholesterol ester storage disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:cholesterol ester storage disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  99. en:classical maple syrup urine disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:classical maple syrup urine disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  100. en:combined deficiency of long chain 3-hydroxyacyl-coa dehydrogenase and enoyl-coa hydratase --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:combined deficiency of long chain 3-hydroxyacyl-coa dehydrogenase and enoyl-coa hydratase | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  101. en:complete mevalonate kinase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:complete mevalonate kinase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  102. en:complication aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:complication aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  103. en:congenital --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:congenital | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  104. en:congenital ichthyosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:congenital ichthyosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  105. en:corpus callosum agenesis neuronopathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:corpus callosum agenesis neuronopathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  106. en:ctrp disease terminology --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:ctrp disease terminology | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  107. en:cystinosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:cystinosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  108. en:decreased phytanic acid oxidase activity --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:decreased phytanic acid oxidase activity | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  109. en:dejerine-sottas disease (disorder) --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:dejerine-sottas disease (disorder) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  110. en:demyelination --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:demyelination | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  111. en:diagnosis aspect --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:diagnosis aspect | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  112. en:dilated cardiomyopathy secondary to phytanic acid storage disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:dilated cardiomyopathy secondary to phytanic acid storage disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  113. en:disorder of ketone metabolism --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:disorder of ketone metabolism | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  114. en:disorders of fatty acid oxidation --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:disorders of fatty acid oxidation | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  115. en:dysfunctions, multiple peroxisomal --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:dysfunctions, multiple peroxisomal | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  116. en:dysfunctions, single peroxisomal --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:dysfunctions, single peroxisomal | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  117. en:dysmyelinating leukodystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:dysmyelinating leukodystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  118. en:dysostosis multiplex group --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:dysostosis multiplex group | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  119. en:dystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:dystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  120. en:electrocardiogram abnormal --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:electrocardiogram abnormal | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  121. en:embryologic --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:embryologic | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  122. en:enzymology --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:enzymology | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  123. en:epidemiologic --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:epidemiologic | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  124. en:ethnologic --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:ethnologic | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  125. en:etiology aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:etiology aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  126. en:exposure as collected domain --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:exposure as collected domain | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  127. en:fabry disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:fabry disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  128. en:familial disease with storage of sterols (other than cholesterol) --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:familial disease with storage of sterols (other than cholesterol) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  129. en:farber lipogranulomatosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:farber lipogranulomatosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  130. en:fucosidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:fucosidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  131. en:galactosemia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:galactosemia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  132. en:gangliosidoses --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:gangliosidoses | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  133. en:gaucher disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:gaucher disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  134. en:gaucher disease, type 1 --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:gaucher disease, type 1 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  135. en:gaucher disease, type 2 (disorder) --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:gaucher disease, type 2 (disorder) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  136. en:gaucher disease, type 3 (disorder) --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:gaucher disease, type 3 (disorder) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  137. en:general peroxisomal dysfunctions --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:general peroxisomal dysfunctions | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  138. en:genetic aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:genetic aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  139. en:genetic disorder of lipid storage --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:genetic disorder of lipid storage | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  140. en:giant axonal neuropathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:giant axonal neuropathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  141. en:glycine encephalopathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:glycine encephalopathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  142. en:glycogen storage disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:glycogen storage disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  143. en:glycoprotein storage disorder --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:glycoprotein storage disorder | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  144. en:gm1 gangliosidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:gm1 gangliosidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  145. en:hartnup disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hartnup disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  146. en:hepatolenticular degeneration --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hepatolenticular degeneration | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  147. en:hereditary and idiopathic peripheral neuropathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hereditary and idiopathic peripheral neuropathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  148. en:hereditary central nervous system demyelinating diseases --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hereditary central nervous system demyelinating diseases | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  149. en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  150. en:hereditary motor and sensory neuropathies --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hereditary motor and sensory neuropathies | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  151. en:hereditary motor and sensory neuropathy type i --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hereditary motor and sensory neuropathy type i | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  152. en:hereditary motor and sensory neuropathy with optic atrophy (disorder) --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hereditary motor and sensory neuropathy with optic atrophy (disorder) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  153. en:hereditary motor and sensory-neuropathy type ii --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hereditary motor and sensory-neuropathy type ii | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  154. en:hereditary peripheral neuropathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hereditary peripheral neuropathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  155. en:hermansky-pudlak syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hermansky-pudlak syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  156. en:historical aspects qualifier --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:historical aspects qualifier | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  157. en:hmsn type viis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hmsn type viis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  158. en:homocystinuria --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:homocystinuria | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  159. en:hunter syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hunter syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  160. en:hyperlysinemia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hyperlysinemia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  161. en:hypoesthesia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hypoesthesia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  162. en:hyporeflexia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:hyporeflexia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  163. en:i-cell disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:i-cell disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  164. en:ichthyosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:ichthyosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  165. en:idiopathic progressive neuropathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:idiopathic progressive neuropathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  166. en:idiopathic progressive polyneuropathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:idiopathic progressive polyneuropathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  167. en:immunology aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:immunology aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  168. en:in blood --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:in blood | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  169. en:in cerebrospinal fluid --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:in cerebrospinal fluid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  170. en:in urine --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:in urine | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  171. en:increased csf protein with normal cell count --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:increased csf protein with normal cell count | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  172. en:increased phytanic acid in body tissues and fluids --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:increased phytanic acid in body tissues and fluids | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  173. en:infantile refsum disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:infantile refsum disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  174. en:kearns-sayre syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:kearns-sayre syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  175. en:krabbe disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:krabbe disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  176. en:late onset globoid cell leukodystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:late onset globoid cell leukodystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  177. en:leigh disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:leigh disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  178. en:lesch-nyhan syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:lesch-nyhan syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  179. en:leucodystrophy without a known biochemical basis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:leucodystrophy without a known biochemical basis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  180. en:leukodystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:leukodystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  181. en:limb atrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:limb atrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  182. en:lipofuscinosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:lipofuscinosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  183. en:lipoidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:lipoidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  184. en:long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:long-chain acyl-coa dehydrogenase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  185. en:long-chain fatty acid transport deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:long-chain fatty acid transport deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  186. en:lysosomal storage disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:lysosomal storage disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  187. en:lysosomal storage diseases, nervous system --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:lysosomal storage diseases, nervous system | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  188. en:malonic aciduria --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:malonic aciduria | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  189. en:mannosidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:mannosidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  190. en:maple syrup urine disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:maple syrup urine disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  191. en:maroteaux-lamy syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:maroteaux-lamy syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  192. en:medium-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:medium-chain acyl-coa dehydrogenase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  193. en:melas syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:melas syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  194. en:menkes disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:menkes disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  195. en:merrf syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:merrf syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  196. en:metabolic aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:metabolic aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  197. en:metachromatic leukodystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:metachromatic leukodystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  198. en:metachromatic leukodystrophy variant --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:metachromatic leukodystrophy variant | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  199. en:microbiological --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:microbiological | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  200. en:mitochondrial trifunctional protein deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:mitochondrial trifunctional protein deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  201. en:morquio syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:morquio syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  202. en:mucolipidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:mucolipidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  203. en:mucolipidosis type iv --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:mucolipidosis type iv | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  204. en:mucopolysaccharidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:mucopolysaccharidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  205. en:mucopolysaccharidosis type i --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:mucopolysaccharidosis type i | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  206. en:multiple acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:multiple acyl-coa dehydrogenase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  207. en:multiple epiphyseal dysplasia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:multiple epiphyseal dysplasia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  208. en:multiple sulfatase deficiency disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:multiple sulfatase deficiency disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  209. en:muscle weakness of limb --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:muscle weakness of limb | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  210. en:myelin sheath alteration --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:myelin sheath alteration | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  211. en:myopathy with abnormal lipid metabolism --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:myopathy with abnormal lipid metabolism | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  212. en:nerve hypertrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:nerve hypertrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  213. en:neuraminidase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:neuraminidase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  214. en:neuraxonal leucodystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:neuraxonal leucodystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  215. en:neuronal ceroid lipofuscinosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:neuronal ceroid lipofuscinosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  216. en:neuropathy in association with hereditary ataxia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:neuropathy in association with hereditary ataxia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  217. en:neuropathy, hereditary motor and sensory, okinawa type --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:neuropathy, hereditary motor and sensory, okinawa type | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  218. en:neuropathy, hereditary thermosensitive --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:neuropathy, hereditary thermosensitive | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  219. en:niemann-pick disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:niemann-pick disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  220. en:nursing therapy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:nursing therapy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  221. en:nutritional management --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:nutritional management | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  222. en:oculocerebrorenal syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:oculocerebrorenal syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  223. en:other disorders of fatty-acid metabolism --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:other disorders of fatty-acid metabolism | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  224. en:other group 2 peroxisomal disorders --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:other group 2 peroxisomal disorders | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  225. en:other hereditary and idiopathic neuropathies --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:other hereditary and idiopathic neuropathies | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  226. en:other peroxisomal disorders --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:other peroxisomal disorders | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  227. en:other specified idiopathic peripheral neuropathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:other specified idiopathic peripheral neuropathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  228. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  229. en:parasitology --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:parasitology | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  230. en:pathological aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pathological aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  231. en:pelizaeus merzbacher like disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pelizaeus merzbacher like disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  232. en:pelizaeus-merzbacher disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pelizaeus-merzbacher disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  233. en:peroxisomal disorder --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:peroxisomal disorder | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  234. en:peroxisome biogenesis disorders --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:peroxisome biogenesis disorders | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  235. en:pex7 gene --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pex7 gene | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  236. en:pharmacotherapeutic --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pharmacotherapeutic | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  237. en:phenylketonuria --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:phenylketonuria | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  238. en:phyh gene --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:phyh gene | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  239. en:physiopathological --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:physiopathological | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  240. en:pigmentary retinal degeneration --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pigmentary retinal degeneration | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  241. en:pigmentary retinal deposits --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pigmentary retinal deposits | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  242. en:primary carnitine deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:primary carnitine deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  243. en:pseudo-hurler polydystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pseudo-hurler polydystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  244. en:psychology qualifier --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:psychology qualifier | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  245. en:pulmonary lipid storage disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pulmonary lipid storage disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  246. en:pycnodysostosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pycnodysostosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  247. en:pyruvate carboxylase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pyruvate carboxylase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  248. en:pyruvate dehydrogenase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:pyruvate dehydrogenase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  249. en:radiotherapeutic --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:radiotherapeutic | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  250. en:rarefaction of retinal pigmentation --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:rarefaction of retinal pigmentation | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  251. en:ravine syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:ravine syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  252. en:refsum disease with increased pipecolic acidemia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:refsum disease with increased pipecolic acidemia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  253. en:refsum disease, adult, 1 --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:refsum disease, adult, 1 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  254. en:refsum disease, adult, 2 --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:refsum disease, adult, 2 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  255. en:refsum disease, phytanoyl coa hydroxylase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:refsum disease, phytanoyl coa hydroxylase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  256. en:rehabilitation aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:rehabilitation aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  257. en:retinal dystrophy in cerebroretinal lipidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:retinal dystrophy in cerebroretinal lipidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  258. en:retinal dystrophy in systemic lipidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:retinal dystrophy in systemic lipidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  259. en:retinitis pigmentosa inversa --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:retinitis pigmentosa inversa | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  260. en:retinopathy, pericentral pigmentary, autosomal recessive --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:retinopathy, pericentral pigmentary, autosomal recessive | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  261. en:rhizomelic chondrodysplasia punctata --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:rhizomelic chondrodysplasia punctata | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  262. en:rna polymerase iii-related leukodystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:rna polymerase iii-related leukodystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  263. en:roentgenographic --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:roentgenographic | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  264. en:sandhoff disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sandhoff disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  265. en:sanfilippo syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sanfilippo syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  266. en:scheie syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:scheie syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  267. en:sensorimotor neuropathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sensorimotor neuropathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  268. en:sensorineural deafness, progressive --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sensorineural deafness, progressive | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  269. en:sensory neuropathy, hereditary --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sensory neuropathy, hereditary | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  270. en:short metacarpal --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:short metacarpal | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  271. en:short metatarsal bones --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:short metatarsal bones | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  272. en:sialic acid storage disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sialic acid storage disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  273. en:sialic acid storage disease, finnish type (disorder) --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sialic acid storage disease, finnish type (disorder) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  274. en:sjogren-larsson syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sjogren-larsson syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  275. en:sly syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sly syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  276. en:spastic paraplegia, hereditary --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:spastic paraplegia, hereditary | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  277. en:sphingolipidosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:sphingolipidosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  278. en:succinyl-coa:3-oxoacid coa transferase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:succinyl-coa:3-oxoacid coa transferase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  279. en:surgical aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:surgical aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  280. en:symptoms show insidious onset in the late first through third decades --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:symptoms show insidious onset in the late first through third decades | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  281. en:talipes cavus --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:talipes cavus | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  282. en:tapetoretinal dystrophy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:tapetoretinal dystrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  283. en:taxonomic --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:taxonomic | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  284. en:tay-sachs disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:tay-sachs disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  285. en:therapeutic aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:therapeutic aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  286. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:thiamin-responsive maple syrup urine disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  287. en:triglyceride storage disease with ichthyosis --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:triglyceride storage disease with ichthyosis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  288. en:tyrosinemia --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:tyrosinemia | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  289. en:unspecified hereditary and idiopathic peripheral neuropathy --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:unspecified hereditary and idiopathic peripheral neuropathy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  290. en:urea cycle metabolism disorder --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:urea cycle metabolism disorder | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  291. en:use of ultrasonography --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:use of ultrasonography | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  292. en:usher syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:usher syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  293. en:very long-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:very long-chain acyl-coa dehydrogenase deficiency | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  294. en:veterinary aspects --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:veterinary aspects | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  295. en:viruses --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:viruses | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  296. en:wolman disease --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:wolman disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  297. en:x-linked retinitis pigmentosa --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:x-linked retinitis pigmentosa | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  298. en:x-linked retinitis pigmentosa heterozygote --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:x-linked retinitis pigmentosa heterozygote | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  299. en:zellweger syndrome --- r_associated #0: 20 --> Refsum (maladie de)
    n1=en:zellweger syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  300. ichthyose --- r_associated #0: 20 --> Refsum (maladie de)
    n1=ichthyose | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  301. ichthyose congénitale --- r_associated #0: 20 --> Refsum (maladie de)
    n1=ichthyose congénitale | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  302. ichtyose --- r_associated #0: 20 --> Refsum (maladie de)
    n1=ichtyose | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  303. ichtyose congénitale --- r_associated #0: 20 --> Refsum (maladie de)
    n1=ichtyose congénitale | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  304. ichtyose congénitale de la peau --- r_associated #0: 20 --> Refsum (maladie de)
    n1=ichtyose congénitale de la peau | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  305. maladie --- r_associated #0: 20 --> Refsum (maladie de)
    n1=maladie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  306. maladie de --- r_associated #0: 20 --> Refsum (maladie de)
    n1=maladie de | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  307. maladie de l'écaille du poisson --- r_associated #0: 20 --> Refsum (maladie de)
    n1=maladie de l'écaille du poisson | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  308. maladie infantile de stockage de l'acide phytanique --- r_associated #0: 20 --> Refsum (maladie de)
    n1=maladie infantile de stockage de l'acide phytanique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  309. maladie
    (médecine)
     --- r_associated #0: 20 --> Refsum (maladie de)
    n1=maladie
    (médecine)
    | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  310. maladies --- r_associated #0: 20 --> Refsum (maladie de)
    n1=maladies | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  311. neuropathie héréditaire motrice et sensitive de type 4 --- r_associated #0: 20 --> Refsum (maladie de)
    n1=neuropathie héréditaire motrice et sensitive de type 4 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  312. neuropathie héréditaire motrice et sensorielle de type 4 --- r_associated #0: 20 --> Refsum (maladie de)
    n1=neuropathie héréditaire motrice et sensorielle de type 4 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  313. neuropathie motrice et sensitive héréditaire de type 4 --- r_associated #0: 20 --> Refsum (maladie de)
    n1=neuropathie motrice et sensitive héréditaire de type 4 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  314. processus pathologique --- r_associated #0: 20 --> Refsum (maladie de)
    n1=processus pathologique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=20
  315. Acide phosphatidique --- r_associated #0: 15 --> Refsum (maladie de)
    n1=Acide phosphatidique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  316. atrophie musculaire spinale (I-II ou III) --- r_associated #0: 15 --> Refsum (maladie de)
    n1=atrophie musculaire spinale (I-II ou III) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  317. déficit en céto-acide décarboxylase --- r_associated #0: 15 --> Refsum (maladie de)
    n1=déficit en céto-acide décarboxylase | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  318. en:Refsum's syndrome --- r_associated #0: 15 --> Refsum (maladie de)
    n1=en:Refsum's syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  319. en:heredopathia atactica polyneuritiformis --- r_associated #0: 15 --> Refsum (maladie de)
    n1=en:heredopathia atactica polyneuritiformis | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  320. hérédopathie ataxique héméralopique polynévritiforme --- r_associated #0: 15 --> Refsum (maladie de)
    n1=hérédopathie ataxique héméralopique polynévritiforme | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  321. mal --- r_associated #0: 15 --> Refsum (maladie de)
    n1=mal | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  322. maladie de Sandhoff --- r_associated #0: 15 --> Refsum (maladie de)
    n1=maladie de Sandhoff | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  323. maladie de refsum-thiébaut --- r_associated #0: 15 --> Refsum (maladie de)
    n1=maladie de refsum-thiébaut | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  324. maladie de surcharge en acide phytanique --- r_associated #0: 15 --> Refsum (maladie de)
    n1=maladie de surcharge en acide phytanique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  325. syndrome de Refsum --- r_associated #0: 15 --> Refsum (maladie de)
    n1=syndrome de Refsum | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=15
  326. Acide phosphoénolpyruvique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=Acide phosphoénolpyruvique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  327. Dejerine-Sottas (syndrome de) --- r_associated #0: 10 --> Refsum (maladie de)
    n1=Dejerine-Sottas (syndrome de) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  328. Peroxysome --- r_associated #0: 10 --> Refsum (maladie de)
    n1=Peroxysome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  329. Refsum (syndrome de) --- r_associated #0: 10 --> Refsum (maladie de)
    n1=Refsum (syndrome de) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  330. acide parinarique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide parinarique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  331. acide pentanedioïque --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide pentanedioïque | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  332. acide peptidique nucléique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide peptidique nucléique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  333. acide peptidonucléique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide peptidonucléique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  334. acide phytique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide phytique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  335. acide phénique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide phénique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  336. acide phényllactique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide phényllactique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  337. acide phénylpyruvique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide phénylpyruvique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  338. acide pimélique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide pimélique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  339. acide pipémidique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide pipémidique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  340. acide périodique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=acide périodique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  341. amyotrophie --- r_associated #0: 10 --> Refsum (maladie de)
    n1=amyotrophie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  342. anosmie --- r_associated #0: 10 --> Refsum (maladie de)
    n1=anosmie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  343. atrophie des muscles --- r_associated #0: 10 --> Refsum (maladie de)
    n1=atrophie des muscles | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  344. atrophie musculaire --- r_associated #0: 10 --> Refsum (maladie de)
    n1=atrophie musculaire | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  345. cardiomégalie --- r_associated #0: 10 --> Refsum (maladie de)
    n1=cardiomégalie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  346. cataracte-ataxie-surdité et retard mental (syndrome) --- r_associated #0: 10 --> Refsum (maladie de)
    n1=cataracte-ataxie-surdité et retard mental (syndrome) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  347. diminution de la sensibilité --- r_associated #0: 10 --> Refsum (maladie de)
    n1=diminution de la sensibilité | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  348. en:Gaucher disease --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:Gaucher disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  349. en:MELAS syndrome --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:MELAS syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  350. en:Zellweger syndrome --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:Zellweger syndrome | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  351. en:hereditary motor and sensory neuropathy type I --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:hereditary motor and sensory neuropathy type I | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  352. en:para-aminobenzoic acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:para-aminobenzoic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  353. en:paraaminobenzoic acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:paraaminobenzoic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  354. en:peroxydases reactions --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:peroxydases reactions | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  355. en:phocenic acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:phocenic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  356. en:phosphoenolpyruvic acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:phosphoenolpyruvic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  357. en:phosphogluconic acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:phosphogluconic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  358. en:phosphoglyceric acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:phosphoglyceric acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  359. en:phosphomevalonic acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:phosphomevalonic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  360. en:phosphonic acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:phosphonic acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  361. en:phosphoric acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:phosphoric acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  362. en:physeteric acid --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:physeteric acid | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  363. en:spinal muscular atrophy --- r_associated #0: 10 --> Refsum (maladie de)
    n1=en:spinal muscular atrophy | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  364. ethnologique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=ethnologique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  365. gangliosidoses --- r_associated #0: 10 --> Refsum (maladie de)
    n1=gangliosidoses | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  366. hypesthésie --- r_associated #0: 10 --> Refsum (maladie de)
    n1=hypesthésie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  367. hypo-esthésie --- r_associated #0: 10 --> Refsum (maladie de)
    n1=hypo-esthésie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  368. hypoesthésie --- r_associated #0: 10 --> Refsum (maladie de)
    n1=hypoesthésie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  369. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 10 --> Refsum (maladie de)
    n1=maladie des urines à l'odeur de sirop d'érable | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  370. maladie du myocarde --- r_associated #0: 10 --> Refsum (maladie de)
    n1=maladie du myocarde | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  371. maladie du sirop d'érable --- r_associated #0: 10 --> Refsum (maladie de)
    n1=maladie du sirop d'érable | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  372. myatrophie --- r_associated #0: 10 --> Refsum (maladie de)
    n1=myatrophie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  373. myocardiopathie --- r_associated #0: 10 --> Refsum (maladie de)
    n1=myocardiopathie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  374. neuropathie motrice et sensorielle héréditaire --- r_associated #0: 10 --> Refsum (maladie de)
    n1=neuropathie motrice et sensorielle héréditaire | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  375. ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose --- r_associated #0: 10 --> Refsum (maladie de)
    n1=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  376. quadriplégie spastique, rétinite pigmentaire et retard mental --- r_associated #0: 10 --> Refsum (maladie de)
    n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  377. refsum --- r_associated #0: 10 --> Refsum (maladie de)
    n1=refsum | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  378. rétinite pigmentaire --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  379. rétinite pigmentaire d'apparition tardive --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire d'apparition tardive | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  380. rétinite pigmentaire et retard mental --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire et retard mental | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  381. rétinite pigmentaire liée au sexe récessive 3 --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire liée au sexe récessive 3 | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  382. rétinite pigmentaire liée à la PDEB (1-bp del, his557-to-tyr) --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire liée à la PDEB (1-bp del, his557-to-tyr) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  383. rétinite pigmentaire liée à la périphérine --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire liée à la périphérine | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  384. rétinite pigmentaire liée à la périphérine (pro219leu) --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  385. rétinite pigmentaire liée à la rhodopsine --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire liée à la rhodopsine | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  386. rétinite pigmentaire sénile --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire sénile | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  387. rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  388. rétinopathie pigmentaire --- r_associated #0: 10 --> Refsum (maladie de)
    n1=rétinopathie pigmentaire | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  389. syndrome cataracte-ataxie-surdité et retard mental --- r_associated #0: 10 --> Refsum (maladie de)
    n1=syndrome cataracte-ataxie-surdité et retard mental | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  390. trouble myocardique --- r_associated #0: 10 --> Refsum (maladie de)
    n1=trouble myocardique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=10
  391. Acide phosphorique --- r_associated #0: 5 --> Refsum (maladie de)
    n1=Acide phosphorique | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  392. acide Para-AminoBenzoïque --- r_associated #0: 5 --> Refsum (maladie de)
    n1=acide Para-AminoBenzoïque | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  393. atrophie musculaire spinale de la mi-enfance et de l'adolescence --- r_associated #0: 5 --> Refsum (maladie de)
    n1=atrophie musculaire spinale de la mi-enfance et de l'adolescence | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  394. atrophie olivoponto-cérébelleuse et dégénérescence rétinienne --- r_associated #0: 5 --> Refsum (maladie de)
    n1=atrophie olivoponto-cérébelleuse et dégénérescence rétinienne | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  395. atrophie olivopontocérébelleuse --- r_associated #0: 5 --> Refsum (maladie de)
    n1=atrophie olivopontocérébelleuse | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  396. enzymologie --- r_associated #0: 5 --> Refsum (maladie de)
    n1=enzymologie | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  397. fonte musculaire --- r_associated #0: 5 --> Refsum (maladie de)
    n1=fonte musculaire | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  398. glycogen storage disease --- r_associated #0: 5 --> Refsum (maladie de)
    n1=glycogen storage disease | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  399. maladie de Krabbe --- r_associated #0: 5 --> Refsum (maladie de)
    n1=maladie de Krabbe | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  400. maladie de Wolman --- r_associated #0: 5 --> Refsum (maladie de)
    n1=maladie de Wolman | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  401. maladie des urines avec odeur de sirop erable --- r_associated #0: 5 --> Refsum (maladie de)
    n1=maladie des urines avec odeur de sirop erable | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  402. peroxydation --- r_associated #0: 5 --> Refsum (maladie de)
    n1=peroxydation | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  403. peroxyde --- r_associated #0: 5 --> Refsum (maladie de)
    n1=peroxyde | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  404. peroxyde d'hydrogène --- r_associated #0: 5 --> Refsum (maladie de)
    n1=peroxyde d'hydrogène | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  405. peroxyde de benzoyle --- r_associated #0: 5 --> Refsum (maladie de)
    n1=peroxyde de benzoyle | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  406. peroxynitrite --- r_associated #0: 5 --> Refsum (maladie de)
    n1=peroxynitrite | n2=Refsum (maladie de) | rel=r_associated | relid=0 | w=5
  407. peroxysomique --- r_associated #0: 5 --> Refsum (maladie de)
    n1=peroxysomique | n2=Refsum (maladie de) | 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